Follow up after childhood cancer: A typology of young people’s health care need

Faith Gibson , Helen Aslett , Gill Levitt , Alison Richardson
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引用次数: 23

Abstract

Background

The paediatric oncology community is focused on providing appropriate care to survivors of childhood cancer, given that despite increases in survival rates it is estimated that 60% will have one or more problems related to their disease or treatment. Agreement and consistency in how follow-up for this group of young people should be designed and delivered has not yet been reached and rarely have young people been asked to contribute to this discussion.

Methodology

The study aimed to find out what young people who are receiving long-term follow-up for childhood cancer would like from their follow-up service. It aimed to illuminate the dimensions of care valued by young people as well as make explicit to professionals health care needs that must be met to provide optimum care into their adult life. The emphasis was on qualitative, participatory methods using reflexive and responsive approaches to give primacy to the voice of participants. Data were generated through a series of workshops, interviews and questionnaires.

Findings

Forty young people (12 male: 30% and 28 female: 70%), participated in the study. Preliminary analysis yielded a descriptive typology that could serve as a basis for classifying and clarifying health care needs: defined as what the young people in this study wanted from a follow-up service. Five categories of health care need were identified: (i) need for a positive relationship with health care professionals; (ii) need for information; (iii) need for communication; (iv) need for parents to be supported; (v) need for health care professionals to have appropriate knowledge.

Conclusions and relevance to practice

Young people in this study were clear about the structure and process of a service that would meet their needs. Assembling data into a typology of health care need presents those delivering and commissioning services a tangible indicator of outcome that can be confidently described as what young people want from any current or future model of follow-up service.

儿童癌症后的随访:年轻人保健需求的一种类型
儿科肿瘤学社区的重点是为儿童癌症幸存者提供适当的护理,因为尽管存活率有所增加,但据估计,60%的儿童将面临与他们的疾病或治疗相关的一个或多个问题。在如何为这一青年群体设计和提供后续行动方面尚未达成一致意见,也很少要求青年参与这一讨论。研究的目的是找出接受儿童癌症长期随访的年轻人希望从他们的随访服务中得到什么。它旨在阐明年轻人所重视的保健方面,并向专业人员明确说明必须满足的保健需求,以便为他们的成年生活提供最佳保健。重点是定性的、参与性的方法,使用反思性和反应性的方法,以参与者的声音为首要。数据是通过一系列讲习班、访谈和问卷调查产生的。研究结果40名年轻人(12名男性占30%,28名女性占70%)参与了这项研究。初步分析得出了一种描述性类型,可以作为分类和澄清医疗保健需求的基础:定义为本研究中的年轻人想从随访服务中得到什么。确定了五类保健需求:(i)需要与保健专业人员建立积极的关系;(ii)对资料的需要;(三)沟通的需要;(iv)需要赡养父母;(v)保健专业人员需要具备适当的知识。结论和与实践的相关性在这项研究中,年轻人对满足他们需求的服务的结构和过程是清楚的。将数据汇编成保健需求的类型,为提供和委托服务的人提供了一个有形的结果指标,可以自信地描述为年轻人从任何当前或未来的后续服务模式中所希望得到的东西。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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