ME: is cognitive behavioural therapy best?

By Siski Green , Monday 6 August 2012

Which treatments can best help to relieve the symptoms of chronic fatigue syndrome? New study fuels the debate
Brain workingsCBT has been found to help improve symptoms and coping strategies

Myalgic encephalomyelitis (ME) the illness also known as chronic fatigue syndrome, affects some 250,000 people in the UK. Symptoms include a live-changing severe fatigue, painful muscles, disrupted sleep and poor memory and concentration. Although viral infection is linked with its onset, no one is sure what causes it. New research indicates that cognitive behavioural therapy (CBT) is the most cost-effective treatment for the disease, along with medical care.

Researchers from King's College London looked at data relating to patients' responses to different treatments and then used criteria from the NHS to ascertain which treatment gave the best value for money. These criteria are based on the years a person lives in good health. If a treatment costs less than £20,000 per year and achieves 'good health' for a patient during that time, it's considered good value. CBT was found to be good value and, although it can’t cure ME it has been found to help improve symptoms and coping strategies.

Graded exercise therapy (GET), where physical activity is tailored to suit the individual and gradually increased over a long period of time, was also found to be of good value.

However, one type of treatment offered to ME sufferers – adaptive pacing therapy – was not found to offer value for money. This is a specific strategy that involves the patient aiming for a balance between rest and activity, enabling them to live within the constraints of the illness. For each year of quality life, CBT costs an estimated £18,000; GET £24,000; and APT £55,000. This means the first two are classifiable as cost effective so it's hoped that the NHS will now invest further in providing them for people with ME.

Understandably, ME patients argue that available treatment shouldn't be based on cost and, according to the ME Association, these study results do not paint a complete picture. "The feedback we get at the ME Association regarding which treatments work best do not match the results of this study," says medical adviser, Dr Charles Shepherd. "Going by our own members' feedback, pacing is by far the most effective and acceptable form of treatment; many members find CBT to be ineffective and GET makes the condition worse in around half of individuals. What we need is more research into the biomedical causes of this illness and forms of treatment based on that."


The opinions expressed are those of the author and are not held by Saga unless specifically stated.

The material is for general information only and does not constitute investment, tax, legal, medical or other form of advice. You should not rely on this information to make (or refrain from making) any decisions. Always obtain independent, professional advice for your own particular situation.

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COMMENTS

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  • lynne dobbs

    Posted: Monday 20 August 2012

    over 10 years ago I was diagnosed with cfs. My therapy was a combination of all the above and all have been useful in understanding and helping to minimise the effects. Today I feel much better and still draw on these therapies albeit not as strongly as I did but now I 'listen' to what my body and my mind are telling me and I ease up so I don't suffer the consequences which can be debilitating.

  • Aileen

    Posted: Sunday 19 August 2012

    There is no way a GET 5 week course at the clinic 55 miles away costs the NHS £24,000! It shouldn't cost more than a few hundred pounds for the person's wages who delivers the course! The NHS has nothing to offer ME patients, and does not offer anything! Apart I must say from a sympathetic ear from our local OT who runs the clinic. After a short course in CBT is offered, and ditto GET, there is nothing else offered!! Pacing costs nothing, no more than the literature given out to the patient.

  • christine davies

    Posted: Wednesday 15 August 2012

    The recommendation of CBT and GET is based on figures provided by the NHS. Those of us who suffer from M.E. have maintained that CBT(which I had for two years) and GET have little effect. THE CBT attempts to get us to accept our condition and live with it as best we can, while it has been shown time and again that GER actually makes many sufferers WORSE. If the raw data from the NHS is flawed then the results of this survey are unreliable, and will further hinder effective treatments once again

  • Dilys McGill

    Posted: Wednesday 15 August 2012

    Dr Shepherd is the Expert. I've had M.E./CFS for 20 years. CBT did not help. Graded exercise is the worst thing possible but pacing does work. Cost does not come into it.

  • Susan Wenger

    Posted: Tuesday 7 August 2012

    "Graded exercise therapy (GET) ... was also found to be of good value." How exactly was GET found to be of good value? People with ME, particularly severe ME, do worse with exercise. Even the mildest exertion (like getting up to go to the bathroom) can exacerbate symptoms.

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