End-of-Life Decision Making by Adolescents, Parents, and Healthcare Providers in Pediatric Oncology
Top Cited Papers
- 1 April 2001
- journal article
- review article
- Published by Wolters Kluwer Health in Cancer Nursing
- Vol. 24 (2) , 122-134
- https://doi.org/10.1097/00002820-200104000-00007
Abstract
Participating in end-of-life decisions is life altering for adolescents with incurable cancer, their families, and their healthcare providers. However, no empirically developed and validated guidelines to assist patients, parents, and healthcare providers in making these decisions exist. The purpose of the work reported here was to use three sources (the findings of three studies on decision making in pediatric oncology, published literature, and recommendations from professional associations) to develop guidelines for end-of-life decision making in pediatric oncology. The study designs include a retrospective, descriptive design (Study 1); a prospective, descriptive design (Study 2); and a cross-sectional, descriptive design (Study 3). Settings for the pediatric oncology studies included a pediatric catastrophic illness research hospital located in the Midsouth (Studies 1 and 2); and that setting plus a children’s hospital in Australia and one in Hong Kong (Study 3). Study samples included 39 guardians and 21 healthcare providers (Study 1); 52 parents, 10 adolescents, and 22 physicians (Study 2); and 43 parents (Study 3). All participants in the studies responded to six open-ended questions. A semantic content analysis technique was used to analyze all interview data. Four nurses independently coded each interview; interrater reliability per code ranged from 68% to 100% across studies. The most frequently reported influencing factors were “information on the health and disease status of the patient,” “all curative options having been attempted,” “trusting the healthcare team,” and “feeling support from the healthcare provider.” The agreement across studies regarding influencing factors provides the basis for the research-based guidelines for end-of-life decision making in pediatric oncology. The guidelines offer assistance with end-of-life decision making in a structured manner that can be formally evaluated and individualized to meet patient and family needs.Keywords
This publication has 39 references indexed in Scilit:
- Medical end-of-life decisions made for neonates and infants in the NetherlandsThe Lancet, 1997
- Foregoing intensive care treatment in newborn infants with extremely poor prognoses:The Journal of Pediatrics, 1996
- Involvement in Health Care Decisions: Parents and Children with Chronic IllnessJournal of Family Nursing, 1996
- The 1992 APON Delphi Study to Establish Research Priorities for Pediatric Oncology NursingJournal of Pediatric Oncology Nursing, 1994
- Do-not-resuscitate orders in a childrenʼs hospitalCritical Care Medicine, 1993
- Agreement between patients and their self-selected surrogates on difficult medical decisionsArchives of internal medicine (1960), 1992
- Patient, parent, and physician perspectives on pediatric oncology roundsThe Journal of Pediatrics, 1988
- Experimental Chemotherapy in Children with Cancer—A Parent'S ViewPediatric Hematology and Oncology, 1987
- Decisions to Withdraw Life Support in the Neonatal Intensive Care UnitClinical Pediatrics, 1983
- On the Elicitation of Preferences for Alternative TherapiesNew England Journal of Medicine, 1982