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Bereaved families’ experiences of end-of-life decision making for general medicine patients
  1. Felicity Moon1,2,
  2. Christine Mooney3,
  3. Fiona McDermott2,
  4. Alistair Miller4 and
  5. Peter Poon3
  1. 1Department of Social Work, Monash Health, Clayton, Victoria, Australia
  2. 2Department of Social Work, Monash University, Caulfield East, Victoria, Australia
  3. 3Department of Supportive & Palliative Care, Monash Health, Clayton, Victoria, Australia
  4. 4Department of General Medicine, Monash Health, Clayton, Victoria, Australia
  1. Correspondence to Felicity Moon, Department of Social Work, Monash Health, Clayton, VIC 3168, Australia; Felicity.moon{at}monash.edu

Abstract

Background Family involvement in decision making for hospitalised patients is associated with improved end-of-life care. Yet, these discussions can be challenging for physicians and families and associated with distress, confusion and conflict. There is a need to understand how best to support families involved in decisions regarding the transition from active to palliative treatment in hospital settings.

Aim To explore bereaved families’ experiences of end-of-life decision making for general medicine patients.

Design A qualitative exploratory study framed by social constructionism using semistructured interviews and thematic analysis.

Setting and participants The general medicine units of one large public hospital in Melbourne, Australia. We recruited 28 bereaved family members of patients who had received end-of-life care.

Findings Patients and families depended on physicians to explain clinical complexity and treatment beneficence; however, trust in medical judgement was mediated by participant’s own interpretations of clinical progress. Families sought to be respected as advocates and experienced distress if physicians disregarded their perspectives and insight concerning patient preferences. Ideally, families supported patients to express their preferences to physicians. Otherwise, families contextualised treatment decisions through their knowledge of patient’s values and quality of life. Families often felt burdened by or excluded from medical decision making and experienced distress and confusion regarding their rights to request or refuse treatment.

Conclusion Our study highlights how families contribute to decision making to ensure end-of-life care treatments reflect patient preferences. Physicians can ease families’ distress around treatment withdrawal by providing a meaningful explanation of complex clinical issues, clarifying decision-making roles and acknowledge families’ desire to protect and advocate for their loved one.

  • hospital care
  • terminal care
  • clinical decisions
  • communication

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Footnotes

  • Contributors FMo and CM conceived the research proposal. FMo, CM and FMc designed the research approach. FMo collected the data. All authors analysed the data. FMo and CM drafted the manuscript with feedback from PP and FMc.

  • Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.

  • Competing interests None declared.

  • Patient consent for publication Not required.

  • Ethics approval Monash Health HREC 15343A.

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Data availability statement Data are available on reasonable request. Summary of deidentified transcripts. Felicity.moon@monashhealth.org.

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