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Jun 7 42 tweets 20 min read
Fiona Fox director of the Science Media Centre has a new book out called Beyond The Hype - The Inside Story of Media's Biggest Controversies.

The chapter on ME/CFS "First they came for the communists" is biased, inaccurate and offensive. #BeyondTheHype

🧵Thread
Fox writes glowingly about a group of #MECFS researchers that are being harassed and discredited by a small group of 'activitists' and is concerned that science is under attack. The chapter title appears to liken these 'activists' to Nazis.
Fox claims the 'activists' are in the minority but over 80 charities and over 100 academics don't trust the research and 15,000 people have expresed no confidence in the treatments.

virology.ws/2018/08/13/tri…
Fox "doesn't fully understand their grievances" but suggests patients reject psychological treatments because it suggests #MECFS is all in the mind. A classic strawman which provokes debate about physical vs mental illness and distracts from the main issues.
Fox fails to explain that a major objection is that the treatments do not fit the patient experience. The hallmark symptom of #MECFS is Post Exertional Malaise, where minimal exertion can cause a flare in symptoms (a crash) that can last for days, weeks or even months.
Graded Exercise and CBT as a treatment for #MECFS is so absurd that an NHS doctor completely disregarded #MECFS as a diagnosis for herself for three months because exercise made her worse and CBT didn't seem appropriate.
Fox says that "some patients report poor outcomes", but doesn't mention that
over 50% of patients consistently report Graded Exercise makes them worse. (11 surveys / 18,000 patients).

Many patients who were previously able to walk ended up in wheelchairs or bedbound.
Post Exertional Malaise (PEM) is now widely acknowledged to be a characteristic feature of #MECFS but the bulk of the evidence being criticised used definitions of #MECFS from the 1990s where PEM is not required.
So patients in these studies may not have had #MECFS and may have had other fatigue-related conditions instead.

This makes it difficult to be sure these studies show the treatments are safe and effective for people with #MECFS.
Fox writes about "good medical evidence" being "attacked and misrepresented" but major health organisations like NICE, NIH, Cochrane, AHRQ have identified significant issues with the evidence.

NICE and the CDC have also withdrawn the treatments.
The £5M PACE trial was the largest trial of its kind but has so many flaws it's taught in University as an example of "How NOT to conduct a clinical trial" and the research into Graded Exercise is "based on science so bad" it's taught in Research Misconduct sessions.
Fox on the other hand believes that because a statistician who worked on PACE told her she uses it in her own training programme as an example of a "good clinical trial" it demonstrates it's a good trial.
PACE had many problems but the biggest is that it was non-blinded and relied on self report data (questionnaires).

This meant patients were aware of the treatment they were receiving which could cause them to consciously or subconsciously feel better and influence the results.
Similar trials of Graded Exercise in #MECFS have the same design flaw - "so problems of bias, make more or less all the trials to date unsuitable as a basis for treatment recommendation.” 

- Prof Edwards expert testimony to NICE explains in more detail.

mecfsresearchreview.me/2021/01/12/the…
Fox writes PACE has been "attacked as ‘scientific and financial fraud’, ‘a piece of crap’ and ‘one of the biggest medical scandals of the 21st century’"

Fraud is difficult to prove but there is evidence of outcome switching which led to inflated treatment effects.
Patients had to meet 4 criteria in order to count as "recovered". Midway through the trial the authors relaxed the thresholds for all 4 criteria.

This made it much easier for patients to count as “recovered” than if they used the criteria defined in their original protocol.
Physical function was lowered to a level similar to patients with congestive heart failure.

And because it was lower than the entry criteria, 13% of patients had already “recovered” on that physical function score before they’d had any therapy at all.

meaction.net/2016/12/14/the…
Minutes obtained by FOI also revealed that activity trackers were dropped mid trial because an unpublished Dutch study reported "no change in this in spite of improvement in fatigue". So patients reported feeling less fatigue but didn't manage to increase their activity.
Fox claims the Health Research Authority "vindicated" PACE and said it was a "good trial" but this is misleading because they couldn't comment on the quality of the trial as it was "outside their remit".

They only said there were many elements of "good practice".
NICE spent 3 years carefully reviewing the evidence for Graded Exercise and CBT and concluded it was all "low" or "very low" quality and the treatments were potentially harmful.

The treatments were not supported by the evidence so they withdrew them.

thesciencebit.net/2021/08/15/the…
Fox quotes the Royal Colleges saying they lobbied NICE after discovering many of their points from the consultation had not made it into the final draft and the evidence base seemed to have been manipulated.
NICE responded to every piece of stakeholder feedback which is available in a public document.

They also re-analysed some evidence after feedback about PEM to make sure the grading was correct.

There is no evidence of evidence being manipulated.
However, there is evidence an individual associated with the Royal College of Psychiatrists asked the Chief Executive of NICE to tamper with evidence in the weeks before the guideline was due to be published.

domsalisbury.github.io/mecfs/nice-mec…
The claim that "three members of the committee had resigned because they had felt unable to sign up to the final guideline" is false. The committee reached a consensus and signed off the guideline before the clinicians resigned.

nice.org.uk/guidance/ng206…
Fox writes about the Royal Colleges objections highlighting that NICE discarded the Cochrane review. NICE explained this was because they didn't agree with their approach to meta analysis but included all the same studies in their own review.

nice.org.uk/guidance/ng206…
NICE also noted the Cochrane review is "contested and that it 'is still based on a research question and a set of methods from 2002, and reflects evidence from studies that applied definitions of #MECFS from the 1990s'." and they were doing a doing a full update.
But Fox wrote that the SMC spoke to Cochrane & "they believed in the quality of the medical research available, and broadly rejected the criticisms circulating on social media and among patient activists". She failed to mention any of the limitations or the full update.
Fox mentions the complaint which led to the update in 2019 and includes a quote drawing parrallels with Animal Rights activists that Cochrane should not be influenced "by unsubstantiated views or commercial pressures".
But an FOI request revealed the Editor in Chief of Cochrane thought the complaint was "thoughtful and reasonable" and noted the author and "the trialists of the included reviews, tend to refer to all criticism of the trials and the review as being the result of ‘activism’."
Harassment has been used to discredit the patient community and deflect legitimate criticism.

The SMC helped organise a campaign in the press that sensationalised the behaviour of a tiny number of individuals as a vicious attack on science and the researchers.
When claims of harassment were tested in court they were found to be "grossly exaggerated". A PACE author, accepted that "unpleasant things have been said to and about PACE researchers only, but that no threats have been made either to researchers or participants”.
The Information commissioner also commented on Professor Anderson drawing parallels with animal rights pressure groups and states his evidence was "an 'over-extension' from his work with completely unrelated animal rights activists".

informationtribunal.gov.uk/DBFiles/Decisi…
An FOI request to Esther Crawley's university also revealed that no incidents of harassment had been recorded despite her claims that colleagues opened her mail and screened her emails.

vadamagazine.com/lifestyle/heal…
Many of the stories focused on Simon Wessely who pioneered the treatments. He has a vested interest in the research but was also on the board of the SMC & their advisory panel a COI that was never disclosed in any of the stories or Foxs book. They even nominated him for an award.
Fox writes about complaints against individual researchers but fails to mention there have been multiple examples of the PACE authors & their associates making complaints when people are publicly critical of the PACE trial or related research.

me-pedia.org/wiki/Intimidat…
It's also important to acknowledge the impact on patients. Alem Matthees health suffered significantly in part from the efforts to release the PACE data. A tribunal would not have been necessary had they just complied with the FOI and released it.

virology.ws/2018/05/07/tri…
Fox writes "The SMC is not in the business of championing one area of research or backing a particular approach". But thats exactly what they did with #MECFS like this fact sheet sent to journalists just before the publication of a PACE re-analysis paper.

sciencemediacentre.org/wp-content/upl…
It describes PACE as a "good quality trial", downplays the criticisms and harm and tries to discredit papers critical of PACE by saying they are published in low impact journals. It also fails to mention opposition from agencies like AHRQ.
Fox and the SMC have been criticised before "Perhaps the biggest criticism of Fox and the SMC is that they push science too aggressively — acting more as a PR agency than as a source of accurate science information." Article in Nature 2013.

nature.com/articles/49914…
This excellent short blog by @_Lucibee highlights how the SMC advised Climategate scientists to ignore personal attacks and restate the science clearly, instead of focusing on the harassment in the case of #MECFS research.

lucibee.wordpress.com/2022/05/30/smc…
References:

AHRQ Impact of Oxford Criteria
effectivehealthcare.ahrq.gov/sites/default/…

NIH comments on Oxford Criteria
prevention.nih.gov/sites/default/…

Graded Exercise Harm Survey meta-analysis
meassociation.org.uk/2017/09/mea-re…

Activity monitors being dropped
lucibee.wordpress.com/2018/05/09/pac…

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More from @ABrokenBattery

May 19
🧵Gulf War Syndrome & Simon Wessely

"For 30 years they have been disowned, ignored and lied to by consecutive governments, with no positive answers to their questions about exposure to toxic substances and gases & the affect it had on them"

bbc.com/news/health-61…
"Even when I was still in the military, I was getting illness after illness... when I questioned whether it could be anything to do with my service in the Gulf or what we were exposed to, the military line was 'You're talking nonsense, there's no evidence.'"
But new research links the nerve agent Sarin to Gulf War Syndrome in >1000 veterans.

Sarin was released into the air when caches of Iraqi chemical weapons were bombed, it is usually deadly but soldiers were exposed to low doses which is thought to be the cause of GWS.
Read 19 tweets
May 12
🧵ME/CFS is often referred to as neglected, under-researched and poorly understood in the media. This is obviously welcome but feels like a disservice when it has also been described as one of the biggest medical scandals of this century.

- Explainer -
This is particularly relevant to #LongCovid where there is growing evidence a subset looks identical to ME/CFS and many meet the diagnostic criteria. It is important to acknowledge the scandal and not repeat the same mistakes.
Graded Exercise Therapy and CBT have been prescribed for people with ME/CFS for decades but have recently been withdrawn by NICE & the CDC because the supporting research was too low in quality and there have been high reports of patient harm.
Read 15 tweets
Apr 18
🧵 Summary of the Countess of Mar's questions in parliament in 2004 about Simon Wessely, his clique of psychiatrists and their "dominance in the thinking about ME/CFS".

Explains why we don't have any treatments for ME/CFS that would probably help a subset of #LongCovid aswell.
The alt name CFS has led to confusion "that has served well the aims of a group of psychiatrists who assert that... ME/CFS is simply medically unexplained chronic fatigue & that it should be classified as a mental disorder over which they should exert control."
"Wessely is politically astute and, in conjunction with his colleagues, has gained respectability in medical and political establishments by producing vast numbers of papers that purport to be about ME."
Read 15 tweets
Feb 12
A few thoughts on the comment in the Lancet about the NICE guideline.

"subjective symptoms are the most valid endpoints"

If blinding is not possible the outcome measures must be objective to reduce expectation bias. Objective measures show no improvement eg. in the PACE trial.
"NICE guideline committee presented
a new non-validated diagnostic definition"

It was based on the 2015 IOM criteria which has PEM as mandatory and is used by the CDC.

More info here.

An FOI revealed that NICE were aware of the IOM criteria and that evidence may need to be downgraded in 2015.

Read 12 tweets
Feb 10
"If Sophia doesn't get better in 6 months... or if she doesn't go to the ME clinic he said i'm going to section her... and if you try and stop me I will have you removed as the nearest relative... if you do not open the door... I will get the Police to smash the door down"
Sophia Mirza was sectioned in 2003 and Police forced entry into her home, she was eventually released but had severely deteriorated and later died. Sophia was the first person to have ME recorded as the cause of death in the UK.

me-pedia.org/wiki/Sophia_Mi…
Content Warning 🚨

More on Sophia can be found in the film Voices from the Shadows including an audio recording of her being sectioned.

Starts at 21 mins

vimeo.com/203285883/8344…
Read 4 tweets
Jan 30
New FOI Documents from the pause of the NICE GL to publication.

RCPsych objected to the evidence review claiming PACE "provides robust evidence", the new GL is "potentially harmful for patients" and that bad experiences likely due to "poor practice".
The RCPhysicians admitted that patients have been "subjected to humiliating treatment at the hands of both trialists and clinicians" because treatment wasn't individualised
The RCPhysicians also objected to the evidence review and suggested "NICE should consider a less rigid approach" and be "less focused on research design" they suggested the National Service Framework for Long Term Conditions which was was written in 2005.
Read 4 tweets

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