Joint hypermobility can be localized to a specific joint, or generalized throughout the joints of the body. When generalized, hypermobility may occur with symptoms such as muscle or joint pain. Joint Hypermobility Syndrome (JHS) and Ehlers Danlos Syndrome (EDS) are severe connective tissue disorders that affect the entire body and have overlapping symptoms. EDS is an inherited connective tissue disorder characterized by abnormal collagen synthesis. Symptoms may include severe joint hypermobility, skin laxity, and tissue fragility accompanied by pain and recurrent joint dislocations. Joint hypermobility can be evaluated using the Beighton Score, a simple scale composed of 5 easy to perform manoeuvres to determine a score between 0 and 9.
Hypermobile joints may be more prone to sprains, soft tissue injuries and dislocations. Strengthening, joint protection techniques and patient education are the key components of therapeutic interventions. Muscle strengthening and balance enhancing exercises are important, as are instructions in maintaining good posture and avoiding extreme range of motion positions.
Orthoses can be used to protect and position painful and or unstable joints during episodes of inflammation. Patients may benefit from knee and ankle supports made out of our rigid thermoplastic materials (Orfit Eco, Orfit Eco Black NS and Orfibrace) and/or from wrist and hand orthoses made from our lightweight thermoplastics (Orfilight, Orfilight Atomic Blue NS, Orfilight Black NS) or our elastic thermoplastic materials (Orfit Classic, Orfit NS, Orfit Natural NS).
Finger orthoses are valuable for maintaining function in joints that are prone to hyperextension. Anti-swan neck orthoses (made from Orficast and/or Orfit Strips) and thumb orthoses that prevent subluxation (made from Orficast) are very helpful.
Joint hypermobility can be managed with an appropriate orthosis that allows the maximum function possible while stabilizing the joint. Check out our videos for valuable splinting instructions.
Scheper, M. C., Engelbert, R. H. H., Rameckers, E. A. A., Verbunt, J., Remvig, L., & Juul-Kristensen, B. (2013). Children with generalised joint hypermobility and musculoskeletal complaints: state of the art on diagnostics, clinical characteristics, and treatment. BioMed research international, 2013.
Engelbert, R. H., Juul‐Kristensen, B., Pacey, V., De Wandele, I., Smeenk, S., Woinarosky, N., … & Simmonds, J. V. (2017, March). The evidence‐based rationale for physical therapy treatment of children, adolescents, and adults diagnosed with joint hypermobility syndrome/hypermobile Ehlers Danlos syndrome. In American Journal of Medical Genetics Part C: Seminars in Medical Genetics (Vol. 175, No. 1, pp. 158-167).
Rombaut, L., Malfait, F., Cools, A., De Paepe, A., & Calders, P. (2010). Musculoskeletal complaints, physical activity and health-related quality of life among patients with the Ehlers–Danlos syndrome hypermobility type. Disability and rehabilitation, 32(16), 1339-1345.
Kumar, B., & Lenert, P. (2017). Joint Hypermobility Syndrome: Recognizing a Commonly Overlooked Cause of Chronic Pain. The American Journal of Medicine.
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