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Practical management strategies for benign hypermobility syndromes
1Department of Internal Medicine, Division of Rheumatology, University of Michigan, Ann Arbor, Michigan, USA.
Hypermobile Ehlers-Danlos syndromes (hEDS) and hypermobility spectrum disorders (HSD) require updated diagnostic and treatment strategies. Rheumatologists can improve patient care by understanding current therapeutic options, including physical and occupational therapy.
Area of Science:
- Rheumatology
- Clinical Medicine
- Genetics
Background:
- Symptomatic hypermobility syndromes, including hypermobile Ehlers-Danlos syndromes (hEDS) and hypermobility spectrum disorders (HSD), frequently present to rheumatologists.
- Patients often experience joint pain and functional disability, posing diagnostic challenges due to limited provider knowledge of associated manifestations and treatments.
Purpose of the Study:
- To review recent updates in diagnostic measures for hEDS/HSD.
- To discuss current therapeutic modalities for rheumatologists managing patients with hEDS/HSD.
Main Methods:
- Review of current literature on diagnostic criteria and therapeutic interventions for hEDS/HSD.
- Assessment of evidence supporting physical therapy, occupational therapy, assistive devices, compressive garments, orthoses, and surgical options.
Main Results:
- Newer diagnostic measures and manifestation assessments for hEDS/HSD are described.
- Evidence supports physical and occupational therapy, with updates on assistive devices, garments, orthoses, and surgical interventions.
- Patient heterogeneity necessitates individualized treatment plans, often focusing on regional complaints over a whole-body approach.
Conclusions:
- Physical therapy and occupational therapy are the primary treatments for hEDS/HSD.
- Individualized, comprehensive treatment strategies are crucial for managing the diverse manifestations of hEDS/HSD.
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