Literature DB >> 12853551

Dying in the ICU: perspectives of family members.

Daren K Heyland1, Graeme M Rocker, Christopher J O'Callaghan, Peter M Dodek, Deborah J Cook.   

Abstract

OBJECTIVE: To describe the perspectives of family members to the care provided to critically ill patients who died in the ICU.
DESIGN: Multicenter, prospective, observational study.
SETTING: Six university-affiliated ICUs across Canada.
METHODS: Patients who received mechanical ventilation for > 48 h and who died in the ICU were eligible for this study. Three to four weeks after the patient's death, we mailed a validated questionnaire to one selected family member who made at least one visit to the patient in the ICU. We obtained self-rated levels of satisfaction with key aspects of end-of-life care, communication, and decision making, and the overall ICU experience. MAIN
RESULTS: Questionnaires were mailed to 413 family members; 256 completed surveys were returned (response rate, 62.0%). In the final hours before the death of the patient, family members reported that patients were "totally comfortable" (34.8%), "very comfortable" (23.8%), or "mostly comfortable" (32.0%). Family members felt "very supported" (57.0%) and "supported" (30.7%) by the health-care team. Most (82.0%) believed that the patient's life was neither prolonged nor shortened unnecessarily. Most family members (90.4%) preferred some form of shared decision making. Overall, 52% of families rated their satisfaction with care as "excellent," 31% rated care as "very good," 10% as "good," 4% as "fair," and 2% as "poor." Overall satisfaction with end-of-life care was significantly associated with completeness of information received by the family member, respect and compassion shown to patient and family member, and satisfaction with amount or level of health care received.
CONCLUSIONS: The majority of families of patients who died in participating ICUs were satisfied with the end-of-life care provided. Adequate communication, good decision making, and respect and compassion shown to both the dying patient and their family are key determinants to family satisfaction.

Entities:  

Mesh:

Year:  2003        PMID: 12853551     DOI: 10.1378/chest.124.1.392

Source DB:  PubMed          Journal:  Chest        ISSN: 0012-3692            Impact factor:   9.410


  39 in total

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Review 2.  Proxy evaluation of health-related quality of life: a conceptual framework for understanding multiple proxy perspectives.

Authors:  A Simon Pickard; Sara J Knight
Journal:  Med Care       Date:  2005-05       Impact factor: 2.983

3.  Attitudes of European physicians, nurses, patients, and families regarding end-of-life decisions: the ETHICATT study.

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5.  The complex roles of relatives in end-of-life decision-making: an ethical analysis.

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Journal:  HEC Forum       Date:  2007-12

6.  Re-visiting visiting hours.

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7.  In their own words: patients and families define high-quality palliative care in the intensive care unit.

Authors:  Judith E Nelson; Kathleen A Puntillo; Peter J Pronovost; Amy S Walker; Jennifer L McAdam; Debra Ilaoa; Joan Penrod
Journal:  Crit Care Med       Date:  2010-03       Impact factor: 7.598

Review 8.  Measuring Experience With End-of-Life Care: A Systematic Literature Review.

Authors:  Jessica Penn Lendon; Sangeeta C Ahluwalia; Anne M Walling; Karl A Lorenz; Oluwatobi A Oluwatola; Rebecca Anhang Price; Denise Quigley; Joan M Teno
Journal:  J Pain Symptom Manage       Date:  2014-12-24       Impact factor: 3.612

9.  Assessment of satisfaction with care among family members of survivors in a neuroscience intensive care unit.

Authors:  David Y Hwang; Daniel Yagoda; Hilary M Perrey; Tara M Tehan; Mary Guanci; Lillian Ananian; Paul F Currier; J Perren Cobb; Jonathan Rosand
Journal:  J Neurosci Nurs       Date:  2014-04       Impact factor: 1.230

10.  Family satisfaction in the ICU: why should ICU clinicians care?

Authors:  Anneliese M Schleyer; J Randall Curtis
Journal:  Intensive Care Med       Date:  2013-04-24       Impact factor: 17.440

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