HARTLEY NURSING AND REHAB

1006 MARKET STREET, POCOMOKE CITY, MD 21851 (410) 957-2252
For profit - Limited Liability company 73 Beds KEY HEALTH MANAGEMENT Data: November 2025 1 Immediate Jeopardy citation
Trust Grade
58/100
#70 of 219 in MD
Last Inspection: July 2024

Within standard 12-15 month inspection cycle. Federal law requires annual inspections.

Overview

Hartley Nursing and Rehab holds a Trust Grade of C, which means it is average compared to other facilities, sitting in the middle of the pack. It ranks #70 out of 219 nursing homes in Maryland, indicating it is in the top half of state facilities, and holds the top spot among three facilities in Worcester County. However, the facility is showing a worsening trend, as the number of issues reported increased from 7 in 2019 to 9 in 2024. Staffing is a concern here, with a rating of 2 out of 5 stars and a turnover rate of 45%, which is near the state average, indicating that staff do not stay long enough to build strong relationships with residents. On a positive note, the facility has not incurred any fines, which is a good sign of compliance with regulations. There is also average RN coverage, which is essential for catching problems that might be missed by less experienced staff. However, there have been critical incidents, such as a resident being able to leave the facility unattended, posing a serious safety risk. Additionally, documentation issues regarding medication and timely reporting of health concerns show areas that need improvement. Overall, while Hartley Nursing and Rehab has some strengths, families should be aware of the concerning staffing issues and past safety incidents when considering this facility.

Trust Score
C
58/100
In Maryland
#70/219
Top 31%
Safety Record
High Risk
Review needed
Inspections
Getting Worse
7 → 9 violations
Staff Stability
⚠ Watch
45% turnover. Above average. Higher turnover means staff may not know residents' routines.
Penalties
✓ Good
No fines on record. Clean compliance history, better than most Maryland facilities.
Skilled Nurses
○ Average
Each resident gets 40 minutes of Registered Nurse (RN) attention daily — about average for Maryland. RNs are the most trained staff who monitor for health changes.
Violations
⚠ Watch
27 deficiencies on record. Higher than average. Multiple issues found across inspections.
★★★★☆
4.0
Overall Rating
★★☆☆☆
2.0
Staff Levels
★★★☆☆
3.0
Care Quality
★★★★☆
4.0
Inspection Score
Stable
2019: 7 issues
2024: 9 issues

The Good

  • Full Sprinkler Coverage · Fire safety systems throughout facility
  • No fines on record

Facility shows strength in fire safety.

The Bad

Staff Turnover: 45%

Near Maryland avg (46%)

Higher turnover may affect care consistency

Chain: KEY HEALTH MANAGEMENT

Part of a multi-facility chain

Ask about local staffing decisions and management

The Ugly 27 deficiencies on record

1 life-threatening
Jul 2024 9 deficiencies
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0582 (Tag F0582)

Could have caused harm · This affected 1 resident

Based on resident medical record review and interviews it was determined the facility failed to notify a resident that his/her Medicare services were ending with the right to appeal. This was evident ...

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Based on resident medical record review and interviews it was determined the facility failed to notify a resident that his/her Medicare services were ending with the right to appeal. This was evident for 1 out of 3 (Resident #1) residents reviewed during the survey. The findings include: Review of Resident #1's medical record on 07/09/2024 at 11:45 AM revealed a Notice of Medicare Non-Coverage form stating that Resident #1's Medicare covered services would end on 01/10/2024 with the right to appeal. Further review of this form revealed that there was no signature documented that Resident #1 had received this notice. During an interview on 07/09/2024 at 11:50 AM Staff #10 stated and verified that the Notice of Medicare Non-Coverage form was not signed by Resident #1. BIMS (Brief Interview for Mental Status) is a tool used to screen and identify the cognitive condition of a resident. The resident's BIMS score is calculated according to their correct answers. A score of 15 out of 15 reveals that the resident's cognitive functions are intact. Review of resident #1 medical record on 07/09/2024 at 12:05 PM revealed that Resident #1 had a BIMS score of 15 out of 15 on 04/19/2024. During an interview on 07/09/2024 at 12:20 PM Resident #1 was able to verbalize his/her name, the current month (July), day (09), and year (2024). Resident #1 stated that he/she was not notified that Medicare services were ending, and a notice was not given to him/her to sign.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Safe Environment (Tag F0584)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation and interview it was determined the facility failed to provide the residents with a clean, comfortable and ...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation and interview it was determined the facility failed to provide the residents with a clean, comfortable and homelike environment. This was evident for 3 residents' (#13, #17 and #11) rooms out of 8 residents rooms observed during the survey. The findings include: 1. During observation rounds on 07/08/2024 at 10:00 AM and on 07/10/2024 at 4:05 PM Resident #13's and #17's room floors were found dirty with streaks of a black colored substance, piles of gray dust like matter and brown colored stains under the residents' beds. During observation rounds and interview on 07/10/2024 at 04:05 PM with the Administrator she stated that Residents #13 and #17 rooms were dirty, and that the facility was working on renovations of the facility resident's rooms. 2. During an initial tour of the facility, this surveyor made the following observations: On 7/8/24 at 10:30am in room [ROOM NUMBER], the upper part of the wall, above the headboard had ripped drywall with large holes in the wall. This damage could be seen immediately upon entering the room. Cracks were noted on several floor tiles. The floor was black in color thru-out the room and a broken and peeling baseboard was noted on the side of the sink. The shower on the back hall was noted with cracked and yellow stained-glass tiles. During an interview on 7/8/24 at 3:30pm the Administrator stated the Director of Maintenance was in the process of stripping floors and repairing rooms. As of exit on 7/11/24 at 1pm, the repairs or stripping of the floor had been completed.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Transfer Notice (Tag F0623)

Could have caused harm · This affected 1 resident

Based on medical record review and staff interview it was determined the facility failed to notify the resident/resident representative in writing of a transfer/discharge of a resident along with the ...

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Based on medical record review and staff interview it was determined the facility failed to notify the resident/resident representative in writing of a transfer/discharge of a resident along with the reason for the transfer. This was evident for 1 (#29) of 2 residents reviewed for hospitalization during the survey. The findings include: Review of Resident #29 's medical record on 7/9/24 at 1:52pm revealed on 3/19/24 the resident was transferred to the hospital for a change in his/her medical condition. Further review of the medical record failed to reveal that the resident and/or the resident representative was notified in writing of the transfer/discharge of the resident along with the reason for the transfer. During an interview with the Director of Nursing and the Administrator on 7/9/24 at 3pm, it was revealed they was unable to locate any documents that the resident and/or the resident representative was notified in writing of the transfer/discharge of the resident along with the reason for the transfer. They stated that the former Administration used The Maryland Notice of Involuntary Transfer and Discharge Forms when a resident was transferred to the hospital. During an interview with the Ombudsman on 7/15/24 at 9am, she stated she doesn't receive the transfer/discharge forms for resident on a consistent basis.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0625 (Tag F0625)

Could have caused harm · This affected 1 resident

Based on medical record review and staff interview it was determined the facility failed to notify the resident/resident representative in writing of the bed hold policy when the resident was transfer...

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Based on medical record review and staff interview it was determined the facility failed to notify the resident/resident representative in writing of the bed hold policy when the resident was transferred/discharged from the facility to an acute care facility. This was evident for 1 (resident #29) of 2 residents reviewed that were transferred to an acute care facility. The findings include: Review of the medical record for Resident #29 on 7/9/24 at 2pm revealed on 3/19/24 the resident was sent to an acute care facility for a change in his/her medical condition. Further review of the medical record failed to produce written evidence that the resident and /or the resident representative were given written notice of the bed hold policy. During an interview with the Social Worker (staff # 17) on 9/26/23 at 5:50pm she stated the resident was given the reason for the transfer; however, she was unable to produce written evidence that the resident /resident representative was given written notice of the bed hold policy. During an interview with the Social Worker staff # 10 on 7/9/24 at 3pm, she revealed she was unable to locate a copy of the bed hold policy that was given to the resident /resident representative.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Comprehensive Care Plan (Tag F0656)

Could have caused harm · This affected 1 resident

Based on medical record review and staff interview it was determined the facility failed to develop a person-centered care plan for residents. This was evident for 2 residents (#11 and 21) out of 24 r...

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Based on medical record review and staff interview it was determined the facility failed to develop a person-centered care plan for residents. This was evident for 2 residents (#11 and 21) out of 24 residents reviewed during the survey. The findings include the following: 1. On 7/9/24 at 3:57pm a review of Resident #11's electronic medical record (EMR) revealed the resident was prescribed Paxil an antidepressant medication for off label use of sexually inappropriate behavior. Further review of the EMR revealed Resident #11 did not have a care plan for Paxil and/or sexually inappropriate behavior. On 7/9/24 at 4:30 pm the Director of Nursing (DON) verified the findings. She stated the Unit manager should have completed a care plan for the use of Paxil. I am unsure why the care plan was not completed. 2. On 7/10/24 at 2pm a review of Resident #21's electronic medical record (EMR) revealed the following physician orders: A. Administer Tylenol (Acetaminophen) 2 tablets by mouth every 6 hours as needed for right knee pain. B. Administer Tramadol 50 MG 1 tablet by mouth every 6 hours as needed for severe pain (7-10) right knee pain. Further review of the medical record revealed Resident #21 received a steroid injection in June of 2024 during a visit to the pain management clinic for right knee pain; however, the medical record failed to reveal a care plan was developed for pain management.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Accident Prevention (Tag F0689)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations, resident medical record review and interviews it was determined the facility failed to complete a smoking...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations, resident medical record review and interviews it was determined the facility failed to complete a smoking assessment for Resident #56. This was evident for 1 resident (#56) out of 2 residents reviewed for smoking during the survey. The findings include: During the facility entrance conference on 07/08/2024 at 11:00 AM the Administrator stated that there were no smoking residents in the building and the facility was a smoke free facility. During observation rounds on 07/10/2024 at 1:20 PM Resident #56 was found smoking outside unattended, on the facility property near a resident facility room window. The facility room window had a sign posted on it stating room [ROOM NUMBER]. Review of Resident #56's medical record on 07/10/2024 at 2:45 PM revealed that the resident was admitted on Hospice 04/18/2024. Continued review of the resident medical record revealed a care plan that was initiated on 03/20/24 documenting that the resident was a smoker. Further review of the resident medical record revealed that there was no smoking assessment completed on this resident. During an interview on 07/10/2024 at 3:05 PM the Administrator stated that the facility is a smoke-free environment. The Administrator further stated that Resident #56 is a smoker and signs him/her out on leave of absence (LOA) every day to go outside to smoke. On 07/10/2024 at 4:20 PM after surveyor intervention, the Director of Nursing provided a smoking assessment dated [DATE] for Residents #56.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0711 (Tag F0711)

Could have caused harm · This affected 1 resident

Based on medical record review and staff interview it was determined that what the Physician and the Nurse Practitioner documented in the resident's (#11) progress notes did not accurately reflect wha...

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Based on medical record review and staff interview it was determined that what the Physician and the Nurse Practitioner documented in the resident's (#11) progress notes did not accurately reflect what was in the resident's medical record. This was evident for 1 of 24 residents reviewed during the survey. The findings include: Resident #11's medical record was reviewed on 7/10/24 at 5:04pm. The review revealed Resident #11 was admitted to the facility with diagnosis that included Anxiety disorder, Depressive disorder. Review of the medical record on 7/10/24 at 6pm revealed Resident #11 was seen by the physician (staff # 15) on 5/17/24 and by the Nurse Practitioner (Staff #14) on 6/12/24 and at that time staff (#15) and staff (#14) documented that the resident was receiving Lexapro for panic attacks; however, according to the Medication Administration Record and the Physician Order the resident Lexapro was discontinued on 5/24/23 by staff (#15). During an interview with the Assistant Director of Nursing (ADON) on 7/10/24 at 6:30pm he verified the findings.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0761 (Tag F0761)

Could have caused harm · This affected 1 resident

Based on observations, interviews and review of facility documentation, the facility failed to properly store medications and biologicals under proper temperature controls. This was evident in 1 out o...

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Based on observations, interviews and review of facility documentation, the facility failed to properly store medications and biologicals under proper temperature controls. This was evident in 1 out of the 2 medication storage refrigerators and freezers observed during the survey. The findings include the following: During observation rounds of the North Hall medication storage room on 07/08/2024 at 05:50 PM with Maintenance Director staff #6 the refrigerator thermometer read 44 degrees Fahrenheit, and the freezer thermometer read 30 degrees Fahrenheit. Several medications and biologicals for facility residents were found in this refrigerator. During an interview on 07/08/2024 at 5:50 PM staff #6 stated that yes, the refrigerator and freezer temperatures were too high, and he would look into this. Review of the facility policy for Monitoring of Cooler/Freezer Temperature on 07/08/2024 at 6:00 PM revealed that all refrigerator storage must be maintained at or below 41 degrees F and that all freezer storage must be maintained at or -4 degrees F.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Food Safety (Tag F0812)

Could have caused harm · This affected 1 resident

Based on observation and interview the facility failed to store food in accordance with professional standards for food safety. This was evident during the kitchen observation of the recertification s...

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Based on observation and interview the facility failed to store food in accordance with professional standards for food safety. This was evident during the kitchen observation of the recertification survey. The findings include: On 07/8/24 10:55AM during an initial tour of the facility with Kitchen Supervisor #9 the following concerns were identified. Inside of the Reach In Refrigerator the following items did not have a date label: 1. Pudding x 9 containers 2. Sandwich x 1 There was no July 2024 temperature log present and the June 2024 temperature log were missing entry dates for 6/12/24 (AM/PM), 6/18/24 (AM and PM), 6/19/24 (AM), 6/20/24 (AM), 6/25/24 (AM), 6/26/24 (AM and PM), 6/27/24 (AM and PM). Inside the Refrigerator the following items did not have a date label: 1. Chunky Salsa-69 ounce container 2. Peaches-x 1 bucket (1/2 full) 3. Bar-b-que sauce x 1 bucket (1/2 full) 4. Vanilla Pudding x 1 bucket (1/4 full) 5. Chocolate Pudding x 1 bucket (1/4 full) 6. Pears x 1 bucket (1/2 full) Inside the Freezer the following items did not have a date label: 1. Large bag of hamburgers with approximately 15-16 hamburgers in the bag 2. Meat Loaf Patties x 2 large bags During an interview with the Kitchen Supervisor #9 at the time of the observation, she stated that the hamburgers and meatloaf patties were placed in the freezer by the activities department. She stated that she will speak to administration regarding the supervision of these items and stated that she just started at the facility in June 2024. The supervisor also stated that the temperature logs are done on both the morning and the evening shifts and she is unable to determine who was responsible for completing the July 2024 temperature log that was not located on the refrigerator, however, she will be providing in-service education to the morning and night shift staff. All concerns were discussed with the Administration team at the time of exit on 7/11/24 at 1pm.
Aug 2019 7 deficiencies 1 IJ
CRITICAL (J)

Immediate Jeopardy (IJ) - the most serious Medicare violation

Accident Prevention (Tag F0689)

Someone could have died · This affected 1 resident

Based on observations, interview with residents and facility staff, and review of residents' medical records, facility policy, and facility quality assurance and performance improvement (QAPI) materia...

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Based on observations, interview with residents and facility staff, and review of residents' medical records, facility policy, and facility quality assurance and performance improvement (QAPI) material, it was determined that the facility failed to have an effective system in place to prevent cognitively-impaired residents from leaving the facility without adequate supervision. This was evident by the facility's failure to: 1) monitor wander guard placement on Resident #59's person and wheelchair, 2) perform an investigation into Resident #59's first elopement attempt on 9/7/18, 3) prevent Resident #59's second elopement on 10/4/18 for almost 40 minutes in the middle of the night, 4) perform and document staff education following either elopement, and 5) secure or monitor the front door during nighttime hours. This was true for 1 (Resident #59) of 8 residents reviewed for elopement. Elopement is the act of a resident leaving the facility unattended when the resident is physically, mental, or cognitively impaired to the extent that s/he is not safe unaccompanied. A wander guard is a device worn by residents who are at risk for elopement that triggers an alarm or a lock when the resident approaches an armed exit. As a result of these findings, a state of immediate jeopardy was declared on 8/2/2019 at 10:50 AM and was removed on 8/5/2019 at 11:59 AM. The findings include: 1) An investigation into facility reported incident MD00132103 was initiated by surveyors on 7/31/2019 at 11:48 AM regarding an elopement by Resident #59 that occurred on 10/4/18. Review of Resident #59's medical record began at this time and revealed that the resident had been admitted to the facility with the diagnoses of alcoholic cirrhosis with ascites and Korsakoff syndrome. Two physicians had certified that the resident was unable to make his/her own decisions at the time of admission into the facility on 9/1/2018. Both alcoholic cirrhosis and Korsakoff syndrome are results of long-term alcohol use. Alcoholic cirrhosis is a condition in which the liver does not function properly due to long-term damage from alcohol. Korsakoff syndrome is a disorder in which the brain suffers damage due to thiamine depravation and is exacerbated by the neurotoxic effects of alcohol. Someone suffering from Korsakoff syndrome experiences loss of memory, apathy, and a lack of insight into all aspects of life. Further review of Resident #59's medical record revealed that the resident had an elopement about one month prior to the reported elopement on 10/4/18. The earlier elopement occurred on 9/7/18 and was detailed in the following nurse's note written on 9/7/18 at 11:42 by the then Assistant Director of Nursing, Registered Nurse (RN) #13: Resident out of building on sidewalk area. Agreed to come back in facility and call his/her significant other. Door alarm did not activate when resident exited. Resident's wander guard not present on him/her. New wander guard placed on right wrist and another placed on his/her wheelchair. Found old wander guard on his/her bedside table. RN #13 was interviewed on 8/1/19 at 10:24 AM. During the interview, RN #13 stated that she saw Resident #59 eloping while looking out her office window in the morning of 9/7/18. She recalled that the resident had already exited the facility and was just barely off the property. She stated that she was able to run outside and redirect Resident #59 into the building without resistance. She also recalled placing two wander guards on the resident, one on his/her wrist and the other on his/her wheelchair. When asked if this information was recorded anywhere else in the medical record, she replied that she believed it was not the facility's practice to change care plans or alter orders when a new wander guard, or multiple wander guards, were placed on a resident. Most likely I only mentioned in a progress note that I put a wander guard on the resident's wheelchair. RN #13 indicated that Resident #59's primary clinical staff were involved in returning Resident #59 to his/her room but that it was not her expectation, in her capacity as Assistant Director of Nursing, for the nursing staff to complete an incident report, obtain new orders, or alter care plans. RN #13 reiterated that this event was not considered an elopement by the facility. Review of physicians' orders for Resident #59 revealed that the resident had an order for Check wander guard every shift for proper functioning with a start date of 9/2/2018 that was active at the time of the elopement. No further note could be found associated with the order that indicated the quantity or locations of wander guards that required checking. Review of Resident #59's care plan failed to reveal that quantity or locations of wander guards on the resident were specified anywhere. Finally, review of the medical record between 9/7/18 and 10/4/18 (the date of the second elopement) failed to reveal observations of the locations of wander guard units on Resident #59 and his/her equipment. Although nursing documented a wander guard check in Resident #59's Treatment Administration Record (TAR) each shift, the location of the wander guard was not included in any of these observations. Ongoing review of the facility's investigation into Resident #59's elopement on 10/4/19 revealed that the resident eloped early in the morning from the front door of the facility (which was armed with a wander guard alarm panel) while using his/her wheelchair. It was also noted in the investigation that the wander guard alarm panel did not alarm when the resident passed it. However, only one wander guard unit was located after the elopement. Because the quantity and location of wander guard units for Resident #59 were not noted anywhere in Resident #59's medical record after the 9/7/18 elopement, it could not be determined if staff were observing one or two wander guard units on Resident #59 when they performed their inspection every shift and documented in Resident #59's TAR. As a result, staff could not show that they had been assessing for the wander guard unit on Resident #59's wheelchair that had been placed by RN #13 expressly to prevent future elopement given the tendency of the resident to remove his/her wander guard bracelet. 2) Review of Resident #59's medical record on 7/31/19 at 11:48 AM revealed that the resident had eloped twice in 2018: on 9/7/18 and on 10/4/18. Review of facility reported incidents sent to the Office of Health Care Quality revealed that only the elopement on 10/4/18 had been reported as an elopement. This was confirmed in interview on 8/1/19 at 9:00 AM with the Director of Nursing (DON), Quality Assurance and Performance Improvement (QAPI) Coordinator, and Assistant Administrator. During the interview, they stated that, because the resident did not leave facility grounds on 9/7/18, they did not consider it an elopement and did not complete an incident report nor send the elopement into the office. Review of the facility's policy regarding elopement revealed the definition of elopement as follows: Elopement is an incident where a resident leaves the facility and he/she is physically, mentally, or cognitively impaired to the extent that she/he is not safe unaccompanied. Any information, investigation, and education that the facility had in relation to this first elopement on 9/7/18 was requested from the facility on 8/1/19 and on 8/2/19. No investigative material or evidence of education performed in relation to this elopement was provided to the survey team prior to survey exit. 3) Review of facility reported incident MD00132103 revealed that Resident #59 eloped in the early morning of 10/4/18. The resident was seen by Geriatric Nursing Assistant (GNA) #5 traveling past the North Hall nurse's station via wheelchair at 1:40 AM. At 1:50 AM, because of a strange noise, Licensed Practical Nurse (LPN) #9 went to the front door to investigate and found the door propped open by a rug. The strange noise revealed itself to be the air conditioning unit blowing into the facility while the front door was continually propped open. A search of the facility began and Resident #59 was discovered to be missing from the facility at 1:59 AM. The resident was located outside the facility on a different street than where the facility was located. The resident had been spotted by police and was returned to the facility accompanied by police at 2:20 AM. The resident's wheelchair was found outside, discarded by the resident under a nearby tree. The wheelchair did not have a wander guard unit attached to it. It was noted in the investigation that the wander guard alarm did not sound and that a single wander guard bracelet was found in a cup of water in Resident #59's room after the elopement. It was not clear if this bracelet had been on the resident's wrist or the resident's wheelchair. The resident was assessed by nursing upon return to the facility and by a physician later that morning and no injuries were noted as a result of this elopement. This review of the incident revealed that the facility reported this elopement to family, physician, county ombudsman, and state agency. Resident #59's medical record was reviewed on 7/31/19 at 11:48 AM. The review revealed an order dated 9/2/18 with the instructions, Resident with wander guard on at all times and was ordered to be performed every shift. This order was renewed on 9/17/18 with no additional instructions. Another order was found with the date 9/5/18 that stated, monitor target behaviors: non-compliance, argumentative, unsafe wandering, paranoia. Monitor every shift. The care plan topic of Falls was found dated 9/2/18 that stated, Resident is at risk for falling related to poor cognition and understanding of safety risks, that included the approach, Teach resident safety measures. Finally, an order for, Activities of Daily Living (ADL) wheelchair mobility: supervision was found dated 9/17/18, indicating that the resident required supervision when propelling himself/herself in a wheelchair. Ongoing review of the medical record revealed that, following the resident's elopement on 9/7/18, three care plan areas were initiated. The first, initiated on 9/7/18, was Ineffective coping related to situation crises, and included the approach, Assess if ineffective coping endangers the resident and/or others. Intervene as necessary. The second, initiated on 9/12/18, was Resident resists care related to not wearing cervical collar and not waiting for assistance with ambulation, and included the approach, Establish clear boundaries for the resident. The third, initiated on 9/17/18, was Elopement: Resident experiences wandering, and included the approaches, Equip resident with a device that alarms when wanders; check for proper functioning of device every shift, and, provide care, activities, and a daily schedule that resembles the resident's prior lifestyle. No care plan topic, assessment, or intervention was found that addressed the resident's ability to remove his/her wander guard bracelet. An interview was conducted with GNA #5 on 8/1/19 at 2:41 PM. During the interview, GNA #5 stated that she did recall Resident #59's elopement in the early morning of 10/4/2018. She confirmed that she observed the resident traveling in his/her wheelchair past the nurse's station in the Front Hall while GNA #5 completed documentation on the computer. When asked if she spoke with the resident, she stated, no, I didn't. She stated that Resident #59 would regularly travel the halls at night to get some coffee or talk to staff on the other unit, and that she didn't think anything of the resident passing by. GNA #5 recalled that only one wander guard unit could be found that night, but that it was found in a glass of water in the resident's room. When asked if the resident required supervision when moving about the facility via wheelchair, GNA #5 stated, No. Finally, when asked if any formal education had been provided to her following the incident, GNA stated that she had been asked to write a statement about the situation and some lessons were learned, but she stated that she had not received formal education following that elopement. When asked to elaborate on what 'some lessons' were, she stated, we just had to keep better eyes on him/her. An interview with the Quality Assurance and Performance Improvement (QAPI) Coordinator was performed on 7/31/19 at 3:07 PM. During the interview, the QAPI Coordinator stated that a Performance Improvement Project (PIP) had been performed by the facility regarding elopement that followed Resident #59's second elopement. The QAPI Coordinator stated, We thought one of the problems might be alarm fatigue. We also wondered if during the admission assessment, if they were capturing the elopement risk. We want to ask families about elopement risk and document events that lead to elopement like 'I want to go home.' We provided education to staff and wander guards are checked every day by nursing. So the four things we did were adjust the wander guard system to produce less false alarms on 10/11/2018, perform elopement risk assessment at admission, increase nursing documentation, and begin monthly tracking of elopement. We also began elopement drills and the first was done on 6/26/2019. The PIP materials were shared with the survey team at this time. The PIP documented the Date Identified as being 10/1/2018, although it can be seen that 10/16/18 was scratched out. The 'Goal / Objective' was, Resident Safety - Confused resident have supervision leaving building. The 'Issues Identified' was, 1) Bell / Alarm Fatigue - increased noise. 2) admission Assessment not triggering Risk of Elopement. The 'Actions' were, 1) Leadership meeting to discuss alarms - decrease sound frequency. 2) QA admission Elopement Risk. 3) Nursing document events possibly leading to increased elopement risk. 4) Monthly tracking elopement events - begin now. Due to the 'Date Identified' being documented as 10/1/2018, prior to Resident #59's elopement on 10/4/2018, the QAPI Coordinator was asked to clarify if this PIP was done in response to Resident #59's elopement or not. The QAPI Coordinator stated, yes, this was in response to Resident #59's elopement on 10/4/2018. The QAPI Coordinator could not identify any quality changes that were made as a result of the first elopement, however did state that she believed a second wander guard was placed on the resident after the first elopement. The QAPI Coordinator provided the survey team with a nursing note that had been written at the time of the first elopement that stated wander guards had been placed on both the resident's right wrist as well as on the resident's wheelchair. When asked how both wander guard bracelets were being tracked, the QAPI Coordinator could not provide any further documentation of how both were being tracked. 4) Interviews were performed with nursing staff including Licensed Practical Nurses (LPNs) #6, #8, and #12 as well as GNAs #2 and #5 on 7/31/2019 around 2:45 PM. Staff were interviewed on the units they were working on. All five staff were asked when they had most recently received elopement inservice training. None could recall when they had their most recent formal training but they did recall that an elopement drill had been performed in April, 2019. LPN #6 and #8 stated that the elopement training had gone well. Following her presentation of the elopement PIP on 7/31/2019 at 3:07 PM, the QAPI Coordinator was asked to provide any evidence of the staff education that she had indicated was given following Resident #59's second elopement. None was provided. An interview was performed on 8/1/19 at 9:00 AM with the Director of Nursing (DON), QAPI Coordinator, and Assistant Administrator. During the interview, it was asked if any education had been provided to facility staff following either of Resident #59's elopements. These facility staff stated that, because the resident did not leave facility grounds, they did not consider the events on 9/7/2018 to be an elopement and did not complete an incident report nor did they perform any staff education regarding the elopement. The DON was unsure at that time if staff education had been performed after Resident #59's second elopement on 10/4/2018. The survey team requested any education to be provided as soon as possible for review. The DON was asked again by the survey team on 8/1/2019 at 11:08 AM to provide any evidence of staff education following Resident #59's elopements. An 'Inservice Attendance Sheet' attached to the facility's elopement policy was given to the survey team at 12:05 PM. However, the date of the inservice was 4/16/2018 and 4/17/2018. 5) Review of the facility's investigation into Resident #59's second elopement revealed the statement, On 10-5-2018 an alarm was placed on front door. This alarm will be turned on each evening around 8 PM and turned off around 7 am. This alarm will be activated any time the door is opened during these hours. An observation of the front door alarm was made on 7/31/2019 at 1:55 PM. The alarm was a small white magnetized box that detected when the door was opened. It was found to make a chiming sound when the door was opened during the day although it could not distinguish if anyone walked through the door. Receptionist #7 was interviewed at the same time and she demonstrated the second, 'Alarm' setting by switching the setting on the white box. This setting made a louder, shriller tone that continued until the door closed. Receptionist #7 stated that the receptionists worked from 7:00 AM to 8:00 PM and that the front door was not monitored when a receptionist was not working. Receptionist #7 also said that the receptionists were responsible for switching the setting from Chime to Alarm each evening at 8:00 PM, as well as for disabling the handicap button that opens the front door automatically. Both are switched back when the receptionist arrives in the morning. Receptionist #7 also indicated that the wander guard alert system was a separate system and alarmed when a resident wearing a wander guard approached the front door. The facility's two nurses' stations were noted to be around 2 corners from the front door. It was noted that the front door alarm could be heard faintly from either nursing station while in both Chime and Alarm modes. However, there was no visual or auditory signal at either nurses' station when the front door alarm went off. The wander guard system was noted to create a local alarm and illuminate a light at both nurses' stations when it was activated. During an interview with the Acting Director of Maintenance that took place on 8/1/2019 at 12:57 PM, the Acting Director stated that the alarm on the front door was installed in March, 2019, five months after Resident #59's elopement on 10/4/2018. The Acting Director of Maintenance stated that he performs monthly reviews of the whole wander guard system to ensure that it is functioning correctly and that there have been no problems with it in either 2018 or 2019. The Acting Director of Maintenance clarified that his reviews involve verifying that the system alarms correctly when a wander guard unit is nearby. During a walk-through with the Administrator that took place on 8/2/2019 at 11:30 AM, the Administrator stated that there was another alarm system that hadn't been reviewed yet by the survey team. He referred to a House Alarm System (separate from the white front door alarm described above) that alarmed locally at the nurses' stations with sound and visual indicators when any of the external doors were opened. This was tested with an emergency exit at the end of the North Hall and it was confirmed that both sound and visual indicators activated at the nurses' station. The Administrator then stated this House Alarm system was also armed at the front door during the night. The walk-through continued to the front door where the Administrator indicated the keypad used to silence the wander guard system when it activated. The Administrator stated that this keypad was used to arm the front door with the House Alarm system each night. The receptionist, who was present at the time, then stated that she does not use that keypad to enable any house alarm. The Administrator then went to the Front Hall nurses' station and attempted to arm the House Alarm at the front door there. He was unable to do so but suggested that this is something that can be investigated. This House Alarm system was not enabled by the time surveyors exited the facility on 8/5/2019 at 12:00 PM, however the white Front Door Alarm and the wander guard systems were still functional. ~~ As a result of these findings, a state of immediate jeopardy was declared on 8/2/2019 at 10:50 AM and the facility was provided with the Immediate Jeopardy Template at that time. The facility submitted a removal plan on 8/2/2019 at 1:18 PM and the State Agency was unable to accept this plan. The facility submitted additional plans at 2:45 PM, 4:21 PM, and 4:46 PM. The facility removal plan was accepted by the State Agency at 4:54 PM. The immediate jeopardy was removed on 8/5/2019 at 11:59 AM. The facility's abatement plan included the following provisions: - Facility staff to be immediately inserviced including nursing, administration, housekeeping, dietary, maintenance, and activities staff regarding the elopement policy, the wander guard policy, monitoring residents at risk for elopement, interventions to prevent elopement, and responding to alarms. This education will be performed by the Staff Development Nurse. - No staff can begin a shift without first receiving the above training. - A schedule will be maintained of all staff who have yet to receive training to ensure that they all receive the training as soon as is practicable. - A response log will be maintained at the front desk that staff must complete when they respond to the local alarm on the facility's front door. - Residents who are at risk for wandering will have a yellow wristband instead of a white wrist band. - Location checks will be performed every 30 minutes for 24 hours for residents after an elopement has occurred. - Care plans will be updated after an elopement to reflect any new interventions. - Alleged date of compliance: 8/4/2019.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0605 (Tag F0605)

Could have caused harm · This affected 1 resident

Based on observation, medical record review, and staff interview, it was determined the facility failed to ensure less restrictive alternatives were tried and documented prior to administering an anti...

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Based on observation, medical record review, and staff interview, it was determined the facility failed to ensure less restrictive alternatives were tried and documented prior to administering an antipsychotic for 1 of 6 residents reviewed during the survey for unnecessary medications (Resident #36). The findings include: Beginning on 7/31/19 10:10 AM, the medical record for Resident #36 was reviewed. According to the diagnostic list on the Care Plan and the Physician Order Sheet, the resident had diagnoses which included dementia as well as other mental, mood, and behavioral disorders. On 8/2/19 at 9:13 AM, a facility reported incident from November 2018 was investigated. It involved Resident #36 and an injury of unknown origin. A nurse's note on 11/10/18 written at 2:40 AM by staff Nurse #10 stated the resident was ambulating (walking) on the unit and looking for his/her mother and father. The nurse stated she explained to the resident that he/she was at the nursing home and the resident became angry at staff, wanting to go home. She wrote that the resident sat down and drank a soda and was noted to have increased confusion. At 4:48 AM, Nurse #10 wrote that the resident was pacing in the hall again, wanting to leave the building and she was able to redirect him/her. At 6:05 AM, Nurse #10 wrote, Resident was discovered by GNA to have a cut above his/her left brow. S/he was standing by the front hall shower room. S/he did not fall, but s/he was unable to tell how. S/he was uncooperative with staff and became agitated. The CRNP (Certified Registered Nurse Practitioner) was made aware. Received: Haldol 2 milligrams (mg) intramuscularly (IM) times one dose now, then apply steri-strips to the cut. Med (medication) was administered. According to https://psychcentral.com/drugs/haldol/, Haldol (haloperidol) is classified as an antipsychotic medication and is used to treat schizophrenia. It relieves symptoms for patients that suffer from delusions, hallucinations, unorganized thought and hostility. On 8/1/19 at 8:19 AM, Nurse #10 was interviewed. When asked to describe the incident, she stated on the morning of the incident the resident was looking for his/her kids and spouse. She said she could tell by the way the resident looked at her that s/he was getting wound up. Nurse #10 was then asked by the surveyor what happened prior to the administration of the Haldol. Nurse #10 said when she saw that the resident was ready to leave the building, she offered him/her peanut butter crackers and a drink, but stated when the resident is like that, s/he doesn't want anything. She said she was then called by the Geriatric Nursing Aides (GNAs) because the resident was bleeding from a cut on his/her head. She stated the resident is difficult to re-direct when s/he is like that and will hit staff. On 8/2/19 at 9:13 AM, the physician order to administer Haldol was found. It stated to administer Haldol (haloperidol lactate) solution; 5 milligrams per milliliter (mg/ml); amount to administer: 2 mg IM X (times) 1 now. The order indicated the injection was given for the diagnosis of unspecified personality and behavioral disorder due to known physiological condition. When the care plans for Resident #36 were reviewed, no care plan was found addressing the need to use anti-psychotic injections, when and why to use them, and what less restrictive nursing interventions were to be tried first. Further review of the medical record revealed there were no orders for PRN (as needed) anti-anxiety or anti-psychotic medications to be offered by mouth when the resident became agitated and/or aggressive. Also, no documentation regarding the resident's occasional resistance to alternative interventions to IM injections (i.e., a rationale for using anti-psychotic injections) was found in physician or nurse practitioner notes until 12/13/19, about one month after the incident. In addition, a review of behavior monitoring sheets by nursing staff revealed the resident was not being monitored for agitation and aggressive behaviors.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Transfer Notice (Tag F0623)

Could have caused harm · This affected 1 resident

Based on review of resident medical records and interview with facility staff, it was determined that the facility failed to ensure that residents and their representatives received written notice of ...

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Based on review of resident medical records and interview with facility staff, it was determined that the facility failed to ensure that residents and their representatives received written notice of resident transfer. This was evident for of 1 resident reviewed for hospitalization 1 (Resident #26). The findings include: Resident #26's medical record was reviewed on 7/30/19 at 12:29 PM. During the review, it was noted that Resident #26 was hospitalized in April, 2019. A review of the facility's documentation surrounding that hospitalization failed to reveal that the resident or his/her representative had been notified of the transfer and the reasons for it in writing. The Director of Nursing (DON) was interviewed on 7/30/19 at 1:15 PM. During the interview, the DON stated that the requirement of written notification was new information to her. She confirmed with this surveyor that the facility had not been providing written notification of transfer to residents or their representatives at time of transfer.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Comprehensive Care Plan (Tag F0656)

Could have caused harm · This affected 1 resident

Based on review of medical records and interviews with facility staff, it was determined that the facility staff failed to develop a care plan to address each residents medical condition. This was evi...

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Based on review of medical records and interviews with facility staff, it was determined that the facility staff failed to develop a care plan to address each residents medical condition. This was evident for 1 of 24 residents investigated during the survey process (Resident #14). The findings include: On 07/31/19 at 8:52 AM while observing Resident #14, it was noted that the Resident had edema (swelling) to both lower legs. While reviewing the Resident's medical record it was noted that there were no routine weights for this resident. Further review of the record revealed that the Resident was taking Lasix daily. Lasix (furosemide) is a diuretic medication that reduces extra fluid in the body caused by conditions such as heart failure, liver disease, and kidney disease. A review of Resident #14's plan of care did not identify any interventions to address the edema or any possible problems the resident might face as a result of any fluid shifts. The Director of Nursing was informed on 8/2/19 prior to the exit interview.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0657 (Tag F0657)

Could have caused harm · This affected 1 resident

Based on observation, medical record review and staff interview, it was determined the facility failed to revise the behavioral care plan to address approaches to agitation and/or aggressive behavior ...

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Based on observation, medical record review and staff interview, it was determined the facility failed to revise the behavioral care plan to address approaches to agitation and/or aggressive behavior and when to use intramuscular (in the muscle) antipsychotic injections. This was evident for 1 of 6 residents reviewed for unnecessary medications and care plans during the survey (Resident #36). The findings include: On 7/31/19 10:10 AM, the medical record for Resident #36 was reviewed. According to the diagnostic list on the resident's care plan and the Physician Order Sheet, the resident had diagnoses which included dementia as well as other mental, mood and behavioral disorders. On 8/2/19 at 9:13 AM, a facility reported incident from November 2018 was investigated. It involved Resident #36 and an injury of unknown origin. A nurse's note on 11/10/18 written at 2:40 AM by Nurse #10 stated the resident was ambulating (walking) on the unit and looking for his/her mother and father. The nurse stated she explained to the resident that he/she was at the nursing home and the resident became angry at staff, wanting to go home. She wrote that the resident sat down and drank a soda and was noted to have increased confusion. At 4:48 AM, Nurse #10 wrote that the resident was pacing in the hall again, wanting to leave the building and she was able to redirect him/her. At 6:05 AM, Nurse #10 wrote, Resident was discovered by GNA to have a cut above his/her left brow. S/he was standing by the front hall shower room. S/he did not fall, but s/he was unable to tell how. S/he was uncooperative with staff and became agitated. The CRNP (Certified Registered Nurse Practitioner) was made aware. Received: Haldol 2 milligrams (mg) intramuscularly (IM) times one dose now, then apply steri-strips to the cut. Med (medication) was administered. According to https://psychcentral.com/drugs/haldol/, Haldol (haloperidol) is classified as an antipsychotic medication and is used to treat schizophrenia. It relieves symptoms for patients that suffer from delusions, hallucinations, unorganized thought and hostility. On 8/1/19 at 8:19 AM, Nurse #10 was interviewed. When asked to describe the incident, she stated on the morning of the incident the resident was looking for his/her kids and spouse. She said she could tell by the way the resident looked at her that s/he was getting wound up. Nurse #10 was then asked by the surveyor what happened prior to the administration of the Haldol. Staff nurse #10 said when she saw that the resident was ready to leave the building, she offered him/her peanut butter crackers and a drink, but stated when the resident is like that, s/he doesn't want anything. She said she was then called by the Geriatric Nursing Aides (GNAs) because the resident was bleeding from a cut on his/her head. She stated the resident is difficult to re-direct when s/he is like that and will hit staff. On 8/2/19 at 9:13 AM, the physician order to administer Haldol was found. It stated to administer Haldol (haloperidol lactate) solution; 5mg/ml; amount to administer: 2 mg IM X (times) 1 now. The order indicated the injection was given for the diagnosis of unspecified personality and behavioral disorder due to known physiological condition. On 8/2/19 at 9:13 AM, the physician order to administer Haldol was found. It stated to administer Haldol (haloperidol lactate) solution; 5 milligrams per milliliter (mg/ml); amount to administer: 2 mg IM X (times) 1 now. The order indicated the injection was given for the diagnosis of unspecified personality and behavioral disorder due to known physiological condition. When the care plans for Resident #36 were reviewed, no care plan was found addressing the need to use anti-psychotic injections, when and why to use them, and what less restrictive nursing interventions were to be tried first.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Infection Control (Tag F0880)

Could have caused harm · This affected 1 resident

Based on observation, medical record review, and staff interview, it was determined that the facility failed implement a system to prevent the spread of communicable diseases and to discreetly notify ...

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Based on observation, medical record review, and staff interview, it was determined that the facility failed implement a system to prevent the spread of communicable diseases and to discreetly notify visitors and staff to take standard precaution for 1 of 1 resident reviewed for isolation precautions during the survey (Resident #55). The findings include: On 7/30/19 at 9:51 AM during a review of the medical record for Resident #55, a physician order was found that stated the resident was to be on contact precautions for Clostridioides difficile (C. diff). According to a C. diff fact sheet published by the CDC (Center for Disease Control) from https://www.cdc.gov/cdiff/pdf/Cdiff-Factsheet-508.pdf, Clostridioides difficile (formerly known as Clostridium difficile ) is a bacterium that causes diarrhea and colitis (an inflammation of the colon). C. diff infections can be deadly . C. diff spreads when people touch surfaces that are contaminated with poop from an infected person or when people don't wash their hands with soap and water.Healthcare professionals can help prevent the spread of C. diff by: .wearing gloves and gowns when treating patients with C. diff-and remembering that hand sanitizer doesn't kill C. diff. Also, when a resident is placed in contact isolation, it means that staff and visitors must wear gowns and gloves while in the resident's room to help prevent the spread of infection to themselves and others. They must know how to appropriately don and remove the gown and gloves and wash their hands with soap and water. On 7/30/19 at 10:04 AM, it was noted there was no information on or near Resident #55's door to alert visitors to see the nurse before entering the resident's or to alert staff to wear the appropriate protective equipment before entering the resident's room. Nurse #1 was in the hallway and was asked if the resident was still on contact precautions. When she said yes, she was asked if she knew why there wasn't a sign. She said she wasn't sure. At 10:06 AM the Director of Nursing (DON) was brought to the room and confirmed that a sign should have been placed on the door.
CONCERN (E)

Potential for Harm - no one hurt, but risky conditions existed

Medical Records (Tag F0842)

Could have caused harm · This affected multiple residents

Based on observation, medical record review and staff interview it was determined the facility failed to provide documentation supporting the use of an intramuscular (in the muscle) antipsychotic inje...

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Based on observation, medical record review and staff interview it was determined the facility failed to provide documentation supporting the use of an intramuscular (in the muscle) antipsychotic injection for 1 of 6 resident reviewed for unnecessary medications during the survey (Resident #36). The findings include: Beginning on 7/31/19 10:10 AM, the medical record for Resident #36 was reviewed. According to the diagnostic list on the Care Plan and the Physician Order Sheet, the resident had diagnoses which included dementia as well as other mental, mood, and behavioral disorders. On 8/2/19 at 9:13 AM, a facility reported incident from November 2018 was investigated. It involved Resident #36 and an injury of unknown origin. A nurse's note on 11/10/18 written at 2:40 AM by Nurse #10 stated the resident was ambulating (walking) on the unit and looking for his/her mother and father. The nurse stated she explained to the resident that he/she was at the nursing home and the resident became angry at staff, wanting to go home. She wrote that the resident sat down and drank a soda and was noted to have increased confusion. At 4:48 AM, nurse #10 wrote that the resident was pacing in the hall again, wanting to leave the building and she was able to redirect him/her. At 6:05 AM, Nurse #10 wrote, Resident was discovered by GNA to have a cut above his/her left brow. S/he was standing by the front hall shower room. S/he did not fall, but s/he was unable to tell how. S/he was uncooperative with staff and became agitated. The CRNP (Certified Registered Nurse Practitioner) was made aware. Received: Haldol 2 milligrams (mg) intramuscularly (IM) times one dose now, then apply steri-strips to the cut. Med (medication) was administered. According to https://psychcentral.com/drugs/haldol/, Haldol (haloperidol) is classified as an antipsychotic medication and is used to treat schizophrenia. It relieves symptoms for patients that suffer from delusions, hallucinations, unorganized thought and hostility. On 8/1/19 at 8:19 AM, Nurse #10 was interviewed. When asked to describe the incident, she stated on the morning of the incident the resident was looking for his/her kids and spouse. She said she could tell by the way the resident looked at her that s/he was getting wound up. Nurse#10 was then asked by the surveyor what happened prior to the administration of the Haldol. Nurse #10 said when she saw that the resident was ready to leave the building, she offered him/her peanut butter crackers and a drink, but stated when the resident is like that, s/he doesn't want anything. She said she was then called by the Geriatric Nursing Aides (GNA's) because the resident was bleeding from a cut on his/her head. She stated the resident is difficult to re-direct when s/he is like that and will hit staff. On 8/2/19 at 9:13 AM, the physician order to administer Haldol was found. It stated to administer Haldol (haloperidol lactate) solution; 5 milligrams per milliliter (mg/ml); amount to administer: 2 mg IM X (times) 1 now. The order indicated the injection was given for the diagnosis of unspecified personality and behavioral disorder due to known physiological condition. When the medical record for Resident #36 was reviewed, no clearly documented rationale for the use of the Haldol injection could be found. When the care plans for Resident #36 were reviewed, no care plan was found addressing the need to use anti-psychotic injections, when and why to use them, and what less restrictive nursing interventions were to be tried first. Further review of the medical record revealed there were no orders for PRN (as needed) anti-anxiety or anti-psychotic medications to be offered by mouth when the resident became agitated and/or aggressive. Also, no documentation regarding the resident's occasional resistance to alternative interventions to IM injections (i.e., a rationale for using anti-psychotic injections) was found in physician or nurse practitioner notes until 12/13/19, about one month after the incident. In addition, a review of behavior monitoring sheets by nursing staff revealed the resident was not being monitored for agitation and aggressive behaviors.
Apr 2018 11 deficiencies
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0657 (Tag F0657)

Could have caused harm · This affected 1 resident

Based on medical record review and staff interview it was determined that the facility failed to revise the Care Plan to include a plan for palliative care for Resident #64. This was evident for 1 of ...

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Based on medical record review and staff interview it was determined that the facility failed to revise the Care Plan to include a plan for palliative care for Resident #64. This was evident for 1 of 25 residents selected for review during the survey. The findings include: On 4/26/18 at 3:30 PM during a review of the medical record for Resident #64, it was noted the resident has been on palliative care at least as far back as January 2018. However, no care plan was found for palliative care. Palliative care focuses on providing relief from the symptoms and stress of a serious illness. This may include extra support for pain, depression, fatigue, anxiety and any other mental or physical symptoms causing distress. The nursing Care Plan addresses multiple areas of diagnoses or risks, sets goals for each area and provides a list of specific interventions for staff to follow. The Assistant Director of Nursing (ADON) confirmed the finding.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0676 (Tag F0676)

Could have caused harm · This affected 1 resident

Based on observation and staff interviews the facility staff failed assist Resident #8 with nutritional needs. This was evident for 1 out of 28 Residents reviewed during the dining service. The findin...

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Based on observation and staff interviews the facility staff failed assist Resident #8 with nutritional needs. This was evident for 1 out of 28 Residents reviewed during the dining service. The findings include: On 04/25/18 while observing the lunch dining service, writer noticed Resident #8 sitting at the table along with 3 other residents. Resident #8 did not look at the meal on the table. The resident just stared around the room. The resident had adaptive utensils but never picked up any of the utensils to eat. No one encouraged the resident to eat. On 4/26/18, writer again noticed Resident #8 in the dining room at the same table not attending to her meal. The resident stared around blankly. Writer at this point notified the dining room staff that the resident needed prompting and cuing assistance to get the nutrients into the resident.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Pressure Ulcer Prevention (Tag F0686)

Could have caused harm · This affected 1 resident

Based on medical record review and staff interview it was determined the facility failed to prevent a pressure ulcer from forming on the left heel of Resident #52. This was evident for 1 of 25 residen...

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Based on medical record review and staff interview it was determined the facility failed to prevent a pressure ulcer from forming on the left heel of Resident #52. This was evident for 1 of 25 residents selected for review during the survey. The findings include: On 4/24/18 at about 1:00 PM during a medical record review, it was noted that Resident #52 had a pressure ulcer to the left heel. According to the medical record, the date the area was found was 4/10/18. The pressure ulcer was documented as a Stage 2 pressure ulcer and the Nursing Skin Assesment documented that it was acquired while the resident was in the facility. Pressure ulcers usually develop when soft tissue is compressed between a bony prominence (such as a hip bone or heel) and the external surface of the skin for prolonged periods of time. Stage 2 pressure ulcers involve partial-skin loss such as would be seen in abrasions or ruptured blisters. Ulcers that are not caused by pressure are not included in the definition of a Stage 2 pressure ulcer. A review of nurses' notes revealed that on 10/9/17 documentation was present stating, Resident advised to not wear shoe related to friction because shoes are too tight and that there is pitting edema LLE (in the lower left extremity); placed slipper on left foot and resident removed it .Nurse reiterated that he/she should not wear ill-fitting shoe but [resident] was insistent that he/she was going to wear it. Shared possible consequences; 'I don't care'. On 11/6/17 another nurses' note stated that the left heel Stage 2 open area remains healed as of 10/31/17. It was, also, documented that the resident was encouraged to wear a slipper on the left foot instead of a hard shoe. According to the resident's Care Plan, nursing staff are to check the resident's skin every shift with close attention to heels. No documentation of nurses checking the skin every shift was found in the medical record. This was confirmed by the Assistant Director of Nursing (ADON). The facility is responsible to follow the interventions of the care plan in order to help prevent the formation or reformation of pressure ulcers
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0761 (Tag F0761)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation and verified by facility staff, it was determined the facility staff failed to ensure that medications and ...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation and verified by facility staff, it was determined the facility staff failed to ensure that medications and blood glucose monitoring strips were labeled with the date when opened. This was evident in 3 carts of 3 carts examined in 1 of 2 nursing stations in the facility. The findings include: An observation conducted on 04/26/2018 at 2:00 PM in the Front/Back Hall nursing station on the Eastern [NAME] Unit revealed the following: 1. The front hall medication cart contained 1 opened vial of EvenCare® G2® blood glucose monitoring strips that was not labeled with the date opened. Per manufacturer instructions the date opened should be recorded on the bottle label and the bottle and any remaining test strips should be discarded after 6 months from the date of opened. 2. The front hall medication cart contained 1 Flovent Diskus that was not labeled with the date opened. Per manufacturer instructions the medication should be discarded after 6 weeks. 3. The back hall medication cart contained 1 opened vial of EvenCare® G2® blood glucose monitoring strips that was not labeled with the date opened. 4. The back hall medication cart contained 1 Incruse inhaler that was not labeled with date opened. Per manufacturer instructions the medication should be discarded after 6 weeks. 5. The supply cart contained 3 opened vial of EvenCare® G2® blood glucose monitoring strips. 2 of the 3 were not labeled with the date opened. These findings were verified by staff #1 and brought to the attention of the Director of Nursing. The facility staff have the responsibility to ensure that all multi-dose medications and blood glucose monitoring strips are labeled with the date when opened.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Food Safety (Tag F0812)

Could have caused harm · This affected 1 resident

2) During a tour of the kitchen on 4/25/2018 at 10:45 AM, Surveyor observed that 3 drain lines in the kitchen area did not have air gaps between the drains and sewer flood rim. An air gap is a space b...

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2) During a tour of the kitchen on 4/25/2018 at 10:45 AM, Surveyor observed that 3 drain lines in the kitchen area did not have air gaps between the drains and sewer flood rim. An air gap is a space between the drain and sewer flood rim (sewers drain) that prevents sewer water from backing up the drain and causing sewer water contamination. The areas in question were the cooks sink, cooks table and one of the two ice machines drains. The findings were brought to the attention of the Kitchen Manager. Factors in these observations can lead to foodborne illnesses if sewer water backed up into an area that is used to prepare food or make ice. Based on observation it was determined that the facility staff failed to serve food to Resident #45 in a sanitary manner. This was evident for 1 out of 28 residents served in the dining room during the survey, and 2) The drains from the kitchen sinks did not have appropriate air gap to ensure that sewer water does not backup to the sink. The findings include: On 04/25/18 while observing the lunch dining service, writer noticed staff #4 assisting Resident # 45 with the meal set-up. Staff #4 was observed holding the resident's roll with bare hands while buttering the bread. It is the facility staff's responsibility to serve food in a manner that prevents food contamination, to lessen the chances outbreaks or illnesses. Food that is not being cooked after bare hand handling should not be served to residents.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0840 (Tag F0840)

Could have caused harm · This affected 1 resident

Based on staff interview and review of medical records the facility failed to follow doctor's orders for daily weights on Resident #34. The finding include: Review of medical records for Resident #34 ...

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Based on staff interview and review of medical records the facility failed to follow doctor's orders for daily weights on Resident #34. The finding include: Review of medical records for Resident #34 on 4/25/2018 at 10:30 AM revealed that the facility staff failed to weigh the resident on 4/21/2018 and 4/22/2018. The doctors order was for daily weight to be done for Resident #34. The Director of Nursing was interviewed on the missing weights and he/she said that the facility is unable to find any supporting documentation that Resident #34 was weighed on the dates in question. The facility staff have a responsibility to follow doctors' orders to ensure that residents are receiving the care necessary to maintain or increase overall health.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Infection Control (Tag F0880)

Could have caused harm · This affected 1 resident

Based on observation, it was determined the facility staff failed to utilize proper hand hygiene techniques consistent with accepted standards of nursing practice. This was evident on 1 of 3 Units. Th...

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Based on observation, it was determined the facility staff failed to utilize proper hand hygiene techniques consistent with accepted standards of nursing practice. This was evident on 1 of 3 Units. The findings include: An observation conducted on 04/26/2018 at 8:00 AM on the [NAME] Unit revealed that staff #2 did not wash his/her hands or use hand sanitizer prior to administering medications to 3 residents. Additionally, following the administration of medications to the 3 residents staff #2 only washed his/her hands for 7-9 seconds. According to Centers for Disease Control and Prevention (CDC) guidelines for healthcare professionals, after wetting hands they should then be rubbed vigorously for at least 15 seconds. Hand washing is one of the most effective ways to prevent the spread of germs from one person to another. The facility staff have the responsibility to ensure that proper hand hygiene techniques are being used.
CONCERN (E)

Potential for Harm - no one hurt, but risky conditions existed

Quality of Care (Tag F0684)

Could have caused harm · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, medical record review and resident and staff interview it was determined: 1) the facility failed to ensure...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, medical record review and resident and staff interview it was determined: 1) the facility failed to ensure that impaired nutrition/hydration status and swallowing issues were reported to the physician in a timely manner and 2) that the resident was being assessed for edema. This was evident for 2 of 25 residents selected for review during the survey, affecting Resident #16 and Resident #214. The findings include: 1. Resident #16 is a [AGE] year-old who is totally dependent on staff for food and drink. A medical record review conducted on 04/25/2018 revealed that on 04/23/2018 at 10 PM Resident #16's physician was notified that the resident had poor intake and had been pocketing food (storing food in the mouth). Orders were given to draw labs in the morning. Labs were collected on 04/24/2018 at 6:30 AM and the pharmacy called at 10:00AM to report the abnormal lab results. The abnormal labs included fluid and electrolyte imbalances and low albumin (a type of protein) and the resident was started on intravenous fluids. A review of the resident's intake and output for 2 weeks prior to notifying the MD the resident displayed the following indicators of poor nutrition and hydration status: 1) Daily food intake ranged from 0 to 1-25% consumed per meal. 2) Daily total urine output ranged between 200 ml to 625ml (extremely low volume). 3) Daily fluid intake ranged from 0 ml to 880 ml with most daily fluid intakes averaging 240ml. 4) Descriptors of the resident's urine included phrases such as amber urine, tea colored, dark/yellow urine, dark urine, thick and amber colored. This pattern started developing as early as 3 months prior to the physician being notified of the poor intake. 2. Resident #214 has multiple diagnoses including Congestive Heart Failure (CHF) and edema. CHF is a condition in which the heart is no longer able to pump blood efficiently. When the heart receives more blood than it can pump back into the body, the blood can back up and begin to seep out of the blood vessels into other tissues. This causes swelling called edema. Edema often shows up first in the legs and ankles. On 4/26/18 at 3:07 PM during an interview, Resident #214 complained of his legs and ankles feeling swollen. The Assistant Director of Nursing (ADON), with the surveyor present, assessed the resident for edema (swelling) of the legs and found he/she had +3 edema. Edema, or swelling, is first evaluated as pitting or non-pitting. When the fingers are pressed against a resident's lower leg for 5 seconds and then released, if there is no lasting indentation but swelling is present, it is non-pitting edema. If after 5 seconds an indentation or pit remains for a while, it is considered pitting edema. Pitting edema is graded on a scale from +1 to +4. Plus 3 edema is considered moderate pitting edema: typically is about 6 millimeters (ml) in depth, and remains about 30 seconds before rebounding after the fingers are no longer pressing against the area. The assessment of edema is significant as it can indicate the worsening of an underlying disease such
CONCERN (E)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0697 (Tag F0697)

Could have caused harm · This affected multiple residents

Based on resident and staff interview and medical record review it was determined the facility failed to adequately manage pain for Resident #113. This was evident for 1 of 25 residents selected for r...

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Based on resident and staff interview and medical record review it was determined the facility failed to adequately manage pain for Resident #113. This was evident for 1 of 25 residents selected for review during the survey. The findings include: Resident #113 has a diagnosis of Rheumatoid Arthritis (RA) with rheumatoid factor. RA is an inflammatory disease that involves the immune system attacking the joints. This can cause symptoms that include pain, swelling, and stiffness which can lead to difficulty or loss of physical function and the ability to perform everyday tasks. Rheumatoid factor is a protein made by the immune system that can attack healthy tissue, so its presence can indicate an autoimmune disease. On 4/24/18 at 9:39 AM, during an interview with Resident #113, when asked if she had any concerns about her care, she stated she was aching all over and did not feel like she had gotten her last dose of Methotrexate. When asked, she stated her level of pain was an '8' on a '0 to 10' pain scale with '0' being no pain and '10' being the worst. A review of the Treatment Administration Record (TAR) and nurses notes over a period of 6 days following admission revealed the resident's perception of pain reached an '8' on day 1; '9' on day 2; and '10' on day 3, 4, 5 and 6. The standard of practice for pain management involves asking the resident what he/she would like the pain level to be and working to meet that goal. On a '0 to 10' pain scale, '1 to 3' is considered mild pain; '4 to 6' is considered moderate pain and '7 to 10' is considered severe pain. Although through the week the resident was given Tylenol, Ibuprofen and Tramadol, as needed, to try to manage the pain, and the Nurse Practitioner (NP) changed the orders at least twice, the resident's pain seemed to always rise to a severe level. Continued review of the medical record for Resident #113 revealed a physician order to administer 10 tablets of 2.5 milligram (mg) Methotrexate Sodium every Wednesday for RA with rheumatoid factor. Further review of the medical record revealed Resident #113 was admitted from the hospital at 5:30 PM on the previous Wednesday evening. When the Assistant Director of Nursing (ADON) was interviewed, she found that the medication list sent from the hospital on the day of admission stated to give the Methotrexate every Wednesday. There was no documentation from the hospital stating whether the resident had received it that day or not. Methotrexate is a drug that was originally used to treat cancer before it was approved to use for RA. It is not prescribed daily because it has the potential for severe toxic effects and taking it once a week decreases the risk of liver and bone marrow damage. It is a standard of nursing practice when an order is unclear to clarify the order. After the surveyor notified the Assistant Director of Nursing (ADON) that the resident thought he/she had missed a dose of Methotrexate, the ADON facilitated a call to the hospital and discovered the resident had not received the medication on the day of admission to this facility. By the time nursing staff notified the physician and received an order to go ahead and administer the medication, the Methotrexate was 6 days late. The standard of practice for pain management involves asking the resident what he/she would like the pain level to be and working to meet that goal.
CONCERN (E)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0760 (Tag F0760)

Could have caused harm · This affected multiple residents

Based on resident and staff interview and medical record review it was determined the facility failed to ensure that Resident #113 did not miss a dose of a significant medication. This was evident for...

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Based on resident and staff interview and medical record review it was determined the facility failed to ensure that Resident #113 did not miss a dose of a significant medication. This was evident for 1 of 25 residents selected for review during the survey. The findings include: Resident #113 has a diagnosis of Rheumatoid Arthritis (RA) with rheumatoid factor. RA is an inflammatory disease that involves the immune system attacking the joints. This can cause symptoms that include pain, swelling, and stiffness which can lead to difficulty or loss of physical function and the ability to perform everyday tasks. Rheumatoid factor is a protein made by the immune system that can attack healthy tissue, so its presence can indicate an autoimmune disease. On 4/24/18 at 9:39 AM, during an interview with Resident #113 when asked if she had any concerns about her care, she stated she was aching all over and did not feel like she had gotten her last dose of Methotrexate. A review of the medical record for Resident #113 revealed a physician order to administer 10 tablets of 2.5 milligram (mg) Methotrexate Sodium every Wednesday for RA with rheumatoid factor. Further review of the medical record revealed that Resident #113 was admitted from the hospital at 5:30 PM on the previous Wednesday evening. When the Assistant Director of Nursing (ADON) was interviewed, she found that the medication list sent from the hospital on the day of admission stated to give the Methotrexate every Wednesday. There was no documentation from the hospital stating whether the resident had received it that day or not. Methotrexate is a drug that was originally used to treat cancer before it was approved to use for RA. It is not prescribed daily because it has the potential for severe toxic effects and taking it once a week decreases the risk of liver and bone marrow damage. It is a standard of nursing practice when an order is unclear to clarify the order. After the surveyor notified the Assistant Director of Nursing (ADON) that the resident thought he/she had missed a dose of Methotrexate, the ADON facilitated a call to the hospital and discovered the resident had not received the medication on the day of admission to this facility. By the time nursing staff notified the physician and received an order to go ahead and administer the medication, the Methotrexate was 6 days late. The facility is responsible to obtain additional information to clarify orders that are unclear, so significant medications can be administered without missing doses. .
CONCERN (E)

Potential for Harm - no one hurt, but risky conditions existed

Medical Records (Tag F0842)

Could have caused harm · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 4) A review of the medical records on [DATE] at 10:30 AM revealed that the facility staff did not do an assessment on Resident #...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 4) A review of the medical records on [DATE] at 10:30 AM revealed that the facility staff did not do an assessment on Resident #34 after a significant weight loss. The residents weight was averaging 157 pounds with sight increase and decrease for the month of April up until [DATE] when the weight dropped to 150 pounds and then on [DATE] the weight was recorded at 133 pounds. During further review of the medical records, the surveyor was unable to find any assessment for Resident #34's weight loss. The Director of Nursing (DON) was interviewed and he/she said that the facility has been having problems with getting accurate weights on the residents. A new policy has just been indicated throughout the facility to ensure the accuracy of weights. Resident #34 was being weighed in his wheelchair with his oxygen bottle attached to the wheelchair and now Resident #34 is weighed without the oxygen bottle attached to his wheelchair. The facility staff did not document the change in weighing the resident. Improper charting of resident weights has the potential to lead to improper medical care and treatments. The DON agreed that resident weights are a very important part of resident assessments and that the facility failed to get accurate weights on residents. 2) Medical Orders forLife Sustaining Treatment (MOLST) helps to ensure that a patient's wishes to receive or decline care are honored. A medical record review conducted on [DATE] at 10:30 AM revealed that Resident #214 was admitted to the [NAME] Unit on [DATE]. At the facility MOLST forms are kept in white binders with the room number written on the outer spine. In the binder that corresponded to Resident #214's room was the MOLST form of the previous resident, now deceased . There was no MOLST form for Resident #214 in the binder. This finding was verified by staff #5. In an interview conducted pn [DATE] at 10:45 AM, the Charge Nurse, staff #1, verified the finding and stated that the resident was originally on another Unit before being hospitalized and that the MOLST orders would be in the computer. It is important to keep hard copies of the MOLST form on the Unit because in the event of a computer outage or planned software updates (access to the electronic medical records would be unavailable) the resident's wishes regarding life sustaining treatments still need to be accessible. 3) A medical record review conducted on [DATE] revealed that between 2017 and 2018 the facility staff were not documenting care plan meetings for Resident #16. This finding was verified by the Director of Nursing who verbalized an awareness that there are documentation issues at the facility. The facility staff have a responsibility to ensure that resident records are in the designated places and that they are documenting completely and accurately. Based on medical record review and staff interview it was determined the facility failed: 1) To document thorough pain assessments for Resident #113. 2) To ensure that a Medical Orders for Life Sustaining Treatment (MOLST) form was present in the correct chart, 3) To document care plan meetings, and 4) To appropriately assess a resident when a significant weight loss occurred. This was evident for 4 residents out of the 25 residents reviewed in Stage 2 of the survey process. This deficient practice affected Residents #113, #214, #16 and #34. The findings include: Resident #113 has a diagnosis of Rheumatoid Arthritis (RA) with rheumatoid factor. RA is an inflammatory disease that involves the immune system attacking the joints. This can cause symptoms that include pain, swelling, and stiffness which can lead to difficulty or loss of physical function and the ability to perform everyday tasks. Rheumatoid factor is a protein made by the immune system that can attack healthy tissue, so its presence can indicate an autoimmune disease. On [DATE] at 9:39 AM, during an interview with Resident #113, when asked if she had any concerns about her care, she stated that she was aching all over and did not feel like she had gotten her last dose of Methotrexate for her RA. When asked, she stated that her level of pain was an '8' on a '0 to 10' pain scale with '0' being no pain and '10' being the worst. A review of the Treatment Administration Record (TAR) and nurses notes over a period of 6 days following admission revealed the resident's perception of pain reached an '8' on day 1; '9' on day 2; and '10' on day 3, 4, 5 and 6 and the was documented as effective. The standard of practice for pain management involves asking the resident what he/she would like the pain level to be and working to meet that goal. On a '0 to 10' pain scale, '1 to 3' is considered mild pain; '4 to 6' is considered moderate pain and '7 to 10' is considered severe pain. A thorough pain assessment includes the onset; location; intensity; description; interventions; how effective the interventions are and/or other descriptors as well. If a '1 to 10' pain scale is used, a scale is typically used to describe how effective the interventions were. Further review of the medical record did not demonstrate that thorough pain assessments were documented. The facility is responsible to thoroughly document pain so that interventions can be modified, as needed.
Understanding Severity Codes (click to expand)
Life-Threatening (Immediate Jeopardy)
J - Isolated K - Pattern L - Widespread
Actual Harm
G - Isolated H - Pattern I - Widespread
Potential for Harm
D - Isolated E - Pattern F - Widespread
No Harm (Minor)
A - Isolated B - Pattern C - Widespread

Questions to Ask on Your Visit

  • "What changes have you made since the serious inspection findings?"
  • "Can I speak with families of current residents?"
  • "What's your RN coverage like on weekends and overnight?"

Our Honest Assessment

Strengths
  • • No fines on record. Clean compliance history, better than most Maryland facilities.
Concerns
  • • Multiple safety concerns identified: 1 life-threatening violation(s). Review inspection reports carefully.
  • • 27 deficiencies on record, including 1 critical (life-threatening) violation. These warrant careful review before choosing this facility.
  • • Grade C (58/100). Below average facility with significant concerns.
Bottom line: Mixed indicators with Trust Score of 58/100. Visit in person and ask pointed questions.

About This Facility

What is Hartley Nursing And Rehab's CMS Rating?

CMS assigns HARTLEY NURSING AND REHAB an overall rating of 4 out of 5 stars, which is considered above average nationally. Within Maryland, this rating places the facility higher than 99% of the state's 100 nursing homes. This rating reflects solid performance across the metrics CMS uses to evaluate nursing home quality.

How is Hartley Nursing And Rehab Staffed?

CMS rates HARTLEY NURSING AND REHAB's staffing level at 2 out of 5 stars, which is below average compared to other nursing homes. Staff turnover is 45%, compared to the Maryland average of 46%. This relatively stable workforce can support continuity of care.

What Have Inspectors Found at Hartley Nursing And Rehab?

State health inspectors documented 27 deficiencies at HARTLEY NURSING AND REHAB during 2018 to 2024. These included: 1 Immediate Jeopardy (the most serious level, indicating potential for serious harm or death) and 26 with potential for harm. Immediate Jeopardy findings are rare and represent the most serious regulatory concerns. They require immediate corrective action.

Who Owns and Operates Hartley Nursing And Rehab?

HARTLEY NURSING AND REHAB is owned by a for-profit company. For-profit facilities operate as businesses with obligations to shareholders or private owners. The facility is operated by KEY HEALTH MANAGEMENT, a chain that manages multiple nursing homes. With 73 certified beds and approximately 66 residents (about 90% occupancy), it is a smaller facility located in POCOMOKE CITY, Maryland.

How Does Hartley Nursing And Rehab Compare to Other Maryland Nursing Homes?

Compared to the 100 nursing homes in Maryland, HARTLEY NURSING AND REHAB's overall rating (4 stars) is above the state average of 3.0, staff turnover (45%) is near the state average of 46%, and health inspection rating (4 stars) is above the national benchmark.

What Should Families Ask When Visiting Hartley Nursing And Rehab?

Based on this facility's data, families visiting should ask: "What changes have been made since the serious inspection findings, and how are you preventing similar issues?" "Can you walk me through typical staffing levels on day, evening, and night shifts?" "Can I visit during a mealtime to observe dining assistance and food quality?" "How do you handle medical emergencies, and what is your hospital transfer rate?" These questions are particularly relevant given the facility's Immediate Jeopardy citations and the below-average staffing rating.

Is Hartley Nursing And Rehab Safe?

Based on CMS inspection data, HARTLEY NURSING AND REHAB has documented safety concerns. Inspectors have issued 1 Immediate Jeopardy citation (the most serious violation level indicating risk of serious injury or death). The facility has a 4-star overall rating and ranks #1 of 100 nursing homes in Maryland. Families considering this facility should ask detailed questions about what corrective actions have been taken since these incidents.

Do Nurses at Hartley Nursing And Rehab Stick Around?

HARTLEY NURSING AND REHAB has a staff turnover rate of 45%, which is about average for Maryland nursing homes (state average: 46%). Moderate turnover is common in nursing homes, but families should still ask about staff tenure and how the facility maintains care continuity when employees leave.

Was Hartley Nursing And Rehab Ever Fined?

HARTLEY NURSING AND REHAB has no federal fines on record. CMS issues fines when nursing homes fail to meet care standards or don't correct problems found during inspections. The absence of fines suggests the facility has either maintained compliance or corrected any issues before penalties were assessed. This is a positive indicator, though families should still review recent inspection reports for the full picture.

Is Hartley Nursing And Rehab on Any Federal Watch List?

HARTLEY NURSING AND REHAB is not on any federal watch list. The most significant is the Special Focus Facility (SFF) program, which identifies the bottom 1% of nursing homes nationally based on persistent, serious quality problems. Not being on this list means the facility has avoided the pattern of deficiencies that triggers enhanced federal oversight. This is a positive indicator, though families should still review the facility's inspection history directly.