Defining the Elements of Early Palliative Care That Are Associated With Patient-Reported Outcomes and the Delivery of End-of-Life Care

Michael Hoerger, Joseph A Greer, Vicki A Jackson, Elyse R Park, William F Pirl, Areej El-Jawahri, Emily R Gallagher, Teresa Hagan, Juliet Jacobsen, Laura M Perry, Jennifer S Temel

Research output: Contribution to journalArticlepeer-review

Abstract

Purpose We describe the key elements of early palliative care (PC) across the illness trajectory and examine whether visit content was associated with patient-reported outcomes and end-of-life care. Methods We performed a secondary analysis of patients with newly diagnosed advanced lung or noncolorectal GI cancer (N = 171) who were randomly assigned to receive early PC. Participants attended at least monthly visits with board-certified PC physicians and advanced practice nurses at Massachusetts General Hospital. PC clinicians completed surveys documenting visit content after each encounter. Patients reported quality of life (Functional Assessment of Cancer Therapy-General) and mood (Hospital Anxiety and Depression Scale and Patient Health Questionnaire-9) at baseline and 24 weeks. End-of-life care data were abstracted from the electronic health record. We summarized visit content over time and used linear and logistic regression to identify whether the proportion of visits addressing a content area was associated with patient-reported outcomes and end-of-life care. Results We analyzed data from 2,921 PC visits, most of which addressed coping (64.2%) and symptom management (74.5%). By 24 weeks, patients who had a higher proportion of visits that addressed coping experienced improved quality of life ( P = .02) and depression symptoms (Depression subscale of the Hospital Anxiety and Depression Scale, P = .002; Patient Health Questionnaire-9, P = .004). Patients who had a higher proportion of visits address treatment decisions were less likely to initiate chemotherapy ( P = .02) or be hospitalized ( P = .005) in the 60 days before death. Patients who had a higher proportion of visits addressing advance care planning were more likely to use hospice ( P = .03). Conclusion PC clinicians' focus on coping, treatment decisions, and advance care planning is associated with improved patient outcomes. These data define the key elements of early PC to enable dissemination of the integrated care model.

Original languageEnglish
Pages (from-to)1096-1102
JournalJournal of clinical oncology : official journal of the American Society of Clinical Oncology
Volume36
Issue number11
DOIs
Publication statusPublished - 2018 Apr 10
Externally publishedYes

Free keywords

  • Adaptation, Psychological
  • Advance Care Planning
  • Affect
  • Aged
  • Boston
  • Clinical Decision-Making
  • Cost of Illness
  • Delivery of Health Care, Integrated/methods
  • Electronic Health Records
  • Female
  • Gastrointestinal Neoplasms/diagnosis
  • Humans
  • Lung Neoplasms/diagnosis
  • Male
  • Middle Aged
  • Palliative Care/methods
  • Patient Participation
  • Patient Reported Outcome Measures
  • Prospective Studies
  • Quality of Life
  • Randomized Controlled Trials as Topic
  • Terminal Care/methods
  • Time Factors
  • Treatment Outcome

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