What are the most important symptoms to assess in hypermobile Ehlers-Danlos syndrome? A questionnaire study based on the Delphi technique. Issue 26 (18th December 2022)

• Record Type: Journal Article
• Authors: Hakimi, Adrien; Bergoin, Cyrille; Mucci, Patrick
• Is Part Of: Disability and rehabilitation. Volume 44:Issue 26(2023)
• Page Start: 8325
• Page End: 8331
• Publication Date: 2022-12-18
• Subjects: Delphi technique -- Ehlers-Danlos symptoms -- Ehlers-Danlos syndrome -- joint hypermobility -- symptom assessment; People with disabilities -- Periodicals; Rehabilitation -- Periodicals; 617.03
• DOI: 10.1080/09638288.2021.2012839
• Languages: English
• ISSNs: 0963-8288

Abstract

Abstract: Purpose: This study aims to determine from questionnaires, submitted to patients with Ehlers-Danlos syndrome hypermobile type (hEDS), what symptoms they perceive as having the most impact on their well-being and, according to them, what symptoms should be assessed. Materials and methods: Three rounds of online questionnaires were conducted following the Delphi method. The first round allowed us to obtain the most important symptoms to assess according to the patients. The second and third round aimed at ranking the categories according to their order of importance. Establishment of a consensus was evaluated using Kendall's coefficient of concordance. Results: A total of 118 responses were analyzed for the first round and 87 for the second and the third round. Ten categories were extracted from the first round. Ranking of the 10 categories in the second round did not reach consensus ( W = 0.33, p < 0.001) nor did the four most important categories in the third round ( W = 0.43, p < 0.001). However, three categories stand out from ranking: "pain", "fatigue and sleep disorders", and "musculoskeletal disorders". Conclusions: These categories seem to be the most important to assess in patients with hEDS, despite the lack of consensus on this ranking. Implications for rehabilitation: Pain, fatigue and sleep disorders, and musculoskeletal disorders should be given high consideration in the assessment of patients with hypermobile Ehlers-Danlos syndrome (EDS). The high phenotypic variability in the hypermobile EDS requires individualized assessment for each patient and a multidisciplinary approach.