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The Draft Report by the Institute..[IQWiG] Does Not Provide Any Evidence That GET and CBT are Safe and Effective treatments for ME/CFS, 2023, Vink et

Discussion in 'Psychosomatic research - ME/CFS and Long Covid' started by Trish, Jan 16, 2023.

  1. Trish

    Trish Moderator Staff Member

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    Location:
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    The Draft Report by the Institute for Quality and Efficiency in Healthcare Does Not Provide Any Evidence That Graded Exercise Therapy and Cognitive Behavioral Therapy Are Safe and Effective Treatments for Myalgic Encephalomyelitis/Chronic Fatigue Syndrome
    by
    Mark Vink
    and
    Alexandra Vink-Niese
    https://www.mdpi.com/2079-9721/11/1/11

    Abstract
    The German Institute for Quality and Efficiency in Healthcare (IQWiG) recently published its draft report to the government about myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). The IQWiG concluded that graded exercise therapy (GET) and cognitive behavioral therapy (CBT) should be recommended in the treatment for mild and moderate ME/CFS based on two CBT and two GET studies.

    In this article, we reviewed the evidence used by IQWiG to support their claims, because their conclusion is diametrically opposed to the conclusion by the British National Institute for Health and Care Excellence (NICE) in its recently updated ME/CFS guidelines.

    Our analysis shows that the trials IQWiG used in support suffered from serious flaws, which included badly designed control groups; relying on subjective primary outcomes in non-blinded studies; alliance and response shift bias, including patients in their trials who did not have the disease under investigation, selective reporting, making extensive endpoint changes and low to very low adherence of treatments.

    Our analysis also shows that the report itself used one CBT and one GET study that both examined a different treatment. The report also used a definition of CBT that does not reflect the way it is being used in ME/CFS or was tested in the studies. The report noted that one study used a wrong definition of post-exertional malaise (PEM), the main characteristic of the disease, according to the report. Yet, it ignored the consequence of this, that less than the required minimum percentage of patients had the disease under investigation in that study. It also ignored the absence of improvement on most of the subjective outcomes, as well as the fact that the IQWiG methods handbook states that one should use objective outcomes and not rely on subjective outcomes in non-blinded studies.

    The report concluded that both treatments did not lead to objective improvement in the six-minute walk test but then ignored that. The report did not analyze the other objective outcomes of the studies (step test and occupational and benefits status), which showed a null effect.

    Finally, the report states that the studies do not report on safety yet assumes that the treatments are safe based on a tendency towards small subjective improvements in fatigue and physical functioning, even though the adherence to the treatments was (very) low and the studies included many patients who did not have the disease under investigation and, consequently, did not suffer from exertion intolerance contrary to ME/CFS patients. At the same time, it ignored and downplayed all the evidence that both treatments are not safe, even when the evidence was produced by a British university.

    In conclusion, the studies used by the report do not provide any evidence that CBT and GET are safe and effective. Consequently, the report and the studies do not provide any support for the recommendation to use CBT and GET for ME/CFS or long COVID, which, in many cases, is the same or resembles ME/CFS, after an infection with SARS-CoV-2.

    I added paragraph breaks.
     
  2. IanMcPhee

    IanMcPhee Senior Member (Voting Rights)

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    That certainly seems very familiar. To the extent you'd think they copied PACE's homework.

    Glad to see there's scientific pushback, and I really hope it gets no further than the draft report, for the sake of German sufferers.
     
    Solstice, Mithriel, Lisa108 and 13 others like this.
  3. Peter Trewhitt

    Peter Trewhitt Senior Member (Voting Rights)

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    It is good that more academics are openly challenging the PACE hegemony.

    This at least makes it harder for the cultists to keep dragging out the militant anti science patient trope. Perhaps the new NICE guidelines are giving other academics more courage or is it that the GET/CBT cheerleaders are being more obviously irrational?
     
  4. MeSci

    MeSci Senior Member (Voting Rights)

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    I think that the Vinks have been very active in the field for some time.
     
    Mark Vink, Solstice, Mithriel and 8 others like this.
  5. Peter Trewhitt

    Peter Trewhitt Senior Member (Voting Rights)

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    Yes, the Vinks have been fantastic research advocates for people with ME, but it feels to me the tone of what is being published is changing, becoming much more challenging of the inappropriately named BPS nonsense.
     
  6. rvallee

    rvallee Senior Member (Voting Rights)

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    So does Cochrane's handbook. And I doubt the previous NICE guidelines actually respected their own rules. And yet there is an entire category of reviews built only on studies that technically don't meet their own standards. Studies that are built on, well, this:
    It's the psychosomatic exemption. Rules and standards, yes, but not for this because we prefer it this way. Hence those are not actual standards, in the end it all comes down to people's judgments and opinions about the evidence, a completely unreliable methodology when dealing with unscientific studies. This is the fatal flaw of evidence-based medicine, it's a popularity contest that actually locks failure in place more than anything else.
     
  7. Peter Trewhitt

    Peter Trewhitt Senior Member (Voting Rights)

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    @rvallee

    The late … (sorry I struggle with names and struggle with finding previous threads here) did some very impressive work pointing out in detail that the Cochrane Exercise Review was not only rubbish but that it significantly deviated from Cochrane’s own published standards. It almost looked as if his work and additional pressure from others would get it withdrawn, but then we ended up, after lots of delay and presumably lots of behind the scenes politicking, with the current limbo of the review not being officially current but still lurking with its status unclear enough that people can go on citing it.
     
  8. rvallee

    rvallee Senior Member (Voting Rights)

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    I'm pretty sure you're actually thinking of Vink, the author of this paper? The CBT review criticism was devastating, but they clearly don't care about their own standards so that's that. I think he and his other collaborator wrote a paper for each. Both reviews ignored Cochrane's own proclaimed "standards", which actually contradicts the idea that they are standards.
     
  9. Peter Trewhitt

    Peter Trewhitt Senior Member (Voting Rights)

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    (Got there in the end.) I was referring to the complaint made by Robert Courtney, see thread here https://www.s4me.info/threads/cochr...arun-et-al-recent-developments-2018-19.10030/
     

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