1. Sign our petition calling on Cochrane to withdraw their review of Exercise Therapy for CFS here.
    Dismiss Notice
  2. Guest, the 'News in Brief' for the week beginning 8th April 2024 is here.
    Dismiss Notice
  3. Welcome! To read the Core Purpose and Values of our forum, click here.
    Dismiss Notice

Caroline Struthers' letter to Cochrane Governing Board

Discussion in 'Psychosomatic news - ME/CFS and Long Covid' started by Peter Trewhitt, Nov 29, 2018.

  1. Peter Trewhitt

    Peter Trewhitt Senior Member (Voting Rights)

    Messages:
    3,666
    Presumably the only potentially hopeful sign was that Larun felt there was a need to leak to the Reuter's journalist that Cochrane were considering withdrawing in some fashion this review, and to brief against them with the false 'bullying patients' narrative.

    Presumably Larun and the BPS crew were feeling threatened in some way, given putting this all in the public domain was not without risk to them.
     
    Last edited: Nov 29, 2018
  2. Patient4Life

    Patient4Life Senior Member (Voting Rights)

    Messages:
    213
    Seems this type of fiasco is right up her ally of work.

     
    SarahandElly, WillowJ, Liessa and 9 others like this.
  3. TiredSam

    TiredSam Committee Member

    Messages:
    10,496
    Location:
    Germany
    This could be based on Cochrane deciding to take at face value the authors' estimate of when the imminent resubmission would be made. If so this leaves plenty of scope for footdragging and Cochrane being surprised that the resubmission is taking longer than the authors' initially estimated.
     
  4. Esther12

    Esther12 Senior Member (Voting Rights)

    Messages:
    4,393
    Looks like the review was updated today, after 5:30 -

    https://www.cochranelibrary.com/cdsr/doi/10.1002/14651858.CD003200.pub7/information#history
     
    WillowJ, Simon M, Sean and 12 others like this.
  5. andypants

    andypants Senior Member (Voting Rights)

    Messages:
    1,334
    Location:
    Norway
    NelliePledge and Esther12 like this.
  6. Hutan

    Hutan Moderator Staff Member

    Messages:
    26,856
    Location:
    Aotearoa New Zealand
  7. Hutan

    Hutan Moderator Staff Member

    Messages:
    26,856
    Location:
    Aotearoa New Zealand
  8. Cheshire

    Cheshire Moderator Staff Member

    Messages:
    4,675
  9. Tijs

    Tijs Established Member

    Messages:
    12
  10. rvallee

    rvallee Senior Member (Voting Rights)

    Messages:
    12,426
    Location:
    Canada
    I'm sure this is the kind of reassuring talk people want to hear from a medical review organisation. That will go down well with their policy that it's perfectly fine for researchers to review their own work and grade it as flawless and perfect and there's nothing wrong with that.

    Found a new slogan for Cochrane: objectivity is overrated. Alternatively: because it feels true.

    Literally centuries of scientific lessons flushed down the toilet. Make phrenology great again?
     
    feeb, 2kidswithME, JaneL and 21 others like this.
  11. Barry

    Barry Senior Member (Voting Rights)

    Messages:
    8,385
    I think we need to work on how to convince people of the how flawed it is to combine subjective outcomes with unblinded trials. There is clearly a good deal of convincing still to do. I seem to recall @Jonathan Edwards saying some time back on PR that quite a few people took a lot of convincing initially when he raised the point. Coming to all this from scratch, once pointed out it seemed terribly obvious to me and still does. But I think there is a lot of inertia in establishment mind set that really doesn't see otherwise. How to change that. For psych therapies aimed at genuine psych conditions, the notion may hold some water, but when targeted toward physical conditions with objective outcomes available, it's junk. Something for 2019.
     
    JaneL, Dolphin, Liessa and 6 others like this.
  12. Andy

    Andy Committee Member

    Messages:
    21,914
    Location:
    Hampshire, UK
    https://healthycontrolblog.wordpres...iew-of-exercise-for-chronic-fatigue-syndrome/
     
    JaneL, Dolphin, Sean and 13 others like this.
  13. NelliePledge

    NelliePledge Moderator Staff Member

    Messages:
    13,259
    Location:
    UK West Midlands
    I think the comment about Cochrane not being responsible for what use is made of their reviews is somewhat disingenuous. What is the point of doing a review if it is not to inform clinical policy and practice which in turn inevitably influences policy and practice on financial support through occupational or social security benefits.
     
    JaneL, rvallee, Skycloud and 16 others like this.
  14. ME/CFS Skeptic

    ME/CFS Skeptic Senior Member (Voting Rights)

    Messages:
    3,507
    Location:
    Belgium
    My quick thoughts:

    1) Tovey confirms that Cochrane planned to temporarily withdraw the Larun et al. GET review because the authors did not adequately respond to criticism in time. This was what the Reuters article was about. "A subsequent meeting with two of the authors” made the Cochrane editors change course.

    Yet Toveys reponse suggests that personal reasons were involved in the authors failure to respond in time and he says that Cochrane only wanted to withdraw the review temporarily, "to give them time without pressure to address the issues raised fully." I suppose it's possible that one of the authors had personal reasons (sickness or deceased family member or something like that) that made it difficult to respond in time and that the Cochrane editors underestimated this.

    2) Tovey says that currently the process of re-submitting, reassessment and peer review is pending, but it is not clear what this means as the authors have already offered a re-submission that was deemed unfit. To me it seems that the authors are allowed to make lots of mistakes and do-overs. Are they now doing a re-re-submission? Is there going to be a re-re-resubmission?

    3) The most controversial point in Tovey’s response concerns the issue of “using only subjective outcomes in unblindable trials”. “To describe this as ‘terrible methodology’ is simply an opinion”, Tovey says, “and it is not shared by independent methodologists who we consulted". Weird.

    Tovey also claims that “objective measures such as resource use were reported when they were identified.” That doesn’t seem right. As Vink showed objective outcomes mostly showed null results and were not considered in the Cochrane assessment of GET. https://journals.sagepub.com/doi/full/10.1177/2055102918805187
     
    Simone, JaneL, WillowJ and 21 others like this.
  15. obeat

    obeat Senior Member (Voting Rights)

    Messages:
    682
    Surely the point about subjective trials is that there is HIGH BIAS in them, and the Cochrane review says it's low bias. Do the independent methodologists consider it low or high?
    What is the current thinking on bias in subjective trials among psychologists @Brian Hughes ?
     
    Simone, JaneL, WillowJ and 17 others like this.
  16. inox

    inox Senior Member (Voting Rights)

    Messages:
    539
    Location:
    Norway
    Haven't been able to read the blogpost yet - but this is more or less exactly what is the current mission statement (or something like that) for Cochrane now.
     
  17. BruceInOz

    BruceInOz Senior Member (Voting Rights)

    Messages:
    414
    Location:
    Tasmania
    It seems to me that the response to point 3 regarding subjective measures in unblinded trials focussed only on the subjective measures and did not consider the consequences of combining that with lack of blinding. I think this is the strongest point with the weakest response. It should be made again but stronger with references to eliminate the "it's just an opinion" rebuttal.
     
  18. inox

    inox Senior Member (Voting Rights)

    Messages:
    539
    Location:
    Norway
    Low reading ability-day today, so still haven't read the bofpost, just some tweets. But really surprised that Tovey would actually put that bit about - "saying that reporting only subjective outcomes in unblindable trials is "terrible methodology" is just an opinion" - in writing. And referencing to some un-named "methodology expert".

    To Struthers?

    I'm glad he did though, even if it makes me nervous about the fate of the ME exercise reviews. Because this will be so obvious wrong (or so I'm hoping....), that it's getting the attention of others.

    https://twitter.com/user/status/1082383175853064192
     
    Simone, Hutan, JaneL and 16 others like this.
  19. ME/CFS Skeptic

    ME/CFS Skeptic Senior Member (Voting Rights)

    Messages:
    3,507
    Location:
    Belgium
    Hilda Bastian is a well respected skeptic who has a blog on Plos One about science and research methodology. Would be great if she got involved as well.
     
    Simone, Hutan, JaneL and 16 others like this.
  20. Esther12

    Esther12 Senior Member (Voting Rights)

    Messages:
    4,393
    Yeah, this response makes me think that Cochrane is even worse than I'd feared and leaves me dreading whatever they're going to do next. So many annoying and misguided things about it. I'm going to have to re-read it with lowered expectations so I can avoid being distracted by my eyes rolling back into my head.
     
    Simone, Hutan, JaneL and 20 others like this.

Share This Page