Incomplete and Inaccurate Medical Record for Pain Medication and Fluid Restriction
Summary
The deficiency involves the facility’s failure to maintain an accurate and complete medical record for a resident with end-stage renal disease on dialysis, COPD, and diabetes, whose daughter was the legal guardian and POA. The resident was admitted to hospice with an order for tramadol 50 mg every six hours as needed for severe pain, along with other medications, and the hospice medication cover sheet was signed by the guardian. A late-entry progress note dated several weeks later documented that tramadol was to be discontinued on the first day of hospice due to non-utilization, but the physician order actually discontinued tramadol nearly two weeks later. During this period, the MAR showed that the resident received a dose of tramadol for severe pain, and the ADON confirmed the discrepancy between the late-entry note and the actual discontinuation order. Further record review showed that the resident’s daughter revoked hospice services the day after hospice admission, and later expressed concerns about tramadol and possible addiction during a care conference. The regional clinical director stated that the guardian believed that revoking hospice would revert the resident’s medications to pre-hospice orders and acknowledged that tramadol should have been discontinued when the family voiced concerns, but it was not discontinued until several days after that conference. The regional clinical director also confirmed uncertainty as to why the former DON entered a late note indicating tramadol was discontinued on the first hospice day when the order was not actually discontinued at that time. These inconsistencies resulted in conflicting documentation regarding tramadol orders and administration in the resident’s medical record. A second component of the deficiency involved incomplete documentation of a prescribed total daily fluid restriction of 2000 ml, divided between dietary and nursing responsibilities. The physician’s order specified 1200 ml for dietary and 800 ml for nursing twice a day, but review of the MAR/TAR for March showed that on two separate days, the morning fluid restriction entries for both dietary and nursing were left blank, with no intake amounts or staff initials. The unit manager LPN confirmed that the MAR/TAR was not completed and should have been, and another LPN later confirmed she had implemented the fluid restriction on those days but acknowledged that the documentation boxes should have contained her initials and the intake amounts. These omissions were contrary to facility policies requiring that all medications, treatments, and services provided be fully documented in the medical record, including date, time, and care-specific details.
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