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中国的埃勒斯-当洛斯综合征的诊断和治疗:首个指南概要。

Diagnosis and treatment of the Ehlers-Danlos syndromes in China: synopsis of the first guidelines.

机构信息

Department of Orthopaedic Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, No. 1 Shuaifuyuan, Beijing, 100730, China.

Beijing Key Laboratory for Genetic Research of Skeletal Deformity, Beijing, 100730, China.

出版信息

Orphanet J Rare Dis. 2024 May 13;19(1):194. doi: 10.1186/s13023-024-03121-0.

Abstract

BACKGROUND

The Ehlers-Danlos syndromes (EDS) are a group of rare hereditary connective tissue disorders. EDS is clinically and genetically heterogeneous and usually involves multiple systems. There are 14 subtypes of EDS with hallmark features including joint hypermobility, skin hyperextensibility, and tissue fragility. The clinical manifestations and their severity differ among the subtypes, encompassing recurrent joint dislocations, scoliosis, arterial aneurysm and dissection, and organ rupture. Challenges in diagnosis and management arise from the complexity of the disease, which is further complicated by its rarity. The development of clinical guidelines and implementation of coordinated multi-disciplinary team (MDT) approaches have emerged as global priorities.

MAIN BODY

Chinese Multi-Disciplinary Working Group on the Ehlers-Danlos Syndromes was therefore established. Healthcare professionals were recruited from 25 top hospitals across China. The experts are specialized in 24 fields, including genetics, vascular surgery, dermatology, and orthopedics, as well as nursing care, rehabilitation, psychology, and nutrition. Based on GRADE methodology, the Guidelines were written by the Group supervised by methodologists, following a systemic review of all 4453 articles in PubMed published before August 9, 2023, using the search term "Ehlers Danlos". A coordinated MDT approach for the diagnosis and management of EDS is highly recommended by the Group, along with 29 specific recommendations addressing key clinical questions. In addition to the treatment plan, the Guidelines also emphasize integrating support from nursing care, rehabilitation, psychology, and nutrition. This integration not only facilitates recovery in hospital settings, but most importantly, the transition from an illness-defined life to a more "normalized" life.

CONCLUSION

The first guidelines on EDS will shorten the diagnostic odyssey and solve the unmet medical needs of the patients. This article is a synopsis of the full guidelines.

摘要

背景

埃勒斯-当洛斯综合征(EDS)是一组罕见的遗传性结缔组织疾病。EDS 具有临床和遗传异质性,通常涉及多个系统。EDS 有 14 个亚型,其特征包括关节过度活动、皮肤过度伸展和组织脆弱。亚型之间的临床表现及其严重程度不同,包括复发性关节脱位、脊柱侧凸、动脉瘤和夹层以及器官破裂。诊断和管理方面的挑战源于疾病的复杂性,而其罕见性则使情况更加复杂。制定临床指南和实施协调的多学科团队(MDT)方法已成为全球优先事项。

主要内容

因此,成立了中国埃勒斯-当洛斯综合征多学科工作组。从中国 25 家顶级医院招募了医疗保健专业人员。这些专家专门从事 24 个领域,包括遗传学、血管外科、皮肤科和骨科,以及护理、康复、心理和营养。该指南采用 GRADE 方法,由专家组在方法学家的监督下撰写,系统回顾了截至 2023 年 8 月 9 日在 PubMed 上发表的所有 4453 篇文章,检索词为“Ehlers Danlos”。专家组强烈推荐采用协调的 MDT 方法来诊断和管理 EDS,并提出了 29 项针对关键临床问题的具体建议。除了治疗方案外,指南还强调整合护理、康复、心理和营养的支持。这种整合不仅有助于在医院环境中康复,而且最重要的是,从以疾病定义的生活过渡到更“正常化”的生活。

结论

第一批 EDS 指南将缩短诊断之旅,解决患者未满足的医疗需求。本文是完整指南的概要。

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