Departments of Hematology and IQ Health, Radboud University Medical Centre, Nijmegen, The Netherlands.
Pediatrics, Department of Clinical Sciences Lund, Lund University, Skåne University Hospital, Lund, Sweden.
Cancer Med. 2024 Oct;13(20):e70225. doi: 10.1002/cam4.70225.
Childhood cancer survivors face high risks of adverse late health effects. Long-term follow-up care for childhood cancer survivors is crucial to improve their health and quality of life. However, implementation remains a challenge. To support implementation of high-quality long-term follow-up care, we explored expected barriers and facilitators for establishing this follow-up care among healthcare providers from four European clinics.
A qualitative study was conducted using four focus groups comprising 30 healthcare providers in total. The semi-structured interview guide was developed based on the Grol and Wensing framework. Data was analyzed following a thematic analysis, combining both inductive and deductive approaches to identify barriers and facilitators across the six levels of Grol and Wensing: innovation, professional, patient, social, organizational and economic and political.
Most barriers were identified on the organizational level, including insufficient staff, time, capacity and psychosocial support. Other main barriers included limited knowledge of late effects among healthcare providers outside the long-term follow-up care team, inability of some survivors to complete the survivor questionnaire and financial resources. Main facilitators included motivated healthcare providers and survivors, a skilled hospital team, collaborations with important stakeholders like general practitioners, and psychosocial care facilities, utilization of the international collaboration and reporting long-term follow-up care results to convince hospital managers.
This study identified several factors for successful implementation of long-term follow-up care for childhood cancer survivors. Our findings showed that specific attention should be given to knowledge, capacity, and financial issues, along with addressing psychosocial issues of survivors.
儿童癌症幸存者面临着诸多不良健康影响的高风险。对儿童癌症幸存者进行长期随访护理对于改善其健康和生活质量至关重要。然而,实施长期随访护理仍然面临挑战。为了支持高质量长期随访护理的实施,我们探索了在来自四个欧洲诊所的医疗保健提供者中建立这种随访护理的预期障碍和促进因素。
采用基于 Grol 和 Wensing 框架的 4 个焦点小组,对总共 30 名医疗保健提供者进行了定性研究。半结构化访谈指南是根据 Grol 和 Wensing 的六个层面(创新、专业、患者、社会、组织和经济与政治)来制定的,以识别障碍和促进因素。数据采用主题分析进行分析,结合归纳和演绎方法,以确定障碍和促进因素。
大多数障碍是在组织层面上发现的,包括人员配备、时间、能力和心理社会支持不足。其他主要障碍包括长期随访护理团队以外的医疗保健提供者对晚期效应的了解有限,一些幸存者无法完成幸存者问卷,以及财务资源有限。主要促进因素包括医疗保健提供者和幸存者的积极性、一支熟练的医院团队、与全科医生等重要利益相关者的合作,以及心理社会关怀设施的利用、国际合作的利用以及向医院管理者报告长期随访护理结果以获得认可。
本研究确定了成功实施儿童癌症幸存者长期随访护理的几个因素。我们的研究结果表明,应特别关注知识、能力和财务问题,同时解决幸存者的心理社会问题。