Literature DB >> 17187541

Parents' reactions to participating in interviews about end-of-life decision making.

Kelly Nicole Michelson1, Tracy K Koogler, Kathleen Skipton, Christine Sullivan, Joel Frader.   

Abstract

BACKGROUND: Although in-depth interviewing is well suited to studying the sensitive topic of end-of-life decision making, no reports have been published assessing the effects on parents of participating in interviews regarding end-of-life decision making for critically ill children.
OBJECTIVE: To examine the reactions of pediatric intensive care unit (PICU) patients' parents to interviews on end-of-life decision making for their child.
METHODS: We conducted semistructured interviews on end-of-life decision making with PICU patients' parents from two tertiary care PICUs. We approached 117 parents of 102 patients. Seventy-four parents (63%) of 69 patients participated.
RESULTS: Forty-three parents (61%) described the interview as "a good experience," 20 (29%) as "a neutral experience," and 1 (1%) as "a bad experience." The parent who judged the interview negatively stated that, "It bothers me a little bit because my son is [out] there having difficulties and I'm in here and not out there." Fifty-four of 59 parents (92%) said they would participate in another similar interview. Most parents (92%) felt the medical community should continue research on end-of-life decision making. Themes identified from the responses included: emotional reaction to the interviews; exposure to end-of-life decision-making issues; impact on parents' views; and impact on future end-of-life decision making. Parents' comments suggested that many perceived the interviews as beneficial.
CONCLUSIONS: This study demonstrates the willingness of many parents of critically ill children to participate in study interviews regarding end-of-life decision making, a topic that most parents felt was important and warranted more research.

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Year:  2006        PMID: 17187541     DOI: 10.1089/jpm.2006.9.1329

Source DB:  PubMed          Journal:  J Palliat Med        ISSN: 1557-7740            Impact factor:   2.947


  4 in total

1.  The Benefits and Burdens of Pediatric Palliative Care and End-of-Life Research: A Systematic Review.

Authors:  Meaghann S Weaver; Kim Mooney-Doyle; Katherine Patterson Kelly; Kathleen Montgomery; Amy R Newman; Christine A Fortney; Cynthia J Bell; Jessica L Spruit; Melissa Kurtz Uveges; Lori Wiener; Cynthia M Schmidt; Vanessa N Madrigal; Pamela S Hinds
Journal:  J Palliat Med       Date:  2019-03-05       Impact factor: 2.947

2.  Parental views on withdrawing life-sustaining therapies in critically ill children.

Authors:  Kelly Nicole Michelson; Tracy Koogler; Christine Sullivan; María del Pilar Ortega; Emily Hall; Joel Frader
Journal:  Arch Pediatr Adolesc Med       Date:  2009-11

3.  Do-not-resuscitate orders and/or hospice care, psychological health, and quality of life among children/adolescents with acquired immune deficiency syndrome.

Authors:  Maureen E Lyon; Paige L Williams; Elizabeth R Woods; Nancy Hutton; Anne M Butler; Erica Sibinga; Michael T Brady; James M Oleske
Journal:  J Palliat Med       Date:  2008-04       Impact factor: 2.947

4.  Caring Decisions: The Development of a Written Resource for Parents Facing End-of-Life Decisions.

Authors:  Vicki Xafis; Lynn Gillam; Jenny Hynson; Jane Sullivan; Mary Cossich; Dominic Wilkinson
Journal:  J Palliat Med       Date:  2015-09-29       Impact factor: 2.947

  4 in total

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