SERIOUS
(G)
Actual Harm - a resident was hurt due to facility failures
Quality of Care
(Tag F0684)
A resident was harmed · This affected 1 resident
Based on observation, record review, policy review, and interviews, the facility failed to promote and manage the delivery of safe nursing care in accordance with accepted Standards of Nursing Practic...
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Based on observation, record review, policy review, and interviews, the facility failed to promote and manage the delivery of safe nursing care in accordance with accepted Standards of Nursing Practice by failing to implement wound care recommendations to promote wound healing for one Resident (#64), in a total sample of 22 residents, which resulted in deterioration of an arterial wound to the Resident's left ankle.
Findings include:
Review of the facility's policy titled Wound and Skin Care Protocols/Definitions, last revised September 2022, included but was not limited to:
-The interdisciplinary plan of care will address problems, goals, and interventions directed toward the prevention and/or treatment of impaired skin integrity/pressure injury/ulcer;
-Monitor and document interventions and outcomes;
-Reclining and dependent residents should have position changes, alternating or low air loss mattress addressed in their care plan;
-Use pillows or foam wedges to keep bony prominences such as knees and ankles from direct contact with each other;
Resident #64 was admitted to the facility in March 2016 with diagnoses including hypertensive chronic kidney disease and a stage 3 pressure ulcer of the right ankle.
Review of the medical record indicated Physician's Orders for the following wound prevention interventions:
-foam booties to bilateral lower extremities at all times; remove every shift to monitor skin integrity
Review of interdisciplinary care plans included but was not limited to:
-Problem: Resident has a potential for bilateral heel deep tissue injury related to history of and decreased mobility (3/8/21)
-Interventions: Bilateral booties while in and out of bed. Remove every shift to monitor skin integrity (3/8/21)
-Goal: Resident will be free of new open areas or pressure areas through next review date (3/8/21)
Review of Weekly Skin Check documentation, dated 12/21/22, indicated nursing staff identified a fragile area to the Resident's right outer ankle.
Review of a Nurse's Note, dated 12/23/22, indicated Resident #64's Physician gave orders for Keflex 500 milligrams (mg) three times a day for 10 days for a right ankle wound infection.
Review of a Wound Evaluation and Management Summary, dated 12/23/22, from the wound consultant Physician, indicated Resident #64 had the following wounds:
1. arterial wound of the right, proximal, lateral ankle
2. arterial wound of the right lateral foot
3. arterial wound of the right shin
The wound Physician's recommendations included but were not limited to off-load [distribute the load to other areas which are not susceptible to pressure] the wounds and implementation of a low air loss mattress.
Further review of the medical record failed to indicate that facility staff notified the Physician of the consultant wound Physician's recommendation of a low air mattress.
On 12/27/22 at 8:27 A.M., the surveyor observed Resident #64 lying in bed sleeping. The Resident's legs were externally rotated with his/her right lateral foot and ankle resting directly on the mattress. There was no air mattress on the Resident's bed and two foam booties were observed placed on a chair in the corner of the room and were not on the Resident's feet.
On 12/27/22 at 1:27 P.M., the surveyor observed Resident #64 seated in a Broda chair (positioning chair) in his/her room. Two foam booties were observed placed on a chair in the corner of the room and were not on the Resident's feet. There was no air mattress applied to the Resident's bed.
On 12/28/22 at 8:27 A.M., the surveyor and Certified Nursing Assistant (CNA) #4 observed Resident #64 sitting upright in bed. The Resident's legs were externally rotated with his/her right lateral foot and ankle resting directly on the mattress. The surveyor observed two foam booties placed on a chair in the corner of the room and were not on the Resident's feet. There was no air mattress applied to the Resident's bed.
On 12/29/22 at 9:07 A.M., the surveyor observed Resident #64 lying upright in bed awake. The Resident's legs were externally rotated with his/her right lateral foot and ankle resting directly on the mattress. The surveyor observed two foam booties placed on a chair in the corner of the room and were not on the Resident's feet. There was no air mattress applied to the Resident's bed.
During an interview on 12/2922 at 2:26 P.M., the surveyor and Unit Manager #1 observed Resident #64 sitting in a Broda chair in his/her room with no booties on his/her feet. Unit Manager #1 said she had just completed a treatment to the Resident's wounds and did not apply the booties as ordered. She confirmed that there was not an air mattress on the Resident's bed.
Review of the December 2022 Medication/Treatment Administration (MAR/TAR) Records indicated Nursing staff signed off that bilateral booties were in place during the surveyor's observations of them not applied and placed on a chair in the Resident's room.
During an interview on 12/30/22 at 9:15 A.M., Unit Manager #1 said that Resident #64 does not have an air mattress in place as recommended by the wound Physician. She said that the Resident was good about wearing the foam booties and staff just needed to apply them. She also said staff should not sign in the medical record that the booties were in place when they were not.
During an interview on 12/30/22 at 1:10 P.M., the wound consultant Physician said he was called by the facility to evaluate wounds on Resident #64's right foot and ankle. He said the Resident should have bilateral booties in place and a pressure reducing mattress to off-load the wounds and was not aware that they were not in place. At 1:21 P.M., the wound Physician accompanied by Unit Manager #1 assessed the Resident. The wound Physician measured the right ankle wound and said that it had gotten bigger. He performed a Doppler test (ultrasound) on the Resident's right foot and said he was unable to obtain a pulse. The wound Physician indicated he wanted the Resident to be sent out to the hospital for evaluation.
During a subsequent interview on 12/30/22 at 2:50 P.M., the wound Physician said Resident #64's right ankle wound had deteriorated more than he expected, and it was very concerning. He said the Resident was in the process of being sent out to the hospital for evaluation.
SERIOUS
(G)
Actual Harm - a resident was hurt due to facility failures
Deficiency F0697
(Tag F0697)
A resident was harmed · This affected 1 resident
Based on observations, interviews, and record review, the facility failed to ensure pain management consistent with professional standards and the resident's goals and preferences was provided to one ...
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Based on observations, interviews, and record review, the facility failed to ensure pain management consistent with professional standards and the resident's goals and preferences was provided to one Resident (#66), out of a total sample of 22 residents. Specifically, for Resident #66, the facility failed to administer medications timely and manage pain effectively during a dressing change.
Findings include:
Review of the facility's policy titled Pain Management Guidelines, last updated September 2022, included but was not limited to:
-Attempts to control pain will be employed and adjusted until the resident reaches an acceptable comfort level. When several medications or varying doses of medication are used to control pain, criteria must be established to identify varying levels of pain.
Resident #66 was admitted to the facility in November 2022 with diagnoses including a history of falls and a pelvic fracture.
Review of the most recent Minimum Data Set (MDS) assessment, dated 11/24/22, indicated the Resident was cognitively intact as evidenced by a Brief Interview for Mental Status (BIMS) score of 14 out of 15, required extensive assistance from staff for bed mobility, transfers, bathing and dressing. The assessment also indicated the Resident reported almost constant pain that made it difficult to sleep and limited day to day activities.
Review of the December 2022 Physician's Orders indicated the following medications for pain management:
-Acetaminophen 500 milligrams (mg), two tablets three times a day for pain (11/18/22)
-Gabapentin 300 mg, one capsule three times a day for pain (12/1/22)
-Morphine Sulfate Solution 20 mg/milliliter (ml), give 0.25 ml sublingually (under tongue) three times a day
During an interview on 12/27/22 at 12:00 P.M., Resident #66 said that he/she is in nearly constant pain and his/her bum burns and hurts. The Resident said the nurses are busy and it takes a long time to get pain medication.
During an interview on 12/28/22 at 2:34 P.M., Resident #66 said he/she has an ulcer on his/her bum and the area burns and hurts constantly. The Resident said he/she tries and puts his/her hands underneath his/her hips to lift up to take the pressure off, but the ulcer hurts whenever he/she moves. The Resident winced as he/she spoke to the surveyor. Resident #66 said he/she cannot reach the side rails or grip the mattress to reposition him/herself and prior to yesterday, staff did not reposition him/her at all and he/she spent all of his/her time on his/her back.
On 12/28/22 at 3:35 P.M., the surveyor obtained consent from Resident #66 to observe the scheduled dressing change to the stage 2 pressure area on his/her coccyx. The Resident told the surveyor and Nurse #4 that he/she is in pain all the time and said, It is like a fire. The Nurse did not pre-medicate the Resident prior to the dressing change to the open area on his/her coccyx. Nurse #4 told the Resident she will have the Nurse that just came on (3:00 P.M. to 11:00 P.M. shift) bring in some pain medication.
During an interview on 12/29/22 at 9:02 A.M., Resident #66 said he/she was feeling pain and burning on his/her coccyx and was waiting for the Nurse to give him/her pain medication. The Resident said it takes a long time for the Nurse to bring pain medication, and I get it when I get it. The Resident was grimacing while speaking to the surveyor.
On 12/29/22 at 9:15 A.M., the surveyor observed Resident #66's call light go on (sounding and light illuminated over door). At 9:44 A.M., a Certified Nursing Assistant (CNA) entered Resident #66's room and asked what the Resident needed. Resident #66 told the CNA that he/she was in pain and needed pain medication. The CNA walked down the hallway to the Nurse at the medication cart. At 9:46 A.M., 44 minutes after the Resident reported that he/she was waiting for the Nurse to administer pain medication, and 31 minutes after pressing the call light, Nurse #3 entered Resident #66's room with pain medication.
Review of a Medication Administration Audit Report run by the Director of Nursing on 12/30/22 indicated Resident #66 received scheduled pain medication up to two and a half hours late on seven occasions from 12/27/22 through 12/29/22.
During an interview on 12/30/22 at 9:15 A.M., Unit Manager #1 said Resident #66 needs to get pain medication timely to ensure his/her pain is managed effectively and should not wait to receive pain relief.
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0552
(Tag F0552)
Could have caused harm · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, record review, and interview, the facility failed to ensure one Resident's (#155) right to be informed of,...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, record review, and interview, the facility failed to ensure one Resident's (#155) right to be informed of, and participate in, his/her treatment plan was honored when his/her Health Care Agent, which was not invoked, made treatment decisions, out of a total sample of 22 residents.
Findings include:
Review of the facility's handbook titled Resident Rights, dated as revised October 2022 indicated resident rights included but was not limited to:
-right to be informed of, and participate in, his/her treatment.
Resident #155 was admitted to the facility in December 2022 with diagnoses that included coronary disease, history of diabetes, and bipolar disorder.
During an interview on 12/27/22 at 9:10 A.M., Resident #155 said he/she had been admitted for short term care. Resident #155 said there was poor communication between him/her and the staff, including the physician. Resident #155 said medication changes had occurred and the facility staff or physician had not informed him/her of the changes, when they occurred. The Resident said he/she thought they no longer had diabetes, unless they ate foods that were high in sugar because they no longer received insulin. Resident #155 said he/she was not clear what medication changes occurred or why.
Review of the medical record indicated Resident #155 signed and consented to the care and treatment at the facility. The medical record indicated he/she was alert and oriented had a Health Care Proxy (HCP) and it was not invoked.
Review of the medication orders from 12/8/22 through 12/28/22 (current orders) indicated the following medication changes:
-Insulin Glargine (diabetic medication) administer 9 units, via an insulin pen, daily was administer from 12/9/22 through 12/20/2022 and then discontinued.
-Insulin Lispro [NAME] KwikPen (diabetic medication) administer 3 units, via an insulin pen, before breakfast, lunch, and dinner was administered from 12/8/22 through 12/20/22 and then discontinued
-Insulin Lispro [NAME] KwikPen (diabetic medication) administer via sliding scale four times per day (before meals and at bedtime) via injection from 12/8/2022 through 12/20/22 and then discontinued
-Metformin 500 milligram (mg) (diabetic medication) orally once a day, started on 12/14/22 through 12/20/22 and increased to 500 mg twice daily on 12/20/22
-Risperidone (antipsychotic) 0.25 mg daily from 12/10/22 through 12/22/22, when it was increased to 0.5 mg daily
-Bupropion (antidepressant) 100 mg daily from 12/9/22 through 12/22/22, then decreased to 50 mg daily on 12/22/22
Record review failed to indicate the Resident was informed of the changes in his/her diabetic medication and psychotropic medications.
Review of the medical record indicated a Family Member had sent a letter to the facility on [DATE] and the facility staff sent a copy of the letter to the Resident's physician on 12/21/22. The Family Member indicated he/she was the go between between the facility and the Resident's outside prescriber (psychiatrist). The Family Member provided a history of the Resident's psychotropic medications and informed the facility of her (the family member's) goals. The Family Member directed the facility to increase the Risperidone and decrease the Bupropion. In addition, the Family Member stated an electrocardiography (EKG) test should be done (EKG was done on 12/22/22).
Record review indicated the Family Member's treatment decisions were implemented beginning on 12/22/22 and there was no indication of the Resident's participation and knowledge. The medical record did not indicate the Family Member's participation in the treatment of the Resident was authorized.
During an interview on 12/27/22 at 11:30 A.M., Unit Manager #3 said there was a Family Member who makes decisions, and he/she deals directly with the Resident's Physician.
During an interview on 12/29/22 at 10:46 A.M., Social Worker #1 said she was aware the Family Member is directing care. She said the facility's practice for a Resident Representative to participate in treatment decisions is for an Authorization for Disclosure of Information form to be completed and consented to by a Resident who does not have an invoked HCP. The Social Worker reviewed the medical record and said that an Authorization for Disclosure of Information form was not completed or consented to by Resident #155.
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Investigate Abuse
(Tag F0610)
Could have caused harm · This affected 1 resident
Based on observations, interviews, and record review, the facility failed to ensure an alleged perpetrator (Nurse #1) did not have access to an alleged victim (Resident #20) following an allegation of...
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Based on observations, interviews, and record review, the facility failed to ensure an alleged perpetrator (Nurse #1) did not have access to an alleged victim (Resident #20) following an allegation of sexual abuse. The total sample was 22 residents.
Findings include:
Resident #20 was admitted to the facility in June 2019.
Review of the Minimum Data Set (MDS) assessment, dated 10/13/22, indicated Resident #20 scored a 15 out of 15 on the Brief Interview for Mental Status, indicating the Resident was cognitively intact.
During an interview on 12/27/22 at 3:45 P.M., Resident #20 said he/she had been raped on 12/24/22 or 12/25/22 by four or five men. The surveyor immediately notified Unit Manager #2. The surveyor observed Unit Manager #2 interview Resident #20. Resident #20 said he/she had been dragged out of their room by four or five men and rectally raped over a barrel. He/she said one of the men was a family member and one of the men was Nurse #1. The Resident said he/she was not sure if Nurse #1 physically participated but had watched the rape occur. The Resident said he/she had been crying off and on for a couple of days and that no one believed him/her.
During an interview on 12/27/22 at 4:02 P.M., Unit Manager #2 said she had notified the Director of Nurses, who entered the room at this time with the Unit Manager and another nurse to complete a skin check for Resident #20.
During an interview on 12/27/22 at 4:08 P.M., Unit Manager #2 said there was no evidence of trauma, and she was notifying the physician.
On 12/27/22 at 4:09 P.M., the surveyor observed Nurse #1, the alleged perpetrator, at the medication cart at the nurses' station.
On 12/27/22 at 4:32 P.M., the surveyor observed Nurse #1 on the unit and going into resident rooms.
During an interview on 12/27/22 at 4:45 P.M., the Director of Nurses said the police had been contacted, laboratory work had been ordered and the Resident would now have two staff members to provide care at a time. When the surveyor inquired who the alleged perpetrators were, the Director of Nurses said the Resident had identified a family member. The surveyor inquired about the allegation in which Nurse #1 was one of the men involved, the Director of Nurses said she was unaware the Resident had mentioned Nurse #1 in the allegation to the Unit Manager and that Nurse #1 was still on the unit.
During an interview on 12/29/22 at 12:55 P.M., Resident #20, with tearful eyes, said he/she kept thinking about the rape. She said Nurse #1 was there for the rape and this made him/her sad because Nurse #1 was a good nurse.
A review of the facility investigation was conducted on 12/30/22 at 8:30 A.M. Review of the investigation included a statement from Unit Manager #2 indicating Resident #20 had made an allegation of sexual abuse and had indicated a family member and Nurse #1 were there during the rape. Review of the investigation included a statement from Nurse #1, which indicated the nurse was informed by Resident #20 on 12/27/22 that he/she was raped by a family member.
Review of the Medication Administration Record indicated on 12/27/22 at 4:28 P.M. Nurse #1 administered 2 units of insulin in the abdomen of Resident #20, 45 minutes after the allegation was made.
During an interview on 12/30/22 at 10:36 A.M., Nurse #1 said he went to the room of Resident #20 on 12/27/22 sometime between 4:00 P.M. and 5:00 P.M. to check their blood sugars. When he entered the room, Resident #20 was tearful and told Nurse #1 that he/she had been raped. Nurse #1 said he immediately went and notified Unit Manager #2 and the Unit Manager said she was already aware.
During an interview on 12/30/22 at 11:20 A.M., the Director of Nurses said Nurse #1 was identified by Resident #20 during the initial interview with Unit Manager #2 on 12/27/22 at 3:45 P.M. and Nurse #1 had continued to have access to Resident #20, until the Director of Nurses was notified by the surveyor on 12/27/22 at 4:45 P.M.
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0658
(Tag F0658)
Could have caused harm · This affected 1 resident
Based on observation, interview, policy review, and record review, the facility failed to ensure Resident #67 was provided care in accordance with professional standards of practice from a total sampl...
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Based on observation, interview, policy review, and record review, the facility failed to ensure Resident #67 was provided care in accordance with professional standards of practice from a total sample of 22 residents. Specifically, the facility failed to ensure:
a. orders were in place for fingerstick blood tests, and
b. bilateral seizure pads were in place and the Resident's foot was elevated on pillows while in bed according to physician's orders.
Findings include:
Review of the facility's policy titled Nursing Care of the Resident with Diabetes Mellitus, last revised December 2015, included but was not limited to:
Glucose Monitoring
-The management of individuals with diabetes mellitus should follow relevant protocols and guidelines;
-The Physician will order the frequency of glucose monitoring;
-Residents whose blood sugar is poorly controlled or those taking insulin may require more frequent monitoring;
-Finger sticks (capillary blood samples (CBG)) measure current blood glucose levels.
Resident #67 was admitted to the facility in December 2020 with diagnoses including diabetes mellitus, type 2 and right leg amputation above the knee.
a. Review of the December 2022 Physician's Orders included but was not limited to the following orders for antidiabetic medication:
-Humalog KwikPen Solution Pen-injector 200 unit/milliliter, inject 8 units subcutaneously before meals for diabetes (ordered 9/28/21);
-Humalog KwikPen Solution Pen-injector 200 unit/milliliter, inject subcutaneously before meals as per sliding scale (initiated 12/15/20):
if 200-250= 2 units;
251-300= 4 units;
301-350= 6 units;
351-400= 8 units;
401-600= 10 units;
CBG greater than 400, call Physician/Nurse Practitioner
Review of September, October, November, and December 2022 Medication/Treatment Administration Records (MAR/TAR) indicated nursing staff measured Resident #67's CBG three times a day.
Further review of the Physician's Orders failed to include an order for fingerstick blood tests three times a day to measure the Resident's CBG.
b. Review of the December 2022 Physician's Orders included but was not limited to the following:
-Seizure pads to bilateral upper side rails at all times, check placement every shift (ordered 12/11/20); and
-Keep LLE (left lower extremity) elevated off bed with pillows (ordered 11/19/20)
On 12/27/22 at 9:25 A.M., the surveyor observed Resident #67 lying in bed with bilateral side rails up and no seizure pads in place. The Resident's left lower extremity was lying directly on the mattress and not elevated with a pillow as ordered by the Physician.
On 12/28/22 at 11:03 A.M., the surveyor observed Resident #67 lying in bed with bilateral side rails up and bilateral seizure pads in place. The Resident's left lower extremity was lying directly on the mattress and not elevated with a pillow as ordered by the Physician.
During an interview on 12/28/22 at 11:04 A.M., the Resident's Health Care Proxy (HCP) asked the surveyor what the blue pads on either side of the Resident's side rails were for. The HCP said she visits the Resident five days per week and had never seen them before today. At 11:07 A.M., Certified Nursing Assistant (CNA) #4 entered the Resident's room. CNA #4 said that she often has Resident #67 on her assignment and has never seen the pads before.
On 12/30/22 at 11:53 A.M., the surveyor observed Resident #67 lying in bed. The Resident's left lower extremity was lying directly on the mattress and not elevated with a pillow as ordered by the Physician.
During interviews on 12/30/22 at 9:15 A.M. and 3:12 P.M., the surveyor and Unit Manager #1 reviewed Resident #67's medical record. She said there should have been orders in place to do finger stick blood sugars to obtain CBGs prior to 12/23/22 and staff should not have done the blood testing without a Physician's order. She said the Resident should have had seizure pads in place and his/her left lower extremity elevated according to Physician's orders.
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0694
(Tag F0694)
Could have caused harm · This affected 1 resident
Based on observation, policy review, interview, and record review, the facility failed to ensure staff provided care for a Peripherally Inserted Central Catheter (PICC - a long catheter inserted throu...
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Based on observation, policy review, interview, and record review, the facility failed to ensure staff provided care for a Peripherally Inserted Central Catheter (PICC - a long catheter inserted through a peripheral vein then into the central vascular system to administer intravenous (IV) treatments over a long period of time) for one Resident (#157), out of a total sample of 22 residents. Specifically, the facility failed to ensure PICC line flushes, assessment, tubing changes, and dressing changes were completed and documented before and after the catheter became occluded (blockage of the access line) which caused a delay in administering the Resident's antibiotics to treat a serious infection.
Findings include:
Review of the facility's policies for PICC/Central Venous Access Device (CVAD) for flushing, for Catheter needleless connector changes, for Catheter dressing change and for clearing Catheter Occlusions (dated as reviewed January 2022) included but was not limited to:
-Flushing is performed to ensure and maintain patency
-A physician's order is required to flush a PICC
-Document date and time of flushing, flushing agents, and amounts, on the Medication/Treatment Administration Record (MAR/TAR)
-Dressing changes and assessment are to be provided at specific intervals and with a specific technique and will occur according to the PICC orders
-A physician's order for the care, maintenance, and schedule of dressing change of the PICC is required
-Assessment of the PICC site should occur before, during, and after medication administration, during dressing changes and at minimum once a shift
-With each site assessment the PICC should be assessed for redness, drainage, swelling, external catheter length, presence of sutures, tenderness, warmth, and patency and documented in the clinical record.
-A catheter occlusion can be caused by a thrombotic buildup, a medical condition known as fibrin - is a fibrous protein involved in the clotting of blood or by non-thrombotic cause - a drug precipitate and/or a mechanical factor, such as kinked tubing, suturing tight and or a poor positioning of the PICC catheter
-An occlusion impacts the access of the device's patency
-To prevent an occlusion from occurring and ensuring the PICC line can be accessed, the licensed nursing staff are required to routinely assess the PICC, and ensure the physician orders for flushes, care, assessment, and treatment are followed. Performing the proper flushing procedure immediately before and after a medication infusion ensures the PICC is working properly and not occluded
-If an occlusion occurs the licensed staff should be competent to do the procedure or contact a prescriber who is competent to clear the occlusion with a thrombolytic agent (a medication that dissolve clots).
-A physician's order is required
-The licensed nurse should document the procedure in the Resident's medical record, including but not limited to: the date and time, site assessment, flushing agent and volume, any complications and the Resident's response.
Resident #157 was admitted in December 2022 with diagnoses including heart failure, chronic kidney disease, and an acute infection of the heart (endocarditis).
Review of the medical record indicated Resident #157 had a double lumen PICC line in the left arm for intravenous (IV) antibiotic administration. Further review indicated orders for Cefepime (an antibiotic) IV at 9:00 A.M. and Vancomycin (an antibiotic) IV at 5:00 P.M.
Review of a Physician's Order, dated 12/9/22, for Care of the PICC line indicated:
- Pre-flush the PICC with 10 milliliters (ml) of Normal Saline (NS) prior to medication administration
- Post flush with 10 ml of NS after medication administration
- Flush all lumens at least every 12 and/or 24 hours and as needed, as the infusion was not continuous
- Document total catheter length and external catheter length on admission
- Document baseline arm circumference every shift and as needed
- Document external catheter length weekly with weekly dressing change
- In addition, per facility policy, care of PICC line includes:
- Change catheter site dressing every week and as needed with transparent dressing
- Monitor IV site every shift and document in the nurses' notes
- Change dressing on admission and change every 24 hours and label with date/time/initials.
Review of the MAR and TAR for 12/9/22 through 12/29/22, failed to indicate the nursing staff had transcribed the physician's orders for the care of the PICC line onto the administration records. The MAR and TAR failed to indicate the PICC had ever been flushed, assessed, and included the external catheter length, arm circumference, or the PICC dressing had been changed as ordered by the physician.
Review of Nursing Notes from 12/9/22 through 12/29/22, revealed no documentation in the nursing notes that included an external catheter length or an arm circumference on any shift, including the 3:00 P.M. -11:00 P.M. shift each day.
Review of a Nurse's Note, dated 12/11/22 at 5:00 P.M., indicated one of the two lumens was occluded / blocked and not accessible for medication administration. The nurse documented she contacted the prescriber who ordered holding the Resident's antibiotics until the occlusion was cleared by the Infusion service.
Review of the Infusion Nurse's Note, dated 12/12/22 at 10:00 A.M., indicated during her visit she removed the PICC line caps and cleared the blockage. The note indicated the Infusion Nurse observed blood clots surrounding the PICC line and she changed the dressing and inserted an IV stat lock (device that holds the IV in place and helps prevent occlusions).
Review of the medical record indicated that after the Resident's PICC line became occluded, there was no additional documentation in the nurses' note or the MAR/TAR that the licensed staff were caring for the PICC line as ordered and as outlined in the facility policy.
During an interview on 12/29/22 at 8:41 A.M., Nurse #5 said she documented the administration of medications and treatment on the MAR. After not finding the treatment and care of the PICC on the MAR, Nurse #5 reviewed the TAR. Nurse #5 said she could not find documentation the flushes, dressing changes, and care of the PICC line had been done. She said there was no other location this information could be documented.
During an interview on 12/29/22 at 11:37 A.M., Unit Manager #3 said she could not explain why the orders for the care and treatment of the PICC had not been entered onto the MAR or the TAR. She said her expectation was for the staff to transcribe the physician's orders onto the administration records. She said she was pretty sure the staff were flushing the PICC line but could not say if they were flushing it as ordered. The surveyor inquired about the note she had written on 12/12/22 regarding the blockage of the PICC. She said she had not observed the PICC at the time of the occlusion and wrote the nurse's note for the nurse. The surveyor inquired when the last time was the staff had changed the Resident's dressing. The Unit Manager said she did not know and when she asked Nurse #5, she said she did not know.
On 12/29/22 at 11:40 A.M., the surveyor observed the Resident's PICC line following the interview. The surveyor observed multiple layers of the transparent dressing to be bunched up. There were layers of tape securing the dressing onto the arm. The dressing was visibly soiled, and a large amount of blood was visible around the PICC site and had seeped onto to the Resident's left upper arm. The date on the dressing was 12/12.
During an interview on 12/29/22 at 11:45 A.M., the surveyor shared the observation with the Unit Manager and Nurse #5, and neither could explain why the dressing had not been changed since the Infusion Nurse had cleared the occlusion/blockage on 12/12/22.
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Respiratory Care
(Tag F0695)
Could have caused harm · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, record review, and policy review, the facility failed to ensure residents were provided respira...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, record review, and policy review, the facility failed to ensure residents were provided respiratory care in accordance with professional standards of practice for two Residents (#22 and #28) receiving Oxygen therapy, out of a sample of 22 residents.
Findings include:
[NAME] NURSING PROCEDURES, 8th edition
Oxygen: all Oxygen delivery systems should be checked at least once each day
-verify the practitioner's order for the Oxygen therapy, because Oxygen is considered a medication or therapy and should be prescribed
-monitor the patient's Oxygen saturation level by pulse oximetry to assess response to Oxygen therapy
- assess the patient frequently for signs and symptoms of hypoxia, such as restlessness, decreased level consciousness, increased heart rate, arrhythmias, perspiration, dyspnea, use of accessory muscles, yawning or flared nostrils, cyanosis, and cool, clammy skin, obtain vital signs, as needed.
DOCUMENTATION: record the date and time of Oxygen administration, the type of delivery device, the Oxygen flow rate, the patient's vital signs, skin color, respiratory effort, and breath sounds.
Review of the facility's policy titled Use of Oxygen, last revised September 2022, included but was not limited to:
-Oxygen is administered only on the order of the Physician;
-Physician's order shall include: liters of flow and vehicle of administration;
-Pre-filled disposable humidifier bottles should be used when indicated. All bottles should be dated and changed every seven days.
1. Resident #22 was admitted to the facility in December 2019 with diagnoses including chronic obstructive pulmonary disease (lung disease that blocks airflow and makes it difficult to breathe).
Review of the Minimum Data Set (MDS) assessment, dated 12/1/22, indicated Resident #22 was cognitively intact as evidenced by a Brief Interview for Mental Status (BIMS) score of 15 out of 15, and received Oxygen therapy while a resident at the facility.
During an interview on 12/27/22 at 12:15 P.M., the surveyor observed Resident #22 lying in bed awake. Oxygen tubing was noted to be connected to the concentrator with a refillable humidifier bottle containing water, with a nasal cannula (a lightweight tube which on one end splits into two prongs which are placed in the nostrils and from which a mixture of air and oxygen flows) in place in the Resident's nostrils. The concentrator was on and set to a flow rate of 4.0 liters/minute. Resident #22 said that he/she uses Oxygen continuously, day and night due to difficulty breathing.
On 12/29/22 at 11:05 A.M., the surveyor observed Resident #22 sitting up in bed. Oxygen tubing was noted to be connected to the concentrator with a refillable humidifier bottle of water, with a nasal cannula in place in the Resident's nostrils. The concentrator was on and set to a flow rate of 4.0 liters/minute.
Review of the medical record indicated the following Physician's Order:
-Administer Oxygen at 2 liters/minute via nasal cannula (nc), prn (as needed) to maintain Oxygen saturation over 92% (2/28/22)
There was no Physician's Order in place for the use of humidified Oxygen including maintenance of the humidification device and no order for Oxygen use continuously.
Review of the December 2022 Medication/Treatment Administration Records failed to indicate staff recorded the date and time of Oxygen administration, and the Oxygen flow rate.
During an interview on 12/30/22 at 9:09 A.M., the Administrator and surveyor observed Resident #22 sitting up in bed. The oxygen tubing was noted to be connected to the concentrator with a refillable humidifier bottle, with a nasal cannula in place in the Resident's nostrils. The concentrator was on and set to a flow rate of 4.0 liters/minute. The Resident said that his/her Oxygen should be set to 2 liters and not 4 liters. The surveyor reviewed Resident #22's medical record with the Administrator. He confirmed that the Physician's orders indicated Oxygen is ordered as needed (prn) at 2 liters/minute and do not indicate humidified Oxygen.
2. Resident #28 was admitted to the facility in June 2022 with diagnoses including chronic obstructive pulmonary disease.
Review of the MDS assessment, dated 11/2/22, indicated Resident #28 was cognitively intact as evidenced by a BIMS score of 15 out of 15 and received Oxygen therapy.
During an interview on 12/27/22 at 1:30 P.M., Resident #28 said that he/she had to tell the Nurse this morning that the humidifier cup (bottle) attached to the oxygen concentrator needed more water. The Resident said he/she has received Oxygen therapy since being admitted to the facility in June. The surveyor observed oxygen tubing connected to the concentrator with a refillable bottle of water, with a nasal cannula in place in the Resident's nostrils. The concentrator was on and set to a flow rate of 2.0 liters/minute.
On 12/28/22 at 2:32 P.M., the surveyor observed Resident #28 lying in bed sleeping. Oxygen tubing was noted to be connected to the concentrator with a refillable bottle of water, with a nasal cannula in place in the Resident's nostrils. The concentrator was on and set to a flow rate of 2.0 liters/minute.
On 12/29/22 at 10:45 A.M., the surveyor observed Resident #28 sitting upright in bed. The oxygen tubing was noted to be connected to the concentrator with a refillable bottle of water, with a nasal cannula in place in the Resident's nostrils. The concentrator was on and set to a flow rate of 2.0 liters/minute.
Review of the medical record indicated the following Physician's Order:
-Oxygen at L via NC to keep saturation above 88% (10/19/21)
The Physician's order failed to indicate a liter flow for Oxygen administration and failed to include the use of a humidifier bottle including maintenance of the humidification device.
Review of the December 2022 Medication/Treatment Administration Records failed to indicate staff recorded the Oxygen flow rate and refilled or replaced the humidifier bottle.
During an interview on 12/30/22 at 9:15 A.M., the surveyor and Unit Manager #1 reviewed Resident #28's medical record. Unit Manager #1 confirmed that the Oxygen order is incomplete and must include a liter flow rate, and there is no order for humidified Oxygen with maintenance instructions.
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Medication Errors
(Tag F0758)
Could have caused harm · This affected 1 resident
2. Resident #25 was admitted to the facility in February 2022 with a diagnosis of anxiety.
Review of the Physician's Orders indicated an order written on 3/24/22 for Ativan (an antianxiety medication)...
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2. Resident #25 was admitted to the facility in February 2022 with a diagnosis of anxiety.
Review of the Physician's Orders indicated an order written on 3/24/22 for Ativan (an antianxiety medication) 0.5 milligrams (mg), give one tablet every 8 hours as needed for anxiety. The order indicated the end date as indefinite.
Review of the medical record indicated this order was in place from 3/24/22 through 11/3/22 (over seven months.)
Review of the Physician's orders indicated an order written on 11/28/22 for Ativan 0.5 mg, give one tablet every 8 hours as needed. The order indicated the end date was indefinite.
Review of the Physician's Progress Notes and Orders failed to indicate a rationale for the extended use of the as needed antianxiety medication or a duration for use.
During an interview on 12/30/22 at 9:38 A.M., Unit Manager #2 reviewed the medical record with the surveyor and said the Ativan should have had a stop date when originally ordered so that the physicians could have evaluated and documented the justification for use.
Based on record review, policy review, and staff interviews, the facility failed to ensure drug regimens were free from unnecessary medications for 2 Residents (#155 and #25), from a sample of 5 residents with potential unnecessary medications. Specifically, the facility failed to ensure
1. For Resident #155, an antipsychotic medication ordered as needed (PRN) was limited to 14 days and was reviewed by the physician with a documented rationale for continued use.
2. For Resident #25, a psychotropic medication ordered as needed (PRN) was limited to 14 days and was reviewed by the physician with a documented rationale for continued use.
Findings include:
Review of the facility's policy titled Antipsychotic Medication Use, dated September 2022, indicated antipsychotic medication will be used based on a comprehensive assessment. Residents who have not used psychotropic drugs are not given those drugs unless such drug therapy is necessary to treat a specific condition, as diagnosed and documented in the clinical record and informed written consent must be obtained and documented prior to the administration of any antipsychotic medication. The policy indicated when psychotropic medications are prescribed, a specific condition or targeted behavior that warrants the use of the medication shall be documented in the medical record.
1. Resident #155 was admitted to the facility in December 2022 with diagnoses that included bipolar disorder.
Record review, including the Hospital Discharge Record, dated 12/8/22, indicated Seroquel 100 milligrams (mg) every 4 hours as needed (PRN) for delirium and anxiety in the hospital setting. The record indicated the Resident cleared considerably and has not voiced anxiety and stated it was controlled.
Review of the Physician's Order for Resident #155, dated 12/8/22, indicated Seroquel 100 mg give one tablet by mouth every four hours as needed (PRN).
The physician's order did not include the required re-evaluation in 14 days.
Review of the Medication Administration Record (MAR), dated 12/8/22, indicated Resident #155 received Seroquel 100 mg by mouth on 12/9/22 12/17/22, 12/19/22, and 12/20/22 for anxiety.
Review of the medical record indicated, on 12/22/22, the Pharmacist notified the physician of the requirement for a medical justification for use and the 14-day timeframe.
During an interview on 12/29/22 at 10:45 A.M., Unit Manager #3 said she was unsure why Resident #155 was receiving PRN Seroquel. She did not know and could not find the physician's justification for the antipsychotic PRN order.
CONCERN
(E)
Potential for Harm - no one hurt, but risky conditions existed
Pressure Ulcer Prevention
(Tag F0686)
Could have caused harm · This affected multiple residents
Based on observations, interviews, and record reviews, the facility failed to ensure pressure relieving devices were utilized following professional standards for 3 Residents (#59, #20, and #66), in a...
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Based on observations, interviews, and record reviews, the facility failed to ensure pressure relieving devices were utilized following professional standards for 3 Residents (#59, #20, and #66), in a sample of 7 residents with pressure ulcers. Specifically, the facility failed to ensure
1. For Resident #59, an ROHO cushion (an inflatable seat cushion) was checked for proper inflation to promote pressure ulcer healing;
2. For Resident #20, the proper use of a gel seating cushion by placing a folded sheet between the Resident and the cushion; and
3. For Resident #66, the pressure relieving air mattress was consistently set to optimize wound healing.
Findings include:
1. Resident #59 was admitted to the facility in June 2021 with an unstageable pressure area to the left buttock.
Review of the Physical Therapy Progress Notes indicated on 6/25/21 Resident #59 was provided with a 3-inch high ROHO cushion related to the pressure area on the buttock.
Review of the wound consultant Physician's Wound Evaluation and Management Summary, dated 12/23/22, indicated Resident #59 had a stage 4 pressure wound to the sacrum (lower back) for greater than 162 days. The wound was noted to be 0.8 centimeters (cm) in length by 0.6 cm in width by 0.2 cm in depth with 20 percent necrotic (dead) tissue and 80 percent granulation tissue (when wound is healing).
Review of the Physician's Orders included an order for the ROHO cushion to be checked every night shift (11:00 P.M. to 7:00 A.M.) for inflation.
Review of the ROHO cushions operating manual indicated the following:
-Do not use a product that is under-inflated or over-inflated, because the product benefits will be reduced or eliminated, resulting in an increased risk to skin and other soft tissue.
-Carefully follow the instructions for inflation, placement, and hand check
-The check would be performed while the person is on the cushion by sliding one hand between the cushion and the pelvic bony prominence; move fingers up and down between the bony prominence and the wheelchair base; check to ensure there is between a 0.5 inch and 1 inch space between the bony prominence and the wheelchair base and adjust the inflation level as necessary.
- After setting up the cushion the first time, perform a hand check frequently, at least once a day.
On 12/27/22 at 12:45 P.M., the surveyor observed Resident #59 to be sitting up in the wheelchair, on an ROHO cushion.
On 12/28/22 at 4:50 P.M., the surveyor observed Resident #59 in bed. The surveyor observed a wheelchair next to the bed with an ROHO cushion which appeared saggy. When pressing two hands flat on the cushion, the center of the cushion lost air (redistributing the air to cells on the outer parts of the cushion) and the surveyor was able to feel the base of the wheelchair.
On 12/29/22 at 10:56 A.M., the surveyor observed Resident #59 to be in his/her room working with Physical Therapy. At this time, the Director of Rehabilitation said the ROHO cushion was used to redistribute the pressure while the Resident was sitting in the wheelchair. The surveyor inquired if the ROHO cushion was inflated properly. The Physical Therapy Assistant pressed on the front left corner of the cushion and said it was inflated. Neither physical therapist completed a hand check to check for proper inflation of the cushion.
During an interview on 12/30/22 at 11:51 A.M., the wound consultant Physician said Resident #59 had a wound that would heal then re-open at times and the Resident was high risk for wounds related to their diagnoses and medications, such as the current use of a steroid. At this time, the surveyor inquired about the ROHO cushion inflation for Resident #59. The wound consultant Physician picked up the ROHO cushion, which visibly flopped to the side, and said the cushion was not inflated properly.
During an interview on 12/30/22 at 1:30 P.M., the Director of Nurses said she had reviewed the physician's order for checking the inflation of the ROHO cushion as the staff on the overnight shift were unable to complete a proper hand check for inflation if the Resident was not in the wheelchair at the time.
2. Resident #20 was admitted to the facility in June 2021 with a diagnosis of cauda equina syndrome (nerve damage at the lower part of the spine).
Review of the medical record for Resident #20 indicated the Resident had a hospitalization in October 2022 and returned with a stage 2 pressure ulcer on the coccyx (bony prominence at end of spine).
Review of the care plans for Resident #20 included interventions of using a pressure reducing cushion on the wheelchair.
During an interview on 12/28/22 at 9:15 A.M., Resident #20 said he/she had an open area on his/her buttock. He/she said their buttock was uncomfortable when sitting up in the wheelchair. The surveyor observed the wheelchair to be in the Resident's room with a pressure relieving cushion on the wheelchair, on top of the pressure relieving cushion was a sheet folded over multiple times.
On 12/28/22 at 3:05 P.M., the surveyor observed Resident #20 seated in the wheelchair. The surveyor observed a folded sheet to be between the Resident and the pressure relieving cushion.
On 12/29/22 at 12:55 P.M., the surveyor observed Resident #20 to be seated in the wheelchair. The surveyor observed a folded sheet to be between the Resident and the pressure relieving cushion.
During an interview on 12/30/22 at 9:04 A.M., Unit Manager #2 said Resident #20 should not have a folded sheet between the Resident and the cushion as this would prohibit the cushion from providing pressure relief.
3. Resident #66 was admitted to the facility in November 2022 with diagnoses including a history of falls and a fractured pelvis.
Review of the medical record indicated Nursing staff identified a 2-centimeter pressure area to Resident #66's coccyx on 12/13/22. The Physician was notified and ordered the following wound care interventions:
-Allevyn (water/bacteria-proof adhesive dressing indicated for moderate to high exudating wounds) to coccyx every 48 hours (12/13/22)
-Santyl 250 unit/grams, apply to wound bed followed by calcium alginate and cover with dry protective dressing, every day shift (12/17/22)
On 12/27/22 at 12:00 P.M., the surveyor observed Resident #66 lying in bed on an air mattress. The air mattress unit was on and set to 240 pounds (lbs.).
On 12/28/22 at 2:34 P.M., the surveyor observed Resident #66 lying upright in bed awake. The air mattress unit was on and set to 180 lbs.
On 12/29/22 at 9:02 A.M., the surveyor observed Resident #66 lying upright in bed. The air mattress unit was on and set to 240 lbs.
Review of Resident #66's weight record indicated on 12/14/22, the Resident weighed 148.6 lbs.
Review of the medical record failed to indicate a Physician's order for the use of the air mattress.
During an interview on 12/20/22 at 9:15 A.M., Unit Manager #1 confirmed there was no order for Resident #66's air mattress. She said there should be a Physician's order in place for its use that includes specific settings to promote healing of Resident #66's pressure ulcer.
CONCERN
(E)
Potential for Harm - no one hurt, but risky conditions existed
Accident Prevention
(Tag F0689)
Could have caused harm · This affected multiple residents
Based on observations, interviews, and record review, the facility failed to maintain an environment free of accident hazards for one Resident (#44), out of a sample of 22 residents. Specifically, the...
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Based on observations, interviews, and record review, the facility failed to maintain an environment free of accident hazards for one Resident (#44), out of a sample of 22 residents. Specifically, the facility failed to ensure that effective care plan interventions were developed and implemented to prevent nine falls in a six month period.
Findings include:
Review of the facility's policies titled Falls Program Policy and Incident Reporting, both last revised September 2022, included but was not limited to:
-Purpose: To prevent the actual occurrence of falls and reduce the risk of any injury from a fall;
-Residents experiencing a fall will receive appropriate care with investigation of cause;
-Care plan will reflect new intervention initiated if fall should occur;
-When an incident involving a resident occurs, a nurse will document the incident in a nursing note and complete an incident report. Be sure the form is complete. These reports shall contain information that is pertinent, factual, accurate, objective, and concise; and
-Incidents involving residents that fall will have a Fall Investigation Form and Post-Fall Evaluation Form completed by a designated member of Nursing Administration
Resident #44 was admitted to the facility in December 2017 with diagnoses including Parkinson's disease, muscle weakness, and cognitive communication deficit.
Review of the Minimum Data Set (MDS) assessment, dated 9/21/22, indicated Resident #44 had moderate cognitive impairment as evidenced by a Brief Interview for Mental Status score of 7 out of 15, required extensive assistance of staff for all activities of daily living, had a history of falls, utilized a wheelchair, and was unsteady and only able to stabilize with assistance when moving from a seated position to standing.
Review of Resident #44's Interdisciplinary Care Plans included but was not limited to:
-Problem: Resident is at risk for falls (9/4/18)
-Interventions: Check on Resident more frequently to see if he/she needs assistance (9/4/18); Dycem to wheelchair seat (under cushion), check placement every shift (9/25/18); Anti-rollback brackets to Resident's wheelchair related to Resident often forgets to apply brake (3/30/21); ensure Resident has his/her Reacher (4/20/21); self-releasing Velcro alarm belt- Resident able to release on command, used as an alert to staff (5/31/22)
-Goal: Resident will be free from any major injuries related to fall through the review date (9/4/18)
Review of the medical record indicated Resident #44 had nine falls from June 2022 to December 2022. Review of the falls indicated:
1. 6/21/22 at 11:30 A.M., the Resident was observed by a Nurse trying to push a bedside table into his/her room from the hallway and slid off the seat of a wheelchair onto the leg and footrest of the wheelchair. The investigation indicated the following interventions were in place at the time of the fall: Velcro alarm seatbelt, shoes and wheelchair. The investigation failed to indicate if Dycem was in place in the wheelchair seat at the time of the fall. An intervention identified on the care plan to prevent future falls was: staff to offer adult coloring books and colored pencils when Resident is in wheelchair.
2. 7/5/22 at 11:00 A.M., the Resident was observed by a Nurse lowering him/herself to the floor in front of their closet. The investigation failed to indicate if Dycem was in place on the wheelchair seat. An intervention identified to prevent future falls was: offer the option to fold clothing on overbed table instead of floor.
3. 7/23/22 at 10:00 A.M., the Resident was observed by a Nurse sliding off the wheelchair while trying to reach and arrange his/her stuff (left side of bed). The Resident landed on his/her buttocks and did not strike his/her head. The investigation indicated the following interventions were in place at the time of the fall: socks, Dycem. An intervention identified to prevent future falls was: non-skid strips to left side of bed.
4. 8/3/22 at 10:45 A.M., the Resident was found lying on his/her back on the floor next to the bed between the bed and closet. The Resident reported reaching for something across from the bed and slipped off the bed. The investigation indicated the following interventions were in place at the time of the fall: socks, Reacher was found on the floor. An intervention identified to prevent future falls was: Reacher velcroed to bedside table; to be kept on right side when Resident in bed.
5. 8/6/22 at 10:30 A.M., Resident found sitting on the floor in the bathroom near the sink. Resident told Nurse he/she slid out of the wheelchair. The investigation indicated the following interventions were in place at the time of the fall: socks, alarm. The investigation failed to indicate if Dycem was on the wheelchair seat at the time of the fall. An intervention identified to prevent future falls was: Dycem to the top of the wheelchair cushion.
6. 8/21/22 at 12:30 P.M., Resident was found kneeling on the floor in the bathroom in front of the wheelchair. The Resident said he/she slid out of the wheelchair while brushing his/her teeth. The investigation indicated the following interventions were in place at the time of the fall: socks, wheelchair, alarms. The investigation failed to indicate if Dycem was in place on the wheelchair seat and on top of the seat cushion at the time of the fall. An intervention identified to prevent future falls was: offer Resident assistance with oral care after lunch.
7. 8/30/22 at 1:00 P.M., Resident was found on the floor beside the bed on right side. Call light was in place, bed alarm was ringing. The Resident's left leg was outwardly rotated, lump on left side of head; sent to hospital for further evaluation. The investigation indicated the following interventions were in place at the time of the fall: socks, bed alarm. An intervention identified to prevent further falls was: Resident returned from the hospital with a diagnosis of a urinary tract infection. An intervention identified to prevent future falls was: continue frequent monitoring.
8. 11/21/22 at 10:30 A.M., Resident found on the floor at the bedside. The investigation indicated the Resident's roommate witnessed the fall and said the Resident removed the alarmed lap belt and fell to the floor. The investigation indicated the following interventions were in place at the time of the fall: lap belt. The investigation failed to indicate if any other interventions were in place at the time of the fall. An intervention identified to prevent further falls was: Resident to remain in hallway.
9. 12/1/22 at 8:45 P.M., Resident found lying on his/her stomach on the floor in the hallway near the nursing station. The investigation indicated the following interventions were in place at the time of the fall: socks, wheelchair. The investigation failed to indicate if Dycem, Velcro alarm seat belt or any other interventions were in place at the time of fall. Interventions identified to prevent further falls were: staff educated to keep floor around Resident as clean as possible to avoid attempting to pick up items, new order urinalysis, culture and sensitivity, psychiatric evaluation.
During an interview on 12/30/22 at 9:15 A.M., the surveyor and Unit Manager #1 reviewed Resident #44's falls and medical record. Unit Manager #1 said most of the fall investigations were not complete and should have included what interventions were in place at the time of the falls to determine what interventions are effective and which are not. She said after reviewing each fall in detail, there were no effective interventions in place to prevent further falls. She said the Resident needs supervision because he/she has cognitive impairment, is impulsive, has poor safety awareness and tries to get up and walk frequently.
On 12/30/22 at 9:35 A.M., Unit Manager #1 and the surveyor observed Resident #44 seated in a wheelchair in the hallway with an alarmed seat belt in place. Unit Manager #1 checked the wheelchair for placement of Dycem underneath and on top of the wheelchair cushion. She showed the surveyor the Dycem underneath the cushion, but said it was not in place on top of the cushion but should be.
CONCERN
(E)
Potential for Harm - no one hurt, but risky conditions existed
Food Safety
(Tag F0812)
Could have caused harm · This affected multiple residents
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations, interviews, and policy review, the facility failed to store food in accordance with professional standard...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations, interviews, and policy review, the facility failed to store food in accordance with professional standards for food service safety and maintain a sanitary kitchen environment.
Findings include:
Review of facility's kitchen policy titled Food Storage and Preparation, dated August 2017, and reviewed with no changes in September 2022, indicated but was not limited to the following:
-All food items will be wrapped properly and tightly, or stored in clean, covered containers clearly marked, including the preparation date and discard date.
-All temperature control for safety foods (TCS), ready to eat (RTE) or leftover foods will be labeled and dated with the date the food was prepared and a discard date.
-All ready to eat salads or leftovers will be discarded within five calendar days from the preparation day, including day one.
-Dry Storage: Once the package has been opened, the product should be stored in a clean sanitized tightly covered container, clearly labeled with common name of the food and dated.
-Preparing salads: cover, label, and date (the date of preparation and the date to be consumed by or discarded) prior to storage.
Review of facility's policy dated Food Safety for Your Loved One, not dated, indicated but was not limited to the following:
-Food or beverages must be labeled and dated to monitor for food safety
-Foods or beverages that have passed the manufacturer's expiration date will be thrown away.
On 12/27/22 at 8:22 A.M., the surveyor observed the following in the main kitchen:
-The inside of the plate warmer (a metal free standing device used to keep plates warm prior to plating the food) had debris including dust and crumbs inside where plates are stored.
-The metal shelf used for drying pots and pans had stains and dust on the metal grates, which hold the pots and pans.
On 12/27/22 at 8:30 A.M., the surveyor observed the walk-in refrigerator. The surveyor observed that various items with loosely (not tightly) unsealed plastic wrap over the top including rice labeled 12/22 (day 5), ham dated 12/25, pork labeled 12/20 (day 7) and uncovered ham not labeled/dated. There was raw bacon, unwrapped, unpackaged in a cardboard box exposed to the air. The surveyor observed plastic containers that held various food items with unsecure lids on them including macaroni dated 12/25, whipped cream open to air (no date) and a container with pears (no date).
During an interview on 12/27/22 at 8:30 A.M., Dietary Aide #1 said the plastic containers do not seal, and the kitchen needs new ones. When shown the various items in the walk-in fridge, he said that the food in the box and with plastic wrap were not covered completely. He also said that it did not look like they were keeping up with the cleaning schedule for the fridge/freezer and was not sure who should have cleaned it. He said the dated items should have been thrown out after 3 days.
During an interview on 12/29/22 at 8:40 A.M., the surveyor observed that the metal rack for drying pans had dust on and between the metal grates. The Food Service Director noticed the dust and said he would have it cleaned. He acknowledged that the second metal drying rack had rust throughout.
On 12/29/22 at 9:00 A.M., the surveyor and the Food Service Director observed the plate warmer to have crumbs and dust inside, where the clean plates were kept. At this time the Food Service Director removed the inside part of the plate warmer and said he had not known this could be removed to be cleaned and it should have been part of the kitchen deep cleaning.
On 12/29/22 at 9:37 A.M. the surveyor observed the following in the [NAME] 2 unit kitchenette:
-Cream of wheat package was loose in a drawer (no expiration date or original box)
-A partial loaf of sliced bread with best by 12/27/22, two days prior
-The toaster had layers of crumbs inside and rust on top between the openings
-A container of Tater Tots was in a disposable cup with a lid in a cabinet above the fridge. It was not dated and not refrigerated.
On 12/29/22 at 9:45 A.M., the surveyor observed the following in the East 1 unit kitchenette:
-The toaster had layers of crumbs inside and there was rust on the top between the openings.
On 12/29/22 at 10:01 A.M., the surveyor observed the following in the East 2 unit kitchenette:
-oatmeal bars with an expiration date of 12/21/22 (8 days past) above the sink cabinet
During an interview on 12/29/22 at 3:20 P.M., while touring the units' kitchenettes, the Food Service Director said items should be thrown out on the expiration dates or the best by dates.
CONCERN
(E)
Potential for Harm - no one hurt, but risky conditions existed
Infection Control
(Tag F0880)
Could have caused harm · This affected multiple residents
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations, interviews, record review, and policy review, the facility failed to establish and maintain an infection ...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations, interviews, record review, and policy review, the facility failed to establish and maintain an infection prevention and control program to help prevent the development and potential transmission of communicable diseases and infections in the facility. Specifically, the facility failed to:
1. Ensure that healthcare personnel performed hand hygiene per the facility policy during a clean dressing change for Resident #66;
2. Ensure that healthcare personnel performed hand hygiene, and donned (put on) and doffed (took off) the appropriate personal protective equipment (PPE) prior to entering resident rooms as indicated by posted signs outside of resident rooms; and
3. Follow infection control procedures while administering a COVID-19 Binax test.
Findings include:
1. Resident #66 was admitted to the facility in November 2022 with diagnoses which included fracture of lumbosacral spine and pelvis.
Review of the facility's policy titled Dry/Clean Dressings, revised September 2013, indicated but was not limited to the following:
-Clean bedside stand. Establish a clean field.
-Place the clean equipment on the clean field. Arrange the supplies so they can be easily reached.
-Tape a biohazard or plastic bag on the bedside stand or use a waste basket below clean field.
-Position resident and adjust clothing to provide access to affected area.
-Wash and dry your hands thoroughly.
-Put on clean gloves. Loosen tape and remove soiled dressing.
-Pull glove over dressing and discard into plastic or biohazard bag.
-Wash and dry your hands thoroughly.
-Open dry, clean dressing(s) by pulling corners of the exterior wrapping outward, touching only the exterior surface.
-Label dressing with date, time and initials. Place on clean field.
-Using clean technique, open other products (i.e., prescribed dressing; dry, clean gauze).
-Wash and dry your hands thoroughly.
-Put on clean gloves.
-Assess the wound and surrounding skin for edema, redness, drainage, tissue healing progress and wound stage.
-Cleanse the wound with ordered cleanser. If using gauze, use clean gauze for each cleansing stroke. Clean from the least contaminated area to the most contaminated area (usually, from the center outward).
-Use dry gauze to pat the wound dry.
-Apply the ordered dressing and secure with tape or boarded dressing per order. Label with date and initials to top off dressing.
-Discard the disposable items into the designated container.
-Remove disposable gloves and discard into designated container. Wash and dry your hands thoroughly.
-Reposition the bed covers. Make the resident comfortable.
Review of current Physician's Orders for Resident #66 indicated:
- Coccyx: Cleanse with normal saline wash, apply Santyl to wound bed followed by Calcium Alginate and cover with DPD every day shift for wound management, dated 12/17/22.
On 12/28/22 at 3:35 P.M., the surveyor obtained permission from Resident #66 to be present during a wound dressing change and observed the following:
-Nurse #3 performed hand hygiene and set up dressing supplies on the overbed table.
-Nurse #3 removed the soiled dressing.
-Nurse #3 removed her soiled gloves and put on a clean pair of gloves.
-Hand hygiene was not performed after removing soiled gloves or prior to putting on new gloves.
-Nurse #3 reached into her pocket for scissors and cut wound supplies.
-Nurse #3 did not change gloves or perform hand hygiene after reaching into her pocket and scissors were not cleansed prior to use.
-Nurse #3 cleansed wound, applied Santyl, applied calcium alginate, and applied dry protective dressing.
-Nurse #3 then assisted Resident to a comfortable position and covered him/her.
During an interview on 12/28/22 at 3:52 P.M., Nurse #3 said she did not perform hand hygiene during the dressing change because she did not bring any hand sanitizer into the room.
During an interview on 12/29/22 at 3:47 P.M., the Director of Nurses (DON) said the expectation is for hand hygiene to be performed during wound care with glove changes.
2. Review of the facility's policy titled Isolation- Categories of Transmission-Based Precautions, revised October 2018, indicated but was not limited to the following:
-When a resident is placed on transmission-based precautions, appropriate notification is placed on the room entrance door so that personnel and visitors are aware of the need for and type of precaution.
-The signage informs the staff of the type of CDC (Centers for Disease Control) precaution(s), instructions for use of PPE, and/or instructions to see a nurse before entering the room.
-Staff will follow PPE donning and doffing process outlined by CDC.
Review of the posted signs indicated:
-Enhanced barrier precautions: everyone must clean their hands, including before entering and when leaving the room. Providers and staff must also wear gloves and a gown for high-contact resident care activities.
- Droplet barrier precautions: everyone must clean their hands, including before entering and when leaving the room. Make sure their eyes, nose and mouth are fully covered before room entry. Remove face protection before room exit.
A. Resident #155 was admitted to the facility in December 2022 with diagnoses which included coronary artery bypass graft (CABG) after cardiac arrest and diabetes.
On 12/28/22 at 11:27 A.M., the surveyor observed two precautions signs on the door entrance of Resident # 155's room indicating both enhanced barrier precautions and droplet precautions were required.
On 12/28/22 at 11:33 A.M., the surveyor observed Social Worker #1 in Resident #155's room talking with the Resident. Social Worker #1 was wearing only a surgical mask.
During an interview on 12/28/22 at 11:38 A.M., the surveyor and Social Worker #1 reviewed the posted precaution signs and Social Worker #1 said she should have put on eye protection prior to entering Resident #155's room.
During an interview on 12/28/22 at 12:22 P.M., the Infection Control Nurse said the expectation for droplet precautions is all staff don eye protection, in the form of goggles or a disposable face shield, prior to entering the room.
B. On 12/27/22 at 9:00 A.M., the surveyor made the following observations on the [NAME] 2 unit:
-room [ROOM NUMBER] had three signs posted that included enhanced barrier precautions, contact precautions and droplet precautions.
-Rooms 204, 205 and 207 had signs indicating enhanced barrier precautions were required.
-room [ROOM NUMBER] had a sign indicating contact precautions were in place
-room [ROOM NUMBER] had two signs, one for enhanced barrier precautions and the other for droplet precautions
On 12/27/22 from 9:00 A.M. through 11:45 A.M., the surveyor observed staff entering and exiting several of the rooms with posted signs. The staff were observed serving meals, administering medication, and providing care. Staff were not consistently observed implementing the infection control practices during the observation. None of the staff were observed performing hand hygiene and did not consistently put on the required PPE prior to entering resident rooms. Observations included:
-On 12/27/22 at 9:15 A.M., a staff member entered room [ROOM NUMBER], which had two signs posted on the door, one for enhanced precautions and the other for droplet precautions. The staff member did not perform handwashing and did not put on any PPE. When the staff member exited no handwashing was performed and she was observed with what appeared to be care items in her hands. The staff member was interviewed about the posted signs, and she said the signs were confusing and they did not help her provide care. She said she did not read the signs before entering a room with a sign.
During an interview on 12/27/22 at 11:30 A.M., Unit Manager #3 was unable to state which Resident on her unit had an infection and what the posted signs meant. She said in the top drawer of the PPE cart the type of infection the resident had was identified.
The surveyor checked the PPE carts outside of room [ROOM NUMBER] and 216 and no information identifying the infection was available in the drawer.
On 12/28/22 at 8:20 A.M., the surveyor observed Nurse #5 approaching room [ROOM NUMBER] with a clipboard in her hand, a cup of water and a cup with medications in it. Nurse #5 stopped outside the door and juggled the items she was carrying and then placed them on top of the PPE cart. The Nurse did not perform hand hygiene before putting on the PPE. She was observed taking a gown out of the cart and tying the neck tie before putting it on. While she was tying the gown the gown was being dragged on the floor. She put the gown over her head and having tied it too tight had to pull and stretched the gown. After putting on the gown the Nurse took out a face shield for eye protection. She did not perform hand hygiene and was observed touching and adjusting the shield and her face mask multiple times without hand hygiene. The Nurse picked up the clipboard, water, and medication cup and entered the room. She put the items she was carrying down on a tray table and took gloves out of a glove container and placed the gloves in her pocket. She gathered the items and went to the Resident where she was observed putting on the gloves without hand hygiene and then administering medication and taking the Resident's blood sugar with a machine she took out of her pocket. During the direct care, the Nurse was observed leaning towards the Resident and her gown was dragging on the floor and on the Resident, as she had not secured the gown in the back. The Nurse was observed walking around the room touching the Resident and other surfaces. She was observed exiting the room without removing her PPE and then re-entering the room several times. When Nurse #5 exited the room, she removed her gown and face mask prior to exiting, but left the soiled gloves on. Nurse #4 was observed cleaning the glucometer and then putting the glucometer in her pocket. Then, the Nurse left the room and returned to the room with tissues for the Resident. The gloves had not been removed and were soiled. Nurse #5 was observed removing her gloves at her medication cart that was located at the nurses' station without performing hand hygiene.
During an interview on 12/28/22 at 8:25 A.M., Nurse #5 said she did not know why the Resident in room [ROOM NUMBER] was on precautions and could not identify the infection. Nurse #5 said she did not understand all the signs that were posted on doorways. She said the Assistant Director of Nurses, or the Infection Control Nurse posts the signs and leaves the unit without an explanation. The surveyor observed Nurse #5 ask Nurse #4 if she knew why and what the Resident in room [ROOM NUMBER] had for an infection. Nurse #4 said she did not know. Nurse #4 said she would review the Resident's medical record, but after reviewing said she was unable to determine an infection or what the plan was. Nurse #5 and Nurse #4 were asked if they had received infection control education. Nurse #4 said there had been education earlier that day. She said education was not done frequently and the education received had been reviewing what was written on the signs. Both nurses said they had not learned anything.
On 12/29/22 at 10:50 A.M., the surveyor observed a Physical Therapist walking a resident down the hall. The resident had been identified as requiring enhanced barrier precautions. The Physical Therapist walked with the resident around the unit and into a day room, where she had the resident perform exercises. The Physical Therapist was observed providing direct care to the resident and was not wearing a gown or gloves as required for direct care of a Resident that is on enhanced barrier precautions.
3. On 12/28/22 at 4:14 P.M., the surveyor observed Nurse #7 prepare a Binax (COVID-19 test) swab at the nurse's medication cart. Nurse #7 walked to a Resident's room with the Binax swab in her ungloved hand. Nurse #7 did not perform hand hygiene before putting on a pair of gloves and before entering the room. Nurse #7 exited the room with the Binax swab in her hand and placed the Binax swab directly on top of her medication cart. Nurse #7 was wearing the same gloves she entered the room with. When Nurse #7 removed her gloves, she put the soiled gloves directly into the trash container on her medication cart and did not perform hand hygiene.
At 4:21 P.M., Nurse #7 announced the test negative and threw the swab directly into the trash container on the medication cart (not a hazard bin per protocol) and did not perform hand hygiene.
During an interview on 12/28/22 at 4:22 P.M., Nurse #7 said that the Binax test takes 15 minutes for the results. She said she had not written down the time she took the swab and thought it had been 15 minutes. Nurse #7 said she had implemented the correct infection control practices during the Binax testing and was unaware that she did not follow infection control practices and protocol.
During an interview on 12/29/22 at 11:00 A.M., the surveyor informed the Infection Control Preventionist that the staff, on the [NAME] 2 unit, did not have knowledge of what the precautions signs were for and were unable to communicate procedures and protocol for minimizing the spread of infectious diseases. The Infection Control Preventionist said she had done a little education. She said because of the survey she had become aware that staff did not understand the posted signs and how to implement infection control practices.
At the time of the interview, the surveyor and the Infection Control Preventionist observed the Physical Therapist in the hallway talking with another staff member. The Resident who had been observed earlier was seated in the day room. The Physical Therapist was telling the other staff member she was not providing direct care and did not need to wear PPE. The surveyor observed the Infection Control Preventionist intervene and explain that a therapist providing treatment is considered a high contact activity and should use gowns and gloves when working with residents on enhanced precautions. The Infection Control Preventionist explained that this was according to the CDC (7/27/22). The Physical Therapist said she did not understand the signs that were posted and disagreed with CDC.