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血友病患儿信息提供方面的经验与需求:一项关于照顾者和医疗服务提供者观点的定性研究

Experiences and Needs Regarding Information Provision in Children With Haemophilia: A Qualitative Study on Caregivers' and Healthcare Providers' Perspectives.

作者信息

Mussert Caroline M A, Kamminga Nadia C W, van Hoorn Evelien S, Eekelaar Tjaisha M, Dehli Silje R, van der Velden-van 't Hoff Carolien, Andeweg Sasja, Reitsma Simone H, Nooteboom Annebelle C M, Diekstra Adinda, Albayrak Armaĝan, Cnossen Marjon H

机构信息

Department of Pediatric Hematology and Oncology, Erasmus MC Sophia Children's Hospital, University Medical Center Rotterdam, Rotterdam, the Netherlands.

Department of Quality and Patient Care, Erasmus MC, University Medical Center Rotterdam, Rotterdam, the Netherlands.

出版信息

Haemophilia. 2025 Jul;31(4):657-667. doi: 10.1111/hae.70063. Epub 2025 May 19.

Abstract

INTRODUCTION

In haemophilia, ever more effective treatment options leading to minimal bleeding make information provision about the disease and its symptoms and when to alert the treatment team increasingly important. However, little is known about how current information provision is perceived and what the needs are.

AIM

Gain in-depth insights into experiences and needs regarding information provision of caregivers of young children with haemophilia, and the perspectives of their healthcare providers (HCPs).

METHODS

A qualitative study was conducted including 15 semi-structured interviews with caregivers and seven interviews with HCPs. Purposive sampling ensured a varied sample regarding the child's age, type and severity of haemophilia, and treatment strategy. A comprehensive thematic content analysis was subsequently conducted using several phases of coding.

RESULTS

Three main themes were identified. First, caregivers and HCPs indicated that current disease knowledge and information provision regarding haemophilia varies and could be improved. Both groups underlined the importance of adequate information provision to support decision-making and alleviate anxiety. Second, the need for standardized, centralized and tailored information was expressed, preferably digital. Current information is experienced as fragmented and incomplete, leading to lack of structure and uncertainties. Lastly, information provision cannot exist without additional coaching by the multidisciplinary treatment team and peers.

CONCLUSION

Both caregivers and HCPs experience unmet needs regarding information provision as currently performed. Empowerment can be provided by standardized, centralized information tailored to disease severity and phase of life. A digital information platform with visual support, could provide a complete, up-to-date, readily available and reliable resource.

摘要

引言

在血友病治疗中,越来越有效的治疗方案使出血风险降至最低,因此提供有关该疾病及其症状的信息以及何时通知治疗团队变得越发重要。然而,对于当前的信息提供情况如何被认知以及需求是什么,我们知之甚少。

目的

深入了解血友病患儿照料者在信息提供方面的经历和需求,以及他们的医疗保健提供者(HCPs)的观点。

方法

开展了一项定性研究,包括对15名照料者进行半结构化访谈以及对7名HCPs进行访谈。目的抽样确保了样本在儿童年龄、血友病类型和严重程度以及治疗策略方面具有多样性。随后使用多个编码阶段进行了全面的主题内容分析。

结果

确定了三个主要主题。首先,照料者和HCPs表示,目前关于血友病的疾病知识和信息提供情况各不相同,且有待改进。两组都强调了提供充分信息以支持决策和减轻焦虑的重要性。其次,表达了对标准化、集中化和量身定制信息的需求,最好是数字化的。目前的信息被认为是零散和不完整的,导致缺乏条理和不确定性。最后,没有多学科治疗团队和同伴的额外指导,信息提供就无法存在。

结论

照料者和HCPs都认为目前的信息提供存在未满足的需求。可以通过根据疾病严重程度和生活阶段量身定制的标准化、集中化信息来提供帮助。一个带有视觉支持的数字信息平台可以提供完整、最新、随时可用且可靠的资源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/903c/12306852/496a9df21afb/HAE-31-657-g003.jpg

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