🧵Diagnostic Criteria and NICE downgrading evidence explainer.
NICE have received criticism about the diagnostic criteria they chose and that studies have been inappropriately downgraded. This will be discussed at tomorrow's roundtable.
The hallmark symptom of ME/CFS is Post Exertional Malaise (PEM), even minimal exertion can cause a flare in symptoms and a reduction in physical capability (a crash) that can last for days, weeks or even months.
There are several diagnostic criteria for ME/CFS. PEM is widely acknowledged in specialist practice as being a characteristic feature. However, not all diagnostic criteria require PEM as mandatory which leaves them open to include people with other fatigue-related conditions.
The criteria that NICE used is largely based on the IOM criteria and requires PEM. The US criteria was created in 2015 after an extensive review of the ME/CFS literature. 15 experts spent a year reviewing over 10,000 peer reviewed studies to produce a report which cost $1M.
A lot of evidence for Graded Exercise used old diagnostic criteria (eg Oxford criteria 1991) where PEM was not required. It's not certain that all the patients in these studies had ME/CFS making it difficult to be sure the treatments are safe and effective for people with ME/CFS
NICE used GRADE (Grading of Recommendations Assessment, Development and Evaluation) an internationally recognised approach to assess the quality of evidence. NICE scored evidence without PEM as 'indirect' and downgraded it acknowledging the uncertainty about diagnosis.
After stakeholder feedback NICE revisited the evidence looking specifically at PEM reported and the application of GRADE and indirectness.
"This did not result in any change to the recommendations." - Government Briefing 17 Aug
The supposedly 'definitive' ÂŁ5M PACE trial, the largest study of behavioural treatments in ME/CFS, is a clear example of this issue.
PACE used the 1991 Oxford criteria which did not require PEM, some participants probably had other fatigue related conditions & didn't have ME/CFS
The Agency for Healthcare Research and Quality (AHRQ) and The National Institute of Health (NIH) recommended that the criteria used in the PACE trial should be retired.
The NIH stated that the criteria could "impair progress" and "cause harm"
The Agency for Healthcare Research also assessed the impact of studies using
the Oxford criteria on their recommendations.
When studies using the PACE criteria were excluded "there would be insufficient evidence of the effectiveness of [Graded Exercise] GET on any outcome"
References:
Government briefing sent from NICE to the Department of Health and Social Care on 17 August
You made a panorama programme in 2010 about Lynn Gilderdale a patient with Severe ME who died by suicide.
Lynne was made worse by Graded Exercise which is currently recommended by the 2007 NICE 2007 Guideline for ME/CFS.
NICE were due to remove Graded Exercise on 18 August but went against their own rigouous process and stopped publication a few hours before after pressure from parts of the medical establishment.
NICE spent 3yrs reviewing the evidence and found the quality was not good enough to recommend Graded Exercise and that it is potentially harmful. Over 50% of patients report that Graded Exercise makes them worse. Many patients have been made significantly more disabled.
After an extensive 3 year review NICE were going to stop recommending Graded Exercise for ME/CFS, due to lack of evidence and possible harm. The day before it was due NICE decided to halt publication after medical bodies were refusing to endorse it.
This thread of updated explainer videos (with clips from experts, MPs and patients) outlines some of the reasons why NICE we're going to drop Graded Exercise and the devastating impact it has had on patients over the last few decades.
The hallmark symptom of ME/CFS is: even minimal exertion can cause a flare in symptoms and a reduction in physical capability (a crash) that can last for days/weeks/months.Â
The 2007 guideline which included Graded Exercise "does not fit" with patient experience - Dr Muirhead
"This document takes an extremely partisan review of the scientific evidence... In my view, following these guide-
lines risks harm to patients. The fact that NHS Scotland appears to have endorsed it is worrying and represents a major departure from evidence based medicine."
"The introduction presents a very negative picture of the illness as neurological and permanent. This does
not apply to the vast majority of people seen in medical practice with chronic fatigue syndrome and is likely to lead to alarm and therapeutic nihilism."
"The departures suggest divisions within the committee over the guideline’s final content, which is an update on 2007 guidance on diagnosing and managing ME/CFS. Three have resigned, and one [Charles] has been removed by NICE."
Michael Beadsworth, a consultant in infectious diseases, Liverpool
Gabrielle Murphy, clinical lead of the fatigue service at the Royal Free
Joanne Bond-Kendall, senior physiotherapist at the ME/CFS service in.
Of course Garner was asked to comment "These resignations can only mean a critical breakdown in the methods for formulating the recommendations. Normally areas of disagreement are solved by formal consensus methods, voting, or informally. That is what the panel is for: to agree"
Trudie Chalder (PACE trial) is training health professionals on Long Covid. Describes Post Exertional Malaise as "Health anxiety" and an "Extreme behavioural response" states "Exercise is clearly not damaging" and recommends "Increasing exercise" #LongCovid#MECFS
Long Covid overlaps with ME/CFS video - Why exercise is harmful with testimony from harmed patient
Trudie Chalder also misrepresented one of her studies in her presentation by missing out the 12 month follow up data. Including it would have shown no significant difference.
Thread of clips from Michael Sharpe's retirement interview on the Today programme - BBC Radio 4 in 2019.
He describes "A small group of campaigners."
At the time over 80 charities (almost all of them) and 100 academics signed an open letter calling for PACE to be reanalyzed.
He claims that campaigners "stalk researchers" and mentions "threats of violence"
When QMUL refused to release the PACE data it went to tribunal. A witness compared ME/CFS activists to animal rights groups and claimed there were serious risks of violence.
However, the tribunal concluded that "It was clear that his assessment was "grossly exaggerated and the only actual evidence was that an individual at a seminar had heckled Professor Chalder”