Rollins School of Public Health, Emory University, Atlanta, Georgia, USA.
Aflac Cancer and Blood Disorders Center at Children's Healthcare of Atlanta, Atlanta, Georgia, USA.
Pediatr Blood Cancer. 2023 Aug;70(8):e30480. doi: 10.1002/pbc.30480. Epub 2023 Jun 3.
Childhood 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.
As 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.
All 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%).
Clinic 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.
儿童癌症幸存者需要定期进行长期的生存者护理。儿童肿瘤学组(COG)建议儿科患者在癌症治疗完成后 2 年开始接受针对晚期影响的基于证据的持续监测。然而,至少有三分之一的幸存者没有参与长期生存者护理。本研究通过儿科癌症幸存者诊所代表的视角评估了后续生存者护理的促进因素和障碍。
作为一项混合实施有效性试验的一部分,12 个参与的儿科癌症幸存者诊所的代表完成了一项关于站点特征的调查,并对其机构提供幸存者护理的促进因素和障碍进行了半结构化访谈。访谈以社会生态学模型(SEM)框架为基础,并利用鱼骨图来了解促进和阻碍幸存者护理的因素。我们进行了描述性统计和对访谈记录的主题分析,以创建两个元鱼骨图。
所有参与的诊所(N=12)都已经存在至少 5 年(平均值=15,中位数=13,范围=3-31),其中一半(n=6,50%)报告每年诊治的幸存者超过 300 人。在鱼骨图中,最主要的促进因素在组织的 SEM 领域,具体包括熟悉的工作人员(n=12,100%)、资源利用(n=11,92%)、专门的生存者工作人员(n=10,83%)和诊所流程(n=10,83%)。常见的障碍涉及组织、社区和政策领域,包括前往诊所的距离/交通(n=12,100%)、技术限制(n=11,92%)、预约问题(n=11,92%)和资金/保险不足(n=11,92%)。
诊所工作人员和提供者的看法对于理解与儿科癌症幸存者诊所的生存者护理提供相关的多层次背景问题非常重要。未来的研究可以帮助开发促进癌症幸存者后续护理的教育、流程和服务。