HAMPSHIRE MEMORIAL HOSPITAL

363 SUNRISE BLVD, ROMNEY, WV 26757 (304) 822-4561
Non profit - Corporation 30 Beds Independent Data: November 2025
Trust Grade
50/100
#70 of 122 in WV
Last Inspection: February 2024

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

Overview

Hampshire Memorial Hospital has a Trust Grade of C, indicating that it is average compared to other nursing homes. It ranks #70 out of 122 facilities in West Virginia, placing it in the bottom half, and #2 out of 2 in Hampshire County, meaning there is only one other local option. The facility is worsening, with issues increasing from 6 in 2022 to 17 in 2024. Staffing is a concern, with a low rating of 1 out of 5 stars; however, a turnover rate of 38% is better than the state average. While there have been no fines, the facility has faced several issues, including not addressing residents' weight loss in care plans and not allowing residents to file grievances anonymously, which raises concerns about resident care and communication.

Trust Score
C
50/100
In West Virginia
#70/122
Bottom 43%
Safety Record
Low Risk
No red flags
Inspections
Getting Worse
6 → 17 violations
Staff Stability
○ Average
38% turnover. Near West Virginia's 48% average. Typical for the industry.
Penalties
✓ Good
No fines on record. Clean compliance history, better than most West Virginia facilities.
Skilled Nurses
○ Average
RN staffing data not reported for this facility.
Violations
⚠ Watch
27 deficiencies on record. Higher than average. Multiple issues found across inspections.
★★☆☆☆
2.0
Overall Rating
★☆☆☆☆
1.0
Staff Levels
★★★☆☆
3.0
Care Quality
★★★☆☆
3.0
Inspection Score
Stable
2022: 6 issues
2024: 17 issues

The Good

  • Full Sprinkler Coverage · Fire safety systems throughout facility
  • No fines on record
  • Staff turnover below average (38%)

    10 points below West Virginia average of 48%

Facility shows strength in fire safety.

The Bad

2-Star Overall Rating

Below West Virginia average (2.7)

Below average - review inspection findings carefully

Staff Turnover: 38%

Near West Virginia avg (46%)

Typical for the industry

The Ugly 27 deficiencies on record

Feb 2024 17 deficiencies
CONCERN (D)

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

Deficiency F0552 (Tag F0552)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and staff interview, the facility failed to inform the resident/responsible party of the risks and benefi...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and staff interview, the facility failed to inform the resident/responsible party of the risks and benefits of receiving an antipsychotic medication. This was found for one (1) of five (5) residents reviewed for unnecessary medications. Resident identifier: #13. Facility census: 27. Findings included: a) Resident #13 Resident #13 was admitted to the facility on [DATE]. On 10/17/23, a physician determined the Resident lacked capacity to make medical decisions due to a diagnosis of Dementia and his wife was appointed as his health care surrogate. Record review found on 01/04/24, the Resident's physician prescribed a new antipsychotic medication Seroquel, oral Tablet, 25 milligrams (mg's) 1 tablet by mouth two (2) times a day for a diagnosis of depression. The Resident was already receiving Lexopro, an antidepressant for a diagnosis of depression. Further review of the medical record found no evidence the responsible party, the Resident's wife, was notified of the risks and benefits of taking Seroquel, an antipsychotic medication. On 02/21/24 at 2:24 PM, the Director of Nursing reviewed the resident's progress notes with the surveyor. The DON states, we really don't have any behaviors documented to add the Seroquel. I think I'll call the physician to address this and maybe he will discontinue the medication. The DON confirmed the physician and the nurse practitioner never addressed the use of Seroquel in their notes. The DON said this happens frequently, those nurses want to give medications for behaviors but they never document anything in their notes. This is an ongoing problem. On 02/21/24 at 4:00 PM, the DON confirmed she could not find any evidence the risks and benefits of starting Seroquel were discussed with the responsible party.
CONCERN (D)

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

Notification of Changes (Tag F0580)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and staff interview, the facility failed to notify the residents' representatives when Resident #20 had a...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and staff interview, the facility failed to notify the residents' representatives when Resident #20 had a significant change in status and when Resident #13 had a significant alteration in treatment. This deficient practice had the potential to affect two (2) of 14 residents reviewed in the long-term care survey sample. Resident identifiers: #20, #13. Facility census: 27. Findings included: a) Resident #20 Review of Resident #20's weights summary in the electronic health record showed the resident weighed 129.6 pounds (lbs.) on 09/01/23. The weights summary identified the resident had lost 10% of weight in six (6) months when compared to the resident's weight of 144.6 lbs. on 04/05/23. Further review of Resident #20's medical records showed a Physician Certification of Capacity/Incapacity dated 04/19/23 that showed the resident lacked sufficient mental capacity to make health care decisions. In 2021, the resident had chosen a family member to make health care decisions for her if she became incapacitated. There was no documentation in Resident #20's medical record that the resident's representative had been notified when the resident had a significant weight loss on 09/01/23. Resident #20 weighed 130.1 lbs. on 10/02/23 and 121.2 lbs. on 11/08/23. Although the weights summary did not identify this change as significant weight loss, the resident had lost 7% of weight in one (1) month. There was no documentation in Resident #20's medical record that the resident's representative had been notified when the resident had a significant weight loss on 11/08/23. The resident continued to lose weight, weighing 116 lbs. on 12/10/23 and 113 lbs. on 01/10/24. On 01/17/24, the resident's representative was notified regarding new orders instituted to address the resident's weight loss. There was no evidence the resident's representative was notified regarding weight loss before 01/17/24. On 02/21/24 at 1:55 PM, Clinical Coordinator #6 confirmed Resident #20's medical records contained no documentation that the resident's representative had been notified of the resident's weight loss before 01/17/24. No further information was provided through the completion of the survey process. b) Resident #13 Resident #13 was admitted to the facility on [DATE]. On 10/17/23, a physician determined the Resident lacked capacity to make medical decisions due to a diagnosis of Dementia and his wife was appointed as his health care surrogate. Record review found on 01/04/24, the Resident's physician prescribed a new medication Seroquel, oral Tablet, 25 milligrams (mg's) 1 tablet by mouth two (2) times a day for a diagnosis of depression. Further review of the medical record found no evidence the responsible party, the Resident's wife, was notified of the physician's order for Seroquel, an antipsychotic medication. On 02/21/24 at 4:00 PM, the Director of Nursing (DON) confirmed she could find no evidence the responsible party was contacted before starting the medication, Seroquel.
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 record review and staff interview, the facility failed to ensure three (3) of three (3) residents reviewed for the care area of beneficiary notices received the required notices when the faci...

Read full inspector narrative →
Based on record review and staff interview, the facility failed to ensure three (3) of three (3) residents reviewed for the care area of beneficiary notices received the required notices when the facility initiated a discharge from Medicare A and the three (3) residents elected to remain at the facility with benefit days remaining. Resident identifiers: #28, #13, and #17. Facility census: 27. Findings included: a) Beneficiary Notices Review of the facility's entrance conference Worksheet indicated three (3) residents who were discharged from Medicare, Part A with benefit days remaining: Resident #28 was discharged from Medicare Part A services on 11/15/23 and remained at the facility with benefit days remaining. Resident #13 was discharged from Medicare Part A services on 11/04/23 and remained at the facility with benefit days remaining. Resident #17 was discharged from Medicare Part A services on 10/29/23 and remained at the facility with benefit days remaining. On 02/20/24 at 3:02 PM, the Director of Nursing (DON) and the Clinical Coordinator, Minimum Data Set (CCMDS) confirmed the facility did not issue a Skilled Nursing Facility Advanced Beneficiary Notice of Non-coverage (SNF ABN) CMS 10055 to Residents #28, #13, #17 when they were discharged from Medicare Part A services.
CONCERN (D)

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

Deficiency F0692 (Tag F0692)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and staff interview the facility failed to assess, monitor and provide timely interventions for residents...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and staff interview the facility failed to assess, monitor and provide timely interventions for residents experiencing weight loss. This was true for two (2) of three (3) residents reviewed for nutrition. Resident Identifiers: #17 and #20. Facility Census: #27 Findings included: a) Policy Review On 02/21/24 at 09:20 AM review of the facility Policy for Resident Weights, revised 05/2023 found the following: Purpose: . that residents maintain acceptable parameters of nutritional status, such as body weight. Weights can be a useful indicator of nutritional status when evaluated within the context of the individuals personal history and overall conditions. A standard protocol is needed to reduce errors. Policy: A. Nursing facility residents will be weighed on admission and weekly (at minimum) for the next consecutive 4 weeks. Thereafter, they will be weighed monthly unless otherwise ordered to help identify any trends such as insidious weight loss. B. Weight loss can be avoidable (resident did not maintain a good nutritional status and the facility did not address it), or unavoidable (resident did not maintain good nutritional status due to clinical condition C. Weighing may also be pertinent if there is significant change in condition, food intake has declined or there is other evidence of altered nutritional status or a fluid/electrolyte imbalance Procedure: . B. Residents will be reweighed for all weight changes of plus or minus 5 pounds, per physician order or at the request of the registered dietician/nurse. C. Residents who experience a weight loss or weight gain of more than 5% in a month are to be evaluated by the registered dietitian b) Resident #17 On 02/20/24 at 02:10 PM record review for Resident #17 shows the following: Medical history: Urinary tract infection Idiopathic peripheral autonomic neuropathy Heart failure Weakness Other specified symptoms and signs involving the circulatory and respiratory systems. Other pulmonary embolism Pneumonia Edema Hypokalemia Hypotension Vitamin B12 deficiency anemia due to intrinsic factor deficiency Resident #17 was admitted on [DATE] weighing 161 pounds Resident #17 was sent out to the hospital on [DATE] and returned on 12/17/23 with no re admission weight obtained. On 12/01/23 Resident #17 weighed 171.5 pounds, a weight gain of 10 pounds, (prior to hospitalization on 12/12/23) On 01/01/24 Resident #17 weighed 153.4 pounds, a weight loss of 18.1 pounds with no re-weigh. This represents a 10.55% weight loss. On 02/08/24 Resident #17 weighed 138 pounds, a weight loss of 15.4 pounds with no re-weigh. This represents a 10.04% weight loss. Resident #17 lost 19.53% of his weight from 12/01/23 until 02/08/24 with no new interventions in place. Further record review shows Resident #17 is on a no added salt diet, soft and bite sized texture, thin liquids consistency. Heart Healthy. There are no supplements ordered. The care plan in place has interventions to refer to Registered Dietitian as needed and Resident to be weighed weekly X 4 weeks to monitor weight loss or gain and then as needed. Review of Nutrition Progress notes finds two progress notes, one dated 10/12/23 and the other 01/08/24. There is one Nutritional Assessment completed on 10/09/23. There are no nutritional notes or assessments completed since the time the weight loss began on 12/01/23. There are no progress notes indicating the Physician has been notified. The above information was confirmed with the Director of Nursing on 02/21/24 at 09:45 AM at which time she stated Resident #17 has a status of Do Not Resuscitate, comfort focused treatments: maximize comfort through symptom management; allow natural death. The DON added, the Resident should not have been weighted; however, the DON was unable to find an order directing no weights. The DON said the Resident's daughter was a nurse practitioner who visits frequently and she has no issues with the Resident's care at the facility. The DON said since the staff did weigh the Resident he should have been reweighted on 1/1/24 and 2/8/24 after the 5 pound weight fluctuation. She agreed that the Physician and Dietitian should have been notified and assessments and/or progress notes maintained concerning the nutritional status of the resident in order to provide professional standards of practice for this resident experiencing weight loss. c) Resident #20 Review of Resident #20's medical records showed a Nutritional Assessment had been performed by the Registered Dietician (RD) on 05/30/23. The resident weighed 137.6 pounds (lbs.). At that time, the resident was receiving tube feeding boluses, 237 milliliters (ml), three (3) times a day, via a percutaneous endoscopic gastrostomy (PEG) tube. The resident received no nutrition by mouth. The RD recommended the resident's tube feeding be changed to infusions to increase the resident's tolerance to feeding. An order was written on 06/05/23 for Glucerna 55 ml an hour for 12 hours via PEG tube daily. Review of Resident #20's weights summary in the electronic health record showed the resident weighed 129.6 lbs. on 09/01/23. The weights summary identified the resident had lost 10% of weight in six (6) months when compared to the resident's weight of 144.6 lbs. on 04/05/23. There was no indication in the medical records that a nutritional assessment had been performed or that any interventions for weight loss had been implemented. Resident #20 weighed 130.1 lbs. on 10/02/23 and 121.2 lbs. on 11/08/23. Although the weights summary did not identify this change as significant weight loss, the resident had lost 7% of weight in one (1) month. There was no indication in the medical records that a nutritional assessment had been performed or that any interventions for weight loss had been implemented. There was no documentation the resident had been reweighed as specified in the facility's policy. The resident continued to lose weight, weighing 116 lbs. on 12/10/23 and 113 lbs. on 01/10/24. On 01/17/24, the RD performed a Nutritional Assessment. The RD recommended the resident's tube feeding amount be increased. On 01/17/24, an order was written for Glucerna 75 ml an hour for 12 hours via PEG tube. On 02/21/24 at 1:55 PM, Clinical Coordinator #6 confirmed Resident #20's medical records contained no documentation that the resident's weight loss had been addressed prior to 01/17/24. Clinical Coordinator #6 confirmed there was no documentation that the RD had been consulted when the resident first experienced significant weight loss on 09/01/23 or that any interventions for weight loss had been implemented. Additionally, Clinical Coordination #6 confirmed there was no documentation the resident had been reweighed as specified in the facility's policy. No further information was provided through the completion of the survey process.
CONCERN (D)

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

Deficiency F0710 (Tag F0710)

Could have caused harm · This affected 1 resident

b) Resident #1 On 02/20/24 at 9:35 AM record review shows Resident #1 had a significant weight loss of greater than 5% in one (1) month two (2) times in five (5) months. According to the facility Res...

Read full inspector narrative →
b) Resident #1 On 02/20/24 at 9:35 AM record review shows Resident #1 had a significant weight loss of greater than 5% in one (1) month two (2) times in five (5) months. According to the facility Resident Weights Policy revised 05/2023 .Procedure: B. Residents will be reweighed for all weight changes of plus or minus 5 pounds, per physician order . Documented weights are as follows with no re-weights when there was a plus or minus of five (5) pounds. 2/8/2024 16:09 203.8 Lbs Mechanical Lift 1/23/2024 16:23 203.8 Lbs Sitting 12/1/2023 09:47 215.4 Lbs Bath 11/2/2023 16:51 217.5 Lbs Bath 10/1/2023 15:57 220.3 Lbs Bath 9/29/2023 11:14 221.5 Lbs Bath 9/22/2023 10:26 224.6 Lbs Mechanical Lift 9/15/2023 14:42 222.8 Lbs Mechanical Lift 9/8/2023 09:26 219.4 Lbs Mechanical Lift 9/7/2023 09:53 220.0 Lbs Bath (Manual) 8/4/2023 12:11 233.5 Lbs Mechanical Lift (Manual) Record review shows Resident #1 had the following weights recorded: 08/04/23 233.5 pounds and on 09/07/23 220 pounds for a weight loss of -5.78% and 12/01/23 215.4 pounds and on 01/23/24 203.8 pounds for a weight loss of -5.85% This reflects a 12.72% weight loss from 08/04/23 until 01/23/24. According to record review, the Physician was not informed of residents' weight loss to evaluate and address medical and nutritional issues. The Physician was not notified of the weight loss on 09/07/23 and the weight loss on 01/23/24 was not reported to the Physician until 02/18/24. A significant weight loss is described as: 5% change in weight in 1 month (30 days) 7.5% change in weight in 3 months (90 days) 10% change in weight in 6 months (180 days) This was confirmed with the Director of Nursing on 02/21/24 at 2:10 PM. Based on record review and staff interview, the facility failed to ensure residents' care after significant weight loss was supervised by the physician. This deficient practice had the potential to affect two (2) of three (3) residents reviewed for the care area of nutrition. Resident identifier: #20, #1. Facility census: 27. Findings included: a) Resident #20 Review of Resident #20's weights summary in the electronic health record showed the resident weighed 129.6 pounds (lbs.) on 09/01/23. The weights summary identified the resident had lost 10% of weight in six (6) months when compared to the resident's weight of 144.6 lbs. on 04/05/23. The resident was receiving feeding via a percutaneous endoscopic gastrostomy (PEG) tube. The resident received no nutrition by mouth. There was no indication in the medical records that the physician had been notified of the resident's weight loss. Resident #20 weighed 130.1 lbs. on 10/02/23 and 121.2 lbs. on 11/08/23. Although the weights summary did not identify this change as significant weight loss, the resident had lost 7% of weight in one (1) month. Again, there was no indication in the medical records that the physician had been notified of the resident's weight loss. The resident continued to lose weight, weighing 116 lbs. on 12/10/23 and 113 lbs. on 01/10/24. On 01/17/24, the physician was notified of the resident's weight loss and a physician's order to increase the resident's tube feeding infusion amount was written. On 02/21/24 at 1:55 PM, Clinical Coordinator #6 confirmed Resident #20's medical records contained no documentation that the physician had been notified of the resident's weight loss prior to 01/17/24.
CONCERN (D)

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

Deficiency F0744 (Tag F0744)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and staff interview the facility failed to ensure a resident who is diagnosed with dementia, received the...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and staff interview the facility failed to ensure a resident who is diagnosed with dementia, received the appropriate treatment and services to attain or maintain his or her highest practicable physical, mental, and psychosocial well-being. The facility failed to identify and address the needs of a resident diagnosed with dementia and develop a person-centered care plan that included individual non-pharmacological approaches to care using meaningful activities to address the resident's customary routines, interests, preferences and choices to enhance the resident's well-being. This was found for one (1) of two (2) residents reviewed for dementia care. Resident identifier: #13. Facility census: 27. Findings include: a) Resident #13 Resident #13 was admitted to the facility on [DATE]. On 10/17/23, a physician determined the Resident lacked capacity to make medical decisions due to a diagnosis of Dementia and his wife was appointed as his health care surrogate. The Resident was admitted to the facility without any psychotropic medications. On 11/05/23, Lexapro 20 milligrams (mg's) daily was ordered for a diagnosis of depression. Progress notes indicated the Resident was having difficulty adjusting to the facility. He would frequently talk of wanting to go home and would wander around the facility asking for his wife. Record review found on 01/04/24, the Resident's physician prescribed a new antipsychotic medication Seroquel, oral Tablet, 25 milligrams (mg's) 1 tablet by mouth two (2) times a day for a diagnosis of depression. The Resident was already receiving Lexapro, an antidepressant for a diagnosis of depression. Review of the Resident's care plan found the facility did not address a diagnosis of dementia and utilizing individualized, non-pharmacological approaches to care with purposeful and meaningful activities to address the resident's well-being. On the morning of 02/21/24 around 11:00 AM, the Resident was observed sitting across from the nurses station watching a show about a rodeo on the computer. Interaction with the Resident found he likes watching rodeo's. He said, those rodeo's are on there (pointing to the computer screen) all the time. Sometimes they go off but they come back on. On 02/21/24 several staff members were interviewed and asked about the Resident's behaviors and how staff interact with him: On 02/21/24 at 11:58 AM, Licensed Practical Nurse (LPN) #10 said the Resident seems more anxious in the evenings. He gets mad when we have to tell him he can't walk alone without our help. He will ball up his fist but he doesn't hit you. Then he will cry and get upset because he threatened to hit us. He says he's sorry. He misses his wife and gets upset because he can't go home. He will say, I have to get home, I can walk home. He hasn't left the facility. I think the Lexapro really helped him. He can be distracted by watching something on the computer. LPN #10 said the resident likes to be out by the nurses station in the evenings. He likes to stay up late and be around other people. We use a geri-chair so he can prop his feet up and sometimes he will doze off and on. On 02/21/24 at 12:05 PM, Registered Nurse (RN) #36 stated, sometimes I call his house when he wants his wife. A step daughter will talk to him. She says his wife is too sick to talk. Watching something on the computer or youtube helps distract him. I have tried food and drinks but that doesn't help at all. A couple of months ago he was on an antibiotic for a urinary tract infection and he had more problems then. He wants to go home and he misses his wife. On 02/21/24 at 12:35 PM, the Residents nurse aide (NA) #3 said he gets upset when family visits. He begs them to take him home, says please don't leave me here I have to get home to my wife. He also gets upset because he can't walk alone anymore. I use coffee and snacks to distract him. He also likes to watch shows about horses and rodeo shows. We turn on youtube for him and he likes to sit here across from the nurses station and watch horse shows. He has never hit me or anyone else that I know about. He really likes to talk about the days when he delivered milk. That was what he worked at and he can really talk about work. 02/21/24 at 12:40 the activity aide #39 said the Resident likes to watch television and shows on you tube. She said he also likes to listen to his faith based programs on the internet. She said members from his congregation visited and told her how to access the religious programs on line. She said this seems to calm him, he just wants to go home at times. He misses his wife. His wife is sick herself and can't visit often. All the above staff denied the Resident had any conflict with any other residents at the facility and all staff confirmed the Resident just wants to go home and he misses his wife. On 02/21/24 at 2:24 PM, the above interviews were shared with the Director of Nursing (DON.) The DON reviewed the progress notes with the surveyor and states, we really don't have any behaviors documented to add the Seroquel. I think I'll call the physician to address this and maybe he will discontinue the medication. The DON confirmed the physician and the nurse practitioner never addressed the use of Seroquel in their notes. The DON said this happens frequently, those nurses want to give medications for behaviors but they never document anything in their notes. This is an ongoing problem. The DON was unable to provide documentation of any non-pharmacological interventions implemented prior to starting Seroquel. The DON was aware the Resident frequently wants to go home and he wanders around the facility looking for a way to get home. At 8:00 AM on 2/22/24, Registered Nurse (RN) #6 the Clinical Coordinator, Minimum Data Set along with the DON present confirmed the resident had never been care planned for a diagnosis of dementia including services to meet the Resident's needs. RN #6 confirmed the non-pharmacological interventions used by staff for distraction when the Resident is missing his wife were never care planned.
CONCERN (D)

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

Menu Adequacy (Tag F0803)

Could have caused harm · This affected 1 resident

Based on observation, record review, resident interview, and staff interview, the facility failed to ensure dietary preferences were honored. Two (2) of six (6) residents reviewed for the care area of...

Read full inspector narrative →
Based on observation, record review, resident interview, and staff interview, the facility failed to ensure dietary preferences were honored. Two (2) of six (6) residents reviewed for the care area of food did not receive the food items indicated on their tray ticket. Resident identifiers: #3, #10. Facility census: 27. Findings included: a) Resident #3 On 02/19/24 at 12:15 PM, Resident #3 was observed eating in her room. Her lunch tray consisted of grilled cheese, tomato soup, and peaches. Resident #3 stated, I can't stand tomato soup. She stated the staff was going to get chicken soup for her. Review of Resident #3's tray ticket indicated she was to receive double noodle chicken soup for that meal. Resident #3 stated she often did not receive the food items she wanted. On 02/19/24 at 12:20 PM, Clinical Coordinator #6 confirmed Resident #3 had received tomato soup when her tray ticket indicated she was supposed to have received chicken noodle soup. No further information was provided through the completion of the survey process. b) Resident #10 On 02/19/24 at 12:12 PM, Resident #10 was observed eating in her room. Her lunch tray consisted of French fries and peaches. She stated her tray had just been delivered and she did not receive a sandwich. She stated the staff was going to get a sandwich for her. Review of Resident #10's tray ticket indicated she was supposed to have received a turkey salad sandwich that meal. Resident #10 stated she often did not receive the food items she wanted. On 02/19/24 at 12:20 PM, Clinical Coordinator #6 confirmed Resident #10 had not received a sandwich for lunch when her meal tray was delivered. No further information was provided through the completion of the survey process.
CONCERN (D)

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

Medical Records (Tag F0842)

Could have caused harm · This affected 1 resident

Based on record review and staff interview the facility failed to ensure complete and accurate medical records were available pertaining to Physicians Order for Scope of Treatment (POST). Resident Ide...

Read full inspector narrative →
Based on record review and staff interview the facility failed to ensure complete and accurate medical records were available pertaining to Physicians Order for Scope of Treatment (POST). Resident Identifier: #17 and #27 Facility Census: #27 Findings Included: a) Resident #17 On 02/19/24 at 03:10 PM, record review shows that the POST form for Resident #17 was not completed in its entirety. The patient information on page one (1) did not have identifying information for a middle initial, last four (4) numbers of the social security number and an address. Section D for Medically Assisted Nutrition was not addressed. Page two (2) of the POST only provided a resident name and the Medical Power of Attorney name. The Primary Care Provider Name or telephone number was provided. This was confirmed with the Director of Nursing on 02/20/24 at 10:40 AM, who agreed that Section D should have been addressed and Resident identification information on page one (1) should be completed in its entirety. b) Resident #27 On 02/19/24 at 03:15 PM, record review shows that the POST form for Resident #27 was not completed in its entirety. Page two (2) of the POST was blank. This was confirmed with the Director of Nursing on 02/20/24 at 10:40 AM, who agreed that at a minimum it should include the residents name, Medical Power of Attorney and Primary Care provider name and telephone number.
CONCERN (E)

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

Grievances (Tag F0585)

Could have caused harm · This affected multiple residents

Based on observation and staff interview the facility failed to provide residents the opportunity to file grievances anonymously by not making grievance forms accessible to residents. This has the pot...

Read full inspector narrative →
Based on observation and staff interview the facility failed to provide residents the opportunity to file grievances anonymously by not making grievance forms accessible to residents. This has the potential to affect more than a limited number of residents. Facility Census: #27 Findings included: a) Facility On 02/20/24 at 11:10 AM observation found that there were no grievance forms accessible to residents to obtain on their own accord. Upon discussion with the Director of Nursing on 02/20/24 at 12:10 PM, she states the forms are kept in her office in a file cabinet. The Residents must go through a staff member to file a grievance. When asked how the Residents file an anonymous grievance, she states they do not. According to the regulation: 483.10(j) Grievances. . Notifying resident individually or through postings in prominent locations throughout the facility of the right to file grievances orally (meaning spoken) or in writing; the right to file grievances anonymously; During a Resident Council meeting on 02/21/24 residents present (14 residents) stated they can not file a grievance anonymously, they must go through a staff member and they might like to file an anonymous complaint sometime. The above was confirmed with the Director of Nursing on 02/22/24 at 9:10 AM.
CONCERN (E)

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

Comprehensive Care Plan (Tag F0656)

Could have caused harm · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and staff interview the facility failed to develop and/or implement the comprehensive care plan for seven...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and staff interview the facility failed to develop and/or implement the comprehensive care plan for seven (7) of fourteen (14) residents reviewed in the long term care survey sample. Resident Identifiers: #1, #27, #24, #11, #13, #20 and #3. Facility Census: #27. Findings included: a) Resident #1 On 02/20/24 at 03:10 PM record review show Resident #1 has a history of weight loss. Weights were documented as: 02/08/24 203.8 01/23/24 203.8 11/02/23 217.5 08/04/23 233.5 Further review of Resident #1's care plan found that there was no care plan developed for weight loss. This was confirmed with the Director of Nursing on 02/20/24 at 03:58 PM who agreed that Resident #1 should be care planned for weight loss. b) Resident #27 On 02/20/24 at 11:50 AM record review shows Resident #27 was admitted on [DATE] with contractures to the left shoulder and elbow. Review of the care plan in place found the contractures were not included on the care plan in place. This was confirmed with the Director of Nursing on 02/20/24 at 03:10 PM and she agreed the contractures should be care planned. c) Resident #24 On 02/21/24 at 10:05 PM record review shows that Resident #24 has a Physicians order for: Lasix Oral Tablet 20 milligrams (MG) (Furosemide) Give 1 tablet by mouth two times a day for edema related to essential (primary) hypertension. A review of the care plan shows there are no care plans in place for hypertension, edema or the use of Lasix for these two diagnosis. This was confirmed with the Director of Nursing on 02/21/24 at 11:01 AM who confirmed the care plan was not correct. d) Resident #11 Review of the current physician's orders found an order written on 4/20/23 for a Cockup brace to right wrist, every eight (8) hours as needed for comfort or support range of motion (ROM) as tolerated. There was no diagnosis for the use of the brace. Review of the current care plan found no mention of a brace to the right wrist. An interview, with the resident's Licensed Practical Nurse (LPN) #10 on 02/21/24 at 8:06 AM, revealed LPN #10 thought the brace was ordered by an orthopedic physician after the Resident broke her wrist. LPN #10 searched the medical record and found a consult dated 04/03/23 which states, cast removed today patient may use cockup brace as needed. Range of motion as tolerated. This order was signed on 04/06/23. On 04/10/23 the physician wrote a new order for, Resident may use cockup brace as needed. ROM as tolerated, every shift. A second order for the brace was written on 04/20/23. Review of the Medication Administration Record (MAR) found the resident wore the brace from 04/10/23 through 04/20/23. Review of the past 3 months of MAR'S for December, 2023, January 2024, and February 2024 found no indication the resident wore the brace, yet the order remained on the MAR. On 02/21/24 at 9:00 AM, the author of the care plan, Registered Nurse (RN) #6 the Clinical Coordinator, Minimum Data Set confirmed the care plan did not mention the use of the brace. RN #6 stated she wasn't sure what the brace was for. e) Resident #13 Resident #13 was admitted to the facility on [DATE]. On 10/17/23, a physician determined the Resident lacked capacity to make medical decisions due to a diagnosis of Dementia and his wife was appointed as his health care surrogate. The Resident was admitted without any psychotropic medications. On 11/05/23, Lexapro 20 milligrams (mg's) daily was ordered for a diagnosis of depression. The Resident was having difficulty adjusting to the facility. He would frequently talk of wanting to go home and would wander around the facility asking for his wife. Record review found on 01/04/24, the Resident's physician prescribed a new antipsychotic medication Seroquel, oral Tablet, 25 milligrams (mg's) 1 tablet by mouth two (2) times a day for a diagnosis of depression. The Resident was already receiving Lexapro, an antidepressant for a diagnosis of depression. Review of the current care plan found no mention of the Resident receiving Seroquel, an antipsychotic medication, for the use of depression. In addition the Resident was diagnosed with Dementia and the care plan did not address a diagnosis of dementia utilizing individualized, non-pharmacological approaches to care with purposeful and meaningful activities to address the resident's well-being. Interviews with the Resident's caregivers found the Resident exhibited the following signs of distress: On 02/21/24 at 11:58 AM, Licensed Practical Nurse (LPN) #10 said the Resident seems more anxious in the evenings. He gets mad when we have to tell him he can't walk alone without our help. He will ball up his fist but he doesn't hit you. Then he will cry and get upset because he threatened to hit us. He says he's sorry. He misses his wife and gets upset because he can't go home. He will say, I have to get home, I can walk home. He hasn't left the facility. I think the Lexapro really helped him. He can be distracted by watching something on the computer. LPN #10 said the resident likes to be out by the nurses station in the evenings. He likes to stay up late and be around other people. We use a geri-chair so he can prop his feet up and sometimes he will doze off and on. On 02/21/24 at 12:05 PM, Registered Nurse (RN) #36 stated, sometimes I call his house when he wants his wife. A step daughter will talk to him. She says his wife is too sick to talk. Watching something on the computer or youtube helps distract him. I have tried food and drinks but that doesn't help at all. A couple of months ago he was on an antibiotic for a urinary tract infection and he had more problems then. He wants to go home and he misses his wife. On 02/21/24 at 12:35 PM, the Residents nurse aide (NA) #3 said he gets upset when family visits. He begs them to take him home, says please don't leave me here I have to get home to my wife. He also gets upset because he can't walk alone anymore. I use coffee and snacks to distract him. He also likes to watch shows about horses and rodeo shows. We turn on youtube for him and he likes to sit here across from the nurses station and watch horse shows. He has never hit me or anyone else that I know about. He really likes to talk about the days when he delivered milk. That was what he worked at and he can really talk about work. 02/21/24 at 12:40 the activity aide #39 said the Resident likes to watch television and shows on you tube. She said he also likes to listen to his faith based programs on the internet. She said members from his congregation visited and told her how to access the religious programs on line. She said this seems to calm him, he just wants to go home at times. He misses his wife. His wife is sick herself and can't visit often. All the above staff denied the Resident had any conflict with any other residents at the facility. Examples of progress notes written by licensed nursing staff indicated the following concerns with the Resident's psychosocial well being: 11/1/23 at 4:56 PM Note Text: (Resident) has made multiple remarks about wanting to go home. He has been looking for a way out. Resident wanders around the facility asking for his wife and when will he be able to go home. New order for Safe Guard bracelet to be applied to his right ankle. Bracelet applied with no problems noted. 11/4/23 at 3:27 AM Note Text: (Resident) has been pacing on occasion this shift. Very forgetful with short term memory. (Resident) has asked for his wife several times and is redirected by staff as needed. 11/5/2023 at 10:40 AM Note Text: (Resident) up ambulating in halls with his walker and looking for his wife. Tearful @ (at) times. (Resident) doesn't understand why his wife is not here now. Appetite has been poor, although he's drinking well. 11/5/2023 at 2:21 PM Note Text: (Resident) continues to pace the halls and asking staff if his wife has been in and where she is at. Tearful at times. Staff try to redirect him and use distraction without success. Resident has a poor appetite and isn't sleeping well. Wife was called and stated to CNA (Certified Nurse Aide) that she wasn't well and that she wanted the staff to try to distract him. The wife stated that it upset her when he called because all he wanted to talk about was coming home. On 02/21/24 at 2:24 PM, the Director of Nursing reviewed the resident's progress notes with the surveyor. The DON states, we really don't have any behaviors documented to add the Seroquel. I think I'll call the physician to address this and maybe he will discontinue the medication. The DON confirmed the physician and the nurse practitioner never addressed the use of Seroquel in their notes. The DON said this happens frequently, those nurses want to give medications for behaviors but they never document anything in their notes. This is an ongoing problem. At 8:00 AM on 2/22/24, Registered Nurse (RN) #6 the Clinical Coordinator, Minimum Data Set confirmed the resident had never been care planned for the use of Seroquel or his diagnosis of Dementia. There was no mention of any behaviors/signs of distress in the care plan and no interventions as to how to address the Residents verbalization of missing his wife and wanting to go home. f) Resident #20 Review of Resident #20's comprehensive care plan showed the following focus, [Resident's name] is at risk for wt (weight) loss, dehydration, due to NPO (nothing by mouth) status with peg (percutaneous endoscopic gastrostomy) tube placement. An intervention was Check for residual prior to feedings and record. The residual is the volume of fluid remaining in the resident's stomach. Nurses withdraw this fluid by attaching a large syringe to the PEG tube and pulling back on the plunger. This is done to make sure the stomach is emptying properly and to prevent complications such as vomiting and aspiration. Resident #20 was receiving a tube feeding infusion for 12 hours one (1) time a day. The medical records contained no documentation that tube feeding residuals were being checked before the feeding was started. During an interview on 02/21/24 at 10:03 AM, Clinical Coordinator #6 stated residuals had not been documented in the resident's medical records prior to initiating daily tube feedings. No further information was provided through the completion of the survey process. g) Resident #3 Review of Resident #3's comprehensive care plan showed the following focus, Psychotropic meds: use of Buspar for anxiety. The interventions were as follows: - Consult with pharmacy. Physician to consider dosage reduction when clinically appropriate, per protocol. - Discuss with physician, family re: ongoing need for use of medication. - Monitor/record occurrence for target behavior symptoms (tearfulness) and document per facility protocol. - Monitor/record/report to physician prn [as needed] side effects and adverse reactions of psychoactive medications: unsteady gait, frequent falls, refusal to eat, dry mouth, depression, suicidal ideations, social isolation, blurred vision, diarrhea, fatigue, insomnia, loss of appetite, weight loss, muscle cramps, nausea, vomiting. Resident #3's comprehensive care plan contained no other focus related to the resident's anxiety. The comprehensive care plan did not include any information regarding situations that caused or exacerbated the resident's anxiety. The comprehensive care plan did not include any non-pharmacological interventions to attempt to relieve the resident's anxiety. During an interview on 02/22/24 at 8:29 AM, Licensed Practical Nurse [LPN] #10 stated Resident #3 is anxious about her health status and exertional activities, such as showers, can also cause her to be anxious. LPN #10 stated non-pharmacological interventions for anxiety that help Resident #3 are talking with her, reassuring her about her medical conditions, and encouraging her to attend activities that she enjoys, such as Bingo. During an interview on 2/22/24 at 8:35 AM, Clinical Coordinator #6 confirmed Resident #3's comprehensive care plan did not contain any information regarding triggers for the resident's anxiety or any non-pharmacological interventions to relieve the resident's anxiety. No further information was provided through the completion of the survey process.
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

b) Resident #7 On 02/21/24 at 09:23 AM, record review shows Resident #7 has a Physicians order for a blood pressure medication with parameters as to when to hold the medication. The order reads: Meto...

Read full inspector narrative →
b) Resident #7 On 02/21/24 at 09:23 AM, record review shows Resident #7 has a Physicians order for a blood pressure medication with parameters as to when to hold the medication. The order reads: Metoprolol Tartrate Tablet 25 MG Give 0.5 tablet by mouth two times a day for HTN (hypertension) give 1/2 tab to equal 12.5 milligram (mg) hold if SBP (systolic blood pressure) <100 or HR <60 A review of the Medication Administration Record (MAR) for 02/01/24 through 02/19/24 shows the medication was held fourteen (14) times. Eight (8) of the fourteen (14) times do not have a documented reason for with holding the medication (heart rate or systolic blood pressure reading). 02/01/24 AM held for a documented heart rate of 52 02/01/24 PM held with no documentation of heart rate or blood pressure 02/02/24 PM held with no documentation of heart rate or blood pressure 02/03/24 PM held for a documented heart rate of 55 02/05/24 AM held for a documented heart rate of 57 02/06/24 PM held with no documentation of heart rate or blood pressure 02/07/24 PM held with no documentation of heart rate or blood pressure 02/10/24 AM held for a documented heart rate of 53 02/11/24 AM held for a documented heart rate of 54 02/11/24 PM held with no documentation of heart rate or blood pressure 02/13/24 PM held with no documentation of heart rate or blood pressure 02/14/24 AM held with no documentation of heart rate or blood pressure 02/15/24 AM held for a documented heart rate of 54 02/19/24 PM held with no documentation of heart rate or blood pressure This was confirmed with the Director of Nursing on 02/21/24 at 12:15 PM. c) Resident #11 Review of the facility's resident matrix (802) on 02/19/24 PM shows the resident has a restraint. Observation on 02/19/24 at 3:01 PM, found Resident #11 was in bed resting. Side rails were present on the right and left side of the bed. Review of the current physician's orders on 02/20/24 found an order for: Side Rails 1/4 rail to the right side of the bed to assist with turning/positioning while in bed. There was no order for a side rail to be in place on the left side of the bed. On 02/20/24 at 4:13 PM, record review found a Minimum Data Set (MDS) with an Assessment Reference Date (ARD) of 11/30/23 which shows the side rails were coded as a restraint. On 1/30/24 a correction MDS was submitted noting the Resident was incorrectly coded as having a restraint. On 02/20/24 at 4:30 PM, observation with Registered Nurse (RN) #50 the staff development coordinator found Resident #11 in bed with both the right and left side quarter rails up on the bed. RN #50 asked the Resident if she used the side rails for turning and repositioning. Resident #11 replied, yes and side she wanted both side rails up on her bed. RN #50 reviewed the current physician's orders for only a quarter rail on the right side to be in place. RN #50 said, we will call the physician and get a new order. Observation on 02/21/24 at 9:47 AM, with Licensed Practical Nurse (LPN) #10 found the resident was again in bed with both the right and left quarter rails in place. Review of the new order, dated 02/20/24, found an order was written for a quarter rail to the right side of the bed to assist in turning and repositioning. The new order dated 02/20/24 is as follows: Side Rails 2/4 to the right side of the bed to assist with turning/positioning while in bed. LPN #10 said, I don't know why that order was written, Resident #11 does use both rails to turn and reposition. I'm getting this fixed right now. Based on record review and staff interview, the facility failed to ensure residents received treatment and care in accordance with professional standards of practice. The facility failed to document vital signs when medications were held for Resident #13 and Resident #7. The facility failed to follow the physician's orders for side rails for Resident #11. This deficient practice had the potential to affect three (3) of 14 residents reviewed in the long-term care survey sample. Resident identifiers: #13, #7, #11. Facility census: 27. Findings included: a) Resident #13 Review of Resident #13's physician's orders showed the following order written on 10/06/23, Lisinopril, oral tablet, 5 mg [milligrams], one time a day related to essential (primary) hypertension. Hold for SBP [systolic blood pressure] < [less than] 100. On 12/13/24 at 8:00 AM, Resident #13's Medication Administration Record (MAR) was marked 5 for Lisinopril administration. According to the MAR code, 5 means hold/see nurse notes. However, there was no nurse note in the progress notes. The area on the MAR to record the resident's blood pressure was marked with an X. The blood pressure was not recorded in the vital signs summary in the resident's medical record. Resident #13 also had the following physician's order written on 10/06/23, Metoprolol, give 25 mg by mouth one time a day related to essential (primary) hypertension. Hold for SBP <100. Hold for pulse <60. On 12/13/23 at 8:00 AM and on 02/19/24 at 8:00 AM, Resident #13's Medication Administration Records were marked 4 for Metoprolol administration. According to the MAR code, 4 means pulse below 60/min [60 beats per minute]. The areas on the MARs to record the resident's pulse rate were marked with an X The pulse rates were not recorded in the vital signs summary in the resident's medical record. During an interview on 02/21/24 at 1:54 PM, Clinical Coordinator #6 confirmed Resident #13's blood pressure and pulse rates had not been documented when medication was held. No further information was provided through the completion of the survey process.
CONCERN (E)

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

Medication Errors (Tag F0758)

Could have caused harm · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** d) Resident #3 The facility's policy titled Psychotropic Drugs with effective date 07/2022 stated, Nursing and Pharmacy will mo...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** d) Resident #3 The facility's policy titled Psychotropic Drugs with effective date 07/2022 stated, Nursing and Pharmacy will monitor and document usage through daily (nursing) and monthly (pharmacy) review of individual patient regimes. Review of Resident #3's medical records showed the resident had a diagnosis of anxiety disorder. On 11/03/23, the resident was prescribed Buspar (buspirone) 5 mg, twice a day, for anxiety. The resident's comprehensive care plan contained the focus, Psychotropic meds: use of Buspar for anxiety. An intervention was the following, Monitor/record occurrence of targeted behavior symptoms (tearfulness) and document per facility protocol. Resident #3's medical records contained no documentation as to whether the resident was experiencing tearfulness. During an interview on 02/21/24 at 2:40 PM, the Director of Nursing confirmed the occurrence of tearfulness episodes for Resident #3 had not been documented and the efficacy of the resident's anti-anxiety medication had not been monitored. No further information was provided through the completion of the survey. Based on record review and staff interview, the facility failed to ensure each resident's drug/medication regimen is managed and monitored to promote or maintain the resident's highest practicable mental, physical, and psychosocial well-being. Resident's #13, #24, #7 and #3 received psychotropic medications without adequate indication for use. Nonpharmacological interventions were not provided prior to starting the medication and the facility failed to monitor medications for side effects and efficacy. This was true for four (4) of five residents reviewed for unnecessary medications. Resident identifiers: #13, #24, #7, and #3. Facility census: 27. Findings included: a) Resident #13 Resident #13 was admitted to the facility on [DATE]. On 10/17/23, a physician determined the Resident lacked capacity to make medical decisions due to a diagnosis of Dementia and his wife was appointed as his health care surrogate. The Resident was admitted without any psychotropic medications. On 11/05/23, Lexapro 20 milligrams (mg's) daily was ordered for a diagnosis of depression. The Resident was having difficulty adjusting to the facility. He would frequently talk of wanting to go home and would wander around the facility asking for his wife. Record review found on 01/04/24, the Resident's physician prescribed a new antipsychotic medication Seroquel, oral Tablet, 25 milligrams (mg's) 1 tablet by mouth two (2) times a day for a diagnosis of depression. The Resident was already receiving Lexapro, an antidepressant for a diagnosis of depression. The medical record contained no documentation of any behaviors five (5) days prior to starting the antipsychotic medication, Seroquel. The last progress note indicating any concerns with the Resident's psychosocial well being was written on 12/30/2023 at 11:02 PM. Note text: Resident rested for short intervals throughout the evening in his bed. Resident is currently in chair awake in hallway. Talkative with staff. Talking and asking for how to get a ride home to his house. Resident became agitated at times with redirection. Resident continues to be confused as to time, place, and situation. Resident continues to have poor safety awareness. Gait continues to be unsteady. Refused snacks when offered. Fluids consumed as Resident desires. Denies any pain or discomfort when asked. On 02/21/24 at 10:37 AM, the Director of Nursing was asked why Seroquel was started? Again on 02/21/24 at 11:52 AM, the DON was asked about the medication and what non-pharmacological interventions were used before starting the Seroquel? Interviews with the Resident's caregivers found the following: On 02/21/24 at 11:58 AM, Licensed Practical Nurse (LPN) #10 said the Resident seems more anxious in the evenings. He gets mad when we have to tell him he can't walk alone without our help. He will ball up his fist but he doesn't hit you. Then he will cry and get upset because he threatened to hit us. He says he's sorry. He misses his wife and gets upset because he can't go home. He will say, I have to get home, I can walk home. He hasn't left the facility. I think the Lexapro really helped him. He can be distracted by watching something on the computer. LPN #10 said the resident likes to be out by the nurses station in the evenings. He likes to stay up late and be around other people. We use a geri-chair so he can prop his feet up and sometimes he will doze off and on. On 02/21/24 at 12:05 PM, Registered Nurse (RN) #36 stated, sometimes I call his house when he wants his wife. A step daughter will talk to him. She says his wife is too sick to talk. Watching something on the computer or youtube helps distract him. I have tried food and drinks but that doesn't help at all. A couple of months ago he was on an antibiotic for a urinary tract infection and he had more problems then. He wants to go home and he misses his wife. On 02/21/24 at 12:35 PM, the Residents nurse aide (NA) #3 said he gets upset when family visits. He begs them to take him home, says please don't leave me here I have to get home to my wife. He also gets upset because he can't walk alone anymore. I use coffee and snacks to distract him. He also likes to watch shows about horses and rodeo shows. We turn on youtube for him and he likes to sit here across from the nurses station and watch horse shows. He has never hit me or anyone else that I know about. He really likes to talk about the days when he delivered milk. That was what he worked at and he can really talk about work. 02/21/24 at 12:40 the activity aide #39 said the Resident likes to watch television and shows on you tube. She said he also likes to listen to his faith based programs on the internet. She said members from his congregation visited and told her how to access the religious programs on line. She said this seems to calm him, he just wants to go home at times. He misses his wife. His wife is sick herself and can't visit often. All the above staff denied the Resident had any conflict with any other residents at the facility. Review of the current care plan found no mention of adding Seroquel, an antipsychotic medication. The care plan addressed the resident did receive an antidepressant. The goal was for the resident to be free from discomfort or adverse reactions related to antidepressant use and he will not exhibit indicators of depression anxiety or sad mood less than daily. The interventions included: Reporting signs and symptoms of depression to the physician Give antidepressants as ordered Consult the pharmacist There was no indication of any specific behaviors exhibited by the resident on the care plan or any interventions to use if the resident exhibited any behaviors. The care plan did not list any side effects of the medication. On 02/21/24 at 2:24 PM, the Director of Nursing reviewed the resident's progress notes with the surveyor. The DON states, we really don't have any behaviors documented to add the Seroquel. I think I'll call the physician to address this and maybe he will discontinue the medication. The DON confirmed the physician and the nurse practitioner never addressed the use of Seroquel in their notes. The DON said this happens frequently, those nurses want to give medications for behaviors but they never document anything in their notes. This is an ongoing problem. The DON was unable to provide documentation of any non-pharmacological interventions implemented prior to starting Seroquel. In addition the DON confirmed the facility was not monitoring for any side effects associated with the use of Seroquel. At 8:00 AM on 2/22/24, Registered Nurse (RN) #6 the Clinical Coordinator, Minimum Data Set confirmed the resident had never been care planned for the use of Seroquel including any behaviors exhibited by the Resident to warrent the use of an antipsychotic. b) Resident #24 On 02/20/24 at 01:50 PM, record review shows Resident #24 has a medical diagnosis of neurocognitive disorder with Lewy Bodies, auditory hallucinations, anxiety disorder, and unspecified hallucinations. This resident has current Physician orders for: Seroquel Oral Tablet 50 milligrams (MG) (Quetiapine Fumarate) Give 1 tablet by mouth two times (BID) a day for behaviors with hallucinations related to auditory hallucinations and Depakote Sprinkles Oral Capsule Delayed Release Sprinkle 125 MG (Divalproex Sodium) Give 4 capsule by mouth two times a day for behaviors with hallucinations related to neurocognitive disorder with Lewy Bodies (Give 4 125 mg capsules to equal 500 mg BID) Upon review of the orders, care plan and progress notes for Resident #24, there is no documentation to monitor side-effects of the anti-psychotropic medication. According to regulation §483.45(e) Psychotropic Drugs: .Anticholinergic side effect is an effect of a medication that opposes or inhibits the activity of the parasympathetic (cholinergic) nervous system to the point of causing symptoms such as dry mouth, blurred vision, tachycardia, urinary retention, constipation, confusion, delirium, hallucinations, flushing, and increased blood pressure. Types of medications that may produce anticholinergic side effects include: Antihistamines, antidepressants, anti-psychotics, antiemetics, muscle relaxants; and Certain medications used to treat cardiovascular conditions, Parkinson's disease, urinary incontinence, gastrointestinal issues and vertigo . This was confirmed with the Director of Nursing on 02/21/24 at 11:01 AM who agreed that there are no monitoring systems in effect for the side effects of anti-psychotic medications. c) Resident #7 On 02/20/24 at 04:00 PM, record review shows resident #7 has a diagnosis of generalized anxiety disorder and recurrent major depressive disorder and is prescribed Zoloft Oral Tablet 150 MG (Sertraline HCl) Give 1 tablet by mouth one time a day related to major depressive disorder, recurrent and Ativan Oral Tablet 0.5 MG (Lorazepam) *Controlled Drug*Give 1 tablet by mouth every 8 hours as needed for anxiousness related to end stage process for 14 Days. Upon review of the care plan and progress notes, there are no systems or documentation in place to monitor side effects of the antidepressant, nor are there any behaviors monitored or documented. This was confirmed with the Director of Nursing on 02/21/24 at 03:10 PM who agreed that there were no behavioral or side effect monitoring systems in place for this resident.
CONCERN (E)

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

Deficiency F0761 (Tag F0761)

Could have caused harm · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation and staff interview, the facility failed to ensure medications were stored in accordance with currently acc...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation and staff interview, the facility failed to ensure medications were stored in accordance with currently accepted professional principles of practice. This was a random opportunity for discovery that had the potential to affect more than a limited number of residents. Facility census: 27. Findings included: a) Expired intravenous fluids On [DATE] at 8:30 AM, observation of the medication room was made with Registered Nurse (RN) #36 in attendance. Two (2) of three (3) bags of intravenous fluids locked in a cart in the medication room were found to have expiration dates of [DATE]. Both of these intravenous fluids bags contained 5% dextrose and 0.45% sodium chloride. RN #36 confirmed the two (2) bags of 5% dextrose and 0.45% sodium chloride were expired. No further information was provided through the completion of the survey. b) Narcotic emergency box During the medication room observation on [DATE] at 8:30 AM, Registered Nurse (RN) #36 opened a locked cabinet. The locked cabinet contained a suitcase-shaped box sealed with zip ties. RN #36 stated the box was a narcotic emergency box, and stated the box contained the items listed on a paper affixed to the box. The box was not affixed to the cabinet and could be removed by anyone who obtained the keys to unlock the medication room and the cabinet containing the narcotic emergency box. According to the label, the box contained as follows: Duragesic (Fentanyl) patches, Morphine for injection, rectal insertion, and oral ingestion, oral methadone, oral hydrocodone and acetaminophen, oral hydromorphone, and oral oxycodone. During an interview on [DATE] at 8:44 AM, the Director of Nursing confirmed the narcotic emergency box was not affixed to the cabinet.
CONCERN (E)

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

Deficiency F0801 (Tag F0801)

Could have caused harm · This affected multiple residents

Based on staff interview and record review the facility failed to employ sufficient staff with the appropriate competencies and skills sets to carry out the functions of the food and nutrition service...

Read full inspector narrative →
Based on staff interview and record review the facility failed to employ sufficient staff with the appropriate competencies and skills sets to carry out the functions of the food and nutrition service when one (1) of eight (8) dietary staff members did not have their Food Handlers/SafeServ certification. Facility Identifier: Facility Facility Census: 27 Findings Included: a) Facility On 02/19/24 at 01:17 PM, the Dietary Manager #49 failed to provide the required Food Handler or Safe/Serve certification for one (1) of the eight (8) staff members on the dietary staff. On 02/20/24 at 09:30 AM a telephone interview with the County Sanitarian at the Hampshire County Health Department states they must have the Food Handlers or Safe/Serve certification in order to work in any food area in this county. This was confirmed with the Director of Nursing on 02/20/24 at 02:45 PM.
CONCERN (E)

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

QAPI Program (Tag F0867)

Could have caused harm · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and staff interview, the facility failed to identify and correct quality deficiencies of which it should ...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and staff interview, the facility failed to identify and correct quality deficiencies of which it should have been aware. The facility's Quality Assessment and Assurance Committee failed to identify and correct deficiencies regarding psychotropic medications. This deficient practice had the potential to affect four (4) of five (5) residents reviewed for the care area of unnecessary medications. Resident identifiers: #13, #24, #7, #3. Facility census: 27. Findings included: a) Quality Assessment and Assurance (QAA) Committee Interview During an interview on 02/22/24 at 9:20 AM, the Director of Nursing (DON) stated the QAA Committee had not known about deficiencies related to prescribing and monitoring psychotropic medications before the survey began. The DON stated the committee had not been aware of antipsychotic medication being prescribed without adequate documented indications. The DON stated the committee was unaware of the failure to address non-pharmacological interventions prior to starting psychotropic medications. The DON also stated the QAA Committee was not aware of the failure to monitor for medication side-effects and for medication efficacy. The DON stated the facility would begin to work on issues related to psychotropic medications now that the issues had been identified during the survey process. The following are examples of the QAA committees failure to monitor psychotropic medications: b) Resident #13 Resident #13 was admitted to the facility on [DATE]. On 10/17/23, a physician determined the Resident lacked capacity to make medical decisions due to a diagnosis of Dementia and his wife was appointed as his health care surrogate. The Resident was admitted without any psychotropic medications. On 11/05/23, Lexapro 20 milligrams (mg's) daily was ordered for a diagnosis of depression. The Resident was having difficulty adjusting to the facility. He would frequently talk of wanting to go home and would wander around the facility asking for his wife. Record review found on 01/04/24, the Resident's physician prescribed a new antipsychotic medication Seroquel, oral Tablet, 25 milligrams (mg's) 1 tablet by mouth two (2) times a day for a diagnosis of depression. The Resident was already receiving Lexapro, an antidepressant for a diagnosis of depression. The medical record contained no documentation of any behaviors five (5) days prior to starting the antipsychotic medication, Seroquel. The last progress note indicating any concerns with the Resident's psychosocial well being was written on 12/30/2023 at 11:02 PM. Note text: Resident rested for short intervals throughout the evening in his bed. Resident is currently in chair awake in hallway. Talkative with staff. Talking and asking for how to get a ride home to his house. Resident became agitated at times with redirection. Resident continues to be confused as to time, place, and situation. Resident continues to have poor safety awareness. Gait continues to be unsteady. Refused snacks when offered. Fluids consumed as Resident desires. Denies any pain or discomfort when asked. On 02/21/24 at 10:37 AM, the Director of Nursing was asked why Seroquel was started? Again on 02/21/24 at 11:52 AM, the DON was asked about the medication and what non-pharmacological interventions were used before starting the Seroquel? Interviews with the Resident's caregivers found the following: On 02/21/24 at 11:58 AM, Licensed Practical Nurse (LPN) #10 said the Resident seems more anxious in the evenings. He gets mad when we have to tell him he can't walk alone without our help. He will ball up his fist but he doesn't hit you. Then he will cry and get upset because he threatened to hit us. He says he's sorry. He misses his wife and gets upset because he can't go home. He will say, I have to get home, I can walk home. He hasn't left the facility. I think the Lexapro really helped him. He can be distracted by watching something on the computer. LPN #10 said the resident likes to be out by the nurses station in the evenings. He likes to stay up late and be around other people. We use a geri-chair so he can prop his feet up and sometimes he will doze off and on. On 02/21/24 at 12:05 PM, Registered Nurse (RN) #36 stated, sometimes I call his house when he wants his wife. A step daughter will talk to him. She says his wife is too sick to talk. Watching something on the computer or youtube helps distract him. I have tried food and drinks but that doesn't help at all. A couple of months ago he was on an antibiotic for a urinary tract infection and he had more problems then. He wants to go home and he misses his wife. On 02/21/24 at 12:35 PM, the Residents nurse aide (NA) #3 said he gets upset when family visits. He begs them to take him home, says please don't leave me here I have to get home to my wife. He also gets upset because he can't walk alone anymore. I use coffee and snacks to distract him. He also likes to watch shows about horses and rodeo shows. We turn on youtube for him and he likes to sit here across from the nurses station and watch horse shows. He has never hit me or anyone else that I know about. He really likes to talk about the days when he delivered milk. That was what he worked at and he can really talk about work. 02/21/24 at 12:40 the activity aide #39 said the Resident likes to watch television and shows on you tube. She said he also likes to listen to his faith based programs on the internet. She said members from his congregation visited and told her how to access the religious programs on line. She said this seems to calm him, he just wants to go home at times. He misses his wife. His wife is sick herself and can't visit often. All the above staff denied the Resident had any conflict with any other residents at the facility. Review of the current care plan found no mention of adding Seroquel, an antipsychotic medication. The care plan addressed the resident did receive an antidepressant. The goal was for the resident to be free from discomfort or adverse reactions related to antidepressant use and he will not exhibit indicators of depression anxiety or sad mood less than daily. The interventions included: Reporting signs and symptoms of depression to the physician Give antidepressants as ordered Consult the pharmacist There was no indication of any specific behaviors exhibited by the resident on the care plan or any interventions to use if the resident exhibited any behaviors. The care plan did not list any side effects of the medication. On 02/21/24 at 2:24 PM, the Director of Nursing reviewed the resident's progress notes with the surveyor. The DON states, we really don't have any behaviors documented to add the Seroquel. I think I'll call the physician to address this and maybe he will discontinue the medication. The DON confirmed the physician and the nurse practitioner never addressed the use of Seroquel in their notes. The DON said this happens frequently, those nurses want to give medications for behaviors but they never document anything in their notes. This is an ongoing problem. The DON was unable to provide documentation of any non-pharmacological interventions implemented prior to starting Seroquel. In addition the DON confirmed the facility was not monitoring for any side effects associated with the use of Seroquel. At 8:00 AM on 2/22/24, Registered Nurse (RN) #6 the Clinical Coordinator, Minimum Data Set confirmed the resident had never been care planned for the use of Seroquel including any behaviors exhibited by the Resident to warrent the use of an antipsychotic. c) Resident #24 On 02/20/24 at 01:50 PM, record review shows Resident #24 has a medical diagnosis of neurocognitive disorder with Lewy Bodies, auditory hallucinations, anxiety disorder, and unspecified hallucinations. This resident has current Physician orders for: Seroquel Oral Tablet 50 milligrams (MG) (Quetiapine Fumarate) Give 1 tablet by mouth two times (BID) a day for behaviors with hallucinations related to auditory hallucinations and Depakote Sprinkles Oral Capsule Delayed Release Sprinkle 125 MG (Divalproex Sodium) Give 4 capsule by mouth two times a day for behaviors with hallucinations related to neurocognitive disorder with Lewy Bodies (Give 4 125 mg capsules to equal 500 mg BID) Upon review of the orders, care plan and progress notes for Resident #24, there is no documentation to monitor side-effects of the anti-psychotropic medication. According to regulation §483.45(e) Psychotropic Drugs: .Anticholinergic side effect is an effect of a medication that opposes or inhibits the activity of the parasympathetic (cholinergic) nervous system to the point of causing symptoms such as dry mouth, blurred vision, tachycardia, urinary retention, constipation, confusion, delirium, hallucinations, flushing, and increased blood pressure. Types of medications that may produce anticholinergic side effects include: Antihistamines, antidepressants, anti-psychotics, antiemetics, muscle relaxants; and Certain medications used to treat cardiovascular conditions, Parkinson's disease, urinary incontinence, gastrointestinal issues and vertigo . This was confirmed with the Director of Nursing on 02/21/24 at 11:01 AM who agreed that there are no monitoring systems in effect for the side effects of anti-psychotic medications. d) Resident #7 On 02/20/24 at 04:00 PM, record review shows resident #7 has a diagnosis of generalized anxiety disorder and recurrent major depressive disorder and is prescribed Zoloft Oral Tablet 150 MG (Sertraline HCl) Give 1 tablet by mouth one time a day related to major depressive disorder, recurrent and Ativan Oral Tablet 0.5 MG (Lorazepam) *Controlled Drug*Give 1 tablet by mouth every 8 hours as needed for anxiousness related to end stage process for 14 Days. Upon review of the care plan and progress notes, there are no systems or documentation in place to monitor side effects of the antidepressant, nor are there any behaviors monitored or documented. This was confirmed with the Director of Nursing on 02/21/24 at 03:10 PM who agreed that there were no behavioral or side effect monitoring systems in place for this resident. e) Resident #3 The facility's policy titled Psychotropic Drugs with effective date 07/2022 stated, Nursing and Pharmacy will monitor and document usage through daily (nursing) and monthly (pharmacy) review of individual patient regimes. Review of Resident #3's medical records showed the resident had a diagnosis of anxiety disorder. On 11/03/23, the resident was prescribed Buspar (buspirone) 5 mg, twice a day, for anxiety. The resident's comprehensive care plan contained the focus, Psychotropic meds: use of Buspar for anxiety. An intervention was the following, Monitor/record occurrence of targeted behavior symptoms (tearfulness) and document per facility protocol. Resident #3's medical records contained no documentation as to whether the resident was experiencing tearfulness. During an interview on 02/21/24 at 2:40 PM, the Director of Nursing confirmed the occurrence of tearfulness episodes for Resident #3 had not been documented and the efficacy of the resident's anti-anxiety medication had not been monitored. No further information was provided through the completion of the survey.
CONCERN (F)

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

Deficiency F0868 (Tag F0868)

Could have caused harm · This affected most or all residents

Based on record review and staff interview, the Quality Assessment Performance Improvement meetings did not include all required members for two (2) of four (4) meetings. This deficient practice had t...

Read full inspector narrative →
Based on record review and staff interview, the Quality Assessment Performance Improvement meetings did not include all required members for two (2) of four (4) meetings. This deficient practice had the potential to affect all residents residing in the facility. Facility census: 27. Findings included: a) Review of Quality Assessment Performance Improvement (QAPI) meeting sign-in sheets On 02/22/24 at 9:04 AM, the Quality Assessment Performance Improvement (QAPI) meeting sign-in sheets were reviewed for the past four (4) quarters. The sign-in sheet for 05/31/23 indicated neither the Medical Director nor a designee for the Medical Director had attended the QAPI meeting. The sign-in sheet for 09/01/23 indicated the Medical Director, the Director of Nursing, the facility vice-president, and the Infection Preventionist had attended the meeting. The meeting was also attended by a member of the therapy/rehabilitation staff. However, another member of staff did not attend the meeting as required. During an interview on 02/22/24 at 9:20 AM, the Director of Nursing confirmed the Medical Director had not attended the QAPI meeting on 05/31/23 and another staff member had not attended the meeting on 09/01/23. No further information was provided through the completion of the survey.
MINOR (C)

Minor Issue - procedural, no safety impact

Staffing Information (Tag F0732)

Minor procedural issue · This affected most or all residents

Based on observation and staff interview, the facility failed to ensure the daily staff posting included the actual amount of hours worked per each shift for Nurse Aides, Licensed Practical Nurses and...

Read full inspector narrative →
Based on observation and staff interview, the facility failed to ensure the daily staff posting included the actual amount of hours worked per each shift for Nurse Aides, Licensed Practical Nurses and Registered Nurses. This had the potential to affect all residents at the facility. Facility census: 27. Findings included: a) Staff posting Observation of the staff posting for 02/19/24 found the facility failed to record the actual number of hours worked per each shift by Nurse Aides, Licensed Practical Nurses and Registered Nurses. At 1:43 PM on 02/20/24, the Director Of Nursing (DON) said she didn't realize the hours had to be recorded for each shift, she thought the hours just needed to be recorded for the day. Review of the daily posted staffing sheets with the DON from 02/06/24 until present found the facility only recorded the hours worked by each discipline for the day, not for each shift.
Jun 2022 6 deficiencies
CONCERN (D)

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

Respiratory Care (Tag F0695)

Could have caused harm · This affected 1 resident

. Based on observation, record review and staff interview, the facility failed to administer oxygen to a Resident at the appropriate flow rate as directed by the physician order. The failed practice w...

Read full inspector narrative →
. Based on observation, record review and staff interview, the facility failed to administer oxygen to a Resident at the appropriate flow rate as directed by the physician order. The failed practice was true for for one (1) of two (2) residents reviewed for oxygen. Resident identifier: #127. Facility census: 27. Findings included: a) Resident #127 An observation on 06/28/22 at 1:18 PM , showed Resident #127 was resting in bed. Resident #127 was being administered oxygen through a nasal cannula at a flow rate of four (4) liters per minute. A record review of Resident #127's medical chart showed a physician order dated 11/01/2017 that stated, oxygen @ 3 liters per min at bedtime for sleep apnea. An observation on 06/30/22 at 8:30 AM, showed Resident #127 was resting in bed. Resident #127 was being administered oxygen through a nasal cannula at a flow rate of four (4) liters per minute. During an interview on 06/30/22 at 8:30 AM, Registered Nurse (RN) #10 stated that Resident #127's oxygen was set at four (4) liters per minute and that was wrong as the flow rate was ordered to be administered at three (3) liters per minute. .
CONCERN (D)

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

Deficiency F0757 (Tag F0757)

Could have caused harm · This affected 1 resident

. Based on record review and staff interview the facility failed to ensure unscheduled/as needed (PRN) narcotics were not in excessive duration. The failed practice was true for one (1) of five (5) re...

Read full inspector narrative →
. Based on record review and staff interview the facility failed to ensure unscheduled/as needed (PRN) narcotics were not in excessive duration. The failed practice was true for one (1) of five (5) residents reviewed for unnecessary medications. Resident identifiers: #12. Facility census: 27. Findings included: a) Resident #12 A record review of Resident #12's medical record showed a physician order dated 07/07/21, stated Percocet Tablet 5-325 MG (oxyCODONE-Acetaminophen) *Controlled Drug* Give 1 tablet by mouth every 6 hours as needed for Moderate Pain. The May and June 2022 Medication Administration Record (MAR) showed Resident #12 had a 0 pain level with no Percocet administered for the date range of 05/01/22 through 06/29/2022. During an interview on 06/30/22 at 10:37 AM, Director of Nursing, (DON) stated, I did not know that physicians had to write a rationale or re-write another prescription to extend PRN narcotics after 14 days. DON stated that the medication should be assessed by the consulting pharmacist and discontinued in 60 days for non use. .
CONCERN (D)

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

Deficiency F0883 (Tag F0883)

Could have caused harm · This affected 1 resident

. Based on record review, staff interview and policy review the facility failed to offer and educate a Resident on the annual influenza vaccination. The failed practice was true for one (1) of five (5...

Read full inspector narrative →
. Based on record review, staff interview and policy review the facility failed to offer and educate a Resident on the annual influenza vaccination. The failed practice was true for one (1) of five (5) residents reviewed for vaccinations. Resident identifier: #10. Facility census: 27. Findings included: Record review of the facility's policy titled, Immunizations in Long Term Care, reviewed on 05/2022, stated, the influenza vaccine is given during appropriate months of October 1st through March 31st. Resident or Resident representative will be given information about the vaccine including the benefits and risks. a) Resident #10 A record review of Resident #10's medical record showed Resident #10 refused all vaccinations. Refusal forms and education provided for each vaccine were located in the medical record and were signed and dated for 03/23/20. There was no refusal form or education found in the medical record that was signed and provided for the annual influenza vaccination for the months of 10/01/21 though 03/31/22. During an interview on 06/29/22 at 10:40 AM , Director of Nursing (DON) stated that Resident #10 refused all vaccines. DON stated that Resident #10 had refused the influenza vaccine year after year. DON stated that Resident #10 was no longer asked or educated about the influenza vaccine each year since Resident #10 refused all vaccines anyway. DON stated that there is no sense to ask Resident #10 about a influenza vaccination when Resident #10 was was just going to refuse. .
CONCERN (E)

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

Grievances (Tag F0585)

Could have caused harm · This affected multiple residents

. Based on observation, resident council meeting and interview, the Resident Council members did not know how to file a grievance or with whom to file a grievance. This had the potential to affect mor...

Read full inspector narrative →
. Based on observation, resident council meeting and interview, the Resident Council members did not know how to file a grievance or with whom to file a grievance. This had the potential to affect more than a limited number of residents. Facility censs: 27. Findings included: a) Grievance Policy and Procedure A review of the facility grievance policy and procedure titled Resident Grievance Policy was conducted on 06/29/22 at 4:16 PM with an effective and approved date of 05/2022. The Grievance Officer was identified as the Social Worker or designee including the Director of Nursing (DON), Minimum Data Set (MDS) Coordinator, or a Registered Nurse (RN) on duty. The procedure stated that an investigation of all grievances will be done within 24 hours, with the resident/responsible party notified in writing of corrective or appropriate action taken. In addition, a file with be kept in Social Workers office with a log kept by the DON of all grievances for three (3) years. b) Resident Council (RC) Meeting On 06/29/22 at 2:59 PM a meeting of the Resident Council was held. The President and 14 residents attended. When asked who was the grievance officer, there were just blank stares with no response. When asked if Council members knew how to file a grievance, the Resident Council President answered No and members shook their heads no. In an interview with the Activity Director on 06/29/22 at 3:45 PM who takes the minutes for the RC meetings stated that she did not know how to file a grievance. If the RC had a concern she referred it to the specific department. On 06/29/22 at 4:16 PM, the DON when asked about the grievance policy, she located a copy of the Grievance Policy and Procedure on the bulletin board across from the DON's office. The DON immediately stated that was not the current policy and removed the policy and placed a new copy on the bulletin board. No grievance forms were found to be available on the unit. There is a form to file the grievance but none were found available for residents on the unit. The DON produced the Grievance log from her office and two (2) grievance forms were found dating back tp 2017. .
CONCERN (E)

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

Deficiency F0725 (Tag F0725)

Could have caused harm · This affected multiple residents

. Based on a review of nursing staffing sheets and interview, the facility failed to indicate Charge Nurse on the nursing schedules. This had the potential to affect more than a limited number of resi...

Read full inspector narrative →
. Based on a review of nursing staffing sheets and interview, the facility failed to indicate Charge Nurse on the nursing schedules. This had the potential to affect more than a limited number of residents. Facility census: 27. Findings included: A review of the nursing schedule dated 04/17/22 through 07/08/22 revealed that no designated Charge Nurse was identified on the schedule. On 06/30/22 at 9:23 AM an schedule. The DON stated that it would be the Registered Nurse (RN) working that shift. When asked if there were two (2) RN's working the same shift who would be charge nurse and how would staff who was the Charge Nurse. The DON stated Staff would not know. I didn't know that needed to be on the schedule. .
CONCERN (E)

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

Deficiency F0868 (Tag F0868)

Could have caused harm · This affected multiple residents

. Based on facility documentation, staff interview, Centers for Medicare and Medicaid Services (CMS) Guidance and policy review the facility's Quality Assessment and Assurance (QAA) Committee did not ...

Read full inspector narrative →
. Based on facility documentation, staff interview, Centers for Medicare and Medicaid Services (CMS) Guidance and policy review the facility's Quality Assessment and Assurance (QAA) Committee did not meet at least quarterly. The failed practice had the potential to affect more than a limited number of residents. Facility census: 27. Findings included: Record review of the facility's policy titled, Quality Assurance Improvement Plan,established date of 05/2019, stated that the QAA Committee Team meets at least every three (3) months. a) QAA Committee Review of the QAA Committee sign in sheets showed the facility's QAA committee met on 12/17/21 and again on 04/29/22. During an interview, on 06/29/22 at 2:20 PM, Director of Nursing (DON) stated the facility's QAA Committee meets every six (6) months or is it four (4) times a year? DON asked which one is it? The requirement of quarterly was revealed and DON then stated, yes, the facility does QAA Committee meetings quarterly. Additional review of the QAA Committee meeting sign in sheets showed that the facility's QAA Committee team last met on 12/15/20 prior to the 12/17/21 and again on 04/29/22 meetings. During an interview on 06/29/22 at 2:50 PM, DON stated that QAA Committee meetings were not done between 12/15/20 and 12/17/21 because QAA Committee meetings were waived during that time. Review of the Centers for Medicare and Medicaid Services (CMS) guidance titled, Blanket 1135 Waived Tags (effective since 03/01/20) stated that F868 was not included as a waived tag. .
Mar 2020 4 deficiencies
CONCERN (D)

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

Assessment Accuracy (Tag F0641)

Could have caused harm · This affected 1 resident

. Based on record review and staff interview, the facility failed to complete an accurate quarterly and annual Minimum Data Set (MDS) assessment related resident weight. This is true for one (1) of 12...

Read full inspector narrative →
. Based on record review and staff interview, the facility failed to complete an accurate quarterly and annual Minimum Data Set (MDS) assessment related resident weight. This is true for one (1) of 12 residents reviewed. Resident identifier: #12. Facility census: 30. Findings included: a) Resident #12 A review of Resident #12's physician order on 03/10/20 9:53 AM, finds a physician order dated 01/09/16, weekly weights times four (4), on admission and readmission, then every month. A review of Resident #12's quarterly and annual Minimum Data Set (MDS) with the assessment reference date (ARD) of 0/19/20, and 10/24/19 on 03/10/20 at 4:00 PM, revealed the resident under section K-200 - B Resident #12 weighed 122 pounds (LBS). A review of Resident #12's weights, finds the resident has not been weighed since 09/22/19. The resident has refused to be weighed since this date. The resident weighed 112.5 LBS on 09/22/19. In an interview on 03/10/20 at 4:21 PM, with Registered Nurse (RN) #12, she stated the weight just populated into that section. She did not know where the weight came from. She said that, she wrote a note revealing the resident was refusing to be weighed. A review of the progress note RN #12 wrote on 01/20/20 at 11:42 AM, revealed a note stating the resident has not been weighed since September 2019, she has refused to be weighed. .
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 resident interview, record review, and staff interview the facility failed to develop and implement a comprehensive person-centered care plan that includes measurable objective and timefram...

Read full inspector narrative →
. Based on resident interview, record review, and staff interview the facility failed to develop and implement a comprehensive person-centered care plan that includes measurable objective and timeframe's to meet a residents medical, nursing, and psychosocial needs. This is true for one (1) of one (1) residents reviewed for pain. Resident identifier: #6. Facility census: 30. Findings include: a) Resident #6 On 03/09/20 at 6:30 PM Resident #6 complained of pain in the right shoulder and back. Review of care plan with a revision date of 12/30/19 includes a problem of pain. Review of the interventions dose not include non-pharmaceutical interventions. During interview Resident #6 explained she would like to have a non-pharmaceutical intervention such as a lotion for pain on her shoulders. On 03/11/20 at 1:00 PM the director of nursing (DON) agreed the current care plan does not include person-centered non-pharmacological interventions. .
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 record review and staff interview, the facility failed to revise a resident's care plan related to the size of the resident's Foley catheter. This is true for one (1) of one (1) residents r...

Read full inspector narrative →
. Based on record review and staff interview, the facility failed to revise a resident's care plan related to the size of the resident's Foley catheter. This is true for one (1) of one (1) residents reviewed for Foley Catheter care. Resident Identifier: #30. Facility census 30. Findings included: a) Resident #30 A review on 03/11/20 at 1:30 PM, finds Resident #30 has a physician order start date of 12/09/19 for a #16 French Foley catheter with 10 cubic centimeter (cc) balloon related to obstructive and reflux Uropathy, not surgically correctable. A review of Resident #30's care plan on 03/11/20 at 1:35 PM, finds a care plan related to urinary/Foley, (Resident name), has an indwelling Foley. The interventions state that Resident #30 has a catheter 18 French Foley catheter with 10 cc balloon in place. The Director of Nursing (DoN) on 03/11/20 at 1:40 PM, confirmed the care plan should have been revised to identify the resident had a 16 French Foley Catheter not a 18 French Foley catheter. .
CONCERN (D)

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

Food Safety (Tag F0812)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** . Based on observation and staff interviews, the facility failed to clean and maintained kitchen equipment to prevent foodborne ...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** . Based on observation and staff interviews, the facility failed to clean and maintained kitchen equipment to prevent foodborne illness. In addition, the facility failed to follow a cleaning schedule for the kitchen and food service equipment. This has the potential to affect more than a limited number of resident. Facility census 30. Findings included: a) Initial kitchen tour On 03/09/20 at 5:30 PM, found the drip pan under the range had hard melted cheese, burnt noodles, burnt pieces of food items and grease completely covering the drip pan. The cook [NAME]#70 was asked when she last cleaned the drip pan, she stated she has been here for a month and she has never cleaned the drip pan. She stated that, she had never been trained to clean the drip pan. In an interview and review of the associate cleaning responsibilities form from starting with breakfast on 03/01/20 through dinner on 03/09/20 at 5:45 PM, [NAME] stated that the range is cleaning the drip pan. A review of the production sheet report on 03/09/20 at 5:45 PM, found for the breakfast/lunch and dinner associate cleaning responsibilities the range top was being signed off or marked they had cleaned the Range top (which the cook stated includes cleaning the drip pan). The Dietary Manager (DM) was not present at this time. The DM #57 on 03/10/20 at 8:50 AM, stated that the form does not have an area where they have been cleaning the drip pans. The D stated the drip pans should be cleaned weekly. The DOD stated that she will need to add this to their equipment cleaning schedule. A review of the facility's policy on 03/11/20 at 9:00 AM, revealed the kitchen staff are to clean the drip pan weekly. The DM provided a new associate cleaning responsibilities on 03/11/20 at 2:00 PM, in which the form revealed the range drip tray was added to clearing responsibilities. .
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

  • "Can I speak with families of current residents?"
  • "What's your RN coverage like on weekends and overnight?"

Our Honest Assessment

Strengths
  • • No major safety red flags. No abuse findings, life-threatening violations, or SFF status.
  • • No fines on record. Clean compliance history, better than most West Virginia facilities.
  • • 38% turnover. Below West Virginia's 48% average. Good staff retention means consistent care.
Concerns
  • • 27 deficiencies on record. Higher than average. Multiple issues found across inspections.
  • • Grade C (50/100). Below average facility with significant concerns.
Bottom line: Mixed indicators with Trust Score of 50/100. Visit in person and ask pointed questions.

About This Facility

What is Hampshire Memorial Hospital's CMS Rating?

CMS assigns HAMPSHIRE MEMORIAL HOSPITAL an overall rating of 2 out of 5 stars, which is considered below average nationally. Within West Virginia, this rating places the facility higher than 0% of the state's 100 nursing homes. A rating at this level reflects concerns identified through health inspections, staffing assessments, or quality measures that families should carefully consider.

How is Hampshire Memorial Hospital Staffed?

CMS rates HAMPSHIRE MEMORIAL HOSPITAL's staffing level at 1 out of 5 stars, which is much below average compared to other nursing homes. Staff turnover is 38%, compared to the West Virginia average of 46%. This relatively stable workforce can support continuity of care.

What Have Inspectors Found at Hampshire Memorial Hospital?

State health inspectors documented 27 deficiencies at HAMPSHIRE MEMORIAL HOSPITAL during 2020 to 2024. These included: 26 with potential for harm and 1 minor or isolated issues.

Who Owns and Operates Hampshire Memorial Hospital?

HAMPSHIRE MEMORIAL HOSPITAL is owned by a non-profit organization. Non-profit facilities reinvest revenue into operations rather than distributing to shareholders. The facility operates independently rather than as part of a larger chain. With 30 certified beds and approximately 29 residents (about 97% occupancy), it is a smaller facility located in ROMNEY, West Virginia.

How Does Hampshire Memorial Hospital Compare to Other West Virginia Nursing Homes?

Compared to the 100 nursing homes in West Virginia, HAMPSHIRE MEMORIAL HOSPITAL's overall rating (2 stars) is below the state average of 2.7, staff turnover (38%) is near the state average of 46%, and health inspection rating (3 stars) is at the national benchmark.

What Should Families Ask When Visiting Hampshire Memorial Hospital?

Based on this facility's data, families visiting should ask: "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?" "Can I speak with family members of current residents about their experience?" These questions are particularly relevant given the below-average staffing rating.

Is Hampshire Memorial Hospital Safe?

Based on CMS inspection data, HAMPSHIRE MEMORIAL HOSPITAL has a clean safety record: no substantiated abuse findings (meaning no confirmed cases of resident harm), no Immediate Jeopardy citations (the most serious violation level indicating risk of serious injury or death), and is not on the Special Focus Facility watch list (a federal program monitoring the lowest-performing 1% of nursing homes). The facility has a 2-star overall rating and ranks #100 of 100 nursing homes in West Virginia. While no facility is perfect, families should still ask about staff-to-resident ratios and recent inspection results during their visit.

Do Nurses at Hampshire Memorial Hospital Stick Around?

HAMPSHIRE MEMORIAL HOSPITAL has a staff turnover rate of 38%, which is about average for West Virginia 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 Hampshire Memorial Hospital Ever Fined?

HAMPSHIRE MEMORIAL HOSPITAL 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 Hampshire Memorial Hospital on Any Federal Watch List?

HAMPSHIRE MEMORIAL HOSPITAL 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.