Journal Article

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

Wu, Nan, Wu, Zhihong, Li, Guozhuang, Zhang, Terry Jianguo, Xu, Kexin

2024

Overview

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.

• Publisher: BioMed Central,BioMed Central Ltd,BMC
• Subject: Aneurysms / Care and treatment / China / Clinical guidelines / Diagnosis / Diagnosis and treatment / Ehlers-Danlos syndrome / Ehlers-Danlos Syndrome - diagnosis / Ehlers-Danlos Syndrome - genetics / Ehlers-Danlos Syndrome - therapy / Ehlers-Danlos syndromes / Human Genetics / Humans / Medical personnel / Medicine / Medicine & Public Health / Multi-disciplinary team approach / Nursing care / Pharmacology/Toxicology / Position Statement / Practice Guidelines as Topic / Scoliosis / Skin