🧵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' £5M 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
New Video: @GeorgeMonbiot describes the treatment of #MECFS as "The Greatest Medical Scandal of the 21st century". Watch the introduction to a new 27 minute explainer video about the scandal from reframing a recognised neurological illness to the withdrawal of harmful treatments.
Watch the full video (27 mins) about #MECFS & the #GreatestMedicalScandal exploring the impact on patients and how bad science was defended by the scientific & media establishment. Includes clips of experts, MPs, patients & news items.
The video is a timeline of key events used to illustrate the scandal. It is broken down into 27 chapters. See image for the list of chapters and how to navigate them.
Timestamps in the description are best, followed by the chapter menu, the progress bar is a bit fiddly.
🧵of news articles, radio and TV about the landmark prevention of future deaths report following the death of Maeve Boothby O'Neill from Severe #ME
Clip from the BBC World Tonight. @BBCJamieCoo talks about the finding from the prevention of future deaths report "The Health Secretary @wesstreeting needs to "urgently address" the "non-existent” care for people with #MECFS & @KarenLHargrave describes her husbands Severe ME
Full segment. BBC World Tonight (5 mins) @BBCJamieCoo interviews @SonyaChowdhury @KarenLHargrave about #MECFS and the landmark future deaths report.
Highlights from today's BBC Breakfast Interview with @BinitaKane and Sarah Boothby (@swastrosarah) about Severe #MECFS and doctors who have had no training not understanding/listening when they see severly ill patients with #MECFS
TW: Full segment - BBC Breakfast about Severe #MECFS and the death of Maeve Boothby-O'Neill.
Mentions, history, lack of understanding, training and research, no provision and calls for urgent action. @BinitaKane and Sarah Boothby (@swastrosarah)
Associated news articles:
The Times: Coroner to report dangers of ME after Boothby O’Neill death
Maeve Boothby O’Neill’s case highlighted an inability to care for patients who suffer with myalgic encephalomyelitis, or chronic fatigue syndrome
"I feel very strongly that if we had done more to understand what is happening in people with ME, we would be in a much better place to deal with all these people who have Long COVID... By one estimate 50% of people with Long COVID have ME"
@oonagh_cousins former Olympic Rower
Dr Weir on severe #MECFS
"they are unable to even get out of bed, and voluntary activities such as speech, chewing, and eating are directly affected by what can be described as an internal battery, which, instead of being charged at 100%, is probably down to about 5 or 10%."
🧵 of clips from the LBC segment about #MECFS and Simon Wessely yesterday
Natasha Devon reading out @GeorgeMonbiot article about #MECFS and the #GreatestMedicalScandal mentiond Wessely, PACE, & the Science Media Centre that portrayed patients as abusive.
Wessely's biopsychosocial model makes ME patients unreliable witnesses to their own bodies. The model says patients are catastrophising and misunderstand the symptoms of recovery and think this an ongoing illness instead of normal aches and pains of recovery - @JohnTheJack 🔥🙏
I spent the first 20yrs in mental health units because of the biopsychosocial approach to #MECFS. I still have PTSD from that period. I have had water poured over me in bed in the last 10 years by a nurse. I shouldn't get PTSD every time I go to hospital. I shouldn't have water
Full article: My child died of ME’: a scandal waiting for its Post Office moment
Sean O’Neill is dreading his daughter’s inquest but hopes it will show the nation how people with the condition are routinely stigmatised and ignored by the NHS