SERIOUS
(G)
📢 Someone Reported This
A family member, employee, or ombudsman was alarmed enough to file a formal complaint
Actual Harm - a resident was hurt due to facility failures
Quality of Care
(Tag F0684)
A resident was harmed · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview and record review, the facility failed to ensure that residents received treatment and care in a...
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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 that residents received treatment and care in accordance with professional standards of practice, the comprehensive person-centered care plan, and the resident's choices for one (#52) of three residents reviewed out of 52 sample residents.
Resident #52 was admitted to the facility after being hospitalized for worsening congestive heart failure. The resident had a history of chronic congestive heart failure and resistance to oral antibiotics. During the hospital stay just prior to the resident's admission the resident was treated for severe edema/ water retention as evidenced by a rapid significant weight gain and swelling in both lower extremities and muscle weakness and fatigue. The hospital treated the resident with intravenous (IV) diuretics and the resident's cardiac condition stabilized enough to discharge the resident. The resident however was not stable enough to undergo a needed surgery to repair a leak in the mitral valve of the heart and the resident was sent to the facility for cardiac monitoring and therapy to strengthen muscle and functional condition.
The hospital sent a discharge summary and discharge orders to the hospital for the facility to monitor the resident's cardiac function. Orders included medication, a cardiac low sodium diet, and monitoring for edema with daily weights taken at the same time each day, a fluid restriction, and assessing the status of edema throughout the resident's body. The facility did not order and provide a cardiac low sodium diet and did not concisely monitor the resident fluid intake, assess the resident weights daily and at the same time of day, or provide daily assessment of the status of the resident edematous symptoms.
Additionally, when the resident started to experience a worsening of cardiac symptoms classically associated with congestive heart failure the facility did not consult with the resident's long time cardiologist for treatment recommendations, or ensure that the resident's primary care physician examined the resident timely when the resident's symptoms worsened.
As a result of the facility failures to develop a baseline care plan and initiate orders to follow hospital discharge orders, the resident's cardiac condition worsened. The resident gained 12.6 pounds while in the care of the facility and complained of feeling weaker and more fatigued. The edema in the resident's legs worsened causing the skin on the lower legs to open and weep fluid. In addition to edema in the lower legs, the hospital 7/17/23 assessment revealed the resident had pitting edema in the groin and presacral edema (edema in the area between the rectum and lowest part of the spine). The resident required hospitalization and parenteral diuresis (IV diuretic medication to aid the body in removing significant water retention).
Findings include:
I. Facility policy
The Care Plans-Baseline policy revised March 2022, was provided by the corporate nurse consultant (CNC) on 7/31/23 at 2:35 p.m. The policy read in pertinent part: A baseline plan of care to meet the resident's immediate health and safety needs is developed for each resident within forty-eight (48) hours of admission.
-The baseline care plan includes instructions needed to provide effective, person-centered care of the resident that meet professional standards of quality care and must include the minimum healthcare information necessary to properly care for the resident including, but not limited to the following: a. Initial goals based on admission orders and discussion with the resident/representative; b. Physician orders .
II. Resident #52
A. Resident status
Resident #52, age [AGE], was admitted to the facility on [DATE] and was discharged to the hospital on 7/19/23. According to the July 2023 computerized physician's orders, diagnoses included biventricular heart failure (a condition affecting both sides of the heart that occurs when the heart muscles cannot not pump enough blood to meet the body's need for blood and oxygen, where blood and fluid collects in the lungs and legs over time); nonthematic mitral (valve) insufficiency (occurs when the mitral valve does not close properly, allowing blood to flow backwards into the heart and as a result, the heart cannot pump efficiently, causing symptoms like fatigue and shortness of breath); presence of an automatic cardiac defibrillator (an internal device capable of restoring normal heartbeat); chronic stage 3 kidney disease; and chronic peripheral venous insufficiency (the body's inability to move blood through the veins of the legs or arms).
The admission minimum data set assessment (MDS) assessment dated [DATE] documented the resident had intact cognition with a brief interview for mental status score of 15 out of 15. The resident needed staff supervision to complete activities of daily living (ADLs).
-The resident received daily diuretics.
B. Resident representative interview
The resident was not available for an interview.
Two resident representatives were interviewed on 7/31/23 at 10:06 a.m. The resident's daughter said Resident #52 had a history of cardiac complications and had been seeing a cardiologist for outpatient care for some time. The cardiologist determined the resident was a candidate for a clip procedure to stop leaking in the mitral value of the heart and repair a malfunctioning heart valve; the resident was scheduled to have the procedure at the end of June 2023. However, the resident started to experience general weakness, fatigue, weight gain, and low blood pressure and the procedure was postponed. Resident #52 went to the hospital for assessment, and was admitted for worsening heart failure and severe edema. The resident was treated with intravenous (IV) diuretic medication with a goal of removing the buildup of fluid. Once the fluid buildup was removed and the resident was determined to be stable, the resident was released from the hospital. It was determined Resident #52 needed time to strengthen his cardiac function and ensure the edema did not return before proceeding with the clip procedure. It was ultimately decided the resident would be admitted to a skilled nursing facility for medical monitoring until he was strong enough to undergo surgery to repair his mitral valve.
The resident representative said that within two days of being in the facility Resident #52 began regaining the water weight (edematous fluid) he had lost while in the hospital. By day three, Resident #52 had gained 4.36 pounds and was retaining fluid in his lower legs. Resident #52 was complaining of weakness and general malaise.
The resident representative said she talked to the resident's physician on 7/8/23; the physician said he would increase Resident #52's diuretic medication to better manage the resident's edema. The following day the nursing staff still did not have an order to increase the diuretic dosage. The physician did not increase Resident#52's diuretic medication until seven days after telling the resident representative he was placing an order to increase the medication (7/15/23).
The resident representative said she spoke to the resident's physician and nursing staff several times relaying Resident #52's complaints of increased weakness, tiredness and increased edema; but felt the physician and nursing staff were not responsive to Resident's #52 and his declining health. The facility was supposed to weigh the resident at the same time, every morning after going to the bathroom. If he gained more than three pounds in a day, they should have notified the cardiologist; that did not happen despite Resident #52 asking staff to comply with that order.
The resident representative said Resident #52 continued to complain that he was not feeling well and that his legs were swelling with fluid, which interfered with his ability to walk and participate in physical therapy; by 7/18/23 the resident weight was 284 pounds and Resident #52 asked to be sent to the hospital. The facility failed to respond timely to Resident #52's declining health.
Resident #52's wife said the resident was determined to get better and was focused on being compliant with the treatment orders and recommendations of his cardiologist as well as the recommendations received at discharge from the hospital. Once at the hospital Resident #52 was started on IV diuretics.
C. Record review
Hospital treatment records dated 6/30/23 documented in pertinent part: Resident #52 was admitted to the (hospital name) on 6/17/23 and discharged on 6/30/23. Primary diagnosis included acute and chronic HFrEF (heart failure with reduced ejection fraction - a condition that occurs when the heart's lower left chamber (left ventricle) doesn't pump blood out to the body as well as it should.) Recommended cardiology follow up for reevaluations within two weeks.
Resident #52 was ultimately discharged to (facility name) in a medically stable improved condition with instruction to follow-up with his cardiologist, neurologist, and PCP (primary care physician) in the upcoming weeks. admission weight was 279 pounds and discharge weight was 268 pounds.
Diet orders: two (2) gram sodium (very low salt) and Limit fluids to two (2) liters (L);
Activity orders: activity as tolerated
Heart failure orders: (Refer to Your Guide to Managing Heart Failure for detailed information)
-Fluid Guidelines (all liquids including food, i.e., soup, ice cream): 2000 milliliters ml/ cubic centimeters (cc) 18 cups or 167 ounces per day;
-Weigh self-daily at the same time of day. Call if weight gain of three (3) pounds (lbs) in one day or five (5) lbs weight gain over a week.
-Call your physician if you have increased cough, shortness of breath, increased leg swelling, or chest tightness or pain.
-Diet: Eat a low salt diet. Avoid excess salt. Your sodium intake should be less than 2000 milligrams (mg) per day.
The facility Nursing admission Data collection and Baseline document, dated 6/30/23, read in pertinent part: admission 6/30/23 at 3:15 p.m. Vital signs; pulse 80 beats per minute and regular; respirations 16; blood pressure 156/65; oxygen saturation 97 percent on oxygen therapy; admission weight was 270.6 pounds at 7:20 p.m. No edema present. Pain level was zero. Cardiovascular condition: heart sounds regular; radial (wrists) and pedal (ankle) pulses detected as normal; (no other conditions documented).
-There was no documentation to identify dietary or hydration needs/restrictions and there was no documentation to identify cardiac conditions for heart failure monitoring or monitor for edema and water weight gain.
-The comprehensive care plan initiated 6/30/23 failed to document the resident's cardiac needs and treatment for heart failure and monitoring for dietary and hydration restriction and monitor for edema and water weight gain.
-The care plan did document a care focus for nutrition problems or potential for nutritional problems related to declining health status secondary to heart failure exacerbation and a relevant medical history of arterial fibrillations, initiated 7/4/23. The goal was for the resident not to be malnourished. Interventions included monitor weights as ordered, initiated; provide diet as ordered; and registered dietitian to evaluate and make diet change recommendations.
The July 2023 CPO revealed the following orders:
-Diet order: regular diet, start date 6/30/23;
-Obtain admission weight and height, start date 6/30/23;
-Obtain daily weight, in the morning for congestive heart failure, start 7/1/23; and,
-Skilled nursing documenting daily every shift.
The hospital discharge orders were not included.
Weight log: The weight log revealed inconsistent weight assessments. The resident's weights were not assessed daily; were not assessed in the morning at the same time of day and not assessed by the same scale. The resident weight was only assessed one time before breakfast and sometimes the staff assessed the resident's weight with a chair scale and sometimes with a standing scale. The resident admission weight was recorded as 270.6 lbs., on day 18 the resident's weight was recorded at 283.2. Resident #52 gained a total of 12.6 lbs. in the 18 days since admission. Medical records revealed the resident entered with edema and by day 16 had 3-4 millimeter (mm) pitting edema with delayed rebound of skin when pressed inward (see below).
On 6/30/23 at 7:21 p.m., the resident's weight was 270.6 lbs., on day of admission;
On 7/1/23, the resident's weight was not assessed;
On 7/2/23 at 4:21 p.m., the resident's weight was 273.0 lbs., an increase of three lbs. in two days;
On 7/3/23 at 4:36 p.m., the resident's weight was 274.6 lbs., an increase of 1.6 lbs. or 4.6 lbs. in three days;
On 7/4/23 at 3:45 p.m., the resident's weight was 271.0 lbs., a decrease of 3.6 lbs. in one day;
On 7/5/23 at 11:37 a.m., the resident's weight was 273.4 lbs., an increase of 2.4 lbs. in one day;
On 7/6/23, the resident's weight was not assessed;
On 7/7/23 at 12:53 p.m., the resident's weight was 273.0 lbs., a decrease of 0.4 lbs. in one day;
On 7/8/23 at 14:05 p.m., the resident's weight was 273.2 lbs., an increase of 0.3 lbs. in one day;
On 7/9/23 at 11:55 p.m., the resident's weight was 279.5 lbs., an increase of 6.3 lbs. in one day;
On 7/10/23, the resident's weight was not assessed;
On 7/11/23 at 12:24 p.m., the resident's weight was 274.4 lbs., a decrease of 5.1 lbs.;
On 7/12/23 and 7/13/23, the resident's weight was not assessed;
On 7/14/23 at 9:30 a.m., the resident weight was 279.6 lbs., an increase of 5.2 lbs. in an undetermined number of days;
On 7/15/23 at 11:17 a.m., the resident's weight was 278.8 lbs., a decrease of 0.8 lbs.;
On 7/16/23 at 12:06 p.m., the resident's weight was 278.8 lbs., no change;
On 7/17/23, the resident's weight was not assessed;
On 7/18/23 at 8:09 a.m., the resident's weight was 283.2 lbs., an increase of 4.4 lbs., in one day.
The resident's medical record contained two fluid intake records, neither documenting that the resident was on a fluid restriction. One record documented fluid intake and the other documented fluid intake with meals. There was no documentation of a daily total fluid intake and it was unclear if the documents were a duplication of the resident fluid intake or if each fluid intake record was a separate account of the amount of fluid the resident drank.
The resident's medical record and progress note from 6/30/23 to 7/18/23 documented, in pertinent part, the following information:
-The physician's admission history and physical exam dated 7/1/23 documented the resident was examined by the facility physician. The note revealed Resident #52 was admitted after a complicated hospital course .was ultimately discharged to (facility name) in medically stable condition. (Resident #52's) main concern was getting enough physical therapy (PT) and occupational therapy (OT) so he could manage at home. He denied chest pain and felt he was breathing at baseline. We reviewed his care plan and medications. He understood a low sodium diet was key to reducing his edema in preparation for possible MVR (mitral valve repair).
-Physical Exam: He is not in acute distress. Appearance: Normal appearance. He is not ill appearing. Swelling present. Normal range of motion. Right lower leg: Edema present. Left lower leg: Edema present.
Nursing progress note dated 7/4/23 at 12:09 p.m. read: Residents blood pressure this morning was 98/51. Blood pressure was rechecked and it was 84/57. Paged physician team and an on-call physician called back and gave verbal orders to discontinue the losartan (medication to lower blood pressure) and to give metoprolol medication (to lower blood pressure) in the mid-afternoon. The physician sent a message for the resident regular facility physician to re-evaluate the resident tomorrow. The on-call physician wants the resident's blood pressure to be checked while sitting, and also encourage fluids.
Nursing progress note dated 7/4/23 at 12:09 p.m. read the on-call physician said, The resident should be on a cardiac low salt diet.
-However, there was no further documentation about the resident's dietary needs for a cardiac low sodium diet. The resident's diet was never changed from a regular diet to a cardiac low sodium diet.
-The resident's physician did not provide a follow up visit until three days later, at that point the resident was experiencing additional cardiac symptoms including redevelopment of pitting edema and complaints of weakness.
Physician visit note dated 7/7/23 revealed the resident was seen for a follow up visit. The note revealed the resident's blood pressure had been improved after medication change, No specific complaints at this time. He is not in acute distress; is not toxic-appearing. Pulmonary effort is normal. Breath sounds: Normal breath sounds. No wheezing or rales. Comments: 2+ (2 mm with delayed rebounds) BLE (bilateral/both lower extremities/legs) edema to just above knees; patient says this has been stable lately (neither worse nor better since admission to SNF) spent additional talking with the patient's family.
-Up to this date the resident's medical record failed to document the status of Resident #52's edema.
-Per the resident's weight log, the resident had an increase of 6.3 lbs. from 7/8/23 to 7/9/23, there was no documentation whether the resident primary care physician or cardiologist had been notified of the resident's weight gain until two days later and the physician did not examine the resident until five days later (see below). The physician visit note dated 7/7/23 failed to document if the physician assessed the resident's weight gain and if any additional medical treatment was necessary.
Daily skilled nursing notes dated 7/10/23 at 6:53 p.m. documented in pertinent part that the resident continued to have impaired balance and weakness. Skin Integrity: weeping to the right lower extremity, edema to the left and right lower extremities.
Nursing progress note dated 7/11/23 revealed Resident #52 had edema to both lower extremities and a couple of blisters, with weeping. The physician gave verbal orders to wrap the resident's legs in kerlix (a bandage rolls that provide wicking action, aeration and absorbency) and apply tubi grips (a tubular bandage that provides consistent and even compression).
Daily skilled nursing notes dated 7/11/23 at 7:05 p.m. documented in pertinent part the resident's Skin Integrity: weeping to right lower extremity, edema to left and right lower
extremities.
-There was no documentation in the daily skilled nursing notes for the section about edema or in any nursing note to document the status of the resident's edema on 7/13/23.
Daily skilled nursing notes dated 7/14/23 at 12:14 a.m. documented in pertinent part: the resident had no edema.
-However, nursing and physician notes before and after this date documented the resident had signs and symptoms of edema.
Physician's visit note dated 7/14/23 documented the resident was seen for a follow up visit for daily weights, monitoring of blood pressure and wound care . The note revealed the resident was seen at the heart failure clinic on 7/5/23. Recommendations from the last visit were to monitor edema and weights.
-During this follow up visit 7/14/23 (Resident #52) told me he felt his legs were more swollen. He has developed clean venous stasis ulcers and is followed by the wound team. Physical exam record review weights reviewed. Medication changes: - Increase Torsemide (Demadex) (medication to help treat fluid retention (edema) and swelling that is caused by congestive heart failure) 20 mg, oral tab; take three tablets by mouth, daily, for chronic congestive heart failure.
Skilled nursing note dated 7/16/23 at 5:12 p.m. documented in pertinent part: Edema is present: in bilateral lower extremity. Edema leaves a slight indentation of 3-4 millimeters (mm), 15 second or less rebound, none noted. Bilateral lower legs red and using Kerlix. Dressing changed as pre-treatment orders.
Nursing progress note dated 7/18/23 at 8:10 a.m. documented Resident voiced some concerns on how he is feeling. Resident feels shaky, and like he is retaining more fluid, he feels bad.
Transfer form dated 7/18/23 at 11:10 a.m. documented the resident was sent to the hospital for further evaluation due to water weight gain of five lbs. in two days.
III. Staff interviews
Licensed practical nurse (LPN) #2 was interviewed on 7/25/23 at 10:30 a.m. LPN #2 had no knowledge of Resident #52. LPN #2 said the nurse should fully assess the resident experiencing a change of condition and document the assessment in the resident progress notes. The nurse should contact the resident's physician and document the contact and any orders. The admitting nurse was responsible for reviewing hospital orders and entering the orders into the resident record.
LPN #3 was interviewed on 7/25/23 at 11:02 a.m. LPN #3 said the skilled nursing assessment was completed. Each shift the nurse should document the resident's status on the form completing a response for each section on the form. If the resident had a change in condition after the skill nursing note was completed the nurse should make an additional entry in the resident record. If there was a change in the resident's condition, the nurse should contact the resident's physician for treatment orders and document that contact. The resident's representative should also be notified.
The registered dietitian (RD) and the RD consultant (RDC) were interviewed on 7/27/23 at 2:20 p.m. The RD said she assessed Resident #52 and talked to the resident about his dietary needs. They discussed the importance of getting good nutrition and a low sodium; however, the RD believed it was important to put the resident on a regular diet due to poor intake and risk of malnutrition. The RD's focus for Resident #52 was to make sure he ate enough food. The resident had a good understanding of low sodium food choices and said he understood he limited his fluid intake.
The CNC was interviewed on 7/27/23 at 11:30 a.m. The CNC said the Nursing admission Data collection and Baseline document was the resident baseline care plan. The document triggered a care focus with interventions for any assessed area where the nurse found concern. If no concern was identified the document would not trigger the need for interventions.
The CNC, director of nursing (DON), nursing home administrator (NHA) and corporate consultant (CC) were interviewed on 7/31/23 at 3:55 p.m. The DON said the admitting nurse would transcribe all medication and treatment orders from the resident's hospital discharge records into the resident record. The resident's physician got a copy of the discharge documents and was responsible for reviewing the resident medication administration record and treatment administration record for accuracy and signing off on the orders. The resident's primary care physician would make the decision whether or not to follow the hospital discharge orders.
The nursing staff should document the resident's health status in the daily skilled nursing note and any additional changes of condition in the resident record.
CONCERN
(D)
📢 Someone Reported This
A family member, employee, or ombudsman was alarmed enough to file a formal complaint
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0697
(Tag F0697)
Could have caused harm · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations, interviews and record review, the facility failed to manage pain in a manner consistent with professional...
Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations, interviews and record review, the facility failed to manage pain in a manner consistent with professional standards of practice, the comprehensive person-centered care plan, and the residents goals and preferences for one (#52) out of 52 sample residents.
Specifically, the facility failed to administer scheduled pain medication, for neuropathy pain, at the correct dosage as ordered by the resident's physician, to Resident #52.
Findings include:
I. Professional reference
According to [NAME] Nursing Drug Handbook 2020, Kizior, R. J. and [NAME], K.J., St. Louis Missouri 2020, revealed the following pharmaceutical information, page (pp). 963-965 read in part: Pregabalin. Use: Management of neuropathic pain associated with diabetic peripheral neuropathy, postherpetic neuralgia. Administration: discontinue gradually over at least one week.
II. Facility policy
The Administering Medications policy revised April 2109, was provided by the corporate nurse consultant (CNC) on 7/31/23 at 2:35 p.m. The policy read in pertinent part: Medications are administered in a safe and timely manner, and as prescribed.
The Pharmacy Services Overview policy revised April 2109, was provided by the corporate nurse CNC on 7/31/23 at 2:35 p.m. The policy read in pertinent part: The facility shall contract with a licensed consultant pharmacist to help it obtain and maintain timely and appropriate pharmacy services that support residents' needs, are consistent with current standards of practice, and meet state and federal requirements.
-Pharmacy services are available to residents 24 hours a day, seven days a week.
-Residents have sufficient supply of their prescribed medications and receive medications (routine, emergency or as needed) in a timely manner.
-Nursing staff communicate prescriber orders to the pharmacy and are responsible for contacting the pharmacy if a resident's medication is not available for administration.
III. Resident #52
A. resident status
Resident #52, age [AGE], was admitted to the facility on [DATE] and was discharged to the hospital on 7/19/23. According to the computerized physician's orders, diagnoses included heart failure, diabetes mellitus with diabetic neuropathy and chronic stage 3 kidney disease.
The admission minimum data set assessment (MDS) dated [DATE] documented the resident had intact cognition with a brief interview for mental status score of 15 out of 15. The resident needed staff supervision to complete activities of daily living (ADL).
-The resident had frequent pain and received scheduled and as needed pain medications to manage the pain. The resident rated his worst pain as an 8 on a pain scale of 1 to 10.
B. Resident representative interview
The resident was not available for an interview.
The resident's representative was interviewed on 7/31/23 at 10:06 a.m The resident representative said there was a pharmacy error and Resident #52 did not get the correct dosage of pregabalin (Lyrica) for neuropathy and Resident #52 complained of increased pain. The resident was prescribed pregabalin 150 milligrams (mg) twice a day, upon admission to the facility he was receiving the correct dose of medication but the facility ran out of medication and the nursing staff gave him 100 mg capsules instead until the pharmacy delivered the correct dose of medication a couple of days later.
C. Record review
The July 2023 CPO documented the following orders:
- Lyrica (pregabalin) oral capsule 150 mg, give 1 capsule by mouth two times a day for pain; start date 6/30/23.
-Lyrica (pregabalin) oral capsule 100 mg, give 100 mg by mouth one time only for neuropathic pain for one day; order date 7/12/23.
--Lyrica (pregabalin) oral capsule 100 mg, give 100 mg by mouth one time only for neuropathic pain for one day; order date 7/13/23.
Review of the July 2023 medication administration records (MAR) revealed: Lyrica (pregabalin) was not administered on 7/12/23, 7/13/23 for the morning and evening dose and 7/14/23 for the morning dose. The resident received a one time dose of Lyrica 100 mg at 7/12/23 at 11:00 p.m. and 7/13/23 at 2:13 p.m.
Physician admission summary dated [DATE] read in pertinent part: Other orders: Pregabalin (Lyrica) 150 mg oral capsule; take one capsule by mouth two times a day for neuropathy.
Medication administration note dated 7/12/23 at 11:46 a.m. read: Lyrica 150 mg (was unavailable). Waiting for the pharmacy to deliver.
Medication administration note dated 7/12/23 at 10:00 p.m. read: Lyrica oral capsule 150 mg, give one capsule by mouth two times a day for pain. (Medication) unavailable. On-call physician notified.
Skilled nursing note dated 7/13/23 at 5:12 a.m. read in pertinent part: Lyrica 150 mg was unavailable. On call physician notified. Obtained an order to give 100 mg by mouth tonight and in the morning. Prescription to be sent to the pharmacy. Lyrica 100 mg provided from emergency medication stock.
IV. Staff interview
Licensed practical nurse LPN #3 was interviewed on 7/25/23 at 11:02 a.m. LPN #3 said the nurse was to administer medication as ordered. The nurse should check the resident's MAR for the order, correct medication, dosage and time; if the medication was unavailable, the nurse should notify the physician that the medication is unavailable and document the communication and any additional orders. The nurse should also contact the pharmacy to reorder the mediation. Medication should be ordered at least three to seven days prior to the medication running out. Some medication could be obtained from the emergency medication storage with pharmacy approval.
The CNC, director of nursing (DON), nursing home administrator (NHA) and corporate consultation (CC) were interviewed on 7/31/23 at 3:55 p.m. The DON said medication should be reordered prior to the medication running out. If medications were unavailable, the nurse should check the emergency medication supply to see if the medication is available in the kit; then contact the pharmacy for an approval code to provide them medication and a prescription refill. When the medication is unavailable, the nurse should contact the prescribing physician for additional orders.
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0761
(Tag F0761)
Could have caused harm · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations and interviews, the facility failed to ensure biologicals were labeled and stored in accordance with accep...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations and interviews, the facility failed to ensure biologicals were labeled and stored in accordance with accepted professional standards for one of four medication storage rooms.
Specifically, the facility failed to discard expired vaccines from the medication storage room.
Findings include:
I. Facility policy
The Storage of Medications policy, dated [DATE], was received on [DATE] at 2:35 p.m. from the corporate nurse consultant (CNC). The policy read in pertinent part:
The nursing staff is responsible for maintaining medication storage and preparation areas. Discontinued, outdated, or deteriorated drugs or biologicals are returned to the dispensing pharmacy or destroyed.
II. Observations
Medication room two-south unit
On [DATE] at 3:03 p.m., the medication room was observed with registered nurse (RN) #1 and the unit manager (UM). After the observation, RN #1 and the UM verified the medication room had the expired biological items including:
Sanofi Pasteur fluzone influenza (flu vaccine), 10 pre-filled syringes that expired [DATE], 97 days prior to the observation.
III. Interviews
RN #1 and the UM were interviewed together immediately after the observation on [DATE] at 3:09 p.m. The UM said the expired vaccines should have been removed from the supply room. The UM said the policy for vaccine storage was to discard or return expired vaccines to the pharmacy. RN#1 disposed of the expired vials immediately.
The assistant director of nursing (ADON) was interviewed on [DATE] at 2:15 p.m. The ADON said the expired vaccines should be removed from storage immediately to prevent expired items being administered.
CONCERN
(E)
📢 Someone Reported This
A family member, employee, or ombudsman was alarmed enough to file a formal complaint
Potential for Harm - no one hurt, but risky conditions existed
Grievances
(Tag F0585)
Could have caused harm · This affected multiple residents
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interviews and record review, the facility failed to provide prompt acceptable resolution to resident/resident represen...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interviews and record review, the facility failed to provide prompt acceptable resolution to resident/resident representative grievances that were important to the residents.
Specifically, the facility failed to resolve grievances for long call wait times in a manner that was satisfactory to the residents in the facility.
Findings include:
I. Facility policy and procedure
The Grievance policy and procedure, reviewed [DATE], was provided by the nursing home administrator (NHA) on [DATE] at 4:48 p.m. It read, in pertinent part, to ensure residents are afforded their right to file a grievance without discrimination or reprisal and that such grievance shall be responded promptly and in written form.
A resident, family member, staff member or visitor may file a grievance at any time with an appropriate staff member or supervisor. There is no set time frame or minimum amount of time in which it must be filed except for those required under the Elder Justice Law.
Upon receipt of a Grievance and Complaint Report or Complaint Concern form, the social services director or designee will begin an exploration into the allegations/concerns. The appropriate department director will be notified of the nature of the complaint and that follow up is necessary. The investigation and report will include, as each may apply: the date and time the incident took place; the circumstances surrounding the incident; where the incident took place; the names of any witnesses and their account of the incident; the resident's account of the incident; the employee's account of the incident; accounts of any other individuals involved; and recommendations for corrective action if not already remedied.
The Grievance and Complaint Investigation Report must be filed with the administrator within five working days of the receipt of the grievance of complaint form.
II. Resident interviews
Resident #41 was interviewed on [DATE] at 1:45 p.m. Resident #41 said she waited several hours for staff to answer her call light. Resident #41 said she used the call light and no staff came. She said it sometimes made her upset and anxious and the staff did not care.
Resident #68 was interviewed on [DATE] at 1:45 p.m. Resident #68 said he waited 45 minutes for staff to answer his call light when he used it to request pain medication.
Resident #1 was interviewed on [DATE] at 3:05 p.m. Resident #1 said it could take staff 20 to 30 minutes or more to answer the call light. Sometimes the certified nursing aids (CNA) came into the room after the 20 to 30 minute wait and did nothing for her; turned off the call light; left the room and then did not come back for another 20-30 minutes. Resident #1 said she did not like it because there were several times they turned off the light and left when she felt uncomfortable and needed personal care.
Resident #233 was interviewed on [DATE] at 4:20 p.m. Resident #233 said she waited in pain for about 45 minutes for staff to come when she needed the bedpan on [DATE]. Resident #233 said there were sometimes after she used her call light that she waited for longer than 20 minutes after activating the call light when she needed to use the bedpan. Resident #233 said sometimes when staff did not answer the call light it made her scared, worried and anxious about having an accident.
III. Record review
A. Grievance log
The grievance log from [DATE] to [DATE] revealed there were 13 grievances for call lights.
B. Call light alert and response times report
A request was made for call light response time for residents who reported long call light wait times during the survey; and for observations during the survey where call light's where staff failed to respond to the resident's call light effectively. The call light response logs (incident details report) revealed the following:
-Resident #4's call light log for [DATE] at 8:37 a.m. revealed the call light was not answered for 30 minutes.
-Resident #233's call light log for [DATE] at 5:10 a.m. revealed the call light was not answered for 44 minutes and not answered for 24 minutes during the same morning at 6:09 a.m.
-Resident #34's call light log for on [DATE] at 9:22 p.m. revealed the call light was not answered for 18 minutes.
-Resident #22's call light log for [DATE] between 8:35 a.m. and 4:47 p.m. revealed the call light was not answered timely five times during that day. The call light activated at 8:35 a.m., was not answered for 48 minutes; the call light activated at 10:11 a.m, was not answered for 45 minutes; the call light activated at 1:46 p.m., was not answered for 26 minutes; the call light activated at 2:17 p.m., was not answered for 55 minutes; and the call light activated at 4:47 p.m., was not answered for 45 minutes.
IV. Staff interviews
CNA #1 was interviewed on [DATE] at 4:08 p.m. CNA #1 said the CNAs were supposed to answer the call lights within three minutes, but sometimes she was busy with other residents and could not answer right away. CNA #1 said she when a call light was activated she would check on the resident and turn off their call. If the resident needed to be changed or toileted, she would help them immediately. If she could not help the resident immediately then she would let the nurse know.
CNA #2 was interviewed on [DATE] at 4:08 p.m. CNA # 2 said she tried to answer the call lights within three minutes, but answering call lights in that time was sometimes difficult when there were a lot of call lights on at the same time. CNA #2 said when that happened she would finish up with the resident she was working with and then answer the next call light as soon as possible. CNA # 2 said if she could not get to the residents she would tell the nurse.
CNA #3 was interviewed on [DATE] at 11:56 a.m. CNA #3 said she tried to answer the call light as soon as possible. If she was in the middle of helping a resident she would finish with them before answering the call light. She said if a resident could wait she would go in and turn off the call light and return after finishing with another resident. CNA #3 said if a resident needed personal care or the bathroom she would find another staff member to help right away.
Licensed practical nurse (LPN) #2 was interviewed on [DATE] at 4:13 p.m. LPN #2 said the resident call light system used pagers which the CNAs had. LPN #2 said the CNAs should answer the call lights within a reasonable time frame, which was considered to be within seven minutes. LPN #2 said there were times when the CNA would be in with a resident and was unable to answer the call lights timely. LPN #2 said when that happened another CNA would help them.
LPN #2 said it would depend on a resident's need, if it was something simple then the CNA could help them quickly. LPN #2 said if it was a more significant need, such as personal care was needed for a resident who required a two-person lift, the CNA might turn off the call light and then leave to get help from another staff member. LPN #2 said there were times when the CNA would forget to turn off the call light when they went to get another staff, which would show an increase in the call light response time.
The director of nursing (DON) was interviewed on [DATE] at 3:56 p.m. The DON said the call light system used pagers and an escalation system. The CNAs, the unit nurses and nurse managers carried pagers. The assistant director of nursing (ADON) and the DON got the call light alerts on their cell phones.
The DON said when a call light was used the CNAs get an alert on their pagers letting them know which room and resident needed attention. The CNAs needed to respond to the call light within three minutes if they did not the unit nurse received an alert page after the three minute mark. If the call light was not answered by six minutes, the nurse manager would then receive an alert pager message; and the ADON would receive an alert after 10 minutes. Then after 15 minutes DON received a notification message a resident's call light was still unanswered.
The DON said when she received the notification on her phone she would call the unit/facility to determine what happened. The DON said she reviewed the call light report weekly and would determine why there were long call light times and provide education for staff who were involved in the long call light times.
The DON said a CNA was to answer the call light within a reasonable time of 10 minutes or less. The DON said for a CNA to answer a call light timely would depend upon several factors such as time of day; if there was an emergency; if someone had a change in condition; if a resident needed a two person assist; or if the CNAs were busy helping another resident. The DON said another reason for the long call light times could be due to the CNA forgetting to turn off the call light before helping the resident, not turning off the call light off prior to leaving the room to finish up with another resident or getting help from another CNA.
CONCERN
(E)
📢 Someone Reported This
A family member, employee, or ombudsman was alarmed enough to file a formal complaint
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0679
(Tag F0679)
Could have caused harm · This affected multiple residents
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations, record review and interviews, the facility failed to ensure meaningful activities designed to support res...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations, record review and interviews, the facility failed to ensure meaningful activities designed to support residents physical, mental, and psychosocial well-being were provided for three (#1, #4 and #41) of six residents out of 52 sample residents.
Specifically, the facility failed to:
-Offer the resident population a consistent and regular scheduled activities program that included both facility-sponsored group and individual activities and independent activities, designed to meet the interests of and support the physical, mental, and psychosocial well-being of each resident, encouraging both independence and interaction in the community;
-To provide residents #1, #4 and #41 meaningful activities; and,
-To offer residents #1, #4 and #41 regularly scheduled activities of choice.
Findings include:
I. Facility policy and procedure
The Activity Documentation policy and procedure, revised on 6/20/23, was provided by the director of nursing (DON) on 7/31/23 at 4:00 p.m.
It revealed, in pertinent part, The community will offer at least three group activities per week, one of which must be offered in the evening (after dinner) that not only meet the requirements of state and federal guidelines, but also the interests, preferences, hobbies and culture of the participants and community. Activities include community sponsored group and assistance in individualized/independent activities.
Activities will create opportunities for participants to have a meaningful life by supporting their domains of wellness (security, autonomy, growth, connectedness, identity, joy and meaning).
Activities will be designed to meet participants' best ability to function, incorporating their strengths and abilities.
The activity department will provide 1:1 (one-to-one) recreation and social visits if the individual was unable to participate in independent leisure, or, upon participant request.
II. Activities programming
A. Resident interviews
Resident #34 was interviewed on 7/24/23 at 9:05 a.m. She stated activities were none existent. She said that staff provided assistance to select television programs. She said that staff had not offered a selection of activities and that she had participated once with an activity but it was not meaningful because it was not interesting to her. She said she had not been invited to participate in other activities.
Resident #57 was interviewed on 7/26/23 at 11:42 a.m. Resident #57 said he had been at the facility for about six weeks, since mid June 2023. Resident #57 said he had not met any other residents for his first three weeks at the facility. Resident #57 said the first time he met other residents was when he attended a group therapy session. He then began to eat meals with the other residents.
Resident #57 said he suggested to staff they have group activities such as an ice cream social, bingo or games in order for residents to meet each other and socialize. Resident #57 said he was not offered one-to-one or group activities since he had arrived. Resident #57's room did not have an activities calendar posted.
Resident #23 was interviewed on 7/27/23 at 9:52 a.m. Resident #23 was unable to speak answers aloud but was able to answer some questions with gestures. Resident #23 shook his head no when asked if he was offered or participated in activities. When Resident #23 was asked how long it had been since he was offered or participated in activities and he held up three fingers indicating he had not been offered activities opportunities in the three months since he arrived in the facility. Resident #23 shook his head yes that he would participate in activities if they were offered. Resident #23's room did not have an activities calendar posted.
B. Record review
The combined July 2023 therapeutic and activity calendar documented the following activities opportunities:
-On 7/5/23 activities offered Bingo at 5:45 p.m.;
-On 7/11/23 activities offered a viewing of a docu-series show at 5:45 p.m.;
-On 7/18/23 activities offered evening devotional at 5:45 p.m.;
-On 7/25/23 activities offered a social with card games at 5:45 p.m
-All other offerings listed on the calendar were therapy-oriented groups activities provided by the therapy department.
C. The activities director (AD) interview
The AD was interviewed on 7/27/23 11:06 a.m. The AD said the activities staff were offering only one group activity a week in the evenings from 5:00 p.m. to 7:00 p.m., due to lack of staff. There were no group activities being offered during the day time hours. The AD was the only staff member in the activities department but when the department was fully staffed there were three to five staff and they were able to provide regular activities programming when they were fully staffed. When fully staffed there would be two group activities every day and one-to-one activities programming would be provided to all residents assessed to need that level of programming on a regular schedule. The one to one activities would be completed by the AD and one other activity staff while the others would provide group programming and offer resident supplies for independent activities. The AD said she was currently the only staff providing one-to-one activities to residents.
The AD said over the last couple of months the activity calendar was merged with the therapeutic group exercise calendar since the activities department was only able to provide one group activity weekly. The therapeutic group exercise programming was a part of the therapy department services; the therapy department provided physical therapy and occupational therapy for residents who received skilled nursing services. The group therapy sessions listed on the combined activities therapy calendar was open to all residents if they wanted to attend.
The AD said when the activity department was fully staffed a separate calendar would be posted to include two recreational and social group activities per day. A paper copy of the calendar would be posted in each of the residents ' rooms so the resident would be aware of what activity was offered by the AD. At present, they did not post an activity calendar in the residents ' rooms.
The AD described independent leisure activities as any activity residents were observed participating in independently such as reading, watching television, talking or visiting with someone.
III. Resident #4
A. Resident status
Resident #4, age [AGE], was admitted on [DATE] and readmitted on [DATE]. According to the July 2023 computerized physician orders (CPO), the diagnoses included ventilator dependence, reduced mobility, dementia, bipolar II disorder and anxiety disorder.
The 5/1/23 minimum data set (MDS) assessment revealed the resident had severe cognitive impairment with a brief interview for mental status score of four out of 15. She required extensive assistance of two people for most activities of daily living (ADLs).
The assessment documented the resident's speech was unclear, but the resident was able to make concrete requests and to respond adequately to simple direct communication.
The 8/7/22 MDS initial assessment indicated it was very important for Resident #4 to listen to music, have animals/pets around, to participate in her favorite activities and religious services. It was somewhat important for Resident #4 to have books, newspapers and magazines to read and to go outside to get fresh air in good weather.
B. Resident observations and interview
-On 7/26/23 at 2:34 p.m., Resident #4 was in bed resting, she appeared to be sleeping.
-From 3:33 p.m. to 3:39 p.m., two staff provided personal care and repositioning. There was no additional stimulation or interactions between the staff and the resident and the resident was not offered or encouraged to participate in any type of recreational activity.
-At 5:02 p.m. Resident #4 was in bed sleeping. Resident #4 did not have any external stimulation or social interactions.
-On 7/27/23 at 9:54 a.m., 11:14 a.m. and 1:49 p.m. Resident #4 was observed in her room sleeping with no external stimulation or social interactions.
-At 2:48 p.m. staff provided personal care and repositioning. There was no additional stimulation or interactions with others.
Resident #4 was interviewed on 7/27/23 at 2:54 p.m. Resident #4 was awake, looking out her window and moving around in bed. Resident #4's television was not on and she did not have any additional stimulation or items for independent activities. Resident #4 was unable to speak aloud but was able to respond to questions by mouthing simple words and by use of gestures.
Resident #4 mouthed yes to wanting to participate in activities including listening to music, visiting with animals and observing or working with art. When asked if she wanted to get out of her room to participate in activities she nodded her head yes. She then pointed to the window and smiled, she nodded her head when asked if she enjoyed looking out of the window. Resident #4's room did not have an activities calendar posted.
C. Resident representative interview
The resident's representative was interviewed on 7/27/23 at 2:10 p.m. The representative said Resident #4 loved music, animals and art. The resident representative said she did not think Resident #4 did any activities right now. She said she would like it if Resident #4 could participate in activities that interested her. She would especially like it if Resident #4 were to be able to get out of her room to participate in activity programming. The resident representative said Resident #4 would not refuse those activities if they were offered to her either for a one-to-one or group activity.
D. Record review
Activities care plan initiated on 8/5/22 revealed Resident #4's interests were reading books, listening to music (rock n ' roll, country, Conway [NAME], and blues), being around animals, watching movies, westerns, or sports on the television (TV). Resident #4 was a Broncos football fan and enjoyed getting fresh air and having her blinds and windows open. Resident #4 was Christian and practiced by listening to gospel music.
The care focus goal initiated on 8/5/22 revealed Resident #4 would participate in independent leisure activities of choice approximately three to five times per week by watching shows of interest on TV, reading or listening to music of interest.
Goal initiated on 2/10/23 revealed Resident #4 would accept therapeutic one-to-one visits approximately three to five times per week which included activities of interest such as listening to music, being spoken to or reading books by nodding her head and making eye contact.
Activities participation documentation revealed Resident #4 participated in a one-to-one activity in the month of July 2023 on 7/17/23; and participated 15 times in independent leisure activities from 7/3/23 to 7/28/23.
-Independent leisure activities were described by the activities director (AD) as any activity residents were observed participating in independently such as reading, watching tv, talking or visiting with someone (see above).
-There was no other documentation in record of Resident #4 participating in one-to-one or group activities of choice.
IV. Resident #41
A. Resident status
Resident #41, age [AGE], was admitted on [DATE] and readmitted on [DATE]. According to the July 2023 CPO, the diagnoses included aphasia (difficulty with language), dysphagia (difficulty with swallowing), cervical disc disorder, and muscle wasting and atrophy.
The 5/23/23 MDS assessment revealed the resident had a moderate cognitive impairment with a brief interview for mental status score of 11 out of 15. She required extensive assistance of two people for most ADLs.
The assessment documented it was very important for Resident #41 to keep up with the news, do her favorite activities, go outside and get fresh air and participate in religious services or practices. It was somewhat important for Resident #41 to have books, newspapers and magazines to read, listen to music and to do things with groups of people.
A. Resident interview and observations
Resident #41 was interviewed on 7/25/23 at 9:42 a.m. Resident #41 was sitting up in bed and said she had not been offered activities in the two months since she had been at the facility. Resident #41 said she would like to go to activities if they had them.
Resident #41 was interviewed again on 7/25/23 at 4:32 p.m. Resident #41 was in her room sitting up in bed, she said she was happy she attended the resident group meeting and felt much better now that she met other residents she could talk to. She said she had not met any other residents prior to the meeting because she never got out of her room to meet residents. Resident #41 said she had not been offered an invitation to activities and was unaware of activities opportunities. The resident said she did not have an activities calendar posted.
Resident #41 was interviewed again on 7/26/23 at 2:03 p.m. Resident #41 said things had been going pretty well, but she still had not been offered an opportunity to participate in activities.
B. Record review
There was no documentation in the resident record showing that Resident #41 had been offered or had participated in activities since during her time in the facility.
V. Resident #1
A. Resident status
Resident #1, age [AGE], was admitted on [DATE]. According to the July 2023 computerized CPO the diagnoses included hemiplegia and hemiparesis following cerebral infarction affecting left dominance (stroke with left side weakness), chronic obstructive pulmonary diseases (lung disease), multiple sclerosis, post polio syndrome, tracheostomy, ventilator dependence, depression and weakness.
The 4/19/23 MDS assessment documented the resident was cognitively intact with a brief interview for mental status score (BIMS) of 15 out of 15. She required two person assistance to extensive assistance with most ADLs. The resident's activity prefrence were not assessed.
B. Resident interview
Resident #1 was interviewed on 7/24/23 at 1:45 p.m. Resident #1 said she used to play Bingo. The activities staff would bring a computer tablet to her bed so she could play with the other residents from her bed. She said it stopped when one of the activities staff members stopped working at the facility and they no longer brought her the tablet so she could participate. The resident said she loved to play Bingo and missed participating.
Resident #1 said she missed letter writing with a family member. An activities staff member used to pick up her outgoing mail every day at 11:00 a.m. since she was unable to leave her room to get the written letter in the mail. The activities staff did so to help the resident participate in a letter writing exchange with a special family member. The resident said this letter writing exchange was a great sense of enjoyment and was very important to her. The activities staff's participation in this social activity was necessary to ensure that her letters got out in the day's mail and arrived to its recipient in a timely fashion so the recipient could respond timely and she could receive letters back in exchange. She looked forward to the recipient's response to her letters. The resident said the staff member who picked up her mail stopped working at the facility three weeks ago and no staff came to pick up her mail in their absence. The resident filed a grievance and they started to pick up her mail; but then that stopped five days later and had not resumed.
Resident #1 said she felt terrible because there were times she would work to find staff to take her mail to the receptionist only to find out the letter was not picked up by the postman.
Resident #1 said sending and receiving mail was the most important thing to her. She had a family member who was only able to visit once a month so they wrote to each other every day. The resident and her family member set up a system of letter writing so they could expect a letter from one another most every day, but without activity staff's assistance that was not happening. The resident said to most people mail may not be that important but for her, it was important because she was in her bed 24 hours a day, 7 days a week and the correct correspondences made her feel connected.
C. Record review
The 7/25/23 comprehensive care plan focus for activities program revealed Resident #1 loved to write letters everyday, visit family and playing games like Bingo with groups of people. Interventions included sending mail daily and providing Resident #1 with assistance setting up a tablet in the resident's room to use for virtual group activities of interest.
The resident's activity record revealed she had three total one-on-one visits in the past 30 days. One for each of the following activities: social, music and drawing in the past 30 days.
-The activity record did not document any resident participation for playing Bingo in the virtual group setting nor did the activities record document that mail assistance was provided to the resident as care planned.
D. Staff interview
The corporate nurse consultant (CNC) was interviewed on 7/31/23 at 3:57 p.m The CNC looked in the resident's record and confirmed that there was no record of mail being sent out and no record of the resident attending Bingo.
VI. Other staff interviews
Certified nurse aide (CNA) #3 was interviewed on 7/27/23 at 11:56 a.m. CNA #3 said group activities such as bingo and movies were held upstairs in the activity room. The residents were offered one-on-one activities in their rooms. CNA #3 said there used to be more activity staff but right now there was only one staff available.
CNA #1 was interviewed on 7/31/23 1:10 p.m. CNA #1 said she had not seen residents participating in any activities in the last two months. CNA #1 said two months ago residents would offer group activities such as bingo, movies, arts and crafts and also one-to-one activities in their rooms. CNA #1 said she was not sure why there had not been any activities recently.
CNA #4 was interviewed on 7/31/23 at 2:37 p.m. CNA #4 said she had been working at the facility for two months and had worked on both long term care and rehabilitation floors. CNA #4 said had not seen one-to-one or group activities being offered to residents since she had started working.
The nursing home administrator (NHA) was interviewed on 7/31/23 at 2:23 p.m. The NHA said there was currently one activity staff and he said the activity department was fully staffed. The NHA said there were two staff in the activity department a month ago. The NHA said group activities were located on the calendar but was unsure as to how many group activities were held daily. The NHA said the therapeutic group activities were counted as activities and all residents were offered therapy. The NHA said for social activities the residents were encouraged to self-initiate and could join other residents in the dining hall during meals.
The NHA said one-to-one activities were offered to residents up to six times a week depending on what was refused or accepted by the resident. The resident's preferences were included in the resident's file.
The NHA said they instituted an ambassador program where each department head was assigned residents to visit each morning. Every resident was visited daily and had the option to share any concerns they had during the visit. The concerns were documented in a spreadsheet and all concerns were addressed at the morning meeting.
CONCERN
(E)
📢 Someone Reported This
A family member, employee, or ombudsman was alarmed enough to file a formal complaint
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0760
(Tag F0760)
Could have caused harm · This affected multiple residents
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and interview, the facility failed to ensure one (#124) of three residents out of 52 sample residents did...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and interview, the facility failed to ensure one (#124) of three residents out of 52 sample residents did not experience a significant medication error.
Specifically, the facility failed to ensure that Resident #124:
-Received the medication selpercatinib, a prescribed kinase inhibitors medication (a medication that blocks the action of an abnormal protein that signals cancer cells to multiply) according to manufacturer's directions when give with a protein pump inhibitor (PPI) medication (a class of medications that blocks gastric acid secretions by dissolving chemical bonds within food molecules); and,
-Received the medication selpercatinib timely within permeates of also giving the medication before meals and doses 12 hours apart per manufacturer's directions.
I. Professional reference
According to the manufacture Eil Lilly and Company Prescribers Information highlights, revised September 2022, retrieved from https://uspl.lilly.com/retevmo/retevmo.html#pi on 7/27/23
Retevmo- selpercatinib capsule is indicated for the treatment of adult patients with locally advanced or metastatic non-small cell lung cancer (NSCLC) with a rearranged during transfection (RET) gene fusion, as detected by an FDA-approved test.
Retevmo may be taken with or without food unless co-administered with a proton pump inhibitor (PPI)
Dosage modifications for concomitant (given with) use of acid-reducing agents
Avoid concomitant use of a PPI, a histamine-2 (H2) receptor antagonist (a medication used to treat gastric intestinal ulcers and for some conditions, in which the stomach produces too much acid), or a locally-acting antacid with Retevmo.
If concomitant use cannot be avoided:
-Take Retevmo with food when co-administered with a PPI.
-Take Retevmo 2 (two) hours before or 10 hours after administration of an H2 receptor antagonist
-Take Retevmo 2 (two) hours before or (two) hours after administration of a locally-acting antacid.
Concomitant use of RETEVMO with acid-reducing agents decreases selpercatinib plasma concentrations, which may reduce RETEVMO anti-tumor activity.
Patient counseling information:
-Advise patients that they will require regular blood pressure monitoring and to contact their healthcare provider if they experience symptoms of increased blood pressure or elevated readings;
-Advise patients that RETEVMO may increase the risk for bleeding and to contact their healthcare provider if they experience any signs or symptoms of bleeding;
-Advise patients to contact their healthcare provider promptly to report any signs and symptoms of tumor lysis syndrome (TLS-caused by massive tumor cells lysis with the release of large amounts of potassium, phosphate and nucleic acid into the the circulatory system) symptom include: nausea, vomiting, diarrhea, muscle cramps or twitches, weakness, numbness or tingling, fatigue, and decreased urination.
-Advise patients and caregivers to inform their healthcare provider of all concomitant medications, including prescription medicines, over-the-counter drugs, vitamins, and herbal products.
According to [NAME], P.A. and [NAME], A.G. et.al., (2021), Fundamentals of Nursing, 10 edition, pp 599 - 609. Nurses play an important role in patient safety, especially in the area of medication administration. The safe administration of medications is also an important topic for current nursing researchers. As a nurse you need to know how to calculate medication doses accurately and understand the different roles that members of the health care team play in prescribing and administering medications.
The National Coordinating Council for Medication Error Reporting and Prevention (2018) defines a medication error as any preventable event that may cause inappropriate medication use or jeopardize patient safety. Medication errors include inaccurate prescribing, administering the wrong medication, giving the medication using the wrong route or time interval, administering extra doses, and/or failing to administer a medication.
-Preventing medication errors is essential.
-Because nurses play an essential role in preparing and administering medications, they need to be vigilant in preventing errors.
Professional standards such as scope of nursing and standards of practice apply to the activity of medication administration. To prevent medication errors follow the seven rights of medication administration consistently every time you administer medication.
-The right medication; the right dose; the right patient; the right route; the right time; the right documentation; and right indication.
II. Facility policy
The Administering Medications policy revised April 2109, was provided by the corporate nurse consultant (CNC) on 7/31/23 at 2:35 p.m. The policy read in pertinent part: Medications are administered in a safe and timely manner, and as prescribed.
Medications are administered in accordance with prescriber orders, including any required time frame.
Medication administration times are determined by resident need and benefit, not staff convenience.
Factors that are considered include:
a. enhancing optimal therapeutic effect of the medication;
b. preventing potential medication or food interactions; and
c. honoring resident choices and preferences, consistent with his or her care plan.
Medications are administered within one (1) hour of their prescribed time, unless otherwise specified (for example, before and after meal orders).
The Medication Regimen Reviews policy revised May 2109, was provided by the corporate nurse consultant (CNC) on 7/31/23 at 2:35 p.m. The policy read in pertinent part: The consultant pharmacist performs a medication regimen review (MRR) for every resident in the facility receiving medication.
-Medication regimen reviews are done upon admission (or as close to admission as possible) and at least monthly thereafter, or more frequently if indicated.
-The goal of the MRR is to promote positive outcomes while minimizing adverse consequences and potential risks associated with medication.
-The MRR involves a thorough review of the resident's medical record to prevent, identify, report and resolve medication related problems, medication errors and other irregularities, for example:
a. medications ordered in excessive doses or without clinical indication;
b. medication regimens that appear inconsistent with the resident's stated preferences;
c. duplicative therapies or omissions of ordered medications;
d. inadequate monitoring for adverse consequences;
e. potentially significant drug-drug or drug-food interactions;
f. potentially significant medication-related adverse consequences or actual signs and symptoms that could represent adverse consequences;
g. incorrect medications, administration times or dosage forms; or
h. other medication errors, including those related to documentation.
-Within 24 hours of the MRR, the consultant pharmacist provides a written report to the attending physicians for each resident identified as having a non-life threatening medication irregularity.
-An 'irregularity' refers to the use of medication that is inconsistent with accepted pharmaceutical services
standards of practice; is not supported by medical evidence; and/or impedes or interferes with achieving
the intended outcomes of pharmaceutical services. It may also include the use of medication without indication, without adequate monitoring, in excessive doses, and or in the presence of adverse consequences.
-If the identified irregularity represents a risk to a person's life, health, or safety, the consultant pharmacist contacts the physician immediately (within one hour) to report the information to the physician verbally, and documents the notification.
-If the physician does not provide a timely or adequate response, or the consultant pharmacist identifies that no action has been taken, he/she contacts the medical director or (if the medical director is the physician of record) the administrator.
-The attending physician documents in the medical record that the irregularity has been reviewed and what (if any) action was taken to address it.
III. Resident #124
A. Resident status
Resident #124, under the age of 65, admitted on [DATE] and discharged on 7/4/23. According to the July 2023 computerized physician orders (CPO), diagnoses included malignant neoplasm (cancer) of the bronchus/lungs, malignant neoplasm of the brain, respiratory failure, epilepsy and gastroesophageal reflux disease (GERD).
The 6/22/23 minimum data set (MDS) assessment revealed the resident had intact cognition with a brief interview for a mental status score of 14 out of 15. The resident needed limited assistance from staff for mobility and completion of activities of daily living (ADL).
B. Record review
1. Physician's orders and medication administration record (MAR)
The June and July 2023 CPO and MARs documented the following orders:
Selpercatinib (Retevmo) oral capsule 80 mg, give two capsules by mouth every 12 hours, for cancer. Give at 8:00 a.m. and 8:00 p.m.
Pantoprazole sodium (protonix -a PPI) oral tablet delayed release 40 mg, give one tablet by mouth one time a day for GERD. Give at 7:00 a.m.
-The CPO and MAR gave the same instruction; failing to give specific instructions for giving the two medications concomitant per manufacturer's directions (see professional reference above).
-Review of the June and July 2023 CPO and MAR revealed the resident's medication was given late consistently for four of 13 morning doses and five of 14 evening doses (see below).
The pantoprazole sodium (PPI medication) was only scheduled for one hour before the selpercatinib medication as directed by the pharmaceutical manufacturer and in most cases the PPI medication was given at the same time as the selpercatinib medication (see below).
The MAR administration time revealed both the selpercatinib and the pantoprazole sodium (PPI medication) were given incorrectly and in direct contradiction to selpercatinib manufacturer's instructions.
On 6/20/23
Selpercatinib was given at 8:53 p.m., this was almost one hour late.
On 6/21/23
Pantoprazole sodium was given at 8:27 a.m., this was almost one hour and 39 minutes late.
Selpercatinib was given at 8:27 a.m.
Selpercatinib was given at 8:40 p.m.
On 6/22/23
Pantoprazole sodium was given at 8:20 a.m., this was over one hour late.
Selpercatinib was given at 8:20 a.m.
Selpercatinib was given at 1:42 p.m. (this was over six hours early from being 12 hours after the previous dose.
On 6/23/23
Pantoprazole sodium was given at 8:10 a.m., this was over an hour late.
Selpercatinib was given at 5:36 p.m., this was over nine hours and 30 minutes late.
Selpercatinib was given at 7:55 p.m., this was less than three hours after the previous dose was administered.
On 6/24/23
Pantoprazole sodium was given at 9:10 a.m., this was over two hours late.
Selpercatinib was given at 10:07 a.m., this was over two hours late.
Selpercatinib was given at 10:20 p.m., this was over two hours late and within the orders to administer doses 12 hours apart, which throws off the 12 hours between administration times.
On 6/25/23
Pantoprazole sodium was given at 9:02 a.m., this was over two hours late.
Selpercatinib was given at 9:05 a.m., this was over an hour late.
Selpercatinib was given at 10:23 p.m., this was over two hours late.
On 6/26/23
Pantoprazole sodium was given at 8:49 a.m., this was one hour and 49 minutes late.
Selpercatinib was given at 8:49 a.m.
Selpercatinib was given at 8:14 p.m.
On 6/27/23
Pantoprazole sodium was given at 7:15 a.m.
Selpercatinib was given at 7:14 a.m.
Selpercatinib was given at 7:13 p.m.
On 6/28/23
Pantoprazole sodium was given at 7:11 a.m.
Selpercatinib was given at 711 a.m.
Selpercatinib was given at 8:38 p.m.
On 6/29/23
Pantoprazole sodium was given at 11:17 a.m., this was over four hours late.
Selpercatinib was given at 11:26 a.m., this was over four hours late.
Selpercatinib was given at 10:29 p.m., this was over two hours late.
On 6/30/23
Pantoprazole sodium was given at 8:48 a.m., this one hour and 48 minutes late.
Selpercatinib was given at 8:47 a.m.
Selpercatinib was given at 8:41 p.m.
On 7/1/23
Pantoprazole sodium was given at 9:02 a.m., this was over two hours late.
Selpercatinib was given at 8:59 a.m.
Selpercatinib was given at 8:12 p.m.
On 7/2/23
Pantoprazole sodium was given at 8:06 a.m., this was over an hour late.
Selpercatinib was given at 8:07 a.m.
Selpercatinib was given at 9:59 p.m., this was three hours late.
On 7/3/23
Pantoprazole sodium was given at 8:58 a.m., this was two hours late.
Selpercatinib was given at 8:58 a.m., this was almost one hour late.
Selpercatinib was given at 8:05 p.m.
2. Nursing notes
Orders note dated 5/2/23 read in pertinent part: The order you have entered
Selpercatinib oral capsule 80 mg, has triggered the following drug protocol alerts/warning(s):
Drug to drug interaction.
Interaction: Severity: Severe. Interaction: Pharmacologic effects and plasma concentrations of selpercatinib may be decreased by proton pump inhibitors (Pantoprazole sodium oral tablet delayed release 40 mg.
-This alert appeared again on the progress notes on 5/9/23, 6/20/23 and 6/21/23 when the resident readmitted to the facility. There was no documentation in the residents records that any facility staff took action to address the drug interaction alert note.
Physician's note dated 5/5/23 read in pertinent part: Resident with a diagnosis of lung cancer metastasis to the brain; started chemo pill again on 4/28/23 after a one-month hiatus. Was referred to SNF (skilled nursing facility) for physical and occupational therapy (PT/OT) to increase strength, mobility, and ADL independence related to her decreased ability to care for herself at home and reduced activity tolerance over the last several weeks. There is a potential drug interaction with another medication, selpercatinib oral capsule. Continue selpercatinib 160 mg twice a day. Continue pantoprazole 40 mg daily.
-The physician's note did not document if the physician looked into the details of the drug interaction or took consideration for the manufacturer's warnings when taking selpercatinib with a PPI medication to take action to make sure the administration orders outlined precautions to lessen the potential drug interactions and outcomes.
3. Comprehensive care plan
The resident's comprehensive care plan initiated 6/23/23 did not contain a care for the resident's cancer treatment or for GERD.
IV. Staff interviews
Licensed practical nurse (LPN) #3 was interviewed on 7/25/23 at 11:02 a.m. LPN #3 said medications should be administered to a resident as close to the prescribed administration time as possible, but no earlier or later than one hour before or after the scheduled administration time. The pharmacy conducts an initial review of resident medications and monthly thereafter to identify any irregularities and alert the facility to recommendations for findings. The nurse was responsible to administer the medication correctly as ordered.
The pharmacist consultant (PC) was interviewed on 7/27/23 at 4:05 p.m. The PC said according to manufacturer's recommendations selpercatinib had a warning related to an adverse interaction.While manufactures recommendations selpercatinib should be given twice a day with each administration being12 hours apart, it was more importantly that when given with a PPI, the selpercatinib should be given two hours before the PPI or 10 hours after the administration of the PPI mediation. When the manufacturer's recommendations were not followed, the effectiveness of selpercatinib as a cancer treatment was reduced by 70 percent.
The CNC, director of nursing (DON), nursing home administrator (NHA) and corporate consultation (CC) were interviewed on 7/31/23 at 3:55 p.m. The DON said she was not familiar with any administration warnings for the resident's selpercatinib medication. The DON said she talked with the resident and the resident's representative specifically about how she was taking the selpercatinib medication and based on the resident selpercatinib to be administered at 8:00 a.m. and 8:00 p.m. so she would received it 12 hours apart. The DON was not aware there were manufacturer's warning instructions when the resident was also taking a PPI.
The CNC said the administering nurse should be aware of medication administration standards and if they were unfamiliar with a medication the nurse should look up the medication for administration instructions.
CONCERN
(E)
📢 Someone Reported This
A family member, employee, or ombudsman was alarmed enough to file a formal complaint
Potential for Harm - no one hurt, but risky conditions existed
Safe Environment
(Tag F0921)
Could have caused harm · This affected multiple residents
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** II. Electrical cords and trip hazards
A. Facility policy
The Safety Precautions, Electrical policy, revised 2011, was provided ...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** II. Electrical cords and trip hazards
A. Facility policy
The Safety Precautions, Electrical policy, revised 2011, was provided by the corporate nurse consultant (CNC) on 7/31/23 at 3:44 p.m. The policy read in pertinent part: Report any and all unsafe electrical hazards to your supervisor immediately.
-However, the policy did not document any methods of how and where electrical cords should be plugged in to prevent electrical cords from creating a trip hazard.
B. Observation
On 7/26/23 and 7/27/23 observations of resident rooms on the second floor unit were conducted. The resident's on the second unit were highly vulnerable individuals requiring the use of complex electrically powered medical equipment for life support. Each resident had several pieces of equipment that required electrical power to remain operational (ventilators, oxygen concentrators, suction machines, nebulizers, tube feeding pumps, pressure relieving mattresses and electrically controlled beds) and their rooms contained other non medical items (televisions, radios, fans) that required electricity to operate. There were not enough electrical outlets for all of the equipment and the electrical outlets were not placed strategically to keep electrical cords out of walkways so that staff and visitors did not trip; trip on a cord and pull it out of the outlet; or trip and fall onto the resident's bed. Some rooms used medical grade surge protectors to extend power cord so they reach outlets and several power cord laid in walkways; cords were not secured in place or affixed to walls to reduce potential trip hazards.
The resident's on the unit were dependent on staff for all care and positioning needs, requiring equipment including ventilator and or use of oxygen treatment.
Observations revealed there were several rooms where electrical cords laid unsecured in walkways where staff and visitors had to walk in order to provide resident care and have conversations with the resident in the room. Of 27 rooms observed on the second floor units there were 13 rooms were an electrical cord (for medical equipment) laid in the walkway causing a trip hazard for staff and visitors leaving the vulnerable resident at risk for injury due to staff getting injured and not being able to continue needed care; equipment being unplugged improperly; due to being improperly pulled out after a staff tripped over it; and/or a person falling on the resident after tripping over the cord.
Based on observations and staff interviews, the facility failed to provide a safe, functional, sanitary and comfortable environment for residents, staff and the public in one of three units.
Specifically, the facility failed to:
-Control foul odors throughout the two-south unit;
-To properly dispose of trash soiled with feces and urine;
-To maintain cleanliness in the dirty utility room; and,
-To keep electrical cords out of walkways, in resident rooms in order to prevent trip hazards.
Findings include:
I. Facility policy
The facility policy for environment maintenance was requested on 7/31/23 and was not received before survey exit on 7/31/23.
II. Observations
Foul odors were detected in the hallway near trash collection bags and outside resident's rooms on the two-north unit on:
7/24/23 at 9:15 a.m., 11:30 a.m., and 12:45 p.m.;
7/26/23 at 11:30 a.m., 1:15, p.m. and 4:15 p.m.;
7/27/23 at 1:25 p.m., and 3:55 p.m.; and,
7/31/23 at 10:35 a.m., and 3:00 p.m.
On 7/25/23 at 11:37 a.m., the dirty utility room was observed in the presence of the respiratory therapy manager (RTM). The trash collection bins were approximately one half full and there were two clear plastic trash bags full of trash soiled with bodily fluid discarded on the counter of the hand washing sink, in the utility room. The trash bags contained trash generated as a result of providing incontinence care to residents. The trash was smeared feces which was visible through the plastic. There was a 12 inch x 12 inch circle size, moist, brown and mucous spot on the floor in the walkway.
III. Staff interviews
On 7/25/23, a family member of the resident in room [ROOM NUMBER], said when he visited the resident, the foul odors were always present in the hallway where the trash disposal bags were frequently left in the hallway outside the resident's room and the odor could be smelled in the resident's room.
Certified nurse aide (CNA) #6 was interviewed on 7/25/23 at 11:40 a.m. CNA #6 said she was unsure why the trash bags were on the counter top and she placed the bags into the trash collection container. The CNA said sometimes the trash collection bags in the hallways were filled to capacity and piled up in the dirty utility room before the end of shift, staff removed trash from the facility for disposal, as time allowed. The CNA said the floors in the soiled utility room were monitored and cleaned by the housekeeping staff.
On 7/26/23 trash collected by the housekeeping department was observed sitting outside the dirty utility room in the hallway adjacent to the two-north nurses desk, next to the emergency equipment cart and vital signs machine.
The unit manager (UM) and the assistant nursing home administrator (ANHA) were interviewed on 7/26/23 at 9:12 a.m. They said they were unaware the housekeeping department left the collected trash in the hallway next to the dirty utility room. The UM and ANHA said the housekeeper should have placed the collected trash into the trash collection bags or removed the trash from the facility for disposal.
CONCERN
(F)
📢 Someone Reported This
A family member, employee, or ombudsman was alarmed enough to file a formal complaint
Potential for Harm - no one hurt, but risky conditions existed
Medical Records
(Tag F0842)
Could have caused harm · This affected most or all residents
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** II. Accurate medical record
A. Facility policy
The Charting and Documentation policy, revised July 2017, was provided by the co...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** II. Accurate medical record
A. Facility policy
The Charting and Documentation policy, revised July 2017, was provided by the corporate nurse consultant (CNC) on 7/31/23 at 2:35 p.m. The policy documented in pertinent part:
All services provided to the resident, progress toward the care plan goals, or any changes in the resident's medical, physical, functional or psychosocial condition, shall be documented in the resident's medical record.
The following information is to be documented in the resident medical record:
Objective observations;
Medications administered;
Treatments or services performed;
Changes in the resident's condition;
Events, incidents or accidents involving the resident; and
Progress toward or changes in the care plan goals and objectives.
B. Resident status
Resident #47 was admitted on [DATE] and readmitted [DATE]. According to the July 2023 computerized physician order (CPO), the diagnoses included acute and chronic respiratory failure, diabetes, tracheostomy, hemiplegia (paralysis) and dysphagia (difficulty swallowing) due to non traumatic intracranial hemorrhage (stroke), weakness and reduced mobility.
The 6/23/23 minimum data sheet (MDS) assessment documented that the resident was rarely understood and a brief interview for mental status score (BIMS) was not completed. She required two person assistance with bed mobility, transfer, toileting, bathing, dressing, personal hygiene and total dependence on eating.
The assessment document that the resident was not receiving physical therapy, occupational therapy or restorative nursing services at the time of the assessment.
C. Record review
The 7/3/23 care plan revealed that the resident had limited physical mobility. One intervention was to provide gentle range of motion as tolerated with daily care.
There was a physical therapy and occupational referral; this was not care planned, or documented as being provided to the resident anywhere in the resident record.
The 1/12/23 occupational therapy discharge summary revealed that the nursing staff were trained on how to provide the resident's recommended restorative nursing program as well as what safety precautions were needed, in order to promote mobility, safety and reduce the risk of further medical complications to the resident.
The 3/24/23 physical therapy progress note revealed that the resident would benefit from a restorative program for maintaining and improving bilateral lower extremities flexibility by passive range of motion and repositioning to decrease risk of skin breakdown.
-There was no documentation in the resident medical record to explain how the resident restorative services benefited the resident, the frequency of services provided and the resident's response to services provided.
D. Staff nterviews
The director of rehabilitation (PTD) was interviewed on 7/27/23 at 1:32 p.m. The PTD said the resident was evaluated a couple times for mobility needs and recommendations for ongoing restorative services were made. At the last evaluation in March 2023, the resident was totally dependent on staff for care. The rehabilitation therapist recommended the resident be placed on a restorative nursing program (RNP) to maintain flexibility and reduce skin breakdown. The RNP included passive range of motion (ROM) and positioning. The restorative nursing staff would be responsible for documenting services.
The director of nursing (DON) and unit manager (UM) were interviewed on 7/27/23 at 1:56 p.m. The DON said she and the UM needed to do some research to see if there was any documentation of services.
The DON was interviewed on 7/27/23 at 2:55 p.m. The DON said that there was no documentation that passive ROM was being provided by the restorative staff. The DON said that passive ROM was included with routine care that certified nurse aide (CNA) performed. The DON said that going forward there would be a separation from routine provision of care and provision of restorative nursing program services so that the restorative nursing care was clearly defined and documented accurately in the resident's record.
The corporate nurse consultant (CNC) was interviewed on 7/31/23 at 11:23 a.m. The CNC provided an updated care plan that reflected interventions that clearly defined the resident restorative nursing program services for type and frequency of ROM services. The intervention was initiated on 7/27/23.
The DON was interviewed on 7/31/23 at 5 p.m. The DON said that there was no documentation of the resident restorative nursing program in the resident's record to explain how often services were provided or how the resident was responding to the service.
Based on record review and interviews, the facility failed to keep confidential resident-identifiable personal information and medical treatments for 27 of 27 residents; and to ensure medical records were complete and accurately documented medical status and response to nursing/medical care and treatment in keeping with accepted standards of practice for a sample of two of four residents reviewed.
Specifically, the facility failed to:
-Keep confidential information specifically protected health information (PHI) out of view of other residents and visitors for 27 of 27 residents on the unit; and,
-Ensure Resident #47's medical record contained accurate and complete documentation regarding the resident's restorative management plan; restorative services provided; and the resident's response to services.
Findings included:
I. Confidentiality of PHI
A. Facility policy
The Confidentiality of Information and Personal Privacy policy, dated October 2017, was requested and received from the corporate nurse consultant (CNC) on 7/27/23 at 9:45 a.m. The policy documented in pertinent part:
The facility will safeguard the personal privacy and confidentiality of all resident personal and medical records;
The facility will strive to protect the resident's privacy regarding medical treatment and personal care;
Access to resident personal and medical records will be limited to authorized staff and business associates.
B. Observations
The facility respiratory therapy department hung a white board on the wall in the common area on the two-south hallway. The white board contained PHI information which was clearly visible to any person (visitors or other resident) entering the unit. The white board contained the following PHI:
-Resident first and last name;
-Resident code status (do not resuscitate/full code);
-Resident room number;
-Resident ventilator settings;
-Resident oxygen settings;
-Resident respiratory therapy treatments and treatment schedule;
-Resident ventilator settings; and ,
-Resident tracheostomy details (size and type) and treatment schedule.
Respiratory therapist (RT) #3 was observed updating the white board on 7/25/23 and 7/26/23 with resident PHI as listed above.
C. Staff interviews
The unit manager (UM) was interviewed on 7/26/23 at 9:35 a.m. The UM said the white board was used by the respiratory therapy department to share pertinent medical information about the residents to whom they provided services. The UM said the board contained resident specific PHI that applied to end of life decisions (code status) and life support care provided. The UM said resident specific healthcare information should be protected from the public such as visitors and other resident family members.
RT #1 was interviewed on 7/26/23 at 11:18 a.m. RT #1 said the white board was helpful to quickly identify which residents had ventilators, the settings and treatments they received and was referenced during shift reports and as needed during her shift. The RT said the resident information was also available to reference in the resident's electronic health record.
The CNC was interviewed on 7/27/23 at 9:45 a.m. The CNC said a board in public view should not include PHI. The CNC said she would review confidentiality of PHI with facility staff.
The respiratory therapy manager (RTM) was interviewed on 7/31/23 at 3:01 p.m. The RTM said the white board had been relocated to an office behind the nurses desk to prevent any confusion regarding what information was considered private and protected.
CONCERN
(F)
📢 Someone Reported This
A family member, employee, or ombudsman was alarmed enough to file a formal complaint
Potential for Harm - no one hurt, but risky conditions existed
Room Equipment
(Tag F0908)
Could have caused harm · This affected most or all residents
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations and interviews, the facility failed to maintain emergency patient care equipment in safe operating conditi...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations and interviews, the facility failed to maintain emergency patient care equipment in safe operating condition.
Specifically, the facility failed to perform daily quality readiness checks on the emergency response cart and to ensure expired items were removed and replaced.
Findings include:
I. Facility policy
The facility policy for maintaining patient care equipment was requested on [DATE] and a copy of the Crash Cart (a cart containing medicine and equipment for use in emergency resuscitations) Checklist, undated, was received from the corporate nurse consultant (CNC) on [DATE] at 11:30 a.m. The checklist documented, the crash cart should be checked daily and contain the following items:
-suction machine,
-record keeping paperwork,
-vitals machine,
-nonrebreather mask,
-nasal cannula high flow,
-nebulizer mask,
-14 French (FR) suction cath kits,
-yankauer suctioning wand,
-spare suction canister with short and long tubing,
-ventilation (AMBU) bag (a device to provide respiratory support to an individual in distress) with mask,
-oxygen regulator,
-oxygen tank wrench, and an
-extension cord.
II. Observations
On [DATE] at 3:15 p.m. the two-south emergency response cart was observed with the unit manager (UM)). Observations revealed the cart contained several expired and missing items (see crash cart checklist above). Expired items included:
-Wolf Medical Supply, 10 cubic centimeters (cc) prefilled normal saline syringes, expired [DATE], 673 days prior to the observation;
-Two 100 militer (ml) medline sterile water solutions, expired, [DATE], 777 days prior to the observation;
-Three B [NAME] Introcan safety IV (intravenous) start catheters needles, 22 gauge (needle width) by one inch, expired [DATE], 25 days prior to the observation; and,
-Two [NAME] IV start catheter needles, expired [DATE], 693 days prior to the observation.
-The UM was unable to locate a wrench to open the oxygen canister on the emergency response cart and had to look for one. A spare wrench was located on the nurses desk.
-In the event of a true emergency the oxygen wrench would not have been easily accessible to staff responding to an emergency without having to leave the emergency area to locate the wrench if oxygen was needed.
-The crash cart did not include a checklist for equipment readiness or documentation of when the cart was last checked for completeness of supply and expression date of the supplies.
III. Interviews
The UM was interviewed on [DATE] at 3:15 p.m. The UM said the expired items (see observations above) could no longer be used and needed to be replaced. The UM removed the expired items and said they would be replaced.
The UM said he did not know if the facility had a checklist or policy and was unaware of when the emergency equipment cart was last checked.
The UM and the assistance director of nursing (ADON) were interviewed together on [DATE] at 3:27 p.m. The ADON said the emergency response carts were checked daily as part of a risk management review. The ADON said the daily checks did not include a checklist and the UM on each unit was responsible to monitor the equipment for readiness.
The UM said he was unaware of the equipment checklist.
IV. Facility follow-up
On [DATE] the emergency equipment cart for two-north and two-south were observed with the UM. The equipment carts included a designated binder with an equipment readiness checklist and the equipment carts were properly stocked.