34
Inspections
71
Deficiencies
3
Actual Harm or Above
60
Occurrences
May 19, 2026
Last Inspection
S/S D/E/F Potential for harmS/S G Actual harm
The most recent inspection of MOUNTAIN VISTA HEALTH CENTER on record is dated May 19, 2026. Across 34 published inspections, state surveyors cited 71 deficiencies, 3 of which reached actual harm or immediate jeopardy.
Colorado publishes inspections on a rolling window, so older surveys may no longer appear. Citation codes 0000 and 9999 are the surveyor's opening and closing comments, not deficiencies, and are excluded from the counts above. Where the state required one, the facility's own plan of correction is shown beneath the finding it answers.
Provider Information
Status
Active
Facility Type
SNF/NF Dual Certification
Administrator
Honl, Brad Nathan
Owner
BAPTIST HOME ASSOCIATION OF THE ROCKY MOUNTAINS, INC.
Phone
(303) 421-4161
Payor Source
Medicare, Medicaid, Private Pay
City
WHEAT RIDGE
ZIP
80033-2112
Inspections & Citations
34 inspections · 71 deficiencies5/19/2026Recertification Survey · ID 22F6C0-L118 deficiencies▼
0000INITIAL COMMENTSSurveyor note▼
Findings
INITIAL COMMENTS (ID Prefix Tag #K000) are informational only and a representation of the facility's general characteristics. This survey was conducted in accordance with the Federal Register at Section 42 CFR 483.70(a). This survey was conducted on May 19, 2026 for compliance with the National Fire Protection Association, (NFPA 101) Life Safety Code (2012) Chapter 19 "Existing Health Care Occupancies." This facility consists of two structures of different construction types that are separated by a common wall having a two-hour fire rating. This structure is a one (1) story with a partial basement and is approximately 45% Type II (000) and was built in 1963. 55% of the structure is Type V (111) (VA) construction. There is a partial basement that has no resident access. The facility is licensed for 168 beds and the census on the date of the survey was 89. The facility is fully protected throughout by a National Fire Protection Association (NFPA) 13 automatic wet-pipe and anti-freeze fire sprinkler systems. The wet-pipe system protects the main level. There is an anti-freeze loop sprinkler system that protects the main entrance canopy. The facility is classified as fully-sprinklered. The results of this survey were discussed with the Plant Operations Director during the exit conference conducted on May 19, 2026.
Plan of correction
The state did not require a plan of correction for this citation.
0161Building Construction Type and Height▼
Findings
K161 Building Construction Type and Height Through observation and document review during the survey, it was determined that the facility failed to provide documentation of the building's construction type as required by the 2012 Life Safety Code (NFPA 101). The deficient practice could affect all smoke zones,168 of 168 residents, and an indeterminable number of staff and visitors. During the review of the facility's life safety documentation conducted in conjunction with the Maintenance Supervisor, the facility failed to produce professional life safety drawings or an architect’s certification detailing the building's construction type, required smoke compartments, hazardous rooms, rated assemblies. Consequently, it could not be verified that the structural frame, bearing walls, floor systems, smoke compartments, and hazardous rooms comply with the fire-resistance ratings stipulated in NFPA 220. 19.1.6 Minimum Construction Requirements. 19.1.6.1 Health care occupancies shall be limited to the building construction types specified in Table 19.1.6.1, unless otherwise permitted by 19.1.6.2 through 19.1.6.7. (See 8.2.1.) 19.3.2.1 Hazardous Areas. Any hazardous areas shall be safeguarded by a fire barrier having a 1-hour fire resistance rating or shall be provided with an automatic extinguishing system in accordance with 8.7.1. 19.3.7 Subdivision of Building Spaces. 19.3.7.1 Smoke barriers shall be provided to divide every story used for sleeping rooms for more than 30 patients into not less than two smoke compartments (see 19.2.4.4), and the following also shall apply:The size of any such smoke compartment shall not exceed 22,500 ft2 (2100 m2), and the travel distance from any point to reach a door in the required smoke barrier shall not exceed 200 ft (61 m). Where neither the length nor width of the smoke compartment exceeds 150 ft (46 m), the travel distance to reach the smoke barrier door shall not be limited. The area of an atrium separated in accordance with 8.6.7 shall not be limited in size. 4.5.8 Maintenance. Whenever or wherever any device, equipment, system, condition, arrangement, level of protection, or any other feature is required for compliance with the provisions of this Code, such device, equipment, system, condition, arrangement, level of protection, or other feature shall thereafter be maintained, unless the Code exempts such maintenance. 4.6.12 Maintenance, Inspection, and Testing. 4.6.12.1 Whenever or wherever any device, equipment, system, condition, arrangement, level of protection, fire-resistive construction, or any other feature is required for compliance with the provisions of this Code, such device, equipment, system, condition, arrangement, level of protection, fire-resistive construction, or other feature shall thereafter be continuously maintained. Maintenance shall be provided in accordance with applicable NFPA requirements or requirements developed as part of a performance-based design, or as directed by the authority having jurisdiction. Deficient items were discussed with the maintenance director during the exit conference.
Plan of correction · submitted by the facility
No residents were identified as being affected when the facility was unable to produce the original architectural drawings for the Life Safety officer. All residents have the potential of being affected if the facility is unable to produce architectural drawing. The original architectural drawings were located and are now being stored on a shelf in the large maintenance supply room. The Maintenance Director/designee will verify the architectural drawings are still stored in the large maintenance supply room and accessible as needed monthly for the next 6 months. Results of the audits will be brought to QAPI monthly for 6 months. The Maintenance Director/designee will utilize a spreadsheet to track audits.
0222Egress Doors▼
Findings
Based on observation and staff interviews, it was determined that the facility failed to arrange and maintain the means of egress in accordance with Life Safety Code Section 19.2 and Chapter 7. The deficient practice affected 3 of 7 smoke compartments. The deficient practice could affect all smoke zones,90 of 168 residents, and an indeterminable number of staff and visitors. 1. During the inspection, observations and interviews with the maintenance director revealed that the exit door patio special care gate handle was installed too high for required restricted access, necessitating access control or delayed egress. 2. During the inspection, observations and interviews with the maintenance director revealed that storage was present in the back corridor hall egress. 3. During the inspection, observations and interviews with the maintenance director revealed that the gaps in elevation at the dining exit exceeded 1/2 inch. NFPA 101 7.1.6.2 Changes in Elevation. Abrupt changes in elevation of walking surfaces shall not exceed 1/4 in. (6.3 mm). Changes in elevation exceeding 1/4 in. (6.3 mm), but not exceeding 1/2 in. (13 mm), shall be beveled with a slope of 1 in 2. Changes in elevation exceeding 1/2 in. (13 mm) shall be considered a change in level and shall be subject to the requirements of 7.1.7 NFPA 101, 7.1.10.1* General. Means of egress shall be continuously maintained free of all obstructions or impediments to full instant use in the case of fire or other emergency. NFPA 101, 19.2.1 General. Every aisle, passageway, corridor, exit discharge, exit location, and access shall be in accordance with Chapter 77.5.1.1 Exits shall be located, and exit access shall be arranged so that exits are readily accessible at all times. NFPA 101 7.2.1.5.10.2 The releasing mechanism shall open the door leaf with not more than one releasing operation, unless otherwise specified in 7.2.1.5.10.3, 7.2.1.5.10.4, or 7.2.1.5.10.6. 7.2.1.7.1 Where a side-hinged door assembly, a pivoted-swinging door assembly, or a balanced door assembly is required to be equipped with panic or fire exit hardware, such hardware shall meet all of the following criteria:(1)It shall consist of a cross bar or a push pad, with the length of the actuating portion of the cross bar or push pad extending not less than one-half of the width of the door leaf measured from the latch stile unless otherwise required by 7.2.1.7.2.(2)It shall be mounted as follows:(a)New installations shall be not less than 34 in. (865 mm) and not more than 48 in. (1220 mm) above the floor.(b)Existing installations shall be not less than 30 in. (760 mm) and not more than 48 in. (1220 mm) above the floor.(3)It shall be constructed so that a horizontal force not to exceed 15 lbf (66 N) actuates the cross bar or push pad and latches. Deficient items were discussed with the maintenance director during the exit conference.
Plan of correction · submitted by the facility
No residents were identified as being affected by having a exit latch above the approved height; with delivered supplies being in a back service hall nor with a gap in elevation exceeding ½ inch. All residents have the potential of being affected by the cited practice. The exit latch has been lowered to the regulated height. The service hallway has been cleared of delivered supplies. The gap has been patched. The Maintenance Director/designee will audit the latch and sidewalk integrity monthly for 6 months. The service hall will be monitored for compliance 3 times per week for 6 months. The results of the audits will be brought to QAPI for 6 months. The Maintenance Director/designee will use a spreadsheet to track audit compliance.
0291Emergency Lighting▼
Findings
Based on observation and staff interviews during record review, it was determined that the facility failed to maintain emergency lighting in accordance with Life Safety Code NFPA 101. The deficient practice affected all smoke compartments. The deficient practice could affect all smoke zones,168 of 168 residents, and an indeterminable number of staff and visitors. During the record review, observations and interviews with the maintenance director revealed that the emergency lighting testing had 7 deficiencies on 4/7/26NFPA 101 7.9.2.1* Emergency illumination shall be provided for a minimum of one and 1/2 hours in the event of failure of normal lighting. Emergency lighting facilities shall be arranged to provide initial illumination that is not less than an average of 1 ft-candle (10.8 lux) and, at any point, not less than 0.1 ft-candle (1.1 lux), measured along the path of egress at floor level. Illumination levels shall be permitted to decline to not less than an average of 0.6 ft-candle (6.5 lux) and, at any point, not less than 0.06 ft-candle (0.65 lux) at the end of 1 1/2 hours. A maximum-to-minimum illumination uniformity ratio of 40 to 1 shall not be exceeded. NFPA 101 7.9.3.1 Required emergency lighting systems shall be tested in accordance with one of the three options offered by 7.9.3.1.1, 7.9.3.1.2, or 7.9.3.1.3.7.9.3.1.1 Testing of required emergency lighting systems shall be permitted to be conducted as follows:(1) Functional testing shall be conducted monthly, with a minimum of 3 weeks and a maximum of 5 weeks between tests, for not less than 30 seconds, except as otherwise permitted by 7.9.3.1.1(2).(2)*The test interval shall be permitted to be extended beyond 30 days with the approval of the authority having jurisdiction.(3)Functional testing shall be conducted annually for a minimum of 1 1/2 hours if the emergency lighting system is battery powered.(4)The emergency lighting equipment shall be fully operational for the duration of the tests required by 7.9.3.1.1(1) and (3).(5)Written records of visual inspections and tests shall be kept by the owner for inspection by the authority having jurisdiction. Deficient items were discussed with the maintenance director during the exit conference.
Plan of correction · submitted by the facility
No residents were identified as being affected by the lack of documentation indicating the emergency lighting was functional. All residents have the potential of being affected by the lack of testing and recording results of emergency light function. At the time of the survey the emergency lights were functional. Those identified by the fire suppression contract company as having issues had previously been repaired by the maintenance department and were operational when tested by the Life Safety officer. The regulatory required testing documentation was provided to the officer at the time of the survey. The maintenance director/designee will maintain written records of monthly testing of the emergency lighting systems monthly per regulation. Results of the testing will be input into the TELS electronic tracking system and audited monthly to assure ongoing compliance. Results of the emergency light testing will be brought to QAPI monthly for 6 months. Tracking will occur with the use of the TELS software and monitored by the maintenance director/designee
0293Exit Signage▼
Findings
Based on observation and staff interviews, it was determined that the facility failed to arrange and maintain exit signage in accordance with Life Safety Code Section 7.10.1.2.1 and Chapter 19. The deficient practice affected all smoke compartments. The deficient practice could affect all smoke zones,168 of 168 residents, and an indeterminable number of staff and visitors. During the record review, observations and interviews with the maintenance director revealed that the emergency lighting testing had 2 deficiencies on 4/7/26NFPA 101 7.9.3.1 Required emergency lighting systems shall be tested in accordance with one of the three options offered by 7.9.3.1.1, 7.9.3.1.2, or 7.9.3.1.3.7.9.3.1.1 Testing of required emergency lighting systems shall be permitted to be conducted as follows:(1) Functional testing shall be conducted monthly, with a minimum of 3 weeks and a maximum of 5 weeks between tests, for not less than 30 seconds, except as otherwise permitted by 7.9.3.1.1(2).(2)*The test interval shall be permitted to be extended beyond 30 days with the approval of the authority having jurisdiction.(3)Functional testing shall be conducted annually for a minimum of 1 1/2 hours if the emergency lighting system is battery powered.(4)The emergency lighting equipment shall be fully operational for the duration of the tests required by 7.9.3.1.1(1) and (3).(5)Written records of visual inspections and tests shall be kept by the owner for inspection by the authority having jurisdiction. Deficient items were discussed with the maintenance director during the exit conference.
Plan of correction · submitted by the facility
No residents were identified as being affected by the functional emergency exit lights which had been repaired prior to the survey. All residents have the potential of being affected by emergency lights that are not functioning properly. The failed emergency lights had been identified and corrected prior to the Life Safety survey and were functioning during the survey. The lights were not deficient nor defective. The maintenance director/designee will maintain written records of monthly visual inspection of the emergency exit lights monthly per regulation. Results of the testing will be input into the TELS electronic tracking system and audited monthly to assure ongoing compliance. Results of the emergency light testing will be brought to QAPI monthly for 6 months. Tracking will occur with the use of the TELS software and monitored by the maintenance director/designee
0300Protection - Other▼
Findings
Based on observation and staff interviews during the survey, it was determined that the facility failed to maintain protection from hazards in rated assemblies in accordance with NFPA 101 chapter 19. The deficient practice affected all smoke compartments. The deficient practice could affect all smoke zones,168 of 168 residents, and an indeterminable number of staff and visitors. 1. During the inspection, observations and interviews with the maintenance director revealed a penetration above the Rehab entrance. 2. During the inspection, observations and interviews with the maintenance director revealed a scab patch above the ceiling in the back corridor hall (near the fire door). 3. During the inspection, observations and interviews with the maintenance director revealed that a penetration (one conduit) above the ceiling entrance for the special care sprinkler pipe has black caulking; provide documentation that it is up-listed. 4. During the inspection, observations and interviews with the maintenance director revealed a gap in the fire wall near the barbershop where a plastic conduit was not filled with fire caulk and a wire was passing through fire doors. 5. During the inspection, observations and interviews with the maintenance director revealed that fire caulking was missing where cables pass through the ceiling in the East kitchen closet. 4.5.8 Maintenance. Whenever or wherever any device, equipment, system, condition, arrangement, level of protection, or any other feature is required for compliance with the provisions of this Code, such device, equipment, system, condition, arrangement, level of protection, or other feature shall thereafter be maintained, unless the Code exempts such maintenance. 4.2.1 Occupant Protection. A structure shall be designed, constructed, and maintained to protect occupants who are not intimate with the initial fire development for the time needed to evacuate, relocate, or defend in place 4.2.3 Systems Effectiveness. Systems utilized to achieve the goals of Section 4.1 shall be effective in mitigating the hazard or condition for which they are being used, shall be reliable, shall be maintained to the level at which they were designed to operate, and shall remain operational. 4.6.12 Maintenance, Inspection, and Testing. 4.6.12.1 Whenever or wherever any device, equipment, system, condition, arrangement, level of protection, fire-resistive construction, or any other feature is required for compliance with the provisions of this Code, such device, equipment, system, condition, arrangement, level of protection, fire-resistive construction, or other feature shall thereafter be continuously maintained. Maintenance shall be provided in accordance with applicable NFPA requirements or requirements developed as part of a performance-based design, or as directed by the authority having jurisdiction. 4.6.12.4 Any device, equipment, system, condition, arrangement, level of protection, fire-resistive construction, or any other feature requiring periodic testing, inspection, or operation to ensure its maintenance shall be tested, inspected, or operated as specified elsewhere in this Code or as directed by the authority having jurisdiction. 8.7.1.1* Protection from any area having a degree of hazard greater than that normal to the general occupancy of the building or structure shall be provided by one of the following means: Enclosing the area with a fire barrier without windows that has a 1-hour fire resistance rating in accordance with Section 8.3 Protecting the area with automatic extinguishing systems in accordance with Section 9.7 Applying both 8.7.1.1(1) and (2) where the hazard is severe or where otherwise specified by Chapters 11 through 43 Deficient items were discussed with the maintenance director during the exit conference.
Plan of correction · submitted by the facility
No residents were identified as being affected by the missing fire caulk in penetrations. All residents have the potential of being affected by penetrations that are not sufficiently caulked. The identified areas cited by the Life Safety officer during the survey have been sealed with fire caulking. Maintenance has investigated the remainder of the building and caulked all holes to the fire walls for proper smoke seal. Maintenance director/designee will visually inspect on a monthly basis fire barriers for unsealed penetrations. Any areas found will be immediately caulked. Results of the inspections will be recorded using the TELS tracking system. Audit results will be tracked and reported for 6 months to QAPI. Tracking will occur with the use of the TELS software and monitored by the maintenance director/designee
0321Hazardous Areas - Enclosure▼
Findings
Based on observation and staff interviews during the survey, it was determined that the facility failed to maintain hazard areas in accordance with NFPA 101, 99, 80, and 58. The deficient practice affected 4 of 7 smoke compartments. The deficient practice could affect all smoke zones,120 of 168 residents, and an indeterminable number of staff and visitors. 1. During the inspection, observations and interviews with the maintenance director revealed that the fire caulking in the fire riser room needed fixing
2. During the inspection, observations and interviews with the maintenance director revealed that the IT room conduit was not filled with fire caulking. 3. During the inspection, observations and interviews with the maintenance director revealed a penetration inside the elevator room. 4. During the inspection, observations and interviews with the maintenance director revealed that the fire-rated door in the dryer room had a detached closer. NFPA 101 8.3.3.2* Fire protection ratings for products required to comply with 8.3.3 shall be as determined and reported by a nationally recognized testing agency in accordance with NFPA 252, Standard Methods of Fire Tests of Door Assemblies; ANSI/UL 10B, Standard for Fire Tests of Door Assemblies; ANSI/UL 10C, Standard for Positive Pressure Fire Tests of Door Assemblies; NFPA 257, Standard on Fire Test for Window and Glass Block Assemblies; or ANSI/UL 9, Standard for Fire Tests of Window Assemblies. NFPA 805.2.5.1 Fire door assemblies shall be visually inspected from both sides to assess the overall condition of door assembly. 5.2.5.2 The following items shall be verified:(1)No open holes or breaks exist in surfaces of either the door or frame.(2)Slats, endlocks, bottom bar, guide assembly, curtain entry hood, and flame baffle are correctly installed and intact.(3)Glazing, vision light frames, and glazing beads are intact and securely fastened in place, if so equipped.(4)Curtain, barrel, and guides are aligned, level, plumb, and true.(5)Expansion clearance is maintained in accordance with manufacturer’s listing.(6)Drop release arms and weights are not blocked or wedged.(7)Mounting and assembly bolts are intact and secured.(8)Attachments to jambs are with bolts, expansion anchors, or as otherwise required by the listing.(9)Smoke detectors, if equipped, are installed and operational.(10)No parts are missing or broken.(11)Fusible links, if equipped, are in the location; chain/cable, s-hooks, eyes, and so forth, are in good condition (i.e., no kinked or pinched cable, no twisted or inflexible chain); and links are not painted or coated with dust or grease.(12)Auxiliary hardware items that interfere or prohibit operation are not installed on the door or frame.(13)No field modifications to the door assembly have been performed that void the label. 8.7.1.1* Protection from any area having a degree of hazard greater than that normal to the general occupancy of the building or structure shall be provided by one of the following means: Enclosing the area with a fire barrier without windows that has a 1-hour fire resistance rating in accordance with Section 8.3 Protecting the area with automatic extinguishing systems in accordance with Section 9.7 Applying both 8.7.1.1(1) and (2) where the hazard is severe or where otherwise specified by Chapters 11 through 43 Deficient items were discussed with the maintenance director during the exit conference.
Plan of correction · submitted by the facility
No residents were identified as being affected by the lack of fire caulking; various penetrations and a detached closure to a fire-rated door. All residents have the potential of being affected by missing fire caulking; defective caulking; penetrations and a detached door closure. The areas identified during the survey have been repaired. Maintenance director/designee will visually inspect on a monthly basis fire barriers for unsealed penetrations. Any areas found will be immediately caulked. Fire-doors with closures will be inspected monthly to assure proper functioning and attachment of the closing device. Results of the inspections will be recorded using the TELS tracking system. Audit results will be tracked and reported for 6 months to QAPI. Tracking will occur with the use of the TELS software and monitored by the maintenance director/designee
0324Cooking Facilities▼
Findings
Based on observation, it was determined that the facility failed to maintain the kitchen hood suppression system as required by NFPA 96. The deficient practice affected all smoke compartments. The deficient practice affected all smoke compartments. The deficient practice could affect 1 out of 7 smoke zones, 30 of 168 residents, and an indeterminable number of staff and visitors. 1. During the inspection, observations and interviews with the maintenance director revealed that the kitchen appliances underneath the kitchen hood are attached (chained) to gas lines, and not attached directly to the wall and directly to the wheel of the kitchen equipment. 2. During the inspection, observations and interviews with the maintenance director revealed that the kitchen hood semi-annual inspection report was missing. Only one cleaning report dated 3/13/26 was provided. NFPA 96 11.2.1* Maintenance of the fire-extinguishing systems and listed exhaust hoods containing a constant or fire-activated water system that is listed to extinguish a fire in the grease removal devices, hood exhaust plenums, and exhaust ducts shall be made by properly trained, qualified, and certified person(s) acceptable to the authority having jurisdiction at leastevery 6 months. 11.4* Inspection for Grease Buildup. The entire exhaust system shall be inspected for grease buildup by a properly trained, qualified, and certified person(s) acceptable to the authority having jurisdiction and in accordance with Table 11.4. 11.4 Table Systems serving moderate-volume cooking operations Semiannually NFPA 96, 12.1.2.3 The fire-extinguishing system shall not require reevaluation where the cooking appliances are moved for the purposes of maintenance and cleaning, provided the appliances are returned to approved design location prior to cooking operations. NFPA 96 (2011) Section 12.1.2.3.1: An approved method shall be provided that will ensure that the appliance is returned to an approved design location. NFPA 54 -2012 Fuel and Gas Code 9.6.1.2 Restraints. Movement of appliances with casters shall be limited by a restraining device installed in accordance with the connector and appliance manufacturer installation instructions. Deficient items were discussed with the maintenance director during the exit conference.
Plan of correction · submitted by the facility
No residents were identified as being affected from kitchen equipment being chained to a gas line nor as the result of having proof of one hood cleaning instead of two. All residents have the potential of being affected by improperly secured equipment and less that the required hood cleaning reports. All kitchen equipment has been inspected for improper securement. Any equipment found to be improperly secured has been rectified and secured by other means. The hood was cleaned in September 2025 and documentation was provided to the Life Safety officer within the requested timeframe of the survey. Maintenance director/designee will audit the kitchen for improperly secured equipment. Any equipment found to be secured to gas lines or other improper places will be detached and secured via other means. All future cleanings will happen every 6 months to maintain compliance. Results of the inspections will be recorded using the TELS tracking system. Audit results will be tracked and reported for 6 months to QAPI. Tracking will occur with the use of the TELS software and monitored by the maintenance director/designee
0345Fire Alarm System - Testing and Maintenance▼
Findings
Based on a record review, observations, inspection, and interviews, it was determined that the facility failed to maintain the fire alarm system components and devices in accordance with the Life Safety Code Section 9.6 and NFPA 72. The deficient practice affected all smoke compartments. The deficient practice could affect all smoke zones, 168 of 168 residents, and an indeterminable number of staff and visitors. 1. During the inspection, observations and interviews with the maintenance director revealed that Family Dining Room - fire-rated door with mag-hold that is not tied into the fire alarm. 2. During the inspection, observations and interviews with the maintenance director revealed that age of single station smoke detectors are greater than 10 years old in rooms 101, 103,100.3. During the inspection, observations and interviews with the maintenance director revealed that magnet on fire door resident room 110 is not attached to fire alarm. 4. During the inspection, observations and interviews with the maintenance director revealed that Room 119 smoke detector is hanging from ceiling by wires. 5. During the inspection, observations and interviews with the maintenance director revealed that fire alarm semi-annual inspection report is missing. The previously approved waiver expired January 7, 2025.6. During the inspection, observations and interviews with the maintenance director revealed that a current 2-year smoke detector sensitivity report without deficiencies was not provided. The previously approved waiver expired January 7, 2025. NFPA 72 2010 Edition: 14.4.8.1 Unless otherwise recommended by the manufacturer's published instructions, single- and multiple-station smoke alarms installed in one- and two-family dwellings shall be replaced when they fail to respond to operability tests but shall not remain in service longer than 10 years from the date of manufacture. NFPA 101: 9.6.1.3 A fire alarm system required for life safety shall be installed, tested, and maintained in accordance with the applicable requirements of NFPA 70, National Electrical Code, and NFPA 72, National Fire Alarm and Signaling Code, unless it is an approved existing installation, which shall be permitted to be continued in use. NFPA 101, Section 9.6.1.5* To ensure operational integrity, the fire alarm system shall have an approved maintenance and testing program complying with the applicable requirements of NFPA 70, National Electrical Code, and NFPA 72, National Fire Alarm and Signaling Code. NFPA 101 19.3.4.1 to comply with section 9.6. Section 9.6.1.3, fire alarm system testing and maintenance to comply with NFPA 72. NFPA 72 14.4.5.3.4; to ensure that each smoke detector or smoke alarm is within its listed and marked sensitivity range, it shall be tested using any of the following methods:(1) Calibrated test method(2) Manufacturer's calibrated sensitivity test instrument(3) Listed control equipment arranged for the purpose(4) Smoke detector/fire alarm control unit arrangement whereby the detector causes a signal at the fire alarm control unit where its sensitivity is outside its listed sensitivity range(5) Other calibrated sensitivity test methods approved by the authority having jurisdiction NFPA 72- 14.4.2.2* Systems and associated equipment shall be tested according to Table 14.4.2.2. (15). Alarm notification appliances (a) Audible: Test shall be performed in accordance with the manufacturer’s published instructions. Appliance locations shall be verified to be per approved layout, and it shall be confirmed that no floor plan changes affect the approved layout. It shall be verified that the candela rating marking agrees with the approved drawing. It shall be confirmed that each appliance flashes 21.8.4 Magnetic door holders that allow doors to close upon loss of operating power shall not be required to have a secondary power source. Deficient items were discussed with the maintenance director during the exit conference.
Plan of correction · submitted by the facility
No residents were identified as being affected by the smoke detectors, mag holds for doors, semi-annual fire inspection report, and 2 year smoke sensitivity report. All residents have the potential of being affected by the smoke detectors age, mag holds for doors not being connected to fire system, fire inspections semi-annual report not being on hand, and the 2 year smoke sensitivity report not being available. The smoke detectors ages have been labeled properly, all mag holds have been removed from the patient rooms and private dining area that are not on the fire system, semi-annual report has been submitted, and the 2 year smoke sensitivity report has been scheduled. Maintenance director/designee will audit all smoke detectors, doors for improper mag holds. The semi annual fire inspections will be scheduled and maintained as well as the 2 year smoke sensitivity report. . Results of the inspections will be recorded using the TELS tracking system. Audit results will be tracked and reported for 6 months to QAPI. Tracking will occur with the use of the TELS software and monitored by the maintenance director/designee
0353Sprinkler System - Maintenance and Testing▼
Findings
Based on a record review, observations, inspection, and interviews, it was determined that the facility failed to meet the protection requirements in accordance with NFPA 101, 25, and 13. The deficient practice affected all smoke compartments. The deficient practice could affect all smoke zones,168 of 168 residents, and an indeterminable number of staff and visitors. 1. During the inspection, observations and interviews with the maintenance director revealed that mixed response types for fire sprinkler head outside rehab therapy. 2. During the inspection, observations and interviews with the maintenance director revealed that Room 306 - paint on fire sprinkler deflector & paint on smoke detector. 3. During the inspection, observations and interviews with the maintenance director revealed that the back corridor hall has a loaded sprinkler head outside electrical room. 4. During the inspection, observations and interviews with the maintenance director revealed that original anti-freeze system non-listed, re-filled with listed anti-freeze 3/10/26. This requires plan review, per FreezeMaster cut sheets. 5. During the inspection, observations and interviews with the maintenance director revealed that expired heads are in the spare sprinkler head box, inside the Fire Riser Room. 6. During the inspection, observations and interviews with the maintenance director revealed that the kitchen freezers - fire sprinklers are dated 2018. Replacement due every 5 years. 7. During the inspection, observations and interviews with the maintenance director revealed that there is a loaded fire sprinkler head in the kitchen above the prep area. 8. During the inspection, observations and interviews with the maintenance director revealed that the kitchen office has a loaded fire sprinkler head
9. During the inspection, observations and interviews with the maintenance director revealed that the kitchen dish wash area has a loaded fire sprinkler head. 10. During the inspection, observations and interviews with the maintenance director revealed that the kitchen service line has a loaded sprinkler head
11. During the inspection, observations and interviews with the maintenance director revealed that there are corroded fire sprinkler heads in the kitchen dishwasher area. 12. During the inspection, observations and interviews with the maintenance director revealed that the activities closet has a painted fire sprinkler head, and the head is to close to the wall. 13. During the inspection, observations and interviews with the maintenance director revealed that there is a fire sprinkler missing escutcheon plate located near the dining emergency exit. 14. During the inspection, observations and interviews with the maintenance director revealed that there is a loaded fire sprinkler head in room 147.15. During the inspection, observations and interviews with the maintenance director revealed that the fire sprinkler escutcheon plate has a gap off the wall in Room 132.16. During the inspection, observations and interviews with the maintenance director revealed that there is a fire sprinkler escutcheon plate missing in the basement breakroom area. 17. During the inspection, observations and interviews with the maintenance director revealed that there are 3 painted fire sprinkler heads in Daniel’s new office (basement). 18. During the inspection, observations and interviews with the maintenance director revealed that the fire sprinkler semi-annual, and 5 year inspection reports were not provided. 5.3.1.1.1.3* Sprinklers manufactured using fast-response elements that have been in service for 20 years shall be replaced, or representative samples shall be tested and then retested at 10-year intervals. NFPA 25 5.3.1.1.1 Where sprinklers have been in service for 50 years, they shall be replaced or representative samples from one or more sample areas shall be tested. NFPA 25 5.2.1.1.2 Any sprinkler that shows signs of any of the following shall be replaced: (1) Leakage, (2) Corrosion, (3) Physical damage, (4) Loss of fluid in the glass bulb heat responsive element, (5)* Loading (6) Painting unless painted by the sprinkler manufacturer. NFPA 101 4.6.12.1 Whenever or wherever any device, equipment, system, condition, arrangement, level of protection, fire-resistive construction, or any other feature is required for compliance with the provisions of this Code, such device, equipment, system, condition, arrangement, level of protection, fire-resistive construction, or other feature shall thereafter be continuously maintained. Maintenance shall be in accordance with applicable NFPA requirements or requirements developed as part of a performance-based design, or as directed by the authority having jurisdiction. NFPA 13 6.2.7.1 Plates, escutcheons, or other devices used to cover the annular space around a sprinkler shall be metallic or shall be listed for use around a sprinkler. NFPA 25, 5.2.1.1.5 Escutcheons and coverplates for recessed, flush, and concealed sprinklers shall be replaced with their listed escutcheon or coverplate if found missing during the inspection. 5.4.1.5 The stock of spare sprinklers shall include all types and ratings installed and shall be as follows:(1)For protected facilities having under 300 sprinklers — no fewer than 6 sprinklers(2)For protected facilities having 300 to 1000 sprinklers — no fewer than 12 sprinklers(3)For protected facilities having over 1000 sprinklers — no fewer than 24 sprinklersNFPA 25 section 14.2.1, in part, inspection of piping and branch line conditions shall be inspected every 5 years for the purpose of inspecting for the presence of foreign organic and inorganic material. NFPA 101 Life Safety Code Standards require automatic sprinkler systems to be continuously maintained in reliable operating condition and are inspected and tested periodically. Section 19.7.6, 4.6.12 FreezeMaster Specification:3.0 System Design Flow rates, pipe sizing, sprinkler spacing, hanging methods and system design must be in accordance with NFPA 13, 13R and 13D. freezemasterTM antifreeze is not listed for use in protecting extra hazard occupancies or flammable liquids, or use with ESFR sprinklers. A. System Limitations 1. Fire sprinkler systems utilizing freezemasterTM antifreeze shall meet the system size limitations as follows: B. Hydraulic Calculations 1. The viscosity of the antifreeze solution at the lowest anticipated temperature of the system shall be considered in the hydraulic design. 2. The friction loss shall be determined using the Hazen-Williams formula for water and the Darcy-Weisbach formula to account for the antifreeze solution fluid properties. 3. The K-factor of the sprinkler shall be adjusted to account for the density of the antifreeze. 4. Where the use of antifreeze in accordance with the listing requires the hydraulic design to be based on the dry system hydraulic design criteria, the hydraulic calculations are to be performed in accordance with the applicable NFPA Standard dry system design even though the system is filled with antifreeze. C. Minimum Design Pressure 1. Pressure meets minimum required pressure for the sprinklers used. D. Expansion 1. It is highly recommended for all systems, including existing, that an expansion tank be used. Without an expansion tank there is potential for system damage and the possibility for water to enter the system and alter the performance of freezemasterTM antifreeze. Reference NFPA 13 for guidance on the addition of expansion tanks in new and existing systems Deficient items were discussed with the maintenance director during the exit conference.
Plan of correction · submitted by the facility
No residents were identified as being affected by the sprinklers that were expired, loaded, painted, corroded and the antifreeze that does not have a plan review that was updated on 3/10/26. And no one was affected by semi-annual and 5 year inspections that were not available. All residents have the potential of being affected by the sprinklers not being regulated by not working properly and also by the antifreeze not being properly installed by a plan review being done. The loaded sprinkler heads have been cleaned properly. The expired sprinklers are being replaced by Cintas and doing a proper Test to confirm expiration and functionality. The plan is being ordered for the antifreeze and as such an extension is requested due to the unknow length of time to have the plan review completed. The semi annual report was submitted to inspector and the 5year is being scheduled Maintenance director/designee will audit sprinkler heads for dates and for cleanliness with the inspection tools. All plans and testing will be scheduled and continued compliance will be maintained. . Results of the inspections will be recorded using the TELS tracking system. Audit results will be tracked and reported for 6 months to QAPI. Tracking will occur with the use of the TELS software and monitored by the maintenance director/designee
0363Corridor - Doors▼
Findings
Based on observation and staff interviews during the course of the survey, it was determined that the facility failed to maintain corridor doors in accordance with the Life Safety Code Section 19.3.6.3. The deficient practice affected 3 of 7 smoke compartments, 90 of 168 residents, and an indeterminable number of staff and visitors. 1. During the inspection, observations and interviews with the maintenance director revealed that Suite 9 - Door does not properly latch shut and maintain smoke seal. 2. During the inspection, observations and interviews with the maintenance director revealed that there is a gap on top of the fire door going into the Therapy Gym. 3. During the inspection, observations and interviews with the maintenance director revealed that the kitchen office - Painted over fire-rated door rating and door stop used on rated door. 4. During the inspection, observations and interviews with the maintenance director revealed that the fire-rated door frame is painted at the kitchen/dining entrance door. 5. During the inspection, observations and interviews with the maintenance director revealed that fire-rated door hardware is not maintained at the kitchen/dining entrance door. 6. During the inspection, observations and interviews with the maintenance director revealed that the fire-rated door closer was removed on the storage room in West Wing. 7. During the inspection, observations and interviews with the maintenance director revealed that the fire doors near Room 117 - one side does not properly latch and seal. NFPA 101, 19.3.6.3.1 19.3.6.3.1* Doors protecting corridor openings in other than required enclosures of vertical openings, exits, or hazardous areas shall be doors constructed to resist the passage of smoke. NFPA 101, 19.3.6.3.2, (2) In smoke compartments protected throughout by an approved, supervised automatic sprinkler system in accordance with 19.3.5.7, the door construction materials requirements of 19.3.6.3.1 shall not be mandatory, but the doors shall be constructed to resist the passage of smoke. Deficient items were discussed with the maintenance director during the exit conference.
Plan of correction · submitted by the facility
No residents were identified as being affected by the doors not being sealed properly, fire ratings being painted over, not latching properly and incorrect closers being attached. All residents have the potential of being affected by the doors not being in proper working conditions and not knowing the proper fire ratings for each door by being painted over. The door seals have been replaced and close properly now. All door frames have had the paint removed from the labels and doors have been adjusted to close properly. Maintenance director /designee will audit doors for proper closure and seals as well as make sure the labels no longer get painted over. Results of the inspections will be recorded using the TELS tracking system. Audit results will be tracked and reported for 6 months to QAPI. Tracking will occur with the use of the TELS software and monitored by the maintenance director/designee
0511Utilities - Gas and Electric▼
Findings
Based on observation and staff interviews, it was determined that the facility failed to maintain wiring in accordance with NFPA 99 and NFPA 70. The deficient practice could affect 1 of 7 smoke compartments, 30 of 168 residents, and an indeterminable number of staff and visitors. 1. During the inspection, observations and interviews with the maintenance director revealed that there is an open junction box above ceiling - back hall corridor to dining area. NFPA 101 9.1.2 Electrical Systems. Electrical wiring and equipment shall be in accordance with NFPA 70, National Electrical Code, unless such installations are approved existing installations, which shall be permitted to be continued in service. Deficient items were discussed with the maintenance director during the exit conference.
Plan of correction · submitted by the facility
No residents were identified as being affected by the open junction box in the ceiling All residents have the potential of being affected by the open junction box in the ceiling by having an electrical incident or even a fire. The junction box has been covered properly and verified others. Maintenance director/designee will audit all junction boxes in the ceilings and on the whole property. Results of the inspections will be recorded using the TELS tracking system. Audit results will be tracked and reported for 6 months to QAPI Tracking will occur with the use of the TELS software and monitored by the maintenance director/designee
0521HVAC▼
Findings
Based on observation and staff interview, it was determined that the facility failed to maintain smoke dampers in accordance with Life Safety Code Section NFPA 105. The deficient practice affected all smoke compartments. The deficient practice could affect all smoke zones,168 of 168 residents, and an indeterminable number of staff and visitors. 1. During the inspection, observations and interviews with the maintenance director revealed that a 4-year fire damper inspection report was not provided. The previously approved waiver expired January 7, 2025. NFPA 105, 6.5.1 Smoke dampers for dedicated and non-dedicated smoke control systems shall be inspected and tested in accordance with NFPA 92A, Standard for Smoke-Control Systems Utilizing Barriers and Pressure Differences. 6.5.2* Each damper shall be tested and inspected one year after installation. The test and inspection frequency shall then be every 4 years, except in hospitals, where the frequency shallbe every 6 years. 6.5.3 Care shall be exercised that all tests are completed in a safe manner wearing the appropriate personal protective equipment. 6.5.4 Full unobstructed access to the damper shall be verified and corrected as required. Deficient items were discussed with the maintenance director during the exit conference.
Plan of correction · submitted by the facility
No residents were identified as being affected by the 4 year fire damper inspection not being available All residents have the potential of being affected by the 4 year fire damper inspection not being done from not ensuring they work properly in case of a fire The fire damper inspection will be scheduled Maintenance director will audit the inspection and insert this into TELs monitoring system to ensure that this happens every 4 years. Results of the inspections will be recorded using the TELS tracking system. Audit results will be tracked and reported for 6 months to QAPI. Tracking will occur with the use of the TELS software and monitored by the maintenance director/designee
0712Fire Drills▼
Findings
Based on the record review, it was determined that the facility failed to conduct fire drills in accordance with the Life Safety Code, Section 19.7.1.6. The deficient practice affected all smoke compartments, 168 of 168 residents, and an indeterminable number of staff and visitors. During the inspection, observations and interviews with the maintenance director revealed that not all required fire drills were completed within the last 12 months. NFPA 101, 19.7.1.6 Drills shall be conducted quarterly on each shift to familiarize facility personnel (nurses, interns, maintenance engineers, and administrative staff) with the signals and emergency action required under varied conditions. Deficient items were discussed with the maintenance director during the exit conference.
Plan of correction · submitted by the facility
No residents were identified as being affected by fire safety drills not being completed for every month All residents have the potential of being affected by the fire safety drill not being completed because of preparedness and practice being implemented The fire drills will be conducted monthly and on various shifts and times. Maintenance director/designee will schedule the fire drills in TELS to be completed monthly at various times and locations to cover all scheduled shifts. Tracking will occur with the use of the TELS software and monitored by the maintenance director/designee
0781Portable Space Heaters▼
Findings
Based on observation and staff interviews it was determined that the facility failed to maintain a fire-safe environment within the facility Life Safety Code, Section 19.7.8. The deficient practice affected 2 of 7 smoke compartments, 60 of 168 residents, and an indeterminable number of staff and visitors. 1. During the inspection, observations and interviews with the maintenance director revealed that there is a space heater located in Deb’s office. 2. During the inspection, observations and interviews with the maintenance director revealed that there is a space heater next to a desk in the Director of Nursing Office. 3. During the inspection, observations and interviews with the maintenance director revealed that there is a space heater under a desk in the office next to the Payroll office. 4. During the inspection, observations and interviews with the maintenance director revealed that there is a space heater located in MDS Nurse Office. Life Safety Code, Section 19.7.8. Portable space-heating devices shall be prohibited in all health care occupancies. Exception: Portable space-heating devices shall be permitted to be used in non-sleeping staff and employee’s areas where the heating elements of such devices do not exceed 212° F (100° C). Deficient items were discussed with the maintenance director during the exit conference.
Plan of correction · submitted by the facility
No residents were identified as being affected by the space heaters under staffs desks All residents have the potential of being affected by the space heaters from being a fire hazard The space heaters have been removedMaintenance director will audit the offices for space heaters and insert this into TELS monitoring system to ensure that this happens monthly. Results of the inspections will be recorded using the TELS tracking system. Audit results will be tracked and reported for 6 months to QAPI Tracking will occur with the use of the TELS software and monitored by the maintenance director/designee
0914Electrical Systems - Maintenance and Testing▼
Findings
Based on documentation review, it was determined that the facility did not maintain proper electrical practices in accordance with NFPA 99 Health Care Facilities Code (2012). The deficient practice affected all smoke compartments, 168 of 168 residents, and an indeterminable number of staff and visitors. 1. During the record review, inspection, observations and interviews with the maintenance director revealed that the facility could not provide a current polarity retention report. NFPA Standard: NFPA 99 Health Care Facilities Code (2012)6.3.3.2 Receptacle Testing in Patient Care Rooms. 6.3.3.2.1 The physical integrity of each receptacle shall be confirmed by visual inspection. 6.3.3.2.2 The continuity of the grounding circuit in each electrical receptacle shall be verified. 6.3.3.2.3 Correct polarity of the hot and neutral connections in each electrical receptacle shall be confirmed. 6.3.3.2.4 The retention force of the grounding blade of each electrical receptacle (except locking-type receptacles) shall be not less than 115 g (4 oz). Deficient items were discussed with the maintenance director during the exit conference.
Plan of correction · submitted by the facility
No residents were identified as being affected by the polarity test not being completed All residents have the potential of being affected by the polarity test not being completed from electrical damage The polarity test has been conducted and will continue to be Maintenance director will audit the polarity tests and insert this into TELS monitoring system to ensure that this happens every 12 months. Results of the inspections will be recorded using the TELS tracking system. Audit results will be tracked and reported for 6 months to QAPI Tracking will occur with the use of the TELS software and monitored by the maintenance director/designee
0918Electrical Systems - Essential Electric Syste▼
Findings
Based on observation and record review during the survey, it was determined that the facility failed to maintain emergency power systems in accordance with Section 9.1.3 ofthe Life Safety Code and the referenced NFPA 110, Standard for Emergency and Standby Power Systems Chapter 8. The deficient practice could affect all smoke zones, 168 of 168 residents, and an indeterminable number of staff and visitors. 1. During the record review, inspection, observations and interviews with the maintenance director revealed that generator weekly, monthly, annual, and fuel testing reports could not be provided. The previously approved waiver expired January 7, 2025. NFPA 110-8.4 Operational Inspection and Testing. 8.4.1* EPSSs, including all appurtenant components, shall be inspected weekly and exercised under load at least monthly. NFPA 110-8.3.7.1 Maintenance of lead acid batteries shall include the monthly testing and recording of electrolyte specific gravity. Battery conductance testing shall be permitted in leu of the testing of specific gravity when applicable or warranted. 8.4.6 Transfer switch shall be operated monthly. NFPA 110, Section 8.3.8. A fuel quality test shall be performed at least annually using applicable ASTM standards or the manufacturer’s recommendations. Deficient items were discussed with the maintenance director during the exit conference.
Plan of correction · submitted by the facility
No residents were identified as being affected by the generator tests not being completed All residents have the potential of being affected by the generator tests not being completed in case we need to use them Generator tests have been scheduled into TELS for weekly, monthly and annual testing per regulationMaintenance director will audit the generator tests and insert this into Tels monitoring system to ensure that this happens weekly, monthly and annually. Results of the inspections will be recorded using the TELS tracking system and audited monthly. Audit results will be tracked and reported for 6 months to QAPI Tracking will occur with the use of the TELS software and monitored by the maintenance director/designee
0920Electrical Equipment - Power Cords and Extens▼
Findings
Through observation during the survey, it was determined that the facility failed to meet the healthcare facilities code requirements in accordance with NFPA 99 and NEC 70. The deficient practice could affect 4 of 7 smoke compartments, 120 of 168 residents, and an indeterminable number of staff and visitors. 1. During the inspection, observations and interviews with the maintenance director revealed that there is an extension cord at the rear entrance. 2. During the inspection, observations and interviews with the maintenance director revealed that a refrigerator is plugged into a daisy-chained surge protector in Room 316.3. During the inspection, observations and interviews with the maintenance director revealed that a microwave is plugged into a surge protector in the MDS Nurse Office. 4. During the inspection, observations and interviews with the maintenance director revealed that an extension cord is plugged in and resting on fire sprinkler pipe and going outside in the boiler room. Flexible cords and cables in accordance with Chapter 4 of NFPA 70, Section 400.8(1), in part, flexible cords and cables shall not be used as a substitute for the fixed wiring of a structure. Furthermore, Health Care Facilities Code section 10.2.3.6 (2), "The sum of the ampacity of all appliances connected to the outlets does not exceed 75 percent of the ampacity of the flexible cord supplying the outlets." Deficient items were discussed with the maintenance director during the exit conference.
Plan of correction · submitted by the facility
No residents were identified as being affected by the power cords and surge protectors that were observed on the property All residents have the potential of being affected by the power cords and surge protectors by starting an electrical fire The surge protectors and improper electrical cords in the boiler room and roof have all been removed Maintenance director will audit the surge protectors, power cords and insert this into Tels monitoring system to ensure that this happens monthly. Results of the inspections will be recorded using the TELS tracking system. Audit results will be tracked and reported for 6 months to QAPI Tracking will occur with the use of the TELS software and monitored by the maintenance director/designee
0923Gas Equipment - Cylinder and Container Storag▼
Findings
Based on observation during the course of the survey it was determined the facility failed to maintain a hazardous area in accordance with NFPA 99. The deficient practice could affect 1 of 7 smoke compartments, 30 of 168 residents, and an indeterminable number of staff and visitors. 1. During the inspection, observations and interviews with the maintenance director revealed that there were both a portable concentrator/combustible and a helium tank stored in the oxygen room. NFPA 99 11.3.1* Storage for nonflammable gases equal to or greater than 85 m3 (3000 ft3) at STP shall comply with 5.1.3.3.2 and 5.1.3.3.3. 5.1.3.3.2 * Design and Construction. Locations for central supply systems and the storage of positive-pressure gases shall meet the following requirements:(1) They shall be constructed with access to move cylinders, equipment, and so forth, in and out of the location on hand trucks complying with 11.4.3.1.1.(2) They shall be secured with lockable doors or gates or otherwise secured.(3) If outdoors, they shall be provided with an enclosure (wall or fencing) constructed of noncombustible materials with a minimum of two entry/exits.(4) If indoors, they shall be constructed and use interior finishes of noncombustible or limited-combustible materials such that all walls, floors, ceilings, and doors are of a minimum 1-hour fire resistance rating. (5)* They shall be compliant with NFPA 70, National Electrical Code, for ordinary locations.(6) They shall be heated by indirect means (e.g., steam, hot water) if heat is required. (7) They shall be provided with racks, chains, or other fastenings to secure all cylinders from falling, whether connected, unconnected, full, or empty. (8)* They shall be supplied with electrical power compliant with the requirements for essential electrical systems as described in Chapter 6.(9) They shall have racks, shelves, and supports, where provided, constructed of noncombustible materials or limited-combustible materials.(10) They shall protect electrical devices from physical damage. NFPA 99 5.1.3.3.3 Ventilation. 5.1.3.3.3.1 Venting of Relief Valves. Indoor supply systems shall have all relief valves vented per 5.1.3.5.6.1(4) through (9). 5.1.3.3.3.2 Ventilation for Motor-Driven Equipment. The following source locations shall be adequately ventilated to prevent accumulation of heat:(1) Medical air sources (see 5.1.3.6)(2) Medical-surgical vacuum sources (see 5.1.3.7) (3) Waste anesthetic gas disposal (WAGD) sources (see 5.1.3.8.1)(4) Instrument air sources (see 5.1.3.9)5.1.3.3.3.3 Ventilation for Outdoor Locations.(A) Outdoor locations surrounded by impermeable walls shall have protected ventilation openings located at the base of each wall to allow free circulation of air within the enclosure.(B) Walls that are shared with other enclosures or with buildings shall be permitted to not have openings. Deficient items were discussed with the maintenance director during the exit conference.
Plan of correction · submitted by the facility
No residents were identified as being affected by the potable concentrators, and helium tank being in the oxygen storage room All residents have the potential of being affected by the improper containers being store in the oxygen room from gas mixing and possible explosions The portable concentrator and the helium tank were removed when the inspector was on sight. Maintenance director will audit the oxygen rooms for improper storage and insert this into Tels monitoring system to ensure that this happens weekly. Results of the inspections will be recorded using the TELS tracking system. Audit results will be tracked and reported for 6 months to QAPI Tracking will occur with the use of the TELS software and monitored by the maintenance director/designee
4/30/2026Licensure Complaint Survey · ID 22F74A-H1No deficiencies▼
0000Initial CommentsSurveyor note▼
Findings
A survey with #CO2971134 was completed on 4/27/26 to 4/30/26. No deficiencies were cited.
Plan of correction
The state did not require a plan of correction for this citation.
4/30/2026Complaint, Recertification Survey · ID 22F6C0-H15 deficiencies▼
0000INITIAL COMMENTSSurveyor note2 building records▼
Findings · record 1 of 2
A recertification survey with complaint #CO2971133, Incident #2978142, Incident #2978145, Incident #2978159 and Incident #2978165 was conducted on 4/27/26 to 4/30/26. Five deficiencies were cited.
Findings · record 2 of 2
An Emergency Preparedness survey was conducted from 4/27/26 to 4/30/26. No deficiencies were cited.
Plan of correction
The state did not require a plan of correction for this citation.
0585Grievances▼
Findings
Based on interviews and record review, the facility failed to ensure two (#71 and #86) of four residents out of 51 sample residents were provided prompt efforts by the facility to resolve grievances. Specifically, the facility failed to effectively resolve Resident #71 and Resident #86’s written grievances (complaints) about call lights previously. Findings include:I. Facility policy and procedureThe Grievances/Complaints Filing policy, dated April 2017, was provided by the nursing home administrator (NHA) on 5/1/26 at 3:41p.m. The policy read in pertinent part,“The Administrator and staff will make prompt efforts to resolve grievances to the satisfaction of the resident and or representative.”The Answering the Call Light policy, dated September 2003, was provided by the nursing home administrator (NHA) on 5/1/26 at 3:41p.m. The policy read in pertinent part,“The facility uses a silent call light system that requires residents to wear a pendant around their neck or on their wrist. The call light system is monitored via electronic devices that alerts staff. “General guidelines included:“Report all defective call lights to the Nurse Supervisor promptly.“Answer the resident's call as soon as possible.“Be courteous in answering the resident’s call.“Steps in the procedure included:“Turn off the call light by claiming and clearing on the tablet.“Identify yourself and listen to the residents request for assistance.“Do what the resident asks of you.“If you have promised the resident you will return with an item or information, do so promptly.“The following information should be documented through the grievance process or incident report, or medical record as it pertains:“If the resident refused the treatment/solution, and the reasons why.“If an issue is identified that prevents a resident from using their all light or the system is not able to clear, the nursing supervisor will implement and document 15 minute checks for the resident affected. Documented checks will be turned in to the director of nursing (DON) or designee.”II. Resident #71A. Resident statusResident #71, age 55, was admitted on 1/27/26. According to the April 2026 computerized physician orders (CPO), diagnoses included type 2 diabetes mellitus (a chronic condition where the body resists insulin or fails to produce enough causing high blood sugar), necrotizing fasciitis (bacterial infection that destroys tissue under the skin and spreads rapidly), and depression. The 2/3/26 minimum data set (MDS) assessment revealed the resident was cognitively intact with a brief interview for mental status (BIMS) of 13 out of 15. B. Resident interviewResident #71 was interviewed on 4/27/26 at 3:11 p.m. Resident #71 said he filed a grievance about long call light wait times on 3/23/26. Resident #71 said he continued to have issues with long call light wait times. C. Record reviewA grievance form, dated 3/23/26, was provided by the DON on 4/30/26 at 6:05 p.m. Resident #71 wrote that the date of incident/concern was over the past few weeks. The grievance form description of concern revealed call lights had gone unanswered for long periods of time. The grievance description revealed Resident #71 had gone out of his room to get assistance from certified nursing aides (CNA) who were on their phones. The grievance description revealed that the CNAs who were available to assist Resident #71 pushed assisting the resident onto a different CNA, instead of helping Resident #71 themselves. The grievance description revealed that the CNAs who were available to assist Resident #71 did not offer to assist him. The grievance description revealed Resident #71 did not feel his CNAs were being professional and he did not feel that he was being treated with dignity and respect. A follow up section was included in the grievance form documentation. The follow up documentation revealed the following items were reviewed and discussed with staff and Resident #71. The form documented the staff were instructedto answer all call lights timely even if the resident calling for help was not assigned to them. The call light iPads were assessed and it was confirmed that they were working properly. -However, Resident #71 said there continued to be long call light wait times (see resident interview above). On 4/20/26 at 6:14 p.m. call light logs for Resident #71 were provided by the DON. According to the logs, the call light response times for April 2026 were as follows:Review of Resident #71’s call light response log from 4/2/26 to 4/30/26 revealed the following call light response times:The call light was activated and not answered for 20 to 39 minutes, 16 times. The call light was activated and not answered for 40 minutes to one hour, seven times. The call light was activated and not answered for one hour and one minute to one hour and 30 minutes, four times. The call light was activated and not answered for over one hour and 30 minutes, six times. III. Resident #86A. Resident statusResident #86, age 77, was admitted on 5/30/23. According to the April 2026 CPO, diagnoses included hyertensive heart disease (heart damage caused by long term untreated high blood pressure), peripheral vascular disease (a circulatory disorder involving narrowed or blocked blood vessels often causing painful leg cramps), polyneuropathy (a malfunction of multiple nerves causing numbness tingling and pain of the feet or hands), personality disorder (one's way of thinking, feeling and behaving deviates from the expectations of the culture, causes distress or problems functioning, and lasts over time), and bipolar disorder (a chronic mental health condition characterized by intense fluctuating mood shifts). The 2/3/26 MDS assessment revealed the resident was cognitively intact with a BIMS of 15 out of 15. B. Resident interviewResident #86 was interviewed on 4/30/26 at 4:36 p.m. Resident #86 said she had filled out a grievance form on 4/3/26 about a call light wait time issue. Resident #86 said that she had used her call light and no one came. Resident #86 said that she then used her hand bell to call for help and no one came. Resident #86 said she had been incontinent and was waiting for help for an extended period. Resident #86 said call light wait times were longer at night because the facility only had two people working on nights. Resident #86 said that sometimes she had to wait for her designated CNA to come help her because the other CNAs would not assist her. Resident #86 said the other CNAs would not assist her, because she was not on their list of residents to assist. Resident #86 said there had been times where she would intermittently ring her bell multiple times and no one would answer. Resident #86 said that she would then get so frustrated that she had to go to the door and yell down the hall for help and that she was not the only one doing it. Resident #86 said that she tried to ask for help when staff were not doing rounds or shift change. Resident #86 said that staff wouldn't come when she was wet and sometimes dirty for hours and hours. Resident #86 said that even after receiving the pendant button, she had to wait in wet and soiled briefs. Resident #86 said that, that morning (4/30/26), she had pressed the call light and no one came. Resident #86 said that she saw someone coming to assist another man across the hallway. Resident #86 said that she waited and waited. Resident #86 said that she had to go to the bathroom and was waiting and waiting. Resident #86 said that she tended to slide down in her wheelchair. Resident #86 said that when she pressed the call light she also needed help getting pulled up in the chair because her lower back was hurting. Resident #86 said that some staff did as little as they could to help. Resident #86 said that she got really frustrated because she was in pain and her back hurt. C. Record review A grievance form, dated 4/2/26 was provided by the DON on 4/30/26 at 6:05 p.m. Resident #86 filled out a grievance form for an incident that occurred on 4/2/26. Resident #86 wrote that at 4:40 p.m. she was feeling cramps indicating that she needed to get to the bathroom and have a bowel movement. Resident #86 wrote that she pressed the call button and pulled the string by the bed and received no response. Resident #86 wrote that she had hoped someone would come before dinner was brought. Resident #86 wrote that she called a few minutes before 5:00 p.m., when staff were usually getting trays and was told "they're coming.” Resident #86 wrote that no one showed up and her tray was brought in some time after 5:00 p.m. Resident #86 wrote that she finished her meal, rolled to the sink to clean up, and still no one came. Resident #86 wrote that it was 7:29 p.m., and her tray was still there. Resident #86 wrote that by then, the night shift was there and getting set up to care for the residents for the evening. Resident #86 wrote that she got tired of waiting for someone to respond and it was too late to call the operator. Resident #86 wrote that she began ringing the bell, hoping someone would respond. Resident #86 wrote that as always, CNA #10 was the only staff member who really worked during the night shift, completed her duties, and usually asked to help with the residents of other employees. Resident #86 wrote that CNA #10 was busy putting people to bed. Resident #86 wrote that a CNA finally came into her room and she advised the CNA of the situation, sitting in her soiled brief since before dinner. Resident #86 wrote that the CNA tried to clear the call light alert from the iPad system. Resident #86 wrote that after a while, she told the CNA that the CNA was busy on the iPad, instead of attending to her needs with a burning bottom and a solid brief. Resident #86 wrote that she told the CNA to tend to her soiled brief instead of trying to clear the call light notification on the iPad. Resident #86 wrote that the CNA told her that the CNA needed to clear the iPad. Resident #86 wrote that she raised her voice at the CNA and the CNA told her not to yell at her. Resident #86 wrote that she told the CNA that she would yell because the CNA was playing with her tablet instead of taking care of her. Resident #86 wrote that she finally told the CNA to leave and the CNA did. Resident #86 wrote that she began ringing the bell again and a tall male CNA came in and said “someone would be there.” Resident #86 wrote that the staff were busy putting people to bed. Resident #86 wrote that apparently that was more important than attending to someone “rotting” in their brief. Resident #86 wrote that the male CNA left. Resident #86 wrote that it was 7:44 p.m. and still no one had come to assist her. Resident #86 wrote that she was tired of being the last consideration for response. Resident #86 wrote that there was always someone else who would come first. Resident #86 wrote that that was why she was sleeping in her wheelchair the past few weeks. Resident #86 wrote that it had been more than a year since anyone had come to assist her in the morning. Resident #86 wrote that it was 7:49 p.m. and she was still sitting in her soiled brief, burning and getting very sore. Resident #86 wrote, someone please do something about the situation. Resident #86 wrote that she felt like the red-headed stepchild and her butt hurt. The actions taken section of the grievance form revealed the facility pulled call light logs and verified times with the times of the grievance. The grievance form revealed the facility planned to get the resident a new call pendant to ensure call lights would go through to the system. Call light logs for Resident #86 were provided by the DON on 4/20/26 at 6:14 p.m. The grievance form revealed the resident/complainant was “satisfied” on 4/5/26. -However, the call light log for Resident #86 revealed the following call light wait times after the grievance form had been marked as the resident/complainant being satisfied on 4/5/26. Call light logs for Resident #86 were provided by the DON on 4/20/26 at 6:14 p.m. Review of Resident #86’s call light response log from 4/1/26 to 4/30/26 revealed the following call light response times:The call light was activated and not answered for 20 to 39 minutes, 21 times. The call light was activated and not answered for 40 minutes to one hour, six times. The call light was activated and not answered for one hour and one minute to one hour and 30 minutes, four times. The call light was activated and not answered for over one hour and 30 minutes, 16 times. IV. Staff interviewsCNA #8 was interviewed on 4/29/26 at 3:50 p.m. CNA #8 said she knew a call light was going off because she looked at her iPad. CNA #8 said the iPad’s battery frequently died and it did not jingle or alert her when a call light was going off. CNA #8 said at one point the facility used a television (TV) screen to show when call lights were going off. CNA #8 pointed to the TV screen above her computer which was blank and had no call light information on it. CNA #8 said that in order to turn the call light off, she had to take the iPad into the resident’s room and get close to the resident to clear the iPad notification. CNA #8 said that unless you were actively looking at the iPad, you were going to miss a call light going off. CNA #8 said that if the resident pulled the cord, or call light, and no one came to help them, the resident could use the hand bell to get the attention of the staff. CNA #8 said that when residents used the bell, she did not know exactly where the ringing was coming from at first, so she had to go look around to help the resident. CNA #9 was interviewed on 4/29/26 at approximately 10:35 a.m. CNA #9 said he was an agency nurse and was new to the facility. CNA #9 said when a resident pushed their call light the light above the door went off and you could see their light. CNA #9 was interviewed on 4/29/26 at 4:08 p.m. CNA #9 said that he had been a CNA for 10 years and that he did not receive any training before starting at the facility because the facility assumed he knew what he was doing. CNA #9 said no one told him how the call light system worked at first and that he did not get a tour of the facility. CNA #9 said previously in the day he thought the call lights were the lights above the doors of the residents’rooms. CNA #9 said he was mistaken about how the call lights worked and that someone showed him that the iPads actually showed when a resident called for assistance. CNA #9 said that in order to clear the call light, the staff had to bring the call light within close proximity of the resident’s call light pendant. CNA #9 said you had to bring the iPad up to the resident wrist band to turn the call light off. The social services director (SSD) was interviewed on 4/30/26 at 5:17 p.m. The SSD said as soon as she received a grievance she made a copy for herself and gave the person responsible for responding to the grievance a copy as well. The SSD said she also spoke about the grievance in the next morning meeting. The SSD said that she ensured the responsible person received the grievance and followed up with that resident. The SSD said that once the grievance was marked as satisfied by the resident, she gave the grievance to the nursing home administrator (NHA) and also kept a copy for her records. The SSD said she would expect the grievance issue to be solved after the grievance process was completed. The SSD said that sometimes extra things came up and the facility had to do additional follow up later on. The DON was interviewed on 4/30/26 at 5:30 p.m. The DON said that the call light system worked through the residents pushing a button/pendant on their wrist or necklace or by the residents pulling the call light cord on the wall. The DON said that this would trigger the iPad to bring up the resident’s name and room number which told staff the was calling. The DON said that staff had to then take the iPad into the resident’s room and clear the call light by placing the iPad close to the pendant, if the resident used the pendant to call staff. The DON said that normal staff members showed the agency staff how the call light system worked. The DON said that the CNAs would tell the agency staff how to clear the iPad alerts and would go into the residents room to clear it for them. The DON said that some residents used hand bells because the facility was having trouble with skynet which was the service that was used to work the tablets. The DON said that sometimes, the call bell service would go down and the call light notifications would not pop up on the iPads, so the facility gave the residents hand bells to alert staff that they needed assistance. The DON said that the facility got a backup battery for their generator so that the system wouldn’t go down. The DON said that when the Skynet system went down, call light notifications did not get to the iPads. The DON said that the call light log records only reflected call light wait times from when the iPad system was up and running, not when the system was down. The DON said that she read through the grievance forms and saw what the resident complained about. The DON said that she pulled the call light logs and interviewed staff to find out whether or not a call light was unable to be cleared, which would be documented in the grievance form. The DON said that when residents complained about call lights not being answered timely, the facility did call light audits. The DON said that Resident #86 would not let staff come into her room or would kick them out of her room and would ring her call bell because she was mad. The DON said that she expected call lights to be answered within five to 10 minutes. The DON said that staff could poke their head into the room and say they were tied up if that were the case, and that they would go help the resident when they could. The DON said that she expected the night shift staff to answer call lights within 15 minutes if they were tied up in a room. The DON said that the facility implemented tablets on the medication carts for the nurses so that if a CNA was tied up in a room, the nurses could help the CNAs and assist the resident if they were able to do so. The DON said that the nurses could not clear the call light notification themselves unless they were truly able to take care of what that resident needed. The DON said that it was important to answer call lights timely so that the resident felt safe and so that the residents were comforted knowing they could get someone’s help remotely or in a time of distress. The DON said that it sounded like the facility needed to implement better onboarding with agency staff. The DON said that she would tell regular staff that when agency staff first got to the facility that they needed to tell agency staff where things were in the facility and how the call lights work. The DON said that the facility would need to make sure that all staff understood the education. The DON said that the facility would do call light audits and go room to room to ensure proper names and room numbers were coming up for each resident. The DON said that the facility would have to do a daily audit of call lights to assess call light wait times.
Plan of correction · submitted by the facility
Resident #86: Was interviewed on 5/19/2026. She stated that staff have been doing a better job answering her light and does not have any complaints. When asked about a long light the previous day she said that she did not experience a long wait and that staff must have forgotten to shut off the light. Facility will continue to interview the resident 5 days per week for 4-weeks to assess her continued satisfaction with staff response time. Additionally, the nursing home administrator (NHA)/designee will monitor resident’s calls once per week for 4 weeks and review the call log with the resident. Any concerns will be brought to the quality assurance performance improvement (QAPI) committee for review. Resident #71: Is currently in the hospital and unable to be interviewed regarding his satisfaction with the call light response. In review of grievances related to call lights since admission on 1/27/2026, he has had no grievances regarding call lights. All residents who use the call system are at risk of being affected by slow response times. Nursing staff, including agency, will receive training on the Quake call light system before they begin shifts by 5/29/2026. The NHA/Designee will assist with call light monitoring daily. Tablets will be set up on nurse medication carts for nurses to monitor and direct staff to answer call lights. Call light response will be a standing agenda item for monthly resident council meetings to seek feedback from the residents. Answering the Call Light policy and procedure was reviewed and updated. Monitoring: Daily at clinical stand-up meetings, social services will present all grievances related to call light responses. Additionally, the DON/designee will review response times for the previous day for 30-days and then weekly for the next 8 weeks. Residents noted with long response times will be interviewed to determine if needs were met. Random visual audits on the neighborhoods will be completed 3x per week for 12 weeks. Call light responses will be discussed at resident council meetings for 3 months. Call light audits will be performed with a call light audit sheet and tracked on a call light audit spreadsheet. Resident interviews will be conducted on a Resident Interview audit form and tracked on a resident interview spreadsheet. The Quake call light response audits will be generated from the call system and tracked on a call light review spreadsheet. Results of the audits and tracking will be brought to the quality assurance performance performance (QAPI) committee monthly for review and further action.
0761Label/Store Drugs and Biologicals▼
Findings
Based on observations and interviews, the facility failed to remove medications and biologicals that were stored and labeled properly according to professional standards in three of five medication carts and two of four medication storage rooms. Specifically, the facility failed to:-Ensure expired medications were discarded; and,-Ensure a drug buster was not stored next to medications. Findings include:I. Professional referencesThe United States Food and Drug Administration (USFDA) Don't Be Tempted to Use Expired Medicines (revised 10/31/24), was retrieved on 5/1/26 from https://www.fda.gov/drugs/special-features/dont-be-tempted-use-expired-medicines. It read in pertinent part, "Expired medical products can be less effective or risky due to a change in chemical composition or a decrease in strength. Certain expired medications are at risk of bacterial growth, and sub-potent antibiotics can fail to treat infections, leading to more serious illnesses and antibiotic resistance. Once the expiration date has passed, there is no guarantee that the medicine will be safe and effective. If your medicine has expired, do not use it."I. Facility policy and procedureThe Storage of Medication policy, undated, was received from the nursing home administrator on 5/1/26 at 3:41 p.m. It revealed in pertinent part, “It is the policy of this facility to ensure all medications housed on our premises will be stored in the pharmacy and or medication rooms according to the manufacturer's recommendations and sufficient to ensure proper sanitation, temperature, light, ventilation, moisture control and security.“All medication rooms are routinely inspected by the consultant pharmacist or discontinued, outdated, defective or deteriorating medications with worn illegible or mislabels.”II. ObservationsOn 4/28/26 at 3:45 p.m. the medication cart #2 on the 100 unit was observed with licensed practical nurse (LPN) #1. The drawer on the medication cart for Resident #54 contained the following:-Mirtazapine (medication used to treat depression) oral tablet 7.5 milligram (mg). The order was discontinued on 4/17/26.-Levothyroxine (medication used to treat hypothyroidism) oral tablet 25 micrograms (mcg). The order was discontinued on 1/15/26. The drawer on the medication cart for Resident #24 contained the following:-Xarelto (medication used as a blood thinner) oral tablet 15 mg. The order was discontinued on 2/20/25. The drawer on the medication cart for Resident #64 contained the following:-Albuterol Ipratropium-Albuterol Inhalation solution 0.5-2.5 mg/3 milliliter (ml) (Ipratropium-Albuterol) The medication did not have an expiration date. On 4/28/26 at 4:35 p.m. the medication cart #1 on the 200 unit was observed with LPN #2. The drawer on the medication cart for Resident #2 contained the following:-Benzonatate (medication used as a cough suppressant) oral tablet 100 mg. The order was discontinued on 4/9/26. The drawer on the medication cart for Resident #66 contained the following:-Ondansetron (medication used to prevent nausea and vomiting) oral tablet 4 mg) The medication expired on 3/31/26. On 4/29/26 at 10:12 a.m. the medication storage room for the secured unit was observed with registered nurse (RN) #2. The cabinets in the medication storage room for the secured unit contained the following:-Twenty-two pre-filled normal saline 0.9% flush syringes 10 ml that expired on 5/13/18.-Three pre-filled normal saline 0.9% flush syringes 10 ml that expired on 7/31/21.-Three vials of ceftriaxone (medication used to treat infections) for injection 1 gram (gm) that expired 1/30/23. The emergency medication, non-narcotic, supply box, for the secured unit expired in March 2026. The supply box contained the following medications:-Humulin R (Short acting regular) insulin-Humulin N (intermediate acting) insulin-Humulin 70/30 (premixed) insulin -Humalog (lisprio) insulin-Cathflo Activase (alteplase)-Lantus (glargine) InsulinOn 4/29/26 at 11:00 a.m. the medication storage room on 200 unit was observed with LPN #3. The medication refrigerator for the 200 unit for Resident #11 contained the following:-Two boxes that contained five pens each of Basaglar KwikPen (insulin glargine) 100 units/ml pen that expired on 9/23/25.-One box that contained five pens of Basaglar KwikPen (insulin glargine) 100 units/ml pen that expired on 10/13/25. The medication refrigerator for the 200 unit for Resident #16 contained the following:-Lumigan 0.01 % (eye drop) that expired on 11/30/25. On 4/29/26 at 11:30 a.m. the medication cart #1 on the rehabilitation unit was observed with RN #1. The following items were found.-A 16-ounce bottle of Drug Buster (activated charcoal-based disposal system designed to quickly deactivate and destroy unwanted pills, capsules, liquids, creams) was in the same drawer as liquid medications. III. Staff interviewsLPN #1 was interviewed on 4/28/26 at 3:30 p.m. LPN #1 said all medications should have been discarded immediately upon reaching the medication expiration date. LPN #1 said any nurse who was assigned to this medication card should be checking the expiration dates on the medications. LPN #2 was interviewed on 4/28/26 at 4:40 p.m. LPN #2 said it was the responsibility of all of the nurses to check the expiration dates on medications during their shift and before medication administration. RN #2 was interviewed on 4/29/26 at 10:20 a.m. RN #2 said she did not work on the secured unit very often. RN #2 said she was unsure as to who was responsible for monitoring expired medications in the medication room. LPN #3 was interviewed on 4/29/26 at 11:10 a.m. LPN #3 said it was the nurses responsibility to ensure all expired medications were removed from the medication storage refrigerator. The director of nursing (DON) was interviewed on 4/30/26 at 1:30 p.m. The DON said the nurses were responsible for checking the expiration dates before administering medication to the residents. The DON said medications should be discarded immediately if it was discontinued, or the nurses should verify with the doctor that the medication was no longer needed. The DON said the night supervisor should be checking medication storage rooms once a week. She said she would advised the night supervisors to check the cabinets and drawers in the medication storage rooms for expired medications. The DON said the night supervisors did not understand the explanation of her instructions. The DON said she would initiate education and training with the supervisors today regarding when and how to check the medication rooms The DON said she also started education and training RN’s and LPN’s to check the medication carts for expired and mislabeled medications. The DON said it was important to keep the medication storage rooms and medications carts free from expired and mislabeled meds to prevent resident harm and to maintain the efficacy of the medication.
Plan of correction · submitted by the facility
The medication carts for residents 54; 24; 64; 2; 16 were searched and any expired medications were removed. Additionally, the medication rooms and medication refrigerators for these residents were searched and any expired medications were removed. Residents 11 and 16 were not identified by the health department. In response, all medication storage areas were searched, and any expired medications were removed by 5/1/2026. The liquids in the cart with the drug buster were removed and reorganized in the cart so they were not in the same drawer. The drug buster was removed from the cart on 5/1/2026The medication rooms were searched for expired medications and supplies. Those found were removed and destroyed by 5/5/2026All residents who have ordered medications are at risk of having expired medications in storage areas and all residents needing supplies are at risk of using expired supplies. Nurses will be educated on the identification and removal of expired medications to include digitally printed and handwritten expiration dates on the medication cards. Medications will be moved from the medication carts to the medication rooms when the expiration is identified. Nurses will be educated to keep chemicals such as Drug Buster, out of the medication cart. Medications in the medication rooms will be destroyed weekly by schedule by the Night House SupervisorsEducation will be completed by 5.22.26; new nurses will receive this education during orientation. Random Medication Room and Medication Cart audits will occur 3 times weekly for 4 weeks, then 2 times weekly for 4 weeks, and 1 time weekly for 4 weeks by the director of nursing (DON)/Designee. Results of the audits and tracking will be brought to the quality assurance performance performance (QAPI) committee monthly for review and further action. Tracking will occur on an Expired Medication and Supplies tracking form.
0805Food in Form to Meet Individual Needs▼
Findings
Based on observations, record review and interviews, the facility failed to ensure 16 residents on a mechanical soft diet received food and fluids prepared in a form designed to meet his or her needs per speech therapy recommendation, physician orders and the residents care plan. Specifically, the facility failed to ensure residents who were prescribed a mechanical soft diet had food prepared according to their diet orders of mechanical soft as indicated on their meal tray cards. Findings include:I. Facility policy and procedureThe Mechanical Soft Food Preparation policy, undated, was provided by the registered dietitian (RD) on 4/28/26 at 5:52 p.m. The policy read in pertinent part, “The facility will prepare mechanical soft foods in a manner that sustains the nutritional value and taste. The foods will be ground to assure the desired consistency. Mechanical soft foods will be made from regular menu items to assure similar taste and nutritional quality. Recipes for regular menu items will be followed during production. Mechanical soft foods must be ground to the proper consistency per resident's needs/requests.”II. Meal service observation and staff interviewsDuring a continuous observation of the dinner meal service on 4/28/26, beginning at 4:11 p.m. and ending at 5:42 p.m., the following was observed:The posted menu documented the dinner meal was a tuna melt grilled sandwich, sweet potato rounds, ambrosia salad (creamy fruit salad) and banana pudding. The mechanically soft altered menu items were a ground grilled tuna melt sandwich and sweet potato rounds. Cook (CK) #1 was interviewed on 4/28/26 at 4:13 p.m. (during meal service). CK #1 said the sweet potatoes in the pan in hot holding were frozen sweet potato rounds and were fried. At 4:26 p.m. CK #1 assembled four meal plates for residents. The plates were placed on a tray for residents whose meal tickets documented they were prescribed mechanical soft diets. The four meal plates included a whole grilled tuna melt sandwich cut in half (triangles) and the fried sweet potato rounds.-The menu extensions provided by the facility documented the mechanical soft modification for the tuna melt sandwich was a ground grilled tuna melt sandwich (see menu extensions below). CK #2 was interviewed on 4/28/26 at 4:28 p.m. (during meal service) CK #2 said he put the raw onions in the food processor before putting them into the tuna salad, but he did not add celery because the facility did not have celery.-The facility was notified the item served was different from the item listed on the extensions. The tuna melt sandwich was served grilled and cut in half instead of ground grilled tuna melt sandwich. CK #2 was interviewed on 4/28/26 at 4:49 p.m. (during meal service). CK #2 said the recipe book for dinner (on 4/28/26) was somewhere, but he made the tuna salad so many times he did not use the recipe. At 4:52 p.m. CK #1 assembled a meal plate of a whole grilled tuna melt sandwich cut in half and sweet potato rounds for a resident whose meal ticket documented a mechanical soft diet order. At 4:53 p.m. CK #1 assembled two meal plates for residents whose meal tickets documented mechanical soft diet orders. The two meal plates included a whole grilled tuna melt sandwich cut in half and fried sweet potato rounds. At 4:54 p.m. the dietary manager (DM) pulled the week five recipe binder. The tuna salad recipe was not present in the binder for the dinner meal on 4/28/26. At 4:55 p.m. CK #1 assembled a meal plate of a whole grilled tuna melt sandwich cut in half and sweet potato rounds for a resident whose meal ticket documented a mechanical soft diet order. At 4:58 p.m. CK #1 assembled a meal plate of a whole grilled tuna melt sandwich cut in half and sweet potato rounds for a resident whose meal ticket documented a mechanical soft diet order. At 5:24 p.m. CK #1 assembled a plate of diced chicken tender, sweet potato rounds and gravy for a resident whose meal ticket documented a mechanical soft diet order. The chicken was diced in one quarter to one half inch pieces.-However, the facility’s mechanical soft diet description failed to indicate the appropriate size mechanical soft meat should be cut into (see description below). At 5:33 p.m. CK #1 assembled three meal plates for residents whose meal ticket documented mechanical soft diet orders. The three meal plates included a whole grilled tuna melt sandwich cut in half and mashed sweet potato. CK #1 was interviewed on 4/28/26 at 5:33 p.m. CK #1 said the facility ran out of sweet potato rounds during meal service. He said the facility substituted canned sweet potato for a mechanical soft diet as a backup.-The facility failed to serve a ground grilled tuna melt sandwich item as part of the mechanically altered diet. The facility failed to chop foods to the desired consistency (see record review below). On 4/28/26 at 6:04 p.m. a test tray for a mechanical soft diet, which was served at the same time as resident room trays, was evaluated by four surveyors during the dinner meal service. The test tray was assembled in the kitchen at 5:41 p.m., arrived on the unit at 6:04 p.m. and was tested for texture. The test tray meal consisted of a whole grilled tuna melt sandwich cut in half and canned sweet potato. The edges of the tuna melt sandwich were hard and crumbly. III. Record reviewThe mechanical soft diet description from the facility’s diet manual was provided by the RD on 4/28/26 at 5:52 p.m. The diet manual documented the following modifications for the mechanically altered food items served during dinner meal service on 4/28/26:Remove desired number of servings to chop for the mechanical soft diets. Use a knife/fork or processor to chop foods to the desired consistency.-The mechanical soft diet description failed to include the residents could have grilled bread or fried items. The mechanical soft menu extensions were provided by the nursing home administrator (NHA) on 4/27/26 at 9:10 a.m. The extensions documented the following modifications for food items served during the dinner meal service on 4/28/26:Three ounces (oz) ground grilled tuna melt sandwich;Four oz sweet potato rounds;Four oz cup of fruit (soft); and,Four oz banana pudding. The recipe for grilled tuna melt was provided on 4/27/28 at approximately 11:00 a.m.. The grilled tuna melt recipe documented for tuna salad include recipe card #4141. After assembling the sandwiches, heat a large skillet/flat top grill to medium heat, place the sandwich margarine side down, brush the other side with melted margarine. Let bread get crisp and carefully flip the sandwiches. Cook to 145 degrees Fahrenheit (F) and serve promptly. Mechanical soft steps: remove the desired number of services to chop for the mechanical soft diets. Use a knife, fork or process to chop foods to the desired consistency.-However, the recipe did not specify what the desired consistency was. IV. Additional staff interviewsThe DM was interviewed on 4/28/26 at 4:43 p.m.(during meal service) The DM said he was trained by the assisted living food service director to make and serve the grilled tuna melt sandwiches and serve the potato rounds (see observations above). The DM said the facility did not use the international dysphagia diet standardisation initiative (IDDSI) diets. The DM pointed to a paper on the table titled IDDSI Menu EC7 (easy to chew level seven) and said that was the facility’s mechanical soft diet. The DM and the RD were interviewed on 4/29/26 at 10:45 a.m. The DM said when the facility had mechanical soft sandwiches the staff ground the meat and not the bread. The DM said because the tuna was ground already the staff did not grind the bread. The DM said the staff assembled the tuna melt sandwiches and then toasted the sandwich.-However, the menu extensions documented ground grilled tuna melt sandwiches (see record review above). The RD said some residents had the modified texture diet for dentition (condition of teeth) because they were missing teeth or they had chewing issues. The director of rehabilitation was interviewed on 4/29/26 at 3:45 p.m. The director of rehabilitation said speech pathology staff conducted the resident swallowing assessments and recommended the diet order based on the assessment. She said the speech therapist was notified if a resident refused a modified texture diet and it was the discretion of the speech therapist to do anOTHER evaluation if needed. The director of rehabilitation said they documented all resident refusals of a diet. She said if a resident refused a texture of a food item on their diet the facility could offer a different option of the same texture. The director of rehabilitation said the risk of not following a prescribed diet was aspiration (food, liquid, saliva, or stomach contents enter the airway and lungs instead of the esophagus, causing coughing, wheezing, or "silent" choking for the resident). CK #2 and the DM were interviewed together on 4/29/26 at 4:30 p.m. CK #2 said he had a full training on food texture when he was hired a year ago. CK #2 said he had some texture coaching with the DM. CK #2 said he referred to the facility's menu program for any mechanical soft modified texture. He said for any alternate menu, he modified the texture based on what the DM taught him. The DM said he taught the cooks how to prepare the texture for any alternate menu as there was no reference in the facility’s menu program. The DM said he had to create any modification texture for the alternate menu based on his experience.
Plan of correction · submitted by the facility
No residents were specifically identified in the statement of deficiencies as being at risk of the facility’s menu and diet textures. Residents were matched from PCC (point click care) to Optima Menu Solutions to ensure these residents were receiving their correct diet textures. Currently 16 residents have a modified texture diet related to poor dentation, dysphasia or other clinical concerns who are at risk of being served the incorrect texture. All cooks will be educated on the modified textures from the Registered Dietitian. The menus will be reviewed and adjusted to conform to the Opima Solution Dietary Management System guidelines. Education will be completed by 5/30/2026 Modified foods will be audited by the dietary manager/designee for correct textures 3 meals daily for 5 days in the first week and then 2 meals daily for 5 days over the following 11 weeks. The auditing will occur prior to the meal being served. Items not within the Opima Solutions recipe modified guideline texture will be pulled and modified to the correct texture. Audits will be reported monthly to the quality assurance performance improvement (QAPI) committee for review and further action. The dietary manager/designee will utilize a spreadsheet to assist with tracking the audit to help assure compliance.
0880Infection Prevention & Control▼
Findings
Based on observations and interviews, the facility failed to maintain an infection control program designed to provide a safe, sanitary, and comfortable environment to help prevent the development and transmission of diseases and infection for two of four units. Specifically, the facility failed to:-Ensure staff donned (put on) personal protective equipment (PPE) when providing care for a resident who was on enhanced barrier precautions (EBP);-Ensure housekeeping staff followed proper cleaning procedures for disinfecting resident rooms and high frequency touched areas; and,-Ensure staff wore personal protective equipment (PPE) when providing care for Resident #56 who was on transmission based precautions (TBP), which included contact and droplet precautions. Findings include:I. EBP failuresA. Facility policy and procedureThe Enhanced Barrier Precautions policy was provided by the nursing home administrator (NHA) on 5/1/26 at 3:41 p.m. The policy read in pertinent part,“It is the policy of American Baptist Homes of the Midwest to reduce transmission of multidrug-resistant organisms through an infection control intervention designed that employs targeted gown and glove use during high contact resident care activities known as Enhanced Barrier Precautions (EBPs).“EBPs are used in conjunction with standard precautions and expand the use of PPE to donning of gown and gloves during high contact resident care activities that provide opportunities for transfer of MDROs to staff hands and clothing. EBPs are indicated for residents with wounds or indwelling medical devices even if the resident is not known to be infected or colonized with an MDRO. Indwelling medical device examples include urinary catheters. For residents whom EBP are indicated, EBPs are employed when performing the following high contact resident care activities:“Dressing, bathing or showering, transferring, providing hygiene, changing linens, changing briefs or assisting with toileting, care of a catheter, or wound care.”The Infection Prevention and Control Program policy, dated September 2025, was provided by the NHA on 5/1/26 at 3:41 p.m. The policy read in pertinent part,“This facility has established and maintains an infection prevention and control program designed to provide a safe, sanitary and comfortable environment and to help prevent the development and transmission of communicable diseases and infections as per accepted by national standards and guidelines.“All staff are responsible for following all policies and procedures related to the program.“The facility will use standard approaches, as defined by the CDC for transmission based precautions, airborne, contact, and droplet precautions. The category of transmission based precautions will determine the type of personal protective equipment (PPE) to be used. “All staff shall use personal protective equipment (PPE) according to established facility policy governing the use of PPE.“High touch objects and environmental surfaces ( bed rails, over-bed table, bedside commode, lavatory surfaces in resident bathrooms) should be cleaned and disinfected with an EPA-registered disinfectant for healthcare use at least daily and when visibly soiled.”B. ObservationsOn 4/28/26 at 10:38 a.m. certified nursing aide (CNA) #4 and CNA #5 went into Resident #52’s room. A bin with PPE was present inside the room. There were signs on top of the bin which read “Enhanced Barrier Precautions.” CNA #5 and CNA #4 provided catheter care to Resident #52. They also cleaned his face and placed his belongings within reach. Then both CNAs left Resident #52’s room.-CNA #4 and CNA #5 failed to put on gowns prior to providing care to Resident #52 who was on EBP.C. Staff interviewsCNA #5 was interviewed on 4/29/26 at 1:01 p.m. CNA #5 said management placed bins with PPE outside a resident’s room when the resident was placed on precautions. CNA #5 said she knew which residents were on precautions because management told them and there were also signs up with bins in front of the resident's door. CNA #5 said if staff were going into a room which required EBPs to change a resident they should wear a gown and gloves. The infection preventionist (IP) was interviewed on 4/30/26 at 2:31 p.m. The IP said isolation precautions were typically set up with new admissions. The IP said the admissions coordinator found out whether or not the resident needed precautions to be in place prior to the resident being admitted and then would inform the IP. The IP said she then would prepare the isolation equipment (bin and signs) for the resident’s arrival to the facility. The IP said if the resident arrived over the weekend, the weekend supervisor would arrange for the bin and signs to be set up. The IP said residents could have isolation equipment in their rooms if that was their preference. The IP said staff should still have been donning PPE before performing direct care activities with the resident. The IP said it was important for staff to wear proper PPE for EBPs because it protected both the staff and the resident. The IP said if a resident had an open line into their body such as a catheter, it was possible to transfer organisms from staff to the resident. The IP said it was also possible to transfer organisms from the resident to staff and then be transferred onto other residents. II. Housekeeping failuresA. Professional referenceAccording to the Centers for Disease Control and Prevention (CDC) Environment Cleaning Procedures retrieved on 5/5/26 fromfrom:https://www.cdc.gov/healthcare-associated-infections/hcp/cleaning-global/procedures.html?CDC_AAref_Val=https://www.cdc.gov/hai/prevent/resource-limited/cleaning-procedures.html“Common high touch surfaces include bedrails, sink handles, call bells, bedside tables, doorknobs, and light switches. According to the Centers for Disease Control and Prevention (CDC) When and How to Clean and Disinfect a Facility on 5/5/26 fromhttps://www.cdc.gov/hygiene/about/when-and-how-to-clean-and-disinfect-a-facility.html#:~:text=During%20use,make%20sure%20germs%20are%20killed.“After you apply the disinfectant to the surface, leave the disinfectant on the surface long enough to kill the germs. This is called the contact/wet time. The surface should stay wet during the entire contact time to make sure germs are killed. B. Facility policy and procedureThe Routine Cleaning and Disinfection policy was provided by the NHA on 5/1/26 at 3:41 p.m. The policy read in pertinent part,“The facility will follow manufacturer recommendations regarding appropriate contact time to ensure adequate disinfection. Routine surface cleaning and disinfection will be conducted with a detailed focus on visibly soiled surfaces and high touch areas to include but not limited to tray tables, bed rails, door knobs and levers and light switches.”C. Record reviewThe housekeeping manufacturer guidelines for each chemical spray was received from the maintenance director on 4/30/26 at 10:19 a.m. The manufacturer guidelines revealed the blue rapid multi surface disinfectant cleaner spray used by housekeeping personnel had a kill time of 10 seconds for COVID-19 and a 30 second kill time for the norovirus, influenza A virus, rhinovirus, murine norovirus, and hepatitis B and C.D. Observations On 4/29/26 at 11:26 a.m. housekeeper (HK) #1 was cleaning room #112, which was a double occupancy room. HK#1 used a blue rapid multi surface disinfectant solution to spray green rags four times each. HK #1 used the green rags to the door knobs, light switches, and bedside tables. The surfaces were not visibly wet for ten seconds. HK #1 did not clean the call bells present in room #112. On 4/29/26 at 10:48 a.m. HK #2 was observed cleaning room the double occupancy room 200. HK #2 did not clean the call bells present in room #200. E. Staff interviewsHK #1 was interviewed on 4/29/26 at 11:46 a.m. HK #1 said if they did not have so many rooms to clean, they would spray the surface and let it sit for longer. Housekeeper #1 said instead, they sprayed cloths and used cloths to wipe surfaces instead, because they had the whole unit to get to. HKr #1 said if all the rooms were filled on the unit, there would be about 70 rooms to clean. HK #1 said there were only four vacant rooms on the unit during the time of survey. HK #1 said call lights were cleaned when performing deep cleans. HK #1 said deep cleans were performed once a week if they had time or when a resident was discharged out of the room. HK #1 was interviewed on 4/30/26 at 12:10 p.m. HK #1 said the dwell time for the blue rapid multi-surface disinfectant spray was 10 seconds. HK #1 said they had noticed the surface drying quicker than 10 seconds and they would start putting more sprays onto the rag so the disinfectant didn’t dry as fast. HK #2 was interviewed on 4/30/26 at 1:35 p.m. HK #2 said the training process was three days long and they were trained by another housekeeper who was no longer at the facility. HK #2 said he sprayed the blue rapid multi-surface disinfectant spray straight onto surfaces and let it sit for 30 seconds before wiping it off. The maintenance director was interviewed on 4/30/26 at 1:44 p.m. The maintenance director said the blue rapid multi-surface disinfectant cleaner spray used by housekeeping staff had a dwell time of 10 seconds for certain viruses and a 30 second dwell time for others. The maintenance director said housekeepers should be wiping all surfaces off except for fabric. The maintenance director said staff should work in a clockwise direction and clean any high touch surface. The maintenance director said surfaces should remain wet for 10 seconds when using the blue rapid multi surface disinfectant cleaner spray. The maintenance director said housekeepers had different techniques when cleaning the rooms. The maintenance director said some housekeepers have a bucket with disinfectant in the top of their cart and others use the spray and rags. The maintenance director said no matter what technique housekeepers used, they needed to ensure the dwell time was being met. The maintenance director said he was going to implement buckets with disinfectant solution for all housekeepers to use in order to ensure surfaces were staying wet for the proper dwell time. The maintenance director said staff needed to ensure the dwell times were being met and if their rags were not wet enough, they were not meeting the dwell time and weren't disinfecting. The maintenance director said he would start watching each housekeeper to ensure proper cleaning was performed.
Plan of correction · submitted by the facility
Resident #56 was not affected by the staff failing to put on personal protective equipment (PPE). No residents were identified nor had infections related to housekeeping room disinfection. All residents have the potential for acquired infections by staff not wearing PPE. All residents have the potential to be affected by housekeeping disinfection procedures. Housekeeping staff will be educated on the proper dwell times of the disinfectants used. The cleaning procedures have been reviewed and changed to ensure proper dwell times are followed. Education occurred on May 1, 2026. The infection control policy was reviewed and remains current. Staff will be educated on isolation precautions, signage, and how to interpret which PPE is indicated. Housekeeping cleaning processes will be audited by the maintenance supervisor/designee 10 times per week for 4 weeks and then 5 times per week for the next 8 weeks. An audit sheet and a tracking log will be used to assure compliance. Staff will be audited for isolation precaution awareness and PPE compliance 3 times per week for 12 weeks. An audit sheet and a spreadsheet log will be used to assure compliance. Audits will be completed by the Infection Preventionist/Designee. Results of the audits will be brought to the quality assurance performance improvement (QAPI) committee for review and further action as needed.
0947Required In-Service Training for Nurse Aides▼
Findings
Based on record review and interviews, the facility failed to ensure certified nurse aides (CNA) received the required 12 hours of annual in-service training for continued competence. Specifically, the facility failed to ensure two CNAs (#2 and #3) of five CNAs received 12 hours of annual training. Findings include:I. Facility policy and procedureThe Required Training, Certification and Continuing Education of Nurse Aides policy and procedure, undated, was received from the nursing home administrator (NHA) on 5/1/26 at 3:41 p.m. It revealed in pertinent part, “It is the policy of this facility to comply with state and Federal regulations and requirements as they pertain to the training, certification and continuing education of its nurse aides. “The facility will provide at least 12 hours of inservice training annually, based on employment date, not calendar year. Documentation of inservice training will be maintained by the Staff Development Coordinator and retained in an employee personnel or education file in accordance with facility policy. It is the responsibility of the employee to attend required in-service training to maintain employment status with the facility. The required 12 hours of annual in-service training include online education completed through the facility designated learning platform. Employees are assigned online training modules on a quarterly basis and completion of these modules within the designated timeframe is mandatory.” II. Training reviewA review of CNA training was reviewed on 4/30/26 at 1:24 p.m. CNA #2 was hired on 3/13/24 and had only completed three hours of the required 12 hours of continuing education units (CEU). CNA #3 who was hired on 5/16/24 and had only completed seven hours of the required 12 hours of CEUs on the platform for education. The facility provided other in-service documentation for CEU however there was no way to determine the contact hours for them as the documentation did not include contact time. III. Staff interviewsThe staff development coordinator was interviewed on 4/30/26 at 3:15 p.m. She said CNAs were required to complete 12 hours minimum of CEU per year. The staff development coordinator said the facility used a platform for education along with inservice training they held. The staff development coordinator said the facility held all staff meetings and had staff signed in to show they were present. The staff development coordinator said she was unable to locate/provide contact hours for the in services provided during all staff meetings. The director of nursing (DON) was interviewed on 4/30/26 at 3:26 p.m. She said it was important for CNAs to complete their 12 hours of CEUs for job safety and residents safety. The DON said starting on May 11th the facility will be having all staff complete 12 hours of CEU prior to their first shift on the floor.
Plan of correction · submitted by the facility
No specific residents were affected by the 2 staff members who did not complete the required education. The 2 staff members identified in the survey have completed their required education as of 5/22/2026. All residents receiving care from certified nursing assistants have the potential to affected by staff lacking required education. The staff development coordinator/designee will develop a training calendar to assure that 12 hours of education is identified and scheduled for the certified nursing assistants. Nursing assistants will receive education on the importance and requirement to receive and complete education. Staff who fail to complete education will be referred to their supervisor for counseling or other disciplinary action. The staff development coordinator will input education hours into the facility’s training software. The staff development coordinator/designee will run a tracking audit from the facility’s computerized training software to validate compliance for nursing assistants. The audit and tracking will occur weekly for 4 weeks; bi-weekly for 4 weeks and then monthly for 4 weeks. Results of the audits and tracking will be brought to the quality assurance performance performance (QAPI) committee monthly for review and further action.
12/9/2025Complaint Survey · ID 1S9X111 deficiency▼
0000INITIAL COMMENTSSurveyor note▼
Findings
A complaint survey, prompted by #CO2608445, Incident #1926122, Incident #2607330 and Incident #2626417 was completed on 10/7/25 to 12/9/25. One deficiency was cited. The actual Survey date was 10/9/25. Per AHFSA guidance from CMS on 11/17/25, the survey end date has been adjusted to the date the CMS-2567 was issued to the provider, on 12/9/25.
Plan of correction
The state did not require a plan of correction for this citation.
0610Investigate/Prevent/Correct Alleged Violation▼
Findings
Based on record review and interviews, the facility failed to investigate and document incidents of physical abuse involving two (#2 and #3) of three residents reviewed out of eight sample residents. Specifically, the facility failed to conduct a thorough investigation of physical abuse involving Resident #3 and Resident #2. Findings include:I. Facility policy and procedureThe Abuse, Neglect and Exploitation policy, dated October 2024, was provided by the nursing home administrator (NHA) on 10/8/25 at 9:52 a.m. via email. It revealed in pertinent part,“An immediate investigation is warranted when suspicion of abuse, neglect or exploitation, or reports of abuse, neglect or exploitation occur.“Written procedures for investigations include: identifying staff responsible for the investigation; investigating different types of alleged violations; identifying and interviewing all involved persons, including the alleged victim, alleged perpetrator, witnesses, and others who might have knowledge of the allegations; focusing the investigation on determining if abuse, neglect, exploitation, and/or mistreatment has occurred, the extent, and cause; and, providing complete and thorough documentation of the investigation.“Analyzing the occurrence(s) to determine why abuse, neglect, occurred, and what changes are needed to prevent further occurrences;“Training of staff on changes made and demonstration of staff competency after training is implemented;“Identification of staff responsible for implementation of corrective actions; The expected date for implementation; and,“Identification of staff responsible for monitoring the implementation of the plan.”II. Incident of physical abuse between Resident #2 and Resident #3 on 8/8/25A. Facility investigationThe 8/8/25 facility investigation documented Resident #2 and Resident #3 kicked each other while in the dining room. The investigation documented the residents were separated. The investigation documented Resident #2 had a history of aggressive behaviors with three prior incidents in the facility. The investigation documented staff and a resident witnessed the incident.-The investigation failed to document what staff were involved in the incident and failed to interview staff. The investigation documented there was no cause of the altercation discovered in the initial investigation. The investigation documented that witness statements were requested.-However, there was no documentation that indicated who the witnesses were or the statements. The investigation documented Resident #2 and Resident #3 returned to their rooms after the altercation and were placed on 15-minute checks. The final report from the facility substantiated the physical abuse. Review of the investigation did not reveal Resident #2 or Resident #3 were interviewed after the incident. B. Resident interviewResident #8 was interviewed on 10/8/25 at 12:50 p.m., who was identified as alert and oriented through facility and assessment. Resident #8 said she witnessed Resident #2 and Resident #3 kicking each other. Resident #8 said Resident #2 was the bully of the facility. Resident #8 said she was seated at the dining room table where the incident occurred at approximately 8:30 a.m. while she was waiting for breakfast. Resident #8 said someone from the dietary staff was there to help and stop the situation. Resident #8 said no one from the facility asked her what happened even though she witnessed the altercation. Resident #8 said the police did talk to her about what happened. Resident #8 said even after the police spoke with her, no one from the facility talked to her about what she saw happen. She said she would have told the administrator that Resident #2 was a bully in the facility.-However, the facility failed to interview Resident #8, who witnessed the resident-to-resident abuse on 8/8/25 (see investigation above). C. Staff interviewsThe social service director (SSD) and the social service assistant (SSA) were interviewed together on 10/8/25 at 12:20 p.m. The SSD said she was not involved with the altercation with Resident #2 and Resident #3. The SSA said she spoke with Resident #3 after the incident but she did not speak to Resident #2. The SSA said she did know that a dietary staff member separated the residents. The SSA was interviewed again on 10/8/25 at 1:30 p.m. The SSA said after further research, she determined Resident #8 witnessed the altercation on 8/8/25. The SSA said she did not interview Resident #8 after the incident as part of the investigation. Licensed practical nurse #1 was interviewed on 10/8/25 at 12:45 p.m. LPN #1 said Resident #2 and Resident #3 did not like each other. LPN #1 said the staff needed to keep an eye on them if they were in the same room to ensure the residents were not fighting. Dietary aide #1 (DA) was interviewed on 10/8/25 at 1:35 p.m. DA #1 said she worked the morning the two men (Resident #2 and Resident #3) had an altercation. DA #1 said Resident #3 liked to tease other residents in a playful manner. DA #1 said Resident #3 was teasing Resident #2 and Resident #2 began yelling shut the (obscenity) up repeatedly. She said Resident #2 came up to Resident #3 and kicked him over and over, and then both residents were kicking each other. DA #1 said she witnessed the altercation and separated the residents. DA #1 said she told both residents to stop as she pulled them apart from kicking each other. DA #1 said no one from the facility interviewed her about the incident. DA #1 said the former NHA did not speak to her about the situation. The nursing home administrator (NHA) was interviewed 10/8/25 at 1:50 p.m. The NHA said the former NHA only worked at the facility for two weeks. The NHA said during that time, the incident on 8/8/25 between Resident #2 and Resident #3 occured. The NHA said after an investigation the facility should interview eyewitnesses, including staff and residents. The NHA said he was unaware Resident #8 was a witness to the situation. The NHA said from now on all witnesses would be interviewed during the investigation.
Plan of correction · submitted by the facility
Residents #2 and #3 were not affected by the lack of witness statements. Resident #2 no longer resides at the facility. All residents have the potential of being negatively affected by incomplete investigations. All leadership members have been educated by the regional nurse on abuse investigations and reporting. The internal policy was reviewed for updates and remains current. All residents with a BIM of 8 or higher were interviewed for abuse with no negative findings. The facility will re-train all staff on abuse/neglect. NHA (nursing home administrator) and/or delegate will interview 5 random residents weekly beginning 12/12/2025 to ensure no abuse allegations are made for 4 weeks then 5 random residents every 2 weeks for eight weeks. The audits will be tracked using a spreadsheet for easy identification of completion. All new employees will be trained on abuse and abuse reportingduring orientation by the SDC (staff development coordinator)/Delegate. NHA will track and trend results of the interviews and present results at QAPI for the next 3 months or until substantial compliance is in place. All allegations of abuse will be investigated per facility policyassuring identified witness statements, other interviews, andsupporting documentation are obtained. The investigation file willbe reviewed by the QAPI Committee as needed to assure the filecontains all required elements. The NHA or designee will reviewthe occurrence log weekly for new occurrences and will follow upon incomplete elements as identified. The results of the ad-hocQAPI Committee reviews and NHA/Designee reviews will bereviewed monthly during the facility QAPI meeting for the next six(6) months beginning January 2026.
7/25/2025Revisit: Complaint Survey · ID WNWR12No deficiencies▼
0000INITIAL COMMENTSSurveyor note▼
Findings
A revisit survey was completed on 7/25/25 for all previous deficiencies cited on 6/11/25. The facility is in compliance with all regulations surveyed.
Plan of correction
The state did not require a plan of correction for this citation.
6/11/2025Complaint Survey · ID WNWR111 deficiency▼
0000INITIAL COMMENTSSurveyor note▼
Findings
A complaint survey, prompted by #CO39932 was conducted on 6/11/25. One deficiency was cited.
Plan of correction
The state did not require a plan of correction for this citation.
0812Food Procurement,Store/Prepare/Serve-SanitaryS/S E▼
Findings
Based on observations, record reviews, and interviews, the facility failed to properly prepare and store food and to maintain sanitary conditions in the main kitchen. Specifically, the facility failed to:-Ensure the main kitchen was clean and sanitary;-Ensure damaged cans were disposed of; and,-Ensure food was labeled and dated. The findings include:I. Ensure the main kitchen was clean and sanitary A. Professional referenceThe Colorado Retail Food Establishment Regulations (3/14/24), retrieved on 6/18/25 read in pertinent part,"Nonfood-contact surfaces shall be constructed of approved materials, in good repair, and be easily maintained in a clean and sanitary condition."Equipment food-contact surfaces and utensils shall be clean to sight and touch. Food contact surfaces of cooking equipment and pans shall be kept free of encrusted grease deposits and other solid accumulations. Nonfood-contact surfaces of equipment shall be kept free of an accumulation of dust, dirt, food residue, and other debris. (Chapter 4)"Receptacles and waste handling units for refuse, recyclables, and returnables used with materials containing food residue and used outside the food establishment shall be designed and constructed to have tight-fitting lids, doors, or covers." (Chapter 5)B. ObservationsThe initial main kitchen tour was conducted on 6/11/25 at 11:00 a.m and the following was observed:-The vents above the stove were greasy and dusty, there was a sticker on the vents that indicated they were serviced on 2/27/25; -There was a yellow puddle of an unidentifiable liquid under the shelf in the dry storage room;- The used aprons were stored next to clean glassware and dishes;-The shelves were covered with light, white dust and felt sticky upon touch;-There was a dark grey trashcan in the preparation area that had no lid and the outside of the trashcan was covered with unknown white splatters and dried on food; -The shelf under the preparation table had dried on food and it was greasy;-The radio, paper towel dispenser, waffle maker, food cart and the food processor had caked on food and were sticky to the touch;-The preparation sink tap was dripping and the sink was leaking underneath. There was a towel put under the sink to trap water;-The outside of the deep fat fryer was greasy and there was dried oil streaks on its side; -The reach-in drink refrigerator had different colored, dried splatters inside on the bottom;-The juice machine vents were sticky and covered in juice. The drip tray had stagnant and crusted liquid inside;-The coffee machine had dried on dark splatters on the sides and there was dried black crud in the corners of the machine;-There was a dark substance on the baseboard throughout the kitchen; -The drain by the ice machine had dirty, dark gunk dried on it; and,-The ice machine lid had fingerprints inside and it had calcified streaks on its side. C. Staff interviewsThe dietary manager (DM) was interviewed on 6/11/25 at 3:20 p.m. She said the staff cleaned the kitchen after meal preparations. The DM said the staff also had daily cleaning tasks to complete. She said the walk-in refrigerator was cleaned daily and all surfaces of the kitchen were wiped down. She said the staff deep cleaned the kitchen once a week, including the reach-in fridges. She said the deep cleaning included scrubbing the floor to get rid off the dark build up on the floor and baseboard. She said deep cleaning also included the deep fryer, drains, vents and all equipment. She said the vents were cleaned by an outside company every two months. She said she had no information on the dripping tap and sink. The dietary director (DD) was interviewed on 6/11/25 at 3:40 p.m. He said the facility lost their utility staff who was responsible for deep cleaning two months ago. He said the kitchen staff was doing deep cleaning now. He said they would start deep cleaning the kitchen right away. He said the vents were cleaned quarterly by an outside company. II. Ensure damaged cans were disposed ofA. Professional referenceThe Colorado Retail Food Establishment Regulations (3/14/25), retrieved on 6/18/25, read in pertinent part, "A food that is unsafe, adultered, or not honestly presented shall be discarded or reconditioned according to an approved procedure. (Chapter 3)"Products that are held by the permit holder for credit, redemption, or return to the distributor, such as damaged, spoiled, or recalled products, shall be segregated and held in designated areas that are separated from food." (Chapter 6)B. ObservationsThe kitchen was observed on 6/11/25 at 11.00 a.m and the following was observed on a shelf in the dry storage area:-Two unopened, dented cans of tuna; and,-One unopened, dented can of mushroom. C. Staff interviewsThe DM was interviewed on 6/11/25 at 3:20 p.m. She said the kitchen staff should have removed the dented cans to the side and then discard it. She said keeping the cans on the shelf was an improper food handling procedure. The DD was interviewed on 6/11/25 at 3:40 p.m. He said that staff should have removed the dented cans from the shelf and moved it to his office. He said the vendor did pick up dented cans and reimbursed the facility for it. III. Ensure food was labeled and datedA. Professional referenceThe Colorado Retail Food Establishment Regulations (3/14/24), retrieved on 6/18/25, read in pertinent part, "Marking the date or day the original container is opened in a food establishment, with a procedure to discard the food on or before the last date or day by which the food must be consumed on the premises, sold, or discarded."Label information shall include the common name of the food." (Chapter 3)B. ObservationsThe initial kitchen tour was conducted on 6/11/25 at 11:00 a.m. and the following was observed:-There was a round, white, plastic container in the dry storage that contained a dark brown food, the container was not labeled or dated;-There was a jar of opened jalapenos on the shelf in the walk-in refrigerator that was not labeled or dated; -There was an opened bag of pancake mix in the dry storage that was not labeled or dated;. -There was a plate of carrots in the walk-in refrigerator that was not labeled or dated;-There was a container of taco shells in the walk-in refrigerator that was not labeled or dated;-There was an opened package of pepperoni in the walk-in refrigerator that was not labeled or dated; and,-There was a tray of lettuce in the reach-in fridge in the preparation area, that was not labeled or dated. C. Staff interviewsThe DM was interviewed on 6/11/25 at 3:20 p.m. She said all produce should have a receiving date indicated on them. She said repackaged food should have a label. She said the label should indicate the name of the item and a date it was. She said all food items without a label should have been discarded by staff. She said nobody would know when to discard spoiled items without proper labeling. She said it was important to ensure food was labeled and dated correctly to prevent foodborne illnesses. She said spoiled food could attract pests to the kitchen. She said she would discard the unlabeled food.
Plan of correction · submitted by the facility
Affected Resident(s):No identified resident was at immediate risk of this alleged deficient practice. Potential Affected Resident(s):All residents who consume food prepared in the kitchen are at risk of this alleged deficient practice. Available staff immediate began cleaning areas addressed during survey, removed and disposed of unlabeled food item and removed dented can from dry food storage area. Measures/Systematic Changes:All dietary staff received education regarding cleaning schedules, label and dating food items, and removing dented cans from the dry storage area. Monitoring:Dietary Manager or designee will round daily to audit completion of the cleaning schedules signed the form and inspect area is clean. Dietary Manager will audit and sign the form that staff did not place dented cans in dry storage area twice each week after deliveries. Dietary Manager or designee will audit and sign tracking form that food items are label and dated in the fridge and dry storage areas daily. NHA (nursing home administrator) will round weekly to audit cleaning schedules are complete and signed by staff and dietary manager, kitchen areas are clean, label and dating is occurring in addition to staff and dietary manager completing tracking form and dented cans are not available for use. Then bi monthly for following 2 months. Results of monitoring shall be reported for at least 3 months at the facility QAPI with ongoing frequency and duration to be determined through analysis and review of results. Completion Date:07/14/2025
5/15/2025Revisit: Complaint Survey · ID DFH612No deficiencies▼
0000INITIAL COMMENTSSurveyor note▼
Findings
A revisit survey was completed on 5/15/25 for all previous deficiencies cited on 3/24/25. The facility is in compliance with all regulations surveyed.
Plan of correction
The state did not require a plan of correction for this citation.
4/18/2025Revisit: Complaint Survey · ID LHCP12No deficiencies▼
0000INITIAL COMMENTSSurveyor note▼
Findings
A revisit survey was completed on 4/18/25 for all previous deficiencies cited on 2/24/25. The facility is in compliance with all regulations surveyed.
Plan of correction
The state did not require a plan of correction for this citation.
3/24/2025Complaint Survey · ID DFH6115 deficiencies▼
0000INITIAL COMMENTSSurveyor note▼
Findings
A complaint survey, #CO39544, Incident #39481, Incident #39482, Incident #39582 and Incident #39583 was conducted on 3/19/25 to 3/24/25. Five deficiencies were cited.
Plan of correction
The state did not require a plan of correction for this citation.
0550Resident Rights/Exercise of RightsS/S D▼
Findings
Based on observation, record review and interviews, the facility failed to promote dignity and respect for one (#12) of three residents out of 14 total sample residents. Specifically, the facility failed to promote dignity and respect by sitting with the Resident #12 at the dining table and providing meal assistance in a dignified manner. Findings include: I. Facility policy and procedure The Activities of Daily Living (ADL's) policy and procedure, dated 2024, was provided by the corporate nurse consultant (CNC) on 3/25/25 at 12:28 p.m. It read in pertinent part, "The facility will, based on the resident's comprehensive assessment and consistent with the resident's needs and choices, ensure a resident's abilities in ADLs do not deteriorate unless deterioration is unavoidable. Care and services will be provided for the following activities of daily living: eating to include meals and snacks ..." II. Resident #12 A. Resident status Resident #12, over the age of 65, admitted 3/10/2020. According to the March 2025, computerized physician orders (CPO), diagnosis included dementia with behavioral disturbance, protein-calorie malnutrition and bilateral cataracts. According to the 1/18/25 minimum data set (MDS) assessment, the resident was severely cognitively impaired and was unable to participate in the brief interview for the mental status (BIMS) assessment. Staff reported the resident had short and long-term memory problems with severely impaired daily decision-making skills and required daily cuing and supervision to make sound decisions. The resident was able to express her needs and had some ability to understand basic conversations. The MDS assessment indicated the resident needed set-up assistance.-However, the resident's medical record revealed the resident needed assistance with meals (see record review below). B. Observations During a continuous observation on 3/19/25, from 11:25 a.m. to 12:24 p.m., Resident #12 was observed at the lunch counter on the unit. The resident was served lunch and had eaten some of her meat but had not eaten anything else. Resident #12 sat not eating her meal for 45 minutes before certified nurse aide (CNA) #3 approached Resident #12 initially to pick up her tray. Without talking with the resident, CNA #3 started to spoon-feed the resident in a rushed manner. CNA #3 was standing in front of the resident and not talking to the resident as she assisted her to eat. After assisting the resident with a couple of bites of food, she called over CNA #4 to finish feeding the resident. CNA #4 approached the resident and sat beside her to finish feeding her. During a continuous observation on 3/20/25, from 11:15 a.m. to 11:43 p.m., Resident #12 was observed during lunch. CNA #3 approached Resident #12 from the front and started to spoon feed her in the same rushed manner as during the observation the day prior (see above). 3. Record review The resident's nutrition care plan, initiated 10/5/21, indicated the resident had a potential nutrition deficiency. Pertinent interventions included: continuing to encourage food and fluid for comfort, honoring the resident's food preferences,providing cueing and supervision during meal service (up to maximum assist on occasion), maintaining eye contact when assisting with meals, offering the resident utensils for self-feeding and offering the resident a meal alternative if she was not eating and informing the kitchen of what she wanted. The physician's assistant (PA) note, dated 2/26/25, documented: continue to assist Resident #12 with eating assistance and nutrition, as needed. The nutrition assessment, dated 1/15/25, documented Resident #12 was eating her meals in the assisted dining room with moderate to maximum assistance and was occasionally independent. The resident had weight gain over the last two quarters despite remaining underweight. Although the weight loss was not desirable,measures to combat weight loss in hospice residents might be ineffective. The staff continued to encourage foods and fluids as the resident desired for comfort. III. Staff interviews CNA #3 was interviewed on 3/20/25 at 11:22 a.m. CNA #3 said they delivered Resident #12's meal to her and let her eat as much independently as she was able. CNA #3 said once the staff noticed the resident stopped eating, they offered verbal prompts and then offered feeding assistance. CNA #3 said the staff should sit at the table with the resident and engage her in conversation about her meal to encourage food and drink intake. Licensed practical nurse (LPN) #2 was interviewed on 3/24/25 at approximatly 5:00 p.m. LPN #2 said when a resident needed feeding assistance, the staff needed to sit with them and encourage the resident to eat as much as possible independently. LPN #1 said the staff increased the level of assistance as needed so that the resident would get enough to eat. The director of nursing (DON) was interviewed on 3/20/25 at 3:55 p.m. The DON said staff should sit and communicate with the resident while assisting them to eat their meal.
Plan of correction · submitted by the facility
Affected Resident(s):R12 was allegedly at risk for this deficient practice. Potential Affected Resident(s):All residents who require meal assistance in the dining area are alleged to be at risk by staff standing to provide meal assistance, not engaging the resident and by staff waiting an extended time to provide meal service after the meal is presented. Measures/Systematic Changes:All staff who provide assistance in the dining area will receive education to sit, converse/cue and engage with the residents while providing the meal assistance once the meal arrives. Monitoring:Dietary or designees will audit staff compliance with sitting during dining assistance cuing residents and having appropriate conversations. Audits will be documented on a spreadsheet to be conducted at a frequency of 2 per week for 3 months. Dietary or designee are responsible for compliance. Results of monitoring shall be reported at the facility QAPI with ongoing frequency and duration to be determined through analysis and review of results. Completion Date:04/30/2025
0609Reporting of Alleged ViolationsS/S D▼
Findings
Based on record review and interviews, the facility failed to report alleged violations of potential abuse, neglect, exploitation or mistreatment and injuries of unknown origin to the state oversight agency in accordance with state laws for two of five alleged abuse violations. Specifically, the facility failed to:-Timely report an allegation of sexual abuse by Resident #6 towards Resident #4, Resident #5, Resident #2 and Resident #3 to the State Agency; and,-Report Resident #7's injury of unknown origin to the State Agency. Findings include: I. Facility policy and procedureThe Abuse, Neglect, and Exploitation policy and procedure, dated October 2024, was received from the director of nursing (DON) on 3/19/25 at 12:45 p.m. It read in pertinent part,"Abuse is defined as the willful infliction of injury with resulting physical harm, pain or mental anguish. Instances of abuse of all residents, irrespective of any mental or physical condition, cause physical harm, pain or mental anguish."Alleged violation is a situation or occurrence that is observed or reported by staff, residents, relatives, visitors, or others but has not yet been investigated and, if verified, could be an indication of noncompliance with the federal requirements related to abuse."Possible indicators of abuse include but are not limited to physical injury of a resident of unknown source."Sexual abuse is a non-consensual sexual contact of any type with a resident."The facility will develop and implement written policies and procedures that establish policies and procedures to investigate any such allegations."An immediate investigation is warranted when suspicion, or reports, of abuse occur."Reporting of all alleged violations to the administrator, State Agency, adult protective services and to all other required agencies within the specified timeframes. If the event that caused the allegation involves abuse or resulted in serious bodily injury or no later, report within two hours. If the event that caused the allegation does not involve abuse or result in serious bodily injury, report within 24 hours."II. Allegation of sexual abuseA. Facility investigation of sexual abuse on 2/23/25 The investigation report revealed the date of the incident was 2/23/25. The incident report documented on 2/24/25 at 6:30 a.m. a certified nurse aide (CNA) reported to the unit manager that Resident #6 exposed his genitals on two different occasions to several residents. Video footage was reviewed and confirmed his indecent exposure on three separate occasions. The incidents were on 2/21/25 at 6:52 p.m., on 2/23/25 at 11:26 a.m. and on 2/23/25 at 11:34 a.m. The alleged incident happened on 2/23/25 at 11:26 a.m, on the east unit in the kitchenette area, where he exposed his genitals to two female residents (Resident #4 and Resident #5). The second incident happened immediately after the first incident on 2/23/25, at 11:34 a.m. Resident #6 wheeled himself to the main dining room. He sat at the same table as two female residents (Resident #2 and Resident #3). He touched Resident #2's arm and then proceeded to expose his genitals. Resident #2 turned her head away from Resident #6. During the facility's investigation, the facility reviewed additional video footage. The facility reported on 2/21/25 at 6:52 p.m. Resident #2 sat at a table in the main dining room alone. Resident #6 wheeled himself to Resident #2's table. Resident #6 lifted his shirt and pulled his pants down. He made motions as if he was fondling himself in front of Resident #2. Resident #6 took Resident #2's hand and tried to place her hand in his genital region. Resident #2 pulled her hand back and Resident #6 grabbed her hand again and made a fondling movement with their hands together. The behavior was repeated several times for over 20 minutes. On two occasions, Resident #6 made motions to his mouth, then to Resident #2's mouth, and then Resident #6 pointed to his genitals in a manner indicating he wanted her to perform oral sex. -The facility did not report the incident until 2/24/25 at 6:53 p.m., which was over 24 hours after Resident #6 exposed his genitals to Resident #4, Resident #5, Resident #3 and Resident #2. B. Resident #6 - assailant
1. Resident statusResident #6, age greater than 65, was admitted on 5/27/22. According to the March 2025 computerized physician orders (CPO), diagnoses included alcoholic cirrhosis of the liver with ascites (chronic liver disease caused by alcohol and fluid accumulates in the abdominal cavity), dementia, psychotic disturbance, mood disturbance and anxiety. The 2/14/25 minimum data set (MDS) assessment revealed the resident was cognitively intact with a brief interview for mental status (BIMS) assessment score of 12 out of 15. He was independent in eating, oral hygiene, toileting, showering and dressing. He used a manual wheelchair. C. Resident #4, Resident #5, Resident #2 and Resident #3 - victims
1. Resident #4Resident #4, age greater than 65, was admitted on 10/13/21. According to the March 2025 CPO, diagnoses included atherosclerotic heart disease, hypertension, contracture of muscle and peripheral vascular disease. The 1/12/25 MDS assessment revealed the resident was cognitively intact with a BIMS score of 13 out of 15. 2. Resident #5Resident #5, age 72, was admitted on 5/12/23. According to the March 2025 CPO, diagnoses included Alzheimer's disease, anxiety disorder, mood disturbance and anxiety disorder. The 1/12/25 MDS assessment revealed a BIMS assessment was not conducted because the resident was rarely or never understood. According to the staff assessment for mental status, the resident had short and long-term memory problems and her cognitive skills for daily decision making were severely impaired. 3. Resident #2Resident #2, age 88, was admitted on 6/3/24. According to the March 2025 CPO, diagnoses included dementia, psychotic disturbance, mood disturbance and anxiety. The 3/3/25 MDS assessment revealed a BIMS assessment was not conducted because the resident was rarely or never understood. According to the staff assessment for mental status, the resident had short and long term memory problems and her cognitive skills for daily decision making were severely impaired. 4. Resident #3Resident #3, age greater than 65, was admitted on 11/21/17. According to the March 2025 CPO, diagnoses included dementia, psychotic disturbance, anxiety disorder and mood disturbance. The 1/4/25 MDS assessment revealed the resident was cognitively impaired with a BIMS score of three out of 15. III. Injury of unknown originA. Resident #7B. Resident statusResident #7, age 85, was admitted on 9/24/24. According to the March 2025 CPO, diagnoses included Alzheimer's disease, dementia with agitation, transient ischemic attack (small stroke), cerebral vascular disease (stroke) and depression. The 12/30/24 MDS assessment revealed a BIMS assessment was not conducted because the resident was rarely or never understood. According to the staff assessment for mental status, the resident had short and long term memory problems and her cognitive skills for daily decision making were severely impaired. She required maximum assistance with personal hygiene and showering. C. Resident's representative interview Resident #7's representative was interviewed on 3/20/25 at 11:09 a.m. The representative said he visited the resident frequently. He said when he visited Resident #7 on 3/1/25 he noticed her hand was swollen when he tried to hold her hand and she said "ow." He said when he noticed her hand, he told the nurse to ask the doctor to take a look at her left hand. He said an x-ray was completed and she had a crack (fracture) in her hand. He said Resident #7 moved frequently throughout the unit in her wheelchair. He said she probably got her hand stuck in between the handrail and wall because he had seen her do that in the past. He said the facility did not say what they did to prevent the injury from happening again. B. Facility investigation of injury of unknown originThe investigation report revealed the date of the incident was 3/5/25. The investigation documented Resident #7 had a fracture of the third metacarpal (the third bone of the hand) on the left hand. The investigation documented that CNA #1 reported the resident went to bed between 7:30 p.m. or 8:00 p.m. CNA #1 said she checked on the resident at 9:00 p.m. because she heard a disturbance. The resident was sitting on the edge of the bed, trying to get out of bed. The resident's bedding was on the floor, the resident took off her brief and was in emotional distress. The investigation included the 3/7/25 provider progress note which revealed Resident #7 had edema to her fingers and the left dorsal (the back) aspect of hand. The x-ray on 3/5/25 revealed the resident had an acute (new) fracture involving the left third metacarpal with mild displacement. The resident was able to bend her finger and used her hand at baseline. She denied pain. The note documented options were discussed with the resident's representative, such as, buddy taping the fingers, an orthopedic consult, elevation and ice. The representative was understanding of the resident's dementia and her goals of care. The representative wished for comfort treatment only at that time and to continue to monitor. The investigation documented, based on the interviews the nurse manager had with the staff and based on the resident's impulsive movement, it was deemed that the fracture happened due to the resident hitting the wall or bed in her room, flailing her arms or any other type of sudden impulsive movement. -The facility was unable to provide documentation that the incident of unknown origin was reported to the State Agency. IV. Staff interview The director of nursing (DON) was interviewed on 3/20/25 at 3:57 p.m. The DON said she was the acting abuse coordinator. She said she did not know Resident #7's representative told the unit nurse about the swelling on 3/1/25. She said she did not know the nurse on 3/2/25 noticed swelling on Resident #7's left hand and the nurse did not report the swelling promptly. The DON said the nurse should have followed the injury of unknown source protocol. The DON said the protocol included completing a skin assessment, asking the other staff on the unit what happened and notifying the physician, abuse coordinator and the family. The DON said she did not report the injury because the resident had a history of hitting the walls. Licensed practical nurse (LPN) #2 was interviewed on 3/24/25 at 6:02 p.m. LPN #2 said if a resident had an injury, he would assess the injury and talk with the resident and staff to determine what happened. He said he would report the injury to the resident's physician and the nurse supervisor for further assessment and treatment recommendations. He said if the cause of the injury could be determined, it would be reported to facility leadership for an immediate investigation. LPN #2 said incidents involving abuse were to be reported immediately to the nursing home administrator (NHA) and the DON for investigation. He said if he observed an allegation of abuse, he was responsible for implementing an immediate intervention to protect the resident from further harm. The interim nursing home administrator (INHA) and the clinical nurse consultant (CNC) were interviewed together on 3/24/25 at 5:10 p.m. The INHA said she was the abuse coordinator as of today (3/24/25). She said the staff had two hours to report possible abuse to the abuse coordinator. The INHA said if a resident had an injury of unknown origin, the injury should be reported as possible abuse. She said when there was an injury of unknown origin, a risk management incident was completed, to include an investigation of interviewing staff, residents and family. The CNC said the nurse who noticed the swelling on 3/2/25 should have notified the physician and the abuse coordinator on 3/2/25.
Plan of correction · submitted by the facility
Affected Resident(s):Resident 6 discharged the community. Potential Affected Resident(s):All residents with reports of alleged abuse, neglect, and exploitation have the ability to be impacted by late reporting. Measures/Systematic Changes:Training will be provided for all staff prior to working in the community on timely reporting guidelines. Monitoring:Administrator or designee will audit of all alleged allegations will be completed as received for timeliness. Results of monitoring shall be reported at the facility QAPI with ongoing frequency and duration to be determined through analysis and review of results. Completion Date:04/30/2025Addendum:The community did not report the alleged incident of unknown injury to the state for R7. As indicated in the citation text the community identified the source of injury as it was deemed that the fracture happened due to the resident hitting the wall or bed in her room, flailing her arms or any other type of sudden impulsive movement. The community selected the incorrect report title when opening the incident report. DON shared history of hitting walls. Training for timely reporting will include:That all alleged violations involving abuse, neglect, exploitation or mistreatment, including injuries of unknown source and misappropriation of resident property are reported immediately, but not later than 2 hours after the allegation is made, if the events that cause the allegation involve abuse or result in serious bodily injury or not later than 24 hours if the events that cause the allegation do not involve abuse. All staff have the ability to report the phone number is listed in the front lobby. Monitoring of injuries of unknown injury occurs daily in the clinical meeting. The DON and NHA review for appropriate occurrence type and as notifications are made to the DON per incident. Monitoring will occur at a minimum of three months on a spreadsheet.
0658Services Provided Meet Professional StandardsS/S D▼
Findings
Based on record review and interviews, the facility failed to ensure one (#1) of two residents out of five sample residents received treatment and care for optimal skin condition of a pressure wound and injury of unknown origin, in accordance with professional standards of practice. Specifically, the facility failed to:-Develop a care plan for treating Resident #1's moisture-associated skin damage (MASD) and preventing pressure injury due to immobility;-Reassess alternative methods of providing Resident #1's pressure-relieving interventions when the resident refused offers to be repositioned; and, -Reassess treatment methods and implement alternative interventions when Resident #1 developed a skin tear and his MASD worsened. Findings include: I. Professional referenceAccording to Wound UK, volume 13, Number 4, 2019, Back to Basics: Understanding Moisture-Associated Skin Damage, retrieved online 4/4/25 from: chrome-extension://efaidnbmnnnibpcajpcglclefindmkaj/https://www.wwic.wales/uploads/files/documents/Professionals/New%20Articles/MASD.pdf "Moisture-associated skin damage (MASD) is the umbrella term for four clinical manifestations, namely incontinence-associated dermatitis (IAD), intertriginous (skin folds) dermatitis (ITD), periwound moisture-associated dermatitis and peristomal moisture-associated dermatitis. Excess moisture and the associated chemical irritants cause MASD. The difference between the four conditions is the type of moisture that induces the skin damage. Urine and faeces cause IAD, and ITD is caused by perspiration."IAD is a form of contact dermatitis. The substances responsible for causing IAD are urine and/or feces. Feces contain enzymes that damage the stratum corneum (outer layer of skin). Liquid feces causes more damage than solid feces as the enzymes are more destructive in the liquid form. The enzymes in feces also exacerbate the effects of urine on the skin, hence, incontinence of urine and feces is more damaging to the skin than either type of incontinence on its own. Skin damage is normally found in the perianal area, although it can extend further depending on the degree of the incontinence and speed with which the contaminants are removed from the skin."According to the All Wales Tissue Viability Nurse Forum, Best Practice Statement on the Prevention and Management of Moisture Lesions, September 2023, retrieved online 4/4/25 from:chrome-extension://efaidnbmnnnibpcajpcglclefindmkaj/https://www.wwic.wales/uploads/files/documents/Professionals/Clinical%20Partners/AWTVNF/All_Wales-Moisture_Lesions_final_final.pdf"To address the issues associated with the development of moisture lesions and the unacceptable consequence of inadequate continence care, the individual's skin and continence status should be assessed regularly. Early recognition and use of appropriate interventions can prevent moisture lesions from occurring in the first place. Skin should be cleansed after each episode of incontinence using pH-friendly skin cleaners and avoiding traditional soap and water, which can strip the skin. A barrier product should be used to protect vulnerable skin from contact with urine and feces. Appropriate devices to divert incontinence should be considered in patients at high risk of developing moisture lesions. Although the treatment for pressure ulcers and moisture lesions is different, patients with moisture-associated skin damage still require pressure relief. This is because the presence of moisture increases the risk of pressure damage occurring. "Individuals with incontinence may also have problems with mobility and, as a result, be at risk of developing pressure ulcers as well as moisture lesions. Consequently, when inspecting an individual's skin, it may be difficult to tell if the damage to the skin is caused by moisture alone or moisture in combination with pressure. If the skin is subjected to moisture and pressure, then the treatment strategy will have to overcome both of these insults to the skin. Therefore, along with guidance on how to prevent and manage moisture on the skin, pressure relief will be an important part of care for the individual. Repositioning together with the use of pressure-relieving equipment are the main methods of preventing pressure damage caused by extended periods of localized pressure on the skin. The use of repositioning should be considered in all at-risk individuals as a prevention strategy and should be undertaken to reduce the duration and magnitude of pressure over vulnerable areas of the body. The repositioning schedule should take into account the daily activities of the individual, their ability to tolerate pressure when in the seated and lying positions and the support surfaces in use. If a moisture lesion does not respond to interventions to minimize the effects of moisture alone, then the clinician should consider whether pressure is contributing to the damage and introduce repositioning and pressure relief into the individual's care." II. Facility policy and procedure The Pressure Injury Prevention Guidelines policy, dated 2024, was provided by the corporate nurse consultant (CNC) on 3/25/25 at 1:00 p.m. It read in pertinent part, "To prevent the formation of avoidable pressure injuries and to promote healing of existing pressure injuries, it is the policy of this facility to implement evidence-based interventions for all residents who are assessed at risk or who have a pressure injury present. "Policy Explanation and Compliance Guidelines: Individualized interventions will address specific factors identified in the resident's risk assessment, skin assessment, and any pressure injury assessment (moisture management, impaired mobility, nutritional deficit, staging, wound characteristics). The goal and preferences of the resident and/or authorized representative will be included in the plan of care." The Skin Assessment policy, dated 2024, was provided by the CNC on 3/25/25 at 1:00 p.m. It read in pertinent part, "A full body, or head to toe, skin assessment will be conducted by a licensed or registered nurse uponadmission/re-admission, daily for three days, and weekly thereafter. The assessment may also beperformed after a change of condition or after any newly identified pressure injury." III. Resident #1 A. Resident status Resident #1, age 72, was admitted on 1/28/25 and discharged 2/23/25. According to the February 2025 computerized physician's orders (CPO) diagnosis included Parkinson's disease (a disease that causes tremors), diabetes and protein deficiency. The 2/2/25 minimum data set (MDS) assessment documented the resident was cognitively intact with a brief interview for mental status (BIMS) score of 15 out of 15. The resident needed substantial to maximal assistance with bed mobility (helper does more than half the effort; and the helper lifts or holds the trunk or limbs and provides more than half the effort). The resident was dependent on staff for all transfers and position changes. The MDS assessment documented that the resident did not have any pressure injury and was not at risk for pressure injury. -However, the resident's electronic medical record (EMR) documented that the resident had MASD upon admission. B. Resident#1's representative interview Resident #1's representative was interviewed on 3/13/25 at approximately 10:00 a.m. The representative said Resident #1 did not have any open pressure injuries upon admission to the facility, but soon after admission, developed an open pressure wound that continued to worsen. The resident's representative said she did not believe that the facility was treating the resident's pressure injury properly and removed the resident from the facility after suspecting that the wound had become infected. The representative said she had the resident sent to the hospital, where the resident received treatment for a stage 3 pressure wound with a suspected infection. C. Record reviewThe resident's comprehensive care plan initiated 1/28/25 failed to document a care focus for treating the resident MASD or potential for pressure injury. Hospital discharge records, dated 1/28/25 and the 1/28/25 facility admission assessment, documented that the resident was admitted to the facility with MASD to the coccyx (base of the tailbone). The admission assessment, dated 1/28/25, revealed that the facility nursing staff assessed the resident's wound within hours of the resident's admission. The MASD measured 11 centimeters (cm) by 10 cm with no measurable depth. The wound was reddened with no open areas. The resident needed assistance with frequent repositioning as well and a pressure-reducing device was placed on the resident's bed and wheelchair. The initial skin assessment, dated 1/29/25, the resident's skin was reassessed within 24 hours of the first assessment by nursing. The nurse documented the resident had MASD on the lower coccyx region with no changes in measurement or condition. The nursing staff continued to monitor, assess and treat the resident's MASD. The skin evaluation note, dated 2/4/25, revealed the resident was assessed for a new skin issue. The nursing staff documentation revealed the resident had a skin tear with no skin loss on the coccyx at the site where MASD existed. There was no sign of infection; however, the resident expressed he had burning pain at the wound site. The note documented the resident had redness to the coccyx and a skin tear down the medial aspect of the intergluteal cleft (the groove between the buttocks). Up to this time, the resident's MASD was being treated with barrier cream and he was being encouraged to participate in frequent turning and repositioning. -There was no assessed measurement for the initial discovery of the resident's skin tear and no indication of what might have caused the skin tear. The nurse practitioner's note, dated 2/6/25, documented the resident was seen for new skin breakdown that was observed as excoriation with a small open area to the coccyx. The note revealed the resident had been refusing to turn and reposition and said it was too hard to be on him due to his Parkinson's diagnosis. The nurse practitioner recommended that the facility consider providing the resident an air mattress to help offload pressure on the resident's coccyx area. The wound care note, dated 2/6/25, documented the resident presented for a follow-up for their wound and an evaluation of MASD on the sacrum/coccyx. The note documented modifying factors included aging and impaired mobility. The MASD wound measured 2.5 cm in length by 0.3 cm in width with no measurable depth. The resident had no pain at the time of the exam. The wound bed had 100% epithelialization (development of new tissue). The periwound (skin surrounding the wound) skin texture was normal. The periwound skin moisture and color were normal. The 2/6/25 wound note also documented the resident's wheelchair cushion was evaluated and the treatment orders provided included: Cleanse and protect the wound; apply Triad cream twice a day (specialized wound care ointment to promote healing); monitor for signs and symptoms of infection; apply moisturizing cream twice a day for dry skin; and provide calorie and protein supplements per registered dietician, as needed to promote wound healing. -The wound care note failed to show evidence that the physician assessed the appropriateness of the resident's mattress for proper pressure relief. The skin evaluation note, dated 2/7/25, documented that the resident's wounds had not been assessed but included measurements of the resident's coccyx wound being 11 cm by 10 cm with no depth and no pain. -These measurements were inconsistent with the wound care specialist note dated 2/6/25 as well as the nurse practitioner notes dated 2/6/25 which revealed they had assessed the resident wound with different results (see above).. The nurse practitioner's note, dated 2/7/25, documented the resident was seen in bed. The NP observed the excoriation and the resident had a small open area on the coccyx area. Barrier cream (Triad) was applied to the area. The resident had requested lidocaine ointment (a topical pain relief medication) for gluteal breakdown pain. A new order was entered for lidocaine topical cream -apply a small amount to the affected area once a day for pain to the superior gluteal fold. The nursing note, dated 2/9/25, documented lidocaine 2% external gel was applied to the coccyx for pain at the site of skin breakdown. The CNA alerted the nurse that the coccyx and buttocks seemed to have increased redness. A skin assessment was done. It was suspected that the resident had an adverse reaction to lidocaine. It was reported to the on-call provider and the lidocaine was discontinued. The nurse practitioner note, dated 2/12/25, documented the resident was assessed for skin breakdown. The resident continued to refuse repositioning but was encouraged to reposition. The resident now has an alternating pressure mattress for coccyx excoriation/breakdown. The note documented the resident had skin breakdown to the gluteal fold with peripheral erythema upon admission, however the breakdown had worsened related to the skin's continued exposure to moisture. It was recommended for the wound care team to evaluate. Nursing was to continue to apply barrier cream to the resident wound twice a day, however the resident was resistant to being moved for skin care. -It took the facility approximately 14 days to place an alternating pressure mattress on the resident's bed despite his wound worsening and refusing turning and repositioning for pressure relief and wound care. The wound care note, dated 2/13/25, documented the resident's coccyx wound was deteriorating. It measured 3 cm length by 0.4 cm width by 0.1 cm depth with a moderate amount of serous drainage (yellowish fluid that is thicker than water). New treatment orders included daily application of calcium alginate (an absorbent dressing that preserves proper moisture level) with a bordered dressing to keep the wound protected. An alternating pressure mattress in place. The wound care note, dated 2/18/25, documented the resident's wound was not healed but was improving. The wound measured 2.0 cm length by 0.4 cm width by 0.1 cm depth. Assessment: Healing is expected to be delayed due to identified factors, including impaired mobility, inevitable effects of aging, and non-compliance. The physician note, dated 2/18/25, documented the resident's buttock/gluteal wound was assessed today, peripherally expanded, with increased central breakdown. The wound was exacerbated by the resident's urinary incontinence, refusal to allow staff to change him after incontinent episodes or provide repositioning assistance to prompt offloading of pressure points of the coccyx at the wound site. The resident said he was unable to use the urinal and could not control voiding at times. The nursing note, dated 2/22/25, documented the CNA was trying to reposition the resident on his side to offload pressure on his coccyx. The resident refused and said he did not ever need to be on his side. The nursing note, dated 2/23/25, documented the resident had a coccyx wound that did not seem to be getting better. The note documented a message was left for the on-call nursing supervisor and wound care nurse. The wound care nurse said she would follow up with the physician in the morning. The family was concerned that the resident's wound was infected and requested that the resident be transported to the hospital for further assessment. IV. Staff interviews Licensed practical nurse (LPN) #2 was interviewed on 2/24/25 at 5:35 p.m. LPN #2 said residents who were bed-bound or in bed a lot and were at risk for pressure injury should be repositioned every two hours to relieve pressure and promote healing. LPN #2 said residents who refused this type of intervention could benefit from an alternating air mattress. LPN #2 said the air mattress would continuously inflate and slightly deflate the air pressure to offload continuous pressure on one point of the body and promote some circulation throughout the body. The director of nursing (DON) was interviewed on 3/20/25 at 2:15 p.m. The DON said Resident #1 was resistant to the care that was recommended to treat his MASD, despite providing the resident education to reposition. The DON said the wound specialist and the nurse practitioner (NP) were monitoring his skin and other health needs. She said he was also being followed by therapy and nursing. The DON said the resident had a standard pressure-relieving mattress but also needed to be willing to reposition. She said, despite his refusal to reposition and accept wound care on a routine basis, the staff were expected to continue to offer him repositioning as that was most important for pressure relief and healing.
Plan of correction · submitted by the facility
Affected Resident(s):Resident #1 discharged 2/23/25. Potential Affected Resident(s):All residents identified with skin issues are at risk from this alleged deficient practice. Measures/Systematic Changes:All residents identified with skin issues will have a care plan with a care focus. Training will be provided for all nursing staff on documenting that all residents with skin issues have a care plan with interventions reassessing interventions routinely. Monitoring:DON (director of nursing) or designee will implement daily tracking log to monitor for interventions, and reassessment with each skin issue. Results of monitoring shall be reported at the facility QAPI with ongoing frequency and duration to be determined through analysis and review of results. Completion Date:04/30/2025Addendum:Monitoring will occur for a minimum of 3 months on a spreadsheet.
0744Treatment/Service for DementiaS/S D▼
Findings
Based on observations, record review, and interviews, the facility failed to ensure a resident who displayed or was diagnosed with dementia received the appropriate treatment and services to attain or maintain his or her highest practical physical, mental, and psychosocial well-being for two (#7 and #14) of three residents reviewed for dementia care out of 14 sample residents. Specifically, the facility failed to develop and implement effective dementia management-focused interventions to prevent Resident #7 and Resident #14 from wandering into other residents' rooms. Findings include: I. Facility policy and procedure The Dementia Care policy and procedure, undated, was provided by the clinical nurse consultant (CNC) on 3/25/25 at 4:31 p.m.. It read in pertinent part, "It is the policy of this facility to provide the appropriate treatment and services to every resident who displays signs of, or is diagnosed with dementia, to meet his or her highest practicable physical, mental, and psychosocial well-being.""The facility will assess, develop, and implement care plans through an interdisciplinary team (IDT) approach that includes the resident, their family, and/or resident representative, to the extent possible. Care and services will be person-centered and reflect each resident's individual goals while maximizing the resident's dignity, autonomy, privacy, socialization, independence, choice, and safety."II. Resident #7A. Resident status Resident #7, age 85, was admitted on 9/24/24. According to the March 2025 computerized physician orders (CPO), diagnoses included Alzheimer's disease, dementia with agitation, transient ischemic attack (heart attack), cerebral vascular disease (stroke) and depression. The 12/30/24 minimum data set (MDS) assessment revealed a brief interview for mental status (BIMS) assessment was not conducted because the resident was rarely or never understood. According to the staff assessment for mental status, the resident had short and long term memory problems and her cognitive skills for daily decision making were severely impaired. She required maximum assistance with personal hygiene and showering. The assessment revealed the resident wandered on one to three days during the seven day assessment look-back period. -The assessment did not reveal if the resident's wandering placed the resident at significant risk of getting to a potentially dangerous place or intruded on the privacy of others. B. Resident's representative interview Resident #7's representative was interviewed on 3/20/25 at 11:09 a.m. The representative said he visited the resident frequently. He said Resident #7 was initially on a non-secured unit at the facility. He said Resident #7 wandered into another resident's room and did not give the other resident privacy. He said the facility suggested the resident move to the secured unit because the facility was concerned the resident could leave the facility or wander into areas she did not know where she was. The representative said Resident #7 wandered in the secure unit. C. Resident observations During a continuous observation on 3/2025, beginning at 12:51 p.m. and ending at 1:46 p.m., the following observations were made:On the north side of the unit, four out of the eight residents' room doors were open. On the south side of the unit, one out of the six residents' room doors was open. At 12:51 p.m. Resident #7 was in the dining area in her wheelchair in front of a dining table. Resident #7 was surrounded by other residents who sat at the communal dining table. From 12:51 p.m. to 1:08 p.m. Resident #7 used her right hand to brush back and forth in a repetitive motion on top of the dining table. She did not have any activities to engage her. From 1:04 p.m. to 1:19 p.m., an unidentified staff member arrived at the unit. The unidentified staff member offered activities to the residents at the communal dining table. The activities included a utensil organization activity, a laundry sorting activity and a coloring activity. Each activity was offered to several residents at the communal dining table. -However, staff did not offer any of the activities to Resident #7. At 1:36 p.m., licensed practical nurse (LPN) #1 closed the open doors on the north side of the unit. During a continuous observation on 3/24/25, beginning at 10:05 a.m. and ending at 11:36 a.m., the following observations were made:On the north side of the unit, six out of the eight residents' room doors were open. On the south side of the unit, four out of the six residents' room doors were open. At 10:11 a.m. Resident #7 went into the first room on the north side of the unit. At 10:15 a.m., LPN #2 redirected Resident #7 out of the room. At 10:20 a.m., LPN #2 offered coloring to the residents sitting at the communal dining table.-However, she did not attempt to engage Resident #7 in the coloring activity. From 10:15 a.m. to 10:34 a.m. Resident #7 continued to wander in and out of the first room on the north side of the unit. At 10:38 a.m., LPN #2 closed the door to room #309. At 10:46 a.m, LPN #2 asked Resident #7 if she wanted to listen to a guitarist. LPN #2 pushed Resident #7 down to the area where a guitarist was setting up to perform. At 10:54 a.m. LPN #2 and CNA #1 took Resident #7 to her room for toileting care. At 11:02 a.m. Resident #7 was taken back to listen to the guitarist. She listened to the guitarist with her eyes closed off and on. At 11:35 a.m. LPN #2 escorted Resident #7 to the communal dining table for lunch. -During the continuous observation, LPN #2 did not attempt to offer coloring to Resident #7 and did not attempt to redirect Resident #7 out of the first room on the north side of the unit after 10:15 a.m. D. Record review Review of Resident #7's wandering care plan, revised 3/21/25, revealed the resident was at risk for wandering due to dementia and anxiety. The behavior could be triggered in the afternoon after her family left the facility. Interventions included encouraging the resident to attend activities in the morning, ensuring the area was safe, addressing wandering by walking with the resident, redirecting the resident away from inappropriate areas, offering ice cream, sitting with the resident, closing the doors of other resident's rooms and administering and monitoring the effectiveness and side effects of medications ordered. The 2/15/25 nurse progress note revealed Resident #7 wandered into another resident's room and was slightly tearful and restless but she was unable to express what was distressing her. The behavior decreased after the certified nurse aide (CNA) changed her brief. The 2/16/25 nurse progress note revealed the resident was tearful and wandered up and down the unit. The resident talked to the nurse or other residents for a while. The resident sobbed but was unable to verbalize what was bothering her or how she could be helped. The resident did not have severe agitation like yesterday (2/15/25) when the resident pushed tables, ran into residents, and knocked things down. Soft redirections were mildly effective. The resident was able to sit at the table for dinner. The 2/18/25 nurse progress note revealed Resident #7 was wandering through the unit in a wheelchair very quickly. The resident cried out, showing signs and symptoms of anxiety. The resident was inconsolable, stated she was tired and refused to lie down. The resident displayed this similar pattern daily after lunch until about 2:00 p.m. The 2/21/25 nurse progress note revealed Resident #7 was wandering the unit in a wheelchair, crying, and said she needed to go to the library. The resident attempted several times to push the door open. The resident was tearful. The resident was able to be redirected for only ten minutes at a time. The resident was offered food, fluid, folding clothes and washing tables. The resident returned to being inconsolable. The 2/28/25 nurse progress note revealed the resident wandered throughout the unit in a wheelchair. The 3/1/25 nurse progress note revealed Resident #7 had a weary expression and was tearful and wandering. The resident could not explain why she was distressed. The resident did not respond to attempts to redirect or distract. The resident was allowed to wander and given tissues when weepy. When dinner arrived, the resident was able to be redirected and ate and drank well. The 3/3/25 nurse progress note revealed the resident was exit seeking and wandering in a wheelchair. The resident was inconsolable with tears, attempting to stand by herself. The resident was able to be redirected for short periods of time. The resident was changed, offered fluid and food, and one-on-one time. The interventions worked intermittently to redirect the resident but the behavior returned. The 3/7/25 nurse progress note revealed Resident #7 was tearful, worried and wandered the unit up and down the hallway in a wheelchair. The resident was able to be redirected for short periods with fluid, food and one-on-one attention. The resident was not aware of other's space, ran over other residents' feet and toes and into their wheelchairs. The 3/9/25 nurse progress note revealed the resident started restless wandering in the afternoon, which was a common behavior for the resident. The 3/14/25 nurse progress note revealed Resident #7 was kept safe when wandering by keeping doors closed and the resident within line of sight. The 3/15/25 nurse progress note revealed the resident wandered in her wheelchair with a distressed look on her face and was tearful. She was unable to coherently verbalize what was bothering her. The resident had a pattern of tearful and distressed behavior almost every day between the hours of 12:30 p.m. to 4:30 p.m. Staff was generally unable to provide comfort, distraction or redirection. Toileting would occasionally calm her behavior but not consistently. -Review of Resident #7's progress notes revealed there was no consistent documentation regarding what interventions were used and which interventions were effective when the resident's wandering was observed. The behavior monitoring and intervention task record revealed Resident #7 was known to have anxiety after her family visited. She was known to respond well to a serving of ice cream after family visits. The resident responded well to sensory activities. The resident responded well to weighted blankets around her shoulders. If the other residents' room doors were closed, Resident #7 did not wander as much and did not try to leave the unit. -There was no documentation in the behavior task record from 3/1/25 to 3/24/25 to indicate if wandering was observed, if interventions were used, and if the interventions were effective. III. Resident #14 A. Resident status Resident #14, age greater than 65, was admitted on 7/1/24. According to the March 2025 CPO, diagnoses included Alzheimer's disease, dementia with agitation and anxiety disorder. The 1/4/25 MDS assessment revealed a BIMS assessment was not conducted because the resident was rarely or never understood. According to the staff assessment for mental status, the resident had short and long term memory problems and his cognitive skills for daily decision making were severely impaired. He required supervision for oral hygiene and moderate to substantial assistance with dressing, personal hygiene, toileting and showeringThe assessment revealed the resident wandered daily during the seven day assessment look-back period. -The assessment did not reveal if the resident's wandering placed the resident at significant risk of getting to a potentially dangerous place or intruded on the privacy of others. B. Resident observationsDuring a continuous observation on 3/24/25, beginning at 10:05 a.m. and ending at 11:36 a.m., the following observations were made:On the north side of the unit, six out of the eight residents' room doors were open. On the south side of the unit, four out of the six residents' room doors were open. At 10:12 a.m. Resident #14 went into room #309. He sat off and on the first bed and held the bed's remote control in his hand. At 10:18 a.m., Resident #14 looked through room #309's window and played with the vertical blinds on the window.-No staff observed Resident #14 in room #309 playing with the vertical window blinds of the bed controller. At 10:20 a.m., LPN #2 offered coloring to the residents sitting at the communal dining table.-However, LPN #2 did not attempt to redirect Resident #14 out of room #309 to participate in the coloring activity. At 10:21 a.m. Resident #14 left room #309 with one of the window blind slats in his hand (an individual strip once combined with others makes a window blind). He walked to the nurse's station and left the window blind slat at the nurse's station. At 10:33 a.m. Resident #14 walked in and out of the second-to-last room on the south side of the unit. At 10:34 a.m. Resident #14 walked in and out of room #309. At 10:38 a.m. LPN #2 closed the door to room #309. At 10:50 a.m. Resident #14 sat on the couch where the guitarist was setting up to perform. He sat on the couch and listened to the with his eyes closed. At 11:27 a.m. Resident #14 joined the other residents at the communal dining table for lunch. -During the continuous observation of Resident #14, LPN #2 did not attempt to offer coloring to the resident, did not redirect Resident #14 out of Room #309and did not ask Resident #14 if he wanted to listen to the guitarist. C. Record review Review of Resident #14's behavior care plan, revised 7/4/24, revealed the resident wandered. The interventions included eliciting family input for the best appropriate approaches. The 2/13/25 social services note revealed Resident #14 pushed on the door trying to leave the unit after a visitor left the unit. The resident was easily redirectable. The 2/14/25 nurse progress note revealed the resident attempted to push, pull and shove doors open on the unit to the outside hallway and outside patio. The 2/18/25 nurse progress note revealed Resident #14 pushed on doors with his hands and used his hands to push against the door. The 2/25/25 nurse progress note revealed the resident pushed and pulled on doors and was able to be redirected with snacks. The 3/3/25 nurse progress note revealed Resident #14 wandered the unit and pushed and pulled on doors. The 3/7/25 nurse progress note revealed the resident pushed and pulled on doors to the outside and was exit-seeking consistently throughout the day. The 3/11/25 nurse progress note revealed Resident #14 pushed and pulled on doors, wandered the unit and checked doors. The 3/14/25 nurse progress note revealed the resident pushed and pulled on doors, wandered to multiple doors, trying them over and over. The 3/18/25 nurse progress note revealed Resident #14 pushed and pulled on doors and wandered up and down the unit, trying each door. -Review of Resident #14's progress notes revealed there was no consistent documentation regarding what interventions were used and which interventions were effective when the resident's wandering was observed. Review of Resident #14's behavior monitoring and intervention task record revealed the resident had wandering behaviors and had exit-seeking behaviors. -There was no documentation in the behavior task record from 3/1/25 to 3/24/25 to indicate if wandering was observed, if interventions were used and if the interventions were effective. IV. Staff interviews LPN #2 was interviewed on 3/24/25 at 2:50 p.m. LPN #2 said she worked mostly in another unit. She said if a resident wandered, she kept an eye on the resident, tried to keep the resident out of other residents' rooms and provided activities to the resident. She said it was important to have interventions for residents who wandered because it helped the residents stay out of other residents' rooms and provided the residents with a purpose. She said one intervention was keeping the resident rooms' doors closed. She said it was an intervention because it prevented one resident from going through another resident's belongings. She said residents who wandered could take another resident's belongings and the items went missing. LPN #2 said she knew if a resident was a wanderer through verbal shift change reports, looking at the resident's care plan, utilizing the Kardex (an abbreviated care plan) and reading report sheets. LPN #2 said she did not document every time a resident wandered into the unit. She said she documented if the resident went into other residents' rooms and if the resident exhibited anxiety or agitation when they wandered. She said she documented her observations as a progress note. LPN #2 said she was familiar with Resident #7. She said night shift staff reported to her that Resident #7 wandered at night and offering ice cream was an effective intervention. LPN #2 said she did not know Resident #14 very well. She said he was wandering today (3/24/25). She said he sat down and watched television after lunch and that helped him not to wander. The CNC was interviewed on 3/24/25 at 5:10 p.m. The CNC said if staff saw a resident wandering into another resident's room, the staff should redirect the resident who was wandering out of the room. She said it was important to redirect the resident because the resident did not have the right to go into another resident's room without an invitation. She said interventions for residents were person-centered and included keeping other residents' doors closed if they were in the communal area, offering activities, walking with the resident and redirecting the resident. She said interventions were important because they kept the resident from going into other residents' rooms. The CNC said nursing knew if a resident wandered during their orientation period and by looking at the resident's care plan and the Kardex. The CNC said if the resident was in the secured unit, there was a level of wandering for all residents who lived in the unit. She said staff also knew if a resident wandered by reviewing a 24-hour report and when they received a verbal report from the previous shift nurse. She said if the resident exhibited new wandering or if the resident went into another resident's room, the nurse should document it as a progress note. The CNC said the interdisciplinary team (IDT) discussed residents' wandering behaviors in order to develop a person-centered intervention for residents. She said she was not familiar with Resident #7. She said she did not know the residents' room doors were left open on the secure unit, and she did not know activities were not offered to Resident #7. She said she was not familiar with Resident #14. She said the staff should have redirected Resident #14 when he was in other residents' rooms. She said the facility was working on additional dementia training in the future for the nursing staff.
Plan of correction · submitted by the facility
Plan of Correction Components: -Preparation, submission and implementation of this Plan of Correction does not constitute an admission of, or agreement with the facts and conclusions in the statement of deficiencies. This Plan of Correction is prepared and executed as a means to continuously improve the quality of care, to comply with all applicable state and federal regulatory requirements and it constitutes the facility’s allegation of compliance. Affected Resident(s):R#7 and R #14 were allegedly wondering in other residents’ rooms. The residents were redirected away from the rooms. Potential Affected Resident(s):All residents who reside on memory care are at risk for this alleged deficient practice an audit will be conducted of each resident to identify those who wander and review interventions for effectiveness. Measures/Systematic Changes:Training will be provided for care staff on memory care to use identified interventions and engage in activities. Monitoring:DON or designee will audit 3 times per week for use of interventions for 12 weeks results of monitoring shall be reported at the facility QAPI via a spreadsheet with ongoing frequency and duration to be determined through analysis and review of results. Completion Date:04/30/2025
0835AdministrationS/S F▼
Findings
Based on record review and interviews, the facility failed to ensure facility resources were administered in a manner that allowed its resources to be used effectively and efficiently to attain or maintain the highest practicable physical, mental, and psychosocial well-being of each resident in the facility. Specifically, the facility failed to:-Provide sufficient leadership to address and or avoid multiple concerns; -Prevent, report and fully investigate allegations of abuse timely to provide immediate protections to residents at risk of being victimized and re-victimized; -Report an injury of unknown origin in a timely manner so that an accurate timeline of events could be established and the injury could be effectively treated and monitored; and,-Implement effective interventions to prevent a female resident with severely impaired cognitive and an inability to consent to a sexual relationship from wandering into a male resident's room to watch him masturbate. Findings include:I. Abuse and neglectDuring the abbreviated survey from 3/19/25 to 3/24/25, it was identified that there were concerns over the timely reporting of an allegation of abuse so that the resident could be immediately protected from a repeat incident of abuse. While staff immediately separated the assailant from his victims in an incident of sexual abuse, the staff did not immediately alert facility leadership so that immediate interventions could be implemented to prevent repeated attempts of abuse by the assailant. Facility leadership were not immediately notified of the incident of sexual abuse occurring. Additionally, the staff's late notifications and failure to identify the incident of sexual abuse as a reportable incident of abuse led to delays in reporting the incident to the proper entities (facility administration, the State Agency and the local police). In this instance of sexual abuse, once the incident was reported to the local police, the resident was arrested and taken to jail for his abusive actions. Cross-reference F609: failure to report an allegation of abuse in a timely manner. II. Injury of unknown originDuring the abbreviated survey from 3/19/25 to 3/24/25, it was identified that there were concerns over the timely reporting of a discovered injury of unknown origin to Resident #7. On 3/2/25, the resident's family member reported swelling, bruising and pain to the nurse on duty. While the injury was documented in the resident's electronic medical record (EMR), the injury was not reported to facility leadership until the injury worsened three days later. There was no record that the injury was monitored for proper healing. The investigation and assessment of the injury started late; it was discovered through the assessment that the resident's fingers were found to be broken (cross-reference F609: failure to report an injury of unknown origin and F658: failure to monitor an injury per professional standards). III. Leadership effortsThe facility nursing home administrator (NHA) had been out on administrative leave since 1/31/25 (seven weeks as of 3/20/25), leaving the facility without a state-licensed administrator to manage the facility's day-to-day operations, particularly the management of incident reporting and investigations. The NHA had the responsibility to lead investigations for allegations of abuse to ensure compliance with identifying potential abuse; responding to an allegation of abuse; preventing ongoing abuse; and reporting abuse to the proper authority, all in a timely manner. IV. Staff interviewsThe director of nursing (DON) was interviewed on 3/19/25 at 12:05 p.m. The DON said the NHA was on administrative leave and she did not know if he was coming back to his position. The DON said the corporate consultants had been providing additional guidance in his absence, but she had taken on the role of abuse incident coordinator. The DON said it was difficult to manage the role of abuse incident coordinator, with all of her other duties. The DON and the corporate nurse consult (CNC) were interviewed on 3/20/25 at 3:11 p.m. The CNC said there was not currently an interim NHA with a state license filling in in the absence of the facility's NHA; however, the corporate office was looking for an interim NHA. The CNC said in the meantime, the CNC and other corporate leadership offered the DON and facility staff support onsite and remotely. The DON said she was acting as the facility abuse coordinator in the absence of the NHA, with assistance from the unit managers and social services staff, to determine needed interventions and complete abuse investigations. The DON said she would be glad to have someone take over the role of abuse coordinator because it was a lot to manage with her clinical duties. The DON said she did not report Resident #7's injury of unknown origin because she knew the resident and even though no one witnessed the injury occur, she assumed the injury was self-inflicted. The DON said she was not well-versed in the regulatory requirements for reporting and investigating abuse and was not able to give details on all types of incidents that needed to be reported. The DON said she did not know that injuries of unknown origin needed to be reported when the source of the injury was not observed, the injury could not be explained, and the injury was suspicious because of the extent of the injury or the location of the injury. V. Follow upThe facility hired a full-time interim nursing home administrator (INHA) on 3/24/25. The INHA had an active State NHA license and prior experience in the industry-An interview with the INHA revealed that she and the CNC had already started training with leadership staff on the components of compliance for abuse identification, reporting, prevention and investigating.
Plan of correction · submitted by the facility
Plan of Correction Components: -Preparation, submission and implementation of this Plan of Correction does not constitute an admission of, or agreement with the facts and conclusions in the statement of deficiencies. This Plan of Correction is prepared and executed as a means to continuously improve the quality of care, to comply with all applicable state and federal regulatory requirements and it constitutes the facility’s allegation of compliance. The community obtained an interim NHA (nursing home administrator) 03/24/2025. The current NHA is on LOA.All residents who report abuse, neglect or exploration are at risk of this alleged deficient practice. Cross reference - audits for F609 for abuse, neglect and exploitation. All staff will be trained regarding timeliness of reporting. The interim NHA, DON and UM (unit manager) will participate in CHCA abuse training. NHA or designee will audit for timeliness of reporting with each alleged allegation on a spreadsheet. Results will be managed with QAPI monthly for 3 months. Addendum:Interim NHA is fulltimeCorporate will monitor by dialing into the community or being present at community to verify NHA participating and directing facility operations. Corporate will document on shared spreadsheet.
2/24/2025Complaint Survey · ID LHCP111 deficiency▼
0000INITIAL COMMENTSSurveyor note▼
Findings
A complaint survey, prompted by Incident #38918, Incident #38952, Incident #39147 and Incident #39149 was conducted on 2/20/25 to 2/24/25. One deficiency was cited.
Plan of correction
The state did not require a plan of correction for this citation.
0610Investigate/Prevent/Correct Alleged ViolationS/S D▼
Findings
Based on record review and interviews, the facility failed to investigate an allegation of physical abuse for two (#10 and #11) of six residents reviewed out of 11 sample residents. Specifically, the facility failed to thoroughly investigate alleged abuse between Resident #10 and Resident #11. Findings include: I. Facility policy and procedure The Abuse, Neglect and Exploitation policy, dated October 2024, was provided by the director of nursing (DON) on 2/25/25 at 1:48 p.m. via email. It read in pertinent part,"Abuse is defined as the willful infliction of injury with resulting physical harm, pain or mental anguish, which can include resident to resident altercations. Instances of abuse of all residents, irrespective of any mental or physical condition, cause physical harm, pain or mental anguish. "Physical abuse includes, but is not limited to, hitting, slapping, punching, biting, and kicking. "Alleged violation is a situation or occurrence that is observed or reported by staff, residents, relatives, visitors or others but has not yet been investigated and, if verified, could be indication of noncompliance with the federal requirements related to abuse."The facility will develop and implement written policies and procedures that establish policies and procedures to investigate any such allegations."An immediate investigation is warranted when suspicion, or reports, of abuse occur."Written procedures for investigations include identifying staff responsible for the investigation, identifying and interviewing all involved persons, including the alleged victim, alleged perpetrator, witnesses, and others who might have knowledge of the allegations, focusing the investigation on determining if the abuse occurred, the extent, and cause and providing complete and thorough documentation of the investigation."II. Resident #10 - assailant A. Resident statusResident #10, age greater than 65, was admitted on 3/15/19. According to the February 2025 computerized physician orders (CPO), diagnoses included Alzheimer's disease and dementia with behavioral disturbance. The 12/9/24 minimum data set (MDS) assessment revealed the resident had severe cognitive impairment with a brief interview for mental status (BIMS) score of one out of 15. She required set-up/clean-up assistance for dressing, oral hygiene, and eating, and supervision for toileting and personal hygiene. She used a manual wheelchair for mobility. B. Record reviewA nursing progress note, dated 2/17/25, revealed Resident #10 was involved in an altercation with another resident over a pack of wet wipes. Resident #10 grabbed the other resident's hand hard and dug her nails into the resident. Both residents were free of harm and injury and were separated. An interdisciplinary team note (IDT), dated 2/19/25, revealed Resident #10 was aggravated by another resident. The other resident (Resident #11) had a pack of wet wipes and Resident #10 wanted them. The other resident (Resident #11) pulled away and Resident #10 grabbed her arm, digging her nails into her arm. Staff immediately removed Resident #10 and kept the two residents separated for several hours.-The 2/17/25 nursing progress note, the 2/19/25 IDT note and the facility investigation revealed conflicting information regarding the incident, whether it was the resident's hand versus her arm that was grabbed (see facility investigation below). III. Resident #11 - victimA. Resident statusResident #11, age greater than 65, was admitted on 11/4/22. According to the February 2025 CPO, diagnoses included Alzheimer's disease and dementia with behavioral disturbance. The 2/3/25 MDS assessment revealed the resident had short term and long term memory problems and had severely impaired cognition and decision-making skills per staff assessment. She required substantial assistance from staff for most activities of daily living (ADL), set-up/clean-up assistance with eating and moderate assistance with toileting. She used a manual wheelchair for mobility. B. Record reviewA nursing progress note, dated 2/17/25, revealed Resident #11 was in a resident to resident altercation that afternoon (2/17/25). Resident #11 had a pack of wet wipes that another resident (Resident #10) wanted. Resident #11 did not give up the wipes, so the other resident (Resident #10) grabbed Resident #11's arm and dug her fingernails into her arm. The two residents were okay and separated. There were no new skin issues. The family and unit manager were aware of the altercation. -However, the investigation had revealed Resident #11's hand was grabbed (see investigation below). A skin check, completed on 2/19/25, revealed no new skin concerns. IV. Facility investigation The investigation of the altercation was provided by the DON on 2/20/25 at approximately 3:00 p.m. The investigation documented that on 2/17/25 at 2:28 p.m. Resident #10 grabbed Resident #11's hand and dug her nails into her skin. The two residents were immediately separated by certified nurse aide (CNA) #1 and were closely monitored. A skin check was performed on Resident #11 with no injuries noted. The residents' providers, resident representatives and the local police department were notified of the incident. Registered nurse (RN) #1, licensed practical nurse (LPN) #1 and CNA #1 were interviewed.-The facility was unable to provide documentation of interviews with other residents who may have witnessed the altercation. The conclusion of the investigation revealed that Resident #10 and Resident #11 were friends who socialized often. The altercation occurred because both residents were cognitively impaired and could not verbalize their needs. D. Staff interviewsCNA #1 was interviewed on 2/24/25 at 4:20 p.m. CNA #1 said she was in the dining room near the residents when the altercation occurred. She said she was talking to other residents when she heard Resident #11 yell, "No!" CNA #1 looked over to see Resident #10 had grabbed Resident #11's left arm. She said afterwards, the two residents were separated. She said Resident #10 was agitated and said, "that was horrible." CNA #1 said Resident #10 rarely got agitated and she had never seen her do anything like that before. She said she thought Resident #11's yelling triggered Resident #10. RN #1 was interviewed by phone on 2/24/25 at 5:04 p.m. RN #1 said she saw video footage of the altercation. She said Resident #10 was originally at another table. She said a resident was shaking Resident #10's wheelchair wheels and agitating her. She said Resident #10 was then moved to a table with her friend, Resident #11. RN #1 said she thought because Resident #10 was already agitated, she lashed out and grabbed Resident #11's right arm. -However, the investigation revealed Resident #11's hand was grabbed, while the 2//17/25 nursing progress revealed the resident's arm was grabbed. RN #1 said she did not think Resident #10's behavior was directed at Resident #11. RN #1 said that when she left work on 2/19/25 (two days after the altercation), Resident #11 had no evidence of injury. The DON was interviewed on 2/24/25 at 5:42 p.m. The DON said she had been temporarily taking over the position of nursing home administrator (NHA), since their NHA was on leave. The DON said she normally started investigating a resident to resident altercation immediately. She said she would interview others and get statements. She said this particular investigation was very short because Resident #10 and Resident #11 were friends and there was no injury.
Plan of correction · submitted by the facility
Preparation, submission and implementation of this Plan of Correction does not constitute an admission of, or agreement with the facts and conclusions in the statement of deficiencies. This Plan of Correction is prepared and executed as a means to continuously improve the quality of care, to comply with all applicable state and federal regulatory requirements and it constitutes the facility’s allegation of compliance. Affected Resident(s):R11 had a skin check the day of, the day after and day five following the incident and the bruise did not appear until day seven and was deemed unrelated to the incident. R11 has had weekly skin checks and has had some additional findings related to aspirin therapy and self reported “bumping” hands and arms. Care plan notes R11 is prone to bruising. The nursing assistant, nurse manager and nurse on the unit all provided statements regarding what they witnessed at the time of the incident, which was added to the investigative file. Potential Affected Resident(s):All residents have weekly skin checks as part of routine care and any reported changes are investigated. All incidents will be thoroughly investigated including witness statements. Measures/Systematic Changes:The Abuse, Neglect and Exploitation Policy was reviewed and remains current. All staff received education regarding the Abuse, Neglect and Exploitation Policy. Any staff member who missed initial training will receive training prior to the start of their next scheduled shift. The interdisciplinary team received education on the components of a thorough investigation and will ensure all components are completed with any identified incident. The 24-hour report is reviewed each business day and reviewed for any potential incident. All reported risk incidents will be reviewed for completion of the components of a thorough investigation. Monitoring:Audits of all risk incidents for completion of the components of a thorough investigation will be reviewed for twelve weeks. Protective action taken, Review of medical record, resident assessed and interviewed, staff interviewed, roommate interviewed if applicable, expanded risk group to other residents who could have been impacted. The Administrator, DON, Social Service Director or designee are responsible for compliance. Results of monitoring shall be reported at the facility Quality Council meeting with ongoing frequency and duration to be determined through analysis and review of results. Monitoring will be documented via a spreadsheet. Completion Date:03/21/2025
Reportable Occurrences
60 records5/24/2026Physical Abuse · ID 26020429006Reported on time: Yes▼
Occurrence summary
SUMMARY OF FINDINGS:On 5/24/26, the healthcare entity investigated a reportable event. The facility acted appropriately to protect their clients by taking immediate protective actions, investigating the event, and implementing a plan to help prevent a future recurrence. The healthcare entity reported physical abuse of a client. Reportedly, client (B) hit client (A) in the nose. During the course of the investigation, the healthcare entity notified law enforcement, assessed the client, conducted interviews, and reviewed video footage. Client (A) did not have any visible injuries and gave varying accounts of the event Client (B) denied the allegations. Video footage showed that client (B) did not hit or attempt to hit client (A). The facility initiated a plan to keep the clients separated in the dining room and completed an updated mental status evaluation for client (A). The event was not substantiated. This public occurrence summary was provided in accordance with 25-1-124, C.R.S., and was based on the report and investigation provided by the licensed healthcare entity. Department investigation of this occurrence was conducted off-site. The healthcare entity occurrence report was submitted within the required timeframe.
Publication
Sent to facility 7/15/2026 · released to the public 7/22/2026.
3/25/2026Physical Abuse · ID 26020429004Reported on time: Yes▼
Occurrence summary
SUMMARY OF FINDINGS:On 3/25/26, the healthcare entity investigated a reportable event. The facility acted appropriately to protect their clients by taking immediate protective actions, investigating the event, and implementing a plan to help prevent a future recurrence. The healthcare entity reported a physical abuse event. Reportedly, client (B) wheeled into client (A)'s room, which upset client (A). Client (A) confronted client (B), and in response, client (B) kicked client (A) causing a skin abrasion. Staff intervened to separate the clients. During the course of the investigation, the healthcare entity conducted assessments and interviews, notified the police and implemented a monitoring plan for peer safety. Staff provided first aid treatment to client (A), and the event was substantiated. This public occurrence summary was provided in accordance with 25-1-124, C.R.S., and was based on the report and investigation provided by the licensed healthcare entity. Department investigation of this occurrence was conducted off-site. The healthcare entity occurrence report was submitted within the required timeframe.
Publication
Sent to facility 6/22/2026 · released to the public 6/29/2026.
2/2/2026Neglect · ID 26020429003Reported on time: Yes▼
Occurrence summary
SUMMARY OF FINDINGS:On 2/3/26, the healthcare entity investigated a reportable event of neglect of two clients. Reportedly, staff #1 delayed providing medications to client (A) and left client (B) without properly flushing their catheter. During the course of the investigation, the healthcare entity suspended staff #1, assessed the clients, conducted interviews, and reviewed records. Neither client experienced pain nor harm due to the delay in receiving services. Both clients reported staff #1 delayed providing care each client became frustrated with staff #1 and had brief verbal exchanges. The facility determined staff #1 demonstrated poor customer service and both clients ultimately received the needed care although the care was delayed. Staff #1’s employment was terminated. The event was not substantiated. This public occurrence summary was provided in accordance with 25-1-124, C.R.S., and was based on the report and investigation provided by the licensed healthcare entity. The department review of the occurrence investigation was conducted off-site. The healthcare entity occurrence report was submitted within the required timeframe. In addition, this event has been identified for further investigation by the Department. An onsite investigation was conducted by a representative from the State agency. For results of that on-site investigation, please reference https://cdphe.colorado.gov/find-and-compare-facilities, specifically the inspection dated 4/30/26, Event ID 22F6C0-H1.
Publication
Sent to facility 5/26/2026 · released to the public 6/2/2026.
1/14/2026Physical Abuse · ID 26020429002Reported on time: Yes▼
Occurrence summary
SUMMARY OF FINDINGS:On 1/14/26, the healthcare entity investigated a reportable event. The facility acted appropriately to protect their clients by taking immediate protective actions, investigating the event, and implementing a plan to help prevent a future recurrence. The healthcare entity reported physical abuse of a client. The client’s family called law enforcement and reported the client had been beaten causing them to lose the ability to walk or talk. During the course of the investigation, the healthcare entity assessed the client, conducted interviews, and reviewed records. The client had no bruising or injuries nor any signs of pain. Due to cognitive impairment the client could not participate in the interview process. Record review showed the client has numerous chronic conditions and receives hospice services. Record review also revealed a steady decline in the client’ abilities which was attributed to the chronic conditions. The facility determined the client had not been beaten or abused. The facility implemented increased safety monitoring and reviewed the care plan. The event was not substantiated. This public occurrence summary was provided in accordance with 25-1-124, C.R.S., and was based on the report and investigation provided by the licensed healthcare entity. Department investigation of this occurrence was conducted off-site. The healthcare entity occurrence report was submitted within the required timeframe.
Publication
Sent to facility 5/14/2026 · released to the public 5/21/2026.
12/17/2025Physical Abuse · ID 25020429007Reported on time: Yes▼
Occurrence summary
SUMMARY OF FINDINGS: On 2/18/25, the healthcare entity investigated a reportable event. The facility acted appropriately to protect their clients by taking immediate protective actions, investigating the event, and implementing a plan to prevent a future recurrence. The healthcare entity reported physical abuse of client (A) by client (B). During the course of the investigation, the healthcare entity separated the clients and monitored them closely after client (B) dug her nails into client’s (A) hand after she took a box of wet wipes. The clients were assessed with no harm or injuries. Due to both clients’ medical conditions, they could not recall the incident. The event was substantiated and care plans were updated. This public occurrence summary was provided in accordance with 25-1-124, C.R.S., and was based on the report and investigation provided by the licensed healthcare entity. Department investigation of this occurrence was conducted off-site. The healthcare entity occurrence report was submitted within the required timeframe.
Publication
Sent to facility 4/28/2025 · released to the public 5/5/2025.
12/12/2025Physical Abuse · ID 25020429050Reported on time: Yes▼
Occurrence summary
SUMMARY OF FINDINGS:On 12/12/25, the healthcare entity investigated a reportable event. The facility acted appropriately to protect their clients by taking immediate protective actions, investigating the event, and implementing a plan to help prevent a future recurrence. The healthcare entity reported physical abuse of a client. Staff witnessed client (B) hit client (A) in the chest with the back of their hand. During the course of the investigation, the healthcare entity separated the clients prior to notifying law enforcement, assessed the client, conducted interviews, and started increased safety monitoring. Client (A) did not have visible injuries nor did they recall the event. The facility determined contact occurred when one client became agitated with the other, but did not result in pain or injury to either client. The facility completed a medication review and educated staff to keep the clients separated. The event was not substantiated. This public occurrence summary was provided in accordance with 25-1-124, C.R.S., and was based on the report and investigation provided by the licensed healthcare entity. Department investigation of this occurrence was conducted off-site. The healthcare entity occurrence report was submitted within the required timeframe.
Publication
Sent to facility 3/17/2026 · released to the public 3/25/2026.
10/10/2025Physical Abuse · ID 25020429049Reported on time: Yes▼
Occurrence summary
SUMMARY OF FINDINGS:On 10/10/25, the healthcare entity investigated a reportable event. The facility acted appropriately to protect their clients by taking immediate protective actions, investigating the event, and implementing a plan to help prevent a future recurrence. The healthcare entity reported physical abuse of a client. When a bruise was discovered on the client's shoulder, they reported it occurred when staff helped them get up. During the course of the investigation, the healthcare entity suspended staff, notified law enforcement, conducted interviews, and assessed the client. The client could not describe anything specific about what happened, denied staff harming them, and reported they bumped their shoulder. Record review showed the client takes a medication that causes an increase in bruising. The facility determined the client may have bumped their shoulder when they were being placed in the lift or being lowered. The facility started using a different type of lift for the client and educated staff. The event was not substantiated. This public occurrence summary was provided in accordance with 25-1-124, C.R.S., and was based on the report and investigation provided by the licensed healthcare entity. Department investigation of this occurrence was conducted off-site. The healthcare entity occurrence report was submitted within the required timeframe.
Publication
Sent to facility 1/26/2026 · released to the public 2/2/2026.
10/1/2025Physical Abuse · ID 25020429047Reported on time: Yes▼
Occurrence summary
SUMMARY OF FINDINGS:On 10/1/25, the healthcare entity investigated a reportable event. The facility acted appropriately to protect their clients by taking immediate protective actions, investigating the event, and implementing a plan to help prevent a future recurrence. The healthcare entity reported physical abuse of a client. Staff witnessed client (B) strike client (A) on the back after client (A) accidentally ran over the foot of client (B). During the course of the investigation, the healthcare entity separated the clients prior to notifying law enforcement, conducted interviews, and assessed the clients. Due to cognitive impairment neither client recalled the event and neither sustained visible injuries. The facility determined physical contact occurred but did not result in pain or injury. The facility reviewed care plans. The event was not substantiated. This public occurrence summary was provided in accordance with 25-1-124, C.R.S., and was based on the report and investigation provided by the licensed healthcare entity. Department investigation of this occurrence was conducted off-site. The healthcare entity occurrence report was submitted within the required timeframe.
Publication
Sent to facility 1/8/2026 · released to the public 1/15/2026.
8/12/2025Sexual Abuse · ID 25020429042Reported on time: Yes▼
Occurrence summary
SUMMARY OF FINDINGS:On 8/13/25, the healthcare entity investigated a reportable event. The facility acted appropriately to protect their clients by taking immediate protective actions, investigating the event, and implementing a plan to help prevent a future recurrence. The healthcare entity reported sexual abuse of a client. The client alleged staff touched them inappropriately in their private area. During the course of the investigation, the healthcare entity suspended both potential alleged assailants, conducted interviews and notified law enforcement. The client was unable to provide additional information due to cognitive impairment, had no visible injuries, and was emotionally distressed. Staff indicate they checked the clients brief and provided peri care during their shift and denied any inappropriate touching. The facility determined staff did not touch the client inappropriately, but rather provided necessary incontinence care. The facility provided the client with daily emotional support and staff did not return to work from their suspension. The event was not substantiated. This public occurrence summary was provided in accordance with 25-1-124, C.R.S., and was based on the report and investigation provided by the licensed healthcare entity. Department investigation of this occurrence was conducted off-site. The healthcare entity occurrence report was submitted within the required timeframe.
Publication
Sent to facility 12/10/2025 · released to the public 12/17/2025.
8/8/2025Physical Abuse · ID 25020429040Reported on time: Yes▼
Occurrence summary
SUMMARY OF FINDINGS:On 8/8/25, the healthcare entity investigated a reportable event of physical abuse of a client. This occurrence has been identified for further investigation by the Department. An onsite investigation was conducted by a representative from the State agency. For results of that on-site investigation, please reference https://cdphe.colorado.gov/find-and-compare-facilities, specifically the inspection dated 10/9/25, Event ID 1S9X11. This public occurrence summary was provided in accordance with 25-1-124, C.R.S., and was based on the report and investigation provided by the licensed healthcare entity. The department investigation of this occurrence was also conducted offsite. The healthcare entity occurrence report was submitted within the required timeframe.
Publication
Sent to facility 11/25/2025 · released to the public 12/2/2025.