BEAUMONT HEALTH CARE CENTER

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to develop and implement comprehensive care plans for residents that included their specific needs as identified in each resident's comprehensive assessment for 2 of 10 residents (Residents #12 and #22) reviewed for person-centered care plans. <BR/>Residents #12 and #22 did not have care plans developed for oxygen therapy. <BR/>This failure could place residents at risk of not receiving proper care or inadequate oxygen support which could result in diminished physical, mental and psychosocial well-being. <BR/>The findings included: <BR/>1. Record review of the face sheet dated 05/14/25 indicated Resident #12 was admitted on [DATE] and was [AGE] years old. Her diagnoses included acute respiratory distress, chronic respiratory failure with hypoxia and chronic obstructive pulmonary disease. <BR/>Record review of the quarterly MDS assessment dated [DATE] indicated Resident #12 MDS had active diagnosis of debility, cardiorespiratory conditions, acute respiratory distress, chronic respiratory failure with hypoxia, chronic obstructive pulmonary disease, shortness of breath with exertion and received oxygen therapy continuous. <BR/>Record review of the undated care plan on 05/14/25 indicated Resident #12 did not have a care plan related to her receiving oxygen therapy. <BR/>Record review of the physician's orders for Resident #12 dated 05/12/25 indicated no order for oxygen administration. <BR/>Record review of the nursing progress notes dated 05/08/25 indicated Resident #12 Resident returned to facility via wheelchair accompanied by 1 personnel from hospital . Dx: chronic pain BLE. Current vitals: BP 122/64, HR 72, RR 21, SP02 98% 2L[PM](of Oxygen) and Temp 98.8 . <BR/>During an observation on 05/12/25 at 09:35 a.m., Resident #12's concentrator setting indicated infusing at the rate of 3 LPM per concentrator and she was asleep in her bed with the oxygen nasal cannula on. <BR/>During an observation on 05/12/25 at 2:07 p.m., Resident #12's concentrator setting indicated infusing at the rate of 3 LPM per concentrator and she was sitting up in her wheelchair. Resident #12 said she was on oxygen for shortness of breath and that it helped her breath better. <BR/>During an observation and interview on 05/12/25 at 2:30 p.m., LVN A verified Resident #12's concentrator was set on 3 LPM. LVN A said Resident #12 did not have an order for administration of oxygen. LVN A said Resident #12 used oxygen for shortness of breath. <BR/>2. Record review of the face sheet dated 05/14/25 indicated Resident #22 was admitted on [DATE] and was [AGE] years old. His diagnoses included essential hypertension, acute cough and chronic obstructive pulmonary disease. <BR/>Record review of the annual MDS assessment dated [DATE] indicated Resident #22 MDS had active diagnosis of medically complex conditions, hypertension, chronic obstructive pulmonary disease. <BR/>Record review of the undated care plan on 05/14/25 indicated Resident #22 did not have a care plan related to him receiving oxygen therapy. <BR/>Record review of Resident #22's physician's orders dated 05/12/25 indicated no order for oxygen administration. <BR/>Record review of Resident #22's nursing progress notes dated 04/25/25 indicated .cough; O2 sat: 87% on room air. Resident placed on 3 L[PM] NC, O2 improved to 93%. <BR/>During an observation on 05/12/25 at 2:17 p.m., Resident #22's concentrator setting indicated infusion at the rate of 2 LPM per concentrator and he was lying in bed watching TV. Resident #22 said he was on oxygen most of the time for shortness of breath. <BR/>During an observation and interview on 05/12/25 2:35 p.m., LVN A verified Resident #22's concentrator was set to 2 LPM. LVN A said Resident #22 did not have an order for administration of oxygen. LVN A said Resident #22 used oxygen for shortness of breath. <BR/>During an observation and interview on 05/14/25 3:35 p.m., the DON verified Resident #12's concentrator was set on 3 LPM and Resident #22's concentrator was set on 2 LPM. The DON said oxygen therapy should have been included on Residents #12 and #22's care plans. After the DON reviewed Resident #12 and 22's care plans, she agreed there were missing care plans specific to the resident current needs of oxygen and did not know why or how it was missed. The DON said no one person was responsible for completing care plans and that it was the responsibility of all administrative nurses of the interdisciplinary team. The DON said she expected the team to complete care plans and to make sure they reflected the current care needs of the resident. <BR/>Record review of facility undated policy titled Comprehensive Care Plan read in part . be developed for each resident that includes measurable objectives and timeframes to meet the resident's medical, nursing, mental and psychosocial needs and ALL services that are been identified in the resident's comprehensive assessment . 3. The comprehensive care plan will describe, at minimum, the following: a. The services that are to be furnished to attain or maintain the resident's highest practicable physical, mental and psychosocial well-being . 4. The comprehensive care plan will be prepared by an interdisciplinary team .

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to ensure that residents receiving enteral feeding received appropriate care and services to prevent complication of enteral feeding for 1 of 1 resident (Resident #42) reviewed for enteral feeding.<BR/>LVN A failed to verify placement of Resident #42's G-tube by checking for residual (fluid and contents that remain in the stomach) before enteral administration of water and medications. <BR/>This failure could place residents receiving enteral nutrition and medications at increased risk of not receiving proper nutrition, infection, and aspiration. <BR/>Findings include:<BR/>Record review of Resident #42's physician orders dated April 2024 indicated she was [AGE] years old and admitted to the facility 11/27/23. Her diagnosis included dysphagia (difficulty or discomfort swallowing) and aphasia (affects the ability to communicate). Orders indicated she was NPO (nothing by mouth) and was to receive all feedings and medications via G-tube (a tube inserted through the stomach that brings nutrition directly to the stomach). <BR/>Record review of a care plan last revised 12/08/23 indicated Resident #42 had a feeding tube related to dysphagia, history of aspiration (breathing in a foreign object such as food), and swallowing problem. Interventions included to verify tube placement prior to use. <BR/>Record review of the most recent quarterly MDS dated [DATE] indicated Resident #42 had severely impaired cognition, was dependent for all ADLs, and received her nutrition and hydration via G-tube. <BR/>During an observation during medication administration on 04/02/24 at 9:18 a.m., LVN A checked placement of Resident #42's G-tube by inserting 10ml of air into the tube and listening at the abdomen for the swish of air. She then administered water flushes and medications through the G-tube. <BR/>During an interview on 04/02/24 at 9:28 a.m., LVN A said she normally checked placement of a G-tube by auscultation (listening for a swish of air inserted into the abdomen with a stethoscope) and checking for residual in the stomach. She said she forgot to check for residual today. She said possible negative outcome of not performing a residual check for placement of the G-tube could be administering medications to a stomach that was too full. She said she had received training on G-tubes at nursing school and during orientation at the facility.<BR/>During an interview on 04/03/24 at 10:15 a.m., the DON said she was not aware of the recommendation in the State Operations Manual Appendix PP - Guidance to Surveyors for Long Term Care Facilities that auscultation was no longer recommended for checking placement of a feeding tube. She said the facility policy indicated placement could be checked by auscultation or aspiration of residual. She said possible negative outcome of not checking placement of a G-tube by residual check could be administration of medications and/or feeding outside of the stomach.<BR/>During an interview on 04/03/24 at 10:20 a.m., the Corporate Nurse said that the corporation was in process of reviewing and updating facility/corporate policies and she would bring the Confirming Placement of Feeding Tube policy to the attention of those updating policies. She said she was the former DON at the facility and all LVNs had received training on G-tubes and other skills during orientation to the facility. The training was given by staff LVNs, the ADON, and the DON. <BR/>Record review of the facility policy titled Confirming Placement of Feeding Tubes revised March 2015 indicated .Observe for placement by: a. verify placement by auscultating stomach or b. verify placement by residual: little to no residual may suggest that the tube has migrated from the stomach to the esophagus.

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to ensure respiratory care was provided according to professional standards of practice for 1 of 14 residents reviewed for respiratory care and services. (Residents #15)<BR/>The facility did not provide Resident #15's oxygen concentrator with a clean filter. The filter was covered with a thick layer of white powdery substance.<BR/>This failure could place residents who required respiratory care at risk of not receiving proper care and treatment and decreased quality of life. <BR/>Findings included:<BR/>Record review of the admission record indicated Resident #15 was admitted on [DATE]. Resident #15 was [AGE] years old male with diagnoses with chronic lung disease<BR/>Record review of quarterly MDS assessment dated [DATE] indicated Resident #15 had moderately impaired cognition, and had not received oxygen during last 7 days. Resident#15 had diagnosis of chronic lung disease. <BR/>Record review of the care plan dated 02/23/23 revealed Resident #15 was resistive to care with a history of non-compliance with O2 use as ordered. Interventions include an order for oxygen as ordered by physician.<BR/>Record review of physician orders dated March 2023 indicated Resident #15 was [AGE] years old and had diagnoses of chronic lung disease. The orders included Administer O2 @ 2 LPM via N/C PRN (as needed) related to Chronic Obstructive Pulmonary disease (lung disease) with acute exacerbation (sudden worsening of symptoms) with a start date of 02/23/2023.<BR/>During an observation and interview on 03/12/23 at 9:00 a.m., Resident #15 was receiving O2 at 2 LPM and filter on the concentrator was covered with a thick layer of white powdery substance. Resident #15 said the nurses change tubing and take care of that machine. <BR/>During an observation on 03/13/23 at 9:38 a.m., Resident #15 concentrator's filter was still covered with a thick layer of white powdery substance. <BR/>During an observation and interview on 03/13/23 at 10:00 a.m., LVN A checked Resident #15 concentrator's filter and said it was dirty and should have been cleaned last night. She said she normally worked the night shift and was trained to clean all filters on Sunday nights. However, she did not work last night. She said the filter being covered with dust could affect the output of the concentrator .<BR/>During an observation and interview on 03/13/23 at 10:20 a.m., the ADON removed Resident #15's filter said she was taking the dirty filter to the DON.<BR/>During an observation on 03/13/23 at 10:35 a.m., the DON said she expected the night nurse to clean filters every Sunday night and they had been trained.<BR/>During the exit meeting on 03/14/23 at 2:02 p.m., the Administrator was given the opportunity to provide additional information related to oxygen concentrators. No additional information was provided.

Based on observation, interview, and record review, the facility failed to store, prepare, distribute, and serve food under sanitary conditions in 1 of 1 kitchen reviewed for dietary services. <BR/>The facility failed to ensure all staff wore hair restraints and restrained all of their hair while plating the food. (05/12/25) <BR/>This failure could place residents who ate meals prepared in the kitchen at risk of foodborne illnesses. <BR/>Findings included: <BR/>During observation on 05/12/25 at 7:50 a.m., the DM was in the kitchen. The DM walked by the stove and by the food prepping tables. The DM operated the dish machine. There was a 2 inches wide area on each side of her neck of unrestrained hair approximately 3 to 4 inches long. <BR/>During an interview and observation on 05/12/25 at 12:27 p.m., the kitchen staff was serving food for lunch in the dining room from steam table and soup cooker. The DM had a 2-inch-wide area on each side of her neck of unrestrained hair approximately 3 to 4 inches long and she was placing the soup in the bowls. [NAME] C was plating from the steam table the 1 inch to 1 1/2-inches of unrestrained hair on top of her hair which extended from her right ear to the left ear. A long braid along the left side of her face was out of the hair net approximately 4 inches long. DM said all hair should be restrained while serving. [NAME] C and the DM went and secured their hair and washed their hands, after surveyor intervention. The DM said she was responsible for ensuring the staff secured their hair. She said a hair could fall in the food if not secured. <BR/>During an interview on 05/14/25 at 8:00 a.m., the Administrator said her expectation was for anyone serving food or in the kitchen to wear hair nets. <BR/>Record review of the undated Dietary Employee Personal Hygiene policy indicated It is the policy of this facility to utilize the following as guidelines for employee personal hygiene to prevent contamination of food by foodservice employees. 4. a. Food employees shall wear hair restraints such as hats, hair covering or nets, beard restraints and clothing that covers body hair, that are designed and worn effectively keep their hair from contacting exposed FOOD, . <BR/> Record review of the FDA food code dated 2022 indicated . Effectiveness. (Hair Restraints)<BR/>1. Code of Federal Regulations, Title 21, Sections 110.10 Personnel. (b) (1) Wearing outer garments suitable to the operation (4) Removing all unsecured jewelry (6) Wearing, where appropriate, in an effective manner, hair nets, head bands, caps, beard covers, or other effective hair restraints.

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to ensure respiratory care was provided according to professional standards of practice for 1 of 14 residents reviewed for respiratory care and services. (Residents #15)<BR/>The facility did not provide Resident #15's oxygen concentrator with a clean filter. The filter was covered with a thick layer of white powdery substance.<BR/>This failure could place residents who required respiratory care at risk of not receiving proper care and treatment and decreased quality of life. <BR/>Findings included:<BR/>Record review of the admission record indicated Resident #15 was admitted on [DATE]. Resident #15 was [AGE] years old male with diagnoses with chronic lung disease<BR/>Record review of quarterly MDS assessment dated [DATE] indicated Resident #15 had moderately impaired cognition, and had not received oxygen during last 7 days. Resident#15 had diagnosis of chronic lung disease. <BR/>Record review of the care plan dated 02/23/23 revealed Resident #15 was resistive to care with a history of non-compliance with O2 use as ordered. Interventions include an order for oxygen as ordered by physician.<BR/>Record review of physician orders dated March 2023 indicated Resident #15 was [AGE] years old and had diagnoses of chronic lung disease. The orders included Administer O2 @ 2 LPM via N/C PRN (as needed) related to Chronic Obstructive Pulmonary disease (lung disease) with acute exacerbation (sudden worsening of symptoms) with a start date of 02/23/2023.<BR/>During an observation and interview on 03/12/23 at 9:00 a.m., Resident #15 was receiving O2 at 2 LPM and filter on the concentrator was covered with a thick layer of white powdery substance. Resident #15 said the nurses change tubing and take care of that machine. <BR/>During an observation on 03/13/23 at 9:38 a.m., Resident #15 concentrator's filter was still covered with a thick layer of white powdery substance. <BR/>During an observation and interview on 03/13/23 at 10:00 a.m., LVN A checked Resident #15 concentrator's filter and said it was dirty and should have been cleaned last night. She said she normally worked the night shift and was trained to clean all filters on Sunday nights. However, she did not work last night. She said the filter being covered with dust could affect the output of the concentrator .<BR/>During an observation and interview on 03/13/23 at 10:20 a.m., the ADON removed Resident #15's filter said she was taking the dirty filter to the DON.<BR/>During an observation on 03/13/23 at 10:35 a.m., the DON said she expected the night nurse to clean filters every Sunday night and they had been trained.<BR/>During the exit meeting on 03/14/23 at 2:02 p.m., the Administrator was given the opportunity to provide additional information related to oxygen concentrators. No additional information was provided.

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to ensure residents were not given psychotropic drugs unless the medication was necessary to treat a specific condition as diagnosed and documented in the clinical record for 1 of 3 residents reviewed for unnecessary psychotropic drugs. (Resident #47)<BR/>The facility failed to ensure Resident #47 had an appropriate diagnosis or adequate indication for the use of Trazadone (an antidepressant used to treat depression) and Zoloft (an antidepressant used to treat depression). <BR/>This failure could place residents at risk for receiving unnecessary medication, having unnecessary medication side effects, and a decreased quality of life. <BR/>Findings included:<BR/>Record review of the physician orders dated April 2024 for Resident #47 indicated she was an [AGE] year-old female admitted on [DATE] with diagnoses included senile degeneration of the brain (mental deterioration associated with aging) and dementia (loss of cognitive functioning). The orders indicated she had the following medications:<BR/>* an order dated 02/23/24 for Trazadone (antidepressant) for dementia; and<BR/>* an order dated 02/23/24 for Zoloft (antidepressant) for dementia.<BR/>During an interview on 04/02/24 at 02:00 p.m. the DON said dementia was not an appropriate indication Resident #47's medications.<BR/>Surveyor requested a medication policy related to medications and diagnoses on 04/03/24 from the DON and no policy was provided.

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interviews and record reviews, the facility failed to ensure the right to formulate an advance directive was provided for 1 of 4 residents reviewed for resident rights. (Resident #5) <BR/>The facility did not have a valid Out of Hospital-Do Not Resuscitate (OOH-DNR) for Resident #5. <BR/>This failure could place residents at risk of lifesaving procedures being performed against their wishes resulting in bruising, broken ribs, and possibly being brought back to life in an unaware and unresponsive state. <BR/>Findings included: <BR/>Record review of physician orders for [DATE] indicated Resident #5 was an [AGE] year-old female readmitted on [DATE]. Her diagnoses included chronic obstructive pulmonary disease (a lung disease that blocks airflow making it difficult to breathe), hypertension (condition in which the force of the blood against the artery walls is too high), and abdominal aortic aneurysm (enlargement of the main blood vessel that delivers blood to the body, at the level of the abdomen). She had an order dated [DATE] for DNR. <BR/>Record review of the current MDS assessment dated [DATE] indicated Resident #5 was alert to person, place, and time with a BIMS of 11 indicating she had moderately impaired cognition. <BR/>Record review of the EMR on [DATE] at 09:33 a.m. indicated Resident #5 had a scanned OOH-DNR dated [DATE] with no printed name of physician and no license number of physician. <BR/>During an observation and interview on [DATE] at 11:05 a.m., Resident #5 was up in her recliner in her room. She said she did not want CPR done.<BR/>During an interview on [DATE] at 02:00 p.m., the DON said she had just started at the facility yesterday, but she knew DNRs should be completed or they can be deemed as invalid. She said missing physician information would make a DNR invalid. She said they would start CPR and possibly bring the person back to life while possibly breaking rib bones.<BR/>During an interview on [DATE] at 03:07 p.m., the former DON/Corporate Nurse said the SW usually did the DNRs.<BR/>During an interview on [DATE] at 03:23 p.m., the SW said DNRs without complete information would be invalid. She said Resident #5's DNR would be invalid due to not having the physician information completed.<BR/>Record review of a Do Not Resuscitate Order policy revised [DATE] indicated Policy Interpretation and Implementation: 2. A Do Not Resuscitate (DNR) order form must be completed and signed by the Attending Physician and resident .

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to ensure each resident's drug regimen was free from unnecessary drugs for 3 of 7 residents (Residents #9, #47, and #104) reviewed for unnecessary medications. <BR/>The facility did not have appropriate indications for medications based on Resident #9's, #47's, and #104's diagnoses.<BR/>This failure could place residents at risk of complications related to receiving unnecessary medications. <BR/>Findings included:<BR/>1.Record review of the physician orders dated April 2024 for Resident #9 indicated she was a [AGE] year-old female readmitted on [DATE] with diagnoses including type 2 diabetes and morbid (severe) obesity due to excess calories. The orders indicated the resident had an order dated 08/16/23 indicated she was to receive Ozempic subcutaneous solution (used to treat weight loss) every Friday related to type 2 diabetes mellitus. <BR/>Record review of a Nurse Note dated 03/22/24 indicated Resident #9 was trying to lose weight and was taking Ozempic to help with weight loss. <BR/>During an observation and interview on 04/01/24 at 09:36 a.m. Resident #9 was a very large built person in a bariatric bed. She said she had started taking Ozempic for weight loss and was hoping it would help some because she wanted to lose weight.<BR/>During an interview on 04/02/24 at 02:00 p.m. the DON said medications should have a diagnosis for the medication. She said the indications for Resident #9 were symptoms and drug classifications, not diagnoses.<BR/>During an interview on 04/02/24 at 03:08 p.m. the former DON/Corporate Nurse said medications should have appropriate diagnoses for their medication indication. She said Resident #9 was taking the Ozempic for weight loss and not for her diabetes.<BR/>2. Record review of the physician orders dated April 2024 for Resident #47 indicated she was a [AGE] year-old female admitted on [DATE] with diagnoses included senile degeneration of the brain and dementia. The orders indicated the resident had an order dated 03/22/24 for valproic acid (anticonvulsant) for dementia. <BR/>During an interview on 04/02/24 at 02:00 p.m. the DON said dementia was not an appropriate indication Resident #47's medications.<BR/>3. Record review of the physician orders dated April 2024 for Resident #104 indicated she was an [AGE] year-old female admitted on [DATE] with diagnoses including paroxysmal atrial fibrillation (a type of irregular heartbeat) and restless leg syndrome. The orders indicated the resident had:<BR/>* an order dated for Eliquis (blood thinner) for blood thinner;<BR/>* an order dated for pramipexole dihydrochloride (used to treat restless leg syndrome) for antiparkinson's.<BR/>During an interview on 04/02/24 at 09:20 a.m. Resident #104 said she did not have Parkinson's, but she took medication for her restless legs. <BR/>During an interview on 04/02/24 at 02:00 p.m. the DON said medications should have an appropriate diagnosis for their use. <BR/>During an interview on 04/02/24 at 03:08 p.m. the former DON/Corporate Nurse said medications should have appropriate diagnoses for their indication. <BR/>Surveyor requested a medication policy related to medications and diagnoses on 04/03/24 from the DON and no policy was provided.