Failure to Provide Advance Directive Information and Document Resident Choices
Summary
The facility failed to inform residents or resident representatives and/or provide written information about the right to accept or refuse medical or surgical treatment and, at the resident’s option, formulate an advance directive. The deficiency affected 6 of 29 sampled residents: R8, R22, R45, R63, R110, and R123. Facility policy stated residents had the right to request, refuse, or discontinue treatment, participate in or refuse experimental research, and formulate an advance directive, and that information about refusing treatment and advance directives would be provided during admission in a manner easily understood by the resident or representative. For R8, the record showed intact cognition with a BIMS of 15/15, but the Resident Legal Document Checklist was incomplete and blank where advance directive information should have been indicated. R8’s MOST form was completed for CPR and full treatment, but sections for antibiotics and IV fluids were left blank, and there was no documented evidence of an advance directive. R8 stated he did not recall being asked about or provided information regarding a living will or advance directive. For R22, the Resident Legal Document Checklist was also blank, the MOST form showed DNR status with other sections left blank, and there was no documented evidence of an advance directive. R22 had severe cognitive impairment with a BIMS of 3/15, and the spouse stated R22 did not have a living will or advance directive and did not recall being asked or given information about one. For R45, the Resident Legal Document Checklist was blank, the MOST form showed DNR status and other treatment sections, but the patient preferences section was left blank, and there was no documented evidence of an advance directive. R45 had intact cognition with a BIMS of 15/15 and stated she did not recall being asked about or provided information regarding a living will or advance directive. For R63, the baseline care plan documented that the resident did not have an advance directive, while the MOST form showed CPR with limited additional interventions and blank sections for fluids/nutrition and antibiotics. The checklist indicated the resident had a POA and living will, but those documents were not located in the medical record or submitted for review. For R110, the MOST form showed DNR and comfort measures, but sections for antibiotics, fluids/nutrition, and patient preferences were blank; the facility’s Advance Directives/Informed Consent form marked a health care surrogate but left the date blank. For R123, the Resident Legal Document Checklist was blank, the MOST form showed CPR with full treatment, and the baseline care plan stated the resident had an advance directive and wished to formulate one, yet no advance directive was documented in the medical record. Interviews with the Admissions Coordinator, SSD, DON, and Administrator showed inconsistent understanding of whether the MOST form was an advance directive and confirmed that written information about advance directives was not provided to residents or representatives.
Penalty
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