Literature DB >> 30880372

Decision-making in childhood cancer: parents' and adolescents' views and perceptions.

Eden G Robertson1,2, Claire E Wakefield3,4, Joanne Shaw5, Anne-Sophie Darlington6, Brittany C McGill3,4, Richard J Cohn3,4, Joanna E Fardell3,4.   

Abstract

PURPOSE: Few studies have addressed the way in which families of children with cancer make treatment decisions, and how we can meet parents' and young peoples' decisional involvement needs. We aimed to explore parents' and adolescents' views and perceptions of making medical decisions in pediatric oncology.
METHODS: We conducted semi-structured interviews with 25 parents of children diagnosed with cancer in the past 12 months, and 5 adolescents diagnosed in the past 12 months. Our interview schedule was underpinned by Elwyn and Miron-Shatz's decision-making model. The model acknowledges the deliberation (process of coming to a decision) and determination (making a choice) phases of decision-making. We conducted a thematic analysis.
RESULTS: Our findings indicate that information provision is not enough to facilitate parents' decision-making involvement. Many parents sought additional information to meet their individual needs and preferences. While many parents and young people desired decisional involvement, they trusted the doctors to make treatment decisions. Feelings of distress, inadequacy, and lack of choice impacted decision-making participation. Regardless, many parents in our study were satisfied with treatment decisions, but this was largely dependent on positive treatment outcomes.
CONCLUSION: Our study contributes to understanding how families of a child with cancer make treatment decisions. Families tend to rely on doctors to make treatment decisions, but often seek additional information to help them feel involved in the decision process. Findings highlight that decision-making in pediatric oncology should focus on involving families in the deliberation phase, rather than just determination of choice.

Entities:  

Keywords:  Decision-making; Experiences; Information; Parents; Pediatric; Preferences; Qualitative

Mesh:

Year:  2019        PMID: 30880372     DOI: 10.1007/s00520-019-04728-x

Source DB:  PubMed          Journal:  Support Care Cancer        ISSN: 0941-4355            Impact factor:   3.603


  42 in total

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4.  Suggestions from adolescents, young adults, and parents for improving informed consent in phase 1 pediatric oncology trials.

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Review 5.  What is known about parents' treatment decisions? A narrative review of pediatric decision making.

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8.  Parents' views on information in childhood cancer care.

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Journal:  Cancer       Date:  2015-09-08       Impact factor: 6.860

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7.  Perception of Pediatric Oncological Patients and Theirzzm321990Parents/Guardians about a Hospital Oral Health Program:zzm321990A Qualitative Study

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8.  The Childhood Cancer Centre Is Coming Home: Experiences of Hospital-Based Home Care.

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10.  COVID-19 and children with cancer: Parents' experiences, anxieties and support needs.

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Journal:  Pediatr Blood Cancer       Date:  2020-11-21       Impact factor: 3.838

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