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Aging & mental health · Jun 2019
Exploring provider-surrogate communication during POLST discussions for individuals with advanced dementia.
- Hyejin Kim, Christine Bradway, Susan E Hickman, and Mary Ersek.
- a Emory Universiry Nell Hodgson Woodruff School of Nursing, Center for Nursing Excellence in Palliative Care , Atlanta , GA , USA.
- Aging Ment Health. 2019 Jun 1; 23 (6): 781-791.
ObjectivesThis qualitative descriptive study explored provider-surrogate communication during Physician Orders for Life-Sustaining Treatment (POLST) discussions for patients with advanced dementia.MethodsData from participant observations and audio-recordings of ten POLST discussions were analyzed using directed content analysis within the context of an existing conceptual model of Communication and Surrogate Decision Making.ResultsSurrogates primarily focused on making sense of the clinical information about life-sustaining treatments during POLST conversations. Providers delivered clinical information about the trajectory of dementia, life-sustaining treatments, and/or features of POLST. They also demonstrated emotional support, by valuing what the surrogate said, acknowledging the surrogate's emotions, listening carefully, understanding the patient as a person, and eliciting questions. However, providers rarely conveyed comprehensive information about the patient's current condition and end-of-life treatment options. Also, open communication of expectations and preferred decision-making roles was rarely observed during the discussions.ConclusionFindings highlight areas that require providers' attention to conduct effective communication, such as delivering comprehensive information about life-sustaining treatments including discussion of risks and benefits in the context of dementia. Findings also support the use of the conceptual model as a framework to examine provider-surrogate communication in the context of POLST discussions, advanced dementia, and non-hospital settings. Additional research is necessary to confirm these findings in larger, more diverse groups of patients, surrogates, and providers.
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