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"Trying to Be a Good Parent" As Defined by Interviews with Parents Who Made Phase I, Terminal Care, and Resuscitation Decisions for Their Children

Overview
Journal J Clin Oncol
Specialty Oncology
Date 2009 Oct 7
PMID 19805693
Citations 93
Authors
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Abstract

Purpose: When a child's cancer progresses beyond current treatment capability, the parents are likely to participate in noncurative treatment decision making. One factor that helps parents to make these decisions and remain satisfied with them afterward is deciding as they believe a good parent would decide. Because being a good parent to a child with incurable cancer has not been formally defined, we conducted a descriptive study to develop such a definition.

Methods: In face-to-face interviews, 62 parents who had made one of three decisions (enrollment on a phase I study, do not resuscitate status, or terminal care) for 58 patients responded to two open-ended questions about the definition of a good parent and about how clinicians could help them fulfill this role. For semantic content analysis of the interviews, a rater panel trained in this method independently coded all responses. Inter-rater reliability was excellent.

Results: Among the aspects of the definition qualitatively identified were making informed, unselfish decisions in the child's best interest, remaining at the child's side, showing the child that he is cherished, teaching the child to make good decisions, advocating for the child with the staff, and promoting the child's health. We also identified 15 clinician strategies that help parents be a part of making these decisions on behalf of a child with advanced cancer.

Conclusion: The definition and the strategies may be used to guide clinicians in helping parents fulfill the good parent role and take comfort afterward in having acted as a good parent.

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References
1.
Catlin E, Guillemin J, Thiel M, Hammond S, Wang M, ODonnell J . Spiritual and religious components of patient care in the neonatal intensive care unit: sacred themes in a secular setting. J Perinatol. 2002; 21(7):426-30. DOI: 10.1038/sj.jp.7210600. View

2.
WHARTON R, Levine K, Buka S, EMANUEL L . Advance care planning for children with special health care needs: a survey of parental attitudes. Pediatrics. 1996; 97(5):682-7. View

3.
Hinds P, Oakes L, Furman W, Foppiano P, Olson M, Quargnenti A . Decision making by parents and healthcare professionals when considering continued care for pediatric patients with cancer. Oncol Nurs Forum. 1997; 24(9):1523-8. View

4.
Swinney R, Yin L, Lee A, Rubin D, Anderson C . The role of support staff in pediatric palliative care: their perceptions, training, and available resources. J Palliat Care. 2007; 23(1):44-50. View

5.
Tomlinson D, Capra M, Gammon J, Volpe J, Barrera M, Hinds P . Parental decision making in pediatric cancer end-of-life care: using focus group methodology as a prephase to seek participant design input. Eur J Oncol Nurs. 2005; 10(3):198-206. DOI: 10.1016/j.ejon.2005.11.003. View