What I Wish I Had Known: Examining Parent Accounts of Managing the Health of Their Child With Intellectual Disability

IF 3 3区 医学 Q2 HEALTH CARE SCIENCES & SERVICES Health Expectations Pub Date : 2025-01-09 DOI:10.1111/hex.70138
Thom Nevill, Jessica Keely, Rachel Skoss, Rachel Collins, Katherine Langdon, Jaquie Mills, Jenny Downs
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Abstract

Background

Appropriate support for the health of children with an intellectual disability by parents and healthcare professionals is pivotal, given the high risk of chronic conditions. However, there is limited research that has collected important insights from parents on their learnings for supporting their child's evolving healthcare needs.

Aim

This study focuses on parents' experiences and learnings from managing and supporting the health of their child with intellectual disability. It aims to understand what parents wish they had known earlier, the essential knowledge and skills they needed to manage their child's health.

Method

A qualitative study was carried out using semi-structured interviews with 21 parents of adolescents and young people with intellectual disability. The children had chronic health conditions that fell into six health domains, including (1) difficulties with movement and physical activity, (2) epilepsy, (3) dental care, (4) respiratory health and infection, (5) behaviour, mental health or sleep and (6) gastrointestinal health.

Results

Thematic analysis yielded five themes: (1) optimising mutual engagement between healthcare professionals and families; (2) planning and practising effective healthcare; (3) having the right information at the right time; (4) finding the support that was needed and (5) navigating healthcare and disability systems. Over time, parents developed specific skills and knowledge for managing their child's health effectively. Some parents expressed regret for not seeking support and information about their child's health conditions earlier. Parents described how mutual engagement between healthcare professionals and parents optimised the management of their child's healthcare.

Conclusion

The study found that managing the health of a child with intellectual disability is complex. The themes were consistent across health comorbidities, indicating important common experiences. The themes aligned with conceptualisations of health literacy, suggesting that improving health literacy skills can help parents better manage their children's health conditions.

Patient or Public Contribution

We developed the project in consultation with members of the public who have lived experience of parenting a child with intellectual disability. They commented on the study aims, interview schedule, participant recruitment and provided feedback on the analysis and discussion.

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我希望我知道的:检查父母如何管理他们智障孩子的健康。
背景:鉴于智力残疾儿童患慢性疾病的高风险,父母和卫生保健专业人员对其健康的适当支持至关重要。然而,从父母那里收集到支持孩子不断发展的医疗保健需求的重要见解的研究有限。目的:本研究的重点是父母在管理和支持智障儿童健康方面的经验和教训。它的目的是了解父母希望他们早点知道的事情,他们需要管理孩子健康的基本知识和技能。方法:采用半结构化访谈法对21名智力障碍青少年家长进行定性研究。这些儿童的慢性健康状况可分为六个健康领域,包括(1)运动和身体活动困难,(2)癫痫,(3)牙齿保健,(4)呼吸健康和感染,(5)行为、心理健康或睡眠,以及(6)胃肠道健康。结果:专题分析得出五个主题:(1)优化医护人员与家庭之间的相互参与;(二)规划和实施有效的医疗保健;(三)在正确的时间获得正确的信息;(4)寻找所需的支持;(5)导航医疗保健和残疾系统。随着时间的推移,父母逐渐掌握了有效管理孩子健康的具体技能和知识。一些家长对没有尽早寻求支持和了解孩子的健康状况表示遗憾。家长们描述了医疗保健专业人员和家长之间的相互参与如何优化了他们孩子的医疗保健管理。结论:研究发现,管理智力残疾儿童的健康是复杂的。这些主题在健康合并症中是一致的,表明了重要的共同经验。这些主题与卫生知识普及的概念一致,表明提高卫生知识普及技能可以帮助父母更好地管理子女的健康状况。患者或公众贡献:我们在与有过养育智障儿童的亲身经历的公众人士协商后制定了这个项目。他们对研究目的、面试日程、参与者招募进行了评论,并对分析和讨论提供了反馈。
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来源期刊
Health Expectations
Health Expectations 医学-公共卫生、环境卫生与职业卫生
CiteScore
5.20
自引率
9.40%
发文量
251
审稿时长
>12 weeks
期刊介绍: Health Expectations promotes critical thinking and informed debate about all aspects of patient and public involvement and engagement (PPIE) in health and social care, health policy and health services research including: • Person-centred care and quality improvement • Patients'' participation in decisions about disease prevention and management • Public perceptions of health services • Citizen involvement in health care policy making and priority-setting • Methods for monitoring and evaluating participation • Empowerment and consumerism • Patients'' role in safety and quality • Patient and public role in health services research • Co-production (researchers working with patients and the public) of research, health care and policy Health Expectations is a quarterly, peer-reviewed journal publishing original research, review articles and critical commentaries. It includes papers which clarify concepts, develop theories, and critically analyse and evaluate specific policies and practices. The Journal provides an inter-disciplinary and international forum in which researchers (including PPIE researchers) from a range of backgrounds and expertise can present their work to other researchers, policy-makers, health care professionals, managers, patients and consumer advocates.
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