16
Inspections
24
Deficiencies
0
Actual Harm or Above
2
Occurrences
June 25, 2026
Last Inspection
S/S D/E/F Potential for harm

The most recent inspection of ADVANCED HEALTH CARE OF COLORADO SPRINGS on record is dated June 25, 2026. Across 16 published inspections, state surveyors cited 24 deficiencies, none of which reached the actual-harm level.

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 (Medicare Only)
Administrator
Beckman, Robert
Owner
AHC OF COLORADO SPRINGS, LLC
Phone
(719) 418-4500
Payor Source
Medicare, Private Pay
City
COLORADO SPRINGS
ZIP
80910-3145

Inspections & Citations

16 inspections · 24 deficiencies
6/25/2026Complaint, Recertification Survey · ID 2363E8-H1No deficiencies
0000INITIAL COMMENTSSurveyor note2 building records
Findings · record 1 of 2
A recertification survey with complaint #CO2655907 was completed on 6/22/26 to 6/25/26. No deficiencies were cited.
Findings · record 2 of 2
An Emergency Preparedness survey was conducted from 6/22/26 to 6/25/26. No deficiencies were cited.
Plan of correction
The state did not require a plan of correction for this citation.
6/25/2026Licensure Complaint, Re-Licensure Survey · ID 2363F7-H1No deficiencies
0000Initial CommentsSurveyor note
Findings
A licensure survey with #CO3046143 was completed on 6/22/26 to 6/25/26. No deficiencies were cited.
Plan of correction
The state did not require a plan of correction for this citation.
12/30/2024Revisit: Recertification Survey · ID NPBN22No deficiencies
0000INITIAL COMMENTSSurveyor note
Findings
A document revisit was completed with all deficiencies being corrected with the exception of any waived deficiency or deficiencies. All waived deficiencies will be corrected at a later date as per the approved waiver. A plan of correction is not required.
Plan of correction
The state did not require a plan of correction for this citation.
9/11/2024Recertification Survey · ID NPBN2112 deficiencies
0000INITIAL COMMENTSSurveyor note
Findings
The Initial Comments (ID Tag K0000) are informational only and are a representation of the facility's general characteristics. The Colorado Division of Fire Prevention and Control conducted this survey in accordance with the Federal Register at Section 42 CFR 483.70 (a). The building is a one story wood framed structure, Type V (111). The facility is classified as fully protected by a National Fire Protection Association (NFPA) 13 automatic sprinkler system. The facility 's fire sprinkler system is a wet and a dry system. This survey of the 34 bed facility was conducted on September 11, 2024 for compliance with the NFPA 101 Life Safety Code, Chapter 19 Existing Health Care Occupancies and Referenced Publications. The facility will meet these requirements with the correction of the deficiencies listed herein. The following deficiencies were discussed with the facility Administrator during the exit conference.
Plan of correction
The state did not require a plan of correction for this citation.
0223Doors with Self-Closing DevicesS/S D
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 Section 19.3.2.11. Dry storage fire door is chained to be held open. Life Safety Code Section 19.3.2.1 requires that sprinkler-protected hazardous areas be separated from other spaces by smoke-resisting construction. Doors installed to protect hazardous areas must be self-closing or automatic closing. This deficiency has the potential to affect occupants, who might include residents, staff, and visitors throughout the facility. The maintenance team discussed deficient items at the exit cinterview.
Plan of correction · submitted by the facility
Resident Specific:Please see systemic changesOther Residents:Please see systemic changesSystemic Changes:Chain and latch have been removed from self-closing door in Kitchen dry storage area. Monitors:Photos taken to confirm Chain Removed. Administrator or designee will report findings at QA meeting and will make changes to the above plan of correction as needed. Date of Compliance: September 24th 2024
0291Emergency LightingS/S D
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 1011. Emergency light in generator enclosure are unable to be tested. NFPA 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. This deficiency has the potential to affect occupants, who might include residents, staff, and visitors within the entire facility. Deficient items were discussed with the administrator and maintenance director at the exit conference.
Plan of correction · submitted by the facility
Resident Specific:Please see systemic changesOther Residents:Please see systemic changesSystemic Changes:New testable outdoor emergency lighting installed in generator area. Monitors:Photos taken to confirm light installed. Will be added to regular testing with other emergency lighting in facility. Administrator or designee will report findings at QA meeting and will make changes to the above plan of correction as needed. Date of Compliance: October 1st 2024
0321Hazardous Areas - EnclosureS/S E
Findings
Based on observation and staff interview during the course of the survey it was determined the facility failed to maintain hazard areas in accordance with NFPA 101 1. Fire stopping systems needed for penetrations along conduit and wiring in ceiling. (Areas ID'd During Survey) 2. Pin hole penetrations in fire stopping systems throughout the mechanical room. 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 8.3Protecting the area with automatic extinguishing systems in accordance with Section 9.7Applying both 8.7.1.1(1) and (2) where the hazard is severe or where otherwise specified by Chapters 11 through 43This deficiency has the potential to affect occupants, who might include residents, staff, and visitors within the entire facility. Deficient items were discussed with the Administrator and Maintenance director at the exit conference.
Plan of correction · submitted by the facility
Resident Specific:Please see systemic changesOther Residents:Please see systemic changesSystemic Changes:Fire Caulking applied to wiring in server room that had not been caulked at install. Pin hole areas identified in existing fire caulking in electrical room have been appropriately filled. Monitors:Photos taken to confirm all caulking areas identified during inspection have been corrected. Administrator or designee will report findings at QA meeting and will make changes to the above plan of correction as needed. Date of Compliance: September 30th 2024
0324Cooking FacilitiesS/S D
Findings
Based on observation it was determined that the facility failed to maintain the kitchen hood suppression system as required by NFPA 101(chapter 19, section 19.3.2.5.3),National Fire Protection Association (NFPA) Standard 96. 1. Missing approved method for securing cooking appliances on casters underneath hood. 2. Missing documentation of kitchen hood suppression inspection 3. Therapy Kitchen needs approved hood system. 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. 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 semiannuallyNFPA 96 14.7 Fire-Extinguishing Equipment for Solid Fuel Cooking. 14.7.1 Solid fuel cooking appliances that produce grease-laden vapors shall be protected by listed fire-extinguishing equipment. 14.7.2 Where acceptable to the authority having jurisdiction, solid fuel cooking appliances constructed of solid masonry or reinforced portland or refractory cement concrete and vented in accordance with NFPA 211 shall not require fixed automatic fire-extinguishing equipment. 14.7.3 Listed fire-extinguishing equipment shall be provided for the protection of grease removal devices, hoods, and duct systems. 14.7.4 Where acceptable to the authority having jurisdiction, solid fuel cooking appliances constructed of solid masonry or reinforced portland or refractory cement concrete and vented in accordance with NFPA 211 shall not require automatic fire-extinguishing equipment for the protection of grease removal devices, hoods, and duct systems. 14.7.5 Listed fire-extinguishing equipment for solid fuel-burning cooking appliances, where required, shall comply with Chapter 10 and shall use water-based agents. 14.7.6 Fire-extinguishing equipment shall be rated and designed to extinguish solid fuel cooking fires. 14.7.7 The fire-extinguishing equipment shall be of sufficient size to totally extinguish fire in the entire hazard area and prevent reignition of the fuel. 14.7.8* All solid fuel appliances (whether under a hood or not) with fire boxes of 0.14 m3 (5 ft3) volume or less shall have at least a listed 2-A rated water spray fire extinguisher or a 6 L (1.6 gal) wet chemical fire extinguisher listed for Class K fires in accordance with NFPA 10, with a maximum travel distance of 6 m (20 ft) to the appliance. NFPA 101: 19.3.2.5.3* Within a smoke compartment, where residential or commercial cooking equipment is used to prepare meals for 30 or fewer persons, one cooking facility shall be permitted to be open to the corridor, provided that all of the following conditions are met:(1)The portion of the health care facility served by the cooking facility is limited to 30 beds and is separated from other portions of the health care facility by a smoke barrier constructed in accordance with 19.3.7.3, 19.3.7.6, and 19.3.7.8.(2)The cooktop or range is equipped with a range hood of a width at least equal to the width of the cooking surface, with grease baffles or other grease-collecting and clean-out capability.(3)*The hood systems have a minimum airflow of 500 cfm (14,000 L/min).(4)The hood systems that are not ducted to the exterior additionally have a charcoal filter to remove smoke and odor.(5)The cooktop or range complies with all of the following:(a)The cooktop or range is protected with a fire suppression system listed in accordance with UL 300, Standard for Fire Testing of Fire Extinguishing Systems for Protection of Commercial Cooking Equipment, or is tested and meets all requirements of UL 300A, Extinguishing System Units for Residential Range Top Cooking Surfaces, in accordance with the applicable testing document's scope.(b)A manual release of the extinguishing system is provided in accordance with NFPA 96, Standard for Ventilation Control and Fire Protection of Commercial Cooking Operations, Section 10.5.(c)An interlock is provided to turn off all sources of fuel and electrical power to the cooktop or range when the suppression system is activated.(6)*The use of solid fuel for cooking is prohibited.(7)*Deep-fat frying is prohibited.(8)Portable fire extinguishers in accordance with NFPA 96 are located in all kitchen areas.(9)*A switch meeting all of the following is provided:(a)A locked switch, or a switch located in a restricted location, is provided within the cooking facility that deactivates the cooktop or range.(b)The switch is used to deactivate the cooktop or range whenever the kitchen is not under staff supervision.(c)The switch is on a timer, not exceeding a 120-minute capacity, that automatically deactivates the cooktop or range, independent of staff action.(10)Procedures for the use, inspection, testing, and maintenance of the cooking equipment are in accordance with Chapter 11 of NFPA 96 and the manufacturer ' s instructions and are followed.(11)*Not less than two AC-powered photoelectric smoke alarms with battery backup, interconnected in accordance with 9.6.2.10.3, and equipped with a silence feature are located not closer than 20 ft (6.1 m) and not further than 25 ft (7.6 m) from the cooktop or range.(12)*The smoke alarms required by 19.3.2.5.3(11) are permitted to be located outside the kitchen area where such placement is necessary for compliance with the 20-ft (7.6-m) minimum distance criterion.(13)*A single system smoke detector is permitted to be installed in lieu of the smoke alarms required in 19.3.2.5.3(11) provided the following criteria are met:(a)The detector is located not closer than 20 ft (6.1 m) and not further than 25 ft (7.6 m) from the cooktop or range.(b)The detector is permitted to initiate a local audible alarm signal only.(c)The detector is not required to initiate a building-wide occupant notification signal.(d)The detector is not required to notify the emergency forces.(e)The local audible signal initiated by the detector is permitted to be silenced and reset by a button on the detector or by a switch installed within 10 ft (3.0 m) of the system smoke detector.(14)System smoke detectors that are required to be installed in corridors or spaces open to the corridor by other sections of this chapter are not used to meet the requirements of 19.3.2.5.3(11) and are located not closer than 25 ft (7.6 m) to the cooktop or range.(15)The smoke compartment is protected throughout by an approved, supervised automatic sprinkler system in accordance with Section 9.7. This deficiency has the potential to affect occupants, who might include residents, staff, and visitors within the entire facility. Deficient items were discussed with the Administrator at the exit conference.
Plan of correction · submitted by the facility
Resident Specific:Please see systemic changesOther Residents:Please see systemic changesSystemic Changes:Wheel chalks installed on two units identified during inspection. Kitchen hood suppression inspection was completed and passed on 4/23/24 by Cintas. Missing report obtained and added to maintenance binderPower cable removed from stove unit and will be Demo only, Monitors:Photos taken to confirm wheel chalks in placeInspection was completed appropriately and missing documentation in placePhoto taken to confirm removal of power supply. Administrator or designee will report findings at QA meeting and will make changes to the above plan of correction as needed. Date of Compliance: October 2nd 2024
0346Fire Alarm System - Out of ServiceS/S F
Findings
Based on observations and records review, it was determined that the facility did not have Fire Alarm out of service guidance in accordance with NFPA 101.1. Fire Alarm Out of Services paperwork not provided NFPA 101 9.6.1.6* Where a required fire alarm system is out of service for more than 4 hours in a 24-hour period, the authority having jurisdiction shall be notified, and the building shall be evacuated, or an approved fire watch shall be provided for all parties left unprotected by the shutdown until the fire alarm system has been returned to service. These deficiencies have the potential to affect occupants, who might include residents, staff, and visitors within the entire facility. Deficient items were discussed with the Administrator at the exit conference
Plan of correction · submitted by the facility
Resident Specific:Please see systemic changesOther Residents:Please see systemic changesSystemic Changes:Fire alarm out of service policy updated and replaced in EOP to reflect 4 hour out of service requirements. Monitors:Photo taken of binder with plolicy updated and placed in EOPAdministrator or designee will report findings at QA meeting and will make changes to the above plan of correction as needed. Date of Compliance: September 26th 2024
0353Sprinkler System - Maintenance and TestingS/S F
Findings
Based on observations and records review, it was determined that the facility failed to maintain the automatic sprinkler system in accordance with National Fire Protection Association NFPA 25 and NFPA 1011. Escutcheon plates throughout facility are broken or not flush with the ceiling 2. Semi-annual report missing high/low-pressure switch and horn and strobe testing 3. Missing 3-year dry valve full trip inspection report 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. 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 254.3.1* Records shall be made for all inspections, tests, and maintenance of the system and its components and shall be made available to the authority having jurisdiction upon request. NFPA 25 4.3.2 Records shall indicate the procedure performed (e.g., inspection, test, or maintenance), the organization that performed the work, the results, and the date. NFPA 25 4.3.3* Records shall be maintained by the property owner. NFPA 13.4.4.2.2.2* Every 3 years and whenever the system is altered, the dry pipe valve shall be trip tested with the control valve fully open and the quick-opening device, if provided, in service. NFPA 13.4.4.2.2.3* During those years when full flow testing in accordance with 13.4.4.2.2.2 is not required, each dry pipe valve shall be trip tested with the control valve partially open. NFPA 13.4.4.2.9 Dry pipe systems shall be tested once every 3 years for air leakage, using one of the following test methods:(1) A pressure test at 40 psi (3.2 bar) shall be performed for 2 hours.(a)The system shall be permitted to lose up to 3 psi (0.2 bar) during the duration of the test.(b)Air leaks shall be addressed if the system loses more than 3 psi (0.2 bar) during this test.(2)With the system at normal system pressure, the air source (compressor or shop air) shall be shut off for 4 hours. If the low air pressure alarm goes off within this period, the air leaks shall be addressed. This deficiency has the potential to affect occupants, who might include residents, staff, and visitors within the entire facility. Deficient items were discussed with the administrator and maintenance director at the exit conference.
Plan of correction · submitted by the facility
Resident Specific:Please see systemic changesOther Residents:Please see systemic changesSystemic Changes:Escutcheon plates throughout the facility are scheduled to be inspected and corrections made to any deficient units found on Friday 10/4/23 by Cintas. Cintas confirmed Hi/Lo switch and strobe test completed 4/2/24 and will provide documentation. New on time inspection also passed on 10/2/24Documentation of 3 year dry valve trip was completed on annual inspection 10/04/2021 and most recently on 10/2/2024. Monitors:Cintas scheduled to inspect and repair any Escutcheons not to code on 10/4/24New on time inspection 10/2/24 passedOriginal report obtained from 2021 and current 3 year completed 10/4/24Administrator or designee will report findings at QA meeting and will make changes to the above plan of correction as needed. Date of Compliance: October 4th 2024
0354Sprinkler System - Out of ServiceS/S F
Findings
Based on observations and records review, it was determined that the facility did not have Sprinkler System out-of-service guidance in accordance with NFPA 101 and NFPA 251. Sprinkler Out of Service needs change to 10 hours and to fit state regulations. NFPA 101, 9.7.6 Sprinkler impairment procedures shall comply with NFPA 25, Standard for the Inspection, Testing, and Maintenance of Water-Based Fire Protection Systems. NFPA 25, 15.5.2 Before authorization is given, the impairment coordinator shall be responsible for verifying that the following procedures have been implemented:(1) The extent and expected duration of the impairment have been determined.(2) The areas or buildings involved have been inspected and the increased risks determined.(3) Recommendations have been submitted to management or the property owner or designated representative.(4) Where a required fire protection system is out of service for more than 10 hours in a 24-hour period, the impairment coordinator shall arrange for one of the following:(a) Evacuation of the building or portion of the building affected by the system out of service(b) *An approved fire watch(c)*Establishment of a temporary water supply(d)* Establishment and implementation of an approved program to eliminate potential ignition sources and limit the amount of fuel available to the fire(5) The fire department has been notified.(6) The insurance carrier, the alarm company, property owner or designated representative, and other authorities having jurisdiction have been notified.(7) The supervisors in the areas to be affected have been notified.(8) A tag impairment system has been implemented. (See Section 15.3.)(9) All necessary tools and materials have been assembled on the impairment site. This deficiency can potentially affect occupants, including residents, staff, and visitors within the entire facility. Deficient items were discussed with the administrator and maintenance director at the exit conference.
Plan of correction · submitted by the facility
Resident Specific:Please see systemic changesOther Residents:Please see systemic changesSystemic Changes:Sprinkler out of service policy updated and replaced in EOP to reflect 10 hour out of service requirements. Monitors:Photo taken of binder with policy updated and placed in EOPAdministrator or designee will report findings at QA meeting and will make changes to the above plan of correction as needed. Date of Compliance: September 26th 2024
0355Portable Fire ExtinguishersS/S D
Findings
Based on observations and records review, it was determined that the facility did not maintain fire extinguishers In accordance with NFPA 10. 1. Therapy kitchen extinguisher exceeds 5ft in height. NFPA 10 6.1.3.8 Installation Height. 6.1.3.8.1 Fire extinguishers having a gross weight not exceeding 40 lb (18.14 kg) shall be installed so that the top of the fire extinguisher is not more than 5 ft (1.53 m) above the floor. This deficiency has the potential to affect occupants, who might include residents, staff, and visitors within this area of the smoke compartment of the facility. Deficient items were discussed with the administrator and maintenance director at the exit conference
Plan of correction · submitted by the facility
Resident Specific:Please see systemic changesOther Residents:Please see systemic changesSystemic Changes:Therapy kitchen extinguisher lowered to below 5’ on the wall. Monitors:Photo taken with measure of lowered unit. Administrator or designee will report findings at QA meeting and will make changes to the above plan of correction as needed. Date of Compliance: September 24th 2024.
0511Utilities - Gas and ElectricS/S E
Findings
Based on observation during the survey, it was determined that the facility failed to maintain proper gas valve protection in accordance with Life Safety Section 9.1and NFPA 54, 7.9.2.1. NFPA 101 and NFPA 70. This was evidenced by the following:1. The Fire Alarm panel breaker needs a lock out tag. 2. Need high altitude orifice sticker for commercial dryer. 3. A grill is stored in the generator enclosureNFPA 70 760.41 NPLFA Circuit Power Source Requirements.(A) Power Source. The power source of non–power-limited fire alarm circuits shall comply with Chapters 1 through 4, and the output voltage shall be not more than 600 volts, nominal. The fire alarm circuit disconnect shall be permitted to be secured in the "on" position. NFPA 101, 9.1.1 Gas. Equipment using gas and related gas piping shall be in accordance with NFPA 54, National Fuel Gas Code. NFPA 54, 11.1.2 High Altitude. Gas input ratings of appliances shall be used for elevations up to 2000 ft (600 m). The input ratings of appliances operating at elevations above 2000 ft (600 m) shall be reduced in accordance with one of the following methods:(1) At the rate of 4 percent for each 1000 ft (300 m) above sea level before selecting appropriately sized appliance(2) As permitted by the authority having jurisdiction.(3) In accordance with the manufacturer ' s installation instructions. NFPA 1 10.11.6 Cooking Equipment. 10.11.6.1 For other than one- and two-family dwellings, no hibachi, grill, or other similar devices used for cooking, heating, or any other purpose shall be used or kindled on any balcony, under any overhanging portion, or within 10 ft (3 m) of any structure. This deficiency has the potential to affect occupants, who might include residents, staff, and visitors within the entire facility. Deficient items were discussed with the administrator and maintenance director at the exit conference.
Plan of correction · submitted by the facility
Resident Specific:Please see systemic changesOther Residents:Please see systemic changesSystemic Changes:Lock out installed on fire alarm breakerObtained work order for high altitude orifice install on 12/7/17Grill removed from generator areaMonitors:Photo taken of installed lock outWork order obtained to confirm hand written install date on dryerPhoto taken to confirm grill removedAdministrator or designee will report findings at QA meeting and will make changes to the above plan of correction as needed. Date of Compliance: September 30th 2024
0781Portable Space HeatersS/S D
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 19.7.81. Space heater in maintenance room. 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). This deficiency can potentially affect occupants, including residents, staff, and visitors within the entire facility. Deficient items were discussed with the maintenance director at the exit conference.
Plan of correction · submitted by the facility
Resident Specific:Please see systemic changesOther Residents:Please see systemic changesSystemic Changes:Heater removed from facility and thrown away,Monitors:Photo taken to confirm unit thrown in dumpster. Administrator or designee will report findings at QA meeting and will make changes to the above plan of correction as needed. Date of Compliance: September 24th 2024
0907Gas and Vacuum Piped Systems - Maintenance PrS/S D
Findings
Based on observations and records review, it was determined that the facility did not maintain oxygen storage in accordance with NFPA 99. 1. Signs needed for "full" and "empty" for racked oxygen storage. NFPA 99 11.6.5.2 If empty and full cylinders are stored within the same enclosure, empty cylinders shall be segregated from full cylinders. NFPA 99 11.6.5.3 Empty cylinders shall be marked to avoid confusion and delay if a full cylinder is needed in a rapid manner. 11.5.2.2 Transfilling Cylinders. 11.5.2.2.1 Mixing of compressed gases cylinders shall be prohibited. 11.7.3.2 Containers shall not be placed in the following areas:(1)Where they can be tipped over by the movement of a door(2)Where they interfere with foot traffic(3)Where they are subject to damage from falling objects(4)Where exposed to open flames and high-temperature devicesThis deficiency can potentially affect occupants, including residents, staff, and visitors within the entire facility. Deficient items were discussed with the maintenance director at the exit conference.
Plan of correction · submitted by the facility
Resident Specific:Please see systemic changesOther Residents:Please see systemic changesSystemic Changes:Signage created to designate signage for full and empty sides. Signage placed on mobile racking and on wall where mobile racking stored. Monitors:Picture taken of new signage attached to cart and wall. Administrator or designee will report findings at QA meeting and will make changes to the above plan of correction as needed. Date of Compliance: September 25th 2024
0918Electrical Systems - Essential Electric SysteS/S F
Findings
Based on observation and record review during the survey, it was determined that the facility failed to maintain the backup emergency generator in accordance with National Fire Protection Association (NFPA) Standard 110. This was evidence by the following: 1. Paperwork needed for battery testing 2. Monthly load testing paperwork needed to verify monthly load testing is to 30%3. Missing annual load testNFPA 110 8.5.4 Records shall be retained for a period of time defined by the facility management or by the authority having jurisdiction. NFPA 110-8.4 Operational Inspection and Testing. 8.4.2* Diesel generator sets in service shall be exercised at least once monthly, for a minimum of 30 minutes, using oneof the following methods: (1) Loading that maintains the minimum exhaust gas tem-peratures as recommended by the manufacturer (2) Under operating temperature conditions and at not lessthan 30 percent of the EPS nameplate kW rating8.4.2.4* Diesel-powered EPS installations that do not meet the requirements of 8.4.2 shall be exercised monthly with the available EPSS load and shall be exercised annually with supplemental loads at not less than 50 percent of the EPS nameplate kW rating for 30 continuous minutes and at not less than 75 percent of the EPS nameplate kW rating for 1 continuous hour for a total test duration of not less than 1.5 continuous hours. These deficiencies have the potential to affect occupants, who might include residents, staff, and visitors within the entire facility. Deficient items were discussed with the Administrator at the exit conference
Plan of correction · submitted by the facility
Resident Specific:Please see systemic changesOther Residents:Please see systemic changesSystemic Changes:Missing testing form located after inspection and placed in maintenance binderMonthly load testing section added to in house form to verify load testing is to 30%+ Annual load test was completed on 1/2/24. Report obtained from Cummins and placed in maintenance binder. Monitors:Testing form in binderForm updated to include monthly requirementsTest was completed and missing documentation in binderAdministrator or designee will confirm at end of month for 3 months that new section being completed and form is properly located in maintenance binder. Administrator or designee will report findings at QA meeting and will make changes to the above plan of correction as needed. Date of Compliance: September 26th 2024
8/15/2024Recertification Survey · ID NPBN11No deficiencies
0000Initial CommentsSurveyor note2 building records
Findings · record 1 of 2
A recertification survey was conducted on 8/12/24 to 8/15/24. No deficiencies were cited.
Findings · record 2 of 2
An Emergency Preparedness survey was conducted from 8/12/24 to 8/15/24. No deficiencies were cited.
Plan of correction
The state did not require a plan of correction for this citation.
4/8/2024Focused Infection Control, Other-Fed Survey · ID 1M1G111 deficiency
0884Reporting - National Health Safety NetworkS/S F
Findings
Based on record review, the facility failed to report complete information about COVID-19 to the Centers for Disease Control and Prevention's (CDC) National Healthcare Safety Network (NHSN) during a seven-day period that reporting was required by regulation. The CDC submitted data from the NHSN to the Centers for Medicare and Medicaid Services (CMS). Based on review of that data, CMS determined that between 04/01/2024 and 04/07/2024, the facility did not report complete information to NHSN about COVID-19 in the standardized format and frequency as specified by CMS and the CDC. This failure to report has the potential to cause more than minimal harm to all residents residing in the facility.
Plan of correction
The state did not require a plan of correction for this citation.
2/12/2024Focused Infection Control, Other-Fed Survey · ID 0F1J111 deficiency
0884Reporting - National Health Safety NetworkS/S F
Findings
Based on record review, the facility failed to report complete information about COVID-19 to the Centers for Disease Control and Prevention's (CDC) National Healthcare Safety Network (NHSN) during a seven-day period that reporting was required by regulation. The CDC submitted data from the NHSN to the Centers for Medicare and Medicaid Services (CMS). Based on review of that data, CMS determined that between 02/05/2024 and 02/11/2024, the facility did not report complete information to NHSN about COVID-19 in the standardized format and frequency as specified by CMS and the CDC. This failure to report has the potential to cause more than minimal harm to all residents residing in the facility.
Plan of correction
The state did not require a plan of correction for this citation.
10/10/2023Focused Infection Control, Other-Fed Survey · ID JLU5111 deficiency
0884Reporting - National Health Safety NetworkS/S F
Findings
Based on record review, the facility failed to report complete information about COVID-19 to the Centers for Disease Control and Prevention's (CDC) National Healthcare Safety Network (NHSN) during a seven-day period that reporting was required by regulation. The CDC submitted data from the NHSN to the Centers for Medicare and Medicaid Services (CMS). Based on review of that data, CMS determined that between 10/02/2023 and 10/08/2023, the facility did not report complete information to NHSN about COVID-19 in the standardized format and frequency as specified by CMS and the CDC. This failure to report has the potential to cause more than minimal harm to all residents residing in the facility.
Plan of correction
The state did not require a plan of correction for this citation.
9/18/2023Focused Infection Control, Other-Fed Survey · ID Q2F2111 deficiency
0884Reporting - National Health Safety NetworkS/S F
Findings
Based on record review, the facility failed to report complete information about COVID-19 to the Centers for Disease Control and Prevention's (CDC) National Healthcare Safety Network (NHSN) during a seven-day period that reporting was required by regulation. The CDC submitted data from the NHSN to the Centers for Medicare and Medicaid Services (CMS). Based on review of that data, CMS determined that between 09/11/2023 and 09/17/2023, the facility did not report complete information to NHSN about COVID-19 in the standardized format and frequency as specified by CMS and the CDC. This failure to report has the potential to cause more than minimal harm to all residents residing in the facility.
Plan of correction
The state did not require a plan of correction for this citation.
8/30/2023Complaint Survey · ID MIMB11No deficiencies
0000INITIAL COMMENTSSurveyor note
Findings
A survey prompted by #CO33360 was conducted on 8/30/23. Deficiencies were not cited.
Plan of correction
The state did not require a plan of correction for this citation.
6/8/2023Revisit: Recertification Survey · ID JHQY22No deficiencies
0000INITIAL COMMENTSSurveyor note
Findings
A document revisit was completed with all deficiencies being corrected. No other deficiencies were cited and no response is needed.
Plan of correction
The state did not require a plan of correction for this citation.
6/5/2023Focused Infection Control, Other-Fed Survey · ID 2X1T111 deficiency
0884Reporting - National Health Safety NetworkS/S F
Findings
Based on record review, the facility failed to report complete information about COVID-19 to the Centers for Disease Control and Prevention's (CDC) National Healthcare Safety Network (NHSN) during a seven-day period that reporting was required by regulation. The CDC submitted data from the NHSN to the Centers for Medicare and Medicaid Services (CMS). Based on review of that data, CMS determined that between 05/29/2023 and 06/04/2023, the facility did not report complete information to NHSN about COVID-19 in the standardized format and frequency as specified by CMS and the CDC. This failure to report has the potential to cause more than minimal harm to all residents residing in the facility.
Plan of correction
The state did not require a plan of correction for this citation.
6/2/2023Revisit: Recertification Survey · ID JHQY12No deficiencies
0000Initial CommentsSurveyor note
Findings
A revisit survey was completed on 6/2/23 for all previous deficiencies cited on 3/16/23. The facility is in compliance with all regulations surveyed.
Plan of correction
The state did not require a plan of correction for this citation.
5/30/2023Focused Infection Control, Other-Fed Survey · ID 1WIS111 deficiency
0884Reporting - National Health Safety NetworkS/S F
Findings
Based on record review, the facility failed to report complete information about COVID-19 to the Centers for Disease Control and Prevention's (CDC) National Healthcare Safety Network (NHSN) during a seven-day period that reporting was required by regulation. The CDC submitted data from the NHSN to the Centers for Medicare and Medicaid Services (CMS). Based on review of that data, CMS determined that between 05/22/2023 and 05/28/2023, the facility did not report complete information to NHSN about COVID-19 in the standardized format and frequency as specified by CMS and the CDC. This failure to report has the potential to cause more than minimal harm to all residents residing in the facility.
Plan of correction
The state did not require a plan of correction for this citation.
4/10/2023Recertification Survey · ID JHQY214 deficiencies
0000INITIAL COMMENTSSurveyor note
Findings
The Initial Comments (ID Tag K0000) are informational only and are a representation of the facility's general characteristics. The Colorado Division of Fire Prevention and Control conducted this survey in accordance with the Federal Register at Section 42 CFR 483.70 (a). The building is a one story wood framed structure, Type V (111). The facility is classified as fully protected by a National Fire Protection Association (NFPA) 13 automatic sprinkler system. The facility 's fire sprinkler system is a wet and a dry system. This survey of the 34 bed facility was conducted on April 10, 2023 for compliance with the NFPA 101 Life Safety Code, Chapter 19 Existing Health Care Occupancies and Referenced Publications. The facility will meet these requirements with the correction of the deficiencies listed herein. The following deficiencies were discussed with the facility Administrator during the exit conference.
Plan of correction
The state did not require a plan of correction for this citation.
0324Cooking FacilitiesS/S D
Findings
Based on observation it was determined that the facility failed to maintain the kitchen hood suppression system as required by NFPA 96, (Chapter 12, Section 12.1.2.3.1) and cooking appliance restraint as required by NFPA 54, 9.6.1.2. Chalks in kitchen on stove wheels | Kitchen stove wheels do not have devices installed to return to same position after pulling out for cleaningNFPA 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, 12.1.2.3.1 An approved method shall be provided that will ensure the appliance is returned to an approved design location. This deficiency has the potential to affect occupants, who might include residents, staff, and visitors within the entire facility. Deficient items were discussed with the Administrator and Maintenance director at the exit conference.
Plan of correction · submitted by the facility
K-324 Resident Specific:Please see systemic changesOther Residents:Please see systemic changesSystemic Changes:Permanent floor chalks have been installed on stove to ensure return position is accurate after cleaning. Monitors:Photos taken to confirm placement of chalks. Administrator or designee will report findings at QA meeting and will make changes to the above plan of correction as needed. Date of Compliance: April 28th 2023
0353Sprinkler System - Maintenance and TestingS/S E
Findings
Based on observations and records review, it was determined that the facility failed to maintain the automatic sprinkler system in accordance with National Fire Protection Association NFPA 25 and NFPA 101No Dry Valve full trip report available during inspectionSprinkler freezer/refrigerator corrosion | Sprinkler heads both freezer/fridge corroded Also unable to identify temperature of headNFPA 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, 4.6.12These deficiencies have the potential to affect occupants, who might include residents, staff, and visitors within the entire facility. Deficient items were discussed with the Administrator and Maintenance director at the exit conference.
Plan of correction · submitted by the facility
K-353 Resident Specific:Please see systemic changesOther Residents:Please see systemic changesSystemic Changes:Dry valve full trip was performed on 10/6/2022. Documents highlighted in maintenance binder. Sprinkler heads in fridge and freezer scheduled to be inspected and replaced as necessary by Cintas. Monitors:Report provided as proof of dry valve trip. Received email confirming Cintas is to inspect and correct sprinkler heads. Administrator or designee will report findings at QA meeting and will make changes to the above plan of correction as needed. Date of Compliance: April 28, 2023
0712Fire DrillsS/S F
Findings
Based on record review, it was determined that the facility failed to conduct fire drills in accordance with the Life Safety Code NFPA 101. Fire Drills not compliant | No Fire Drill 3rd shift (4th qrt)/2nd shift (2nd qrt)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. NFPA 101, 19.7.1.4* Fire drills in health care occupancies shall include the transmission of a fire alarm signal and simulation of emergency fire conditions. NFPA 101, 4.7.4. Drills shall be held at expected and unexpected times and under varying conditions to simulate the unusual conditions that can occur in an actual emergency. This deficiency has the potential to affect occupants, who might include residents, staff, and visitors within the entire facility. Deficient items were discussed with the Administrator and Maintenance director at the exit conference.
Plan of correction · submitted by the facility
K-712 Resident Specific:Please see systemic changesOther Residents:Please see systemic changesSystemic Changes:Annual schedule in place to ensure quarterly drills completed are appropriately performed per standards. Schedule is only available to Maintenance Supervisor and Administrator. Q1 drills complete and Q2-Q4 are mapped. Monitors:Administrator or designee audit schedule monthly over the next quarter to ensure drills are being completed in accordance to above schedule. Administrator or designee will report findings at QA meeting and will make changes to the above plan of correction as needed. Date of Compliance: April 28th 2023
0912Electrical Systems - ReceptaclesS/S F
Findings
Through documentation review, it was determined that the facility did not maintain proper electrical practices in accordance with NFPA 99 Health Care Facilities Code (2012). This was evidenced by:Written records of the continuity of the grounding circuit, polarity of hot and neutral connections, and retention force of the grounding blade for receptacles in patient care need to be updated to verify all areas accounted for. 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). This deficiency has the potential to affect occupants, who might include residents, staff, and visitors within the entire facility. Deficient items were discussed with the Administrator and Maintenance director at the exit conference.
Plan of correction · submitted by the facility
K-912 Resident Specific:Please see systemic changesOther Residents:Please see systemic changesSystemic Changes:Tracking form implemented to ensure all residents room receptacles appropriately tested on a yearly basis. Monitors:New tracking form added to maintenance binder. Administrator or designee will review form monthly X 3 to ensure information is being reported on time and accurately. Administrator or designee will report findings at QA meeting and will make changes to the above plan of correction as needed. Date of Compliance: April 28th 2023
3/16/2023Recertification Survey · ID JHQY112 deficiencies
0000Initial CommentsSurveyor note2 building records
Findings · record 1 of 2
A recertification survey was conducted 3/13/23-3/16/23. Two deficiencies were cited.
Findings · record 2 of 2
An Emergency Preparedness survey was conducted from 3/13/23 to 3/16/23. No deficiencies were cited.
Plan of correction
The state did not require a plan of correction for this citation.
0656Develop/Implement Comprehensive Care PlanS/S D
Findings
Based on record review and interviews, the facility failed to develop and implement a comprehensive person-centered care plan that included measurable interventions and objectives for one (#12) of three out of 18 sample residents. Specifically, the facility failed to develop a person centered care plan for Resident #12's mental illness that included interventions, behaviors, and non-pharmaceutical approaches. Findings include: I. Resident #12 A. Resident status Resident #12, age 74, was admitted to the facility on 2/8/23. According to the March 2023 computerized physician orders (CPO), diagnoses included bipolar II disorder and unspecified dementia without psychotic disturbance. The 2/11/22 minimum data set (MDS) assessment showed the resident had moderate cognitive impairment with a score of ten out of 15. No behaviors were indicated. B. Record review The mood care plan, revised on 2/17/23 revealed the resident was taking an anticonvulsant for bipolar II disorder. The goals were to be without injury related to use of an anticonvulsant. The approaches were to administer the medication as ordered and report to the medical director. There were no interventions, behaviors, or non-pharmaceutical approaches related to mood. The psychotropic drug usage care plan, revised on 2/17/23 revealed the resident required the use of an antipsychotic medication related to a diagnosis of psychosis. The goals were for the resident to not exhibit any adverse side effects related to the medication. The approaches were:-offer counseling-encourage resident to express needs, wants, and feelings-encourage family to visit-monitor for changes in behavior-educate family and resident on side effects-review regime and conduct gradual dose reduction as appropriate-review medication for appropriate does, diagnosis, and usage per psycho pharmacological review-administer medication as ordered. -The resident's care plan failed to identify individualized behaviors, person centered interventions, and non-pharmaceutical approaches. The March 2023 medication administration records (MAR) revealed the following physician orders for psychotropic medications:-Divalproex (Depakote) 250 MG one time a day for bipolar ordered on 2/8/23;-Divalproex (Depakote) 500 MG to equal 1000 MG one time a day at bedtime for bipolar ordered on 2/8/23;-Lamotrigine (Lamictal) 25 MG one time a day for bipolar ordered on 2/8/23; and,-Quetiapine (Seroquel) 25 MG to equal 75 MG at bedtime for psychosis ordered on 2/8/23. The hospital nursing record dated 2/6/23, two days prior to admission to the facility, revealed the resident was experiencing dysphoric mood (depression, irritability, aggression and anger). The resident was prescribed Depakote 500 MG for mania associated with bipolar disorder. Target behavior tracking from 2/12/23 to 3/13/23 revealed: -Divalproex and Lamictal for behaviors of erratic mood swings or erratic behaviors started on 2/8/23 with no behaviors marked. -Quetiapine for behaviors of hallucinations/auditory or visual started on 2/8/23 with no behaviors marked. -Review of resident's progress notes dated 3/15/23 through 2/8/23 failed to reveal any notes regarding care conferences or care planning. II. Resident interview and representative interview The resident was interviewed on 3/15/23 at 10:30 a.m. He acknowledged he has a diagnosis of bipolar disorder and stated that no therapy or counseling has been offered to him, and he would have liked for it to have been offered. He stated he had never been invited to a care conference meeting since being at the facility. The resident's representative was interviewed on 3/16/23 at 8:52 a.m. She stated that the resident had been receiving psychological services in the community but had not been offered since admitting to the facility. She was aware there were routine care conferences held but she had to ask to attend, but the resident nor her were invited. She said that the staff had interviewed the resident regarding if he was experiencing depression but they did not ask her about his history of behaviors, interventions, or what approaches had worked for him in the past. The last significant episode he had was two years prior. He had been experiencing manic behaviors and depression, resulting in a fall and hospitalization. While at the hospital, he had been treated with Prozac (depression medication) which increased his manic behaviors. He had another injury and required 24- hour supervision while at the hospital. Manic behaviors for him manifested as excessive energy, "bouncing off the walls", apathy, and chronic depression. III. Staff interviews Registered nurse (RN) #2 was interviewed on 3/14/23 at 10:47 a.m. RN #2 stated the resident did not have any behaviors that he knew of. RN #2 pulled up the resident's target behavior tracking and could not tell which behavior was being tracked for Lamotrigine and the Divalproex because the tracker was combined. He acknowledged he could effectively track the behavior with one tracker for two medications. He could not explain what behaviors he was to be watching for according to the behaviors listed on the target behavior tracker. CNA #1 was interviewed on 3/14/23 at 11:00 a.m. CNA #1 stated resident had behaviors of confusion but no other behaviors that she was aware of. The admissions coordinator (AC) was interviewed on 3/14/23 at 11:19 a.m. She stated she did the admission and intake with the new residents. She would interview the resident and their family regarding any behaviors and would look in the resident's hospital records. She included that information on their target behavior tracker. If a resident had started taking several psychotropic medications at the same time, then they would be included on the same tracker. She could not explain how the staff would know which behavior they were tracking for which medication. RN #1 was interviewed on 3/15/23 at 10:44 a.m. RN #1 stated the resident had memory problems but no other behaviors she was aware of and she could not explain the behaviors she was tracking the resident for. She said what she thought erratic behavior meant a person was dangerous, she did not know what mood swings or hallucinations looked like for the resident. Management had not elaborated what behaviors staff were to be watching for on the tracker or in the resident care plan. The DON was interviewed with the AC present on 3/15/23 at 11:03 a.m. The DON stated the behaviors management wanted nursing staff to track were on the target behavior tracker. These were the behaviors that have been determined to be associated with the medication on the tracker. The AC did the interview with the family and the resident at time of admission. She would ask what behaviors they have associated with their mental illness and what did that look like. When the information was vague, the DON or AC would contact the psychologist that came to the facility to meet with the resident to help determine what their behaviors were. The MDS coordinator entered the care plan in the resident's electronic medical record and gathered her information from the staff and the records, she worked remotely. They acknowledged that they had not contacted their psychologist to meet with Resident #12 for counseling, to clarify behaviors or interventions for the resident. The MDS coordinator was interviewed with DON on 3/15/23 at 1:29 p.m. The MDS coordinator stated that if a resident was stable with their mental illness, she dis not include their behaviors or interventions in the resident's care plan. The MDS coordinator did not indicate why the behaviors on the target behavior tracker had not been included in Resident #12's care plan. The DON stated that even if the resident had a diagnosis of mental illness, if they were not showing behaviors, had not had any episodes for years, and were reportedly stable then the care plan would not include behaviors, approaches or non-pharmacological interventions for that diagnosis. The DON and the MDS coordinator acknowledged Resident #12's care plan did not include person centered information regarding behaviors, interventions and approaches.
Plan of correction
The state did not require a plan of correction for this citation.
0689Free of Accident Hazards/Supervision/DevicesS/S D
Findings
Based on observations, interviews and record review, the facility failed to provide adequate supervision and assistance devices to prevent accidents for one (#7) of two residents reviewed for falls out of 18 sample residents. Specifically the facility failed to timely implement appropriate and effective interventions to prevent five falls in a two week period. Findings include: I. Facility policy The Fall Prevention policy, updated 9/28/22, was provided by the director of nursing (DON) on 3/15/23 at 4:30 p.m., read in part:"Safety interventions will be implemented and monitored with appropriate documentation as indicated ...Based upon the calculated score of the Fall Risk Assessment, the fall risk protocol and care plan will be completed and the appropriate interventions initiated. The admitting nurse/nurse manager will be responsible for insuring that interventions are initiated and communicated to appropriate staff for follow through ...The assigned licensed nurse will be responsible for ensuring safety checks are in place as care planned and will initial the TAR (treatment administration record) indicating checks are completed and document in nursing notes for verification." II. Resident #7 A. Resident status Resident #7, age 79, was admitted on 2/20/23. According to the March 2023 clinical physician orders (CPO) diagnoses included encounter for orthopedic aftercare following surgical amputation, right below knee amputation, diabetes mellitus and heart failure. The 2/26/23 minimum data set (MDS) assessment revealed the resident's cognition was intact with a brief interview for mental status (BIMS) score 15 out of 15. She required extensive assistance with bed mobility and dressing, limited assistance with transfers and toilet use, supervision with eating, and she was independent with personal hygiene. B. Record review The comprehensive care plan, dated 2/27/23, included the following: Patient will improve self-care and mobility function and achieve discharge goals as identified on MDS (minimum data set) section GG. Approaches included: functional performance will be evaluated with discharge from skilled services. Functional discharge goals will be determined on admission. Baseline functional performance will be determined upon admission. Patient identified at risk for falls related to: Mobility and/or functional deficits. Impaired safety awareness and balance deficits. Goal: Risk of falls and/or injury related to falls will be minimized throughout stay. Approaches included: Monitor for adverse side effects of medication regimen; consult with MD (physician) as needed. Ensure proper placement of call light and assistive devices for ease of access. PT (physical therapy) and/or OT (occupational therapy) evaluation and treatment to address functional deficits. Educate patient and/or family regarding fall risks and safety needs. Encourage patient to call for assistance with transfers and ambulation. Assist with transfers and ambulation as needed.-The risk for falls care plan was not revised with new interventions after Resident #7's falls. Patient requires/receives staff assist with ADL (activities of daily living) completion r/t (related to) limited mobility and generalized weakness due to s/p (status post) Rt BKA (right below knee amputation). Goal: Patient will increase strength and endurance to regain independence per skilled therapy goals throughout stay. Patient will present a clean and neat appearance, clean clothing, properly adjusted, hair combed and neat throughout stay. Approaches included: Oxygen as ordered. Monitor of s/s (signs and symptoms) of lethargy/fatigue/dizziness r/t (related to) medication use; notify MD (physician) if s/s (signs and symptoms) occur. Monitor labs as ordered; notify MD (physician) of abnormal results. Monitor vital signs as ordered; notify MD (physician) of abnormal results. Functional mobility is expected to improve throughout the patient's stay. More or less assistance may be needed depending on progress, acute illness, time of day and/or psychosocial needs. Ensure call light is within patient's reach. Assist with ambulation or wheelchair mobility as needed. Monitor for s/s (signs and symptoms) of pain; assess pain at least every shift and PRN (as needed). Encourage patient to rest in between activities. PT (physical therapy) & OT (occupational therapy) to evaluate and treat per MD (physician) order. Staff to allow for and encourage patient choices and preferences. Staff to encourage independence/participation with ADLs (activities of daily living) as able. Falls On 2/28/23 a nurse documented: "Pt (patient) stated she slipped out of w/c (wheelchair) and hit face on carpet, noted abrasion to bridge of nose, no other visible injuries noted. Given cool washcloth for abrasion. ROM (range of motion) good and neuro checks initiated d/t (due to) unwitnessed fall and are wnl (within normal limits). Pt (patient) on scheduled hydrocodone (pain medication). Pt (patient) is assisted back into bed with call light within reach. On call DON (director of nursing) notified of fall." On 3/4/23 a nurse documented: "pt (patient) was trying to transfer from w/c (wheelchair) to recliner. Pt (patient) has BKA (below knee amputation) and thought her leg was whole. When trying to 'step' out of w/c (wheelchair), she fell on her right side. She was found sitting up on the floor and was upset that she did this. No increased pain than pt (patient) already has. Assessment negative. Neuro's (neurological assessment) started and wnl (within normal limits) so far." On 3/9/23 a nurse documented: "Pt (patient) found sitting upright against the side of the sink in the bedroom. W/C (wheelchair) was in front of the bathroom door. She stated she slid from W/C (wheelchair)."Pt (patient) assessed for injury with no injuries noted at this time. Neurological assessment in place and are WNL (within normal limits), ROM (range of motion) intact. Assisted back to bed. Bed in lowest position with call light in reach. DON (director of nursing) notified." On 3/10/23 a nurse documented: "patient found sitting on floor by her room door. Assessed for injury and no noted. Patient denied any pain or discomfort, patient very drowsy. Assisted back to bed. Neuro checks commenced per facility policy." Follow-up note revealed: "Patient found sitting on floor by the door to her room. Her w/c (wheelchair) was noted to be in the bathroom. When asked what happened she stated that she was going to the bathroom."On 3/14/23 a nurse documented: "Pt (patient's) neuro checks are completed this shift. Pt (patient) continues to self-transfer, pt (patient) is seen hopping on 1 (one) leg with transfer and did not look safe. Encouraged pt (patient) to call for assistance with transfers and/or to use a slide board to which pt (patient) refuses. Notified pt (patient) that her scheduled pain medication was decreased this eve from 5mg to 2.5mg. Pharmacy also notified." On 3/15/23 a nurse documented: "Pt (patient) found sitting upright on the fall mat next to the bed. She stated she was trying to get into the W/C from the bed."Follow-up note revealed: "Assessed for injury with none noted at this time. Assisted back to bed. Neuros initiated and are WNL (within normal limits), ROM (range of motion) intact. DON (director of nursing) notified. Call light in reach, fall mats in place and bed in lowest position." C. Resident observations and interviewResident #7 was observed on 3/15/23 between 11:00 a.m. and 2:30 p.m. She was in her room seated in her wheelchair at the table. At 11:30 a.m. the resident brought a pillow from her bed and placed it on the table. At 12:00 p.m., Resident #7 was observed sleeping at the table, with her head on a pillow. Resident #7 was interviewed on 3/15/23 at 12:01 p.m. She said she fell last night and a "couple times" before that. She said she realized she was weak and needed help, however she did not remember to use the call light. The resident's lunch meal was delivered to her room by a certified nurse aide (CNA) #2, and the tray was placed on the table. The CNA removed the pillow and placed it on the bed. At 1:15 p.m. the resident was observed sleeping with head down on the table, her lunch meal tray was pushed back. The resident said she was not hungry. At 2:25 p.m. the resident closed the door to her room. CNA #1 was asked to check on the resident. At 2:30 p.m. the CNA said the resident was trying to transfer herself from wheelchair to bed. During the observations, the staff did not offer the resident assistance to use the restroom or if she needed to rest in bed. III. Staff interviews Registered nurse (RN) #1 was interviewed on 3/15/23 at 11:42 a.m. She said Resident #7 was very impatient and frequently transferred herself from her wheelchair to the toilet and to her bed. She said the resident did not remember to use the call light. She said the resident was not aware she was an amputee and was at high risk for falls. She said she was not aware of any new fall prevention approaches except for reminding the resident to use the call light. CNA #2 was interviewed on 3/15/23 at 11:45 a.m. She said the standard was to check on each resident every two hours. She said she was not aware of Resident #7 falls. She said she reminded the resident to use her call light when she needed help. The director of therapies (DOT) was interviewed on 3/15/23 at 2:12 p.m. She said the unit nurse communicated with the therapy team about residents' falls. She said the interdisciplinary team was reviewing falls during morning stand-up meeting and appropriate approaches were discussed. She said Resident #7 refused the "do not get up on your own - call for help" signs placement in her room. She said one of the approaches to prevent falls for Resident #7 was initiating a "check light," the call light system was automatically turned on every 15 minutes to alert staff to check on the resident. The DON was interviewed on 3/15/23 at 4:30 p.m. She said she was aware of the resident's frequent falls. She said the resident did not remember she had her right lower leg amputated and tried to transfer herself to and from the toilet, and to and from bed. She said the resident did not use her call light for assistance. She said the interdisciplinary team recommended the check light. She said the resident's call light should be set to activate at every 15 minutes intervals for the staff to check on her, however this was not initiated until this afternoon.
Plan of correction
The state did not require a plan of correction for this citation.

Reportable Occurrences

2 records
3/4/2026Misappropriation of Property · ID 2602Q655001Reported on time: Yes
Occurrence summary
SUMMARY OF FINDINGS:On 3/4/26, 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 misappropriation of property event. Client (A) initially alleged staff (1) took $10 from him. During the course of the investigation, the healthcare entity helped conduct a search, reviewed records and conducted interviews. Staff found six dollars in client (A)'s pocket, which client (A) was not aware of at the time. Client (A) said the last time they saw the money was prior to admission. With a family interview, the family reported client (A) did not have $10 in their possession. Staff (1) denied the allegation. Later, client (A) said they were not able to identify a person or establish a timeline. No other clients reported having a concern with missing items. Options were available for clients to secure their valuables. Staff were reminded to educate clients on keeping valuables safe and about their options. 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 5/19/2026 · released to the public 5/26/2026.
9/3/2024Neglect · ID 2402Q655001Reported on time: Yes
Occurrence summary
SUMMARY OF FINDINGS: On 9/3/24, 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 a neglect event. Reportedly, a representative from Adult Protective Services opened an investigation related to concerns about former client (B)’s care. During the course of the investigation, the healthcare entity conducted record reviews and interviews. Client (B) discharged back in mid-August to the hospital post a mental and medical change after a dialysis appointment. He subsequently passed in the hospital at a later date. No further details were known about the care concerns with client (B). Nursing staff checked on current clients and ensured their needs were met. Based on the facility investigation, care was offered, medications were provided, and assessments were conducted. There were no findings to support an allegation of staff neglect. 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 3/31/2025 · released to the public 4/7/2025.