A clinical practice guideline for primary care physiotherapy in patients with haemophilia

IF 3 2区 医学 Q2 HEMATOLOGY
Haemophilia Pub Date : 2024-07-10 DOI:10.1111/hae.15065
Johan Blokzijl, Martijn F. Pisters, Magnus Aspdahl, Wypke de Boer, Ruth Elise Dybvik Matlary, Danielle Douma-van Riet, Piet de Kleijn, Sébastien Lobet, Paula Loughnane, Paul McLaughlin, Melanie Bladen, Sheila Roche, David Stephensen, Leo van Vlimmeren, Lize F. D. van Vulpen, Merel A. Timmer, the EAHAD physiotherapy committee
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Abstract

Introduction

As a result of centralisation of haemophilia care to a limited number of intramural settings, many persons with haemophilia have to travel long distances to attend their haemophilia specialised treatment centre. However, regular physiotherapy treatment can be provided by primary care physiotherapists in the personʼs own region. Due to the rarity of the disease most primary care physiotherapists have limited experience with this population. This study aims to provide a clinical practice guideline for primary care physiotherapists working with persons with bleeding disorders.

Method

A list of the most urgent key-questions was derived from a previous study. Literature was summarised using the grading of recommendations assessment, development, and evaluation (GRADE) evidence-to-decision framework. Recommendations were drafted based on four 90 min consensus meetings with expert physiotherapists. Recommendations were finalised after feedback and >80% consensus of all stakeholders (including PWH, physiotherapists, haematologists and the corresponding societies).

Results

A list of 82 recommendations was formulated to support primary care physiotherapists when treating a person with a bleeding disorder. These recommendations could be divided into 13 categories: two including recommendations on organisation of care, six on therapy for adult patients with bleeding disorders and five on therapy adaptations for paediatric care. Therapy recommendations included treatment after a joint- or muscle bleed, haemophilic arthropathy, chronic synovitis, non-haemophilia related conditions and orthopaedic surgery.

Conclusion

An evidence-based practice guideline, based on current evidence from literature and clinical expertise, has been developed for primary care physiotherapists treating a person with haemophilia. To improve care, the recommendations should be implemented in daily practice.

Abstract Image

血友病患者初级物理治疗临床实践指南。
导言:由于血友病治疗集中在数量有限的院内机构,许多血友病患者不得不长途跋涉前往血友病专科治疗中心就诊。不过,患者所在地区的初级物理治疗师可以提供定期的物理治疗。由于这种疾病的罕见性,大多数初级保健物理治疗师对这类人群的治疗经验有限。本研究旨在为从事出血性疾病治疗的初级保健物理治疗师提供临床实践指南:方法:从先前的一项研究中得出了一份最紧迫的关键问题清单。采用建议评估、发展和评价分级(GRADE)证据到决策框架对文献进行总结。在与物理治疗师专家举行的四次 90 分钟共识会议基础上起草了建议。所有利益相关者(包括公共卫生人员、物理治疗师、血液病专家和相应的学会)反馈意见并达成 80% 以上的共识后,最终确定了建议:结果:制定了一份包含 82 项建议的清单,为初级保健物理治疗师治疗出血性疾病患者提供支持。这些建议可分为 13 类:两类包括关于护理组织的建议,六类关于成人出血性疾病患者的治疗,五类关于儿科护理的治疗调整。治疗建议包括关节或肌肉出血后的治疗、血友病关节病、慢性滑膜炎、与血友病无关的疾病和骨科手术:根据当前的文献证据和临床专业知识,为初级保健物理治疗师治疗血友病患者制定了循证实践指南。为改善护理,应在日常实践中落实这些建议。
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来源期刊
Haemophilia
Haemophilia 医学-血液学
CiteScore
6.50
自引率
28.20%
发文量
226
审稿时长
3-6 weeks
期刊介绍: Haemophilia is an international journal dedicated to the exchange of information regarding the comprehensive care of haemophilia. The Journal contains review articles, original scientific papers and case reports related to haemophilia care, with frequent supplements. Subjects covered include: clotting factor deficiencies, both inherited and acquired: haemophilia A, B, von Willebrand''s disease, deficiencies of factor V, VII, X and XI replacement therapy for clotting factor deficiencies component therapy in the developing world transfusion transmitted disease haemophilia care and paediatrics, orthopaedics, gynaecology and obstetrics nursing laboratory diagnosis carrier detection psycho-social concerns economic issues audit inherited platelet disorders.
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