Clinic reported facilitators and barriers to pediatric cancer survivor care delivery among survivorship clinics: A fishbone analysis

Author:

Krauss Victoria1ORCID,Mertens Ann23ORCID,Marchak Jordan Gilleland23,Haardörfer Regine1,Meacham Lillian R.23,Lewis Rebecca Williamson2ORCID,Wright Robert1,Adisa Oyinda1,Kommajosula Apoorva1,Escoffery Cam1

Affiliation:

1. Rollins School of Public Health Emory University Atlanta Georgia USA

2. Aflac Cancer and Blood Disorders Center at Children's Healthcare of Atlanta Atlanta Georgia USA

3. Department of Pediatrics Emory University Atlanta Georgia USA

Abstract

AbstractBackgroundChildhood cancer survivors need regular, long‐term survivor care. The Children's Oncology Group (COG) recommends that pediatric patients receive ongoing, evidence‐based surveillance for late effects, beginning 2 years after the completion of cancer therapy. However, at least a third of survivors are not engaging in long‐term survivorship care. This study assessed facilitators and barriers to follow‐up survivorship care through the perspectives of pediatric cancer survivor clinic representatives.MethodsAs part of a hybrid implementation‐effectiveness trial, a representative from 12 participating pediatric cancer survivor clinics completed a survey about site characteristics and a semi‐structured interview on facilitators and barriers to survivor care delivery at their institution. Interviews were grounded in the socio‐ecological model (SEM) framework and utilized a fishbone diagram to understand what facilitates and impedes survivor care. We ran descriptive statistics and conducted thematic analyses of the interview transcripts to create two meta‐fishbone diagrams.ResultsAll participating clinics (N = 12) have existed for at least 5 years (mean = 15, median = 13, range = 3–31), and half (n = 6, 50%) reported seeing more than 300 survivors annually. In the fishbone diagram, the top facilitators were in the SEM domain of organization, specifically with familiar staff (n = 12, 100%), resource utilization (n = 11, 92%), dedicated survivorship staff (n = 10, 83%), and clinic processes (n = 10, 83%). Common barriers were across the domains of organization, community, and policy, which included distance/transportation to the clinic (n = 12, 100%), technology limits (n = 11, 92%), scheduling issues (n = 11, 92%), and insufficient funding/insurance (n = 11, 92%).ConclusionClinic staff and provider perceptions are instrumental in understanding multilevel contextual issues related to survivor care delivery for pediatric cancer survivor clinics. Future research can aid in developing education, processes, and services to promote cancer survivor follow‐up care.

Funder

National Cancer Institute

Centers for Disease Control and Prevention

Winship Cancer Institute

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Reference27 articles.

1. Cancer facts & figures 2022.American Cancer Society;2021.

2. COG.Long‐term follow‐up guidelines for survivors of childhood adolescent and young adult cancers. Version 5.0.Children's Oncology Group (COG);2018.

3. Patterns of Loss to Follow-Up Care Among Childhood Cancer Survivors

4. Survivor clinic attendance among pediatric- and adolescent-aged survivors of childhood cancer

5. Longitudinal risk-based health care for adult survivors of childhood cancer

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