Parental distress and desire for information regarding long-term implications of pediatric cancer treatment

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Abstract

Background: Parents of children with cancer have unmet information needs regarding future limitations resulting from cancer or its treatment. Prior research has demonstrated that, in early care discussions, clinicians focus on the acute effects of therapy rather than long-term limitations, partly due to worries of causing distress. The validity of concerns regarding distress is unknown. In the current study, the authors evaluated parental distress associated with information regarding future limitations, and the extent to which distress is associated with information preferences. Methods: The authors surveyed 355 parents of children with cancer within 3 months of diagnosis, and the children’s physicians at Dana-Farber Cancer Institute/Boston Children’s Cancer and Blood Disorders Center and the Children’s Hospital of Philadelphia. The primary outcome was parental distress associated with information regarding long-term limitations. Results: Approximately 46% of parents found information regarding future limitations to be extremely or very upsetting. In multivariate analysis, parents were more likely to consider information regarding future limitations distressing if they also found prognostic information upsetting (odds ratio [OR], 5.36; P

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Greenzang, K. A., Cronin, A. M., Kang, T. I., & Mack, J. W. (2018). Parental distress and desire for information regarding long-term implications of pediatric cancer treatment. Cancer, 124(23), 4529–4537. https://doi.org/10.1002/cncr.31772

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