13
Inspections
13
Deficiencies
1
Actual Harm or Above
7
Occurrences
February 10, 2026
Last Inspection
S/S D/E/F Potential for harmS/S G Actual harm
The most recent inspection of WASHINGTON COUNTY NURSING HOME on record is dated February 10, 2026. Across 13 published inspections, state surveyors cited 13 deficiencies, 1 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
Schuetz, Libbie Jo
Owner
WASHINGTON COUNTY
Phone
(970) 345-2211
Payor Source
Medicare, Medicaid, Private Pay
City
AKRON
ZIP
80720
Inspections & Citations
13 inspections · 13 deficiencies2/10/2026Complaint Survey · ID 1E397D-H12 deficiencies▼
0000INITIAL COMMENTSSurveyor note▼
Findings
A survey for Incident #2735884 was conducted on 2/10/26. Two deficiencies were cited.
Plan of correction
The state did not require a plan of correction for this citation.
0684Quality of Care▼
Findings
Based on record review and interviews the facility failed to ensure one (#1) of three residents received treatment and care in accordance with professional standards of practice out of three sample residents. Specifically, the facility failed to ensure Monitor Resident #1’s blood sugar after long acting insulin was administered to ensure the effectiveness of the medication. Findings include:I. Professional ReferenceAccording to the manufacturer, Sanofi, Patient Information Lantus Insulin Glargine Injection, 2025, retrieved on 2/20/26 from https://www.lantus.com/new-to-insulin/starting-insulin “The most common side effect of insulin, including Lanus, is low blood sugar (hypoglycemia), which may be serious and life threatening. It may cause harm to your heart or brain. Symptoms of serious low blood sugar may include shaking, sweating, fast heartbeat, and blurred vision.”II. Resident #1A. Resident statusResident #1, age 86, was admitted on 1/6/26. According to February 2026 computerized physician orders (CPO), diagnoses included type 2 diabetes mellitus with diabetic chronic kidney disease and unspecified dementia, unspecified severity, with mood disturbance. The 1/21/26 minimum data set (MDS) revealed that the resident had severe cognitive impairment with a brief interview for mental status (BIMS) score of six out of 15. The resident required partial to moderate assistance with activities of daily living. The assessment indicated the resident’s insulin order changed. B. Record review Review of Resident #1’s electronic medical record (EMR) revealed the resident’s blood sugar level measured on 1/8/26 with the value of 439 milligrams per deciliter (mg/dL). Review of the January 2026 CPO revealed the following physician's order:Lantus, subcutaneous solution pen injection 100 unit/ milliliter (ml). Inject 5 units one time a day for type 2 diabetes, ordered on 1/8/26. Review of Resident #1’s EMR did not reveal documentation regarding the resident was monitored after being administered Lantus, which was a newly prescribed medication, to evaluate the effectiveness of the treatment and necessary monitoring for possible side effects of the new medication. C. Staff interviewsThe physician was interviewed on 2/10/26 at 1:00 p.m. The physician said the nurse called to report the high blood sugar value for Resident #1 on 1/8/26. The physician said she ordered of Resident #1 to receive 5 units of Lantus. The director of nursing (DON) was interviewed on 2/10/26 at 1:03 p.m. The DON said upon a review of Resident #1’s EMR, there was no follow up for re-evaluation of Resident #1 elevated blood sugar value post receiving the 5 units of Lantus per physician’s order by licensed practical nurse (LPN) #2. The DON said In addition she confirmed that there is no documentation regarding the incident and receiving the order in the Resident #1 and Resident #3 electronic health records.
Plan of correction · submitted by the facility
1. For resident #1, he received the ordered five units of Lantus. Follow up was not documented, but the nurse on duty did monitor him for side effects that evening and re-checked his blood sugar at approximately 2230. At that time his blood sugar was 352mg/dL. Resident #1’s blood sugar was checked the next morning, 1/10/2026 at 10:21am, and was 174 mg/dL. Blood sugar monitoring parameters for resident #1 were updated to include “notify provider and document follow-up”.2. Seven other residents receive insulin and had the potential to be affected by this deficient practice. All seven charts were reviewed by the Director of Nursing to determine if blood sugars were monitored after receiving insulin in response to an episode of hyperglycemia since January 1, 2026. There were no other incidents identified. 3. The policy for hyperglycemia was updated to include monitoring and documenting blood sugar after administering insulin in response to an episode of hyperglycemia. All orders to monitor blood sugars were updated to ensure they have clear parameters for when to notify the physician and to document follow-up. The DON (Director of Nursing) provided education to all nurses (by 3/6/26) on steps to take after a resident receives a dose of insulin for hyperglycemia and the importance of documenting the follow-up monitoring and actions taken. 4. The DON will audit blood sugar monitoring and insulin administrations, and document on a spreadsheet, for appropriate monitoring and follow-up documentation weekly for four weeks and then monthly for two months. The results of the audits will be reported to the QA committee monthly and new corrective action taken if concerns are identified. 5.3/6/26
0880Infection Prevention & Control▼
Findings
Based on observations and staff interviews, the facility failed to maintain an infection control and prevention program designed to provide a sanitary environment to help prevent the development and transmission of communicable diseases and infections. Specifically, the facility failed to follow proper infection control practices during insulin injection via insulin pen by using Resident #3 insulin pen to inject insulin to Resident #1. Findings include:I. Professional referenceThe Centers for Disease Control and Prevention (CDC), Considerations for Blood Glucose Monitoring and Insulin Administration (revised 8/7/24) was retrieved on 2/17/26 from https://www.cdc.gov/injection-safety/hcp/infection-control/. It read in read in pertinent part, “Insulin pens and other medication cartridges and syringes are for single patient use only. Never use them for more than one person. II. Facility policy and procedureThe Insulin Pen Use Policy, dated November 2025, read in pertinent part “Insulin pens contain multiple doses of insulin but are used for a single elder only.” III. Resident #1A. Resident statusResident #1, age 86, was admitted on 1/6/26. According to February 2026 computerized physician orders diagnoses included type 2 diabetes mellitus with diabetic chronic kidney disease and unspecified dementia, unspecified severity, with mood disturbance. The 1/21/26 minimum data set (MDS) revealed that the resident had severe cognitive impairment with a brief interview for mental status (BIMS) score of six out of 15. The resident required partial to moderate assistance with activities of daily living. The MDS assessment indicated there was a change in the insulin order. B. Record reviewThe facility’s investigation, dated 1/9/26, documented Resident #1 was prescribed 5 units of Lantus (insulin). Licensed practical nurse (LPN) #2 looked in the emergency kit of the facility and it did not contain Lantus. LPN #2 then used Resident #3’s insulin pen for Lantus, using a new needle, to inject the 5 units of Lantus to Resident #1. On 1/9/26 the LPN #2 was re-educated and disciplined by the director of nursing (DON) regarding proper use of the insulin pen. -However, the re-education for the LPN #2 failed to address infection control in regards to safe medication administration pertaining to infection control, specifically bloodborne pathogens. In addition, the re-education dated 1/9/26 for all other nurses failed to address infection control in regards to safe medication administration pertaining to infection control, specifically bloodborne pathogens. IV. Staff interviewsLPN #1 was interviewed on 2/10/26 at 12:50 p.m. LPN #1 said the facility had an emergency kit for medication. LPN #1 said the emergency kit was supplied with both short and long acting insulin for emergency use. She said if a new high risk medication (blood thinner, insulin, antibiotic) was ordered by the physician and the medication was not in the emergency kit, the pharmacy could deliver the medication with a STAT status within two hours at the latest. LPN #1 said that if the medication was not available at the pharmacy, there were two nearby hospitals that could provide the medication. LPN #1 said the pharmacy was 45 minutes away. She said there was a hospital within 30 minutes of the facility. The DON was interviewed on 2/10/26 at 1:03 p.m. The DON said she completed an investigation on 1/9/26 when she learned about the incident which occurred in the evening of 1/8/26. The DON said insulin pens should never be used for more than one person because of risk for contamination with blood borne pathogens. She said all of the other nurses received training on The Insulin Pen Use policy. The DON said Resident #1 and Resident #3 were tested for hepatitis B and C with negative results.
Plan of correction · submitted by the facility
1. The shared insulin pen was destroyed per drug destruction policy. For resident #1 a new insulin pen was ordered and delivered by the pharmacy. Resident #1’s POA (Power of Attorney) and Physician were notified of the incident with the shared insulin pen. Following the post-exposure plan, labs were ordered by the physician to test for blood borne pathogens on both elders who were administered insulin with the same pen. The labs were drawn on 1/12/26 and the results were received on 1/15/26. All labs results were negative. 2. There were seven other residents identified who receive insulin. All seven charts were reviewed by the Director of Nursing to determine if they could have been affected by this deficient practice. There were no other instances identified where an extra dose of insulin was ordered since January 1, 2026.3. Long acting insulin was obtained for the emergency drug kit to ensure it is available for future incidents of hyperglycemia, if needed. All nurses were re-educated by the Director of Nursing (by 3/6/26) regarding the insulin pen policy and the potential spread of blood borne pathogens if an insulin pen is used for more than one person. 4. The DON will audit insulin administrations, and document on a spreadsheet, to ensure compliance with the insulin policy weekly for four weeks and then monthly for two months. The results of the audits will be reported to the QA committee monthly and new corrective action taken if concerns are identified. 5.3/6/26
12/9/2024Revisit: Recertification Survey · ID 4WHJ12No deficiencies▼
0000INITIAL COMMENTSSurveyor note▼
Findings
A revisit survey was completed on 12/9/24 for all previous deficiencies cited on 9/25/24. The facility is in compliance with all regulations surveyed.
Plan of correction
The state did not require a plan of correction for this citation.
12/9/2024Revisit: Federal Monitoring Survey Survey · ID BEUJ12No deficiencies▼
0000INITIAL COMMENTSSurveyor note▼
Findings
A revisit survey was completed on 12/9/24 for all previous deficiencies cited on 10/24/24. The facility is in compliance with all regulations surveyed.
Plan of correction
The state did not require a plan of correction for this citation.
11/20/2024Revisit: Recertification Survey · ID 4WHJ22No 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.
10/17/2024Recertification Survey · ID 4WHJ212 deficiencies▼
0000INITIAL COMMENTSSurveyor note4 building records▼
Findings · record 1 of 4
INITIAL COMENTS (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). The campus comprises four single-story Type V (111) buildings, with each building accommodating 10 beds. The facility designated as building A1 is fully protected by automatic fire suppression systems that comply with National Fire Protection Association (NFPA) 13 standards. The attic space, mechanical area, and screen porch are safeguarded by a dry-piped automatic sprinkler system and are classified as fully sprinklered. The emergency power system for all four buildings is supported by a 200 kW, 208-volt diesel-powered generator located in a separate structure on the campus. Each building is equipped with two automatic transfer switches and a remote annunciator panel. Constructed in 2016, the facility is licensed for 40 beds. This recertification survey, conducted on October 17, 2024, assessed compliance with the NFPA 101 Life Safety Code (2012) Chapter 19, "Existing Health Care Occupancies." All deficiencies cited during the survey were discussed with the Administrator and Maintenance Director during the exit conference held at the conclusion of the on-site assessment.
Findings · record 2 of 4
INITIAL COMENTS (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). The campus comprises four single-story Type V (111) buildings, with each building accommodating 10 beds. The facility designated as building B1 is fully protected by automatic fire suppression systems that comply with National Fire Protection Association (NFPA) 13 standards. The attic space, mechanical area, and screen porch are safeguarded by a dry-piped automatic sprinkler system and are classified as fully sprinklered. The emergency power system for all four buildings is supported by a 200 kW, 208-volt diesel-powered generator located in a separate structure on the campus. Each building is equipped with two automatic transfer switches and a remote annunciator panel. Constructed in 2016, the facility is licensed for 40 beds. This recertification survey, conducted on October 17, 2024, assessed compliance with the NFPA 101 Life Safety Code (2012) Chapter 19, "Existing Health Care Occupancies." All deficiencies cited during the survey were discussed with the Administrator and Maintenance Director during the exit conference held at the conclusion of the on-site assessment.
Findings · record 3 of 4
INITIAL COMENTS (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). The campus comprises four single-story Type V (111) buildings, with each building accommodating 10 beds. The facility designated as building C1 is fully protected by automatic fire suppression systems that comply with National Fire Protection Association (NFPA) 13 standards. The attic space, mechanical area, and screen porch are safeguarded by a dry-piped automatic sprinkler system and are classified as fully sprinklered. The emergency power system for all four buildings is supported by a 200 kW, 208-volt diesel-powered generator located in a separate structure on the campus. Each building is equipped with two automatic transfer switches and a remote annunciator panel. Constructed in 2016, the facility is licensed for 40 beds. This recertification survey, conducted on October 17, 2024, assessed compliance with the NFPA 101 Life Safety Code (2012) Chapter 19, "Existing Health Care Occupancies." All deficiencies cited during the survey were discussed with the Administrator and Maintenance Director during the exit conference held at the conclusion of the on-site assessment.
Findings · record 4 of 4
INITIAL COMENTS (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). The campus comprises four single-story Type V (111) buildings, with each building accommodating 10 beds. The facility designated as building D1 is fully protected by automatic fire suppression systems that comply with National Fire Protection Association (NFPA) 13 standards. The attic space, mechanical area, and screen porch are safeguarded by a dry-piped automatic sprinkler system and are classified as fully sprinklered. The emergency power system for all four buildings is supported by a 200 kW, 208-volt diesel-powered generator located in a separate structure on the campus. Each building is equipped with two automatic transfer switches and a remote annunciator panel. Constructed in 2016, the facility is licensed for 40 beds. This recertification survey, conducted on October 17, 2024, assessed compliance with the NFPA 101 Life Safety Code (2012) Chapter 19, "Existing Health Care Occupancies." All deficiencies cited during the survey were discussed with the Administrator and Maintenance Director during the exit conference held at the conclusion of the on-site assessment.
Plan of correction
The state did not require a plan of correction for this citation.
0353Sprinkler System - Maintenance and TestingS/S F▼
Findings
STANDARD not met as evidenced by: Based on observation, it was determined that the facility failed to maintain the automatic sprinkler system per National Fire Protection Association (NFPA) Standard 13 and Standard 25. This deficient practice could affect all residents, staff, and visitors should the automatic sprinkler system fail to operate promptly and effectively due to non-code-compliant maintenance. Two gauges in the Fire Sprinkler Raiser room were manufactured in 2018. They shall be calibrated or replaced every five years. NFPA 101 2012 Edition Life Safety Code Standards require automatic sprinkler systems to be continuously maintained in reliable operating conditions and are installed, inspected, and tested periodically. 19.7.6, 4.6.12, NFPA 13, NFPA 25, 9.7.5The Director of Maintenance acknowledged the deficiency in the maintenance of the automatic sprinkler system during the facility's record review.
Plan of correction · submitted by the facility
Tag-K 353 Sprinkler gauges Plan for correcting specific deficiencyReplacement gauges have been ordered by Nebraska Fire and Safety. Procedure for implementing POCThe gauges will be replaced by NE Fire and Safety. Maintenance will create a spreadsheet listing the manufacture date of all gauges. MonitoringMaintenance Director or designee will maintain of spreadsheet listing each gauge and the manufacture date or calibration date. All gauges will be replaced or calibrated prior to their expiration date. Maintenance will review the spreadsheet monthly for upcoming expiration dates. Title of person responsibleMaintenance Director or designee will oversee this POC. Completion dateCompliance will be reached by 11/23/2024
0918Electrical Systems - Essential Electric SysteS/S F▼
Findings
STANDARD is not met, as evidenced by: Based on record review and staff interviews during the survey, it was determined that the facility failed to maintain emergency power systems in accordance with section 19.2.9.1 of the Life Safety Code and the referenced 2010 NFPA 110, Section 8.3.8 Maintenance and Operational Testing. This deficient practice has the potential to affect all residents, staff, and visitors in the event of power loss. The annual diesel fuel quality test, conducted using applicable ASTM Standards, failed due to samples containing levels of gasoline. NFPA 110, Section 8.3.8 a fuel quality test shall be performed at least annually using approved ASTM standards. The generator deficiency was discussed with the Director of Maintenance during the survey and the exit conference with the Administrator.
Plan of correction · submitted by the facility
Tag-K 918 Fuel Quality Plan for correcting specific deficiencyUniversal Fuel Services of CO will remove and dispose of oxidized diesel and water. Procedure for implementing POCUniversal Fuel Services of CO came on 10/31/2024 to remove and dispose of oxidized diesel and water. They have flushed the tank using 75 gallons of new diesel and removed that. A post-test was completed to verify compliance. Universal Fuel Servies of CO will come at least every 3 years and polish the fuel which will help maintain the quality of the fuel. MonitoringStand-by-power will come and test the diesel quality annually. If any fuel quality issues are identified corrective action will be taken. Title of person responsibleMaintenance Director or designee will oversee this POC. Completion dateCompliance was reached on 10/31/24
9/25/2024Recertification Survey · ID 4WHJ114 deficiencies▼
0000Initial CommentsSurveyor note2 building records▼
Findings · record 1 of 2
A recertification survey was conducted from 9/22/24 to 9/25/24. Four deficiencies were cited.
Findings · record 2 of 2
An Emergency Preparedness survey was conducted from 9/22/24 to 9/25/24. No 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 interviews, observations and record review, the facility failed to promote care for residents in a manner and in an environment that maintained or enhanced their dignity and respect for one (#35) of three residents reviewed for dignity out of 19 sample residents. Specifically, the facility failed to ensure Resident #35's fall intervention sensor alarm was discussed with the resident on how it made her feel. Findings include:I. Facility policy and procedureThe Elder rights policy, revised 7/8/24, was provided by the nursing home administrator (NHA) on 9/25/24/at 2:53 p.m. It read in pertinent part,"All elders will be treated equally regardless of age, race, ethnicity, religion, culture, language, physical or mental disability, socioeconomic status, sex, sexual orientation, or gender identity or expression. The campus will ensure that all staff members are educated on the rights of elders and the responsibility of the campus to properly care for its elders."II. Resident statusResident #35, age above 65, was admitted on 6/30/23. According to the September 2024 computerized physician orders (CPO), diagnosis included unspecified dementia, abnormal posture, insomnia, repeated falls and abnormal weight loss. The 6/30/24 minimum data set (MDS) assessment revealed the resident had moderate cognitive impairments with a brief interview for mental status score (BIMS) of 11 out of 15. She had no behaviors and did not reject care. She used a walker and a wheelchair. She required assistance with transfers and moving between surfaces. She was able to propel herself in her wheelchair and reposition herself in bed. She was always continent of bowels and bladder. She had two or more falls with injury since admission. A motion sensor alarm was used daily. III. Resident interviewsResident #35 was interviewed on 9/23/23 at 10:04 a.m. She said she felt like she was treated differently than the other residents. She said the facility used an alarm to track her movements which restricted her movements. She said when she tried to reposition herself in bed, the alarms would activate. She said she would stop moving around or have to crawl between the touch call lights that were on her bed. She said there were also two motion sensor alarms, one at the foot of the bed and one on the other side of the room that would activate when she placed her feet on the ground. She said no one had ever asked her how the alarms made her feel. She said everyone in the house knew when she was moving around. Resident #21 was interviewed on 9/25/24 at 11:49 a.m. Resident #21 said the jingle that was heard throughout the house, was Resident #35's motion sensor alarm notifying everyone that she was moving. She said staff would immediately respond to the alarm. IV. ObservationsOn 9/23/24 at 10:00 a.m. observations of Resident #35's room revealed she had two motion sensor alarms. One at the foot of the bed and one across from the bed. On 9/24/24 at 9:34 a.m. Resident #35 was observed sitting in the common area in a recliner watching television. Two push call lights were observed. One on top of each arm of the chair. The resident tried to reposition herself and the push call light, on the right arm of the chair, fell off and activated. Staff immediately responded and asked her if she needed anything. V. Record reviewThe September 2024 CPO revealed the resident had an order to monitor the motion sensor for proper placement and functioning every day and night shift for motion sensor use, ordered on 8/14/24. An incident note, dated 3/4/24 at 10:21 a.m., documented a motion sensor alarm was placed in Resident #35's room to alert staff when she was attempting to get up. A health status noted, dated 6/4/24 at 3:30 a.m., documented Resident #35 was restless most of the night as evidence of the motion sensor alarming frequently throughout the night.. When staff entered the room to ask how she was or what she needed, the resident was either quiet with no response or when asked if she was alright she responded yes. A behavior note, dated 6/20/24 at 1:00 a.m., documented Resident #35 was fidgety and up to the toilet four times since going to bed and the sensor alarm rang often throughout the night. A behavior note, dated 8/25/24 at 12:04 a.m,. documented Resident #35 had been restless as evidence of the sensor alarm chiming frequently since the resident went to bed at 6:30 p.m. VI. Staff interviewsCertified nurse aide (CNA) #4 was interviewed on 9/24/24 at 9:49 a.m. CNA #4 said she did not know why Resident #35 had two touch call lights and was not aware of a motion sensor alarm. She said she usually worked in a different house. CNA #5 was interviewed on 9/24/24 at 10:05 a.m. CNA #5 said Resident #35's motion alarm was used to notify the staff that she was attempting to get out of her bed, wheelchair or recliner. She said the alarm was audible for everyone to hear. She said the alarm sounded in the common area of the facility. She said she did not feel the motion alarm was very effective. The director of nursing (DON) was interviewed on 9/25/24 at 10:47 a.m. The DON said Resident #35 was a difficult resident to keep free from falling. She said the facility had placed the two push call lights near the resident. She said the resident would climb around them. She said the facility then decided to place the two motion sensors along with the push call lights in the resident's room. She said the resident was able to climb around the motion sensors as well. She said the alarms were activated frequently due to the resident putting her feet on the ground or bumping the push call lights when moving. The DON said she was not aware of how the alarms affected the resident or made her feel. She said she never asked her. She said the social services director (SSD) may have spoken with her but she was not sure. She said she would speak with the resident about how it made her feel and figure out something different. The NHA was interviewed on 9/25/24 at 11:26 a.m. The NHA said she was not aware of how the motion alarms made the resident feel. She said she had never asked her. She said when the facility first decided to use the motion sensor alarm the resident was willing to try them. The NHA said they had never reassessed how the resident felt about the alarms. The SSD was interviewed on 9/25/24 at 1:22 p.m. The SSD said she was not involved with the initiation of the motion sensor alarms and had not interviewed Resident #35 on how she felt.
Plan of correction · submitted by the facility
F-550 Dignity
1. Elder 35 was affected by this deficient practice. Elder 35 was interviewed by NHA and Resident Service Director (RSD) in regards to how she feels about the motion sensors. She reported that they went off too easily when she moved around. The motion sensors were adjusted to a lower position so they won’t alarm until the elder puts her feet on the floor. The elder was agreeable to this change. 2. Other elders have the ability to be affected by this deficient practice. All elders with motion sensors have been interviewed and adjustments have been made according to their preferences and safety. 3. All staff education was completed on 10/22/24 about this deficient practice. All staff were educated on elders’ rights to maintain dignity. Consent will be obtained for all elders who are in need of motion sensors prior to being put in place and added to their care plan. The RSD, or designee will interview all elders with current motion sensors and consents monthly for 3 months and quarterly thereafter. The RSD will maintain a spreadsheet with the elder’s name, date, interview findings, and care plan changes made. Elders will be asked about how they feel in regards to the motion sensor, if they feel it is helping to maintain their safety, and if they are agreeable to continue to have the motion sensor in place. Adjustments will be made to the elders’ care plan based on interview findings. 4. The RSD, or designee will report results of the above systematic changes to the QAPI committee monthly until substantial compliance is met. 5. Compliance date: 10/25/24
0656Develop/Implement Comprehensive Care PlanS/S E▼
Findings
Based on record review and staff interviews, the facility failed to develop and implement a comprehensive care plan for three (#38, #24 and #3) of five residents reviewed for care plans out of 19 total sample residents. Specifically, the facility failed to: -Ensure Resident #38 had a care plan for the use of an anticoagulant medication;-Ensure Resident #24 had a care plan for the use of supplemental oxygen; and,-Ensure Resident #3 had a care plan for the use of a diuretic medication. Findings include:I. Facility policy and procedureThe Care Plan policy, revised 8/12/24, was provided by the nursing home administrator (NHA) on 9/25/24 at 2:53 p.m. It read in pertinent part, "A comprehensive, person-centered care plan that includes measurable objectives and timetables to meet the resident's physical, psychosocial and functional needs is developed and implemented for each resident."The care plan interventions are derived from a thorough analysis of the information gathered as part of the comprehensive assessment."The comprehensive, person-centered care plan includes measurable objectives and timeframes describing the services that are to be furnished to attain or maintain the resident's highest practicable physical, mental, and psychosocial well-being."Care plan interventions are chosen only after data gathering, proper sequencing of events, careful consideration of the relationship between the resident's problem areas and their causes, and relevant clinical decision making. When possible, interventions address the underlying source(s) of the problem area(s), not just symptoms or triggers."Assessments of residents are ongoing and care plans are revised as information about the residents and the residents' conditions change."II. Resident #38A. Resident statusResident #38, age greater than 65, was admitted on 5/20/24. According to the September 2024 computerized physician orders (CPO), diagnoses included atrial fibrillation (irregular heartbeat), gross hematuria (blood in the urine), personal history of other venous (vein) thrombosis (blood clot) and embolism (blockage inside a blood vessel), cardiac murmur and long term current use of anticoagulants. The 9/1/24 minimum data set (MDS) assessment revealed the resident had severe cognitive impairment with a brief interview for mental status score (BIMS) score of six out of 10. She required moderate assistance with bathing, repositioning, dressing, personal hygiene, transfers and toilet use. The assessment indicated the resident received an anticoagulant medication daily. B. Record reviewThe September 2024 CPO revealed the resident had a physician's order for Eliquis (a blood thinner) 5 mg (milligrams) twice a day with a start date of 7/10/24. -There was no care plan addressing the use of the anticoagulant medication or its side effects. C. Staff interviewsLicensed practical nurse (LPN) #2 was interviewed on 9/24/24 at 1:41 p.m. LPN #2 said she was not sure if the use of an anticoagulant medication needed to have a care plan or not. She said the nurses gave input when there was a new admission but the management team was responsible for updating the residents' care plans. She said nurses did not have a lot to do with care plans. The director of nursing (DON) was interviewed on 9/25/24 at 10:47 a.m. The DON said a care plan should be in place to address the use of Resident #38's anticoagulant. She said the care plan should include watching for signs and symptoms of side effects related to anticoagulant medication use, such as excessive bruising, excessive bleeding and blood in the urine and stool. She said it was very important to monitor for these side effects, especially if the resident was scheduled for surgery. The DON said she would immediately ensure a care plan was initiated for the use of the anticoagulant medication. The NHA was interviewed on 9/25/24 at 11:21 a.m. The NHA said a care plan should be in place for Resident #38's anticoagulant medication use. She said an anticoagulant was a significant medication with risk factors and needed a reason for use. She said the care plan should address the monitoring of side effects or complications. She said having a care plan in place was important so all staff would know how to care for the resident and the risks involved. She said the minimum data set (MDS) coordinator was responsible for initiating the comprehensive care plans. The NHA said she did not know how the implementation of a care plan for the use of Resident #38's anticoagulant medication was missed. III.Resident #24A. Resident status Resident #24, age greater than 65, was admitted on 11/19/21. According to the September 2024 CPO, diagnoses included Parkinson's (chronic brain disorder that affects movement), dementia (decrease cognitive thinking), hypoxemia (low levels of oxygen in the blood) and hypertension (increased blood pressure). The 7/21/24 MDS assessment revealed the resident was moderately cognitively impaired with a BIMS score of 10 out of 15. The assessment indicated the resident required supplemental oxygen but it did not reveal if oxygen was to be administered continuously or intermittently. B. Record review-Review of Resident #24's comprehensive care plan failed to reveal a care plan focus for supplemental oxygen use. The September 2024 CPO revealed the following physician's orders for oxygen:Supplemental oxygen per nasal cannula at 2 liters per minute (LPM) to keep oxygen at or above 90% (percent), ordered 2/1/23. May apply oxygen to continuous positive airway pressure (CPAP) machine at night if oxygen saturations (level of oxygen in the blood) were below 90%, ordered 2/16/23. The Kardex (a tool used by the certified nurse aides (CNA) to provide consistent care) failed to document how much supplemental oxygen Resident #24 was to receive. C. Staff interviewsCNA #3 was interviewed on 9/24/24 at 1:56 p.m. CNA #3 said CNAs did a verbal report during shift change and that was how staff knew how much oxygen a resident should be on. LPN #1 was interviewed on 9/24/24 at 2:16 p.m. LPN #1 said she would look at the physician's orders to know how many liters of oxygen a resident should be on. LPN #1 said the use of supplemental oxygen should be care planned. LPN #1 said she was unable to locate oxygen on Resident #24's care plan. CNA #1 was interviewed on 9/25/24 at 11:16 a.m. CNA #1 said staff had access to residents' Kardex and she said the oxygen liter flow should be documented on the Kardex. CNA #1 reviewed the Kardex for Resident #24 and said she was unable to identify how much oxygen Resident #24 should be receiving. CNA #1 said she knew Resident #24 was on oxygen because she had gotten the information in report. The DON was interviewed on 9/25/24 at 12:20 p.m. The DON said it was her assistant director of nursing (ADON)/MDS coordinator's responsibility to ensure care plans were updated. The DON said care plans should include all care provided to a resident, including supplemental oxygen use. IV. Resident #3A. Resident statusResident #3, age greater than 65, was admitted on 11/20/2020. According to the September 2024 CPO, diagnoses included dementia and hypertensive chronic kidney disease. The 8/7/24 MDS assessment revealed the resident was significantly cognitively impaired with a BIMS score of one out of 15. The MDS did not indicate Resident #3 was taking a diuretic medication. B. Record reviewThe incontinence care plan, revised 12/9/2020, revealed Resident #3 had mixed bladder incontinence. Pertinent interventions included encouraging fluids during the day to promote prompted voiding responses. The hypertension care plan was revised 12/9/24. Pertinent interventions included monitoring for edema, monitoring and documenting any abnormalities in urinary output and giving anti-hypertensive medications as ordered. The September 2024 CPO revealed a physician's order for Lasix (furosemide) 40 mg with instructions to give one tablet by mouth one time a day for edema, ordered 1/16/24. The 8/14/24care plan conference notes revealed Resident #3's care plan was reviewed by the director of nursing (DON) and assistant director of nursing (ADON) but no changes were noted at that time.-The comprehensive care plan did not include a care plan focus related to chronic kidney disease or diuretic medication monitoring. C. Staff interviewsLPN #1 was interviewed on 9/25/24 at 9:49 a.m. LPN #1 said Resident #3 did not have any fluid restrictions. LPN #1 said Resident #3 was prescribed Lasix and potassium and explained that Lasix was a diuretic medication. LPN #1 said Resident #3 had good fluid intake and drank well, so the nursing staff did not have to push more fluids for the resident but needed to monitor her for edema. LPN #1 said interventions related to Resident #3's hydration status would be found in the care plan. LPN #1 said all facility staff worked on the residents' care plans but they were primarily maintained by the ADON.The ADON was interviewed on 9/25/24 at 1:10 p.m. The ADON said she maintained the majority of residents' care plans but that the management team worked on them as well. The ADON said she had not put any specific care plan focus into any residents' comprehensive care plans for medications such as diuretics. The ADON said it was important to have a diuretic care plan because of the resident's risk of dehydration or fluid overload. The ADON said Resident #3 should also have a care plan focus for her chronic kidney disease.
Plan of correction · submitted by the facility
F-656 Care Plans1. A care plan focus has been created for Elder 38 for anticoagulant use. A care plan focus has been created for Elder 24 for oxygen use. A care plan focus has been created for Elder 3 for diuretic use. 2. Other elders can be affected by this deficient practice. A full audit of all elders’ orders was completed to identify all elders who are on an anticoagulant, utilize supplemental oxygen, or are taking a diuretic. Care plans were audited to ensure there are care plan focuses for those orders. 3. All staff education was completed on 10/22/24 about this deficient practice. This education includes the importance of care planning for any elders taking medications or requiring therapies, specifically anticoagulants, supplemental oxygen and diuretics. The All staff education will also include what should be included in these care plans, as well as when the care plan should be created or initiated. Upon admission, the DON or designee will review the admission orders and ensure that the appropriate care plan focuses are present for any anticoagulant, supplemental oxygen, or diuretic use. The DON or designee will review the order listing report at least weekly for any new anticoagulant, oxygen, or diuretic orders and create appropriate care plans as needed. A spreadsheet will be maintained to track monitoring and compliance. 4. The DON or designee will monitor the above systematic changes by reviewing the order listing report weekly for 4 weeks and monthly for 3 months. The DON or designee will report identified issues or trends to QAPI monthly until substantial compliance is met. 5. Compliance date: 10/25/24
0757Drug Regimen is Free from Unnecessary DrugsS/S D▼
Findings
Based on record review and interviews, the facility failed to ensure drug regimens were free from unnecessary medications for one (#38) of five residents reviewed for unnecessary medications out of 19 sample residents. Specifically, the facility failed to ensure Resident #38 was adequately monitored and side effects were documented for the use of an anticoagulant medication. Findings include:I. Facility policy and procedureThe Anticoagulant policy, revised 8/24/24, was provided by the nursing home administrator (NHA) on 9/25/24 at 2:53 p.m. It read in pertinent part, "As part of the initial assessment, the physician and staff will identify individuals who are currently anticoagulated. For example, those with a recent history of deep vein thrombosis (DVT), or heart valve replacement, atrial fibrillation or those who have had recent joint replacement surgery."Assess for any signs or symptoms related to adverse drug reactions due to the medication alone or in combination with other medications."Assess for evidence of effects related to the subtherapeutic or greater than therapeutic drug level related to that particular drug (for example, a resident with an above therapeutic level of an anticoagulation medication should be assessed for bleeding)."The staff and physician will monitor for possible complications in individuals who are being anticoagulated, and will manage related problems. If an individual on anticoagulation therapy shows signs of excessive bruising, hematuria, hemoptysis (bleeding from the mouth), or other evidence of bleeding, the nurse will discuss the situation with the physician before giving the next scheduled dose of anticoagulant. The physician will order measures to address any complications, including holding or discontinuing the anticoagulant as indicated."II. Resident #38A. Resident statusResident #38, age greater than 65, was admitted on 5/20/24. According to the September 2024 computerized physician orders (CPO), diagnoses included atrial fibrillation (irregular heartbeat), gross hematuria (blood in the urine), personal history of other venous (vein) thrombosis (blood clot) and embolism (blockage inside a blood vessel), cardiac murmur and long term current use of anticoagulants. The 9/1/24 minimum data set (MDS) assessment revealed the resident had severe cognitive impairment with a brief interview for mental status score (BIMS) score of six out of 10. She required moderate assistance with bathing, repositioning, dressing, personal hygiene, transfers and toilet use. The assessment indicated the resident received an anticoagulant medication daily. B. Record reviewThe September 2024 CPO revealed the resident had a physician's order for Eliquis (a blood thinner) 5 mg (milligrams) twice a day with a start date of 7/10/24. -There was no care plan addressing the use of the anticoagulant medication or its side effects. Cross reference F656 for failure to have a care plan for the use of an anticoagulant medication. III. Staff interviewsLicensed practical nurse (LPN) #2 was interviewed on 9/24/24 at 1:41 p.m. LPN #2 said the nurses should be monitoring for side effects of the anticoagulant medication, such as increased bleeding or a change in cognition. She said she could not remember the other signs to monitor for when a resident was on an anticoagulant medication. The director of nursing (DON) was interviewed on 9/25/24 at 10:47 a.m. The DON said the care plan should include watching for signs and symptoms of side effects related to anticoagulant medication use, such as excessive bruising, excessive bleeding and blood in the urine and stool. She said it was very important to monitor for these side effects, especially if the resident was scheduled for surgery. The DON said she would immediately ensure Resident #38 was being monitored for possible side effects or complications related to the use of the anticoagulant medication. The NHA was interviewed on 9/25/24 at 11:21 a.m. The NHA said an anticoagulant was a significant medication with risk factors and needed a reason for use. She said the care plan should address the monitoring of side effects or complications. She said there should be a physician's order to monitor the resident for side effects and/or complications related to the use of an anticoagulant medication.
Plan of correction · submitted by the facility
F-757 Unnecessary Drugs
1. An order for side effect tracking for Elder 38’s anticoagulant has been added to their active orders. 2. Other elders can be affected by this deficient practice. An audit of all elders on anticoagulants has been completed and side effect tracking put in place. 3. All staff education was completed on 10/22/24 about this deficient practice. Upon admission, the DON or designee will review orders to identify if there are any anticoagulant medications and ensure side effect monitoring is in place. All nurses will be educated on the procedure for placing side effect monitoring on anticoagulant orders. 4. The DON or designee will monitor anticoagulant side effect monitoring by reviewing the order listing report weekly for 4 weeks and monthly for 3 months. A spreadsheet will be maintained to track the anticoagulation medication side effect monitoring, which will include the elders name, date, medication, and that side effect monitoring is in place. The DON or designee will report identified issues or trends to QAPI monthly until substantial compliance is met. 5. Compliance date: 10/25/24
0880Infection Prevention & ControlS/S D▼
Findings
Based on observations, record review and interviews, the facility failed to maintain an infection control program designed to provide a safe, sanitary and comfortable environment to help prevent the possible development and transmission of infectious diseases. Specifically, the facility failed to ensure nursing staff followed proper infection control procedures for a resident on enhanced barrier precautions (EBP). Findings include:I. Professional referenceThe Centers for Disease Control and Prevention (CDC) Implementation of Personal Protective Equipment (PPE) Use in Nursing Homes to Prevent Spread of Multidrug-resistant Organisms (MDROs) (4/2/24), was retrieved on 9/26/24 from https://www.cdc.gov/long-term-care-facilities/hcp/prevent-mdro/PPE.html. It read in pertinent part,"Enhanced Barrier Precautions (EBP) are an infection control intervention designed to reduce transmission of resistant organisms that employs targeted gown and glove use during high contact resident care activities."EBP may be indicated (when contact precautions do not otherwise apply) for residents with wounds or indwelling medical devices, regardless of MDRO colonization status."II. Facility policy and procedureThe Infection Prevention and Control Program policy, revised 8/12/24, was received from the nursing home administrator (NHA) on 9/25/24 at 2:50 p.m. It read in pertinent part, "The designated infection preventionist serves as a consultant to our staff on infectious diseases, elder room placement, implementing of isolation precautions, staff and elder exposures, surveillance, and epidemiological investigations of exposures of infectious diseases."Staff shall use personal protective care equipment (PPE) according to established campus policy governing the use of PPE."-The policy did not include specifics for EBP.III. Resident interviewResident #29 was interviewed on 9/24/24 at 2:29 p.m. Resident #29 said he had a urinary catheter. Resident #29 said the nursing staff helped him with his catheter care by emptying his catheter bag whenever he needed it and switching from a night bag to a leg bag each morning. Resident #29 said the nursing staff only wore gloves when they helped him perform catheter care. Resident #29 said he had not seen the nursing staff wear gowns while helping him perform catheter care. IV. ObservationsOn 9/23/24 at 10:06 a.m. there was no PPE observed in or outside Resident #29's room. On 9/24/24 at 2:29 p.m. there was no PPE observed in or outside Resident #29's room. V. Record reviewThe incontinence care plan, revised 9/14/23, revealed Resident #29 had a urinary catheter in place. Pertinent interventions included changing Resident #29's catheter as needed, cleansing the catheter daily, and assisting Resident #29 with emptying his catheter bag and catheter care every shift and as needed.-Review of the resident's electronic medical record (EMR) did not reveal any information regarding the use of EBP or PPE while performing care. VI. Staff interviewsCertified nurses aide (CNA) #6 was interviewed on 9/24/24 at 3:05 p.m. CNA #6 said the nursing staff helped Resident #29 with his urinary catheter, which included switching from his night bag to his leg bag, cleaning the bag, changing his urinary catheter, and helping Resident #29 dress his bottom half. CNA #6 said she applied gloves whenever she needed to provide catheter care for Resident #29. CNA #6 said she did not wear a gown or any other PPE while providing catheter care. Licensed practical nurse (LPN) #1 was interviewed on 9/25/24 at 9:49 a.m. LPN #1 was not sure what EBP entailed. LPN #1 said for urinary catheter care she only needed to wear gloves. LPN #1 said if a resident had any sort of infection she would be more likely to wear PPE. LPN #1 said the CNAs helped Resident #29 change his catheter bag each morning and wiped the catheter area with alcohol. LPN #1 said the CNAs only wore gloves to perform this care but that she would advise them to wear a gown just in case any urine splattered during the process. LPN #1 said the CNAs were not required to wear a gown unless the resident had something that was contagious. The infection preventionist (IP) and the NHA were interviewed together on 9/25/24 at 1:10 p.m. The IP and NHA said did not know what EBP were or what they entailed. The IP said she did not know the nursing staff needed to wear PPE unless the resident had an infection. The IP acknowledged the facility did not have a system in place to notify if residents were on EBP.
Plan of correction · submitted by the facility
F-880 Infection Prevention and Control
1. Enhanced Barrier Precautions (EBP) has been added to Elder 29’s care plan. 2. Other elders can be affected by this deficient practice. All elders have been reviewed for their need for EBP and their care plans have been updated. 3. All staff education was completed on 10/22/24 about this deficient practice. This education included what EBP is, what elders need EBP, how to identify additional elders who may need EBP. The DON or designee will review new admissions weekly as well as current elder’s orders and conditions for the need for EBP and ensure it is in place and included in the elder’s care plan. 4. The DON or designee will review orders weekly for 4 weeks and monthly for 3 months for any that would indicate the need for EBP and ensure it is in place. A spreadsheet will be maintained listing any orders or conditions noted that would require EBP and whether it’s been put in place. The DON or designee will complete random observation audits with staff to ensure that they are following EBP with the required elders. The DON or designee will report identified issues or trends to QAPI monthly until substantial compliance is met. 5. Compliance date: 10/25/24
6/5/2024Complaint Survey · ID GD5E11No deficiencies▼
0000INITIAL COMMENTSSurveyor note▼
Findings
A complaint survey, prompted by #CO36226 was conducted on 6/5/24. No deficiencies were cited.
Plan of correction
The state did not require a plan of correction for this citation.
8/14/2023Revisit: Recertification Survey · ID DYL122No 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.
7/18/2023Revisit: State Licensure Survey · ID 3L2V12No deficiencies▼
0000Initial CommentsSurveyor note▼
Findings
A revisit survey was completed on 7/18/23 for all previous deficiency cited on 5/17/23. The facility is in compliance with all regulations surveyed.
Plan of correction
The state did not require a plan of correction for this citation.
7/18/2023Revisit: Recertification Survey · ID DYL112No deficiencies▼
0000Initial CommentsSurveyor note▼
Findings
A revisit survey was completed on 7/18/23 for all previous deficiencies cited on 5/17/23. The facility is in compliance with all regulations surveyed.
Plan of correction
The state did not require a plan of correction for this citation.
Reportable Occurrences
7 records1/8/2026Diverted Drugs · ID 26020162002Reported on time: Yes▼
Occurrence summary
SUMMARY OF FINDINGS:On 1/9/26, the healthcare entity investigated a reportable event of diverted drugs. 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 2/10/26, Event ID 1E397D-H1. 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 4/13/2026 · released to the public 4/20/2026.
8/15/2024Misappropriation of Property · ID 24020162005Reported on time: Yes▼
Occurrence summary
SUMMARY OF FINDINGS:On 8/15/24, 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 misappropriation of client property. During the course of the investigation, the healthcare entity placed four staff identified members on suspension pending the outcome of the investigation. The healthcare entity became aware that the client was possibly giving staff money. Staff and client interviews revealed client (A) was writing checks for the staff to purchase items from the store for them. All four staff confirmed this and stated they had receipts for all purchases made. The police were notified and conducted their own investigation. The healthcare entity concluded client (A) was of sound mind and the staff members involved did not willfully take or misuse the client’s money. 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 3/9/2025 · released to the public 3/17/2025.
5/11/2024Physical Abuse · ID 24020162003Reported on time: Yes▼
Occurrence summary
SUMMARY OF FINDINGS: On 5/11/24, 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 physical abuse event. During the course of the investigation, the healthcare entity reported male client (A) started yelling at female client (B) after she took a food item from him. He then grabbed female client (B)’s wrist causing an abrasion. Client (B) was visibly upset when staff separated the clients. First aid treatment was provided and safety monitoring was initiated. Through interviews, client (A) reported she took his granola bar and he wanted to break her wrist. Client (A) moved to a different area for monitoring and client (B)’s medications were adjusted to help with behavioral management. 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 3/2/2025 · released to the public 3/10/2025.
5/11/2024Misappropriation of Property · ID 24020162004Reported on time: Yes▼
Occurrence summary
SUMMARY OF FINDINGS: On 5/11/24, 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 misappropriation of property event. During the course of the investigation, the healthcare entity reported female client (B) took a granola bar from male client (A)’s walker bag without permission and started eating it. Client (A) physically reacted to the situation causing an injury to client (B). Refer to event ID# 24020162003 for details on the physical incident. Staff separated the clients and provided additional monitoring. Client (A) was moved to a different house. Education was provided to client (B) about not taking things without permission. 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 2/25/2025 · released to the public 3/4/2025.
3/22/2024Physical Abuse · ID 24020162002Reported on time: Yes▼
Occurrence summary
SUMMARY OF FINDINGS:On 3/22/24, 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 an alleged physical abuse event involving two clients. During the course of the investigation, the healthcare entity reported client (A) allegedly hit client (B) in the nose. Client (B) suffered an abrasion. Staff kept the clients separated and provided first aid treatment. The altercation occurred over an argument about a cup of pop and cigarettes. From further interviews, the facility concluded the abrasion might have been caused during the exchange of the metal cup. A room move occurred to keep the clients separated and an alternative smoking area was arranged. 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 2/11/2025 · released to the public 2/18/2025.
2/23/2024Brain Injury · ID 24020162001Reported on time: No▼
Occurrence summary
DESCRIPTION OF OCCURRENCE: On 2/23/24, a resident experienced an unwitnessed fall while he was in the bathroom. A staff member, present in the room at the time, heard a loud noise and found the resident on the floor unconscious. The resident was immediately assessed by the registered nurse (RN) and he was noted to be guarding his right elbow. His range of motion was noted within normal limits and he was provided with first aid at the time. The resident was transported to the hospital for further evaluation and treatment. A CT scan of the head showed he had a brain bleed and additional x-rays showed a fractured right hip. AGENCY/FACILITY ACTION: The facility conducted an internal investigation and notified the physician and family/guardian. Record review showed the resident was assessed upon admission to have moderate cognitive impairment and he had a history of falls. He was ambulatory with the use of a walker and was receiving physical therapy. The record review further showed safety interventions were in place prior to the fall and he had been in the bathroom independently per his baseline. The facility reported the resident’s family declined further treatment and elected comfort measures upon his discharge back to the facility. The resident remained bed bound and was monitored closely by staff. The facility concluded the patient had been independent in the bathroom at the time of the incident. Staff was outside of the bathroom, although present in the room, had allowed the resident his privacy. The record review showed the resident subsequently passed away in the facility.
DEPARTMENT FINDINGS: In accordance with Colorado Revised Statute 25-1-124, the Department conducted an off-site investigation of this reportable event submitted by the agency/facility. This public summary is based on information provided by the agency/facility to the Occurrence section of the Department. The provider reports the information submitted to the Department is accurate and complete. Prior to the next onsite investigation of the agency/facility, this occurrence will be reviewed by the State Agency. The facility/agency complied with licensing standards for conducting an internal investigation of this Occurrence event and submitting a report of the findings to the Department. However, the licensing standard for timely reporting was not met
Publication
Sent to facility 11/25/2024 · released to the public 12/2/2024.
1/9/2023Sexual Abuse · ID 23020162001Reported on time: Yes▼
Occurrence summary
DESCRIPTION OF OCCURRENCE:
On 01/09/23 a male resident's family member reported the resident told his wife he did not need her anymore because he had an intimate physical relationship with the alleged staff during showers. The resident was in his 60s and was mildly cognitively impaired.
FACILITY / AGENCY ACTION:
The facility conducted an internal investigation and notified the police, physician, families/guardians and ombudsman. The staff member was suspended. The resident denied the allegation when interviewed. The staff member denied ever sexually touching or interacting with the resident. The staff member said the resident had said she was his girlfriend and always corrected him saying she was married and was not his girlfriend. Other staff were interviewed and said the resident prefers the accused staff member provide care to him but denied ever witnessing anything inappropriate by the staff member. The allegation could not be substantiated. Staff will work in pairs when caring for the resident. The staff member was assigned to a different unit.
DEPARTMENT FINDINGS:
In accordance with Colorado Revised Statute 25-1-124, the Department conducted an off-site investigation of this reportable event and investigative findings submitted by the agency/facility. This public summary is based on information provided by the agency/facility to the Occurrence Section of the Department and is accurate and complete at this time. Prior to the next onsite investigation of the agency/facility, this occurrence will be reviewed.
The occurrence report indicated the agency/facility acted appropriately in response to this occurrence by complying with licensing standards of reporting and investigating this occurrence.
Publication
Sent to facility 8/1/2023 · released to the public 8/8/2023.