Eichinger Josef K, Byrd Rebecca L, Bailey Evan P, Reis Robert J, Daylor Victoria, Schiessl Maggie, Gensemer Cortney, Friedman Richard J, Patel Sunil J, Norris Russell A
Department of Orthopaedics and Physical Medicine, Medical University of South Carolina, Charleston, South Carolina.
Department of Regenerative Medicine and Cell Biology, Children's Research Institute, Medical University of South Carolina, Charleston, South Carolina.
J Bone Joint Surg Am. 2025 Jul 10;107(16):1848-1856. doi: 10.2106/JBJS.24.01106.
Hypermobile Ehlers-Danlos syndrome (hEDS) is a collagen disorder affecting multiple organ systems, including the musculoskeletal system. We sought to determine the type and severity of orthopaedic manifestations experienced by these patients. The purpose of this study was to identify the most common orthopaedic manifestations in patients with hEDS and to examine the patient-reported helpfulness of treatments. Of note, collagen disorders such as hEDS may affect the success rates of orthopaedic interventions. The success or failure of treatment is not currently fully understood for this patient population.
A total of 1,999 patients who were enrolled in an international EDS registry were contacted to complete a 260-question survey regarding their experience with nonoperative and operative treatments for musculoskeletal instability and/or pain. Participants reported their demographic characteristics, hEDS diagnosis characteristics, symptomatic joints, nonoperative and operative treatments, and satisfaction with each treatment.
Over a 30-day period, 1,075 responses were received. Participants were predominately female (95.3%) and had a median age of 40.0 years (interquartile range width, 17.0 years). The majority (60.8%) of respondents reported a mental health burden every day, with the remainder reporting a mental health burden weekly (24.4%), monthly (11.0%), or never (3.80%). Compared with those who underwent standard physical therapy (n = 378), individuals who underwent physical therapy tailored to EDS (n = 602) more frequently reported improved posture (78.6% versus 43.1%; p < 0.001), greater helpfulness (p < 0.001), and a longer duration of attending therapy (p < 0.001). A total of 1,120 primary and 261 revision operations for joint or spine instability and/or pain were reported. The reported complication rates were 35.7% and 42.9% for joint and spine surgeries, respectively. Physical therapy was the only nonoperative treatment for which the median reported helpfulness sometimes equaled or exceeded that of a joint or spine surgery.
This study offers insights into the demographics and management of hEDS. The high rate of surgical complications reported by patients indicates the need for a better understanding of surgical indications and treatment options. These findings should guide physicians in managing hEDS and highlight the importance of incorporating this knowledge into clinical practice to improve the management of orthopaedic manifestations in patients with hEDS.
Prognostic Level V . See Instructions for Authors for a complete description of levels of evidence.
过度活动型埃勒斯-当洛综合征(hEDS)是一种影响包括肌肉骨骼系统在内的多个器官系统的胶原蛋白紊乱疾病。我们试图确定这些患者所经历的骨科表现的类型和严重程度。本研究的目的是识别hEDS患者中最常见的骨科表现,并检查患者报告的治疗效果。值得注意的是,诸如hEDS之类的胶原蛋白紊乱疾病可能会影响骨科干预的成功率。目前对于该患者群体治疗的成败尚未完全了解。
联系了1999名登记在国际埃勒斯-当洛综合征注册库中的患者,以完成一项关于他们对肌肉骨骼不稳定和/或疼痛的非手术和手术治疗体验的260个问题的调查。参与者报告了他们的人口统计学特征、hEDS诊断特征、有症状的关节、非手术和手术治疗,以及对每种治疗的满意度。
在30天内收到了1075份回复。参与者以女性为主(95.3%),中位年龄为40.0岁(四分位间距为17.0岁)。大多数(60.8%)受访者报告每天都有心理健康负担,其余受访者报告心理健康负担为每周(24.4%)、每月(11.0%)或从不(3.80%)。与接受标准物理治疗的患者(n = 378)相比,接受针对埃勒斯-当洛综合征量身定制的物理治疗的患者(n = 602)更频繁地报告姿势改善(78.6%对43.1%;p < 0.001)、更大的治疗效果(p < 0.001)以及更长的治疗持续时间(p < 0.001)。共报告了1120例针对关节或脊柱不稳定和/或疼痛的初次手术和261例翻修手术。报告的关节和脊柱手术并发症发生率分别为35.7%和42.9%。物理治疗是唯一一种报告的中位治疗效果有时等于或超过关节或脊柱手术的非手术治疗方法。
本研究为hEDS的人口统计学和管理提供了见解。患者报告的高手术并发症发生率表明需要更好地了解手术适应症和治疗选择。这些发现应指导医生管理hEDS,并强调将这些知识纳入临床实践以改善hEDS患者骨科表现管理的重要性。
预后V级。有关证据水平的完整描述,请参阅作者指南。