CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0578
(Tag F0578)
Could have caused harm · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to ensure a current or accurate advance directive ( a written statemen...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to ensure a current or accurate advance directive ( a written statement of a person's wishes regarding medical treatment) regarding the resuscitation status for three residents (Resident #21, #152, and #202) out of 13 sampled residents. The facility's census was 44.
1. Record review of the facility's policy titled Advance Directives, dated [DATE], showed:
- Advance directives will be respected in accordance with state law and facility policy;
- Upon admission, the resident will be provided with written information concerning the right to refuse or accept medical or surgical treatment and to formulate an advance directive if he or she chooses to do so;
- If the resident is incapacitated and unable to receive information about his or her right to formulate an advance directive, the information may be provided to the resident's legal representative;
- Information about whether or not the resident has executed an advance directive shall be displayed prominently in the medical record;
- The Attending Physician will provide information to the resident and legal representative regarding the resident's health status, treatment options and expected outcomes during the development of the initial comprehensive assessment and care plan;
- The plan of care for each resident will be consistent with his or her documented treatment preferences and/or advance directive;
- The Interdisciplinary Team will review annually with the resident his or her advance directives to ensure that such directives are still the wishes of the resident. Such reviews will be made during the annual assessment process and recorded on the resident assessment instrument (MDS, minimum data set, a federally mandated assessment instrument completed by the facility).
2. Record review of resident #21's medical record showed:
- Face sheet showed do not resuscitate (DNR);
- DNR outside the hospital form dated [DATE], signed by the resident's Power of Attorney (POA; the person responsible to make decisions for the individual when the individual cannot make a decision) showed DNR;
- Physician's Order Sheet (POS), dated [DATE] to [DATE], showed order start date [DATE] with no end date for Full Code (resuscitate);
- Comprehensive care plan, last updated/revised [DATE], showed full code.
3. Record review of resident #152's medical record showed:
- Face sheet showed no code status;
- POS, dated [DATE] - [DATE], showed no code status and no order for a code status;
- Cardiopulmonary Resuscitation (CPR; combines chest compressions with artificial ventilation) Directive, dated [DATE], showed wishes for CPR signed by the POA.
4. Record review of resident #202's medical record showed:
- Face sheet showed no code status;
- POS, dated [DATE] - [DATE], showed no code status and no order for a code status;
- Comprehensive care plan, updated/revised [DATE], showed no code status;
- CPR Directive, dated [DATE], showed wishes for CPR signed by the POA.
5. During an interview on [DATE] at 10:50 A.M., the Director of Nursing said she would expect there to be an order for the code status of the resident. The orders and the advance directive should match.
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 interview and record review, the facility failed to issue a Centers for Medicare and Medicaid Services (CMS) Skilled Nursing Facility Advance Beneficiary Notice (SNF ABN: a SNF will issue a S...
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Based on interview and record review, the facility failed to issue a Centers for Medicare and Medicaid Services (CMS) Skilled Nursing Facility Advance Beneficiary Notice (SNF ABN: a SNF will issue a SNF ABN if there is reason to believe that Part A may not cover or continue to cover your care or stay because it isn't reasonable or necessary, or is considered Custodial care) Form 10055 for two residents (Resident #21 and #23) out of two sampled current residents and one sampled closed record. The facility's census was 44.
1. Record review of Resident #21's medical record showed:
- Medicare Part A (Med A) skilled services start date of 4/19/21 and end date of 5/24/21;
- The facility initiated a discharge from Medicare Part A services on 5/21/21 when benefit days were not exhausted;
- The facility did not issue a CMS SNF ABN Form 10055.
2. Record review of Resident #23's medical record showed:
- Medicare Part A skilled services start date of 2/26/21 and end date of 5/11/21;
- The facility initiated a discharge from Medicare Part A services on 5/8/21 when benefit days were not exhausted;
- The facility did not issue a CMS SNF ABN Form 10055.
3. During an interview on 7/27/21 at 3:03 P.M., the Assistant Administrator said he would expect a resident or the responsible party of a resident who discharges from Med A services and remains in the facility to be provided with the SNF ABN form.
4. The facility did not provide a policy for liability/denial notification.
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Transfer Notice
(Tag F0623)
Could have caused harm · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to document notification in writing to the resident and/or responsible...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to document notification in writing to the resident and/or responsible party of the reason for transfer to the hospital for two residents (Resident #21, and #34) out of 13 sampled residents and one resident (Resident #17) out of two sampled closed records. The facility's census was 44.
1. Record review of the facility's policy titled, Bed-Holds and Returns, dated March 2017, showed prior to a transfer, written information will be given to the residents and the resident representatives that explains the details of the transfer (per the Notice of Transfer).
2. Record review of Resident #17's nursing progress notes showed:
- The resident to have a responsible party;
- The resident transferred to a hospital on 4/19/21 and readmitted to the facility on [DATE].
Record review of the resident's medical record showed no documentation of notification in writing to the responsible party of the transfer.
3. Record review of Resident #21's nursing progress notes showed:
- The resident to have a responsible party;
- The resident transferred to a hospital on 4/10/21 and readmitted to the facility on [DATE];
- The resident transferred to a hospital on 6/7/21 and readmitted to the facility on the same day;
- The resident transferred to a hospital on 6/16/21 and readmitted to the facility on the same day.
Record review of the resident's medical record showed no documentation of notification in writing to the responsible party of the transfers.
4. Record review of Resident #34's nursing progress notes showed:
- The resident transferred to a hospital on 3/8/21 and readmitted to the facility on [DATE];
- The resident transferred to a hospital on 5/30/21 and readmitted to the facility on [DATE].
Record review of the resident's medical record showed no documentation of notification in writing to the resident and/or responsible party of the transfers to the hospital.
5. During an interview on 7/27/21 at 3:03 P.M., the Assistant Administrator said he would expect the hospital transfer sheet to include the reason for transfer and to be provided to the resident and/or responsible party.
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0655
(Tag F0655)
Could have caused harm · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to ensure the resident and/or the representative received a written su...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to ensure the resident and/or the representative received a written summary of the baseline care plan (an initial plan for delivery of care and services) for three residents (Residents #50, #152, and #202) and the facility failed to complete a baseline care plan within 48 hours of admission for one resident (resident #152) out of 13 sampled residents. The facility's census was 44.
1. Record review of the facility's policy titled, Care Plans - Baseline, dated [DATE], showed:
- A Baseline plan of care to meet the resident's immediate needs shall be developed for each resident within 48 hours of admission;
- The Interdisciplinary Team will review the healthcare practitioner's orders and implement a baseline care plan to meet the resident's immediate care needs including but not limited to initial goals based on admission orders, physician orders, dietary orders, therapy services, social service and PASARR (preadmission screening and resident review) recommendation if applicable;
- The baseline care plan will be used until the staff can conduct the comprehensive assessment and develop an interdisciplinary person-centered care plan;
- The resident and their representative will be provided a summary of the baseline care plan that included but is not limited to the initial goals of the resident, a summary of the resident's medications and dietary instructions, any services and treatments to be administered by the facility and personnel acting on behalf of the facility and any updated information based on the details of the comprehensive care plan, as necessary.
Record review of the facility's policy titled, Resident Participation - Assessment/Care Plans, dated [DATE], showed:
- The resident and his or her representative are encouraged to participate in the resident's assessment and in the development and implementation of the resident's care plan;
- The care planning process will: Facilitate the inclusion of the resident and/or representative, include an assessment of the resident's strengths and his or her needs, incorporate the resident's personal and cultural preferences in establishing goals of care;
- Resident assessments are begun on the first day of admission and completed no later than the fourteenth day after admission.
2. Record review of Resident #50's medical record showed:
- admitted on [DATE];
- Physician's Order Sheet (POS), dated [DATE] through [DATE], showed diagnosis of non-Covid (not Covid-19 virus related) acute respiratory disease (an infection of the lungs that interferes with breathing), anxiety disorder (excessive and persistent worry and fear about everyday situations), dry eye syndrome (tears do not provide adequate moisture), pneumonia (an infection of the lungs), cognitive communication deficit (difficulty using spoken languages).
Record review of the resident's admission Minimum Data Set (MDS; a federally mandated assessment required to be completed by the facility), dated [DATE], showed the resident to have a diagnosis of anxiety and to be moderately cognitively impaired.
Record review of the medical record showed a baseline care plan completed on [DATE].
During an interview on [DATE] at 12:21 P.M., the resident voiced concerns about his/her medication not being given correctly because the facility does not have it available. The resident said the facility did not discuss his/her care plan with him/her upon admission.
Record review of the resident's nurse progress note, dated [DATE], showed the care plan was provided to the guardian.
During an interview on [DATE] at 10:01 A.M.,the Public Administrator's office deputy said they do not have an electronic copy of the care plan in their record.
4. Record review of Resident #152's medical record showed:
- admitted on [DATE];
- POS, dated [DATE] through [DATE], showed diagnoses of malignant neoplasm of prostate (cancer), hypertension (high blood pressure), stress incontinence (leaking urine with activity), alcohol abuse, chronic pain, type two diabetes mellitus with hyperglycemia (high blood sugar).
Record review of the resident's admission MDS, dated [DATE], showed the resident to have diagnoses of cancer, diabetes, seizures, hypertension, and to be severely cognitively impaired.
Record review of the medical record on [DATE] at 9:39 A.M., showed no baseline care plan completed.
During an interview on [DATE] at 8:57 A.M., the resident said he/she did not know anything about a care plan.
During an interview on [DATE] at 11:45 A.M., the Director of Nurses (DON) said she does the baseline care plan and usually discusses it with the family or resident but she does not document it or have them sign anything. Resident #152's baseline care plan is not complete yet as she has 21 days to complete the care plan, she could complete it now.
Record review of the facility policy showed the baseline plan of care to meet the resident's immediate needs shall be developed for each resident within 48 hours of admission.
Record review of the resident's medical record on [DATE] at 2:00 P.M., showed a baseline care plan, dated [DATE], 17 days after admission.
The facility did not develop a baseline care plan with 48 hours.
5. Record review of Resident #202's Face Sheet showed:
- admission date [DATE];
- Diagnosis of urinary tract infection;
- Emergency contact - family member.
Record review of the resident's Cardiopulmonary Resuscitation (CPR; an emergency lifesaving procedure performed when the heart stops beating) Directive showed wish for CPR to be provided to resident, signed by family member, shown as Power of Attorney (POA; the authority to act for another person in specified or all legal or financial matters) dated [DATE].
Record review of the resident's comprehensive care plan, dated [DATE], showed:
- Care areas with onset date [DATE] and completion date [DATE];
- Baseline care plan not provided.
Record review of the resident's medical record showed no documentation that the baseline care plan was reviewed with the resident representative.
6. During an interview on [DATE] at 3:03 P.M., the DON said she would expect the baseline care plan to be discussed with the representative and a copy provided after [DATE], prior to that date the requirement was waived. She would expect it to be documented that it was discussed with the resident or representative.
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
ADL Care
(Tag F0677)
Could have caused harm · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to provide consistent resident care for activities of daily living (AD...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to provide consistent resident care for activities of daily living (ADLs) for four residents (Resident #6, #18, #45, and #46) out of 13 sampled residents. This practice could potentially affect all residents. The facility's census was 44.
1. Record review of the facility's policy titled, Activities of Daily Living (ADLs), Supporting, dated March 2018, showed:
- Residents will be provided with care, treatment and services as appropriate to maintain or improve their ability to carry out ADLs;
- Residents who are unable to carry out ADLs independently will receive the services necessary to maintain good nutrition, grooming and personal and oral hygiene;
- Residents will be provided with care, treatment and services to ensure that their ADLs do not diminish unless the circumstances of their clinical condition(s) demonstrate that diminishing ADLs are unavoidable;
- Appropriate care and services will be provided for residents who are unable to carry out ADLs independently, with the consent of the resident and in accordance with the plan of care, including appropriate support and assistance with hygiene (bathing, dressing, grooming, and oral care, mobility (transfer and ambulation including walking), elimination, dining (meals and snacks), and communication (speech, language, and any functional communication systems).
2. Record review of Resident #6's annual Minimum Data Sheet (MDS; a federally mandated assessment instrument required to be completed by facility staff), dated 1/21/21, showed:
- Section G- Functional Status the resident requires total assistance of one for all personal care;
- Section L-Oral/Dental Status the resident has inflamed, bleeding gums, loose natural teeth.
Record review of the resident's quarterly MDS, dated [DATE], showed:
- Section G the resident to require total assistance of one for all personal care;
- Section L no documentation for dental needs.
During observation and interview on 7/20/21 at 12:09 P.M., on 7/21/21 at 10:20 A.M., and on 7/22/21 at 8:45 A.M., the resident's teeth covered with thick brown substance and the gums to be red. The resident said the staff do not provide oral care.
During an interview on 7/21/21 at 1:59 P.M., Certified Nurse Assistant (CNA) L said sometimes the CNAs might swab Resident #6's mouth with a wet swab but do not brush his/her teeth. The CNAs don't really do oral care during the day.
During a telephone interview on 7/22/21 at 11:01 A.M., the resident's responsible party said his/her only concern with the resident's care is that the resident's teeth always seemed to be dirty and nasty.
During observation and interview on 7/23/21 at 10:04 A.M., the resident's teeth covered with thick brown substance and the gums to be red. The resident said the staff have not provided oral care. The resident does not remember ever being offered dental care.
During an interview on 7/23/21 at 10:50 A.M., the Director Of Nursing (DON) said she expects oral care to be provided daily for residents who need assistance.
During observation and interview on 7/27/21 at 8:38 A.M., the resident's teeth covered with thick brown substance and the gums to be red. The resident said the staff have not provided oral care.
3. Record review of Resident #18's annual MDS, dated [DATE], showed:
- Section G the resident to require total assistance of one for all personal care;
- Section L no documentation for dental needs.
Record review of the resident's quarterly MDS, dated [DATE], showed:
- Section G the resident to require total assistance of one for all personal care;
- Section L no documentation for dental needs.
Record review of resident's Physician's Order Sheet (POS), dated 7/1/21 through 7/31/21, showed diet is nothing by mouth (NPO).
Record review of the resident's comprehensive care plan, dated 5/12/21, showed staff to provide with oral care every shift and as needed.
During observations on the following dates and times showed the resident's lips were dry, with peeling skin and the tongue dry with resident open mouth breathing.
- On 7/20/21 at 11:00 A.M. and 3:12 P.M.;
- On 7/21/21 at 9:27 A.M., 10:27 A.M. and 3:43 P.M.;
- On 7/22/21 at 8:51 A.M., 11:50 A.M. and 3:50 P.M.;
- On 7/23/21 at 9:00 A.M. and 12:38 P.M.;
- On 7/26/21 at 11:00 A.M., 2:10 P.M. and 4:00 P.M.;
- On 7/27/21 at 9:10 A.M., 11:20 A.M. and 2:45 P.M.
4. Record review of Resident #45's annual MDS, dated [DATE], showed:
- Section G the resident requires total assistance of one for all personal care;
- Section L no documentation for dental needs.
Record review of the resident's Quarterly MDS, dated [DATE], showed:
- Section G the resident requires total assistance of one for all personal care;
- Section L no documentation for dental needs.
During the following observations, Resident #45's teeth were covered with a dirty, thick tan substance:
- On 7/20/21 at 11:30 A.M. and 3:17 P.M.;
- On 7/21/21 at 9:21 A.M., 11:45 A.M. and 3:50 P.M.;
- On 7/22/21 at 9:00 A.M., 1:36 P.M. and 4:05 P.M.;
- On 7/23/21 at 9:10 A.M. and 11:18 A.M.;
- On 7/26/21 at 11:20 A.M., 2:16 P.M. and 4:07 P.M.;
- On 7/27/21 at 9:17 A.M., 11:32 A.M. and 2:32 P.M. e.
5. Record review of Resident #46's annual MDS, dated [DATE], showed:
- Section G the resident requires total assistance of one for all personal care;
- Section L the resident to have no natural teeth or tooth fragments.
Record review of the resident's quarterly MDS, dated [DATE], showed:
- Section G the resident requires total assistance of one for all personal care;
- Section L no documentation for dental needs.
Record review of resident's Physician's Order Sheet (POS), dated 7/1/21 through 7/31/21, showed:
-Diagnoses of 2019-nCoV acute respiratory disease, essential hypertension, type 2 diabetes mellitus with hyperglycemia, cerebral infarction, unspecified dementia without behavioral disturbance, undifferentiated schizophrenia (disorder that affects a person's ability to thin, feel or behave clearly), chronic obstructive pulmonary disease (COPD), pain in unspecified joint, pseudobulbar affect (inappropriate laughing or crying due to a nervous system disorder), Parkinson's disease (disease of the central nervous system that affects movement, often including tremors), aphasia (loss of ability to understand or express speech caused by brain damage), pressure ulcer of other site stage 2, and pressure ulcer other site unspecified stage;
-Diet is pureed diet with nectar thickened liquids for pleasure if resident requests three times a day.
Record review of resident's comprehensive care plan, dated 4/06/21, showed provide me with oral care every shift and as needed.
During the following observations, the resident's lips and tongue looked dry and the water pitcher on nightstand was empty:
- On 7/21/21 at 9:25 A.M., 11:30 A.M. and 3:45 P.M.;
- On 7/22/21 at 8:47 A.M., 11:53 A.M. and 3:57 P.M.;
- On 7/23/21 at 9:03 A.M. and 12:42 P.M.;
- On 7/26/21 at 11:08 A.M., 2:14 P.M. and 4:03 P.M.;
- On 7/27/21 at 9:07 A.M., 11:25 A.M., 1:27 P.M. and 2:40 P.M.
6. During an interview on 9/23/21 at 9:05 A.M., Registered Nurse (RN) K said oral care should be performed each shift and as needed.
During an interview on 9/23/21 at 9:24 A.M., CNA C said oral care should be done at least every shift.
During an interview on 7/23/21 at 10:50 A.M., the DON said she expects oral care to be provided daily for residents who need assistance.
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Pressure Ulcer Prevention
(Tag F0686)
Could have caused harm · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to ensure care to prevent and promote healing of a pressure ulcer for ...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to ensure care to prevent and promote healing of a pressure ulcer for one resident (Resident #17) out of two sampled closed records. The facility's census was 44.
Record review of the facility's policy titled, Pressure Ulcers(damage to the skin and/or underlying tissue as a result of pressure)/Skin Breakdown-Clinical Protocol, dated March 2014, showed:
- The nurse shall describe and document/report the following: Full assessment of pressure sore including location, stage, length, width and depth, presence of exudates or necrotic tissue, pain assessment, resident's mobility status, current treatments, and all active diagnoses;
- The staff will examine the skin of a new admission for ulcerations or alterations in skin;
- The physician will help identify factors contributing or predisposing residents to skin breakdown;
- The physician will authorize pertinent orders related to wound treatments;
- The physician will help staff characterize the likelihood of wound healing;
- During resident visits, the physician will evaluate and document the progress of wound healing-especially for those with complicated, extensive, or non-healing wounds;
- The physician will help the staff review and modify the care plan as appropriate, especially when wounds are not healing as anticipated or new wounds develop despite existing interventions.
Observations from 7/20/21 to 7/28/21 showed Resident #17 out of the facility due to hospitalization.
Record review of Resident #17's Physician's Order Sheet, dated 7/1/21-7/31/21, showed diagnoses of Type-2 diabetes mellitus (a chronic metabolic disorder affecting blood sugar) with hyperglycemia (elevated blood sugar), acute kidney failure, hypertension (high blood pressure), dementia (loss of cognitive ability), unspecified pain, dehydration, presence of cardiac pacemaker, and urinary incontinence.
Record review of the resident's Skin Integrity Assessments signed by the Director of Nursing (DON) showed:
- On 4/9/21, right heel measurements 6 centimeter (cm) by 4.8 cm by 0.3 cm, heavy amount of exudate (bodily fluid of protein, cells, or debris), necrotic (death of a portion of tissue), unstageable due to slough (dead matter separated from living tissue) and/or eschar (dead matter cast off from the surface of the skin);
- On 4/9/21, coccyx (small bone at the base of the spinal column) measurements 3.1 cm by 1.2 cm by 0.1 cm, light amount of exudate, granulation tissue (healing tissue), Stage II (partial thickness loss of dermis presenting as a shallow open ulcer with a red pink wound bed, without slough);
- On 4/18/21, right heel measurements 6 cm by 4.8 cm by 0.3 cm, heavy amount of exudate, necrotic tissue, unstageable due to slough and/or eschar;
- On 4/18/21, coccyx wound resolved;
- On 6/23/21, pressure ulcer right hip first observed, clarified with physician from buttocks to hip. No measurements. Pressure ulcer coccyx first observed 6/23/21, no measurements;
- No nursing assessment dated [DATE] as noted in progress notes;
- Coccyx wound measurements on 4/9/21 do not match measurements in 4/9/21 progress notes.
Record review of the resident's Weekly Pressure Injury Log showed:
- On 5/12/21, right heel unstageable-eschar/necrotic, measurements 7 cm by 4 cm by 0.5 cm, odor present, no drainage or culture. Left heel unstageable-eschar/necrotic, measurements 4 cm by 4.5 cm by 0.5 cm, odor and drainage present, no culture. Coccyx Stage II, measurements 3 cm by 2 cm by 0.2 cm, no odor, drainage, or culture;
- The facility did not provide the weekly skin assessment for 5/19/21;
- On 5/26/21, right heel unstageable-eschar/necrotic, measurements 7 cm by 4.3 cm by 0.5 cm, odor and drainage present, no culture. Left heel unstageable-eschar/necrotic, measurements 4 cm by 4 cm by 0.5 cm, odor and drainage present, no culture;
- The facility did not provide the weekly skin assessment for 6/2/21;
- The weekly skin assessment for 6/9/21 did not include this resident;
- The facility did not provide the weekly skin assessment for 6/16/21;
- On 6/23/21 (incorrectly dated 6/23/20), coccyx Stage II, measurements 2.5 cm by 2 cm by 0.1 cm, no odor or drainage present, no culture. Right heel Stage IV (Full thickness tissue loss with exposed bone, tendon or muscle), measurements 7 cm by 4 cm by 0.5 cm, odor and drainage present, no culture. Left heel Stage IV, measurements 4 cm by 4.3 cm by 0.5 cm, odor and drainage present, no culture. Right hip Stage II, measurements 1.5 cm by 0.5 cm by 0.1 cm, odor and drainage present, no culture;
- The facility did not provide the weekly skin assessment for 6/30/21.
Record review of the resident's progress notes showed:
- On 3/26/21, the resident admitted to the facility on contact isolation for Methicillin-resistant Staphylococcus aureus (MRSA; a bacteria that is resistant to most antibiotics) from a previous wound. Left heel wound scabbed over and right heel wound quarter sized, minimal drainage and blood noted;
- On 3/30/21, the resident with shortness of breath, 2 liters oxygen administered, unable to respond to nurse and daughter;
- On 3/31/21, hospital contacted and informed resident was admitted . MRSA wound swab awaiting culture from right heel. Left heel noted with unblanchable (area of tissue with redness slow to get blood supply to return) redness and wound to coccyx noted by their team;
- On 4/9/21, hospital contacted for status update. Right heel culture negative for MRSA, but positive for Vancomycin-resistant Staphylococcus aureus (VRSA; a bacteria that is resistant to most antibiotics). Resident on contact precautions for previous exposure. No antibiotic noted at this time. Blood cultures negative at this time for all testing conducted. Resident returned to the facility. Coccyx wound measurements 4.5 cm by 3.2 cm. Right foot with 3.1 cm by 1.2 cm black over flap area, unstageable;
- On 4/18/21, pressure ulcer to right heel noted to have large amount of serous (thin or watery) drainage. Measurements 6 cm by 4.8 cm by 0.3 cm. Doctor made aware and new order noted;
- On 4/19/21, staff reported resident catheter found on side of resident's floor. Nurse observed catheter/G tube on side of bed. Nurse unable to place tube back in. New order to send resident to hospital for tube replacement;
- On 4/21/21, resident returned to facility. Ulcer to right heel skin prepped and left open to air;
- On 4/23/21, Resident sent to hospital from dialysis after oxygen levels lowered;
- On 5/3/21, resident returned to facility. Unstageable pressure ulcers noted to bilateral heels, Stage II noted to coccyx-see nursing assessment;
- On 6/23/21, Stage II pressure ulcer noted to right buttocks, physician aware, new order noted. Measurements 1.5 cm by 1.2 cm by 0. cm;
- On 7/4/21, Stage II pressure ulcer to right buttocks and bilateral heels. Resident responding to name with slight moaning, has been drooling with slurred speech. New order to send to hospital;
- On 7/13/21, spoke with hospital nurse, admitted for urinary tract infection (UTI) and lethargy (drowsiness). Received one unit of blood 7/12/21 for low count of 7.6, wound culture to heels positive for E coli (bacteria), Proteus (bacteria), Pseudomonas (bacteria), Faecalis (bacteria), plus one more. Antibiotic being determined. Surgical debridement to be completed at a later time;
- On 7/22/21, hospital contacted, resident currently stable, wounds are actively healing, but resident has slow healing process.
Record review of the resident's progress notes showed:
- The resident went to dialysis (a procedure to remove waste products and excess fluid from the blood when the kidneys stop working properly) on Tuesday/Thursday/Saturday for the dates 3/27/21 and 3/30/21;
- The resident hospitalized from [DATE] through 4/9/21;
- The resident went to dialysis on Monday/Wednesday/Friday for the dates 4/12/21, 4/14/21, 4/16/21, 4/19/21, 4/21/21, and 4/23/21;
- The resident hospitalized from [DATE] through 5/3/21;
- The resident went to dialysis on 5/27/21, 6/4/21, 6/7/21, 6/23/21, and 6/25/21;
- The resident hospitalized on [DATE] to present.
Record review of the resident's March 2021 Medication and Treatment Administration Record (MAR/TAR), showed no treatment orders for right heel wound or coccyx wound for four days after re-admitted from hospital to the facility on 3/26/21 through 3/30/21.
Record review of the resident's April 2021 MAR/TAR, showed:
- An order, dated 4/9/21, for skin prep to right heel twice daily (BID) at 8:00 A.M. and 8:00 P.M.;
- On 4/14/21 at 8:00 A.M. the facility staff documented as the treatment not given due to resident unavailable and on 4/15/21 due to other reason;
- An order, dated 4/18/21, for Santyl Ointment (debridement medication) 250 unit/gram (unit/gm). Cleanse open area to right heel with normal saline, apply Santyl ointment and dry dressing once daily to bilateral heels;
- The facility staff documented as the treatment not given 4/22/21 due to resident unavailable.
Record review of the resident's May 2021 MAR/TAR, showed:
- An order, dated 4/18/21, for Santyl Ointment 250 unit/gm. Cleanse open area to right heel with normal saline, apply Santyl ointment and dry dressing once daily to bilateral heels;
- The facility staff documented as the treatment not given 5/3/21 and 5/5/21 due to resident unavailable;
- An order, dated 5/3/21, for Santyl Ointment 250 unit/gm. Cleanse open area to bilateral heels with normal saline, apply Santyl Ointment and dry dressing once daily to bilateral heels;
- The staff documented as the treatment not given 5/10/21, 5/12/21, 5/14/21, 5/17/21, 5/19/21, 5/21/21, 5/24/21, and 5/27/21 due to resident unavailable;
- No orders to care for Stage II coccyx wound. The weekly pressure injury log dated 5/12/21 documentation showed the resident had a Stage II coccyx wound.
Record review of the resident's June 2021 MAR/TAR, showed:
- An order, dated 5/3/21, for Santyl Ointment 250 unit/gm. Cleanse open area to bilateral heels with normal saline, apply Santyl Ointment and dry dressing once daily to bilateral heels;
- The facility staff documented as the treatment not given 6/7/21, 6/11/21, 6/14/21, 6/16/21, 6/18/21, 6/21/21, and 6/28/21 due to resident unavailable, and 6/23/21 and 6/24/21 due to unable to retain;
- An order, dated 6/24/21, for Collagen Matrix Fenest External Sheet (repairs tissue) 2 cm by 2 cm, cleanse pressure ulcer to right buttocks with normal saline, apply collagen dressing and secure with tape once daily;
- The facility staff documented as the treatment not given 6/24/21 and 6/28/21 due to resident unavailable;
- No orders to care for Stage II coccyx wound. The weekly pressure injury log dated 5/12/21 and 6/23/21 documentation showed the resident had a Stage II coccyx wound.
Record review of the resident's July 2021 MAR/TAR, showed:
- An order, dated 5/3/21, for Santyl Ointment 250 unit/gm. Cleanse open area to bilateral heels with normal saline, apply Santyl Ointment and dry dressing once daily to bilateral heels;
- The facility staff documented as the treatment not given 7/3/21 due to resident unavailable;
- An order, dated 6/24/21, for Collagen Matrix Fenest External Sheet 2 cm by 2 cm, cleanse pressure ulcer to right buttocks with normal saline, apply collagen dressing and secure with tape once daily;
- The facility staff documented as the treatment not given 7/3/21 due to resident unavailable;
- The facility staff continued to not obtain orders to care for coccyx wound.
During an interview on 7/27/21 at 3:03 P.M., the Assistant Administrator (AA) and DON said the DON is handwriting a lot of things right now because they are getting ready to change computer systems. The DON is not putting wound care assessments in the computer, there is limited charting in the system right now. The facility stopped doing it three to six months ago, will have to look to see exactly when. When asked if the DON would expect a resident with a wound to have treatment orders for the wound, the DON said there are wounds that you don't treat, so there would not necessarily be orders. The AA said if there is a change in orders, he would expect that to be on the physician's orders.
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0744
(Tag F0744)
Could have caused harm · This affected 1 resident
Based on observation, interview, and record review, the facility failed to assess, develop, and implement an individualized approach to providing dementia care services for three residents (Residents ...
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Based on observation, interview, and record review, the facility failed to assess, develop, and implement an individualized approach to providing dementia care services for three residents (Residents #16, #45, and #46) out of 13 sampled residents. The facility's census was 44.
1. Record review of Resident #16's annual Minimum Data Set (MDS-a federally mandated assessment, required to be completed by the facility), dated 5/6/21, showed the resident to have a diagnosis of Alzheimer's (progressive mental deterioration), dementia (disorder marked by memory disorders, personality changes, and impaired reasoning), anxiety (persistent worry and fear about everyday situations), psychotic disorder (a disconnection from reality), and to be moderately cognitively impaired.
Record review of the resident's Physician's Order Sheet (POS), dated 7/1/21 to 7/31/21, showed:
- Diagnoses of Alzheimer's disease, dementia without behavioral disturbance, dementia with behavioral disturbance, anxiety disorder;
- An order, dated 4/4/19, for Cymbalta (a medication used to treat depression) 30 milligrams (mg) once daily for dementia;
- An order, dated 10/18/18, for Seroquel (a medication used to treat schizophrenia, bipolar disorder and depression) 25 mg, 1/2 tablet two times daily for vascular dementia with behavioral disturbance.
Record review of the resident's medication administration record (MAR), dated 7/1/21 through 7/27/21, showed Seroquel and Cymbalta administered as ordered.
Record review of the resident's comprehensive care plan, last reviewed 5/19/21, showed:
- Problem: Dated 10/18/18, a history of confrontations, outbursts and violent behavior;
- Approach: Dated 2/20/19, Visits as needed, medications as ordered - Seroquel as needed for diagnosis and medication management, Dated 2/25/20, Document episodes if they occur, Dated 4/20/20 the physician documented that a reduction in medications may cause an increase in symptoms, redirect as needed, validation and redirection;
- Problem: a history of depression;
- Approach: Dated 2/20/19, Medication as ordered - Cymbalta.
The care plan failed to utilize individualized, non-pharmacological approaches to care, failed to provide current, specific interventions for confrontations, outbursts and violent behavior, and failed to provide current, specific interventions for depression to enhance Resident #16's ability to attain, or maintain the highest practicable level of functioning.
Record review of the resident's progress notes, dated 1/29/21 through 6/2/21, showed no documentation of confrontations, outbursts or violent behaviors. The facility did not provide notes dated after 6/2/21.
Observations showed:
- On 7/20/21 at 12:42 P.M., Resident #16 to be calm, to sit in wheelchair at the dining room table, voicing that his/her legs hurt;
- On 7/21/21 at 10:22 A.M., the resident to be lying in bed, calm, eyes closed;
- On 7/22/21 at 8:55 A.M., the resident to be lying in bed, calm, eyes closed;
- On 7/27/21 at 8:47 A.M., the resident to be eating breakfast, calm.
During an interview on 7/21/21 at 1:59 P.M., Certified Nurse Assistant (CNA) L said Resident #16 sleeps a lot.
2. Record review of Resident #45's POS, dated 7/1/21 through 7/31/21, showed:
- Diagnoses included unspecified dementia without behavioral disturbance;
- An order, dated 9/24/20, for Namenda oral tablet 10 mg 1 tab by mouth twice daily (for dementia).
Record review of the MAR, dated 7/1/21 through 7/27/21, showed Namenda administered as ordered.
Record review showed no care plan for dementia and care plan last reviewed 7/5/21.
3. Review of Resident #46's POS, dated 7/1/21 through 7/31/21, showed:
- Diagnoses included unspecified dementia without behavioral disturbance, major depressive disorder, undifferentiated schizophrenia (disorder that affects a person's ability to think, feel or behave clearly);
-Remeron SolTab oral tablet disintegrating 15 mg 1 tab per G-tube at bedtime (for dementia) (order start date 6/30/21).
Record review of the MAR, dated 7/1/21 through 7/27/21, showed Remeron administered as ordered.
Record review of the resident's comprehensive care plan, dated 4/6/21, showed no care plan for depression.
During an interview on 7/27/21 at 1:44 P.M., CNA C said the care plan on the computer explains how to take care of each resident.
During an interview on 7/27/21 at 3:03 P.M., the Director of Nursing (DON) said she would expect there to be a care plan for antipsychotic and antidepressants medications.
The facility did not provide a policy for dementia care planning.
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Pharmacy Services
(Tag F0755)
Could have caused harm · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to ensure a sufficient supply of prescribed medications were available...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to ensure a sufficient supply of prescribed medications were available to meet the needs of two residents (Resident #46 and #50) out of 13 sampled residents. The facility's census was 44.
1. Record review of the facility's policy titled, Medication and Treatment Orders, dated July 2016, showed Drugs and biological's that are required to be refilled must be reordered from the issuing pharmacy not less than three days prior to the last dosage being administered to ensure that refills are readily available.
2. Record review of Resident #46's admission Minimum Data Set (MDS-a federally mandated assessment, required to be completed by the facility), dated 7/6/21, showed Resident #46 to have diagnoses of stroke (damage to brain from interrupted blood supply), heart failure (chronic condition in which the heart doesn't pump blood as well as it should), hypertension (high blood pressure), diabetes mellitus (condition affecting the way the body processes blood sugar), dementia (disease causing impairment of brain functions such as memory loss and judgment), schizophrenia (disorder that affects a person's ability to think, feel or behave clearly) and chronic obstructive pulmonary disease (COPD: constriction of the airway) and to be moderately cognitively impaired. The MDS showed resident was not on a scheduled or as needed (PRN) pain medication.
Record review of Resident #46's medical record showed admitted on [DATE].
Record review of the resident's Physician's Order Sheet (POS), dated 7/1/21 through 7/31/21, showed:
- Diagnoses of Novel Coronavirus (2019-nCoV acute respiratory disease), type 2 diabetes mellitus with hyperglycemia, heart failure, cerebral infarction, unspecified dementia without behavioral disturbance, major depressive disorder, undifferentiated schizophrenia (disorder that affects a person's ability to think, feel or behave clearly), chronic obstructive pulmonary disease, pain in unspecified joint, pseudobulbar affect (inappropriate laughing or crying due to a nervous system disorder), abnormal weight loss, Parkinson's disease (disease of the central nervous system that affects movement, often including tremors), aphasia (loss of ability to understand or express speech caused by brain damage), constipation, pressure ulcer of other site stage 2, and pressure ulcer other site unspecified stage;
- An order, dated 3/10/21, for Hydrocodone-Acetaminophen (pain medication) oral tablet 5-325 milligram (mg) per gastrostomy tube (G-tube: a surgically placed device used to give direct access to the stomach for supplemental feeding and medications) 1- 2 tabs max daily- four times a day (for pain).
Record review of the resident's medication administration record (MAR), dated May 2021, showed Hydrocodone-Acetaminophen 30 missed attempts out of 124 opportunities due to medication not available.
Record review of the MAR, dated June 2021, showed Hydrocodone-Acetaminophen 34 missed attempts out of 103 opportunities due to medication not available;
Record review of the MAR, dated July 2021, showed Hydrocodone-Acetaminophen 38 missed attempts out of 108 opportunities due to medication not available.
During an interview on 7/27/21 at 3:03 P.M., the Director of Nursing (DON) and Assistant Administrator said if medications are not available, it is ordered from the pharmacy, they have two deliveries a day so it should be delivered on the next available delivery. If the prescription requires a prescription, the facility writes an order and sends it to the pharmacy. The pharmacy calls to get a verbal or signature for the prescription to be delivered on the next delivery day. If the script is available the resident shouldn't go more than 8 hours without the medication, but if there is a lag in the script it could be longer.
3. During an interview on 7/20/21 at 1:27 P.M., Resident #50 said he/she is not getting his/her medication for his/her blood cancer. He/she is starting to feel the effects of not having it. He/she was supposed to see his/her cancer doctor on 4/14/21 but the facility didn't take him/her so now he/she can't get his/her medication.
Record review of the resident's admission MDS, dated [DATE], showed Resident #50 to have a diagnosis of anxiety and to be moderately cognitively impaired.
Record review of Resident #50's medical record showed admitted on [DATE].
Record review of the resident's POS, dated 7/1/21 through 7/31/21, showed:
- Diagnoses of non-Covid (not Covid-19 virus related) acute respiratory disease (an infection of the lungs that interferes with breathing), anxiety disorder (excessive and persistent worry and fear about everyday situations), dry eye syndrome (tears do not provide adequate moisture), pneumonia (an infection of the lungs), cognitive communication deficit (difficulty using spoken languages);
- An order, dated 6/28/21, for Imatinib mesylate (a chemotherapy medication used to treat chronic myeloid leukemia, cancer of the blood and for pneumonia in patients with severe acute respiratory syndrome SARS-Covid ) 100 mg two tablets daily to be given for a diagnosis of pneumonia.
Record review of the resident's medication administration record (MAR), dated July 2021, showed:
- Imatinib Mesylate to be given daily 7/1/21 through 7/11/21:
- Imatinib Mesylate to be unavailable in the facility 7/12/21 - 7/15/21;
- Imatinib Mesylate to be given on 7/16/21;
- Imatinib Mesylate to be unavailable in the facility 7/17/21 through 7/20/21.
Seven missed attempts out of 21 opportunities due to medication not available, one erroneous recorded administration on 7/26/21 when medication not to be available in facility, total eight missed attempts out of 21 opportunities.
During an interview on 7/21/21 at 1:43 P.M., the Director of Nursing (DON) said the documentation of the given medication on 7/16/21 is an error and it should have been corrected as not available, she will correct it. The DON explained the medication is not covered by the resident's insurance without a prior authorization (PA). The facility was trying to get a PA for it when the resident informed them he/she receives the medication through a grant program. The DON contacted the grantor and they verified the resident's eligibility and will provide the medication at least through 2021. The medication was ordered on 7/16/21 and had just been received to the facility on 7/21/21. The resident will be re-evaluated at the end of the year for continued eligibility. The DON said the resident did not miss any appointments.
During an interview on 7/22/21 at 9:52 A.M., the resident's oncologist's medical assistant (MA) said the resident has a diagnosis of chronic myeloid leukemia. The resident did miss an appointment with them on 4/14/21. In April 2021, the Grantor for the medication notified the office that the grant was going to end for non-compliance of information updates. The MA called the facility and spoke with the DON to request the information needed to continue the medication, he/she got the impression that the DON did not care and the DON did not provide the information. The MA gave the DON the information about who to call to continue the medication grant. The MA said he/she felt like he/she was talking to a wall. The MA called the responsible party (RP) who did not return the call. On 5/7/21, the MA was notified that the resident had been discontinued from the grant for non-compliance of information updates. On 7/16/21, the facility called the MA to get the information about the grant, the MA said it was a painful conversation.
During an interview on 7/22/21 at 10:01 A.M., a representative at the RP's office said there is no record of any complications related to medication availability for Resident #50.
During an interview on 7/27/21 at 3:03 P.M., the DON said medications are ordered from the pharmacy, the pharmacy does two deliveries a day so the medication should be delivered during the next available delivery. If the pharmacy can't get it quickly, they have a contract with another pharmacy and they can deliver anytime. The Assistant Administrator said if the medication requires a prescription and they run out of medication, we write an order and send it to the pharmacy, they call to get verbal or signature, they go ahead and fill the prescription and deliver it on the next delivery. If the script is available it shouldn't go more than eight hours, if there is a lag in the script it could be longer.
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Drug Regimen Review
(Tag F0756)
Could have caused harm · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to ensure the Consultant Pharmacist performed a review of each residen...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to ensure the Consultant Pharmacist performed a review of each resident's medical record each month, reported irregularities to the Attending Physician, Medical Director and Director of Nursing (DON) in a separate written report and the attending physician reviewed and acted on any identified irregularities and Gradual Dose Reduction (GDR) recommendations and document the action taken to address the irregularity or GDR for four residents (Residents #11, #14, #16, and #23) and failed to ensure each medication to be clinically indicated for one resident (#50) out of six sampled residents for unnecessary medications. The facility's census was 44.
1. Record review of the facility's policy titled, Medication and Treatment Orders, dated July 2016, showed:
- Drug and biological orders must be recorded on the Physician's Order Sheet (POS) in the resident's chart;
- Such orders are reviewed by the consultant pharmacist on a monthly basis.
2. The facility failed to provide a clear set of documentation that the Consultant Pharmacist does a complete review of all resident's medications and provides written recommendations with responses from the physician for the recommendations.
3. Record review of Resident #11's medical record showed:
- admitted on [DATE];
- Diagnoses of chronic kidney disease, stage 5, dependence on renal dialysis, unspecified convulsions, major depressive disorder, type 2 diabetes mellitus (a chronic condition that affect the way the body processes blood sugar) with foot ulcer, bipolar disorder (a disorder associated with episodes of mood swings ranging from depressive lows to manic highs), generalized anxiety disorder;
- An order, dated 1/11/18, for Celexa (can treat depression) 40 mg (milligram) 1 tab by mouth every day for major depressive disorder;
- An order dated, 12/4/19, for Depakote (can treat seizures and bipolar disorder, an anticonvulsant) delayed release 250 mg take 1 tablet by mouth twice a day with a 500 mg tablet for a total dose of 750 mg for bipolar disorder;
- An order, dated 12/4/19, for Depakote 500 mg take 1 tablet by mouth twice a day with a 250 mg tablet for a total dose of 750 mg for bipolar disorder;
- An order, dated 1/11/18, for Venlafaxine (can treat depression, generalized anxiety disorder) HCL (hydrogen chloride) ER (extended-release) 150 mg 1 tablet by mouth every day for major depressive disorder;
- An order, dated 1/11/18, for Zyprexa 7.5 mg 1 tablet by mouth every day for bipolar disorder;
- No documentation to show the physician reviewed the recommendation, dated 8/24/20.
Record review of the Consultant Pharmacist's Medication Regimen Review listing residents reviewed with no recommendations showed no reviews for the resident in September 2020, or December 2020. A written recommendation from the pharmacist to the physician to consider gradual dose reduction on 8/24/20 for Celexa 40 mg daily since 1/11/18, Venlafaxine ER 150 mg daily since 1/11/18, and Zyprexa 7.5 mg daily since 1/11/18 with no response on pharmacist recommendation.
4. Record review of Resident #14's medical record showed:
- admitted on [DATE];
- Diagnoses of dementia (a group of thinking and social symptoms that interferes with daily functioning) with behavioral disturbances, major depressive disorder, hypertension (elevated blood pressure), abnormal weight loss, pain disorder exclusively related to psychological factors;
- An order, dated 5/14/20, for Quetiapine fumarate (antipsychotic, can treat schizophrenia ,a serious mental illness that affects how a person thinks, feels, and behaves, bipolar disorder, a disorder associated with episodes of mood swings ranging from depressive lows to manic highs, and depression) 50 mg take 1 tablet by mouth once daily;
- An order, dated 4/26/19, for Risperdal (antipsychotic, can treat schizophrenia, bipolar disorder, and irritability caused by autism, a serious developmental disorder that impairs the ability to communicate and interact) 0.5 mg give 1 tablet by mouth at bedtime;
- An order, dated 5/1/19, for Zoloft (can treat depression, obsessive-compulsive disorder, posttraumatic stress disorder, premenstrual dysphoric, a state of unease or generalized dissatisfaction with life, disorder, social anxiety disorder, and panic disorder) 50 mg give 1 tablet by mouth daily;
- No documentation to show the physician reviewed the recommendation, dated 8/24/20.
Record review of the Consultant Pharmacist's Medication Regimen Review listing residents reviewed with no recommendations showed no reviews for the resident in September 2020, or December 2020. A written recommendation from the pharmacist to the physician to consider gradual dose reduction on 8/24/20 for sertraline (Zoloft) 50 mg since 5/1/19 and risperidone (Risperdal) 0.5 since 5/1/19 with no response on pharmacist recommendation.
5. Record review of Resident #16's medical record showed:
- admitted [DATE];
- POS, dated 7/1/21 - 7/31/21, showed:
- Diagnoses of Cerebral infarction (stroke), Alzheimer's disease (a disease that causes progressive mental deterioration), Dementia (a disorder of the mental processes caused by brain disease or injury and marked by memory disorders, personality changes, and impaired reasoning), Anxiety disorder (more than temporary worry or fear), Type two diabetes mellitus (an impairment in the way the body regulates and uses sugar);
- An order, dated 10/18/18, for Risperdal 25 mg 1/2 tablet two times daily;
- An order, dated 8/12/20, for Tramadol (used for pain) 50 mg two times daily;
- An order, dated 4/4/19, for Cymbalta (used for depression) 30 mg one time daily.
Record review of the Consultant Pharmacist's Medication Regimen Review listing residents reviewed with no recommendations showed no reviews for the resident in August 2020, September 2020, December 2020, or June 2021. There are no GDR attempts for Risperdal, Tramadol, or Cymbalta for more than one year.
6. Record review of Resident #50's medical record showed:
- admitted on [DATE];
- The POS, dated 7/1/21 to 7/31/21, showed:
- Diagnoses of non-covid acute respiratory disease, anxiety (a feeling of worry, nervousness, or unease), dry eye syndrome (tears aren't able to provide adequate lubrication for your eye), pneumonia, (an infection that inflames the air sacs in one or both lungs), cognitive communication deficit (impairment of understanding);
- An order, dated 6/28/21, for Risperidone (an antipsychotic medication used to treat schizophrenia (a serious mental illness that affects how a person thinks, feels, and behaves), bipolar disorder (mental disorder that causes unusual shifts in mood) and depression (a serious medical illness that negatively affects how you feel, the way you think and how you act) 0.25 milligrams (mg) two times daily for pneumonia;
- An order, dated 6/28/21, for Imatinib Mesylate (a chemotherapy medication used to treat chronic myeloid leukemia) 100 mg two times daily for pneumonia, a diagnosis of pneumonia is not an indication for Imatinib Mesylate use.
Record review of the Consultant Pharmacist's Medication Regimen Review listing residents reviewed with no recommendations showed reviews for the resident in April 2021, May 2021 and June 2021 and showed Resident #50 not to be included in the July 2021 report and no written recommendations.
During an interview on 7/22/21 at 2:40 P.M., the DON said the Consultant Pharmacist reviews every resident's medication each month.
During an interview on 7/23/21 at 8:46 A.M., the Registered Pharmacist with the facility pharmacy said they contract the monthly reviews out to an outside consulting agency.
During an interview on 7/23/21 at 9:33 A.M., the Registered Pharmacist with the consulting agency said:
- The medications for Resident #50 would be reviewed during his/her next review;
- They use the primary diagnosis for some medications;
- They only send reports for psychotic medications, unless there is a problem with the stop date on them, lab work that needs to be done, sometimes there is a delay, we make recommendations if there is an abnormal lab result;
- Sometimes responses are delayed, if there isn't a response it is discussed with the DON.
7. Record review of resident #23's medical record showed:
- admitted on [DATE];
- The POS, dated 7/1/21 to 7/31/21, showed:
- Diagnoses of anxiety disorder (intense, excessive and persistent worry and fear about everyday situations), major depressive disorder-recurrent (long-term loss of pleasure or interest in life), major depressive disorder-recurrent-in partial remission (symptoms of a major depressive episode are present but full criteria are not met, or there is a period without any significant symptoms lasting less than 2 months following the end of the major depressive episode);
- An order, dated 6/6/17, for Seroquel (an antipsychotic medication that works by changing the actions of chemicals in the brain) 300 mg, give 1/2 tablet by mouth two times daily for major depressive disorder-recurrent.
Record review of the Consultant Pharmacist's Medication Regimen Review listing residents reviewed with no recommendations showed no reviews for Resident #23 in August 2020, and September 2020, a written recommendation on 10/23/20 to reduce quetiapine (generic name for Seroquel) 500 mg with a denial marked, not signed by the physician, and no review in December 2020.
During an interview on 7/27/21 at 3:03 P.M., the Director of Nursing said we send the psychiatrist the recommendation from the pharmacist and then we send the response from the psychiatrist to the pharmacist. The psychiatrist makes reductions when she agrees that they need to be made. They are documented in her notes. The pharmacist has access to our system so they can read notes.
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Medication Errors
(Tag F0758)
Could have caused harm · This affected 1 resident
Based on observation, record review and interview, the facility failed to ensure one resident (Resident #16) received a gradual dose reduction attempt at least annually. This failure had the potential...
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Based on observation, record review and interview, the facility failed to ensure one resident (Resident #16) received a gradual dose reduction attempt at least annually. This failure had the potential to keep any resident on a psychoactive medication from receiving the lowest possible dosage of medication due to not monitoring if a medication is treating the target symptom (or behavior). The facility's census was 44.
Record review of the facility's policy titled, Antipsychotic Medication Use, dated December 2016, showed:
- Antipsychotic medications may be considered for resident with dementia but only after medical, physical, functional, psychological, emotional psychiatric, social and environmental causes of behavioral symptoms have been identified and addressed;
- Antipsychotic medications will be prescribed at the lowest possible dosage for the shortest period of time and are subject to gradual dose reduction and re-review;
- Residents will only receive antipsychotic medications when necessary to treat specific conditions for which they are indicated and effective;
- The attending physician and other staff will gather and document information to clarify a resident's behavior, mood, function, medical condition, specific symptoms, and risks to the resident and others;
- The attending physician will identify, evaluate and document, with input from other disciplines and consultants as needed, symptoms that may warrant the use of antipsychotic medications;
- The attending physician and facility staff will identify acute psychiatric episodes, and will differentiate them from enduring psychiatric conditions;
- Residents who are admitted from the community or transferred from a hospital and who are already receiving antipsychotic medications will be evaluated for the appropriateness and indications for use;
- The interdisciplinary team will complete PASRR (preadmission screening for mentally ill and intellectually disabled individuals), if appropriate, re-evaluate the use of antipsychotic medication at the time of admission and/or within two weeks (at the initial MDS assessment) to consider whether or not the medication can be reduced, tapered, or discontinued, based on assessing the resident's symptoms and overall situation, the physician will determine whether to continue, adjust, or stop existing antipsychotic medication;
- Diagnosis of a specific condition for which antipsychotic medications are necessary to treat will be based on a comprehensive assessment of the resident;
- Antipsychotic medications shall generally be used only for the following conditions/diagnoses as documented in the record, consistent with the definition(s) in the Diagnostic and Statistical Manual of Mental Disorders (current or subsequent editions): Schizophrenia, Schizo-affective disorder, Schizophrenia disorder, Delusional disorder, Mood disorders (bipolar disorder, depression with psychotic features, and refractory major depression), Psychosis in the absence of dementia, Medical illnesses with psychotic symptoms and/or treatment-related psychosis or mania (e.g. high-dose steroids), Tourette's disorder, Huntington disease, Hiccups (not induced by other medications), or Nausea and vomiting associate with cancer or chemotherapy;
- Diagnoses alone do not warrant the use of antipsychotic medication. In addition to the above criteria, antipsychotic medications will generally only be considered if the following conditions are also met: The behavioral symptoms present a danger to the resident or others AND the symptoms are identified as being due to mania or psychosis (such as auditory, visual, or other hallucinations, delusions, paranoia or grandiosity, or behavioral interventions have been attempted and included in the plan of care, except in an emergency;
- Antipsychotic mediation will not be used if the only symptoms are one or more of the following: wandering, poor self-care, restlessness, impaired memory, mild anxiety, insomnia, inattention or indifference to surroundings, sadness or crying alone that is not related to depression or other psychiatric disorders, fidgeting, nervousness or uncooperativeness;
- The staff will observe, document, and report to the attending physician information regarding the effectiveness of any interventions, including antipsychotic medications;
- The physician shall respond appropriately by changing or stopping problematic does or medications, or clearly documenting (based on assessing the situation) why the benefits of the medication outweigh the risks or suspected or confirmed adverse consequences.
Record review of Resident #16's medical record showed an admission date of 4/27/18.
The Physician's Order Sheet (POS), dated 7/1/21 - 7/31/21, showed:
- Diagnoses included Cerebral infarction (stroke), Alzheimer's disease (a disease that causes progressive mental deterioration), Dementia (a disorder of the mental processes caused by brain disease or injury and marked by memory disorders, personality changes, and impaired reasoning), Anxiety disorder (more than temporary worry or fear), Type two diabetes mellitus (an impairment in the way the body regulates and uses sugar);
- An order for Risperdal (antipsychotic) 25 mg 1/2 tablet two times daily dated10/18/18;
- An order for Tramadol (narcotic, works by changing the way the brain and nervous system respond to pain) 50 mg two times daily, dated 8/12/20;
- An order for Cymbalta (used for depression) 30 mg one time daily, dated 4/4/19.
Observations showed:
- On 7/20/21 at 12:42 P.M., Resident #16 to be calm, to sit in wheelchair at the dining room table, voicing that his/her legs hurt;
- On 7/21/21 at 10:22 A.M., the resident to be lying in bed, calm, eyes closed;
- On 7/22/21 at 8:55 A.M., the resident to be lying in bed, calm, eyes closed;
- On 7/27/21 at 8:47 A.M., the resident to be eating breakfast, calm.
Record review of the resident's Annual Minimum Data Set (MDS-a federally mandated assessment, required to be completed by the facility), dated 5/6/21, showed Resident #16 with a diagnoses of Alzheimer's disease (progressive mental deterioration), Dementia (disorder marked by memory disorders, personality changes, and impaired reasoning, Anxiety (persistent worry and fear about everyday situations), and Psychotic disorder (a disconnection from reality), to be moderately cognitively impaired, no mood disorders and no behaviors.
Record review of the resident's Medication Administration Record (MAR), dated 7/1/21 through 7/27/21, showed Risperdal, Tramadol and Cymbalta administered as ordered.
Record review of the Consultant Pharmacist's Medication Regimen Review listing residents reviewed with no recommendations showed no GDR attempts for Risperdal, Tramadol, or Cymbalta for more than one year.
Record review of the progress notes provided by the facility staff showed no GDR attempts for the Risperdal, Tramadol or Cymbalta. There were no notes addressing any previous GDR attempts and no reasoning to indicate why a GDR would not be advised.
CONCERN
(E)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0624
(Tag F0624)
Could have caused harm · This affected multiple residents
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to document preparation and orientation for transfer to the hospital f...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to document preparation and orientation for transfer to the hospital for five residents (Resident #11, #16, #21, #34, and #37) out of 13 sampled residents and one resident (Resident #17) out of two sampled closed records. The facility's census was 44.
1. Record review of Resident #11's progress notes showed:
- The resident transferred to the hospital on 6/5/21 and readmitted to the facility on the same day;
- The resident transferred to the hospital on 6/8/21 and readmitted to the facility on [DATE].
Record review of the resident's medical record did not contain documentation which showed the resident was prepped and oriented for transfers out of the facility.
2. Record review of Resident #16's progress notes showed the resident transferred to the hospital on 2/11/21 and readmitted to the facility on [DATE].
Record review of the resident's medical record did not show documentation which showed the resident was prepared and oriented for transfer out of the facility.
3. Record review of Resident #17's progress notes showed:
- The resident transferred to the hospital on 4/19/21 and readmitted to the facility on [DATE];
- The resident transferred to the hospital on 7/4/21 and remained in the hospital on 7/28/21.
Record review of the resident's medical record did not contain documentation which showed the resident was prepped and oriented for transfers out of the facility.
4. Record review of Resident #21's progress notes showed:
- The resident transferred to a hospital on 4/10/21 and readmitted to the facility on [DATE];
- The resident transferred to a hospital on 6/7/21 and readmitted to the facility on the same day;
- The resident transferred to a hospital on 6/16/21 and readmitted to the facility on the same day.
Record review of the resident's medical record did not show documentation which showed the resident was prepared and oriented for transfers out of the facility.
5. Record review of Resident #34's progress notes showed:
- The resident was transferred to the hospital on 3/9/21 and readmitted to the facility on [DATE];
- The resident was transferred to the hospital on 5/30/21 and readmitted to the facility on [DATE];
- The resident was transferred to the hospital on 7/7/21 and readmitted the same day.
Record review of the resident's medical record did not contain documentation which showed the resident was prepped and oriented for transfers out of the facility.
6. Record review of Resident #37's progress notes showed the resident was transferred to the hospital on 1/22/21 and readmitted to the facility on [DATE].
Record review of the resident's medical record did not contain documentation which showed the resident was prepped and oriented for transfer out of the facility.
7. During an interview on 7/27/21 at 3:03 P.M., the Assistant Administrator said he wasn't sure he would use the word oriented, but would expect that they would be informed. He understands it should be documented.
8. The facility did not provide a policy for preparation and orientation of the resident for transfer out of the facility.
CONCERN
(E)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0625
(Tag F0625)
Could have caused harm · This affected multiple residents
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to inform the resident and/or resident's representative of their bed h...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to inform the resident and/or resident's representative of their bed hold policy at the time of transfer to the hospital for five residents (Resident #11, #16, #21, #34, and #37) out of 13 sampled residents and one resident (Resident #17) out of two sampled closed records. The facility's census was 44.
1. Record review of the facility's policy titled, Bed-Holds and Returns, dated March 2017, showed:
- Prior to transfer and therapeutic leaves, residents or resident representatives will be informed in writing of the bed-hold and return policy;
- Prior to a transfer, written information will be given to the residents and the resident representatives that explains in detail the rights and limitation of the resident regarding bed-holds; the reserve bed payment policy as indicated by the state plan (Medicaid residents); the facility per diem rate required to hold a bed (non-Medicaid residents), or to hold a bed beyond the state bed-hold period (Medicaid residents);
- The resident will be permitted to return to an available bed in the location of the facility that he or she previously resided. If there is not an available bed in that part, the resident will be given the option to take an available bed in another distinct part of the facility and return to the previous distinct part when a bed becomes available.
2. Record review of Resident #11's medical record showed:
- The resident transferred to the hospital on 6/5/21 and readmitted to the facility on the same day;
- The resident transferred to the hospital on 6/8/21 and readmitted to the facility on [DATE];
- The facility did not provide documentation of the bed-hold notice to the resident or the resident's representative.
3. Record review of Resident #16's medical record showed:
- The resident transferred to the hospital on 2/11/21 and readmitted to the facility on [DATE].
- The facility did not provide documentation of the bed-hold notice to the resident or the resident's representative.
4. Record review of Resident #17's medical record showed:
- The resident transferred to the hospital on 4/19/21 and readmitted to the facility on [DATE];
- The resident transferred to the hospital on 7/4/21 and remained in the hospital on 7/28/21;
- The facility did not provide documentation of the bed-hold notice to the resident or the resident's representative.
5. Record review of Resident #21's medical record showed:
- The resident to have a responsible party;
- The resident transferred to a hospital on 4/10/21 and readmitted to the facility on [DATE];
- The resident transferred to a hospital on 6/7/21 and readmitted to the facility on the same day;
- The resident transferred to a hospital on 6/16/21 and readmitted to the facility on the same day;
- The facility did not provide documentation of the bed-hold notice to the resident or the resident's representative.
6. Record review of Resident #34's medical record showed:
- The resident transferred to the hospital on 3/9/21 and readmitted to the facility on [DATE];
- The resident transferred to the hospital on 5/30/21 and readmitted to the facility on [DATE];
- The resident transferred to the hospital on 7/7/21 and readmitted on the same day;
- The facility did not provide documentation of the bed-hold notice to the resident or the resident's representative.
7. Record review of Resident #37's medical record showed:
- The resident transferred to the hospital on 1/22/21 and readmitted to the facility on [DATE];
- The facility did not provide documentation of the bed-hold notice to the resident or the resident's representative.
8. During an interview on 7/27/21 at 3:03 P.M., the Assistant Administrator said he would expect the bed hold policy to be provided to the resident or the responsible party when they are transferred.
CONCERN
(E)
Potential for Harm - no one hurt, but risky conditions existed
Assessment Accuracy
(Tag F0641)
Could have caused harm · This affected multiple residents
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to accurately assess and document on the Minimum Data Se...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to accurately assess and document on the Minimum Data Sets (MDS; a federally mandated assessment instrument required to be completed by the facility's staff) for five residents (#6, #11, #34, #37 and #50) during the time of the individual assessments. The facility's census was 44.
1. The facility did not provide a policy for accurate MDS completion.
2. Record review of Resident #6's medical record showed:
- The resident admitted on [DATE];
- Diagnoses of acute respiratory disease (a sudden condition in which breathing is difficult and the oxygen levels in the blood abruptly drop lower than normal), contracture (shortening and hardening of muscles, tendons, or other tissue, often leading to deformity and rigidity of joints), cerebral palsy (a condition marked by impaired muscle and/or other disabilities, typically caused by damage to the brain before or at birth), and urinary tract infection (UTI; an infection in the urinary system).
Record review of the resident's monthly weights showed:
- admission weight on 11/18/16 to be 234 pounds (lbs);
- 1/27/21 to be 244 lbs;
- 2/25/21 to be 245 lbs;
- 3/31/21 to be 242 lbs;
- 4/2/21 to be 244 lbs;
- 5/3/21 to be 245 lbs;
- 6/27/21 to be 248 lbs;
- No weight recorded for July, 2021.
Record review of the resident's medical record showed no documentation of UTI in 2021.
Record review of the resident's MDSs showed the last three assessments included a quarterly dated 10/23/20, an annual dated 1/21/21 and another quarterly on 4/23/21. Those MDSs showed:
- Section G- Functional Status as total dependence with assistance of one for all personal hygiene including oral care;
- Section I2300- Active Diagnoses indicated an active diagnosis of an UTI on the 1/21/21 and 4/23/21 MDS;
- Section K0300- Nutritional Status indicated significant weight loss, current weight on 10/23/20 was 240 lbs. On 1/21/21 and 4/23/21 the resident's current weight was 244 lbs.;
- Section L0200- Oral/Dental Status indicated no dental concerns on 10/23/20 and 4/23/21, and inflamed, bleeding gums or loose natural teeth on 1/21/21.
Observations and interviews showed:
- On 7/20/21 at 12:09 P.M., the resident in bed with head of bed up, feeding self, teeth covered with brown tinged scum and brown in color, gums red and inflamed;
- On 7/21/21 at 10:20 A.M., on 7/22/21 at 8:45 A.M., on 7/23/21 at 10:04 A.M., and on 7/27/21 at 8:38 A.M., the resident in bed with head of bed up, teeth covered with brown tinged scum and brown in color, gums red and inflamed;
- During interviews on each occasion the resident said the staff did not provide oral care.
During an interview on 7/23/21 at 10:50 A.M., the Director of Nursing (DON) said Resident #6 has not had a UTI since 2018 as far as she knows.
2. Record review of Resident #11's progress notes showed:
- On 2/10/21, resident ambulating in dayroom, reports that he/she became dizzy and fell. Complaint of (C/O) back pain. Dime sized abrasion to right knee, bruising noted to right knee;
- On 2/23/21, resident yelling in room, found on the floor in bathroom. No injuries noted.
Record review of the resident's quarterly MDS, dated [DATE], Section J1800-Health Conditions-Falls showed no falls.
3. Record review of Resident #34's progress notes showed on 3/9/21 at 6:01 A.M. loud crash heard and resident moaning. Upon further investigation, it was noted that resident was sitting on floor in front of bed. Resident stated that he/she was attempting to get up and sit in his/her chair. Resident stated that he/she wanted to go to the hospital. Resident denies pain at this time, but does state mild discomfort to right knee. Emergency Medical Services (EMS) contacted and advised that paramedics were in route.
Record review of the resident's quarterly MDS, dated [DATE], Section J1800 showed no falls.
4. Record review of Resident #37's progress notes showed on 1/22/21 at 9:26 A.M., Certified Nurse Aide (CNA) reported resident had fallen in shower, nurse entered shower and found resident lying supine on back of the head with blood coming out. Resident stated the shower chair. Call out to EMS and in route to nearest hospital.
Record review of the resident's quarterly MDS, dated [DATE], Section J1800 showed no falls.
5. Record review of Resident #50's medical record showed:
- admitted on [DATE];
- Diagnoses of non-Covid (not Covid-19 virus related) acute respiratory disease (an infection of the lungs that interferes with breathing), anxiety (a feeling of worry, nervousness, or unease), dry eye syndrome (tears aren't able to provide adequate lubrication for your eye), pneumonia, (an infection that inflames the air sacs in one or both lungs), cognitive communication deficit (impairment of understanding);
- The Physician's Order Sheet (POS), dated 7/1/21 to 7/31/21, showed an order dated 6/28/21 for Imatinib Mesylate Oral Tablet (a medication used to treat chronic myeloid leukemia, cancer of the blood) 100 milligrams, two tablets by mouth daily.
Record review of the resident's MDSs showed:
- admission MDS, dated [DATE], section I0100 showed no diagnosis of cancer, section O0100 showed no chemotherapy agents,
- Quarterly MDS, dated [DATE], section I0100 showed no diagnosis of cancer, section O0100 showed no chemotherapy agents.
During an interview on 7/20/21 at 12:21 P.M., the resident said he/she is supposed to be getting medicine for his/her blood cancer and the facility didn't get it. He/she missed an appointment on 4/14/21 to have the grant that pays for his/her medicine continued and now the facility doesn't have it.
During an interview on 7/22/21 at 9:52 A.M., the nurse at the physician's office which treats the resident's cancer said the resident did miss an appointment but that is not why the medication was not continued. The medication has been provided through a grant for about a year and the facility must communicate with the grantor to continue receiving the medication. The resident has a diagnosis of chronic myeloid leukemia.
6. During an interview:
- On 7/23/21 at 10:50 A.M. the DON said she would expect the MDS assessment to be completed accurately;
- On 7/27/21 at 3:03 P.M. the DON said not only should the MDS be completed accurately, but care areas that no longer apply to be removed.
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 interview and record review, the facility failed to develop and implement an individualized comprehensive care plan for...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to develop and implement an individualized comprehensive care plan for 11 residents (Resident #6, #11, #14, #16, #18, #21, #34, #45, #46, #50, and #202) out of 13 sampled residents and one resident (Resident #17) out of two sampled closed records. The facility's census was 44.
1. Record review of Resident #6's Physician's Order Set (POS), dated 7/1/21 - 7/31/21, showed:
- Diagnoses of cerebral palsy (a condition marked by impaired muscle coordination and/or other disabilities, typically caused by damage to the brain before or at birth) and contracture (a permanent tightening of the muscles, tendons, skin, and nearby tissues that causes the joints to shorten and become very stiff).
Record review of the resident's annual Minimum Data Sheet (MDS; a federally mandated assessment instrument required to be completed by facility staff), dated 1/21/21, showed:
- Section G-Functional Status (assess the need for assistance with activites of daily living ADLs): the resident to require total assistance of one for all personal care;
- Section H-Bladder and Bowel (assess for incontinence or at risk for developing incontinence): the resident to be always incontinent of bowel and bladder.
Record review of the resident's Quarterly MDS, dated [DATE], showed:
- Section G: the resident requires total assistance of one for all personal care;
- Section H: the resident always incontinent of bowel and bladder.
Record review of the resident's comprehensive care plan, last reviewed 7/21/21, showed the care plan did not address the need for assistance with ADLs or personal care.
2. Record review of Resident #11's POS, dated 7/1/21 - 7/31/21, showed:
- Diagnoses of bipolar disorder (a disorder associated with episodes of mood swings ranging from depressive lows to manic highs), major depressive disorder (a persistent feeling of sadness and loss of interest, affects how you feel, think and behave), generalized anxiety disorder (severe, ongoing anxiety that interferes with daily activities);
- Celexa (antidepressant medication) 40 mg (milligram) 1 tablet by mouth every day;
- Venlafaxine HCL (hydrogen chloride) ER (extended-release) (an antidepressant medication) 150 mg 1 tablet by mouth every day;
- Zyprexa (an antipsychotic medication for bipolar disorder) 7.5 mg 1 tablet by mouth every day.
Record review of the resident's comprehensive care plan, dated 6/6/21, showed the care plan did not address the black box warning (alert the public and health care providers to serious side effects of the medication, such as injury or death) for the medications, Celexa, Venlafaxine HCL ER, or Zyprexa.
3. Record review of Resident #14's POS, dated 7/1/21 - 7/31/21, showed:
- Diagnoses of dementia (chronic or persistent disorder of the mental processes caused by brain disease or injury and marked by memory disorders, personality changes, and impaired reasoning) with behavioral disturbances, major depressive disorder;
- Quetiapine Fumarate (an antipsychotic medication) 50 mg take 1 tablet by mouth once daily;
- Risperdal (an antipsychotic medication) 0.5 mg give 1 tablet by mouth at bedtime (HS);
- Zoloft (an antidepressant medication) 50 mg give 1 tablet by mouth daily in morning(AM).
Record review of the resident's comprehensive care plan, dated 7/12/21, showed:
- The care plan did not address the black box warning for the medications, Quetiapine fumarate, Risperdal, or Zoloft;
- The care plan did not address the resident's depression.
4. Record review of Resident #16's POS, dated 7/1/21 - 7/31/21, showed:
- Diagnoses of Alzheimer's disease (a disease that causes progressive mental deterioration), dementia, anxiety disorder (Intense, excessive, and persistent worry and fear about everyday situations), Type two diabetes mellitus (an impairment in the way the body regulates and uses sugar);
- An order, dated 2/17/21, for Novolog (a medication used for diabetes) three times a day, dosed according to blood sugar scale;
- An order, dated 2/15/21, for Glucagon (a medication used to raise blood sugar) emergency injection one mg intramuscular (injected into a muscle) as needed;
- An order, dated 10/18/18, for Risperdal 25 mg 1/2 tablet two times daily;
- An order, dated 8/12/20, for Tramadol (pain medication) 50 mg two times daily;
- An order, dated 4/4/19, for Cymbalta (an antidepressant medication) 30 mg one time daily.
Record review of the resident's comprehensive care plan, last reviewed 5/19/21, showed:
- The care plan did not address the resident's Type two diabetes;
- The care plan did not address the resident's anxiety;
- The care plan did not address the black box warning for the medications, Risperdal, Tramadol or Cymbalta.
5. Record review of Resident #17's progress notes, dated 3/26/21, showed:
- The resident admitted to the facility on [DATE] with Gastrostomy (G-tube; a tube placed in the stomach for nutrition and medication administration) in place. G-tube site covered with a dry dressing with scant blood noted;
- Dialysis (a process of purifying the blood of a person whose kidneys are not working normally) on Tuesday, Thursday, and Saturday, on nephro (nutritional supplement) 55 milliliters (ml) per hour, flush 100 ml every six hours, dialysis port (device used to acess the blood during dialysis) to the right side, clear dressing in place, no drainage or redness noted.
Record review of the resident's POS, dated 7/1/21 through 7/31/21, showed:
- An order, dated 4/11/21, for gauze dressing pad four inches (in) by four in. Cleanse G-tube site with soap and water, apply dry dressing change once weekly, daily every one day(s);
- An order, dated 4/11/21, check G-tube placement prior to each medication administration four times daily;
- An order, dated 6/6/21, for Glucerna (nutritional supplement) 1.5 cal oral/liquid tube feeding at 60 cubic centimeters (cc) per hour continuous. Pump may use auto flush set at 100 cc of water (H2O) every six hours three times daily (TID);
- An order, dated 3/26/21, for Eliquis (an anticoagulant medication) 2.5 milligram (mg) via G-tube twice daily (BID) for diagnosis of presence of cardiac pacemaker;
- No orders for dialysis care.
Record review of the resident's comprehensive care plan, dated 5/19/21, showed the plan did not address the care for G-tube, anticoagulant use, or dialysis.
6. Record review of Resident #18's POS, dated 7/1/21 through 7/31/21, showed:
- Diagnoses included novel coronavirus (2019-nCoV; highly contagious respiratory disease) acute respiratory disease, rash and other nonspecific skin eruption, shortness of breath, other sites of candidiasis (yeast infection), candidiasis of skin and nail;
- Ipratropium-Albuterol Inhalation Solution 0.5-2.3 (3) mg/3 ml four times a day as needed for shortness of breath (order start date 6/6/2018);
- Lotrimin AF External Cream 1%. Cleanse back with soap and water, pat dry, apply cream three times a day (for rash and other nonspecific skin eruption) (order start date 4/20/2021);
- Nystop External Powder 100000 unit/gram. Wash under bilateral breast and axilla with soap and water, pat dry and apply power generously to side as needed (Other sites of candidiasis) (Order start date 10/23/2020).
Record review of the resident's comprehensive care plan, dated 5/12/21, showed:
- The care plan did not address the shortness of breath;
- The care plan did not address the rash and other nonspecific skin eruption;
- The care plan did not address the other sites of candidiasis.
7. Record review of Resident #21's medical record showed:
- admitted [DATE];
- POS, dated 7/1/21 through 7/31/21, showed:
- Diagnoses included acute respiratory disease (a sudden condition that makes breathing difficult), muscle weakness, hemiplegia following cerebral infarction (stroke with paralysis on one side), seizures (a burst of uncontrolled electrical activity between brain cells that causes temporary abnormalities in muscle tone or movements like stiffness, twitching or limpness, behaviors, sensations or states of awareness), chronic pain (long-term pain), hypertension (high blood pressure), major depressive disorder (overwhelming sadness);
- An order, dated 10/19/18, for a regular diet;
- An order, dated 6/6/21, for Jevity 1.5 (a nutritional supplement), to run at 55 ml/per hour between 5:00 P.M. and 6:00 A.M., (total of 13 hours at 55 ml/hr =715 ml of feeding) then off, flush at 150 ml every four hours (total of 487 ml of water flush), hold feeding if able to aspirate stomach contents greater than 60 ml during feeding;
- No order for G-tube and the care or maintenance of the G-tube.
Observations showed:
- On 7/23/21 at 10:02 A.M., resident to lay in bed;
- A mechanical feeding pump with tubing connected to the resident's G-tube;
- The pump not turned on;
- A 1000 ml bottle of Jevity 1.5 hung on a pole and attached into the pump;
- The bottle of Jevity dated dated 7/22/21 5:00 P.M.;
- 400 ml of the Jevity feeding remained in the bottle (based on the rate of the feeding and the time alloted to run the feeding, there should have been 245 ml remaining);
- A 1000 ml bag for water flush hung on the pole;
- A total of 600 ml remained in the bag and the bag not dated.
Observations showed:
- On 7/27/21 at 8:40 A.M. showed resident to lay in bed;
- The mechanical feeding pump tubing not be connected to G-tube;
- The feeding pump not turned on;
- A 1000 ml bottle of Jevity attached to the feeding pump with 1000 ml fluid present, dated 7/26/21 at 4:15 P.M.;
- A 1000 ml bag of fluid hung with 1000 ml fluid present, dated 7/26/21.
During an interview on 7/22/21 at 2:40 P.M., the Director of Nursing (DON) said resident #21 had a G-tube inserted during a hospital stay in April, 2021, the resident had been alert and oriented, experienced multiple seizures, was hospitalized and returned to the facility on 4/19/21 with a G-tube in place.
Record review of the resident's comprehensive care plan, last reviewed 5/19/21, showed the care plan did not address the G-tube feeding, care, or maintenance.
8. Record review of Resident #34's POS, dated 7/1/21 - 7/31/21, showed:
- Diagnoses of shortness of breath, chronic obstructive pulmonary disease (COPD; a group of lung diseases that block airflow and make it difficult to breathe), and major depressive disorder, generalized anxiety disorder;
- Escitalopram Oxalate (an antidepressant medication for major depressive disorder) 10 mg 1 tab by mouth every day.
Record review of the resident's comprehensive care plan, dated 3/3/21, showed:
- The care plan did not address the black box warning for the medication Escitalopram oxalate;
- The care plan did not address the resident's depression.
9. Record review of Resident #45's POS, dated 7/1/21 through 7/31/21, showed:
-Diagnoses of dysuria (painful or difficult urination), neuromuscular dysfunction of bladder unspecified (bladder dysfunction caused by neurologic damage), hematuria (blood in urine), unspecified abnormalities of gait and mobility, constipation, enlarged prostate without lower urinary tract symptoms, iron deficiency anemia (low iron in blood), hypokalemia (low potassium), essential hypertension, acute kidney failure (kidneys unable to filter waste from the blood), urinary tract infection (infection of the urinary system), unspecified viral hepatitis C (infection caused by a virus that attacks the liver and leads to inflammation) without hepatic coma, acute tubule-interstitial nephritis (inflammation of the tubules of the kidneys), unspecified dementia without behavioral disturbance, metabolic encephalopathy (problem in the brain caused by a chemical imbalance in the blood), severe sepsis with septic shock (widespread infection causing organ failure and dangerously low blood pressure), abnormal weight loss, non-pressure chronic ulcer unspecified part of unspecified lower leg with unspecified severity, other seizures (sudden uncontrolled electrical disturbance in the brain), venous insufficiency (improper functioning of the vein valves in the leg causing swelling and skin changes), unspecified abdominal pain, dementia in other disease classified elsewhere without behavioral disturbances;
-Keppra oral table 500 mg 1 tab by mouth twice daily (for seizures) (order started 4/14/21);
-Namenda oral table 10 mg 1 tab by mouth twice daily (for dementia) (order started 9/24/20);
-Tylenol oral tablet 325 mg 2 tabs by mouth every 6 hours as needed for pain (order started 5/4/20).
Record review of the resident's comprehensive care plan, dated 7/5/2021, showed the care plan did not address the resident's seizures, dementia, pain, and the viral hepatitis C.
10. Record review of Resident #46's POS, dated 7/1/21 through 7/31/21, showed:
- Diagnoses of 2019-nCoV acute respiratory disease, essential hypertension, type 2 diabetes mellitus with hyperglycemia, heart failure, cerebral infarction, unspecified dementia without behavioral disturbance, major depressive disorder, undifferentiated schizophrenia (disorder that affects a person's ability to think, feel or behave clearly), chronic obstructive pulmonary disease (COPD), pain in unspecified joint, pseudobulbar affect (inappropriate laughing or crying due to a nervous system disorder), abnormal weight loss, Parkinson's disease (disease of the central nervous system that affects movement, often including tremors), aphasia (loss of ability to understand or express speech caused by brain damage), hyperlipidemia (high cholesterol), constipation, hyperkalemia (high potassium), pressure ulcer of other site stage 2, and pressure ulcer other site unspecified stage;
- Hydrocodone-Acetaminophen (pain medication) oral tablet 5-325 mg 1 tab per G-tube- 2 tabs max daily- four times a day (for pain) (order start date 3/10/21);
- Remeron SolTab (an antidepressant medication) oral tablet disintegrating 15 mg 1 tab per G-tube at bedtime (for dementia) (order start date 6/30/21);
- Seroquel (an antipsychotic medication) oral tablet 25 mg take 1 tab by mouth at 6 P.M. daily per G-Tube (for schizophrenia) (order start date 3/31/20);
- Valproic Acid 250 mg/5 Ml Solution give 15 Ml via G-tube twice daily (for schizophrenia) (order start date 5/17/17);
- Labs: Depakote level, complete metabolic panel, complete blood count, lipid panel, hemoglobin A1c, thyroid stimulating hormone, free thyroxine, and folic acid yearly.
Record review of the resident's comprehensive care plan, dated 4/6/21, showed:
- The care plan did not address the resident's depression, schizophrenia, diabetes mellitus;
- The care plan for pain showed: Medication as ordered Fentanyl Patches (pain patch) (dated 3/24/19) (Resident is not on Fentanyl Patches and takes hydrocodone for pain);
- The care plan addressed anxiety (Resident has no diagnosis for anxiety).
11. Record review of Resident #50's medical record showed:
- admitted on [DATE];
- POS, dated 7/1/21 through 7/31/21, showed:
- Diagnoses of non-Covid (not Covid-19 virus related) acute respiratory disease (an infection of the lungs that interferes with breathing), anxiety disorder (excessive and persistent worry and fear about everyday situations), dry eye syndrome (tears do not provide adequate moisture), pneumonia (an infection of the lungs), cognitive communication deficit (difficulty using spoken languages);
- An order, dated 6/28/21, for Imatinib mesylate (a chemotherapy medication used to treat chronic myeloid leukemia) 100 milligrams (mg) two tablets daily to be given for a diagnosis of pneumonia.
Record review of the medication administration record (MAR), dated July 2021, showed Imatinib Mesylate to be given daily 7/1/21 through 7/11/21, unavailable in the facility 7/12/21 - 7/15/21, given on 7/16/21, unavailable in the facility 7/17/21 through 7/20/21.
During an interview on 7/22/21 at 9:52 A.M., the resident's oncologist's medical assistant (MA) said the resident has a diagnosis of chronic myeloid leukemia.
Record review of the resident's comprehensive care plan, last reviewed on 7/22/21, showed the care plan did not address the resident's cancer or chemotherapy treatment.
12. Record review of Resident #202's progress notes showed:
- On 7/13/21 at 12:42 A.M., resident observed on floor in dining hall after laying flat in w/c. Resident unable to state whether he/she hit his/her head. No trauma, redness, swelling observed;
- On 7/16/21 at 4:30 P.M. resident was sitting across from the nursing station when he decided to throw himself/herself out of his/her chair according to several staff members. Resident has a small hematoma above the right eyebrow. He/she also has a resolving hematoma to the left forehead. Resident denies having any pain.
Record review of the resident's comprehensive care plan, dated 7/21/21, showed the care plan did not address falls.
13. During an interview on 7/23/21 at 10:50 A.M., the Director of Nursing (DON) said if a resident has a G-tube, there should be a care plan. She would expect a resident with a fall to have a care plan with interventions.
During an interview on 7/27/21 at 3:03 P.M., the DON said she would expect there to be a care plan for antipsychotics and antidepressants. When asked if she would expect there to be a care plan for cellulitis, she said if it is short term, that may not be needed, just because there is an order for treatment doesn't mean it would be on the care plan. If it is long term with a wound or several months, there should be a care plan. When asked if she would expect there to be a care plan for seizures, she said just because they have a diagnosis for seizures doesn't mean they need a care plan for seizures. If we are dealing with breakthrough seizures, yes, but they wouldn't need one just because they are on medication. A care plan should reflect how you are going to care for the patient. If they have been on medication for a long period of time and the condition is under control, She said she wouldn't do a care plan. Not all diagnoses need interventions. She would expect a care plan to be updated each time there is a seizure.
CONCERN
(E)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0657
(Tag F0657)
Could have caused harm · This affected multiple residents
Based on observation, interview, and record review, the facility failed to revise and update comprehensive care plans with specific interventions to meet the individual needs of seven residents (Resid...
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Based on observation, interview, and record review, the facility failed to revise and update comprehensive care plans with specific interventions to meet the individual needs of seven residents (Resident #11, #16, #20, #21, #34, #37, and #46) and failed to invite two residents (#23 and #34) to participate in the care planning process out of 13 sampled residents. The facility's census was 44.
1. Record review of the facility's policy titled, Change in a Resident's Condition or Status, dated December 2016, showed a significant change of condition is a major decline or improvement in the resident's status that requires interdisciplinary review and/or revision to the care plan.
The facility did not provide a policy for updating care plans.
2. Observation of Resident #11 on 7/20/21, 7/21/21, 7/22/21, and 7/23/21 showed the resident in wheelchair to propel his/herself around facility.
During an interview on 7/217/21 at 8:42 A.M., the resident said he/she can't use a 4-wheel roller walker. The resident fell backward with it and can't have it anymore. Therapy has to get him/her a new walker.
Record review of the resident's progress notes dated 6/10/21 showed the nurse reminded the resident to use wheelchair for ambulation.
Record review of the resident's comprehensive care plan, dated 6/6/21, showed:
- I use a walker for ambulation - I am at risk for falls - updated 6/5/21 trip and fall with head injury;
- Interventions - make sure I do not forget my walker, remind resident to stand for a few seconds;
- No interventions for resident to use wheelchair.
The facility did not update the care plan with new interventions to use wheelchair for ambulation.
3. During an interview on 7/20/21 at 1:15 P.M., Resident #16 said his/her legs hurt and he/she can't walk. The facility staff give him/her pain medicine.
Record review of the resident's Physician's Order Sheets (POS), dated 7/1/21 - 7/31/21, showed an order for Tramadol (a medication used to treat pain) 50 mg by mouth two times a day.
Record review of the resident's nurse progress notes showed a note, dated 6/2/21, the resident to be found kneeling down on floor, resident stated I was trying to get her glasses, resident denies any pain nor discomfort and refused care. Call being placed to physician, continue monitoring.
Record review of the resident's comprehensive care plan, last reviewed 5/19/21, showed:
- Acute and Chronic Pain, onset 5/17/18;
- No new interventions after 5/17/18;
- I am at risk for falls, onset 5/17/18;
- No new interventions after 5/17/18.
The facility did not update the care plan with new interventions for pain control and falls.
4. Record review of Resident #20's progress notes showed:
- On 6/8/21, Stage II pressure ulcer noted to coccyx;
- Medical Director (MD) aware, new order noted;
- The pressure ulcer measured 2 centimeters (cm) x 4 cm x 0.2 cm.
Record review of the resident's POS, dated 7/1/21 through 7/31/21, showed:
- Order started 5/9/21 and discontinued 6/7/21, Collagen Matrix (dressing which stimulate new tissue growth) 2x2 pad. Cleanse open area to left gluteal fold with normal saline (NS), apply collagen pad and gauze, change daily;
- Order started 6/9/21 and discontinued 6/30/21, Collagen Matrix 4x4. Cleanse open area to coccyx with NS, apply collagen dressing, cover with border gauze, change daily;
- Order started 7/1/21 and discontinued 7/15/21, Collagen Matrix 2x2. Cleanse open areas to right and left gluteal fold with NS, apply Collagen pad and cover with gauze, change daily;
- Order started 7/16/21, Collage Matrix 2x2. Cleanse open areas to right gluteal fold with NS, apply collagen pad and cover with gauze, change daily.
Record review of resident's comprehensive care plan, last reviewed 5/17/21, showed:
-Two at high risk for impaired skin integrity care plan areas;
-High risk for impaired skin integrity onset dated 3/18/18 with interventions dated the same;
-High risk for skin breakdown onset dated 11/06/18 with last intervention dated 2/21/20;
-No new interventions for newly developed or healed pressure ulcers.
5. Record review of Resident #21's progress notes showed:
- On 5/12/21, Resident found lying on floor next to bed, resident unable to state cause of fall. Resident very combative with staff in trying to assist back to bed, resident denies any pain or discomfort, call being placed to physician exchange, Power of Attorney (POA) will be notified, call light in reach of patient, resident refused vital signs (VS);
- On 5/13/21, CNA notified this nurse patient was laying on the floor next to the bed. On assessment no apparent injuries noted, range of motion within normal limits (ROM WNL), no bruises or bleeding noted. Resident assisted back to bed with five assistance. Resident combative. Bed low and locked with call light in reach. Staff asked to do frequent checks for safety. MD and family notified. VS refused, unable to assess neuro checks. Resident combative and uncooperative.
Observations showed:
- On 7/20/21 at 12:40 P.M., the resident to lay in bed, gastric tube (G-tube; a tube inserted through the wall of the abdomen directly into the stomach used to give drugs and liquids, including liquid food) in place;
- On 7/21/21 at 10;18 A.M., the resident to lay in bed, G-tube connected to feeding, pump not running;
- On 7/22/21 at 8:56 A.M., the resident to lay in bed, G-tube in place;
Record review of the resident's comprehensive care plan, last reviewed 5/19/21, showed:
- I am at risk for falls, onset 11/29/16;
- No new interventions after 11/29/16.
- History of confrontations and repetitive bizarre stories believe that my nails can grow mushrooms if I plant my nail clippings, onset 2/28/20;
- No new interventions after 2/28/20;
- Regular diet, onset 3/24/19;
- No new interventions after 3/24/19;
- Therapeutic diet related to diabetes mellitus (a disease in which the body's ability to produce or respond to the hormone insulin is impaired, resulting in abnormal elevated levels of glucose in the blood), onset 2/16/17;
- No new interventions after 2/16/17.
The facility did not update the care plan with individualized interventions for falls, combative behaviors and diet.
6. During an interview on 7/20/21 at 12:13 P.M., Resident #23 said he/she is own responsible party (RP), he/she is not invited to care plan meetings.
During an interview on 7/21/21 at 1:43 P.M., the DON said the facility is not having care plan meetings with everyone right now but the care plan is reviewed in detail, especially if there are any changes, with the resident each time they are done. She does not usually document that.
During an interview on 7/21/21 at 1:54 P.M., Resident #23 said the facility staff do not, and have never, invited the resident to a care plan meeting or discussed the care plan with him/her.
The facility did not involve the resident to participate in the care planning process.
7. During an interview on 7/20/21 at 11:48 A.M., Resident #34 said he/she has never heard of a care plan meeting. The facility staff have never discussed the resident's medication with him/her.
The facility did not involve the resident to participate in the care planning process.
Record review of the Resident 34's progress notes showed:
- On 3/9/21, the resident was found sitting on floor in front of bed. Resident said he/she was attempting to get up and sit in his/her chair. Mild pain in right knee, emergency medical services (EMS) were contacted;
- On 7/7/21, the resident found sitting on floor with a moderate amount of blood surrounding. Laceration to right lower leg. Resident said he/she hit his/her head with noticeable lump to area. EMS here to assist resident up and to bed. Left facility enroute to hospital.
Record review of the resident's comprehensive care plan, dated 3/3/21, showed:
- History of falls, onset 11/20/19;
- No interventions dated after 11/20/19.
The facility did not update the care plan with individualized interventions for falls.
8. Record review of Resident #37's progress notes showed on 1/22/21, the resident had fallen in shower, found resident lying supine, back of head with blood coming out. Called EMS and in route to nearest hospital.
Record review of the resident's comprehensive care plan, dated 6/23/21, showed:
- Three fall care plan areas;
- High risk for falls onset dated 6/19/18 with interventions dated the same;
- I am at risk for falls onset dated 1/18/17 with interventions dated the same;
- I use a walker for ambulation, I am a risk for falls onset dated 1/18/17 with interventions dated the same.
- No new interventions for fall on 1/22/21 with head injury, diagnosis of subarachnoid hemorrhage (bleeding between the brain and the tissue covering the brain).
The facility did not update the care plan with individualized interventions for falls.
9. Record review of Resident #46's POS, dated 7/1/21 - 7/31/21, showed an order dated, 3/10/21, for Hydrocodone (pain medication)-acetaminophen (pain and fever reducer medication) 5/325 milligram (mg) per gastrostomy tube (G-Tube) four times a day.
Record review of the resident's comprehensive care plan, last reviewed 4/06/21, showed:
- Problem: Chronic Pain related to medical conditions, onset 11/07/6 and edited 08/02/17;
- Goal: I will voice relief of my pain or that my pain level is tolerable with current medication, dated 08/02/1;
- Approach: I will report relief of pain, dated 08/02/17;
- Medication as ordered Fentanyl (strong narcotic pain medicine) patches, dated 03/24/19.
The facility did not update the care plan with new interventions for pain control.
During an interview on 7/27/21 at 3:03 P.M., the DON said she would expect care plans to be updated with new interventions for each care area when there is a change.
CONCERN
(E)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0658
(Tag F0658)
Could have caused harm · This affected multiple residents
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to ensure resident care and services were provided accor...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to ensure resident care and services were provided according to acceptable standards of care for six residents (Residents #11, #18, #21, #34, #50, and #152) out of 13 sampled residents. The facility's census was 44.
1. Record review of the facility's policy titled, Medication and Treatment Orders, dated July 2016, showed orders for medications and treatments will be consistent with principles of safe and effective order writing.
Record review of the facility's policy titled, Medication Orders, dated November 2014, showed:
- The purpose of this procedure is to establish uniform guidelines in the receiving and recording of medication orders;
- Each resident must be under the care of a licensed physician authorized to practice medicine in this state and must be seen by the physician at least every 60 days;
- A current list of orders must be maintained in the clinical record of each resident;
- Orders must be written and maintained in chronological order;
- Physician orders/progress notes must be signed and dated every 30 days.
2. Observation on 7/27/21 at 2:12 P.M. showed Resident #11's dialysis fistula (an access made by joining an artery and vein in your arm for preparation for dialysis process) at his/her upper right arm. The site had bruises on the skin.
During an interview on 7/27/21 at 2:12 P.M., the resident said he/she has a dressing on his/her dialysis site (fistula) when he/she returns from dialysis. The nurses do not check the site when he/she returns from dialysis, such as bleeding issues. The dialysis center takes care of it.
Record review of the resident's Physician's Order Sheet (POS), dated 7/1/21 - 7/31/21, showed:
- Diagnoses of chronic kidney disease, stage 5 (end stage) and dependence on renal dialysis;
- No orders to assess the fistula after dialysis.
Record review of the resident's medication administration/treatment record showed no assessment of the resident's fistula after dialysis.
Record review of the facility's policy titled, End-Stage Renal Disease, Care of a Resident with, dated September 2010, showed residents with end-stage renal disease (ESRD; last stage of kidney failure and requires dialysis treatment) will be cared for according to currently recognized standard of care.
Record review of [NAME] & [NAME], Inc, dated 2010, showed
- After dialysis, assess the vascular access for any bleeding or hemorrhage;
- Assess for patency at least every 8 hours;
- Palpate the vascular access to feel for a thrill or vibration that indicates arterial and venous blood flow and patency;
- Notify the healthcare provider promptly if you suspect clotting.
3. Record review of Resident #18's POS, dated 7/1/21 through 7/31/21, showed:
- admitted [DATE] with diagnoses of acute respiratory disease (an infection of the lungs that interferes with breathing), constipation, gastrostomy status (G-tube; a tube inserted through the wall of the abdomen directly into the stomach that can be used to give drugs and liquids, including liquid food);
- An order, dated 11/25/19, for Jevity 1.2 (a nutritional supplement), 55 cubic centimeters (cc) per hour continuous pump, flush at 50 cc of water every hour via pump.
Observation on 7/27/21 at 8:50 A.M. showed the resident lay in bed;
- The mechanical feeding pump on hold;
- The feeding pump set for 50 cc/hr (5 cc less than ordered, a total loss of nutrition of 120 cc/24 hour;
- The Jevity bottle when first opened contains 1000 cc;
- The Jevity 1.2 hung on pole attached to the mechanical feeding pump;
- The Jevity bottle dated for 7/26/21 at 1:00 P.M. and contained 950 cc in bottle (the resident only received 50 cc in a 19 hour period-a total loss of nutrition of 995 cc);
- The water/fluids hung on pole and attached to the mechanical feeding pump. The fluids contained 850 cc and dated 7/26/21 at 6:00 P.M. (the resident only received 150 cc of water).
Record review of the resident's nurse progress notes showed the last progress note dated 6/07/21 related to the care of the resident.
4. Record review of Resident #21's POS, dated 7/1/21 through 7/31/21, showed:
- admitted [DATE] with diagnoses of acute respiratory disease (a sudden condition that makes breathing difficult), hemiplegia following cerebral infarction (stroke with paralysis on one side), hypertension (high blood pressure), major depressive disorder (overwhelming sadness);
- An order, dated 6/6/21, for Jevity 1.5 (a nutritional supplement), 55 cc per hour between 5:00 P.M. and 6:00 A.M., total 715 cc to be delivered, then off, flush at 150 cc every four hours, total 450 cc, hold feeding if able to aspirate stomach contents greater than 60 cc during feeding;
- No order for G-tube care and maintenance.
During an interview on 7/22/21 at 2:40 P.M., the Director of Nursing (DON) said resident #21 had a G-tube inserted during a hospital stay in April, 2021, the resident had been alert and oriented, experienced multiple seizures, was hospitalized and returned to the facility on 4/19/21 with a G-tube in place.
Observations showed:
- On 7/23/21 at 10:02 A.M., resident lay in bed, Jevity 1.5 hanging at bedside with 400 cc feeding remaining in bottle, started with 1000 cc, dated 7/22/21 5:00 P.M., 115 cc less than ordered delivered;
- On 7/27/21 at 8:40 A.M., resident #21 lay in bed, Jevity bottle hanging with 1000 cc fluid present, dated 7/26/21 at 4:15 P.M., 1000 cc bag of fluid also hanging dated 7/26/21. Pump not on.
During an interview on 7/27/21 at 9:01 A.M., the DON said she didn't know about the feeding, she said maybe they had to hang a new bottle. She didn't know why it is still full.
During an interview on 7/27/21 9:08 A.M., RN K said he/she hung the bottle of Jevity and the bag of fluids before he/she left yesterday (7/26/21). He/she knows it was not run last night, but the night shift nurse could not tell him/her why it was not run. He/she believes they forgot it.
Record review of the resident's nurse progress notes showed the last progress note dated 7/23/21 with no documentaion of reason for less than ordered Jevity delivered on that date.
5. Observation of Resident #34 on 7/20/21, 7/21/21, 7/22/21, 7/23/21 showed nasal cannula (a device used to deliver supplemental oxygen to a person in need of respiratory help) to provide supplemental oxygen at 2.5 Liters/minute.
During an interview on 7/27/21 at 9:14 A.M., the Assistant Director of Nursing (ADON) said he/she would find the rate for oxygen therapy through the computer on the resident's orders. Oxygen tubing should be changed maybe every 72 hrs. It would show on the order when to change the tubing.
Record review of the resident's POS, dated 7/1/21 - 7/31/21, showed:
- Diagnoses of shortness of breath, chronic obstructive pulmonary disease (COPD, a group of lung diseases that block airflow and make it difficult to breathe), generalized anxiety disorder, cough;
- No orders for oxygen therapy.
Record review of the resident's comprehensive care plan, dated 3/3/21, showed:
- COPD - oxygen as ordered;
- No instructions on the care of oxygen therapy.
6. Record review of Resident #50's medical record showed:
- admitted on [DATE];
- POS, dated 7/1/21 through 7/31/21, showed:
- Diagnosis of anxiety disorder (excessive and persistent worry and fear about everyday situations), pneumonia (an infection of the lungs);
- An order, dated 6/28/21, for Imatinib Mesylate (a chemotherapy medication used to treat chronic myeloid leukemia) 100 milligrams (mg), two tablets by mouth daily.
Record review of resident #50's Medication Administration Record showed:
- On 7/1/21 through 7/31/21 the Imatinib Mesylate not given;
- On 7/12/21 through 7/15/21 and on 7/17/21 through 7/20/21, reason documented as the medication not given, medication not available in facility.
During an interview on 7/27/21 at 1:43 P.M., the DON said the documented administration of Imatinib Mesylate on 7/16/21 is an error, the medication was not available in the facility.
7. Record review of Resident #152's admission nurse progress note, dated 7/3/21 at 3:14 P.M., showed the resident to arrive at the facility with a G-tube, a neck brace, and a condom catheter (an external urinary catheter collection device that fits over the penis like a condom).
Record review of the resident's medical record showed an admission date of 7/3/21.
POS dated 7/1/21 through 7/31/21 showed:
- Diagnoses of malignant neoplasm of prostate (cancer), hypertension (high blood pressure), stress incontinence (leaking urine with activity), alcohol abuse, chronic pain, seizures, type two diabetes mellitus (condition that affects the way the body processes blood sugar),with hyperglycemia (high blood sugar);
- An order, dated 7/4/21, Jevity 1.5 Cal/Fiber (nutritional supplement with fiber) at 60 cc per hour continuously and water 150 cc every four hours via auto pump three times a day (TID);
- An order, dated 7/13/21, may use Jevity 1.2 until Jevity 1.5 is delivered to the facility;
- No order for G-tube care and maintenance;
- No order to administer medications via the G-tube;
- No order for a neck brace use or discontinued use;
- No order for condom catheter use or discontinued use;
Record review of the resident's Medication Administration Record (MAR) dated 7/1/21 - 7/27/21 showed medications to be administered through the G-tube.
Record review of the resident's admission MDS, dated [DATE], showed Resident #152 to have a diagnoses of cancer, diabetes, seizures, and hypertension and to be severely cognitively impaired.
Observations of Resident #152 showed:
- On 7/20/21 at 12:50 P.M., the resident sat near the nurse station in a wheelchair, wore a neck brace, no catheter;
- On 7/27/21 at 8:45 A.M. the resident sat in a wheelchair in the dining room, the resident wore a neck brace and no catheter.
During an interview on 7/20/21 at 1:00 P.M., the ADON said Resident #152 was admitted with the neck brace because he has a fracture in the first cervical vertebra (C-1), she does not think the resident has a catheter and does have a G-tube.
During an interview on 7/22/21 at 4:31 P.M. the DON said Resident #152 was admitted with a condom catheter in a comatose state. The catheter has been removed because the resident is now able to walk.
8. During an interview on 7/27/21 at 3:03 P.M., the DON said she would expect all orders for medication and treatments to be followed as written, there's to be an order for oxygen use if oxygen is used, G-tube feeding administration orders to be followed, wound care orders to be followed, and she would expect orders to be updated and changed as needed. The dialysis port is assessed when the resident returns from dialysis, but it isn't documented. They look for change in condition, low blood pressure, bleeding, pain, heat, any complication. As a nurse, they should know that. There is not a daily assessment of the site. The dialysis center does an ultrasound of the resident's site monthly and a clean out every three months, so the facility staff doesn't check the thrill and bruit.
CONCERN
(E)
Potential for Harm - no one hurt, but risky conditions existed
Food Safety
(Tag F0812)
Could have caused harm · This affected multiple residents
Based on observation, interview, and record review, the facility failed to store, prepare, distribute, and serve food under sanitary conditions. The facility's census was 44.
Observation of the kitche...
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Based on observation, interview, and record review, the facility failed to store, prepare, distribute, and serve food under sanitary conditions. The facility's census was 44.
Observation of the kitchen on 7/22/21 at 9:30 A.M. showed:
- The first refrigerator along the wall to the right of the kitchen entrance had food debris in the bottom, residue running down the front of the doors, and both door seals loose at the bottom;
- The freezer had food debris in the bottom and residue running down the front of the doors;
- The refrigerator in the corner had food debris in the bottom and residue running down the front of the doors;
- The toaster had a buildup of grime and food residue on the front and sides;
- The steam table had food residue running down the front and sides;
- The stove had food residue running down the front and sides;
- The bottom shelf of the food prep table had a buildup of grime and food residue.
Record review of the steam table temperature logs showed:
- On 7/19/21, no temperatures recorded for the lunch and supper meals;
- On 7/20/21 and 7/22/21, no temperatures recorded for the supper meal.
During an interview on 7/22/21 at 9:45 A.M., the Dietary Supervisor (DS) said there is no kitchen cleaning schedule. The cooks should know they are supposed to deep clean on Wednesdays and Saturdays, and clean up between meal services. The DS said he/she leaves before the supper meal, but the cooks are supposed to be writing the temperatures down.
During an interview on 7/27/21 at 3:03 P.M., the Assistant Administrator (AA) said he would expect the staff to know what to clean and when it needs to be cleaned, not necessarily a written schedule of who does what. He expected the DS and kitchen staff to keep all equipment clean and operational. The DS and kitchen staff should monitor and check food temperatures before the food goes out and keep a log. If the temperatures are out of range, they are to notify the DS, administration or call the Director of Nursing.
Record review of the facility's policy titled, Nutrition Services, dated December 2016, showed:
- Policy Statement: Store, prepare, distribute and serve food in accordance with professional standards for food service safety;
- Centers for Medicaid and Medicare Services (CMS) recognizes the U.S. Food and Drug Administration's (FDS) Food Code and the Centers for Disease Control and Prevention's (CDC) food safety guidance as national standards to procure, store, prepare, distribute and serve food in long term care facilities in a safe and sanitary manner.
CONCERN
(E)
Potential for Harm - no one hurt, but risky conditions existed
Antibiotic Stewardship
(Tag F0881)
Could have caused harm · This affected multiple residents
Based on interview and record review, the facility failed to implement an antibiotic stewardship program to include an infection surveillance program and antibiotic use protocols. This deficient pract...
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Based on interview and record review, the facility failed to implement an antibiotic stewardship program to include an infection surveillance program and antibiotic use protocols. This deficient practice had the potential to affect all residents in the facility. The facility's census was 44.
Record review of the facility's Infection Prevention and Control Program (IPCP) showed the facility did not establish an Antibiotic Stewardship Program which includes antibiotic use protocols and a system to monitor antibiotic use. The facility did not have the following:
- An infection surveillance program;
- Protocols to review clinical signs and symptoms and lab reports to determine if the antibiotic is indicated or if adjustments to therapy should be made and to identify what infection assessment tools or management algorithms are used for one or more infections;
- A process for periodic review of antibiotic use by prescribing practitioners;
- Protocols to optimize the treatment of infections by ensuring that residents who require antibiotics are prescribed the appropriate one;
- A system for the provision of feedback reports on antibiotic use, antibiotic resistance patterns based on lab data, and prescribing practices for the prescribing practitioners and for the Quality Assurance and Assessment (QAA) committee.
The Director of Nursing (DON) provided a red binder which contained:
- One sheet, dated 3/12/19, of infections,
- One lab infection control detail report, dated 9/1/20-9/30/20, for a former resident's urine cultures;
- One lab infection control detail report, dated 9/1/20-11/30/20, for the same former resident's urine cultures;
- One sheet, titled Nursing Home Antimicrobial Stewardship Guide, dated 2021, which showed one resident with hospital acquired pseudomonas with cough, prescribed Doxycycline from 2/20/21-3/31/21, one resident with nursing home acquired cellulitis rash, prescribed cephalexin from 6/23/21-6/28/21, one resident with nursing home acquired cellulitis rash with drainage, prescribed doxycycline from 6/23/21-6/28/21, cephalexin from 3/17/21-3/24/21, cephalexin from 6/9/21-6/16/21, cipro from 4/1/21-4/8/21, and clindamycin from 5/5/21-5/15/21, and one resident with nursing home acquired leg redness from toe, prescribed cephalexin from 5/4/21-5/11/21.
Infection Surveillance did not include whether the resident was on isolation precautions, prescribing clinician, medication dosage, and whether the antibiotic ordered was appropriate to treat the infection or if a change in medication was needed.
During an interview on 7/27/21 at 3:03 P.M., the Assistant Administrator (AA) said they are working with the lab and pharmacy to monitor, track, and watch for infections. The AA said they still look at previous month infections at monthly meetings. The DON has a spreadsheet which shows the antibiotic, if there was a culture, and signs and symptoms being treated. The AA said they look for trends quarterly.
The facility did not provide a policy for Antibiotic Stewardship.
CONCERN
(E)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0883
(Tag F0883)
Could have caused harm · This affected multiple residents
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to provide information and education to two residents (Resident #6 and...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to provide information and education to two residents (Resident #6 and #23) or the resident's representative, of the two types of pneumococcal vaccine (a method of preventing a specific type of lung infection (pneumonia) that is caused by the pneumococcus bacterium), and offer both pneumococcal vaccines, and failed to provide information and education and accurately document the influenza vaccine administration for four residents (#6, #20, #37, and #23) out of five residents sampled for immunization status. The facility's census was 44.
1. Record review of the facility's policy titled, Vaccination of Residents, dated 10/2019, showed:
- All residents will be offered vaccines that aid in preventing infectious diseases unless the vaccine is medically contraindicated or the resident has already been vaccinated;
- Prior to receiving vaccinations, the resident or legal representative will be provided information and education regarding the benefits and potential side effects of the vaccinations. (See current vaccine information statements at https://www.cdc.gov/vaccines/hcp/vis/index.html for educational materials.);
- Provision of such education shall be documented in the resident's medical record;
- All new residents shall be assessed fro current vaccination status upon admission;
- The resident or the resident's legal representative may refuse vaccines for any reasons;
- If the vaccines are refused, the refusal shall be documented in the resident's medical record;
- If the resident receives a vaccine, at least the following information shall be documented in the resident's medical record: site of administration, date of administration; lot number of the vaccine, expiration date, name of person administering vaccine;
- Certain vaccines (influenza and pneumococcal vaccines) may be administered per the physician-approved facility protocol (standing orders) after the resident has been assessed by the physician for medical contraindications for each vaccine. The resident's attending physician must provide a separate written order for any other vaccination, and such orders shall be recorded in the resident's medical record;
- Inquiries concerning this policy should be referred to the Infection Preventionist or the Administrator.
2. Record review of the facility's policy titled, Pneumococcal Vaccine, dated October 2019, showed:
- All resident will be offered pneumococcal vaccines to aid in preventing pneumonia/pneumococcal infections;
- Prior to or upon admission, resident will be assessed for eligibility to receive the pneumococcal vaccine series, and when indicated, will be offered the vaccine series within 30 days of admission to the facility unless medically contraindicated or the resident has already been vaccinated;
- Assessments of pneumococcal vaccination status will be conducted within five working days of the resident's admission if not conducted prior to admission;
- Administration of pneumococcal vaccine or revaccinations will be made in accordance with current Centers for Disease Control and Prevention (CDC) recommendations at the time of the vaccination.
3. Record review of the facility's policy titled, Influenza Vaccine, dated October 2019, showed:
- All residents who have no medical contraindications to the vaccine will be offered the influenza vaccine annually to encourage and promote the benefits associated with vaccinations against influenza;
- The facility shall provide pertinent information about the significant risks and benefits of vaccines to residents ( or residents' legal representatives);
- Between October first and March 31 each year, the influenza vaccine shall be offered to residents, unless the vaccine is medically contraindicated or the resident has already been immunized;
- Prior to the vaccination the resident (or legal representative) will be provided information and education regarding the benefits and potential side effects of the influenza vaccine, provision of such education shall be documented in the resident's medical record;
- The date of vaccination, lot number, expiration date, person administering, and the site of vaccination will be documented in the resident's medical record;
- A resident's refusal of the vaccine shall be document on the Informed Consent for Influenza Vaccine and placed in the resident's medical record;
- The Infection Preventionist will maintain surveillance data on influenza vaccine coverage and reported rates of influenza among residents;
- Administration of the influenza vaccine will be made in accordance with current CDC recommendations at the time of the vaccination.
4. Record review of the U.S. Department of Health and Human Services Centers for Disease Control (CDC) Pneumococcal Vaccine Timing for Adults, dated 11/30/15, showed the following:
- CDC recommends two pneumococcal vaccines for adults: 13-valent pneumococcal conjugate vaccine (PCV 13, Prevnar 13) and 23-valent pneumococcal polysaccharide vaccine (PPSV 23, Pneumovax 23);
- CDC recommends vaccination with PCV 13 for all adults 65 years or older and adults 19 through [AGE] years old with certain medical conditions (such as chronic heart or lung disorders, including congestive heart failure, diabetes mellitus (a chronic health condition which increases blood sugars which leads to dangerous complications), chronic obstructive pulmonary disease (COPD :a condition involving constriction of the airway and difficulty or discomfort in breathing);
- CDC recommends vaccination with PPSV 23 for all adults 65 years or older and adults 19 through [AGE] years old with certain medical conditions.
5. During an interview on 7/23/21 at 10:50 A.M., the Director of Nursing (DON) said she is responsible for offering pneumonia vaccine and providing education if no records can be verified. It depends on what the doctor says if any other vaccine or screening is offered to them.
7. Record review of Resident #6's medical record showed:
- The resident admitted on [DATE];
- The resident [AGE] years old;
- Diagnoses of acute respiratory disease (a sudden condition in which breathing is difficult and the oxygen levels in the blood abruptly drop lower than normal), contracture (shortening and hardening of muscles, tendons, or other tissue, often leading to deformity and rigidity of joints), acute embolism and thrombosis of deep vein (occurs when a blood clot, develops in a blood vessel and reduces the flow of blood) of low extremities bilaterally (both legs), essential hypertension (high blood pressure), cerebral palsy (a condition marked by impaired muscle and/or other disabilities, typically caused by damage to the brain before or at birth), pressure ulcer of unspecified site, stage 2 (a condition when the skin breaks open, wears away, or forms an ulcer, which is usually tender and painful, the sore expands into deeper layers of the skin), urinary tract infection (an infection in the urinary system), hypocalcemia (low calcium), vitamin B12 deficiency anemia due to intrinsic factor deficiency (a condition in which the body does not have enough healthy red blood cells, due to a lack of vitamin B12);
- The resident's quarterly Minimum Data Set (MDS), a federally mandated assessment instrument required to be completed by the facility's staff), dated 4/23/21, Section O, showed pneumococcal vaccine response not offered, influenza vaccine last given 10/27/20.
Record review of the Immunization Record, dated 2/3/21, showed:
- Staff documented the resident's pneumococcal vaccine response as not up to date, offered and declined, no reason documented;
- Influenza vaccine last given 10/7/19 with a handwritten correction dated 10/27/20;
- Staff did not document PCV 13 and PPSV 23 offered to the resident or representative;
- Staff did not document education provided to the resident or representative regarding the benefits and potential side effects of the pneumococcal vaccines;
- Staff did not document education provided to the resident or representative regarding the benefits and potential side effects of the influenza vaccine.
8. Review of Resident #20's medical record showed:
- The resident admitted on [DATE];
- The resident [AGE] years old;
- Diagnoses of stroke (damage to the brain from interruption of its blood supply), anemia, hypertension diabetes mellitus (condition that affects the way the body processes blood sugar), hemiplegia and hemiparesis (muscle weakness or partial paralysis on one side of the body that can affect the arms, legs and facial muscles), seizure disorder (disorder in which nerve cell activity in the brain is disturbed causing seizures), benign prostatic hypertrophy (prostate gland enlargement that causes urination difficulty), abnormal weight loss, pain, disorder of skin and subcutaneous tissue unspecified, gastrostomy tube (feeding tube placed through the abdomen into the stomach), stage 2 pressure ulcer to right gluteal cleft and gastroesophageal reflux disease (condition where acid from the stomach comes up into the esophagus causing acid reflux or heartburn);
- The resident's quarterly MDS, dated [DATE], Section O, showed pneumococcal vaccine response yes, influenza vaccine last given 10/27/20.
Record review of the Immunization Record, dated 2/3/21, showed:
- Staff documented the resident's pneumococcal vaccine response as given in 2019, type of pneumococcal vaccine not identified;
- Influenza vaccine last given 10/7/19 with a handwritten correction dated 10/27/20;
- Staff did not document PCV 13 and PPSV 23 offered to the resident or representative;
- Staff did not document education provided to the resident or representative regarding the benefits and potential side effects of the pneumococcal vaccines;
- Staff did not document education provided to the resident or representative regarding the benefits and potential side effects of the influenza vaccine.
9. Review of Resident #23's medical record showed:
- The resident admitted on [DATE];
- The resident [AGE] years old;
- Diagnoses of hypertension, cerebral infarction (stroke), major depressive disorder (depression), herpes simplex myelitis (a rare nervous system disease), pain, osteoporosis (bones become brittle and fragile), anxiety (a feeling of worry, nervousness, or unease) psychosis (a severe mental disorder in which thought and emotions are so impaired that contact is lost with external reality), tremor (involuntary quivering movement), insomnia (unable to sleep);
- The resident's quarterly MDS, dated [DATE], Section O, showed pneumococcal vaccine response yes, influenza vaccine last given 10/27/20.
Record review of the Immunization Record dated 1/21/20 showed:
- Staff documented the resident's pneumococcal vaccine response as not up to date, offered and declined, no reason documented;
- Influenza vaccine last given 10/7/19 with a handwritten correction dated 10/27/20;
- Staff did not document PCV 13 and PPSV 23 offered to the resident or representative;
- Staff did not document education provided to the resident or representative regarding the benefits and potential side effects of the pneumococcal vaccines;
- Staff did not document education provided to the resident or representative regarding the benefits and potential side effects of the influenza vaccine.
10. Review of Resident #37's medical record showed:
- The resident admitted on [DATE];
- The resident [AGE] years old;
- Diagnoses of hypertension, hypothyroidism (the thyroid gland doesn't produce enough thyroid hormone), cellulitis (serious bacterial skin infection) of right lower limb, type 2 diabetes mellitus (chronic condition that affects the way the body processes blood sugar) with diabetic neuropathy (nerve damage affects the legs and feet), chronic pain, elevated prostate specific antigen (can be a sign of prostate cancer), chronic obstructive pulmonary disease (COPD);
- The resident's quarterly MDS, dated [DATE], Section O, showed pneumococcal vaccine response yes, showed influenza vaccine last given 10/27/20.
Record review of the Immunization Record, dated 2/3/21, showed:
- Staff documented the resident's influenza vaccine last given 10/7/19 with a handwritten correction dated 10/27/20;
- Staff did not document education provided to the resident or representative regarding the benefits and potential side effects of the influenza vaccine.
During an interview on 7/23/21 at 10:50 A.M., the DON said she is responsible for giving the pneumonia vaccine to residents who have not had it, she provides education. If the vaccine is needed, she orders it from the pharmacy and gives it when it arrives to the facility. The DON said if she is able to get records from where the resident comes from she uses them, it depends on what the doctor says if another vaccine is offered to the resident. The influenza vaccines are not correctly documented in the medical records, she crossed out the incorrect date and handwrote the correct date.
CONCERN
(F)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0801
(Tag F0801)
Could have caused harm · This affected most or all residents
Based on observation, interview, and record review, the facility failed to have a clinically qualified nutritional professional designated as the Food and Nutritional Service Manager for one of one fo...
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Based on observation, interview, and record review, the facility failed to have a clinically qualified nutritional professional designated as the Food and Nutritional Service Manager for one of one food service kitchen, which prepared food for all residents. This practice potentially affected all of the residents who were served food prepared by the facility. The facility's census was 44.
During an observation and interview in the kitchen on 7/22/21 at 9:30 A.M., the Dietary Supervisor (DS) said he/she has worked for the facility for two years, he/she isn't certified, and has never attended classes or received any formal education.
Record review of the facility's current employee list, dated 7/20/21, showed a hire date of 1/10/18 for the DS.
During an interview on 7/27/21 at 3:03 P.M., the Assistant Administrator (AA) said he thought the DS had until November 2021 to get certified. The AA said the DS and the Registered Dietician Consultant (RDC) are working together to make sure it happens.
During an interview on 8/9/21 at 12:33 P.M., the RDC said the DS will be enrolled in a class scheduled for September to get his/her certification completed.
Record review of the facility's policy titled, Nutrition Services, dated December 2016, showed:
- The facility must employ sufficient staff with the appropriate competencies and skills sets to carry out the functions of the food and nutrition services, taking into consideration resident assessments, individual plans of care and the number, acuity and diagnoses of the facility's resident population in accordance with the facility assessment;
- If a qualified dietician or other clinically qualified nutrition professional is not employed full-time, the facility must designate a person to serve as the director of food and nutrition services who - for designations prior to November 28, 2016, meets the following requirements no later than five years after November 28, 2016, or no later than one year after November 28, 2016 for designations after November 28, 2016 is: (A) a certified dietary manager or (B) a certified food service manager, or (C) has similar national certification for food service management and safety from a national certifying body or (D) has an associate's or higher degree in food service management or in hospitality, if the course study includes food service or restaurant management, from an accredited institution of higher learning. In states that have established standards for food service managers or dietary managers, meets State requirements for food service managers or dietary mangers and receives frequently scheduled consultations from a qualified dietician or other clinically qualified nutrition professional.