• Nicholas Braus, Toby C Campbell, Kristine L Kwekkeboom, Susan Ferguson, Carrie Harvey, Anna E Krupp, Tara Lohmeier, Michael D Repplinger, Ryan P Westergaard, Elizabeth A Jacobs, Kate Ford Roberts, and William J Ehlenbach.
• Department of Medicine, University of Wisconsin School of Medicine and Public Health, Madison, WI, USA.
• Intensive Care Med. 2016 Jan 1; 42 (1): 546254-62.

PurposeTo evaluate the effects of a palliative care intervention on clinical and family outcomes, and palliative care processes.MethodsProspective, before-and-after interventional study enrolling patients with high risk of mortality, morbidity, or unmet palliative care needs in a 24-bed academic intensive care unit (ICU). The intervention involved a palliative care clinician interacting with the ICU physicians on daily rounds for high-risk patients.ResultsOne hundred patients were enrolled in the usual care phase, and 103 patients were enrolled during the intervention phase. The adjusted likelihood of a family meeting in ICU was 63% higher (RR 1.63, 95% CI 1.14-2.07, p = 0.01), and time to family meeting was 41% shorter (95% CI 52-28% shorter, p < 0.001). Adjusted ICU length of stay (LOS) was not significantly different between the two groups (6% shorter, 95% CI 16% shorter to 4% longer, p = 0.22). Among those who died in the hospital, ICU LOS was 19% shorter in the intervention (95% CI 33-1% shorter, p = 0.043). Adjusted hospital LOS was 26% shorter (95% CI 31-20% shorter, p < 0.001) with the intervention. Post-traumatic stress disorder (PTSD) symptoms were present in 9.1% of family respondents during the intervention versus 20.7% prior to the intervention (p = 0.09). Mortality, family depressive symptoms, family satisfaction and quality of death and dying did not significantly differ between groups.ConclusionsProactive palliative care involvement on ICU rounds for high-risk patients was associated with more and earlier ICU family meetings and shorter hospital LOS. We did not identify differences in family satisfaction, family psychological symptoms, or family-rated quality of dying, but had limited power to detect such differences.

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