Delayed consultant follow-up and improper CGM monitoring
Summary
The facility failed to follow professional standards of practice for a resident with Parkinson's disease and dementia when a neurology consultant recommended a trial of Carbidopa/Levodopa, but the Nurse Practitioner did not receive or review the consultant summary in a timely manner. The resident returned from the neurology appointment with documentation noting deterioration in function and memory and recommending Carbidopa/Levodopa 25/100 mg twice daily, then three times daily. Nursing documentation indicated the NP was notified the evening of the appointment, but the medication was not initiated until 22 days later after the resident's family member brought the neurology report to the facility and the NP reviewed it. The facility also failed to obtain and review a urology consultant report for a resident with benign prostatic hyperplasia, urinary tract infections, and urinary retention. The NP had written an order requesting the urology visit summary be obtained and placed in the provider book for review, and nursing documentation showed a call was made to the urology office requesting the report. However, the report was not present in the medical record when reviewed by surveyors, and the consultant note from the 12/12/25 visit was not received in the building until 57 days after the visit. The urology note included recommendations related to recurrent urinary tract infections, including cranberry supplements and consideration of suppressive antibiotics and methenamine hippurate. The facility failed to monitor and manage a resident's continuous glucose monitor according to the manufacturer's instructions and had no policy for CGM use. The resident, who was legally blind and had diabetes mellitus with insulin use, was being monitored by staff using the CGM system rather than finger sticks, but staff members stated they did not know who monitored the sensors, who changed them, how often they were changed, or where supplies came from. The DON stated the facility did not use CGM systems in the building and was not aware the resident's blood glucose was being monitored only through the CGM. The resident stated the sensor was changed every two weeks by self, but did not demonstrate cleaning the site or rotating the sensor location, and staff did not know the care or maintenance requirements for the device.
Penalty
Resources
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