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Thursday 9 May 2013Plenary Session 1—Primary Care & Chronic Disease
  1. J Randall Curtis1,2,3
  1. 1A. Bruce Montgomery—American Lung Association Endowed Chair in Pulmonary and Critical Care Medicine
  2. 2Director, UW Palliative Care Center of Excellence
  3. 3Section Head, Pulmonary and Critical Care Medicine Harborview Medical Center, University of Washington, Seattle, Washington, USA


Description and Learning Objectives There are major challenges confronting clinicians, researchers, and policy-makers regarding improving communication about palliative and end-of-life care with patients and families. There is also mounting evidence that the intensity of care at the end-of-life is increasing, despite the fact that most patients report they would prefer not to die in high-intensity medical settings. Recent research suggests that improved communication about palliative and end-of-life care is associated with reduced intensity of care at the end of life, improved quality of life for patients and families, improved quality of dying for patients, and reduced psychological symptoms for families. Yet, the most effective and cost-effective ways to achieve improved communication are not clear. One important step to improving communication is being able to reliably measure the quality of this communication. We will review recent studies identifying some successful methods to measure the quality of communication about palliative and end-of-life care and some interventions that have been documented to successfully improve these communication skills. We will also review preliminary results of a recently completed randomised trial of a communication skills building workshop for physicians and nurse practitioners using patient-level outcomes data to assess outcomes. Finally, we will discuss methods to help clinicians develop a personalised approach for conducting communication about palliative and end-of-life care in their own clinical practice.

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