Georges Naasan1, Nicole D Boyd1, Krista L Harrison1, Sarah B Garrett1, Talita D'Aguiar Rosa1, Brenda Pérez-Cerpa1, Shamiel McFarlane1, Bruce L Miller1, Christine S Ritchie1. 1. Global Brain Health Institute (GN, KLH, TDAR, BP-C, SM, BLM, CSR), University of California, San Francisco; Department of Neurology (GN, BLM), Mount Sinai Hospitals, Ichan School of Medicine, New York, NY; Division of Geriatrics (NDB, KLH, SBG), Department of Medicine, University of California, San Francisco; Philip R. Lee Institute for Health Policy Studies (SBG), University of California, San Francisco, CA; Department of Neurology (TDAR), University of Louisville, Kentucky; Hospital Civil de Guadalajara (Hospital Civil Fray Antonio Alcade) (BP-C), Guadalajara, Jalisco, Mexico; and The Mongan Institute and the Division of Palliative Care and Geriatric Medicine (CSR), Department of Medicine, Massachusetts General Hospital, Boston, MA.
Abstract
Background and Objectives: To determine the frequency of and challenges to documentation of advance care planning (ACP) in people with dementia, we conducted a chart review of 746 deceased patients seen at a tertiary memory care center between 2012 and 2017. Methods: The rates of documented advance directives (ADs), Physician Order for Life-Sustaining Treatment (POLST), and Do Not Resuscitate (DNR) status were calculated from review of institutional electronic health records. Regression analysis was used to determine associations between ACP documentation and patient characteristics. Results: At the time of death, approximately half of the patients had a documented AD and/or DNR status and 37% had a documented POLST; 30% of patients did not have any ACP documentation. Whereas most of the ADs were documented more than 5 years before time of death, POLST and DNR status were documented more frequently within 2 years of time of death. People who presented to clinic at a younger age and who primarily spoke English were more likely to have documented ADs. People living in zip codes with lower household incomes were 2-4.5 times less likely to have a POLST or DNR documentation. Discussion: ACP is underutilized in people with dementia, even among those seen in a specialty memory care center. ACP should be introduced early on for people with dementia to ensure patients have a voice in their care.
Background and Objectives: To determine the frequency of and challenges to documentation of advance care planning (ACP) in people with dementia, we conducted a chart review of 746 deceased patients seen at a tertiary memory care center between 2012 and 2017. Methods: The rates of documented advance directives (ADs), Physician Order for Life-Sustaining Treatment (POLST), and Do Not Resuscitate (DNR) status were calculated from review of institutional electronic health records. Regression analysis was used to determine associations between ACP documentation and patient characteristics. Results: At the time of death, approximately half of the patients had a documented AD and/or DNR status and 37% had a documented POLST; 30% of patients did not have any ACP documentation. Whereas most of the ADs were documented more than 5 years before time of death, POLST and DNR status were documented more frequently within 2 years of time of death. People who presented to clinic at a younger age and who primarily spoke English were more likely to have documented ADs. People living in zip codes with lower household incomes were 2-4.5 times less likely to have a POLST or DNR documentation. Discussion: ACP is underutilized in people with dementia, even among those seen in a specialty memory care center. ACP should be introduced early on for people with dementia to ensure patients have a voice in their care.
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