CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Abuse Prevention Policies
(Tag F0607)
Could have caused harm · This affected 1 resident
Based on interview and review of pertinent documentation provided by the facility, it was determined that the facility failed to ensure licensed staff credentials were verified upon hire for 2 of 5 ne...
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Based on interview and review of pertinent documentation provided by the facility, it was determined that the facility failed to ensure licensed staff credentials were verified upon hire for 2 of 5 newly hired licensed staff reviewed (Staff Member #2 and #4).
This deficient practice was evidenced by the following:
On 4/7/25 at 9:47 AM, the surveyor requested from the Licensed Nursing Home Administrator (LNHA) the employee files of six randomly selected new hire employees for which five of the selected were licensed staff.
The surveyor reviewed the facility provided files for the five licensed staff. There was no license verification printout from the corresponding licensing entity to verify the staff license was active prior to or upon their date of hire (doh). However, 3 of the 5 licensed staff had a criminal background check (CBC) that contained a license verification. The following two staff had a CBC but the CBC did not contain information that their license was active prior to or upon their doh:
Staff Member #2 (SM #2), a Licensed Practical Nurse/Infection Preventionist, with a doh of 2/7/25, did not have documented evidence that a license verification was performed prior to their doh.
Staff Member #4 (SM#4), a Certified Nurses Aide, with a doh 10/22/24, did not have documented evidence that a license verification was performed prior to their doh.
On 4/8/25 at 11:07 AM, the surveyor interviewed the Scheduling & Payroll Manager (SPM) regarding the process for new hires and license verification. The SPM stated that she would do a license check and background check. She added that she would get a copy of the license and check it on the website. She would then keep the copy of the license until the criminal background check came back then shred it. She stated that the background check was done prior to the start date. The SPM stated that she verified the licenses but that she did not print it out and keep it in their file.
On 4/9/25 at 10:12 AM, the surveyor interviewed the Director of Nursing (DON) regarding the process for new hires and license verification. The DON stated that the Human Resources department performed a background check and license verification prior to being hired. She added that the license was checked on the website and it would be printed out for proof and placed in their employee file and that it was done to make sure their license was active and to make sure there was not anything on their license that would be a flag. The surveyor showed the DON the two employee files that did not have evidence of license verification. The DON confirmed that there was no documented evidence that SM #2 and #4's licenses were verified.
The facility did not provide any documented evidence that SM #2 and #4's licenses were verified prior to their doh.
On 4/9/25 at 12:59 PM, the surveyor notified the LNHA, DON, Clinical Lead of New Jersey (CLoNJ) and Regulatory Compliance Advisor (RCA) the concern that SM #2 and #4 did not have their licenses verified prior to their doh.
On 4/10/25 at 11:23 AM, in the presence of DON, CLoNJ and RCA, the LNHA stated that an audit was done with license verification and that the SPM was educated.
The LNHA did not provide any additional information.
A review of the facility's Abuse Prohibition Policy, with a revised date of 10/24/22, included the following:
3. The Center will screen potential employees for a history of abuse .and checking with the appropriate licensing boards and registries.
A review of the facility's HR200 Hiring Policy, with a review date of 7/1/22, included the following:
Process
3. Post-Offer, Pre-Hire:
3.1 Internal candidate:
3.1.1 Verify all hiring requirements were obtained, current and appropriate for the new position .
3.2 External candidate:
3.2.1 Verify credentials, licenses, certificates, or other documents required for the position .
N.J.A.C. 8:39-43.15(a)
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Transfer Notice
(Tag F0623)
Could have caused harm · This affected 1 resident
Based on observation, interview, and record review, it was determined that the facility failed to notify the Office of the State Long-Term Care Ombudsman (LTCO) for 1of 1 resident reviewed for hospita...
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Based on observation, interview, and record review, it was determined that the facility failed to notify the Office of the State Long-Term Care Ombudsman (LTCO) for 1of 1 resident reviewed for hospitalization, Resident #18.
This deficient practice was evidenced by the following:
On 4/6/25 at 10:43 AM, the surveyor observed the Resident #18 sitting on the wheelchair in the day room, and the resident stated that they were hospitalized before.
A review of the admission Record (an admission summary) reflected that the resident was admitted to the facility with diagnoses which included, but not limited to; type 2 diabetes mellitus with severe non-proliferative diabetic retinopathy with macular edema, bilateral, complete traumatic amputation of left great toe, subsequent encounter, essential (primary) hypertension.
A review of the Quarterly Minimum Data Set (MDS), an assessment tool, with an assessment reference date (ARD) of 9/12/24, revealed a Brief Interview for Mental Status (BIMS) score of 15 out of 15 indicating intact cognition.
A review of the resident's medical record revealed the resident was transferred to the hospital twice on October 2024 for left toe gangrene and for hypotension (low blood pressure).
Further review of the medical records revealed that there was no documented evidence that the LTCO was notified of the resident's transfers to the hospital.
On 4/7/25 at 1:29 PM, the surveyor requested from the Licensed Nursing Home Administrator (LNHA), the binder for acute transfer and bed hold policy, and LTCO notifications for 2024.
On 4/9/25 at 9:00 AM, the LNHA stated that she spoke to the Social Worker (SW), who stated that she did not know she had to do notifications in 2024, however, she started them in 2025. The binder for the LTCO notification of transfers for 2025 was provided. The facility staff could not provide any documentation to show that the LTCO had been notified of the resident's transfers to the hospital in October of 2024.
On 4/9/25 at 9:43 AM, the surveyor interviewed the Director of SW (DSW), who had been working in facility since October 2023. The DSW stated, I will be honest, I do not have the emergency transfer notification, bed hold, bed rates and Ombudsman notifications for 2024, and that the DSW was unaware about the logs until this year. The DSW further stated that If I knew that, I would have done it.
On 4/9/25 at 10:40 AM, the surveyor interviewed the Director of Nursing (DON), and the DON stated, In my knowledge, we notify family of transfer, as far as bed hold and rates, the SW does that in my knowledge of it. The DON further stated that LNHA did make us aware either last Sunday or Monday that the bed hold and LTCO notifications for 2024, were not done. The DON also stated that I am aware of the regulations.
On 4/9/25 at 1:10 PM, the surveyor notified the LNHA, DON, Regulatory Compliance Advisor, and Clinical Lead of New Jersey regarding above concerns.
On 4/10/25 at 8:25 AM, the LNHA confirmed that there was no documented evidence that the LTCO was notified of the resident's acute transfer to hospital on October 2024.
A review of the facility's Discharge and Transfer Policy, dated 3/24/25, reflected that the written notice must also be provided to the Ombudsman .using the Notice of Hospital Transfer .
NJAC 8:39-4.1(a)31
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0625
(Tag F0625)
Could have caused harm · This affected 1 resident
Based on observation, interview, record review, and policy review, it was determined that the facility failed to notify the resident and/or the resident's representative in writing of the reason for t...
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Based on observation, interview, record review, and policy review, it was determined that the facility failed to notify the resident and/or the resident's representative in writing of the reason for transfer or discharge for 1 of 1 resident transferred to the hospital, Resident #18.
This deficient practice was evidenced by the following:
On 4/6/25 at 10:43 AM, the surveyor observed the Resident #18 sitting on the wheelchair in the day room.
A review of the admission Record (an admission summary) reflected that the resident was admitted to the facility with diagnoses which included, but not limited to; type 2 diabetes mellitus with severe non-proliferative diabetic retinopathy with macular edema, bilateral, complete traumatic amputation of left great toe, subsequent encounter, essential (primary) hypertension.
A review of the Quarterly Minimum Data Set (MDS), an assessment tool, with an assessment reference date (ARD) of 9/12/24, revealed a Brief Interview for Mental Status (BIMS) score of 15 out of 15 indicating intact cognition.
A review of the resident's medical record revealed the resident was transferred to the hospital twice on October 2024 for left toe gangrene (It happens when the blood flow to an area of tissue is cut off) and for hypotension (low blood pressure).
Further review of the medical records revealed that there was no documented evidence that the bed hold notifications for October 2024 for Resident #18 was done when the resident was transferred to hospital.
On 4/7/25 at 1:29 PM, the surveyor requested from the Licensed Nursing Home Administrator (LNHA), the binder for acute transfer and bed hold policy, and notifications for 2024.
On 4/9/25 at 9:43 AM, the surveyor interviewed the Director of SW (DSW), who had been working in facility since October 2023. The DSW stated, I will be honest, I do not have the emergency transfer notification, bed hold, bed rates and Ombudsman notifications for 2024, and that the DSW was unaware about the logs until this year. The DSW further stated that If I knew that, I would have done it.
On 4/9/25 at 10:01 AM, the surveyor interviewed the [NAME] Wing Unit Manager (UM), who stated that the Director of Nursing (DON), Responsible Party (RP), and the Doctor were notified verbally of the resident's transfer to hospital, and if they were not in the facility, a phone call will be made. The surveyor asked the UM if nursing was giving the written bed hold policy and pay rate to the resident or RP, and the UM responded No, and I do not know anything about that.
On 4/9/25 at 10:40 AM, the surveyor interviewed the DON, and the DON stated, In my knowledge, we notify family of transfer, as far as bed hold and rates, the Social Worker does that in my knowledge of it. The DON further stated that LNHA did make us aware either last Sunday or Monday that the bed hold notifications for 2024, were not done. The DON also stated that I am aware of the regulations.
On 4/9/25 at 1:10 PM, the surveyor notified the LNHA, DON, Regulatory Compliance Advisor, and Clinical Lead of New Jersey regarding above concerns. The LNHA stated that the Business Office Manager (BOM) was responsible in completing the transfer notifications and bed holds.
On 4/9/25 at 1:22 PM, in the presence of the LNHA and Scheduling/Payroll Manager who called the BOM via phone, and the BOM stated, Once the person goes out, I see their insurance, Medicaid is a bed hold, Medicare I discharge out of the system because of their policy. I update the census to where they went. The bed hold notification would be provided if person is private pay, and then scanned in the system in their chart. The surveyor asked what about the other residents with other insurances, and BOM replied, They do not have bed hold days, I believe I am aware of the regulation. The surveyor asked if she knew where Resident #18's bed hold notifications were and she replied that it should be in the resident's medical record.
On 4/10/25 at 8:25 AM, the LNHA confirmed that there was no documented evidence that the bed hold notifications and policy was provided in written form to the resident and/or RP on October 2024. The LNHA further stated, Education will be done that notifications will be given regardless of payer.
On 4/10/25 at 10:26 AM, the LNHA stated, I will educate the BOM upon her return, regarding bed hold policy for all residents regardless of payer.
A review of the facility's Bed-Holds Policy, dated 1/16/23, reflected that when a resident is transferred out .the designee will provide the resident and their representative .with the written Bed Hold Policy Notice and Authorization form regardless of payer.
NJAC 8:39-4.1(a)31
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0658
(Tag F0658)
Could have caused harm · This affected 1 resident
REPEAT DEFICIENCY
Based on observation, interview, record review, and review of other pertinent facility provided documentation, it was determined that the facility failed to a.) ensure that the physi...
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REPEAT DEFICIENCY
Based on observation, interview, record review, and review of other pertinent facility provided documentation, it was determined that the facility failed to a.) ensure that the physician orders were followed and orders for blood work was transcribed and followed for 1 of 20 residents, (Resident #59), and b.) adhere to appropriate disposal of unused medication for 1 out of 3 residents, (Resident #65), observed during the medication pass, according to the standard of clinical practice and facility policy.
This deficient practice was evidenced by the following:
Reference: New Jersey Statutes Annotated, Title 45. Chapter 11. Nursing Board. The Nurse Practice Act for the State of New Jersey states: The practice of nursing as a registered professional nurse is defined as diagnosing and treating human responses to actual and potential physical and emotional health problems, through such services as case-finding, health teaching, health counseling, and provision of care supportive to or restorative of life and wellbeing, and executing medical regimens as prescribed by a licensed or otherwise legally authorized physician or dentist.
1. On 4/6/25 at 9:40 AM, Surveyor #1 (S#1) observed Resident #59 lying on bed with eyes closed.
S#1 reviewed the medical records of Resident #59 and revealed:
A review of the admission Record (AR, an admission summary) or face sheet reflected that the resident was admitted with diagnoses that included but were not limited to; chronic systolic (congestive) heart failure, type 2 diabetes mellitus with other ophthalmic complication, anemia (low red blood cells count) in chronic kidney disease, and end stage renal disease (a medical condition in which the kidneys can no longer adequately filter waste products from the blood, functioning at less than 15% of normal levels).
A review of the most recent comprehensive Minimum Data Set (MDS), an assessment tool, with an assessment reference date (ARD) of 2/5/25, revealed in Section C Cognitive Patterns, a brief interview for mental status (BIMS) score of 14 of 15, which reflected that the resident's cognitive status was intact.
A review of the active Physician's Orders (PO) revealed:
-start date 7/1/23, Retacrit (generic name epoetin alfa-epbx, medication used to treat anemia) injection solution 10000 unit/ml (milliliters) inject 10000 unit subcutaneously in the evening every Saturday for anemia. CBC (complete blood count, is a commonly ordered blood test used to evaluate one's overall health and detect a wide range of disorders, including anemia and infection) and BMP (basic metabolic panel is a helpful and common test that measures several important aspects of blood, like electrolytes and blood sugar) weekly on Thursday mornings prior to administration of epoetin and please fax results to pharmacy, hold for hgb (hemoglobin, is a protein in red blood cells that carries oxygen. The hgb test measures how much hgb is in the blood. Normal results; Male: 13. 8 to 17. 2 grams per deciliter (g/dL) or 138 to 172 grams per liter (g/L) Female: 12. 1 to 15. 1 g/dL or 121 to 151 g/L Low hgb level may be due to: Anemia) over 10.
-start date 10/19/23, A1C (An A1C test measures the average amount of sugar in blood over the past few months) one time a day every three months starting on the 19th for one day for medication (med) regime.
-start date 8/21/24, CBC and CMP (comprehensive metabolic panel is a blood test that measures proteins, enzymes, electrolytes, minerals and other substances in the body. A healthcare provider can use the results to diagnose, screen for or monitor health conditions or side effects of medications) every two weeks. 11-7, check for lab (laboratory) slip. 7-3, follow up with result. Every shift every 14 days for anemia.
The above PO were plotted in the electronic Medication Administration Record (eMAR) and revealed:
-A review of the October 2024 eMAR reflected that on 10/19/24, the order for A1C was left blank. There was no documented evidence that the PO for A1C was followed.
-A review of the January 2025 eMAR reflected that on dates 1/4/25, 1/11/25, and 1/18/25, there were check marks and electronically signed by nurses.
-A review of the chart codes/follow up codes in the January 2025 eMAR revealed that a check mark meant administered.
A review of the Lab Reports revealed that on 12/26/24 collection date, hgb result was 10.3 g/dl and on 1/13/25 collection date, the hgb result was 10.5 g/dl.
Further review of the Lab Reports revealed that there was no A1C blood work was done on 10/19/24.
On 4/7/25 at 12:18 PM, S#1 interviewed Registered Nurse #1 (RN#1) about the above findings and concerns regarding the order for blood work and epoetin. RN#1 confirmed by checking the lab book that there was no lab done for 10/19/24 for A1C.
At that same time, RN#1 reviewed the eMAR for January 2025, and the lab results for CBC specifically for hgb. RN#1 stated that the 1/4/25, 1/11/25, and 1/18/25 epoetin order should have been followed and med should not been administered because the results for hgb were above 10. RN#1 confirmed that the nurses should have held the med. He also confirmed that the check mark on those dates meant that the epoetin was administered.
On 4/8/25 at 12:12 PM, the survey team met with the Licensed Nursing Home Administrator (LNHA), Director of Nursing (DON), and Clinical Lead of New Jersey (CLoNJ). S#1 discussed the above concerns for Resident #59.
On 4/9/25 at 12:37 PM, the survey team met with the LNHA, DON, CLoNJ and the Regulatory Compliance Advisor (RCA). The LNHA stated that regarding the med epoetin and lab reports, I am going to have a meeting with lab Representative to put a process with routine lab and to see if they can send preprinted routine lab and put them in lab book. The LNHA also stated that an audit will be done.
On 4/10/25 at 11:43 AM, the CLoNJ stated that the survey team could proceed with decision making and that there was no additional information.
A review of the facility's Lab and Radiology Integration Clinical System Process, dated 6/2024, that was provided by the LNHA, revealed under Guidance/Expectations for Lab/Radiology Order Entry:
Lab/Radiology orders will be entered in the electronic medical record .
Centers can order one time only labs/rad (radiology) or recurring lab/rad orders (standing orders).
Centers must print the lab/rad requisition prior to the lab/rad date and maintain in a folder for the lab/rad practice .
A review of the facility's Physician/Advanced Practice Provider (APP) Orders, with a review/revision date of 2/24/25, that was provided by the LNHA, revealed under Policy: Orders will be accepted only from authorized, credentialed physicians/APP or from order authorized credentialed practitioners in accordance with state regulations regarding prescriptive privileges .
Purpose: To ensure all physician orders are received from a credentialed practitioner before implementing .
On 4/10/25 at 12:02 PM, the survey team met with the LNHA, DON, CLoNJ and RCA for an exit conference, and there was no additional information provided by the LNHA and her team.
2. On 4/8/25 at 9:15 AM, during the medication (med) pass, Surveyor #2 (S#2) observed Registered Nurse #2 (RN#2) assigned to the med cart (med-cart) located on the [NAME] Wing Unit Low side prepare and administer medications (meds) to Resident #65. S#2 observed RN#2 remove a tablet (tab) of Amlodipine (a med used to control blood pressure) 2.5 mg (milligram) from the packaging and dropped it on the surface of the med-cart. RN#2 then stated that they could not give that to the resident as it was contaminated. RN#2 then proceeded to dispose of the tab into the open topped trash receptacle mounted on the side of the med-cart. S#2 asked RN#2 if that was the usual way to dispose of meds, and RN#2 stated, yes, contaminated meds are thrown in the garbage and not given to the resident. S#2 then observed RN#2 prepare another tab for administration to the resident.
S#2 completed the med-pass observation of RN#2.
S#2 reviewed the medical records for Resident #65 which revealed the following:
A review of Order Summary Report (OSR) and an eMAR that reflected a PO for Amlodipine 2.5 mg to be given at 9:00 AM.
A review of AR reflected that Resident #65 was admitted with diagnoses of, but not limited to, essential hypertension (high blood pressure) and type 2 diabetes (a chronic condition when the body cannot use insulin effectively).
A review of Resident #65's quarterly MDS, with an ARD of 3/13/25, reflected, in Section C, that the resident had a BIMS score of 15 out of 15, which indicated that Resident #65 was cognitively intact.
On 4/8/25 at 12:14 PM, the survey team met with the DON, LNHA, and CLoNJ to discuss the above concerns with med disposal. S#2 asked if it was common practice to dispose of meds that were not taken by a resident in the open trash container mounted on the side of the cart. The DON and CLoNJ both stated, no, they should be disposed in the (name redacted) (drug disposal system). S#2 asked if meds placed in the open trash could potentially be accessed by another resident or other unauthorized person. The DON stated yes, it could be possible.
On 4/9/25 at 10:18 AM, S#2 interviewed the facility Consultant Pharmacist (CP) by telephone. S#2 discussed the concerns with the med pass observation including disposal of unused meds. S#2 asked the CP if any education was done for the nursing staff on med pass, specifically med disposal, and the CP stated that any education was usually done one on one with staff at the med-cart, none done as a class, and nothing referencing disposal of unused med. The CP also stated that it was standard practice to use a self-contained drug disposal system (name redacted) to safely dispose of meds.
On 4/9/25 at 12:38 PM, the survey team met with the LNHA, DON and CLoNJ, and the DON stated that (name redacted) approved self-contained drug disposal systems were placed in all med-carts and staff education was conducted for proper disposal of meds.
A review of the facility's Disposal of Medications Policy, dated 1/24, reflected, under POLICY, 3. Methods of disposition of pharmaceutical hazardous and non-hazardous waste are consistent with applicable state and federal requirements, local ordinances, and standards of practice. Under PROCEDURES, 1.b. Authorized personnel who have access to meds should deposit pharmaceutical waste in the appropriately labeled container.
The facility did not provide any further pertinent information on med disposal.
NJAC 8:39-11.2(b); 27.1(a); 29.2(a)(d); 29.4(g)(h)(i)
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 F0660
(Tag F0660)
Could have caused harm · This affected 1 resident
Complaint NJ #184234
Based on interview, observation, and record review, it was determined the facility failed to; a.) update a resident's discharge goals based on the resident's representative (RR) w...
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Complaint NJ #184234
Based on interview, observation, and record review, it was determined the facility failed to; a.) update a resident's discharge goals based on the resident's representative (RR) wishes, b.) hold an interdisciplinary care plan meeting to collaborate with the RR on an updated discharge planning process, c.) and document in the electronic medical record , for 1 of 2 residents, (Resident #9), reviewed for discharge planning.
This deficient practice was evidenced by the following:
On 4/7/25 at 9:25 AM, the surveyor reviewed the electronic medical record (EMR) of Resident #9.
A review of the admission Record (or face sheet, an admission summary) documented that the resident had diagnoses that included but were not limited to, dementia, and adult failure to thrive (a decline in overall health and well-being in older adults).
A review of the quarterly Minimum Data Set (MDS), an assessment tool, with an assessment reference date (ARD) of 3/13/25, revealed a Brief Interview for Mental Status (BIMS) score of 99, which reflected the resident was unable to complete the interview.
A review of the physician's progress note (PN) dated 3/27/25, by the primary physician indicated the RR wanted the resident to be transferred to an assisted living facility.
A review of other PN and assessments including care plan (CP) meeting notes from January to April 2025, revealed, no additional documentation of the RR's desire for Resident #9 to be referred for discharge (d/c) to another facility.
On 4/7/25 at 9:42 AM, the surveyor spoke with Resident #9's RR over the phone, who stated they wanted the resident to be referred to another facility for transfer since February 2025. The RR stated there was paperwork that needed to be completed by the facility which was not done until recently. The RR stated they came to the facility and spoke with the Admissions Director (AD) on several occasions for the required paperwork to be completed. The RR stated that they had not discussed with any other facility staff and only dealt with the AD. The RR further explained that a representative from the referred facility attempted to contact the facility for requested paperwork and received no response.
On 4/7/25 at 11:49 AM, the surveyor observed Resident #9 sitting in a chair in the day room for an activity. The resident was alert, verbally responsive, and pleasantly conversant with the recreational aide.
On 4/8/25 at 11:26 AM, the surveyor interviewed the AD who stated the Social Worker (SW) was responsible for following up on a resident and/or RR request to be referred to another facility. The AD stated it would be expected for the facility to follow up as soon as they were notified of a resident and/or RR request for referral to another facility.
At that same time, the surveyor asked the AD about Resident #9. The AD stated that they recently submitted via fax requested paperwork for Resident #9 to another facility as requested by the RR. The AD provided the faxed documentation which was dated 4/4/25. The AD stated he could not recall when the RR first verbalized their wishes for the resident to be referred for transfer to another facility and stated the SW would have additional information.
On 4/8/25 at 11:34 AM, the surveyor interviewed the SW who stated the RR spoke with the AD when visiting the facility and did not come to her. The SW stated she was first made aware by the AD that the RR was requesting Resident #9 to be referred for d/c to another facility in mid-March 2025, and that was when she approached the RR. The SW stated at the time that RR verbalized their wish to refer the resident to be transferred to another facility and specified an assisted living facility they were interested in. The SW stated she was not aware of when the RR had previously verbalized their wish for the resident to be referred for transfer to another facility.
On that same date and time, the surveyor asked the SW after she spoke with the RR if she followed up with their wishes for a referral to another facility. The SW stated that she did not follow up. The SW stated that Resident #9 required a higher level of care than what could be provided at an assisted living facility and did not think the resident would be approved. The SW stated a representative for the other facility did come to the facility, she cannot recall when, she spoke with them, and they did not request any paperwork. The SW stated she believed the resident would not be accepted into the facility. The SW stated she did not document in the EMR when she spoke with the RR in mid-March 2025, and there was no documentation regarding their verbalized wishes for Resident #9 to be referred for transfer. The SW acknowledged that she did not follow up regarding the RR's wishes and an interdisciplinary (IDT) CP meeting was not held with the RR to further discuss a d/c plan of care for Resident #9.
On 4/8/25 at 12:14 PM, the surveyor notified the Licensed Nursing Home Administrator (LNHA), the Director of Nursing (DON) and the Clinical Lead of New Jersey (CLoNJ) about the concern for Resident #9's RR requesting for the resident to be referred to another facility with no documentation or follow up. The surveyor asked what the facility's protocol was for when a RR requested for a resident to be referred to another facility. The DON stated that once a RR expressed and decided on a facility for a resident to be referred, the SW would follow up with the other facility and collaborate with that facility to provide the needed paperwork.
On 4/9/25 at 12:37 PM, the LNHA, the DON, the CLoNJ, and the Regulatory Compliance Advisor (RCA) met with the survey team. There was no additional information provided by the facility. The surveyor asked what the process for d/c was if a resident requested to be transferred to another facility. The LNHA stated the physician, the SW, the business office, and the IDT would be notified to work with the resident/RR and the referred facility. The LNHA acknowledged it would also be expected for it to be documented in the EMR regarding a resident and/or RR wishes and update the plan of care.
A review of the facility's Person-Centered Care Plan Policy, with a last revised date of 10/24/22, under Purpose revealed: .To promote positive communication between patient, patient representative, and team to obtain the patient's and RR input into the plan of care, ensure effective communication, and optimize clinical outcomes .
A review of the facility's Discharge Planning Process Policy, with a last revised date of 11/15/22, under Policy revealed: The Center's d/c planning process must be consistent with the patient's discharge rights.
Under Process of the policy revealed: .
1. The interprofessional care team will use the d/c planning process to:
1.1 Identify d/c needs and develop a d/c plan to meet those needs .
1.4 Involve the patient and RR to establish goals of care and treatment preferences .
1.7 Provide ongoing support, encouragement, and education to patients and patient representatives, and families from admission through d/c from the Center .
1.8.2 If the patient indicates an interest in returning to the community, the Center must document any referrals to local contact agencies or other appropriate entities made for this purpose .
1.8.4 If d/c to the community is determined to not be feasible, the Center must document who made the determination and why .
NJAC 8:39-4.1; 27.1 (a); 46.6 (b)
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Respiratory Care
(Tag F0695)
Could have caused harm · This affected 1 resident
Based on observation, interview, record review, and review of other pertinent facility documentation, it was determined that the facility failed to, a.) maintain the necessary respiratory care and ser...
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Based on observation, interview, record review, and review of other pertinent facility documentation, it was determined that the facility failed to, a.) maintain the necessary respiratory care and services of residents by following the physician orders and b.) verify the duplicate order for one 1 of 1 resident, (Resident #39), reviewed for respiratory care, in accordance with professional standards of practice and facility policy.
This deficient practice was evidenced by the following:
Reference: New Jersey Statutes Annotated, Title 45. Chapter 11. Nursing Board. The Nurse Practice Act for the State of New Jersey states: The practice of nursing as a registered professional nurse is defined as diagnosing and treating human responses to actual and potential physical and emotional health problems, through such services as case-finding, health teaching, health counseling, and provision of care supportive to or restorative of life and wellbeing, and executing medical regimens as prescribed by a licensed or otherwise legally authorized physician or dentist.
On 4/6/25 at 9:45 AM, the surveyor observed Resident #39 lying on bed, with head of bed elevated, on oxygen (O2) 2 LPM (liters per minute) via nasal cannula (N/C, a medical device that provides supplemental O2 therapy, the device has two prongs and sits below the nose. The two prongs deliver O2 directly into nostrils) via concentrator (a device that supply an O2) with tubing dated 3/31/25.
A review of the admission Record (an admission summary) or face sheet revealed diagnoses which included but not limited to; encephalopathy (refers to brain disease, damage, or malfunction) unspecified, unspecified combined systolic (congestive) and diastolic (congestive) heart failure, and dementia in other diseases classified elsewhere, unspecified severity, without behavioral disturbance, psychotic disturbance, mood disturbance, and anxiety.
A review of the most recent comprehensive Minimum Data Set (MDS), an assessment tool, with an assessment reference date (ARD) of 2/18/25, revealed in Section C Cognitive Patterns the cognitive skills for daily decision making was coded 3, which reflected that the resident's cognition was severely impaired.
A review of the April 2025 electronic Medication Administration Record (eMAR) revealed the following active Physician's Orders (PO):
-start date 3/21/25, O2 PRN (as needed) at 1 LPM via N/C to maintain sats (saturation is a measure of how much O2 is in the blood. For healthy adults, a normal O2 sats level is between 95% and 100%), if sats are less than 92% PRN post treatment (tx): evaluate heart rate (HR), respiratory rate (RR), pulse oximetry, skin color, and breath sounds.
-start date 3/21/25, O2 PRN at 1 LPM via N/C to maintain sats if sats are less than 92% every shift.
Further review of the above April 2025 eMAR revealed that there were duplicate PO for O2 PRN. The above PO for O2 PRN that included monitoring of HR, RR, pulse oximetry, skin color, and breath sounds were blank.
Furthermore, the above PO for O2 PRN every shift monitoring was not followed as evidenced by the following O2 sats and O2 at 1 LPM was administered:
On 4/1, 4/2, 4/3, 4/5, and 4/6/25, Day Shift (7:00 AM - 3:00 PM) O2 sats were above 92%.
On 4/1, 4/2, 4/3, 4/4, 4/5, and 4/6/25, Evening Shift (3:00 PM - 11:00 PM) sats were above 92%.
On 4/1, 4/2, 4/3, 4/4, 4/5, and 4/6/25, Night Shift (11:00 PM - 7:00 AM) sats were above 92%.
A review of the medical records revealed that there was no documented evidence as to why the PRN O2 was administered beyond the parameters and did not follow the PO.
On 4/7/25 at 12:08 PM, both the surveyor and the Registered Nurse (RN) observed the resident seated in a wheelchair with other residents in the dayroom with no O2 in use.
Afterward, both the surveyor and the RN went to resident's room, and the RN informed the surveyor that the resident's O2 was a PRN order. The RN stated that nurses had to check O2 sats every shift and verify the order when to administer the O2. He further stated, usually when O2 sats was low, it should be documented in the eMAR.
On 4/7/25 at 12:26 PM, the surveyor notified the RN of the above findings and concerns with regard to the duplicate order for O2 PRN and not following the PO for PRN O2. The surveyor also notified the RN of the observation that the resident was on 2 LPM during the 1st day of tour on 4/6/25. The RN stated that the nurse should have been followed the order for 1 LPM and that the order to document if the resident's 02 was below 92% prior to administering the O2. He further stated that the blanks should have been filled out with O2 saturation. The RN stated that the PO should have been followed and the nurse should clarify the duplicate orders.
On 4/8/25 at 12:12 PM, the survey team met with the Licensed Nursing Home Administrator (LNHA), Director of Nursing (DON), and Clinical Lead of New Jersey (CLoNJ), and the surveyor discussed above concerns and findings with Resident #39's PRN O2 duplicate orders and not following the PO.
On 4/9/25 at 12:37 PM, the survey team met with the LNHA, DON, CLoNJ, and Regulatory Compliance Advisor (RCA). The LNHA stated, we started an audit to ensure the O2 was matching the eMAR. The CLoNJ stated we did an audit on PRN O2 orders.
At that same time, the surveyor asked about the concerns with double entry for PO PRN O2 and as to why the PO was not followed, the LNHA and the DON did not respond.
On 4/10/25 at 11:43 AM, the CLoNJ stated that the survey team could proceed with decision making and that there was no additional information.
A review of the facility's Oxygen: High Pressure Cylinders Policy, with a review/revision date of 12/16/24, that was provided by the LNHA, revealed under policy that high pressure cylinders are set up a licensed nurse, respiratory therapist, or rehabilitation therapist with a physician's/advanced practice provider's order .
On 4/10/25 at 12:02 PM, the survey team met with the LNHA, DON, CLoNJ and RCA for an exit conference, and there was no additional information provided by the LNHA and her team.
NJAC 8:39-27(b)
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Staffing Information
(Tag F0732)
Could have caused harm · This affected 1 resident
Based on observation, interview, and review of pertinent facility documents, it was determined that the facility failed to ensure that the 24-hour staffing report was accurately posted and in a promin...
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Based on observation, interview, and review of pertinent facility documents, it was determined that the facility failed to ensure that the 24-hour staffing report was accurately posted and in a prominent place within the facility readily accessible and visible to the residents and the visitors.
This deficient practice was evidenced by the following:
On 4/6/25 at 9:00 AM, the surveyor entered the facility. The surveyor observed that the Nursing Home Resident Care Staffing Report (NHRCSR) that was posted on the table across from the receptionist desk was dated 4/3/25, day shift. The NHRCSR was not up to date.
On 4/8/25 at 12:31 PM, the surveyor notified the Licensed Nursing Home Administrator (LNHA), Director of Nursing (DON) and Clinical Lead of New Jersey(CLoNJ) the concern that the staffing report that was posted and observed on 4/6/25 was dated 4/3/25, and was not up to date. The LNHA stated that it should be posted every day.
On 4/9/25 at 9:44 AM, the surveyor interviewed the Scheduling & Payroll Manager (SPM) regarding posting of the NHRCSR. The SPM stated that she would print out the NHRCSR and post it in the morning. She added that the later shifts were behind the day shift. The surveyor asked who was responsible for posting it when she was not at the facility. The SPM stated that prior to the new LNHA starting she posted it on the weekend but that now she only worked Monday through Friday and did not know who posted it on the days she was not at the facility.
On 4/9/25 at 12:55 PM, in the presence of the DON, CLoNJ, and Regulatory Compliance Advisor, the LNHA stated that the Receptionist would post the report on the weekend and that staff were educated.
The LNHA did not provide any additional information.
A review of the facility's Posting Staffing Policy, with a review date of 8/7/23, included the following:
Policy
In accordance with federal and state regulations, Centers will post the census, shift hours, number of staff and total actual hours worked by licensed and unlicensed nursing staff who are directly responsible for patient care for each shift and on a daily basis.
Process
1. The DON or designee will post the number of staff and actual hours worked of nursing staff directly responsible for the care of patients
2. The posting should include the:
2.1 Center name;
2.2 Current date;
2.3 Patient census at the beginning of each shift;
2.4 Center specific shifts .
3. The posting should be: .
3.3 Completed on a daily basis at the beginning of each shift; .
N.J.A.C. 8:39-41.2 (a)(b)(c)
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
Pharmacy Services
(Tag F0755)
Could have caused harm · This affected 1 resident
NJ#176708
Based on observation, interview, and review of facility documents, it was determined that the facility failed to provide pharmaceutical services in accordance with professional standards to...
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NJ#176708
Based on observation, interview, and review of facility documents, it was determined that the facility failed to provide pharmaceutical services in accordance with professional standards to ensure accurate accountability of controlled substances, have sufficient secure procedures in place to prevent further diversion of controlled substances, and to educate all staff on accountability procedures for controlled substances. This deficient practice was identified for 1 of 2 years of controlled substances accountability reviewed.
The deficient practice was evidenced by the following:
Reference: New Jersey Statutes Annotated, Title 45. Chapter 11. Nursing Board. The Nurse Practice Act for the State of New Jersey states: The practice of nursing as a registered professional nurse is defined as diagnosing and treating human responses to actual and potential physical and emotional health problems, through such services as case-finding, health teaching, health counseling, and provision of care supportive to or restorative of life and wellbeing, and executing medical regimens as prescribed by a licensed or otherwise legally authorized physician or dentist.
Reference: New Jersey Statutes Annotated, Title 45, Chapter 11. Nursing Board. The Nurse Practice Act for the State of New Jersey states: The practice of nursing as a licensed practical nurse is defined as performing tasks and responsibilities within the framework of case finding; reinforcing the patient and family teaching program through health teaching, health counseling, and provision of supportive and restorative care, under the direction of a registered nurse or licensed or otherwise legally authorized physician or dentist.
On 4/7/25 at 11:42 AM, the surveyor reviewed the contents of the facility provided binder containing completed DEA 222 forms (forms from the Drug Enforcement Agency that are used to order Schedule II controlled substances from the provider pharmacy). The binder revealed completed DEA 222 forms with the most recent date of 5/30/24.
On 4/9/25 at 10:18 AM, the surveyor interviewed the facility Consultant Pharmacist (CP) by telephone. The CP stated that they have been servicing the facility since 2022. The surveyor asked the CP what procedures they do regarding controlled substance accountability. The CP stated that they do monthly audits at the medication carts (med-cart) and compare the count of controlled substance medications present in the cart to the count sheet (a form that tracks each time a dose was removed from the med-cart), to check for discrepancies. The surveyor asked if the CP audits the DEA 222 forms. The CP stated no, not unless they are asked to.
On that same date and time, the surveyor asked the CP if they knew that there were no records of DEA 222 forms since 5/30/24, and if that was of any concern. The CP stated that they were not aware and that it was unusual. The surveyor asked the CP if they were aware of a controlled substance diversion issue that was discovered on April 2024, and the CP stated yes, they were aware that something occurred with a nurse removing controlled substances. The surveyor asked the CP if they were aware of or assisted in any plans or procedures put in place to prevent diversion of controlled substances. The CP stated, no, they were not aware of any other plans or procedure put in place.
On 4/9/25 at 10:49 AM, the surveyor interviewed the Director of Nursing (DON) regarding the requested 4/2/24 documents regarding the facility reported incident of drug diversion and what the facility implemented to prevent recurrence of the incident. The DON stated that she was not fully familiar with what occurred as she only started at the facility February 2025, but will find out. The surveyor asked if there were any further records of DEA 222 forms after 5/30/24 and if there were any records of 4/2/24 pertaining to the controlled substance diversion including, but not limited to, investigations, reports, inventories, interventions, plans of correction, education, or policies and procedures.
On 4/9/25 at 11:30 AM, the DON stated to the surveyor that they were unable to provide any further DEA 222 forms for the period after 5/30/24, and she was in process of obtaining more for the facility. The DON also stated that they would look for any other investigative documents for the diversion and it there were any corrective plans put in place.
On 4/9/25 at 12:30 PM, the DON provided copies of an educational in-service sign in sheet and Action Plan (AP) from 4/3/24, referencing the incident. The DON also provided copies of investigations and employee statements that were previously provided with the original Facility Reported Event (FRE) on 4/2/24.
The surveyor reviewed the documents provided by the DON. The AP did not reflect any conclusions or preventive actions put in place. The in-service sign in sheet reflected the names of ten employees of the nursing department.
The surveyor reviewed the investigative documents for the FRE. The documents revealed that the initial investigation was performed and appropriate reporting to the required agencies was done. The documents included a statement from the employee involved that reflected a statement of apology for a mistake and unprofessionalism.
On 4/9/25 at 1:53 PM, the survey team met with the DON to discuss concerns with controlled substance accountability. The surveyor asked the DON what the process was for current controlled substances (CDS) when they were discontinued or the resident was discharged (d/c), The DON stated that if the CDS was completed, the count sheet was placed in the resident's hard copy chart for medical records. If the CDS was discontinued or resident d/c, the CDS will be destroyed by the DON and another nurse and there will be a log to document it. The DON stated she was not sure what the previous process was.
On the same date and time, the surveyor interviewed the Unit Manager (UM) who was present at the time of the FRE. The surveyor asked the UM what the process was for removing CDS. The UM stated that the DON and floor nurse would reconcile the amount of CDS from the count sheet and then destroy the remaining CDS. The UM also confirmed that the not all nurses signed the in service sign in sheets. The UM acknowledged that all nurses should have been signed the in service sign in sheets for drug diversion.
On 4/9/25 at 2:15 PM, the DON provided CDS count sheets showing signatures indicating removal and destruction. The surveyor reviewed the sheets which reflected only the years 2022 and 2023. The DON confirmed there were no count sheets available for 2024. The DON also confirmed, based on the education sign in sheet that not all the nurses were educated on correct disposal of CDS.
On 4/10/25 at 11:24 AM, the survey team met with the Licensed Nursing Home Administrator (LNHA), the DON, The Clinical Lead of New Jersey (CLoNJ), and Regulatory Advisor (RA) to discuss the above concerns with the lack of staff education on CDS diversion prevention and lack of a specific plan to prevent further diversion prior to surveyor's inquiry.
A review of the facility's Controlled Drugs: Management of Policy, with a revision date of 1/31/25, reflected, Centers will upload Controlled Substance Declining Inventory Sheets to the patient medical record upon discontinuing of the medication, d/c, or completion.
The facility did not provide any further pertinent information.
NJAC 8:39-29.7(c)
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Drug Regimen Review
(Tag F0756)
Could have caused harm · This affected 1 resident
Based on interviews, record review, and a review of pertinent facility documents, it was determined that the facility's Consultant Pharmacist (CP) failed to identify irregularity for 1 of 3 residents,...
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Based on interviews, record review, and a review of pertinent facility documents, it was determined that the facility's Consultant Pharmacist (CP) failed to identify irregularity for 1 of 3 residents, (Resident #62), during the medication pass observation.
This deficient practice was evidenced by the following:
On 4/8/25 at 9:31 AM, the surveyor observed the Licensed Practical Nurse (LPN) assigned to the medication cart (med-cart) located on the East Wing Unit, High Side, prepare and administer due medications (meds) to Resident #62.
The surveyor observed the LPN prepare and administer Linzess (a medication (med) used to treat irritable bowel syndrome with constipation). The med was scheduled to be given at 9:00 AM per the physician's orders (PO) and the LPN was within the accepted time based on the order. The surveyor observed on the Linzess med container labeling that reflected to take on an empty stomach. The surveyor asked the LPN about the labeling. The LPN stated they noticed it and was going to call the physician to ask about it.
The surveyor concluded the med-pass.
The surveyor reviewed the electronic medical record for Resident #62.
A review of Resident #62's admission Record (or facesheet, an admission summary) reflected that the resident was re-admitted to the facility with diagnoses of, but not limited to, essential hypertension (high blood pressure) and type 2 diabetes (a chronic condition when the body cannot use insulin effectively).
A review of Resident #62's comprehensive Minimum Data Set (MDS), an assessment tool, with an assessment reference date (ARD) of 1/11/25, reflected, in Section C Cognitive Patterns, that the resident had a Brief Interview for Mental Status (BIMS) score of 15 out of 15, which indicated that Resident #62 was cognitively intact. Section H Bowel and Bladder, revealed that the resident was occasionally incontinent of bowel and did not have constipation.
A review of the resident's Order Summary Report (OSR, a listing of the resident's active meds and other orders) revealed the following:
An order for Linzess Oral Capsule 145 mcg (microgram) Give 1 capsule by mouth one time a day for chronic constipation, with a start date of 10/22/24.
A review of the resident's electronic medication administration record (eMAR) revealed that the order for Linzess was scheduled for administration at the 9:00 AM administration period.
A review of the CP report, revealed that the CP did document that the resident's chart was reviewed for the period of October 2024 through present, and did not reflect any irregularities with the Linzess orders or the time Linzess was scheduled.
On 4/8/25 at 12:14 PM, the survey team met with the Licensed Nursing Home Administrator (LNHA), Director of Nursing (DON) and Clinical Lead of New Jersey (CLoNJ) to provide concerns observed during the med-pass, specifically the timing of Linzess and the lack of documentation of this irregularity by the CP.
On 4/9/25 at 10:18 AM, the surveyor interviewed the CP by telephone. The surveyor asked the CP if they were familiar with Linzess. The CP stated, yes, they were. The surveyor asked the CP if they were familiar with the administration of Linzess regarding timing and food. The CP stated that it should be given in the morning, but they would have to check the information regarding food.
On 4/9/25 at 12:38 PM the survey team met with the LNHA, DON, CLoNJ and Regulatory Compliance Advisor (RCA). The LNHA stated that the administration time for the Linzess was changed to be given at least 30 minutes before breakfast and the staff was educated on administration of meds according to manufacturer guidelines.
A review of the facility's Disposal of Medications Policy, dated 1/24, reflected under Procedures:
1. The DON and the CP will monitor for compliance with federal and state laws regarding the disposal of meds.
A review of the facility's Medication Administration Policy, dated 1/25, reflected under Policy: Meds are administered as prescribed in accordance with manufacturers' specifications, .
Procedures, Medication Administration:
3. Med administration timing parameters include the following:
a. Meds to be given on an empty stomach or before meals are to be scheduled for administration 30 minutes to 2 hours prior to meals.
A review of the manufacturer package insert for Linzess, reflected under 2 DOSAGE AND ADMINISTRATION, 2.2 Preparation and Administration Instructions, Take LINZESS on an empty stomach, at least 30 minutes prior to a meal, at approximately the same time each day.
The facility did not provide any further pertinent information for this concern.
NJAC 8:39-29.3(a)(1)
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0868
(Tag F0868)
Could have caused harm · This affected 1 resident
Based on interview and record review, it was determined that the facility failed to a.) assure that the required staff attended the quarterly Quality Assurance (QA) meetings for 2 of 4 quarterly QA me...
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Based on interview and record review, it was determined that the facility failed to a.) assure that the required staff attended the quarterly Quality Assurance (QA) meetings for 2 of 4 quarterly QA meetings and b.) ensure there was a scheduled frequency of meetings and reporting according to the regulation and facility's policy.
This deficient practice was evidenced by the following:
On 4/8/25 at 3:09 PM, the surveyor reviewed the QAPI (Quality Assurance Performance Improvement) Plan, dated 1/1/25, and the Center Quality Assurance Performance Improvement Process Policy that was provided by Licensed Nursing Home Administrator #1 (LNHA#1) on 4/7/25 at 8:20 AM, and revealed that the facility QAPI members will meet at least quarterly.
The LNHA also provided the QAPI sign in sheets and revealed:
7/24/24=10 attendees signed and did not include their titles.
8/22/24=nine attendees signed and did not include their titles.
9/25/24=12 attendees signed and did not include their titles.
10/29/24=11 attendees signed and did not include their titles.
11/26/24=11 attendees signed and did not include their titles except for LNHA#2.
12/12/24=12 attendees signed and did not include their titles except for the LNHA#2.
2/28/25=11 attendees signed and did not include their titles except for LNHA#1, Director of Nursing (DON), Infection Preventionist (IP), Social Services (SS), and Minimum Data Set Coordinator (MDSC).
3/26/25=six attendees signed and did not include their titles except for LNHA#1, DON, Medical Director (MD), IP, Unit Manager (UM), and Clinical Lead of New Jersey (CLoNJ).
Further review of the above sign in sheets for QAPI revealed that there was no QAPI sign in sheet for January 2025 and that on all meetings the MD was present.
On 4/9/25 at 11:19 AM, the surveyor interviewed the CLoNJ regarding the QAPI sign in sheets. The CLoNJ confirmed after reviewing the sign in sheets that on 10/29/24, 11/26/24, and 12/12/24, QAPI sign in sheets, there was no DON present. The CLoNJ stated that the IP was the covering DON at that time, and the CLoNJ was the covering IP. The CLoNJ acknowledged that she did not sign on 10/29/24 and 11/26/24 QAPI sign in sheets.
On that same date and time, the surveyor asked the CLoNJ if she was aware of the regulation that the IP must physically work onsite in the facility, cannot be an off-site consultant or perform the IP work at a separate location such as a corporate office or affiliated short term acute care facility, and the CLoNJ responded that she was unaware of that. The surveyor notified the CLoNJ of the concern that the facility had no January 2025 QAPI sign in sheets.
On 4/10/25 at 8:50 AM, the surveyor asked LNHA#1 why the only provided QAPI Meeting Schedule was for 2025 when the surveyor asked for the planned QAPI Meeting Schedules for 2023, 2024, and 2025, and LNHA#1 responded that she did not find any schedule for 2023 and 2024. She further stated that the 2023 and 2024 quarterly schedule should be the same with 2025 schedule provided to the surveyor. LNHA#1 also stated that there was no January 2025 quarterly QAPI schedule because she was not the Administrator at that time.
A review of the provided 2025 QAPI Meeting Schedule for 2025 revealed:
All Meetings start at 9:30 AM
January 2025 (no schedule provided)
4/22/25 (Quarterly)
7/17/25 (Quarterly)
10/16/25 (Quarterly)
On 4/10/25 at 9:39 AM, the surveyor met with LNHA#1 for QAPI meeting, and the surveyor notified LNHA#1 of the above findings and concerns. LNHA#1 stated that the 2025 QAPI Meeting Schedule should be the same schedule that the facility should follow as scheduled for January, April, July, and October respectively for a quarterly meetings. She also acknowledged that there should be a planned quarterly QAPI meeting schedule.
A review of the undated facility's Center Quality Assurance Performance Improvement Process Policy, that was provided by LNHA#1, revealed:
Process:
1. The Administrator, along with the DON, directs the development and documentation of the Center QAPI Plan .and effectively Quality Assessment and Assurance (QAA) Committee.
2. The QAA Committee:
2.1 Functions under the authority of the Administrator and the Governing Body and is composed of:
2.1.1 Administrator,
2.1.2 DON,
2.1.3 MD,
2.1.4 IP, or designee,
2.1.5 Consultant Pharmacist (recommended),
2.1.6 Patient and/or family representatives (if appropriate),
2.1.7 Three additional staff representatives including, but not limited to, department heads, certified nursing assistants, rehabilitation services, hospice, home health, etc.
2.2 Meets at least quarterly.
On 4/10/25 at 12:02 PM, the survey team met with the LNHA, DON, CLoNJ and Regulatory Compliance Advisor for an exit conference, and there was no additional information provided by the LNHA and her team.
N.J.A.C. 8:39-33.1(a)(b)
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0883
(Tag F0883)
Could have caused harm · This affected 1 resident
Based on observation, interview, and record review, it was determined that the facility failed to offer a resident a pneumococcal vaccine. This deficient practice was identified for 1 of 5 residents, ...
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Based on observation, interview, and record review, it was determined that the facility failed to offer a resident a pneumococcal vaccine. This deficient practice was identified for 1 of 5 residents, (Residents #57), reviewed for immunizations.
This deficient practice was evidenced by the following:
On 4/9/25 at 11:12 AM, the surveyor reviewed the electronic medical record (EMR) of Resident #57 for immunizations.
A review of the admission Record (or facesheet, an admission summary) documented that Resident #57 was recently admitted and had diagnoses that included but were not limited to; dementia, chronic atrial fibrillation (an irregular, rapid heart rate that commonly causes poor blood flow), and hypertension (high blood pressure).
A review of the most recent comprehensive Minimum Data Set (MDS), an assessment tool, with an assessment reference date of 3/11/25, indicated a Brief Interview for Mental Status (BIMS) test was not completed as the resident was documented as being rarely/never understood. Section O of the MDS indicated the resident's pneumococcal vaccination was up to date.
A review of the immunizations listed in the EMR revealed documentation for a pneumovax dose which indicated the resident refused. Additional review revealed the refusal was documented on 4/23/24.
On 4/9/25 at 11:36 AM, the surveyor reviewed the hard copy chart of Resident #57, which revealed there was no documentation of administration or declination for the pneumococcal vaccine.
On 4/9/25 at 11:46 AM, the surveyor interviewed the Infection Preventionist (IP), who stated she was responsible for assessing and reviewing the residents' immunizations. The IP explained she would review the state online database for resident's vaccination records and asked residents and/or the resident's representative (RR) about vaccination status upon admission. The IP stated vaccines would be offered to residents if they wished to receive them. An informed consent form would be signed if the resident desired or declined a vaccine. The IP stated immunizations would be documented under the immunizations section of the EMR.
The surveyor asked the IP about Resident #57's pneumococcal vaccination documentation and history. The IP stated Resident #57 was newly admitted to the facility in March 2025, and had previous stays at the facility. The IP stated it was previously documented in the EMR that the pneumococcal vaccine had been previously refused. The IP confirmed the documentation was from the resident's previous stay in 2024. The IP stated that she did not discuss with the resident and/or RR to offer the pneumococcal vaccine upon admission. The IP was not sure if it was part of the facility policy to offer a vaccine to every resident upon a new admission, even if they had documentation from a previous stay at the facility. The IP stated she would have to follow up about the process and that if it's something she should be doing, then she would.
On 4/9/25 at 12:59 PM, the survey team met with the Licensed Nursing Home Administrator (LNHA), the Director of Nursing (DON), the Clinical Lead of New Jersey (CLoNJ), and the Regulatory Compliance Advisor (RCA). The surveyor asked if it would be expected for staff to assess a resident who were newly admitted for immunizations and for them to be offered an opportunity to receive a vaccine, whether they had a previous stay or not. The DON replied Yes. The surveyor notified the facility's management of the concern that the resident was not offered a pneumococcal vaccine.
On 4/10/25 at 11:22 AM, the LNHA, the DON, the CLoNJ, and the RCA met with the survey team. The DON stated that the IP was doing an audit on all resident to review immunizations and ensure up to date documentation of their refusal or consent for vaccination. There was no additional information provided by the facility.
A review of the facility's Pneumococcal Vaccine Policy, with a last revised date of 9/13/24, under Process revealed: .
1. Upon admission, obtain the pneumococcal vaccination history of all patients .
2. Based on the patient's pneumococcal vaccination history, offer (unless the vaccination is medically contraindicated or the patient has already been vaccinated) the appropriate vaccination following the recommended schedule .
N.J.A.C. 8:39-19.4 (i)
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0887
(Tag F0887)
Could have caused harm · This affected 1 resident
Based on interview and record review, it was determined that the facility failed to offer a resident a coronavirus-19 (COVID-19) vaccine. This deficient practice was identified for 1 of 5 residents, (...
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Based on interview and record review, it was determined that the facility failed to offer a resident a coronavirus-19 (COVID-19) vaccine. This deficient practice was identified for 1 of 5 residents, (Residents #57), reviewed for immunizations.
This deficient practice was evidenced by the following:
On 4/9/25 at 11:12 AM, the surveyor reviewed the electronic medical record (EMR) of Resident #57 for immunizations.
A review of the admission Record (or facesheet, an admission summary) documented that Resident #57 was recently admitted and had diagnoses that included but were not limited to; dementia, chronic atrial fibrillation (an irregular, rapid heart rate that commonly causes poor blood flow), and hypertension (high blood pressure).
A review of the most recent comprehensive Minimum Data Set (MDS), an assessment tool, with an assessment reference date of 3/11/25, indicated a Brief Interview for Mental Status (BIMS) test was not completed as the resident was documented as being rarely/never understood. Section O of the MDS did not indicate if the resident was up to date or not with the COVID-19 vaccine.
A review of the immunizations listed in the EMR revealed documentation for a COVID-19 booster 2023-2024, dose which indicated the resident refused. Additional review revealed the refusal was dated 4/23/24.
On 4/9/25 at 11:36 AM, the surveyor reviewed the hard copy chart which revealed there was no documentation of administration or declination for the COVID-19 booster vaccine.
On 4/9/25 at 11:46 AM, the surveyor interviewed the Infection Preventionist (IP), who stated she was responsible for assessing and reviewing the residents' immunizations. The IP explained she would review the state online database for resident's vaccination records and asked residents and/or the resident's representative (RR) about vaccination status upon admission. The IP stated vaccines would be offered to residents if they wished to receive them. An informed consent form would be signed if the resident desired or declined a vaccine. The IP stated immunizations would be documented under the immunizations section of the EMR.
The surveyor asked the IP about Resident #57's COVID-19 vaccination documentation and history. The IP stated Resident #57 was newly admitted to the facility in March 2025 and had previous stays at the facility. The IP stated Resident #57 was newly admitted to the facility in March 2025 and had previous stays at the facility. The IP stated it was previously documented in the EMR that the COVID-19 booster vaccine had been previously refused. The IP confirmed the documentation was from the resident's previous stay in 2024. The IP stated that she did not discuss with the resident and/or RR to offer the COVID-19 booster vaccine upon admission. The IP was not sure if it was part of the facility policy to offer a vaccine to every resident upon a new admission, even if they had documentation from a previous stay at the facility. The IP stated she would have to follow up about the process and that if it's something she should be doing, then she would.
On 4/9/25 at 12:59 PM, the survey team met with the Licensed Nursing Home Administrator (LNHA), the Director of Nursing (DON), the Clinical Lead of New Jersey (CLoNJ), and the Regulatory Compliance Advisor (RCA). The surveyor asked if it would be expected for staff to assess a resident who were newly admitted for immunizations and to be offered an opportunity to receive a vaccine, whether they had a previous stay or not. The DON replied Yes. The surveyor informed the facility's management of the concern that the resident was not offered a COVID-19 booster vaccine.
On 4/10/25 at 11:22 AM, the LNHA, the DON, the CLoNJ, and the RCA met with the survey team. The DON stated that the IP was doing an audit on all residents to review immunizations and ensure up to date documentation of their refusal or consent for vaccination.
There was no additional information provided by the facility.
A review of the undated facility's COVID-19 Vaccination Policy, under Policy revealed: .
1. The facility will offer the COVID-19 Vaccine to our healthcare workers and the residents as soon as it becomes available .
2. Consents for vaccination must be obtained, If the vaccine is refused, a declination must be signed .
The policy did not further address offering of COVID-19 booster doses.
N.J.A.C. 8:39-5.1(a)
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0941
(Tag F0941)
Could have caused harm · This affected 1 resident
Based on interview and review of pertinent facility documents, it was determined that the facility failed to ensure facility staff had mandatory training that included effective communications for 3 o...
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Based on interview and review of pertinent facility documents, it was determined that the facility failed to ensure facility staff had mandatory training that included effective communications for 3 of 5 Certified Nurse Aides (CNAs), reviewed for mandatory education (CNA #1, #4 and #5).
This deficient practice was evidenced by the following:
On 4/7/25 at 9:47 AM, the surveyor requested from the Licensed Nursing Home Administrator (LNHA) the annual education that was done for five randomly selected CNAs based on their date of hire.
On 4/7/25 at 1:04 PM, the surveyor interviewed the Infection Preventionist/Educator Licensed Practical Nurse (IP/E/LPN) regarding the education process. The IP/E/LPN stated that she started in February and that the education was done in person and in an electronic system. She added that all of the education was in the electronic system since the in person educations were entered into the electronic system.
On 4/8/25 at 12:45 PM, the IP/E/LPN provided the Student and Group Transcript Report for the five CNAs with the date range of April 9, 2024 to April 8, 2025. The reports were not based on the annual year from each CNAs date of hire (doh).
A review of the facility provide Transcripts included the following:
CNA #1, with a doh of 2/18/19, did not have effective communications training.
CNA #4, with a doh of 2/5/24, did not have effective communications training.
CNA #5, with a doh of 11/26/25, did not have effective communications training.
On 4/8/25 at 1:01 PM, the surveyor interviewed the Director of Nursing (DON) regarding the process for education. The DON stated that the company had a process for yearly mandatory education and a calendar provided and followed. The DON stated that some education was done in the electronic system, skills fair and inservices. She added that the tracking was in the electronic system.
On 4/9/25 at 11:01 AM, the IP/E/LPN and Clinical Lead of New Jersey (CLoNJ) confirmed that they could not locate any additional inservice sign in sheets that the CNAs may have attended that were not entered into the electronic system.
On 4/9/25 at 1:03 PM, the surveyor notified the LNHA, DON, CLoNJ and Regulatory Compliance Advisor (RCA) the concern that CNA #1, #4, and #5 did not have effective communications training.
On 4/10/25 at 11:25 AM, in the presence of DON, CLoNJ, and RCA, the LNHA stated that the IP/E/LPN received education to ensure that CNAs receive annual education which included the mandatory topics.
The LNHA did not provide any additional information.
A review of the facility's In-service Training Policy, with a review date of 7/1/22, included the following:
Policy .[Facility] will provide in-service training for all personnel on a regularly scheduled basis. All mandatory in-service requirements must be completed annually as a condition of continued employment.
In-service training programs are planned and conducted to develop and improve the skills of all personnel in accordance with federal and state law, in accordance with the facility assessment, and consistent with the staff members' expected roles.
All mandatory in-service training content is located on the learning management system and is supported by various policies and procedures. Employee's training completion will be tracked via a transcript which is located within the learning management system.
Other in-service training and competency results completed outside of the learning management system will be stored in the employee's personnel file.
Process .2. Training topics include, but are not limited to, the following:
2.1 Effective communication;
N.J.A.C. 8:39-13.4
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0942
(Tag F0942)
Could have caused harm · This affected 1 resident
Based on interview and review of pertinent facility documents, it was determined that the facility failed to ensure facility staff had mandatory training that included rights of the resident and the r...
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Based on interview and review of pertinent facility documents, it was determined that the facility failed to ensure facility staff had mandatory training that included rights of the resident and the responsibilities of a facility to properly care for its residents for 2 of 5 Certified Nurse Aides (CNAs), reviewed for mandatory education (CNA #4 and #5).
This deficient practice was evidenced by the following:
On 4/7/25 at 9:47 AM, the surveyor requested from the Licensed Nursing Home Administrator (LNHA) the annual education that was done for five randomly selected CNAs based on their date of hire (doh).
On 4/7/25 at 1:04 PM, the surveyor interviewed the Infection Preventionist/Educator Licensed Practical Nurse (IP/E/LPN) regarding the education process. The IP/E/LPN stated that she started in February and that the education was done in person and in an electronic system. She added that all of the education was in the electronic system since the in person educations were entered into the electronic system.
On 4/8/25 at 12:45 PM, the IP/E/LPN provided the Student and Group Transcript Report for the five CNAs with the date range of April 9, 2024 to April 8, 2025. The reports were not based on the annual year from each CNAs doh.
A review of the facility provide Transcripts included the following:
CNA #4, with a doh of 2/5/24, did not have resident's rights training.
CNA #5, with a doh of 11/26/25, did not have resident's rights training.
On 4/8/25 at 1:01 PM, the surveyor interviewed the Director of Nursing (DON) regarding the process for education. The DON stated that the company had a process for yearly mandatory education and a calendar provided and followed. The DON stated that some education was done in the electronic system, skills fair and inservices. She added that the tracking was in the electronic system.
On 4/9/25 at 11:01 AM, the IP/E/LPN and Clinical Lead of New Jersey (CLoNJ) confirmed that they could not locate any additional inservice sign in sheets that the CNAs may have attended that were not entered into the electronic system.
On 4/9/25 at 1:03 PM, the surveyor notified the LNHA, DON, CLoNJ and Regulatory Compliance Advisor (RCA) the concern that CNA #4 and #5 did not have resident's rights training.
On 4/10/25 at 11:25 AM, in the presence of DON, CLoNJ and RCA, the LNHA stated that the IP/E/LPN received education to ensure that CNAs receive annual education which included the mandatory topics.
A review of the facility's In-service Training Policy, with a review date of 7/1/22, included the following:
Policy .[Facility] will provide in-service training for all personnel on a regularly scheduled basis. All mandatory in-service requirements must be completed annually as a condition of continued employment.
In-service training programs are planned and conducted to develop and improve the skills of all personnel in accordance with federal and state law, in accordance with the facility assessment, and consistent with the staff members' expected roles.
All mandatory in-service training content is located on the learning management system and is supported by various policies and procedures. Employee's training completion will be tracked via a transcript which is located within the learning management system.
Other in-service training and competency results completed outside of the learning management system will be stored in the employee's personnel file.
Process .2. Training topics include, but are not limited to, the following: .
2.2 Resident's rights and facility responsibility for proper care of residents; .
N.J.A.C. 8:39-13.4 (c)3
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0944
(Tag F0944)
Could have caused harm · This affected 1 resident
Based on interview and review of pertinent facility documents, it was determined that the facility failed to ensure facility staff had mandatory training that outlined and informed staff of the elemen...
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Based on interview and review of pertinent facility documents, it was determined that the facility failed to ensure facility staff had mandatory training that outlined and informed staff of the elements and goals of the facility's QAPI (quality assurance and performance improvement) program for 3 of 5 Certified Nurse Aides (CNAs), reviewed for mandatory education (CNA #1, #4 and #5).
This deficient practice was evidenced by the following:
On 4/7/25 at 9:47 AM, the surveyor requested from the Licensed Nursing Home Administrator (LNHA) the annual education that was done for five randomly selected CNAs based on their date of hire (doh).
On 4/7/25 at 1:04 PM, the surveyor interviewed the Infection Preventionist/Educator Licensed Practical Nurse (IP/E/LPN) regarding the education process. The IP/E/LPN stated that she started in February and that the education was done in person and in an electronic system. She added that all of the education was in the electronic system since the in person educations were entered into the electronic system.
On 4/8/25 at 12:45 PM, the IP/E/LPN provided the Student and Group Transcript Report for the five CNAs with the date range of April 9, 2024 to April 8, 2025. The reports were not based on the annual year from each CNAs doh.
A review of the facility provide Transcripts included the following:
CNA #1, with a doh of 2/18/19, did not have QAPI training.
CNA #4, with a doh of 2/5/24, did not have QAPI training.
CNA #5, with a doh of 11/26/25, did not have QAPI training.
On 4/8/25 at 1:01 PM, the surveyor interviewed the Director of Nursing (DON) regarding the process for education. The DON stated that the company had a process for yearly mandatory education and a calendar provided and followed. The DON stated that some education was done in the electronic system, skills fair and inservices. She added that the tracking was in the electronic system.
On 4/9/25 at 11:01 AM, the IP/E/LPN and Clinical Lead of New Jersey (CLoNJ) confirmed that they could not locate any additional inservice sign in sheets that the CNAs may have attended that were not entered into the electronic system.
On 4/9/25 at 1:03 PM, the surveyor notified the LNHA, DON, CLoNJ and Regulatory Compliance Advisor (RCA) the concern that CNA #1, #4, and #5 did not have QAPI training.
On 4/10/25 at 11:25 AM, in the presence of DON, CLoNJ and RCA, the LNHA stated that the IP/E/LPN received education to ensure that CNAs receive annual education which included the mandatory topics.
The LNHA did not provide any additional information.
A review of the facility's In-service Training Policy, with a review date of 7/1/22, included the following:
Policy .[Facility] will provide in-service training for all personnel on a regularly scheduled basis. All mandatory in-service requirements must be completed annually as a condition of continued employment.
In-service training programs are planned and conducted to develop and improve the skills of all personnel in accordance with federal and state law, in accordance with the facility assessment, and consistent with the staff members' expected roles.
All mandatory in-service training content is located on the learning management system and is supported by various policies and procedures. Employee's training completion will be tracked via a transcript which is located within the learning management system.
Other in-service training and competency results completed outside of the learning management system will be stored in the employee's personnel file.
Process .2. Training topics include, but are not limited to, the following: .
2.4 Quality assurance and performance improvement (QAPI) training on the elements and goals of the QAPI program;
N.J.A.C. 8:39-33.1
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0947
(Tag F0947)
Could have caused harm · This affected 1 resident
Based on interview and review of facility documentation, it was determined that the facility failed to ensure that a) Certified Nurses Aides (CNA) received 12 hours of mandatory annual in-service trai...
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Based on interview and review of facility documentation, it was determined that the facility failed to ensure that a) Certified Nurses Aides (CNA) received 12 hours of mandatory annual in-service training for 1 of 5 CNAs reviewed (CNA #4); b) CNA education included resident abuse prevention training for 1 of 5 CNAs reviewed (CNA #4); and c) dementia management training for 2 of 5 CNAs reviewed (CNA #4 and CNA #5).
This deficient practice was evidenced by the following:
On 4/7/25 at 9:47 AM, the surveyor requested from the Licensed Nursing Home Administrator (LNHA) the annual education that was done for five randomly selected CNAs based on their date of hire (doh).
On 4/7/25 at 1:04 PM, the surveyor interviewed the Infection Preventionist/Educator Licensed Practical Nurse (IP/E/LPN) regarding the education process. The IP/E/LPN stated that she started in February and that the education was done in person and in an electronic system. She added that all of the education was in the electronic system since the in person educations were entered into the electronic system.
On 4/8/25 at 12:45 PM, the IP/E/LPN provided the Student and Group Transcript Report for the 5 CNAs with the date range of April 9, 2024 to April 8, 2025. The reports were not based on the annual year from each CNAs doh.
A review of the facility provide Transcripts included the following:
CNA #4, with a doh of 2/5/24, had three hand hygiene modules which were all dated 1/14/25, and listed as administrator entered and totaled 21 minutes and 1 abuse, and neglect module which was dated 4/8/25, which was done after surveyor's inquiry, and listed as administrator entered which was six minutes.
CNA #4 did not have 12 hours of education. CNA #4 did not have resident abuse prevention training prior to the surveyor requesting the information. CNA #4 did not have dementia management training.
CNA #5, with a doh of 11/26/25, did not have dementia management training.
On 4/8/25 at 1:01 PM, the surveyor interviewed the Director of Nursing (DON) regarding the process for education. The DON stated that the company had a process for yearly mandatory education and a calendar provided and followed. The DON stated that some education was done in the electronic system, skills fair and inservices. She added that the tracking was in the electronic system.
On 4/9/25 at 11:01 AM, the IP/E/LPN and Clinical Lead of New Jersey (CLoNJ) confirmed that they could not locate any additional inservice sign in sheets that the CNAs may have attended that were not entered into the electronic system.
On 4/9/25 at 1:03 PM, the surveyor notified the LNHA, DON, CLoNJ, and Regulatory Compliance Advisor (RCA) the concern that CNA #4 did not have 12 hours of annual education and did not have resident abuse prevention and dementia training and CNA #5 did not have dementia management training.
On 4/10/25 at 11:25 AM, in the presence of DON, CLoNJ, and RCA, the LNHA stated that the IP/E/LPN received education to ensure that CNAs receive 12 hours annual education which included the mandatory topics.
The LNHA did not provide any additional information.
A review of the facility's In-service Training Policy, with a review date of 7/1/22, included the following:
Policy .[Facility] will provide in-service training for all personnel on a regularly scheduled basis. All mandatory in-service requirements must be completed annually as a condition of continued employment.
In-service training programs are planned and conducted to develop and improve the skills of all personnel in accordance with federal and state law, in accordance with the facility assessment, and consistent with the staff members' expected roles.
All mandatory in-service training content is located on the learning management system and is supported by various policies and procedures. Employee's training completion will be tracked via a transcript which is located within the learning management system.
Other in-service training and competency results completed outside of the learning management system will be stored in the employee's personnel file.
Process .2. Training topics include, but are not limited to, the following: .
2.3 Abuse, neglect, and exploitation to include;
2.3.1 Activities constituting abuse, neglect, exploitation, and misappropriation of resident property;
2.3.2 Procedures for reporting incidents of abuse, neglect, exploitation, and misappropriation of resident property; and
2.3.3 Dementia management and resident abuse prevention;
3. In addition, there are requirements regarding in-service training for nurse aides .
3.1 Ensure continuing competence for no less than 12 hours per year;
3.2 Dementia management and resident abuse prevention;
N.J.A.C. 8:39-13.4 (c)2, (c)4; 43.17 (b)
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 F0725
(Tag F0725)
Could have caused harm · This affected multiple residents
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** NJ#171811 and #175736
Based on observation, interview, record review, and review of other pertinent facility documentation, it w...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** NJ#171811 and #175736
Based on observation, interview, record review, and review of other pertinent facility documentation, it was determined that the facility failed to provide sufficient nursing staff to ensure resident's highest practical wellbeing by failing to ensure that residents received timely and appropriate incontinence care. This deficient practice was identified for 7 of 20 residents, (Residents #9, #18, #30, #39, #58, #59, and #276), reviewed.
This deficient practice was evidenced by the following:
1. On 4/6/25 at 9:40 AM, the surveyor observed Resident #59 inside room [ROOM NUMBER], lying on bed with eyes closed.
On 4/6/25 at 9:58 AM, the surveyor asked the assigned Licensed Practical Nurse (LPN) to accompany the surveyor in Resident #59's room.
Inside the resident's room, the surveyor observed the resident was awake and allowed the LPN to check resident's incontinence brief. The surveyor observed the LPN performed handwashing, donned (put on) gloves, and repositioned the resident. Both surveyor and LPN observed resident with double incontinence brief.
During an interview, the LPN informed the surveyor that the resident was cognitively impaired and incontinent of bladder and bowel (B & B) elimination. The LPN further stated that the resident should not have a double incontinence brief.
The surveyor reviewed the medical records of Resident #59 and revealed:
A review of the admission Record or face sheet (AR, an admission summary) reflected that the resident was admitted with diagnoses that included but were not limited to; chronic systolic (congestive) heart failure, type 2 diabetes mellitus with other ophthalmic complication, anemia (low red blood cells count) in chronic kidney disease, and end stage renal disease (a medical condition in which the kidneys can no longer adequately filter waste products from the blood, functioning at less than 15% of normal levels).
A review of the most recent comprehensive Minimum Data Set (cMDS), an assessment tool, with an assessment reference date (ARD) of 2/5/25, revealed in Section C Cognitive Patterns, a brief interview for mental status (BIMS) score of 14 of 15, which reflected that the resident's cognitive status was intact. The cMDS also included that the resident was coded #3 for B & B continence, which reflected that the resident was always incontinent.
A review of the personalized care plan (CP) revealed that there was no documented evidence that the resident should have a double incontinence brief as a plan of care.
Further review of the medical records revealed that there was no documented evidence as to why the resident should have a double incontinence brief.
On 4/8/25 at 8:50 AM, the surveyor interviewed assigned Certified Nursing Aide #1 (CNA#1) of Resident # 59. CNA#1 informed the surveyor that most of the time she had 17 residents in her assignment. CNA#1 stated it was hard to finish with residents' incontinence care if she had 17 residents, but she ensures that she would finish even if she had to leave the facility late at 3:30 PM. She further stated that her time starts 7:00 AM. The CNA confirmed that on her assignments, rooms #2, #4, #8, #10, and #12 were all incontinent of B & B. She further stated that Resident #59 was incontinent of both B & B elimination.
On that same date and time, the surveyor asked CNA#1 if she noticed at any given time the resident with double incontinence brief or any other resident with double incontinence brief. CNA#1 stated yes, a few times and it was not right. CNA#1 further stated it was 11-7 CNA who does that because of short staff. She also stated that at times there were only one or two CNAs in the whole unit to take care of the resident and the aides did not want the bed to get wet that was why the CNA put double incontinence brief. The CNA confirmed that she was aware of the New Jersey staffing law for 7-3 shift should be 1 CNA to 8 residents.
On 4/8/25 at 9:51 AM, the surveyor interviewed CNA#2 via phone conference. CNA#2 informed the surveyor that he was a per diem CNA who works three times per week and usually on a weekend. CNA#2 confirmed that he worked this weekend Saturday going to Sunday morning, (4/5/25), for 11-7 shift with 17 residents. CNA#2 confirmed Resident #59 was on his assignment and that he put double incontinence brief to the resident. CNA#2 stated also that the resident was incontinent.
2. On 4/6/25 at 9:45 AM, the surveyor observed Resident #39 lying on bed inside room [ROOM NUMBER], with head of bed elevated, on oxygen (O2) 2 LPM (liters per minute) via nasal cannula (a medical device that provides supplemental O2 therapy, the device has two prongs and sits below the nose).
A review of the AR revealed diagnoses which included but not limited to; encephalopathy (refers to brain disease, damage, or malfunction) unspecified, unspecified combined systolic (congestive) and diastolic (congestive) heart failure, and dementia in other diseases classified elsewhere, unspecified severity, without behavioral disturbance, psychotic disturbance, mood disturbance, and anxiety.
A review of the most recent cMDS, with an ARD of 2/18/25, revealed in Section C, the cognitive skills for daily decision making was coded 3, which reflected that the resident's cognition was severely impaired. The cMDS also revealed that the resident was coded #3 (always incontinent of both B & B elimination).
A review of the personalized CP revealed that there was no documented evidence that the resident should have a double incontinence brief as a plan of care.
Further review of the medical records revealed that there was no documented evidence as to why the resident should have a double incontinence brief.
On 4/8/25 at 8:50 AM, CNA#1 confirmed that Resident #39 was incontinent of both B & B elimination.
On 4/8/25 at 9:55 AM, CNA#2 confirmed that he was the aide of Resident #39, and that the resident was incontinent. He further stated that the resident had double incontinence brief and he did not notify the nurse about it.
3. On 4/8/25 at 10:37 AM, the surveyor met with four residents during the resident council meeting. Four of four residents, included Residents #18 and #30, both stated that short staff especially on weekends, affected care by responding to the toileting needs of residents.
On that same date and time, Resident #30 stated that one time the CNA put a double incontinence brief on them, and on that same day, when the resident refused, it then stopped and did not happen again. The resident unable to state the name of the CNA and what shift.
At that same time, Resident #18 confirmed that they experienced double incontinence brief a few times in 3-11 shift. Resident #18 unable to state the name of the CNA. Resident #18 also stated that the issue was that there was no enough staff that was why aide was putting double incontinence brief to residents.
On 4/8/25 at 12:12 PM, the survey team met with the Licensed Nursing Home Administrator (LNHA), Director of Nursing (DON), and Clinical Lead of New Jersey (CLoNJ). The surveyor discussed the above concerns and findings with Residents #39, #59, and Resident Council Meeting concerns with double incontinence brief.
On 4/9/25 at 12:37 PM, the survey team met with the LNHA, DON, CLoNJ, and the Regulatory Compliance Advisor (RCA). The DON stated for double incontinence brief we did start an in service and I did rounds at 4:30 AM to check the residents to make sure no double incontinence brief.
On 4/10/25 at 11:43 AM, the CLoNJ stated that the survey team could proceed with decision making and that there was no additional information.
A review of the facility's Continence Management Policy, with a review/revision date of 6/15/22, that was provided by the LNHA, revealed under Policy that patients will be assessed for the need for continence management as part of the nursing assessment process .
Purpose:
-To provide appropriate treatment and services for patients with urinary incontinence to minimize urinary tract infections and restore continence to the extent possible.
-To provide appropriate treatment and services for patients incontinent of bowel to restore continence to the extent possible.
Practice Standards:
6. Provide routine incontinence care .
On 4/10/25 at 12:02 PM, the survey team met with the LNHA, DON, CLoNJ and RCA for an exit conference, and there was no additional information provided by the LNHA and her team.
4. On 4/6/25 at 10:39 AM, the surveyor observed Resident #9 lying on bed with eyes closed.
On 4/6/25 at 10:49 AM, the surveyor proceeded to the nurse's station and asked for a nurse to accompany the surveyor to Resident #9's room. The LPN accompanied the surveyor to Resident #9's room.
Inside the resident's room, the surveyor observed the resident was awake and allowed the LPN to check resident's incontinence brief. After donning gloves, the LPN opened Resident #9's incontinent brief and both the surveyor and LPN observed the resident had a white absorbent pad with elastic on both sides of the pad inside the incontinent brief. The resident had double incontinent brief. The LPN stated that the white absorbent pad looked like a sanitary pad. She added that she did not work on this side of the unit and was not sure why the resident would have a sanitary pad.
The surveyor reviewed the medical record of Resident #9 and which revealed:
A review of the AR reflected that the resident was admitted with diagnoses that included but were not limited to; dementia (a group of conditions characterized by impairment of at least two brain functions, such as memory loss and judgment), hypothyroidism (abnormally low activity of the thyroid gland, resulting in metabolic changes in adults), and anemia.
A review of the most recent quarterly MDS (qMDS), with an ARD of 3/13/25, revealed in Section C, the resident's cognitive skills for daily decision making was severely impaired. The qMDS also included that the resident was coded #3 for Bladder & Bowel continence, which reflected that the resident was always incontinent.
Further review of the medical record revealed that there was no documented evidence as to why the resident should have a double incontinence brief or an additional absorbent pad.
5. On 4/6/25 at 10:39 AM, the surveyor observed Resident #58 lying on bed with eyes closed.
On 4/6/25 at 10:57 AM, the surveyor asked the LPN to accompany the surveyor to observe Resident #58's incontinence brief.
Inside the resident's room, the surveyor observed the resident was awake and allowed the LPN to check resident's incontinence brief. After donning gloves, the LPN opened Resident #58's incontinence brief and the both the surveyor and LPN observed the resident had a white absorbent pad with elastic on both sides of the pad inside the incontinence brief. The resident had a double incontinence brief. The surveyor asked the LPN if that was considered double incontinence briefing. The LPN stated that she did not know and that she had never seen that before. She added that it looked like a sanitary pad.
The surveyor reviewed the medical record of Resident #58 which revealed:
A review of the AR, reflected that the resident was admitted with diagnoses that included but were not limited to; dementia (a group of conditions characterized by impairment of at least two brain functions, such as memory loss and judgment), hypertension (high blood pressure) and hyperlipidemia (an abnormally high concentration of fats or lipids in the blood).
A review of the most recent qMDS, with an ARD of 3/17/25, revealed in Section C, the resident's cognitive skills for daily decision making was moderately impaired. The qMDS also included that the resident was coded #3 for Bladder & Bowel continence.
Further review of the medical record revealed that there was no documented evidence as to why the resident should have a double incontinence brief or an additional absorbent pad.
On 4/7/25 at 11:32 AM, the surveyor interviewed the Central Supply Staff (CSS) regarding the observation of the absorbent pad that had elastic on both sides. The CSS stated that the facility had a sanitary pad but that it did not have elastic on the sides.
On 4/8/25 at 12:34 PM, the surveyor notified the LNHA, DON, and CLoNJ the concern that Resident #9 and #58 had a double incontinence brief applied.
A review of the facility's provided policy titled Staffing/Center Plan, with a review date of 8/7/23, included the following:
Policy
Centers will provide qualified and appropriate staffing levels to meet the needs of the patient population. The staffing plan will include all shifts, seven days per week.
Purpose
To assure that appropriate staffing levels are scheduled and maintained.
Process
1. The Center meets or exceeds the staffing levels mandated by state and federal staffing requirements.
2. Staffing levels are reviewed on an ongoing basis by Center staff to evaluate compliance and provide appropriate levels of care by qualified employees .
4. The Center maintains appropriate staffing levels, with qualified personnel, 24 hours/day, seven days/week on each shift to assure that patients are safe and their needs are met .
NJAC 8:39-25.2(b)
CONCERN
(E)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0730
(Tag F0730)
Could have caused harm · This affected multiple residents
Based on observation, interview, and review of facility documentation, it was determined that the facility failed to ensure that the Certified Nursing Aide (CNA) received an annual performance review ...
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Based on observation, interview, and review of facility documentation, it was determined that the facility failed to ensure that the Certified Nursing Aide (CNA) received an annual performance review for 5 of 5 CNA files reviewed.
This deficient practice was evidenced by the following:
On 4/7/25 at 9:47 AM, the surveyor requested from the Licensed Nursing Home Administrator (LNHA) the performance reviews for five randomly selected CNAs.
On 4/8/25 at 1:40 PM, the Director of Nursing (DON) notified the surveyor that she could not locate the performance reviews for the five CNAs.
On 4/9/25 at 1:06 PM, the surveyor notified the LNHA, DON, Clinical Lead of New Jersey (CLoNJ), and Regulatory Compliance Advisor (RCA) the concern that the performance reviews were not done.
On 4/9/25 at 1:26 PM, in the presence of the CLoNJ, the DON confirmed that they did not have performance reviews for the five CNAs.
On 4/10/25 at 11:25 AM, in the presence of the LNHA, CLoNJ and RCA, the DON stated she was auditing the nursing staff to see when their last annual performance evaluation was done and would get them completed.
The LNHA did not provide any additional information.
A review of the facility, Performance Appraisal Policy, with a review date of 7/1/22, included the following:
Managers will meet with their regular full-time, regular part-time, and regular casual employees at least annually to conduct a performance appraisal or have a performance based conversation. In-service education will be provided based on the outcome of these reviews.
N.J.A.C. 8:39-43.17 (b)
CONCERN
(E)
Potential for Harm - no one hurt, but risky conditions existed
Medication Errors
(Tag F0758)
Could have caused harm · This affected multiple residents
5. On 4/6/25 at 9:46 AM, Surveyor #3 (S#3) observed Resident #21 asleep in bed.
A review of Resident #21's AR reflected that the resident was admitted to the facility with diagnoses which included bu...
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5. On 4/6/25 at 9:46 AM, Surveyor #3 (S#3) observed Resident #21 asleep in bed.
A review of Resident #21's AR reflected that the resident was admitted to the facility with diagnoses which included but were not limited to; psychotic disorder with delusions (a type of mental illness where a person experiences persistent, false beliefs (delusions) that they firmly hold despite evidence to the contrary), bipolar disorder (a mental illness characterized by extreme and persistent shifts in mood, energy, and activity levels), and dementia (a group of conditions characterized by impairment of at least two brain functions, such as memory loss and judgment).
A review of Resident #21's qMDS, with an ARD of 1/31/25, reflected that the resident had a BIMS score of 3 out of 15, which indicated that the resident's cognition was severely impaired. The qMDS also included that the resident received an antipsychotic (a mood altering medications specifically used to manage psychosis, a mental disorder characterized by a disconnection from reality) med.
A review of Resident #21's April 2025 eMAR included the following PO:
-Seroquel Oral Tab 50 mg, give 1 tab by mouth at HS for Delusional disorder.
Monitor Behavior While Resident is Taking Seroquel every shift.
[There was not a target behavior listed to monitor for the Seroquel]
There was an additional order, Behavior documentation for exit seeking
and wandering on 3-11 and 11-7 shifts every evening and night shift. This was not the behavior that the Seroquel was ordered for.
On 4/7/25 at 11:38 AM, S#3 interviewed the RN regarding the process for behavior monitoring and Resident #21. The RN stated that there was an order in the eMAR every shift and if there was a behavior would write y (yes) and write a note that went to the progress note section [in the electronic record]. S#3 asked what Resident #21's target behaviors were that were monitored. The RN stated that had not seen the resident have any behaviors since March. She added that the resident had a wandergard but that she did not see the resident wandering. S#3 asked the reason why Resident #21 was receiving Seroquel. The RN stated can find out.
On 4/7/25 at 11:58 AM, the RN stated that Resident #21 was on Seroquel mostly for wandering on 3-11 or 11-7 shift.
On 4/7/25 at 12:01 PM, S#3 interviewed the LPN/UM regarding behavior monitoring. The LPN/UM stated that the resident was seen by the PNP and that the PNP would tell us what behavior to monitor or it was based on our interaction with the resident. The LPN/UM stated that Resident #21 wandered and hallucinated and would look for the resident's brother in the afternoon. She further stated that based on the resident's notes, the resident had behavior monitoring for exit seeking and wandering.
On 4/8/25 at 9:54 AM, S#3 showed the LPN/UM Resident #21's eMAR with the two orders for behavior monitoring. The LPN/UM stated that the resident was monitored for exit seeking and confirmed that the order for monitoring for Seroquel did not have the target behavior that should be monitored. She further stated that the Seroquel was ordered for delusional disorder and that the target behavior should be delusions. The LPN/UM confirmed that the target behavior of delusions should have been in the order.
On 4/8/25 at 12:36 PM, S#3 notified the LNHA, DON and CLoNJ the concern that Resident #21's behavior monitoring order did not include a target behavior for the antipsychotic med.
On 4/9/25 at 12:52 PM, in the presence of the LNHA, CLoNJ, and RCA, the DON stated that she started an audit of residents' orders for psychotropic meds updated the order for behavior monitoring.
The LNHA did not provide any additional information.
NJAC 8:39-27.1(a)
4. On 4/6/25 at 10:15 AM, Surveyor #2 (S#2) observed Resident #57's door closed. The resident's privacy curtain was closed, and the resident was being assisted by staff with morning care.
On 4/8/25 at 10:15 AM, S#2 reviewed the paper medical records and the electronic medical record (EMR) of Resident #57.
The AR documented that the resident was newly admitted to the facility and had diagnoses that included but were not limited to; dementia, drug induced subacute dyskinesia (a movement disorder that develops within days to weeks after initiating or increasing the dose of certain medications), chronic atrial fibrillation (an irregular, rapid heart rate that commonly causes poor blood flow), and hypertension (high blood pressure).
A review of the cMDS, with an ARD of 3/11/25, indicated a BIMS test was not completed as the resident was documented as being rarely/never understood.
A review of the PO revealed:
-dated 3/8/25, indicated to obtain dental, ophthalmology, podiatry, physiatry, psych[psychiatry], and wound consults as needed/indicated and treatment for patient health and comfort.
-dated 3/13/25, indicated benztropine mesylate (a med used to help with tremors, improve muscle control and reduce stiffness) oral tab 0.5 mg, give 1 tab by mouth BID. The med order had an indicated diagnosis of depression.
-dated 3/13/25, indicated Depakote (a med used to treat types of seizures and used to treat certain mood episodes in adults) oral tab delayed release 500 mg, give 1 tab by mouth BID for depression.
-dated 3/8/25, indicated lorazepam (a med used to treat anxiety disorders) oral tab 0.5 mg, give 1 tab by mouth in the evening for anxiety.
-dated 3/13/25 indicated olanzapine (an antipsychotic meds used to treat mental health conditions such as schizophrenia and bipolar disorder) oral tab 15 mg, give 1 tab by mouth at bedtime for depression.
-dated 3/8/25, indicated Sertraline (an antidepressant med) oral tab 100 mg give 1 tab by mouth one time a day for depression.
There were no PO for monitoring of target behaviors and adverse effects for psychotropic med.
A review of the CP for Resident #57, included a focus area for complications r/t the use of psychotropic meds of olanzapine, lorazepam, and sertraline, dated 3/18/25. Interventions of the CP included:
-Complete behavior monitoring flow sheet; date initiated 3/18/25.
-Gradual dose reduction as ordered; date initiated 3/18/25.
- Monitor for continued need of med r/t behavior and mood; date initiated 3/18/25.
- Monitor for side effects and consult physician and/or pharmacist as needed; date initiated 3/18/25.
- Obtain psych evaluation as ordered; date initiated 3/18/25.
A review of the March 2025 and April 2025 eMAR and electronic Treatment Administration Record (eTAR) revealed there were no entries for monitoring of target behaviors and side effects of psychotropic meds.
A review of the EMR revealed there was no documentation of the resident's target behaviors.
On 4/8/25 at 11:00 AM, S#2 interviewed the Licensed Practical Nurse (LPN), who was assigned to care for Resident #57. The LPN stated residents who received psychotropic meds were monitored for behaviors which were documented in the EMR. The LPN further explained that behavior monitoring was documented in the eMAR and there should be a separate order from the meds for behavior monitoring. LPN#1 stated that monthly psychotropic summaries would also be completed in the EMR.
At that same time, S#2 asked the LPN about psychiatric consults for residents, the LPN replied that residents with psychotropic meds ordered would have a routine psychiatric consult and/or psychology consult. The LPN stated the psychiatric consultant visited the facility at least once a week to see residents. S#2 asked the LPN if Resident #57 had a psychiatry consult. The LPN stated she was not sure as it was the first time she was assigned to the resident and would have to look in the EMR.
On 4/8/25 at 11:20 AM, S#2 interviewed the LPN/UM about Resident #57 and their psychotropic meds. The LPN/UM stated the resident had not really exhibited behaviors since their admission and had not had any outbursts. She further explained Resident #57 had a history of being resistive to care and outbursts. S#2 asked about management for psychotropic med use. The LPN/UM stated that residents who had psychotropic med ordered would have routine psychiatric consults. The LPN/UM stated Resident #57 should have one. The LPN/UM reviewed with S#2 the EMR and confirmed there was no documentation that the resident had a psychiatric consult. The LPN/UM checked the list of residents referred to the psychiatric consultant since March 2025 and found Resident #57 was not on the list. The LPN/UM could not speak to what happened and stated she did not know how it was missed.
On that same date and time, S#2 asked the LPN/UM about the indicated diagnoses for the resident's olanzapine, depakote, and benztropine mesylate. The LPN/UM reviewed the med orders and stated that they were not typical indications for the med and would have to review with the physician to clarify.
At that time, S#2 asked the LPN/UM about behavior monitoring, and she explained that it was documented for residents with antipsychotic and antianxiety med orders. The LPN/UM stated that a PO for behavior monitoring would be documented in the EMR, and it was a separate entry order from the psychotropic med. S#2 also asked about monthly psychotropic summaries as mentioned by the LPN. The LPN/UM replied that before they were being completed and that she was not sure now if it was still part of the facility's process. The LPN/UM stated she would have to follow up with the DON.
On 4/8/25 at 12:14 PM, S#2 notified the LNHA, the DON, and the CLoNJ of the concerns for the diagnosis of the resident's psychotropic meds, there was no psychiatry consult as per the facility's protocol, no behavior monitoring, and no adverse effect monitoring.
On 4/9/25 at 12:37 PM, the LNHA, the DON, the CLoNJ, and the RCA met with the survey team. The DON stated that they reviewed the hospital records which only documented diagnoses of depression and stated they would have to reach out the resident's sending facility to further determine the resident's history and specific target behaviors. Additionally, a psychiatric consultant would be in to visit with the resident, and all residents on psychotropic meds were audited.
There was no additional information provided by the facility.
A review of the facility's Behaviors: Management of Symptoms Policy, with a last revised date of 7/1/24, under Purpose it documented: To identify, prevent, and manage behavioral symptoms by .Monitoring outcomes of CP interventions.
Under Practice Standards it detailed: .
2. Staff will monitor for and document in the medical records any exhibited behavioral symptoms .
3. Identify, to the extent possible, potential underlying causes of behavioral symptoms (e.g., pain, delirium, environmental factors, etc.) .
5. The Center will ensure that necessary behavioral health services are person-centered and reflect the patient's goals of care, while maximizing the patient's dignity, autonomy, privacy, socialization, independence, choice, and safety .
6. When med is ordered for behavioral symptoms .
6.2 Complete the Psychotropic/Therapeutic Med Use Evaluation when a patient is newly prescribed a psychotherapeutic med and then quarterly .
6.3 Complete the Abnormal Involuntary Movement Scale (AIMS) per nursing schedule for patients receiving anti-psychotic meds .
Based on observation, interview, review of the medical record, and review of other facility documentation, it was determined that the facility failed to adequately monitor target behaviors for the use of a psychotropic (affecting the brain and nervous system, altering mood, thoughts, perception, and behavior) medications for 5 of 5 residents, (Residents #12, #21, #24, #49, and #57), reviewed for unnecessary medications.
This deficient practice was evidenced by the following:
1. On 4/6/25 at 10:29 AM, Surveyor #1 (S#1) observed Resident #12 walking all around the room, alert, and well groomed.
S#1 reviewed Resident #12's medical record which revealed the following:
A review of the admission Record (AR, an admission summary) reflected that the resident was admitted to the facility with diagnoses which included, but not limited to; metabolic encephalopathy (brain dysfunction from metabolic imbalances), unspecified dementia, unspecified severity without behavioral disturbance, psychotic disturbance, mood disturbance and anxiety, adjustment disorder with anxiety, and depression unspecified.
A review of the quarterly Minimum Data Set (qMDS), an assessment tool, with an assessment reference date (ARD) of 4/2/25, reflected that the resident had a Brief Interview for Mental Status (BIMS) score of 99 (unable to complete interview-rarely understood), and a staff assessment reflected severely impaired cognitive status. The MDS indicated that the resident did not exhibit behavior symptoms within the look-back period and had received in the last seven days an antipsychotic medication (med) daily.
A review of the resident's individualized care plan (CP), dated 3/20/25, reflected the resident received psychotropic drugs due to behavioral episodes of verbal aggression towards staff, physical aggression towards staff, and episodes of resistance with care, history of violent behaviors.
A review of the physician's order (PO) indicated the resident was prescribed the antipsychotic medications (meds):
-Quetiapine Fumarate (Seroquel) oral Tablet (tab) 25 mg (milligram) give 1 tab by mouth at bedtime (HS) for psychosis ordered 6/28/24, and discontinued (d/c) on 11/20/24.
-Seroquel oral tab 25 mg (Quetiapine Fumarate) give 25 mg by mouth at HS every other day for Psychosis, ordered on 11/20/24.
-Monitor and document behaviors every shift ordered on 7/17/24.
There was no target behaviors indicated.
On 4/7/25 at 12:19 PM, S#1 interviewed the Registered Nurse (RN) regarding psychotropic meds. The RN stated, sometimes the resident might be aggressive, will tap you really hard on the arm to get attention. The RN further stated that the resident was on Seroquel at HS, usually they just tell you to monitor their behavior. S#1 asked if there should be a target behavior listed on the order with Seroquel and the RN stated, Yes, I will try to find out. The antipsychotic should have behaviors listed.
On 4/7/25 at 12:29 PM, S#1 interviewed the Licensed Practical Nurse/Unit Manager (LPN/UM) of the [NAME] Wing Unit. The LPN/UM stated the Psychiatric doctor will send the LPN/UM recommended orders, then the LPN/UM will call the primary medical doctor (PMD), and if the PMD agreed with the recommended orders, the order will be be in. The LPN/UM further stated that the new orders were for increase behavior and mood changes, some people had different behavior monitoring, for antipsychotics, there should be a target behaviors.
At that time, S#1 reviewed with the LPN/UM the orders in the electronic Medication Administration Record (eMAR), and both S#1 and the LPN/UM did not see target behaviors. The LPN/UM stated, I honestly do not know why it was not there, and that the she I will speak to the Psychiatric Nurse Practitioner (PNP) from the Psychiatric consulting group to determine what appropriate target behaviors should be monitored. She further stated that the changes in mood was not enough to describe target behavior.
On 4/7/25 at 12:30 PM, S#1 reviewed the Psychiatric Consult Notes (PCN) dated 4/4/25, completed by the PNP which revealed, Pt (patient) is a poor historian. Information received from pt, staff, and medical chart No evidence of hallucinations No manic or psychotic behaviors reported.
2. On 4/6/25 at 10:21 AM, S#1 observed Resident #24 lying in bed and alert. The resident stated, My doctor said sleep is important.
S#1 reviewed Resident #24's medical record which revealed the following:
A review of the AR reflected that the resident was admitted to the facility with diagnoses which included, but not limited to; adjustment disorder with anxiety, other symptoms and signs involving emotional state, hallucinations, unspecified, unspecified dementia, unspecified severity, without behavioral disturbance, psychotic disturbance, mood disturbance, and anxiety, depression, unspecified, adjustment disorder with mixed anxiety and depressed mood, and unspecified dementia, unspecified severity, with psychotic disturbance.
A review of the most recent comprehensive MDS (cMDS), with an ARD of 3/11/25, revealed a BIMS score of 9 out of 15, indicating moderate cognitive impairment. The cMDS did not reflect that the resident had behaviors exhibited.
A review of the resident's individualized CP initiated 6/25/24, reflected the resident at risk for complications related to (r/t) the use of psychotropic drugs.
A review of the PO revealed the resident was prescribed the antipsychotic med, Quetiapine Fumarate oral tab 25 mg, give 0.5 tab by mouth two times a day (BID) for psychosis (0.5 tab=12.5 mg), ordered on 12/5/2.
There was no target behaviors indicated.
A review of the PCN dated 4/4/25, completed by the PNP which revealed, Pt reports feeling, okay. No recent mood changes reported. No current evidence of hallucinations or delusions noted this visit. No recent mood changes reported.
On 4/7/25 at 12:41 PM, S#1 interviewed the LPN/UM, who confirmed no target behaviors listed in the eMARS, and stated, Yes, these psychotropic orders should have target behaviors listed as well.
3. On 4/6/25 at 10:47 AM, S#1 observed the Resident #49 in the room lying in bed, bed lowest to the floor, screaming intermittently, and the resident stated, I'm fine.
S#1 reviewed Resident #49's medical record which revealed the following:
A review of the AR reflected that the resident was admitted to the facility with diagnoses which included, but not limited to; unspecified psychosis not due to a substance or known physiological condition, generalized anxiety disorder; depression, unspecified, Alzheimer's disease with early onset, dementia in other diseases classified elsewhere, severe, with other behavioral disturbance, other Alzheimer's disease, and traumatic hemorrhage of left cerebrum with loss of consciousness of unspecified duration, subsequent encounter.
A review of the qMDS, with an ARD of 1/8/25, revealed the resident unable to complete interview, was coded as rarely understood, and a staff assessment reflected severely impaired cognitive status.
A review of the resident's individualized CP initiated 10/5/2020, reflected the resident exhibits distressed/fluctuating mood and behavioral symptoms r/t Psychiatric Disorder Dementia with yelling out in the hallway and periods of sadness.
A review of the PO revealed the resident was prescribed the antipsychotic meds:
-Risperidone oral tab 0.5 mg, give 0.5 mg by mouth two times a day for Unspecified Psychosis ordered 1/23/24, d/c on 3/3/25.
-Risperidone oral tab 0.5 mg, give 0.5 mg by mouth two times a day for Psychosis, monitor for increase in behaviors and changes in mood ordered 3/3/25.
-Monitor behavior while resident is taking Risperidone every shift 2/26/24.
There was no target behaviors listed.
A review of the PCN dated 3/28/2, completed by the PNP which revealed, No evidence of hallucinations. No manic or psychotic behaviors reported . Continue to monitor for mood and behavioral changes: agitation, aggressiveness, hallucinations or delusions.
On 4/8/25 at 12:13 PM, the survey team met with the License Nursing Home Administrator (LNHA), Director of Nursing (DON), and Clinical Lead of New Jersey (CLoNJ), and S#1 notified them of the above concerns regarding anti-psychotic meds.
On 4/9/25 at 10:40 AM, S#1 interviewed the DON, and the DON stated, I am aware of the psychotropic behavior monitoring, and target behaviors not being done.
On 4/9/25 at 12:38 PM, the survey team met with the Regulatory Compliance Advisor, LNHA, and CLoNJ, and the DON stated, I started the house wide audit of all residents, reached out to the psychiatrist to do monthly meeting and each week I will audit for behavior monitoring.
CONCERN
(E)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0919
(Tag F0919)
Could have caused harm · This affected multiple residents
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations and interviews on 4/8/2025 and 4/9/2025 in the presence of the Senior Maintenance Director (SMD), it was d...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations and interviews on 4/8/2025 and 4/9/2025 in the presence of the Senior Maintenance Director (SMD), it was determined that the facility failed to ensure that all devices used to identify call bell notifications were properly functioning. This deficient practice had the potential to affect 40 residents and was evidenced by the following:
An observation at 11:19 AM revealed that when testing the call bell system for resident room [ROOM NUMBER], there was no audible notification of the call bell activation at the nurse's station.
In an interview at the time, there were three staff members at the nurse's station. The surveyor asked the staff members if they can hear anything. The three staff members stated no. The surveyor notified them they were testing the call bell system for resident room [ROOM NUMBER]. The staff members then stated that something must be wrong because they can usually hear audible notification of call bell activations at the nurse's station.
An observation at 11:20 AM revealed that when testing the call bell system for resident room [ROOM NUMBER], there was no audible notification of the call bell activation at the nurse's station.
An observation at 11:30 AM revealed that when testing the call bell system for resident room [ROOM NUMBER], there was no audible notification of the call bell activation at the nurse's station.
In an interview at the time, the SMD confirmed that there was no audible notification of the call bell activation and stated that the entire East wing (21 resident rooms) was served by the call bell system.
The facility's Administrator was notified of the deficient practices at the Life Safety Code exit conference on 4/9/2025 at 2:00 PM.
N.J.A.C 8:30-31.2 (e)
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
Safe Environment
(Tag F0584)
Could have caused harm · This affected most or all residents
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** NJ#171811
REPEAT DEFICIENCY
Based on observation, interview, and review of pertinent facility documentation, it was determined t...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** NJ#171811
REPEAT DEFICIENCY
Based on observation, interview, and review of pertinent facility documentation, it was determined that the facility failed to provide a safe, clean, and comfortable homelike setting. This deficient practice was identified for 2 of 2 units, and was evidenced by the following:
1. On 4/6/25 at 9:40 AM, Surveyor #1 (S#1) observed Resident #59 inside room [ROOM NUMBER], lying on bed with eyes closed. The nightstand table bottom door had no cover, and the cover piece was on the side of the table. The bottom part of the nightstand table had multiple personal items that include two bedpans, papers, and plastics. The regular chair inside the room had multiple blackish and brownish stains. The adjoining toilet room (with room [ROOM NUMBER]) vent had accumulation of grayish substances, and the tissue paper holder was broken. The two tissue paper rolls were on top of the toilet bowl.
The closet door was broken and uneven.
Outside the room, in the hallway, S#1 observed multiple vents with accumulation of grayish substances.
On 4/6/25 at 10:08 AM, during the Entrance Conference meeting with S#1 with the Licensed Nursing Home Administrator (LNHA), the LNHA informed the surveyor that there were two units in the facility. The LNHA further stated that the East Wing Unit which was the rooms with even numbers and the [NAME] Wing Unit which was the odd room numbers.
On 4/7/25 at 12:13 PM, S#1 asked Registered Nurse #1 (RN#1) to accompany the surveyor to Resident #59's room.
Inside the resident's room, both S#1 and RN#1 observed the regular chair with brownish and blackish stains. RN#1 unable to identify what were those stains and stated that it should have been cleaned. S#1 and RN#1 also observed the curtains in the window with scattered brownish stains and RN#1 stated that it should have been cleaned. RN#1 also confirmed that the aircon had an accumulation of dust, and RN#1 stated that it should have been cleaned.
On that same date and time, S#1 asked RN#1 confirmed that the nightstand table bottom door should have been fixed. Prior to leaving the room the surveyor asked RN#1 who had the closet on the right side was and why the door was uneven. RN#1 opened the closet on the right side, RN#1 confirmed it was uneven and stated that it should have been fixed by the Maintenance Person (MP). RN#1 also confirmed that the closet belong to Resident #59.
Outside the resident's room, in the hallway both S#1 and RN#1 observed accumulation of grayish substance on the multiple vents, and RN#1 stated that should have been cleaned by Maintenance department. RN#1 also confirmed that the grayish substances were accumulation of dust.
2. On 4/6/25 at 9:45 AM, S#1 observed Resident #39 inside room [ROOM NUMBER], lying on bed, with head of bed elevated, with oxygen in use. Inside the resident's room, the surveyor observed the window curtains were stained with brownish discoloration and ripped. The adjoined toilet room (with room [ROOM NUMBER]) tissue paper holder was broken and the vent with accumulation of grayish substances.
On 4/7/25 at 12:08 PM, S#1 was accompanied by RN#1 inside Resident #39's room. Both S#1 and RN#1 observed the ripped curtains, the adjoined toilet room with broken tissue holder, and RN#1 confirmed that the vent inside the toilet room with accumulation of dust. RN#1 also confirmed the ripped curtains with unknown brown stain should have been fixed by the MP, and the curtains should have been cleaned.
3. On 4/7/25 at 10:54 AM, S#1 reviewed the last three months Resident Council Minutes that was provided by the LNHA and revealed:
-4/2/25 minutes included that nine residents attended the meeting that included Residents #4, #11, #18, and #30. The staff who attended were the Director of Recreation, Food Services Director, and Assistant Director of Nursing/Infection Preventionist (ADON/IP). The ADON/IP informed the residents that the facility currently did not have a Maintenance Director.
On 4/8/25 at 10:51 AM, during the Resident Council Meeting, Residents #11 and #18 both stated that they were unaware if facility had new MP because the regular MP was out for medical reason.
On 4/8/25 at 12:12 PM, the survey team met with the LNHA, Director of Nursing (DON), and the Clinical Lead of New Jersey (CLoNJ). S#1 discussed the environment concerns with rooms [ROOM NUMBERS] in East unit, vents in the hallway, and the Resident Council Meeting concerns.
On 4/9/25 at 12:37 PM, the survey team met with the LNHA, DON, CLoNJ, and the Regulatory Compliance Advisor (RCA). The LNHA informed S#1 that rooms [ROOM NUMBERS] tissue holder was replaced, aircon was cleaned, the closet door was fixed, vent was cleaned, and the vendor was asked for a quote for the whole building curtain replacements. The LNHA had no response with regard to Resident #59's nightstand table and further stated that she had to go back to check the nightstand table of Resident #59.
On 4/10/25 at 9:39 AM, S#1 met with the LNHA for Quality Assurance Performance Improvement (QAPI) meeting. The LNHA stated that there were multiple areas of concerns surveyors identified that were not identified by the facility team during the most recent QAPI meeting, and that included issues with vents and homelike environment.
On 4/10/25 at 11:43 AM, the CLoNJ stated that team could proceed with decision making and that there was no additional information.
4. On 4/6/25 at 10:10 AM, Surveyor#2 (S#2) toured the East Wing Unit Bath/Shower room and observed the following:
-Next to the toilet, there was a used towel folded in half on the floor.
-On sink #1, there was an open tube of toothpaste and on the other side of the sink there were two toothbrushes which were used and saturated with dried toothpaste.
- On sink #2, there was a pile of towels on one side and a blue colored pajama set on the other side. A chair in front of the sink had a tied clear plastic bag with towels in it.
On 4/6/25 at 10:14 AM, S#2 interviewed Certified Nurse Aide (CNA) #1 who stated that nursing staff checked the bath/shower room after it was used by a resident to clean up, dispose of used linen, and make sure nothing was left by the resident. CNA #1 was not sure of how often housekeeping cleaned the bath/shower room. CNA#1 accompanied the surveyor to check the bath/shower room and confirmed the above observations. CNA #1 was not sure who used the bath/shower room last and stated it was probably a resident who was independent and had frequently left their belongings in the bath/shower room.
On 4/6/25 at 11:05 AM, S#2 interviewed the Licensed Practical Nurse/Unit Manager (LPN/UM), who stated it was expected for the shower room to be cleaned as soon as the resident was done using it. The LPN/UM further explained the staff would return a resident to their room, then would go to bath/shower room to remove any linens and belongings left by the resident. The LPN/UM stated for independent residents, it was expected for staff to check the bathroom after it was used. S#2 discussed with the LPN/UM the observed concerns in the bath/shower room.
On 4/6/25 at 11:12 AM, S#2 accompanied by the LPN/UM toured the bath/shower room. The LPN/UM confirmed the observed concerns as the bath/shower room had not been cleaned from S#2's previous observation. The LPN/UM donned gloves and started cleaning up the items left in the bathroom.
On 4/8/25 at 12:14 PM, S#2 notified the DON, the LNHA, and the CLoNJ of the above concerns.
On 4/10/25 at 11:22 AM, the survey team met with the LNHA, the DON, the CLoNJ, and the RCA, and the LNHA stated the East unit bath/shower room was deep cleaned and education was provided to nursing staff. The LNHA further stated that the LPN/UM and the ADON/IP would do daily rounds.
5. On 4/6/25 at 8:55 AM, the survey team entered the facility, walking from the back of the building parking lot to the front of the building, Surveyor #3 (S#3) observed residents' rooms from the outside, with ripped curtains on the East Wing Unit.
On 4/10/25 at 8:20 AM, S#3 observed in the East Wing Unit, Rooms #12, #28 and #34 with window curtains ripped and facility management were made aware.
6. On 4/6/25 at 9:45 AM, S#3 observed the Resident #64 sitting on the wheelchair in the day room, with family members also in the dayroom visiting the resident.
On 4/6/25 at 9:55 AM, S#3 observed in the [NAME] Wing Unit, room [ROOM NUMBER]-B (Resident #64) and room [ROOM NUMBER] doorways with peeling wood on the bottom, and sharp wood exposed in room [ROOM NUMBER] doorway.
On 4/6/25 at 10:05 AM, S#3 interviewed RN#2, who had been working in the facility since September 2024. RN#2 confirmed the peeled wood was sharp to touch and had been like that, since RN#2 had been working at the facility. S#3 asked if the wood should be that way and RN#2 responded, No, and that MP do rounds in the morning and we notify the MP verbally what needed to be done or fix.
On 4/8/25 at 11:15 AM, S#3 interviewed the Director of Maintenance (DoM) from another facility regarding S#3's concerns above. The surveyor also notified the DoM regarding the ripped curtains in the residents' rooms observed upon entrance, and DoM was unaware of the ripped window curtains.
7. On 4/6/25 at 10:21 AM, S#3 observed Resident #24 in room [ROOM NUMBER]-B, lying in bed. S#3 observed the edges of the window curtains torn. The resident stated, The curtains have been like that for three months.
On 4/6/25 at 10:36 AM, S#3 interviewed CNA#2, who stated she had been working in the facility for two months, and confirmed the curtains were ripped. CNA#2 further stated that the curtains were ripped since she started working at the facility. CNA#2 further stated that she told the nurses about it, and I do not know what was next.
On 4/8/25 at 12:13 PM, S#3 notified the LNHA, DON and the CLoNJ regarding the above concerns of peeled wood and ripped curtains.
8. On 4/7/25 at 12:04 PM, while observing the facility East Wing Unit, S#4 observed broken molding near the floor in a doorway between a janitor closet and the nurses' station.
On the same date and time, S#4 observed air circulation vents located in the ceiling of the East Wing Unit. The vent covers were observed to have an accumulation of gray substance both inside and outside of the vent cover.
At 12:56 PM, S#4 observed the air circulation vents located on the [NAME] Wing Unit of the facility. S#4 observed the same accumulation of a gray substance on the vents located on the [NAME] Wing Unit.
The vents observed with the accumulation of gray substance included but not limited to:
East Wing Unit:
Small vent outside room [ROOM NUMBER].
Large vent at the end of the high side hall.
Small vent in the hall outside the beauty parlor.
Small vent in the hall outside the nursing station.
Large vent at the end of low side hall.
Small vent outside room [ROOM NUMBER].
Large vent near the doorway to the low side hall.
Small vent in hall outside the admissions office.
West Wing Unit:
Large vent at the end of the high side hall.
Small vent in the hall outside room [ROOM NUMBER].
Large vent at the entrance to the high side hall.
Small vent in the hall outside the clean utility room.
Small vent in the hall outside room [ROOM NUMBER].
On 4/8/25 at 12:12 PM, the survey team met with the LNHA, DON, and the CLoNJ to discuss the above concerns with the air circulation vents located on both wings of the building and the broken molding on the East Wing Unit.
On 4/9/25 at 12:37 PM, the survey team met with the RCA, DON, LNHA, and CLoNJ, and the LNHA stated, Regarding the ripped window curtains, we notified the vendor to replace curtains and the doorways with wood issues have been fixed. The LNHA further stated that a new cleaning schedule was initiated after surveyor's inquiry.
A review of the facility's Accommodation of Needs Policy, with a review/revision date of 2/1/23, that was provided by the DON, revealed that the resident/patient has the right to a safe, clean, comfortable, and homelike environment including, but not limited to, receiving treatment and support for daily living safely .
Under Process of the policy revealed: .1. The center must provide .1.2 Housekeeping and maintenance services necessary to maintain a sanitary, orderly, and comfortable interior .
Reasonable accommodations of individual needs and preferences means the facility's efforts to individualize the patient's physical environment. This includes the physical environment of the patient's bedroom and bathroom, as well as individualizing as much as feasible the facility's common living areas. The facility's physical environment and staff behaviors should be directed toward assisting the patient in maintaining and/or achieving independent functioning, dignity, and well being to the extent possible in accordance with the patient's own needs and preferences .
On 4/10/25 at 12:02 PM, the survey team met with the LNHA, DON, CLoNJ and RCA for an exit conference, and there was no additional information provided by the LNHA and her team.
NJAC 8:39-31.2(e), 31.4(a)(f)
CONCERN
(F)
Potential for Harm - no one hurt, but risky conditions existed
Food Safety
(Tag F0812)
Could have caused harm · This affected most or all residents
Based on observation, interview, and review of pertinent facility documents, it was determined that the facility failed to maintain sanitation in a safe and consistent manner to prevent food borne ill...
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Based on observation, interview, and review of pertinent facility documents, it was determined that the facility failed to maintain sanitation in a safe and consistent manner to prevent food borne illness.
This deficient practice was evidenced by the following:
On 4/6/25 at 9:21 AM, the surveyor, in the presence of the Cook, observed the following during the kitchen tour:
1. In the juice refrigerator, there was an unlabeled and undated glass bottle containing an orange-colored sauce. The [NAME] stated that it was a staff member's food item and not an item for the residents. The [NAME] acknowledged it should not have been in the refrigerator and removed the bottle.
2. On a food prep countertop, there was a compact blender. The blender cup was sealed on to the machine and was observed wet inside. The [NAME] checked and confirmed the blender cup was wet inside. The [NAME] stated that items after washing were supposed to be left to air dry as it prevented bacteria growth. The [NAME] removed the blender cup and placed it to be re-washed.
On 4/7/25 at 9:13 AM, the surveyor notified the Dietary Manager (DM) and the Regional District Manager (RDM) of the above concerns observed during the kitchen tour on the previous day. The DM acknowledged staff food items should not be stored in the kitchen and equipment after washing should be air-dried prior to storing.
On 4/8/25 at 12:14 PM, the surveyor notified the Licensed Nursing Home Administrator (LNHA), the Director of Nursing (DON), and the Clinical Lead of New Jersey (CLoNJ) of the above concerns observed in the kitchen.
On 4/9/25 at 9:45 AM, the surveyor interviewed the Licensed Practical Nurse/Unit Manager (LPN/UM) about the nutrition refrigerators on the units. The LPN/UM stated the refrigerators stored outside food belonging to residents and snacks provided by the kitchen. The LPN/UM explained the nurses and the certified nurse aides (CNAs) were responsible for ensuring items placed in the refrigerators were dated and labeled with the resident's name. The LPN/UM stated food items were disposed after 72 hours as indicated by signage on the refrigerator.
The surveyor inspected the [NAME] unit nutrition refrigerator with the LPN/UM and observed the following:
3. In the refrigerator, there was an undated and unlabeled box which consisted fast-food restaurant chicken. The LPN/UM confirmed the box was unlabeled and undated.
4. In the refrigerator, there was a black plastic bag containing three food containers filled with food items. The items were unlabeled and undated. The LPN/UM disposed of the bag in the garbage bin.
5. In the refrigerator, there was a black bag with a carton of eggs which was less than half full. The bag and the carton were unlabeled and undated. The LPN/UM confirmed the items were unlabeled and undated.
6. In the refrigerator, there were two bottles of water, with a first name written on their labels. The LPN/UM stated that it was a staff member's name, and it should not have been stored in the nutrition refrigerator.
7. In the freezer, there was a frozen half full 20 ounces soda bottle which was undated and unlabeled.
8. In the freezer, there was an uncovered Styrofoam cup with a clear colored frozen item. The cup was undated and unlabeled.
9. In the freezer, there was a sandwich bag with grapes, which was undated and unlabeled.
The LPN/UM stated she could not say who the items belonged to. She acknowledged the food items should have been labeled with the resident's name and dated when placed in the refrigerator. The LPN/UM stated the items would be removed and disposed.
On 4/9/25 at 9:54 AM, the surveyor inspected the East unit nutrition refrigerator with the LPN/UM and observed the following:
10. In the refrigerator, there were two take-out food containers, which were undated and unlabeled. The LPN/UM stated the items would be disposed.
The LPN/UM stated that the dietary staff would stock the refrigerator with snacks, and they usually checked the refrigerators for outdated items. She acknowledged it would be expected for outside food items to be labeled with a resident's name and dated when it was stored in the refrigerator by staff.
11. In the freezer, the bottom floor of the freezer was soiled with dark in color marks and there was a crumpled paper label.
The LPN/UM was unsure of who was responsible for cleaning the nutrition refrigerators and would have to find out from the DON.
On 4/9/25 at 12:37 PM, the LNHA, the DON, the CLoNJ, and the Regulatory Compliance Advisor (RCA) met with the survey team. The LNHA stated the item found in the kitchen refrigerator was hot sauce that belonged to one of the kitchen staff, which was removed, and the staff were in-serviced. The blender cup was re-washed and airdried. Additionally, in-service education was provided to dietary staff.
On 4/9/25 at 12:59 PM, the surveyor notified the LNHA, the DON, the CLoNJ, and the RCA of the concerns observed in the nutrition refrigerators. The surveyor asked who was responsible for ensuring items were dated and labeled. The LNHA replied that it was the nurses' responsibility. The surveyor asked who was responsible for cleaning the refrigerators and if there was a routine cleaning schedule. The LNHA stated the process going forward would be for housekeeping to clean the outside of the refrigerator and dietary staff would clean the inside of the refrigerator. The LNHA who started at the facility approximately two weeks ago, could not speak to who was previously responsible for cleaning the refrigerators and for when the refrigerators were last cleaned.
On 4/10/25 at 9:57 AM, the surveyor interviewed the DM and RDM about the dietary department's responsibility for nutrition refrigerators. The DM stated dietary staff checked refrigerator temperatures and any food items belonging to the kitchen were stocked and removed as needed. The DM stated the dietary staff were not responsible for cleaning the nutrition refrigerators or checking that outside food items were stored appropriately.
The RDM stated dietary staff cleaned out the refrigerators yesterday after the surveyor informed the facility's management of the concerns observed. The RDM further explained that the staff storing food items in the nutrition refrigerator were responsible for ensuring the items were dated and labeled. The DM was not sure who was responsible for cleaning the refrigerators prior to surveyor's inquiry and that it was not part of the dietary staff's responsibility.
On 4/10/25 at 11:22 AM, the LNHA, the DON, the CLoNJ, and the RCA met with the survey team. The DON stated the refrigerators were deep cleaned after surveyor's inquiry. There was no additional information provided.
A review of the facility's Warewashing Policy, with a last revised date of February 2023, under the Policy Statement revealed, All dishware, serviceware, and utensils will be cleaned and sanitized after each use.
Under Procedures revealed: .
4. All dishware will be air dried and properly stored .
A review of the facility's Food Storage: Cold Foods Policy, with a last revised date of February 2023, under the Procedures revealed, All foods will be stored wrapped or in covered containers, labeled and dated, and arranged in a manner to prevent cross contamination.
A review of the facility's Food Brought in for Patients/Residents Policy, with a last revised date of 1/26/24, under Process revealed: .
1.2. Food items that require refrigeration must be labeled with the resident's name and date the food was brought in .
1.3 Food items must be stored in a closed container to prevent contamination .
1.5 Food will be held in refrigerator for three (3) days following date on label and will be discarded by staff upon notification to resident .
NJAC 8:39-17.2(g)
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
Administration
(Tag F0835)
Could have caused harm · This affected most or all residents
Refer to F584 and S0560
Based on observations, interviews, and record review, it was determined that the facility failed to ensure the staff, as well as herself, the Licensed Nursing Home Administrato...
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Refer to F584 and S0560
Based on observations, interviews, and record review, it was determined that the facility failed to ensure the staff, as well as herself, the Licensed Nursing Home Administrator (LNHA), implemented the facility's policies and procedures including the promotion of a homelike environment and sufficient staffing in order to provide the appropriate needs of residents. This failure had the potential to affect all 71 residents who currently live in the facility.
The evidence was as follows:
On 5/21/25 at 9:00 AM, during revisit #1, to standard of 4/10/25, the survey team entered the facility and observed the posted Nursing Home Resident Care Staffing Report (NHRCSR) dated 5/21/25-Day Shift, current census was 71, shift hours of 7:00 AM-3:00 PM (7-3), and the staff to resident ratio of 1 Certified Nurse Aide (CNA):10.1 Residents.
On that same date at 9:14 AM, Surveyor #1 (S#1) met with the LNHA for a brief entrance conference with regard to the revisit, and the LNHA acknowledged that the completion date for the submitted plan of correction (POC), the reason for the revisit, was on 5/20/25. S#1 asked the LNHA for the facility's POCs, and she stated that she would get back to the surveyor with their binder for POCs.
At 10:11 AM, S#1 interviewed the Scheduling and Payroll Manager (SPM) who confirmed that today's census was 71 with one bed hold, and that the ratio was 1CNA:10 Residents. The SPM further stated that she was aware of the New Jersey (NJ) Mandated law for staffing, 1CNA:8 Residents for 7-3 shift, 1CNA:10 Residents in the evening (3:00 PM-11:00 PM), and 1CNA:14 Residents at night (11:00 PM-7:00 AM). The SPM acknowledged that the facility's CNA were mostly per diem, and at times not meeting the required staffing. The SPM also acknowledged that the facility follows the NJ Mandated law for staffing as part of their policy and procedure for staffing the facility.
At 10:32 AM, S#1 interviewed the Director of Nursing (DON), who informed the surveyor that it was since yesterday (5/20/25) in the afternoon that they were aware that there will be a short staffing problem for today (5/21/25), for 7-3 shift for CNA due to a call out. The DON further stated that she was unable to communicate to the LNHA about the short staff and the need of an agency CNA. The DON also stated that it was only the LNHA who had access to post the need of the facility for CNA.
At that same time, the DON informed S#1 that the facility had issues with acquiring the curtains as part of the facility's POC. The DON stated that the facility ordered the curtains and were delivered maybe two weeks ago. The DON further stated that if they were delivered, the expectation was, the damaged curtains should have been replaced. The DON acknowledged the concerns of the surveyors that the concerns from the standard survey on 4/10/25, for curtains were not corrected, and that the facility should provide a homelike environment to residents as facility's policy and protocol.
Furthermore, the DON stated that she acknowledged the concerns of the surveyors about environment concerns that included housekeeping and maintenance issues. She further stated that the Maintenance and Housekeeping Departments were working on it, and the expectation was it should have been done by the completion date. The DON also stated that the facility shared a Maintenance Director from another sister facility. Surveyor #2 (S#2) asked the DON why the facility had no full time Maintenance Director, and the DON responded that she would get back to the surveyors why the facility had no full time Maintenance Director, if it was in their facility assessment, and policy.
At 11:22 AM, S#1 interviewed the LNHA. The LNHA confirmed that she was the one who can post the need of the facility with regard to CNA in order to have agency fills up their need. The LNHA also stated that the facility can contact her at anytime for that need. The LNHA confirmed that she was not notified yesterday that a CNA called out and for her to be able to find a replacement and post the need of a CNA.
At that same time, the LNHA confirmed that she was aware of the facility's policy and procedure with regard to sufficient staffing and homelike environment, and as an administrator, it was her responsibility to ensure that policy and procedures were implemented and followed. The LNHA also stated that she was aware of the completion date on 5/20/25, and that the curtains should have been addressed as well as the other environment concerns, and staffing.
Furthermore, Surveyor #3 (S#3) notified the LNHA of the concerns with East wing unit shower room was dirty, molding not fixed near the nursing station. S#2 asked the LNHA why the provided audit tool/forms were signed by the LNHA as checked and no concerns if she was aware that they were not fixed. The LNHA stated that it was the Department heads who visually check the units for environmental tours and the LNHA received the verbal confirmation that they were fixed and no problem.
A review of the Position Title: Administrator signed by the LNHA on 7/15/24, revealed: position summary; the administrator is responsible for planning and is accountable for all activities and departments of the center subject to rules and regulations promulgated by government agencies to ensure proper health care services to residents. The administrator administers, directs, and coordinates all activities of the center (facility) to assure that the highest degree of quality of care is consistently provided to residents.
Essential Functions:
4. Assures all aspects of the center physical plant and environment are maintained at a high level .
6. Follows company administrative policies .
Clinical Excellence:
3. Assures that staffing levels in all departments are appropriate to meet the needs of all patients and residents .
Center Risk Manager Activities:
1. Responsible for implementation and oversight of the facility's risk management and quality assurance program and committee.
Job Skills:
4. Thorough knowledge of administrative management techniques, supervisory practices, procedures and principles.
A review of the Facility Assessment, last activity 8/20/24, revealed that the facility's Core Staffing & Personnel Audit, required one Maintenance Staff.
A review of the facility's Accommodation of Needs Policy, with a revised date of 2/1/23, revealed: the resident/patient .has the right to a safe, clean, comfortable, and homelike environment including, but not limited to, receiving treatment and support for daily living safely .
Under Process of the policy revealed: .1. The center must provide .1.2 Housekeeping and maintenance services necessary to maintain a sanitary, orderly, and comfortable interior .
On 5/21/25 at 12:58 PM, the survey team met with the LNHA, DON, and Market Clinical Head, and the Regional Senior Maintenance Director for an exit conference. S#1 notified the facility management of the above findings and concerns.
NJAC 8:39-9.2(a); 14.2