CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0582
(Tag F0582)
Could have caused harm · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on staff interview, facility documentation review, and clinical record review the facility staff failed to issue an ABN (A...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on staff interview, facility documentation review, and clinical record review the facility staff failed to issue an ABN (Advanced Beneficiary Notice) timely for one Resident (Resident #292) in a sample of 18 Residents.
The findings included:
Resident #292 was admitted to the facility on [DATE], with a most recent readmission date of 6/20/19. Diagnoses for Resident #292 included but were not limited to: acute pancreatitis, pancreatic cancer, and obstruction of bile duct.
Resident #292's most recent MDS (minimum data set) (an assessment tool) with an ARD (assessment reference date) of 6/27/19 was coded as an admission assessment. Resident #292 was coded as having had a BIMS (brief interview for mental status) score of 14, which indicated cognitively intact. He was coded as being dependent upon one staff person for extensive assistance with bed mobility, transfers, walking, dressing, toilet use and personal hygiene.
Review of the SNF ABN (skilled nursing facility advance beneficiary notice) for Resident #292, revealed that it was signed on 7/5/19 and indicated that the Resident's skilled care would end on 7/9/19. However, an option was not identified as to if the Resident wanted to continue to receive services and have the fiscal intermediary make the coverage determination.
On 9/5/19 during a clinical record review it was revealed that Resident #292 came off of skilled care (Medicare Part A reimbursed stay) on 7/4/19 and became self pay on 7/5/19, which was prior to the issuance of the ABN.
The ABN is to be issued prior to skilled care services ending, which would have allowed Resident #292 or his representative, to make a decision about continuation of services and have Medicare make the coverage determination; or the option to continue services and pay privately for them. Resident #292 was not given this option since the notice was issued after the payer change had taken place.
On 9/5/19 at 12:31 PM an interview was conducted with Employee H, the social worker. The social worker was asked if Resident #292 went private pay on 7/5/19 why the SNF ABN indicated skilled services would end on 7/9/19. Employee H, stated I don't know I will have to look at my notes she then turned to her computer and started reviewing her notes. The social worker stated, on 7/4/19 I spoke with the son and discussed going hospice. I then asked when his skilled services ended, the social worker stated he was supposed to come off on 7/10/19. When asked how she knew this she stated because I issued the NOMNC on 7/9/19 and the ABN started 7/10/19. The social worker then stated, well a significant change MDS was done on 7/9/19.
On 9/5/19 at 1:38 PM the Social Worker, (employee H) came into the conference room with the survey team and stated these are my PPS (prospective payment system) (reimbursement by Medicare) sheets, he was scheduled to discharge on [DATE] but they said they wanted to stay until 7/12/19. When the social worker was asked to explain what she reviews with Residents, the social worker stated, it says if they stay past their last covered non-covered day they have to become private pay. She was then asked to read the ABN form options. She read it and replied, I forgot to have him sign it.
The survey team asked social worker to identify what the options were telling the Resident; and she stated this form is new, we tell the people they can't choose option 1. She was then asked to say that again, she said, well, I have been told to tell them if they choose option 1 they are going to loose anyway and it is no need to check it, I usually go to option 2 that they will be billed private pay for the room. During this interview the facility Administrator came into the room and was advised that the social worker was advising Resident's not to choose option 1. The Social worker then said I was told to say that if they choose #1 to bill Medicare but when Medicare looks and sees that the services have stopped they aren't going to cover the cost of the room, so why bother with option 1. The social worker and Administrator were advised that option 1 gives the resident the option to continue to receive the services and have the fiscal intermediary make the coverage determination.
On 9/5/19 at 2:20 PM the facility Administrator, Employee A stopped this writer, (Surveyor E) in the lobby and stated the ABN notices have been an ongoing issue with her, referencing Employee H, the social worker. The Administrator had in her hand the employee file of Employee H and showed the surveyor two disciplinary actions as well as, education that had been provided to Employee H, with regard to the ABN notices.
On 9/5/19 at 2:36 PM the Administrator came into the conference room with the survey team and provided this writer with a copy of the education Employee H, the social worker, received on 6/26/18 regarding the CMS (Centers for Medicare & Medicaid Services) SNF ABN form. The training included the following information to include but not limited to:
* a flow chart of when to issue the SNF ABN form.
* the statement The NOMNC [notice of medicare non-coverage] is given > 2 calendar days before the last covered day or 3 days prior to discharge from skilled services. *this applies to ABNs as well*
* the statement, the revised SNF ABN will be mandatory for use on May 7, 2018.
* CMS guidance on the form, including how and when to use the form
* the facility policy.
On 9/5/19 at 2:36 PM an interview was conducted with the facility Administrator, Employee A, in the conference room with the entire survey team present. When the Administrator was asked when the issue had been identified, the Administrator stated, it was identified during a mock survey in January. I asked for another mock survey in May and the same issues were identified. She was re-educated with these documents. When Employee A was asked who supervises the Social Worker, the Administrator stated I do. When asked since this has been identified as an issue in the past what was being done to monitor her progress, the Administrator stated, I was doing an audit ever week, she has to give me the ones she completes. The Administrator was asked if she had identified any issues, she stated 1 or 2 with dates.
Review of the facility policy titled, Notification of Non-Coverage: Medicare Part A Skilled Nursing Facility Advanced Beneficiary Notice (SNF ABN) stated in the purpose statement: To notify the resident, who has Medicare Part A or Part B coverage that it is the facilities opinion that individualized service required does not meet Medicare coverage criteria required for payment and the resident may be responsible for charges. Provides the resident the right to appeal to the fiscal intermediary. All Residents who are discharged from Medicare Part A without utilizing their 100 day benefit and remain in the building must be issued an SNF ABN. This may be issued to the resident or resident representative and must have a signature with a date completed on or before the date of discharge. This includes SNF to hospice.
CMS defines the use of the SNF ABN in the section 70.3 of the Medicare Claims Processing Manual in chapter 30 on page 84, it read A SNF ABN is evidence of beneficiary knowledge about the likelihood of a Medicare denial, for the purpose of determining financial liability for expenses incurred for extended care items or services furnished to a beneficiary and for which Medicare does not pay. If Medicare is expected to deny payment (entirely or in part) on the basis of one of the exclusions listed in §70 of this chapter for extended care items or services that the SNF furnishes to a beneficiary, a SNF ABN must be given to the beneficiary in order to transfer financial liability for the item or service to the beneficiary. The table on page 85 stated, In the situation in which a SNF proposes to stop furnishing all extended care items or services to a beneficiary because it expects that Medicare will not continue to pay for the items or services that a physician has ordered and the beneficiary would like to continue receiving the care, the SNF must provide a SNF ABN to the beneficiary before it terminates such extended care items or services.
No further information was provided.
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
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, staff interview, clinical record review, and facility documentation review, the facility staff failed for ...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, staff interview, clinical record review, and facility documentation review, the facility staff failed for 1 resident (Resident #39) in the survey sample of 18 residents, to implement their abuse policy for an injury of unknown origin. Specifically, they failed to report and investigate.
The Findings included:
Resident #39 was a [AGE] year old who was admitted to the facility on [DATE]. Resident #39's diagnoses included Coronary Artery Disease, High Blood Pressure, and Dementia.
On 9/4/19 a review was conducted of Resident #39's clinical record. A Licensed Practical Nurse's (LPN H) progress note dated 7/21/19 at 9:14 P.M. read, Tonight during medpass resident came up to me and showed me a skin tear he had on his right elbow. Skin tear is 1.5 cm x 0.25 cm. Red in color and bleeding. Resident could not explain what happened, and denied any pain. Skin tear was cleaned per protocol and dressing was applied. Provider notified. LPN H was not available for an interview.
In addition, the following number of incidents, over time, were documented:
7/25/17: Skin tear to right hand from fall
4/13/18: Skin tear to right inner calf
5/31/18: Skin tear to right lower leg from bumping into something into his room
8/23/18: bruising to left wrist and right upper arm
9/14/18: injury to right knee, right upper arm, right elbow
10/4/18: hematoma of the left lateral forearm
10/12/18: 2 skin tears right lateral leg and right knee
3/20/19: skin tear on right lower leg just below knee
6/1/19: abrasion to right temporal. Skin tears right lower arm and left inferior arm
6/4/19: 2 skin tears right posterior leg
6/26/19: skin tear to left shin and new skin tear to right elbow
7/1/19: skin tear to left upper anterior arm
7/17/19: laceration noted above left temporal above left eye. 2 skin tears noted to left leg. Staples were placed in ER to left forehead wound
The clinical record did not contain any documentation of reporting, or investigating of the injury that occurred on 7/21/2019.
On 9/4/19 a review was conducted of facility documentation. There was no documentation that the injury of unknown origin had been reported to the state agency.
The facility Abuse Prevention and Management Policy dated 8/15/19 was reviewed. An excerpt read, The facility is committed to developing and denationalizing policies and procedures for screening and training employees, protection of residents and for the prevention, identification, investigation, and reporting of abuse, neglect, mistreatment, and misappropriation of property.
On 9/5/19 at approximately 3:30 P.M. an interview was conducted in the conference room, with the facility Administrator (Employee A) and Surveyors B, D, and E present. The Administrator was asked why the injury of unknown origin had not been reported, and investigated, and why their abuse policy hadn't been implemented. The Administrator stated that she usually reports when she has something solid.
No further information was received.
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Report Alleged Abuse
(Tag F0609)
Could have caused harm · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, staff interview, clinical record review, and facility documentation review, the facility staff failed for ...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, staff interview, clinical record review, and facility documentation review, the facility staff failed for 1 resident (Resident #39) in the survey sample of 18 residents, to report an injury of unknown origin to the State Survey Agency.
The Findings included:
Resident #39 was a [AGE] year old who was admitted to the facility on [DATE]. Resident #39's diagnoses included Coronary Artery Disease, High Blood Pressure, and Dementia.
On 9/4/19 a review was conducted of Resident #39's clinical record. A Licensed Practical Nurse's (LPN H) progress note dated 7/21/19 at 9:14 P.M. read, Tonight during medpass resident came up to me and showed me a skin tear he had on his right elbow. Skin tear is 1.5 cm x 0.25 cm. Red in color and bleeding. Resident could not explain what happened, and denied any pain. Skin tear was cleaned per protocol and dressing was applied. Provider notified. LPN H was not available for an interview.
In addition, the following number of incidents, over time, were documented:
7/25/17: Skin tear to right hand from fall
4/13/18: Skin tear to right inner calf
5/31/18: Skin tear to right lower leg from bumping into something into his room
8/23/18: bruising to left wrist and right upper arm
9/14/18: injury to right knee, right upper arm, right elbow
10/4/18: hematoma of the left lateral forearm
10/12/18: 2 skin tears right lateral leg and right knee
3/20/19: skin tear on right lower leg just below knee
6/1/19: abrasion to right temporal. Skin tears right lower arm and left inferior arm
6/4/19: 2 skin tears right posterior leg
6/26/19: skin tear to left shin and new skin tear to right elbow
7/1/19: skin tear to left upper anterior arm
7/17/19: laceration noted above left temporal above left eye. 2 skin tears noted to left leg. Staples were placed in ER to left forehead wound
The clinical record did not contain any documentation of reporting of the injury that occurred on 7/21/2019.
On 9/4/19 a review was conducted of facility documentation. There was no documentation that the injury of unknown origin had been reported to the state agency.
The facility Abuse Prevention and Management Policy dated 8/15/19 was reviewed. An excerpt read, The facility is committed to developing and denationalizing policies and procedures for screening and training employees, protection of residents and for the prevention, identification, investigation, and reporting of abuse, neglect, mistreatment, and misappropriation of property.
On 9/5/19 at approximately 3:30 P.M. an interview was conducted in the conference room, with the facility Administrator (Employee A) and Surveyors B, D, and E present. The Administrator was asked why the injury of unknown origin had not been reported, and investigated, and why their abuse policy hadn't been implemented. The Administrator stated that she usually reports when she has something solid.
No further information was received.
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Investigate Abuse
(Tag F0610)
Could have caused harm · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, staff interview, clinical record review, and facility documentation review, the facility staff failed for ...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, staff interview, clinical record review, and facility documentation review, the facility staff failed for 1 resident (Resident #39) in the survey sample of 18 residents, to investigate an injury of unknown origin.
The Findings included:
Resident #39 was a [AGE] year old who was admitted to the facility on [DATE]. Resident #39's diagnoses included Coronary Artery Disease, High Blood Pressure, and Dementia.
On 9/4/19 a review was conducted of Resident #39's clinical record. A Licensed Practical Nurse's (LPN H) progress note dated 7/21/19 at 9:14 P.M. read, Tonight during medpass resident came up to me and showed me a skin tear he had on his right elbow. Skin tear is 1.5 cm x 0.25 cm. Red in color and bleeding. Resident could not explain what happened, and denied any pain. Skin tear was cleaned per protocol and dressing was applied. Provider notified. LPN H was not available for an interview.
In addition, the following number of incidents, over time, were documented:
7/25/17: Skin tear to right hand from fall
4/13/18: Skin tear to right inner calf
5/31/18: Skin tear to right lower leg from bumping into something into his room
8/23/18: bruising to left wrist and right upper arm
9/14/18: injury to right knee, right upper arm, right elbow
10/4/18: hematoma of the left lateral forearm
10/12/18: 2 skin tears right lateral leg and right knee
3/20/19: skin tear on right lower leg just below knee
6/1/19: abrasion to right temporal. Skin tears right lower arm and left inferior arm
6/4/19: 2 skin tears right posterior leg
6/26/19: skin tear to left shin and new skin tear to right elbow
7/1/19: skin tear to left upper anterior arm
7/17/19: laceration noted above left temporal above left eye. 2 skin tears noted to left leg. Staples were placed in ER to left forehead wound
The clinical record did not contain any documentation of investigating the injury that occurred on 7/21/2019.
On 9/4/19 a review was conducted of facility documentation. There was no documentation that the injury of unknown origin had been reported to the state agency.
The facility Abuse Prevention and Management Policy dated 8/15/19 was reviewed. An excerpt read, The facility is committed to developing and denationalizing policies and procedures for screening and training employees, protection of residents and for the prevention, identification, investigation, and reporting of abuse, neglect, mistreatment, and misappropriation of property.
On 9/5/19 at approximately 3:30 P.M. an interview was conducted in the conference room, with the facility Administrator (Employee A) and Surveyors B, D, and E present. The Administrator was asked why the injury of unknown origin had not been reported, and investigated, and why their abuse policy hadn't been implemented. The Administrator stated that she usually reports when she has something solid.
No further information was received.
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Pharmacy Services
(Tag F0755)
Could have caused harm · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on staff interview, facility documentation review, and clinical record review, the facility staff failed to provide one Re...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on staff interview, facility documentation review, and clinical record review, the facility staff failed to provide one Resident (Residents #14) with physician ordered medications in a survey sample of 18 Residents.
The findings included:
For Resident #14, the facility failed to provide an antibiotic medication which was unavailable for 3 doses.
Resident #14, was admitted to the facility on [DATE]. Diagnoses included; metabolic encephalopathy, weakness, heart failure, diabetes, chronic obstructive pulmonary disease, hypothyroidism, essential hemorrhagic thrombocytopenia, and obstructive uropathy.
Resident #14's most recent MDS (minimum data set) with an ARD (assessment reference date) of 7-9-19 was coded as an admission assessment. Resident #14 was coded as having a BIMS (brief interview of mental status) score of 14 out of a possible 15, revealing no cognitive impairment. Resident #14 was also coded as requiring extensive assistance of staff to perform activities of daily living, such as bed mobility, transferring, locomotion, and toileting.
Review of Resident #14's clinical record revealed no evidence the following antibiotic medication was administered on the days and times indicated:
Erythromycin 5 mg (milligram)/per gram (0.5%) eye ointment (1 cm (centimeter) ribbon) right eye for blepharitis four times daily at (8 to 10-a.m., 12 to 2 p.m., 4 to 6 p.m., and 9 to 10 p.m.) for seven days, ordered to start 8-27-19.
Valid physician's orders were evident for the medication in question, and was written by the doctor on the morning of 8-27-19.
The Medication Administration History report was requested and received. The facility audit document revealed the times that the medication was actually administered, and notes written by nursing staff about that administration. On 8-27-19, the document showed that the order was put into the system after the 8:00 a.m., administration time, and before the 12 noon administration time.
The 12 noon administration time was in the system for the medication to be administered, however, the 8:00 a.m., dose was not in the order history. For 8-27-19, at 12:00 noon, 4:00 p.m., and 9:00 p.m., the document revealed that the medication was not administered, and the nurse documented awaiting from pharmacy, pharmacy called. This means that the medication was unavailable for those 3 doses.
On 9-5-19 the DON (director of nursing) was interviewed in the conference room and stated she was aware that medications had not been given.
On 9-5-19 at approximately 4:15 p.m., at the end of day debrief, the Administrator and DON were made aware. No further information was provided.
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0760
(Tag F0760)
Could have caused harm · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on staff interview, facility documentation review, and clinical record review, the facility staff failed to ensure one Res...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on staff interview, facility documentation review, and clinical record review, the facility staff failed to ensure one Resident was free from significant medication errors for one resident (Residents #14) in a survey sample of 18 Residents.
The findings included:
For Resident #14, the facility failed to administer antibiotic medication for an active eye infection as ordered by a physician.
Resident #14, was admitted to the facility on [DATE]. Diagnoses included; metabolic encephalopathy, weakness, heart failure, diabetes, chronic obstructive pulmonary disease, hypothyroidism, essential hemorrhagic thrombocytopenia, and obstructive uropathy.
Resident #14's most recent MDS (minimum data set) with an ARD (assessment reference date) of 7-9-19 was coded as an admission assessment. Resident #14 was coded as having a BIMS (brief interview of mental status) score of 14 out of a possible 15, revealing no cognitive impairment. Resident #14 was also coded as requiring extensive assistance of staff to perform activities of daily living, such as bed mobility, transferring, locomotion, and toileting.
Review of Resident #14's clinical record revealed a valid physician's order, written by the doctor on the morning of 8-27-19 for the following medication.
Erythromycin 5 mg (milligram)/per gram (0.5%) eye ointment (1 cm (centimeter) ribbon) right eye for blepharitis four times daily at (8 to 10-a.m., 12 to 2 p.m., 4 to 6 p.m., and 9 to 10 p.m.) for seven days, ordered to start 8-27-19.
The Medication and Treatment Administration Record (MAR/TAR) was reviewed and revealed nursing signatures indicating the medication had been administered from 8-27-19 at 12 noon through 9-2-19 at 9 p.m. This particular document showed nurse initials on it which indicated that the Resident missed only one dose of the antibiotic which was ordered four times per day for 7 days.
The Medication Administration History report was requested and received. The facility audit document revealed the times that the medication was actually administered, and notes written by nursing staff about that administration. On 8-27-19, the document showed that the order was put into the system after the 8:00 a.m., administration time but before the 12 noon administration time. The 12 noon administration time was in the system for the medication to be administered, however, the 8:00 a.m., dose was not in the order history.
On 8-27-19, at 12:00 noon, 4:00 p.m., and 9:00 p.m., the document revealed that the medication was not administered, and the nurse documented awaiting from pharmacy, pharmacy called. This means the medication was unavailable for those 3 doses. The document also revealed that the antibiotic medication was not administered therapeutically nor timely, for 5 of the 6 days when it was administered.
During the seven days it was ordered to be given, the Erythromycin eye ointment antibiotic was at times, administered too closely to the previous dose, or was administered too early, or too late, or was omitted entirely. The medication should have been given for 7 days, on time, and at equally spaced intervals, and was not. The medication was discontinued after the evening dose on 9-2-19 after only 6 days of administration.
The medication was ordered four times daily (8 am, 12 pm (noon), 4 pm, and 9 pm).
The following shows the medication actual administration times:
(Day 1) 8-27-19 - omitted for 3 doses, (due to being unavailable). The fourth dose was never scheduled at the end of the 7 days to complete the regimen, nor were the other 3 missed doses scheduled.
(Day 2) 8-28-19 - administration begins - 9:27 a.m., 3:34 p.m., 4:18 p.m., 8:40 p.m. Late for the noon dose, and too close to the 4p dose. (6 hrs, 44 minutes, 4 hrs) between doses.
(Day 3) 8-29-29 - 9:14 a.m., 2:22 p.m., 4:42 p.m., 10:53 p.m. Late for the noon dose, and too close to the 4p dose, and late for the 9p dose. (5 hrs, 2hrs, 6 hrs) between doses.
(Day 4) 8-30-19 - 7:58 a.m., 3:54 p.m., 4:14 p.m., 1:05 a.m. Late for the noon dose, and too close to the 4p dose, late for the 9p dose. (8 hrs, 20 minutes, 8 hrs) between doses.
(Day 5) 8-31-19 - 10:04 a.m., 12:49 p.m., 6:45 p.m., 8:20 p.m. Late for the 8a dose, too close to the noon dose, and too close to the 9p dose. (2.75 hrs, 6 hrs, 1.5 hrs) between doses.
(Day 6) 9-01-19 - 7:52 a.m., 11:49 p.m., 4:11 p.m., 8:43 p.m. This was the only day in 6 days relatively evenly spaced, and relatively on time.
(Day 7) 9-02-19 - 7:37 a.m., 2:57 p.m., 4:36 p.m., 11:42 p.m. Too long between the 8a and noon dose, the noon dose was late, too close between the noon dose, and the 4p dose, and too long between the 4p dose and the 9p dose, and late for the 9p dose. (7.5 hrs, 1.5 hrs, 7 hrs) between doses.
Guidance for the administration of Erythromycin eye antibiotic is given by The National Institutes of Health (NIH) & Medline.gov, and are as follows;
Using medication: Using antibiotics correctly and avoiding resistance. What's important to consider when taking antibiotics? Antibiotics should be taken for as long as the doctor has prescribed them. Just because the symptoms of the illness subside, it doesn't mean that all of the germs have been killed. Remaining bacteria may cause the illness to start up again. Medications can only work properly if they are used correctly. It's important to know the following things when taking antibiotics:
When should you take antibiotics? Some antibiotics are always meant to be taken at the same time of day, others are meant to be taken before, with or after a meal. If you are supposed to take the medicine three times a day, for example, it usually needs to be taken at set times so that the effect is spread out evenly over the course of the day. You could remember the regular times of 6 a.m., 2 p.m. and 10 p.m. for an antibiotic that needs to be taken every 8 hours, for example.
How should this medicine be used? Ophthalmic erythromycin comes as an ointment to apply to the eyes. It is usually applied up to six times a day for eye infections. Use erythromycin eye ointment exactly as directed. Do not use more or less of it or use it more often than prescribed by your doctor. You should expect your symptoms to improve during your treatment. Call your doctor if your symptoms get worse or do not go away, or if you develop other problems with your eyes during your treatment. Use ophthalmic erythromycin until you finish the prescription, even if you feel better. If you stop using ophthalmic erythromycin too soon, your infection may not be completely cured and the bacteria may become resistant to antibiotics.
What should I do if I forget a dose? Apply the missed dose as soon as you remember it. However, if it is almost time for the next dose, skip the missed dose and continue your regular dosing schedule. Do not apply extra ointment to make up for a missed dose.
Further review of the MAR indicated that the Resident could have only ever received 6 days of the antibiotic, instead of the 7 days which was ordered by the physician, as it was discontinued on 9-2-19 after the 9p.m. dose.
Physician's progress notes were reviewed and revealed no indication that the physician was ever notified or aware of the 4 missing doses of antibiotic for Resident #14.
Review of the facility's policy entitled, Medication Administration Procedure revealed that the purpose of the procedure was The applying, dispensing, or giving of drugs or medicines as prescribed by a physician. The document further stated; Chart medications during the med pass in a consistent manner before going to the next resident.
On 9-5-19 the DON (director of nursing) was interviewed in the conference room and stated she was aware that medications had not been given and were late.
On 9-5-19 at approximately 4:15 p.m., at the end of day debrief, the Administrator and DON were made aware of the failure of staff to administer the antibiotic medication as ordered. No further information was provided.
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0806
(Tag F0806)
Could have caused harm · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, resident interview, staff interview, facility documentation review, and clinical record review, the facili...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, resident interview, staff interview, facility documentation review, and clinical record review, the facility staff failed to provide a diet to accommodate food preferences for 1 resident (Resident #342) in a sample size of 18 residents.
The Findings included:
For Resident #342, the facility staff failed to provide a diet to accommodate her food preferences as a vegetarian.
Resident #342, an [AGE] year old female, was admitted to the facility on [DATE].
On 09/04/2019 at approximately 1:45 PM, during initial tour, Resident #342 voiced her concern that she is a vegetarian however the facility was still serving her meat. She stated that she had received a barbeque sandwich earlier at lunch, adding the food is good but I am a vegetarian and the choices are very limited, they have been putting meat on some of my meal trays, I won't eat that, they have not offered me anything different. Resident #342 stated that she met with the Dietician the previous afternoon, 9/3, and had indicated that she is vegetarian and prefers to adhere to a vegetarian diet.
On 09/04/2019 at approximately 2:10 PM, a staff interview was conducted with Dining Room Supervisor (Employee G) who confirmed the current dinner ticket for Resident #342 reflected a mechanical soft, no added salt diet. Employee G stated it was possible Resident #342 could have received a barbeque sandwich at lunch, however he could not confirm it because the lunch tickets had been thrown away. Employee G stated he was unaware that she was a vegetarian and would not know by looking at the meal tickets currently being generated by Dining Services.
On 09/04/2019 at approximately 2:20 PM, a staff interview was conducted with the Director of Dining Services (Employee D) who provided a Resident Dining Details Report dated 9/4/2019 and confirmed that Resident #342 received a mechanical soft, no salt added diet for breakfast and lunch on 09/04/2019. Employee D stated that diet changes need to be communicated to Dietary Services using a Nutrition Services Communication Form because the Resident Dining Details Report is generated the day prior to the Kitchen providing meals to the residents. Employee D indicated that when a diet change is received using the Nutrition Services Communication Form, the Dining Services staff will manually change the pre-printed, individual meal tickets to ensure that the affected resident receives the appropriate diet as ordered.
On 09/04/2019 at approximately 2:30 PM, a staff interview was conducted with the RD (Registered Dietician, Employee F) who confirmed she had assessed Resident #342 in the afternoon of 09/03/2019 and Resident #342 requested a vegetarian diet. An order for a Mechanical Soft, Vegetarian diet was entered for Resident #342 on 09/03/2019 at 6:52 PM. The RD stated, I put an order in for the diet modification and that alerts nursing staff in the computer, nursing acknowledges the order and notifies the kitchen by putting in a Nutrition Services Communication Form, this is done immediately so the Resident's next meal will be correct.
On 09/04/2019 at approximately 2:40 PM, a staff interview was conducted with RN A who confirmed that she was aware of the change to Resident #342's diet as she had electronically acknowledged the order in the medical record on 09/03/2019 at 6:52 PM. RN A stated, I did not fill out a slip [Nutrition Services Communication Form] for the Kitchen, normally I would but the Dietician should have done it, she made the order.
On 09/05/2019 at approximately 1:50 PM, the DON (Director of Nursing, Employee B) was interviewed regarding the communication process and expectations for ordered dietary changes. She stated, I had a mandatory nursing meeting just this past Friday, 8/30, and I spoke about the procedure for the dietary slips [Nutrition Services Communication Form] which is, whoever activates or acknowledges the order is responsible to notify Dietary. The DON confirmed that RN A attended the meeting and stated, she [RN A] is a Nurse Supervisor and is expected to know this procedure, I would have expected her to complete the Nutrition Services Communication Form and take it to Dietary.
CONCERN
(E)
Potential for Harm - no one hurt, but risky conditions existed
Food Safety
(Tag F0812)
Could have caused harm · This affected multiple residents
Based on observation, staff interview, and facility documentation review, the facility staff failed to store, prepare, distribute and serve food in accordance with professional standards in 2 of 2 kit...
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Based on observation, staff interview, and facility documentation review, the facility staff failed to store, prepare, distribute and serve food in accordance with professional standards in 2 of 2 kitchens serving nursing home Residents.
The findings included:
1. The facility staff failed to properly dry dishes to prevent the development of microorganism growth.
On 9/4/19 at approximately 1:00 PM during observation of the facility main kitchen observation revealed wet nesting of ramekins. When asked what is the proper way to dry the ramekins, Employee D, the director of dining services stated, that he expects facility kitchen staff to place ramekins separate on a sheet pan like we do over here and pointed to other dishes that were air drying separately.
On 09/05/19 at 11:16 AM an interview was conducted in the conference room in the presence of the survey team with Employee D, Director of Dining Service and Employee E, the Executive Chef. When asked what the concern was with the ramekins wet nesting, Employee D stated, because they don't effectively air dry and bacteria can grow between them. When asked what they expectation is, Employee D stated, form them to be properly air dried.
Review of the facility policy titled, Dietary Services dish machine and manual ware washing policy stated on page 2, to avoid recontamination of clean and sanitary items: a. air dry all items on a drain board or drying rack.
According to the 2017 Food Code published by the U.S. Public Health Service, FDA U.S. Food & Drug Administration chapter 4, section 4-901.11, titled Equipment and Utensils, Air-Drying Required pages 151-152 stated: After cleaning and SANITIZING, EQUIPMENT and UTENSILS: (A) Shall be air-dried or used after adequate draining as specified in the first paragraph of 40 CFR 180.940 Tolerance exemptions for active and inert ingredients for use in antimicrobial formulations (food-contact surface SANITIZING solutions), before contact with FOOD; and (B) May not be cloth dried except that UTENSILS that have been air-dried may be polished with cloths that are maintained clean and dry.
2. The facility staff failed to store and maintain kitchen equipment in a clean and sanitary manner.
On 9/4/19 at approximately 13:05 during observation of the facility kitchen a metal pan was observed with multiple, various serving utensils such as ladles, spoons, etc. Observed was a significant amount of debris in the bottom of the metal pan as well as dried rice on some of the utensils. The Director of Dining Services agreed he observed it as well and asked the Executive Chef, (Employee E) to have facility dining staff to re-wash the items.
When the Chef was asked how often the pan and utensils are washed he stated the expectation is daily but they are not being washed daily.
On 9/4/19 it was observed that the electric meat slicer was open to air had dust as well as food crumbs on the surface. The Director of Dining Services, (Employee D) and the facility Executive Chef stated, we would have to re-clean it, there is a little bit of dust on it.
Observation of the sugar storage bin revealed heavy build up of grime on the lid. When the Director of Dining Services was asked about this observation he stated, it needs to be cleaned obviously. The Dining Director then asked the Executive Chef how often this is cleaned, the Executive Chef stated they clean it weekly. When the surveyor asked the Executive Chef if it had been cleaned in the past week, he stated no.
Review of the facility kitchen cleaning scheduled revealed, that the daily hot prep cleaning list stated daily cleaning, clean and cover slicer.
Review of facility document provided titled, Cold Prep Tasks stated, Sugar/flour bin lids sent to dish when needed.
According to the 2017 Food Code published by the U.S. Public Health Service, FDA U.S. Food & Drug Administration chapter 4, section 4-601.11 titled Equipment, Food-Contact Surfaces, Non-food Contact Surfaces, and Utensils read: (A) EQUIPMENT FOOD-CONTACT SURFACES and UTENSILS shall be clean to sight and touch. (B) The FOOD-CONTACT SURFACES of cooking EQUIPMENT and pans shall be kept free of encrusted grease deposits and other soil accumulations. (C) Non-FOOD-CONTACT SURFACES of EQUIPMENT shall be kept free of an accumulation of dust, dirt, FOOD residue, and other debris.
3. The facility staff failed to maintain a sanitizing solution that would sanitize food surface areas to prevent food contamination.
On 9/4/19 at 1:13 PM during an observation of the main kitchen in the food prep area located by the floor mixer, a red sanitizing bucket was observed with a cleaning cloth in the solution. The Director of Dining Services was asked what this was used for and he stated, it is used to wipe down food contact surfaces. The Director of Dining Services was then asked to check the sanitation level and it revealed a sanitation level of 0 ppm. The Director of Dining Services re-checked the solution in the red sanitizer bucket and when asked what it showed he stated less than 150 ppm. When asked what it should be, he stated at least 200 ppm.
On 9/4/19 at 1:30 PM during observation of the convalescent kitchen a red sanitizing bucket was observed. The Director of Dining Services again stated, it is used to wipe down food contact surfaces. The Director of Dining Services was then asked to check the sanitation level and it was observed to test less than 150 ppm, when the Director of Dining Services was asked, he stated it is a little weaker than I like. He then asked the staff member to replace it with new sanitizing solution.
On 09/05/19 at 11:16 AM an interview was conducted in the conference room in the presence of the survey team with Employee D, Director of Dining Service and Employee E, the Executive Chef. When asked the purpose of the red sanitation buckets, Employee D stated, it is used to sanitize the surfaces, countertops. When asked why you would want sanitizer in the bucket, Employee E stated, to properly be able to clean and sanitize at the proper ppm to make sure food contact surfaces are sanitized before use. When asked what the risk is of not using a proper parts per million sanitation solution, Employee E stated, the risk of bacteria and to prevent food borne illness. When asked about the red sanitizing buckets observed on 9/4/19, Employee E, agreed that the sanitizer buckets contained less than 150 ppm of sanitizing solution.
Review of the facility policy titled, Dietary services cleaning and sanitizing food contact surfaces read, Food service employee who prepare, serve food or who clean areas where foods is [sic] prepared and served will be trained on the proper procedures used to clean and sanitize food contact surfaces. Manufacturer's instructions regarding the use and maintenance of equipment, use of chemicals for cleaning and sanitizing food contact surfaces will be followed. Wash, rinse, and sanitize food contact surfaces of sinks, tables, cutting boards, equipment, utensils, thermometers, carts and equipment, before each use, between uses, any time contamination occurs or is suspected.
Review of a product specification document provided by the Director of Dining Services, titled Oasis 146 Multi-Quat Sanitizer read, to sanitize food contact surfaces, food processing equipment and other hard surfaces in (food processing locations, dairies or restaurants): Use Oasis 146 Multi-Quat sanitizer to sanitize pre-cleaned hard non-porous surfaces of food processing equipment, countertops in federally inspected restaurants. Apply a use-solution of (150-400 ppm [parts per million] active quat). Expose all surfaces to the sanitizing solution.
According to the 2017 Food Code published by the U.S. Public Health Service, FDA U.S. Food & Drug Administration chapter 3, section 3-304.14, page 77 stated: cloths in-use for wiping counters and other equipment surfaces shall be: held between uses in a chemical sanitizer solution at a concentration specified under 4-501.114
4. The facility staff failed to store food in a manner to maintain the integrity of the product.
On 9/4/19 at approximately 1:20 PM during observation of the walk-in freezer multiple items were observed to be in open, unclosed bags, and were not labeled to indicate what the product was or when it was placed in the freezer. Items were identified by the Director of Dining Services and the Executive Chef as breaded shrimp which contained no label or date. French Fries which were open to air and contained no label or date. Chicken tenders which were open to air and contained no label or date.
On 9/4/19 at 1:20 PM during the observation, when the Director of Dining Services was asked about the importance of labeling, he stated, it is important so that we know how fresh the product is, and if we can use it or not and if it is safe to use.
Review of the facility policy titled , Dietary Services Dating and Labeling Food Supplies Policy it read, All foods, including ready-to-eat and TCS foods, that are prepared on site, must be labeled and dated with the product name and expiration date. All foods, including ready-to-eat and TCS foods will be labeled and dated when opened. Products will be labeled by using a use by date.
Review of the facility policy titled Dietary Services Food Storage Policy stated, food must be stored in a way to prevent cross-contamination and to comply with all required regulations. Page 2 of this document stated, dates and labels should be facing forward to allow for easier identification and ease of following FIFO (first in, first out). Place food in covered containers or packages, except during cooling, and store in the walk-in refrigerator or cooler.
According to the 2017 Food Code published by the U.S. Public Health Service, FDA U.S. Food & Drug Administration chapter 3, section 3-302.12, pages 73-74 stated: Except for containers holding food that can be readily and unmistakably recognized such as dry pasta, working containers holding food or food ingredients that are removed from their original packages for use in the food service establishment, shall be identified with the common name of the food.
According to the 2017 Food Code published by the U.S. Public Health Service, FDA U.S. Food & Drug Administration chapter 3, section 3-302.15, page 64 stated: Package Integrity. FOOD packages shall be in good condition and protect the integrity of the contents so that the FOOD is not exposed to ADULTERATION or potential contaminants.
No further information was provided.