Identifying and Managing Patients with Hypermobility Syndromes

This presentation focused on the recognition, assessment, and management of hypermobility syndromes, including Hypermobile Ehlers-Danlos Syndrome (hEDS) and Hypermobility Spectrum Disorders (HSD). Brendan McCann, DC, PSP, discussed common signs and symptoms such as chronic pain, fatigue, proprioceptive deficits, autonomic dysfunction, and recurrent injuries, while emphasizing the importance of accurate diagnosis and a multidisciplinary approach to care.

The session highlighted assessment strategies, including Beighton scoring and patient history evaluation, as well as individualized treatment approaches centered on stability, motor control, strengthening, load management, and patient education. Dr. McCann also addressed common clinical challenges and stressed the importance of evidence-informed, patient-centered care to improve long-term outcomes for hypermobile patients.

Learning Objectives

1. Identify the clinical characteristics and common presentations associated with hypermobility syndromes, including Hypermobile Ehlers-Danlos Syndrome (hEDS) and Hypermobility Spectrum Disorders (HSD).
2. Apply appropriate assessment strategies, including Beighton scoring and patient history evaluation, to improve recognition and diagnosis of hypermobility-related conditions.
3. Describe evidence-informed management approaches focused on stability, motor control, strengthening, load management, and patient education for individuals with hypermobility syndromes.
4. Recognize common clinical challenges and implement patient-centered, multidisciplinary strategies to support improved functional outcomes and long-term care.