Volume 30, Issue 5 pp. 747-755
PAPER

Longitudinal predictors of caregiver resilience outcomes at the end of childhood cancer treatment

Lamia P. Barakat

Corresponding Author

Lamia P. Barakat

Department of Pediatrics, Division of Oncology, Children's Hospital of Philadelphia, Perelman School of Medicine, Philadelphia, Pennsylvania, USA

Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA

Correspondence

Lamia P. Barakat, Division of Oncology, Children's Hospital of Philadelphia, 3615 Civic Center Blvd., ARC 1427A, Philadelphia, PA 19104, USA.

Email: [email protected]

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Rebecca E. Madden

Rebecca E. Madden

Department of Pediatrics, Division of Oncology, Children's Hospital of Philadelphia, Perelman School of Medicine, Philadelphia, Pennsylvania, USA

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Gabriela Vega

Gabriela Vega

Nemours Children's Health System, Orlando, Florida, USA

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Martha Askins

Martha Askins

Department of Pediatrics, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA

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Anne E. Kazak

Anne E. Kazak

Nemours Children's Health System, Orlando, Florida, USA

Sidney Kimmel Medical School, Thomas Jefferson University, Philadelphia, Pennsylvania, USA

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First published: 11 January 2021
Citations: 13

Abstract

Objective

Caregiver resilience in the context of childhood cancer treatment has been described using cross-sectional and retrospective studies, but little is known about prospective predictors of resilience outcomes. We examined associations of demographics, cancer-related variables, and intrapersonal and interpersonal factors at diagnosis (family psychosocial risk, perceived social support, and healthcare self-efficacy) and psychosocial services provided during treatment with caregiver resilience outcomes at the end of treatment.

Methods

For a study validating a family psychosocial risk screener, 314 primary caregivers completed the measures at diagnosis of their child (aged 0–17 years) and when cancer treatment ended. Resilience outcomes were ratings of distress, posttraumatic stress, and posttraumatic growth. Multiple regression analyses evaluated the relative contribution of hypothesized predictors.

Results

Caregivers endorsed clinically significant distress, moderate posttraumatic growth, and low posttraumatic stress based on norms. Posttraumatic growth was not associated with posttraumatic stress or distress, which were significantly associated with each other. Over and above resilience at diagnosis, family psychosocial risk was associated with resilience at the end of treatment. Perceived social support, healthcare self-efficacy, and psychosocial services provided demonstrated associations with resilience in univariate analyses, but demographics and cancer-related variables did not.

Conclusions

Resilience and family psychosocial risk at diagnosis were the strongest predictors of caregiver resilience outcomes at the end of the treatment. Intrapersonal and interpersonal predictors were weaker and varied by resilience measure. Consistent with psychosocial standards of care, broad evaluation of caregiver risks, resources, and resilience processes and outcomes is recommended at diagnosis and through the treatment trajectory including the end of treatment.

CONFLICT OF INTERESTS

The authors declare that there is no conflict of interests.

DATA AVAILABILITY STATEMENT

The data that support the findings of this study are available from the corresponding author upon reasonable request.

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