Richmond Rehab | Physio, Exercise & Massage

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Joint Hypermoblity Syndrome

Formally known as Benign Joint Hypermobility Syndrome (BJHS), Joint Hypermobility Syndrome (JHS) is a heritable disorder of the connective tissues. People typically present with very elastic skin, a large amount of flexibility and often with a history of joint injuries.

What Is The Prevalence Of Hypermobility

  • Affects 10-20% of the population in Western countries and higher still in Indian, Chinese, & Middle Eastern populations

  • More common in children and decreases with age

  • Hypermobility is more common in women than men

  • There are wide variations between ethnic groups

What Are The Causes Of Hypermobility?

JHS is commonly found to have a hereditary factor, in particular a genetic variation in collagen. Collagen is found throughout the body in structures such as the skin, ligaments, and the heart valves. If collagen is weaker than it should be, there can be increased laxity in these structures which can lead to issues.


Does It Really Matter If I’m Stretchy?

We believe it is important to screen patients for hypermobility that could be contributing to their symptoms. Ross and Grahame (2011) describe the following factors that highlight this importance:

  • Inappropriate and potentially harmful labelling of treatments may be applied on the basis of an erroneous diagnosis such as rheumatoid arthritis, hypochondriasis, or somatisation.

  • Over zealous physical manipulation causing avoidable damage, such as dislocations, connective tissue ruptures, or fracture of fragile bone.

  • Exercise therapy may be excessively forceful or ineffectual.

  • Anecdotal evidence exists that orthopaedic operations on patients with connective tissue disorders, leading to poorer outcomes.

  • Chronic pain may sometimes lead to a potentially reversible downward spiral or immobility, reconditioning, dependency, and despair.


What Are Some Of The Clues Suggesting Joint Hypermobility?

Hypermobility In Children & Adolescents

  • Coincidental congenital dislocation of the hip

  • Late walking, with bottom shuffling instead of crawling

  • Recurrent ankle sprains

  • Poor ball catching and handwriting skills

  • Tiring easily compared with peers

  • So called growing pains of chronic widespread pain

  • Joint dislocations

Hypermobility In Adults

  • Non-inflammatory joint or spinal pain

  • Joint dislocations

  • Multiple soft tissue injuries

  • Increase in pain or progressive intensification of pain that is largely unresponsive to pain medications

  • Progressive loss of mobility owing to pain or kinesiophobia (pain avoidance through movement avoidance)

  • Premature osteoarthritis

  • Autonomic dysfunction such as dizziness or faintness

  • Functional gastrointestinal disorders (sluggish bowel, bloating, rectal evacuator dysfunction)

  • Laxity in other supporting tissues such as hernias, varicose veins, or uterine or rectal prolapse


How is Hypermobility Diagnosed In Physiotherapy?

A huge part of a physiotherapy assessment is the subjective assessment, the interview your physio does with you at the start of a session. It helps us to learn about your injury, family history, previous problems etc… If we consider some of the clues from the previous section, a thorough subjective assessment can help build a Physio’s suspicion that hyper mobility may be a factor in your complaint.

When looking at things that can be tested to confirm a suspicion of hypermobilty, a physiotherapist will typically use a screening test called the Beightons Score. This test assesses the amount of movement in your elbows, knees, hands & trunk. Scored out of 9, with a score of > 4 typically considered to be a positive finding for hypermobility (Clinch et al. 2011). Though the Beightons Score is a great tool to quickly give an impression of a patients mobility, it does have limitations as it doesn’t look at the wider system such as the shoulder, hip or ankle.

Beightons Score

If your physiotherapist holds concerns about your level of hypermobility, they may refer you back to your GP who may request blood tests and / or refer you to a Rheumatologist for a more thorough investigation.


How Can Physiotherapy Help?

The role of a physiotherapy can vary greatly depending on the presentation of a patient. The team at Richmond Rehab are passionate about having a positive influence in the areas we can help with, and directing patients to a more appropriate service when required. We believe that simply identifying patients with JHS and educating them about how it can influence their symptoms is an essential step in helping a patient manage their symptoms. When a patient has a good understanding, they then have the power to modify their behaviours and rely on passive treatment less.

Depending on the severity of presentation, your physiotherapist may opt for some supportive taping in the short term and possibly bracing for long-term management if required.

The one thing that all Physio’s should do however, is to develop an exercise program suitable for your specific presentation. Palmer et al. (2013) reports that exercise interventions can create improvements with JHS over time without any adverse effects. The mode of exercise was inconclusive however, with generalised exercise performing better than joint-specific exercise and that further studies in the area are indicated.

Is Massage Or Manipulation Helpful?

The difficulty for patients in pain with undiagnosed JHS is that they are not best placed to decide which treatments are best suited for them. Typically looking for a relief in pain, they often bounce from therapist to therapist seeking short-term relief from passive treatments.

In relation to helping to ease the pain, manual therapies can have their place, however they do little to create any longterm changes. Instead they can create a reliance on practitioners to help ease a patients pain and potentially lead to a lot of costly appointments over time.

We believe it is imperative to identify hypermobile patients as early as possible to allow us to develop an appropriate management plan that is guided by evidence. We may refer JHS patient for manual therapy if they require temporary relief, however our focus is always on education and self-management in the longterm.


So What Are We Saying?

The purpose of this article is to illustrate to you that more mobility isn’t necessarily a good thing. Sure it’s great to have a good level of mobility to move well, but there are limits. If you’ve always thought of yourself as being quite bendy and have been struggling with ongoing musculoskeletal pain, it might be time you had a chat with your physio or GP.

We’d be thrilled to see more patients educated about their bodies and taking a proactive approach to managing their health. When you’re informed you can make better decisions about which treatments are best for you and how you’d like to spend your hard earned money.


References

Clinch, J., Deere, K., Sayers, A., Palmer, S., Riddoch, C., Tobias, J. H., & Clark, E. M. (2011). Epidemiology of generalized joint laxity (hypermobility) in fourteen‐year‐old children from the UK: A population‐based evaluation. Arthritis & Rheumatism, 63(9), 2819-2827.

Lawrence, A. (2005). Benign hypermobility syndrome. J Indian Rheumatol Assoc, 13, 150-155.

Palmer, S., Bailey, S., Barker, L., Barney, L., & Elliott, A. (2014). The effectiveness of therapeutic exercise for joint hypermobility syndrome: a systematic review. Physiotherapy, 100(3), 220-227.

Ross, J., & Grahame, R. (2011). Joint hypermobility syndrome. Bmj, 342.

van der Giessen, L. J., Liekens, D., Rutgers, K. J., Hartman, A., Mulder, P. G., & Oranje, A. P. (2001). Validation of beighton score and prevalence of connective tissue signs in 773 Dutch children. The Journal of rheumatology, 28(12), 2726-2730.