基于共识的儿童多重先天性关节挛缩康复建议:综合知识转化方法。

IF 3.4 2区 医学 Q2 GENETICS & HEREDITY
Noémi Dahan-Oliel, Sarah Cachecho, Clarice Araujo, Alicja Fąfara, Francis Lacombe, Ani Samargian, Camille Costa, Maureen Donohoe, Ann Flanagan, Bart Kowalczyk, Courtney Krakie, Lisa Wagner, Carolina Navalón, Verity Pacey, Unni Steen, Misha Walker, Trudy Wong, André Bussières
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引用次数: 0

摘要

背景:多发性先天性关节挛缩症(AMC)是一组罕见的疾病,其特征是出生时就存在多个关节挛缩。早期康复对于减少关节挛缩和最大化自主和参与是必不可少的。然而,几乎没有可靠的科学证据来指导最佳实践。本项目旨在针对以下优先领域的AMC患儿的康复管理提出基于共识的建议:早期干预和运动发育、肌肉和关节功能、矫形器、活动能力、生活领域的参与、疼痛、社会心理健康和围手术期康复。结果:这个多阶段的项目采用了集成的知识翻译方法。基于对AMC儿童康复优先领域的范围审查结果,以及描述AMC康复当前实践的临床医生调查,职业治疗、物理治疗、骨科、物理和社会工作方面的三个专家临床医生小组,以及有生活经验的人和来自10个国家的研究人员制定了基于共识的康复建议。符合建议、评估、发展及评估分级架构(GRADE)准则。修改后的德尔菲过程由更广泛的国际AMC专家小组完成,以修改和验证建议(第1轮= 41名,第2轮= 37名专家)。一个由五名成员组成的外部审查小组使用《研究和评估指南II》(AGREE II)工具对这些建议进行了评估。经过两轮德尔菲分析,最终的16条建议的平均满意率达到96.6%。总体质量在AGREE II工具上被评为96.6%。与临床医生和管理人员的访谈确定了使用理论领域框架在实践中实施建议的促进因素和障碍。结论:广泛的利益相关者、医疗保健用户和提供者制定了基于共识的、专家验证的AMC儿童康复建议。预期拟议的建议将有助于改善以儿童和家庭为中心的做法和保健成果。未来的工作包括制定知识翻译策略,以促进这些建议在实践中的分享和实施。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Consensus-based recommendations for the rehabilitation of children with arthrogryposis multiplex congenita: an integrated knowledge translation approach.

Background: Arthrogryposis multiplex congenita (AMC) is a group of rare disorders characterized by multiple joint contractures present at birth. Early rehabilitation is essential to minimize joint contractures and maximize autonomy and participation among individuals with AMC. However, there is little robust scientific evidence to inform best practice. This project aimed to develop consensus-based recommendations for the rehabilitation management of children with AMC in the following priority areas: early intervention and motor development, muscle and joint function, orthotics, mobility, participation in areas of life, pain, psychosocial wellbeing, and perioperative rehabilitation.

Results: This multi-phase project used an integrated knowledge translation approach. Based on the results from scoping reviews on the priority areas identified for the rehabilitation of children with AMC, and a clinician survey describing current practices in AMC rehabilitation, three panels of expert clinicians in occupational therapy, physical therapy, orthopedics, physiatry, and social work, as well as people with lived experience and researchers from 10 countries developed consensus-based recommendations for rehabilitation, in concordance with the Grading of Recommendations, Assessment, Development and Evaluations framework (GRADE) criteria. A modified Delphi process was completed with a wider group of international AMC experts to revise and validate the recommendations (Round 1 = 41 and Round 2 = 37 experts). A five-member external review panel appraised the recommendations using the Appraisal of Guidelines for Research and Evaluation II (AGREE II) tool. The final 16 recommendations reached a mean agreement rate of 96.6% after two Delphi rounds. The overall quality was rated at 96.6% on the AGREE II tool. Interviews with clinicians and managers identified facilitators and barriers to implementation of the recommendations in practice using the Theoretical Domain Framework.

Conclusion: Consensus-based, expert validated recommendations for the rehabilitation of children with AMC were developed by a wide range of stakeholders, healthcare users and providers. The proposed recommendations are expected to contribute to improving child- and family-centered practice and health outcomes. Future work includes a knowledge translation strategy to promote sharing and implementation of the recommendations in practice.

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来源期刊
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases 医学-医学:研究与实验
CiteScore
6.30
自引率
8.10%
发文量
418
审稿时长
4-8 weeks
期刊介绍: Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases. In addition, the journal may consider articles on clinical trial outcome reports, either positive or negative, and articles on public health issues in the field of rare diseases and orphan drugs. The journal does not accept case reports.
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