Cannabis spray being tested for pain, anxiety & depression in Cardiff

Wales online article, by Mark Smith, 23 August 2016: People with depression, anxiety and arthritis could use a cannabis spray being tested in Cardiff

The testing is happening at an NHS facility in Cardiff

cannabis1
A cannabis-based vapouriser is being tested in Wales.

We’ve learned that an NHS facility in Cardiff is testing the vapouriser to determine the cannabinoid concentration of the formula.

Two years ago, Wales became the first UK nation to legalise a cannabis based drug for Multiple Sclerosis sufferers.

The new vapouriser is a MediPen, which is inhaled like an e-cigarette.

The MediPen, which is inhaled like an e-cigarette, has been described as a “completely legal and harm-free way to unleash the miraculous health benefits of cannabis”
It has been described as a “completely legal and harm-free way to unleash the miraculous health benefits of cannabis”.

It uses a substance known as cannabidiol, an oil extracted from the cannabis plant that does not contain any of the psychoactive chemicals which get a person high.

It claims to be able to reduce anxiety, depression and even relieve the pain of arthritis and fibromyalgia.

We understand that the cannabidiol (CBD) vaporiser, which can already be bought online, is undergoing quality control measures in Cardiff and Vale University Health Board.

But the exact location cannot be released by the NHS due to a non-disclosure agreement which prevents them from sharing client information.

READ MORE
How many of us would buy cannabis if it was sold in high street shops?

All contracts scrutinised
A spokesman for Cardiff and Vale University Health Board said:

“As a University Health Board we undertake a number of commercial activities, such as quality control with private companies, including Medipen.

“Due to commercial in confidence we are not able to provide any further details.

“All Cardiff and Vale University Health Board contracts are scrutinised for ethical, legal and commercial sensitivities and any breach of this will be fully investigated by the Health Board.”

MediPen believes that by testing products with the help of the NHS, the public’s perception of cannabis will change.

It says it wants to “end the criminalisation of over one million medicinal users” and make cannabis-based medication readily available to those who need it.

Managing director Jordan Owen said:

“Our contract is for the purposes of safety, quality control and to ensure the consistency of cannabinoid concentration throughout each batch.

“This is something that is extremely important in an industry subject to so many negative connotations, by testing our proprietary formula through a reputable body such as the NHS we are confident that this will have a very positive impact on the public’s perception of cannabis.

“This is a huge leap forward”

“This is a huge leap forward for the UK’s rapidly growing legal cannabis industry and we are confident that by breaking down the negative connotations surrounding cannabis this will have a positive effect on our countries draconian prohibition laws that are having a detrimental impact on the lives of millions of medicinal cannabis users across the UK.”

The MediPen, which is described as a “sleek and stylish portable handheld device ”, can be bought online for as little as £50 and has 17 flavours.

It says it uses cannabis plants grown in the Netherlands with the sole aim of maximising CBD content whilst eliminating any traces of tetrahydrocannabinol, the primary ingredient in marijuana responsible for the high.

See also: abc.net.au, 13 August 2016 Medicinal cannabis scheme will make ‘life worth living’ for Canberra resident

Fatigued, frequently ill and experiencing ever-changing symptoms, Sue Curry has spent years living with a debilitating illness.

“It’s like having the flu, a concussion, multiple sclerosis,” she said.

Her illness, Chronic Fatigue Syndrome or Myalgic Encephalomyelitis (ME), is poorly understood and has no certain pharmacological treatment.

“When we are hit severe, you don’t see us anymore,” Ms Curry said…

 

Posted in News | Tagged , , , , , | Comments Off on Cannabis spray being tested for pain, anxiety & depression in Cardiff

Catalogue of writings by Prof Hooper & Margaret Williams

A website containing a catalogue of all the articles on ME written by Margaret Williams and Professor Malcolm Hooper can be found at: www.margaretwilliams.me/

The articles in this catalogue have been available on the internet or elsewhere for many years but now for the first time have been brought together in one place. The intention is to provide a valuable historical resource for researchers, advocates, patients and anyone interested in the illness Myalgic Encephalomyelitis/Chronic Fatigue Syndrome. These articles illustrate how the “Wessely School” have ignored the biomedical science on ME/CFS for almost 30 years.

Margaret Williams is the pen-name used by someone who spent her professional life in the British National Health Service (NHS), latterly in a senior clinical capacity for many years until severe ME put an end to her career. For professional and personal reasons she does not wish her own name to be in the public domain.

Malcolm Hooper is Professor Emeritus of Medicinal Chemistry at the University of Sunderland in the UK, and is an advocate for ME/CFS patients. He chaired the International Invest in ME Conference in 2008, 2010, and 2011. He is also the Chief Scientific Adviser to the British Gulf War Veterans Association.

hooper

With contributions from Eileen Marshall (1994-2007) and others.

Posted in News | Tagged , , | Comments Off on Catalogue of writings by Prof Hooper & Margaret Williams

The role of inflammation & over active immune system in depression

BBC news report, by James Gallagher, Rachael Buchanan & Andrew Luck-Baker, 24 August 2016: Depression: A revolution in treatment? The Inflamed Mind, BBC Radio 4

It’s not very often we get to talk about a revolution in understanding and treating depression and yet now doctors are talking about “one of the strongest discoveries in psychiatry for the last 20 years”.

It is based around the idea that some people are being betrayed by their fiercest protector. That their immune system is altering their brain.

The illness exacts a heavy toll on 350 million people around the world, among them Hayley Mason, from Cambridgeshire:

“My depression gets so bad that I can’t leave the bed, I can’t leave the bedroom, I can’t go downstairs and be with my partner and his kids.

The 30-year-old added: “I can’t have the TV on, I can’t have noise and light, I have suicidal thoughts, I have self-harmed, I can’t leave the house, I can’t drive.

“And just generally I am completely confined to my own home and everything else just feels too much.”

Anti-depressant drugs and psychological treatments, like cognitive behavioural therapy, help the majority of people.

But many don’t respond to existing therapies and so some scientists are now exploring a new frontier – whether the immune system could be causing depression.

“I think we have to be quite radical,” says Prof Ed Bullmore, the head of psychiatry at the University of Cambridge.

He’s at the forefront of this new approach:

“Recent history is telling us if we want to make therapeutic breakthroughs in an area which remains incredibly important in terms of disability and suffering then we’ve got to think differently.”

The focus is on an errant immune system causing inflammation in the body and altering mood.

And Prof Bullmore argues that’s something we can all relate to, if we just think back to the last time we had a cold or flu.

He said: “Depression and inflammation often go hand in hand, if you have flu, the immune system reacts to that, you become inflamed and very often people find that their mood changes too.

“Their behaviour changes, they may become less sociable, more sleepy, more withdrawn.

“They may begin to have some of the negative ways of thinking that are characteristic of depression and all of that follows an infection.”

It is a subtle and yet significant shift in thinking. The argument is we don’t just feel sorry for ourselves when we are sick, but that the chemicals involved in inflammation are directly affecting our mood.

Find out more
You can listen to The Inflamed Mind documentary on BBC Radio 4 at 21:00 BST and then here on iPlayer.

Inflammation is part of the immune system’s response to danger. It is a hugely complicated process to prepare our body to fight off hostile forces.

If inflammation is too low then an infection can get out of hand. If it is too high, it causes damage.

And for some reason, about one-third of depressed patients have consistently high levels of inflammation. Hayley is one of them: “I do have raised inflammation markers, I think normal is under 0.7 and mine is 40, it’s coming up regularly in blood tests.”

There is now a patchwork quilt of evidence suggesting inflammation is more than something you simply find in some depressed patients, but is actually the cause of their disease. That the immune system can alter the workings of the brain.

Joint pain
To explore this revolutionary new idea in depression, we visited an arthritis clinic at Glasgow Royal Infirmary.

It is perhaps an unexpected location, but it was in clinics like this that doctors noticed something unusual.

Rheumatoid arthritis is caused by the immune system attacking the joints. And when patients were given precise anti-inflammatory drugs that calmed down specific parts of the immune response, their mood improved.

Prof Iain McInnes, a consultant rheumatologist, said:

“When we give these therapies we see a fairly rapid increase in a sense of well-being, mood state improving quite remarkably often disproportionately given the amount of inflammation we can see in their joints and their skin.”

It suggests the patients were not simply feeling happier as they were in less pain, but that something more profound was going on.

Prof McInnes added: “We scanned the brains of people with rheumatoid arthritis, we then gave them a very specific immune targeted therapy and then we imaged them again afterwards.

“What we are starting to see when we give anti-inflammatory medicines is quite remarkable changes in the neuro-chemical circuitry in the brain.

“The brain pathways involved in mediating depression were favourably changed in people who were given immune interventions.”

One possible explanation is that inflammatory chemicals enter the brain. There they interrupt the production of serotonin – a key neurotransmitter that’s linked to mood.

To hear more we visited Carmine Pariante’s laboratory at King’s College London. The professor of biological psychiatry has been piecing together the evidence on inflammation and depression for 20 years.

He told the BBC: “Nearly 30% to 40% of depressed patients have high levels of inflammation and in these people we think it is part of the causal process.

“The evidence supporting this idea is that high levels of inflammation are present even if someone is not depressed, but is at risk of becoming depressed.

“We know from studies that if you have high levels of inflammation today you’re at higher risk of becoming depressed over the next weeks or months even if you are perfectly well.”

He’s shown that not only are depressed patients more likely to have high levels of inflammation, but those with an overactive immune system are also less likely to respond to anti-depressants.

This is a big deal because a third of patients don’t get any benefit from drug treatments.

But there’s something confusing here. The immune system responds to infection and that doesn’t seem to fit the usual story of depression.

Take Jennifer Streeting, a trainee midwife in London, who traces her mental health problems back to when she was 14.

“My nana passed away and my mum had breast cancer and if you ask my therapist now she puts it down to grief and not really dealing with that at the time, I think there was just a lot going on.”

Prof Pariante argues it is actually these awful moments in our lives that change our immune system, priming it to increase the risk of depression years later.

He said: “We think the immune system is the key mechanism by which early life events produce this long-term effect.

“We have some data showing adult individuals who have a history of early life trauma, even if they have never been depressed, have an activated immune system so they are in a state of risk.”

The hope is that drugs targeting the immune system will provide much needed treatments for patients, particularly for those like Jennifer who seem to have tried them all.

“I had sertraline, I had Prozac, there was another one, I got started on citalopram, I was put on duloxetine, mirtazapine as well. I was on three at one point.”

She is now on a combination of drugs that seem to be working for her, but it has been a long journey.

“It is totally trial and error,” said Prof Pariante.

He added: “We are not able to predict right from the beginning whether someone will respond.

“We think by measuring inflammation in the blood we’ll actually be able to identify individuals that do require more complex, intensive antidepressant treatment, maybe a combination of an antidepressant and and anti-inflammatory.”

Most of us have common anti-inflammatories like ibuprofen at home, but doctors warn against experimenting at home, while clinical trials are taking place to prove whether this will work in patients.

The world’s largest medical research charity, the Wellcome Trust, has brought together universities and the pharmaceutical industry.

The aim is to consolidate the evidence to accelerate the field; ultimately they want to find a new treatment for depression and develop a test to identify those who will benefit.

Cambridge University’s Prof Bullmore is leading the consortium. But we interviewed him at his other employer, GlaxoSmithKline.

The company’s immuno-inflammation laboratory is where scientists are developing new molecules which they hope will become effective medicines for inflammatory disorders.

That process will take more than a decade, but Prof Bullmore says there may already be a drug out there.

“One of the exciting things about immunopsychiatry is that because of the success of immunology in other areas of medicine there are already many drugs that are far beyond this stage of development.

“They may already be licensed or in late-stage clinical trials so the timeline from start of work on that project to delivering a medicine that might make a difference to patients could be much shorter.”

Progress
Raiding the cupboards is already showing signs of success. Those early clues in arthritis mean the anti-inflammatory drug sirukomab is now being trialled in depressed patients.

So are drugs targeting the immune system about to transform the treatment of depression?

Prof Bullmore argues: “I don’t think they are going to be a panacea, I don’t think we’re talking about a scenario in future where every patient with symptoms of depression is going to be offered an anti-inflammatory drug.

“I don’t think that makes sense and frankly that sort of blockbuster one-size-fits-all approach to development of drugs for psychiatry has not been helpful to us in the past.

“We have to take a more personalised or stratified approach, not everyone that is depressed is depressed for the same reason.”

That will require a blood test to identify which patients will benefit from immune-based therapies.

Depression is a disease that affects hundreds of millions of people. Even if anti-inflammatories help just a small proportion of them – that would still be a huge number of patients. But if immunotherapy becomes a success, its biggest impact may be on the way we think about the disease, making people less likely to believe sufferers should just “pull themselves together”.

“I hate that phrase, if I could I would,” says Jennifer.

She adds: “Just as if someone had diabetes and their insulin levels weren’t working correctly, you wouldn’t say, ‘Oh snap out of it, stop having a hypo.'”

Hayley feels the same:

“If there was a way to say depression was a physical problem I think it would make a massive difference, I think people would treat depression as something that is not made up and going on in the head.

“It would be seen as a genuine condition, it would validate a lot of people’s feelings.”

Prof Pariante concludes:

“It is groundbreaking because, for the first time, we are demonstrating that depression is not only a disorder of the mind, in fact it is not even only a disorder of the brain, it is a disorder of the whole body.”

Posted in News | Tagged , , , , , , , | Comments Off on The role of inflammation & over active immune system in depression

BMJ reports tribunal orders PACE trial release of data

British Medical Journal news report, by Ingrid Torjesen, 22 August 2016: Tribunal orders university to release data from PACE chronic fatigue study

A tribunal has ruled that Queen Mary University of London must release data from a trial looking at treatment of chronic fatigue syndrome, which found that cognitive behavioural therapy and graded exercise therapy helped to alleviate the symptoms of the condition.1

The findings of the PACE (Pacing, graded Activity, and Cognitive behaviour therapy: a randomised Evaluation) trial, published in the Lancet in 2011,2 were questioned by some academics and patients, who argued that the PACE programme could harm patients.

In March 2014 Alem Matthees, a patient in Australia, submitted a freedom of information request to Queen Mary University of London, where some of the PACE researchers were based, asking for the anonymised patient data to allow analysis of the data according to the study’s original published protocol. The university refused the request, so Matthees filed a complaint with the information commissioner for England. The commissioner ruled in October 2015 that the data had to be released, but the university appealed that decision.

The university’s main arguments for not releasing the data were that they were not sufficiently anonymised and that it did not have permission from participants to publish the data. To require disclosure would damage trust and jeopardise future studies, the university said.

The tribunal dismissed the appeal, saying that it was satisfied that the data had “been anonymised to the extent that the risk of identification is remote.” It added, “There is a strong public interest in releasing the data given the continued academic interest so long after the research was published and the seeming reluctance for Queen Mary University to engage with other academics they thought were seeking to challenge their findings.

“There is insufficient evidence to persuade us that disclosure of the disputed information would cause sufficient prejudice to QMUL’s [Queen Mary University of London’s] research programme, reputation, and funding streams.”

A spokesperson for the university said,

“This has been a complex case and the tribunal’s decision is lengthy. We are studying the decision carefully and considering our response, taking into account the interests of trial participants and the research community.”

Keith Geraghty, honorary research fellow at the University of Manchester, said that he had contacted the PACE researchers to request access to the data to run an independent analysis, but his request “was first ignored, then later refused.”

He added, “I now understand that the authors shared the data with a select few academics who they picked to co-write papers, but they have failed to share the data with the broader scientific community.

Selectively sharing this publicly funded data with collaborators, but refusing to share data with anyone else, is not in the best interests of patients or science, and it creates a perception that the PACE team do not want independent critical analysis of this trial.”

He added that it was “regrettable” that the UK Medical Research Council, which partly funded the £5m (€5.8m; $6.5m) study, “did not specify that the trial data be made available to other researchers.”

Jonathan Edwards, emeritus professor of connective tissue medicine at University College London, said that the tribunal had made the right decision. He noted,

“The reasons given for not providing the information requested are essentially groundless. It is also clearly appreciated that critics of the PACE trial are not young sociopaths—they include senior medical scientists like myself, concerned about poor science.”

References

General Regulatory Chamber. First-tier tribunal. Appeal number EA/2015/0269. 2016. www.informationtribunal.gov.uk/DBFiles/Decision/i1854/Queen%20Mary%20University%20of%20London%20EA-2015-0269%20(12-8-16).PDF

White PD, Goldsmith KA, Johnson AL, et al. PACE trial management group. Comparison of adaptive pacing therapy, cognitive behaviour therapy, graded exercise therapy, and specialist medical care for chronic fatigue syndrome (PACE): a randomised trial. Lancet 2011;377:823-36. doi:10.1016/S0140-6736(11)60096-2 pmid:21334061

Posted in News | Tagged , , | Comments Off on BMJ reports tribunal orders PACE trial release of data

CFS misdiagnosis – how a teen diagnosed her own rare illness

The Times article, by Mike Pattenden, 16 August 2016: How a teen diagnosed her own rare illness

Should you google your symptoms? This 13-year-old did, and it helped to save her life

Amelia FergusonHave you had a niggling pain bothering you for a while? Whatever you do, don’t google your symptoms, it can be fatal — metaphorically speaking. That persistent headache isn’t cancer, it’s too much caffeine, and you have a stiff neck because you slept in an odd position, not because you have meningitis. Whatever dire diagnosis your search turns up, it’s probably best ignored.

Unless, of course, you happen to discover that you are suffering from a super-rare condition with which only a handful of people in the country have been diagnosed. This is what happened to Amelia Ferguson. Two years ago the 13-year-old started feeling dizzy and experiencing cold hands and feet, stomach pains and shooting pains in her legs. Her parents first put it down to exam stress but within weeks their daughter’s symptoms had escalated to include joint and bone pain, nausea, reflux and constipation. Her weight was plummeting, she was virtually unable to walk and weak as a kitten.

While all tests for serious illness came back negative, her parents, Kyrste and David, were alarmed at her deterioration and sought answers from private practitioners, including a neurologist, an acupuncturist, two homeopaths and a chiropractor.

“We were begging for her to be taken seriously,” says Kyrste. “She was disappearing before our eyes and it was heartbreaking.”

Amelia was admitted to Queen Mary’s Hospital for Children in Carshalton, Surrey, which diagnosed chronic fatigue syndrome and put her on a drip. By the summer of 2014 she was almost completely bed-ridden. At her lowest she was unable to swallow.

“I was no longer able to live my life properly so I’d spend seven or eight hours lying there searching for a cure,” she says, speaking from the family home in Esher. “I didn’t feel like I was getting the right treatment. Painkillers weren’t working and nor was the treatment so I went down another pathway that would help me get my life back. I had lots of symptoms that I could see just didn’t fit with chronic fatigue syndrome. I knew that it was something else.”

“We wanted to believe it was chronic fatigue. Half a dozen specialists were in agreement,” says David, a financial adviser. “They kept saying, ‘We’ve seen this before, trust us, stop worrying.’ We wanted to believe it, but she was fading before our eyes and we were racking our brains for a solution.”

While her parents racked their brains, Amelia took to her iPad. Instead of watching teen vloggers or cat virals, though, she began sifting through medical research. Her father had conducted some postgraduate research in clinical science and gave her some tips but he was too busy at work to put in the necessary hours of painstaking research himself.

In December Amelia found a medical paper about a 13-year-old girl in Australia who presented with the same symptoms and the same chronology — the Australian girl’s symptoms began shortly after she had received the HPV (cervical cancer) vaccine, just as Amelia’s had. It suggested that Amelia might have pandysautonomia, a rare autoimmune autonomic neuropathy.

Amelia wrote a 1,700 word summation of her clinical history, attached the medical paper and her conclusions with it, and sent it to Professor Russell C Dale, a paediatric neurologist at the University of Sydney. He referred her to Dr Ming Lim at the Evelina London Children’s Hospital, part of Guy’s and St Thomas’, who rushed her in for tests and came to the same conclusion. “Her condition was life-threatening and it was clear she needed urgent care,” Lim tells me. He put Amelia on a course of immunotherapy using steroids and immunoglobulins.

If Lim had any doubts that Amelia was responsible for her prognosis, he was soon disabused when he got to know her. “I’ve never heard of a child diagnosing themselves like this, not just that but to show the initiative to contact the author of the specific medical paper with a detailed summation of her condition is incredible.

“Combing through the medical literature, sifting through the useful information and understanding the language was a huge leap for someone her age. She wants to write a medical paper about pandysautonomia and I’d say, having treated her for so long, she’s more than capable.”

So was it a miracle that a 13-year-old was able to successfully diagnose a condition so rare that it affects approximately one in ten million people? Online self-diagnosis has widespread disapproval within the medical establishment, yet there seems little doubt that those of Amelia’s generation will increasingly rely on internet resources for medical information (between 1 and 5 per cent of searches are medically directed).

None of which stops doctors googling merrily away themselves.

“We do google, absolutely,” admits Lim. “When Amelia contacted me the first thing I did was google her condition and conduct a search of the latest medical papers. On the TV programme GPs: Behind Closed Doors, you can see them doing it all the time.”

Maybe the best person to turn to for advice is Amelia, who is now 15. She’s currently in remission, though still weak from the ravages of pandysautonomia and the side-effects of the drugs, so she can’t yet be fully discharged from the Evelina. She intends to embark on a career in medicine but just wants to get back to playing sport regularly first.

“I think you have to trust doctors to some degree but if you have been in their care for some time and you have a gut feeling that something is not right you should take matters into your own hands and try to find the answer,” she says.

“But when you start googling you have to take everything with a pinch of salt. There are some very useful sites out there but some people, no offence, write a lot of nonsense. You have to be sure who’s writing knows what they’re talking about.”

Next time you type “lump” into Google, try to remember that.

 

Posted in News | Tagged , , , , | Comments Off on CFS misdiagnosis – how a teen diagnosed her own rare illness

Dr Myhill told not to prescribe antiviral for post viral CFS

Health rising blog post, 23 August 2016: Dr Myhill Stripped of her Right to Prescribe Valtrex off label

From an email Dr. Myhill sent to her patients 13 August 2016:

We have a problem with me prescribing valacyclovir.

Yesterday I attended my annual appraisal. This is something all doctors have to do in order to revalidate with the General Medical Council. The appraisal is done by another doctor who looks at all aspects of one’s medical practice to make sure that professional standards are being maintained..

My appraiser was concerned about the idea of me prescribing valacyclovir for EBV post viral chronic fatigue syndromes. Whilst valacyclovir is licensed for acute viral infection it is not licenced for post viral chronic fatigue . What this means is that should anything go wrong, (and that may not even be the prescribing which is at fault), then I would be blamed and be left without any defence. My appraiser would also be part responsible.

If I should go ahead and prescribe valaciclovir for post viral CFS then I would not be revalidated and then I would lose all prescribing rights. The fact that I would be following the guidelines as developed by Dr Martin Lerner is of little or no consequence.

The bottom line is that I cannot prescribe valacyclovir for post viral CFS until either the drug company (Glaxo Smith Kline) has a license to use this drug for post viral chronic fatigue syndrome or I can get ethical committee approval to do this.

Of course I shall be writing to the drug company and also to local ethics committee to see this can be put in place.

In the interim I cannot prescribe valacyclovir for post viral chronic fatigue syndrome. This is very disappointing because I now have several patients who have seen marked benefit as a result of this drug in the prevention of viral flares.”

Find Dr. Lerner’s Guidelines here

Posted in News | Tagged , , , , | Comments Off on Dr Myhill told not to prescribe antiviral for post viral CFS

9 potential diagnostic tests for ME/CFS

shoutoutaboutme blog post, by Russell Logan, 31 July 2016: 9 potential diagnostic tests for ME/CFS: Highlights of the IACFS submission to NIH RFI on new research strategies

Though there are as yet no readily available, well-accepted, objective diagnostic tests for ME and CFS, work is ongoing in several key areas to develop one.

One objective measure, the 2-day CPET, is gaining acceptance and has been used with success in legal presentations. A drawback to this measure is its potential for harming patients.

And there are good subjective or self-reported diagnostic measures, though these are of limited value in clinical diagnosis.

In its response to the recent NIH solicitation for input into new research strategies for ME/CFS, the International Association for Chronic Fatigue Syndrome/ Myalgic Encephalomyelitis (IACFS/ME) documented emerging opportunities, research needs, and continuing challenges, but in particular highlighted promising work on developing a diagostic test or biological marker for the illness.

The IACFS/ME authors — Lily Chu, Fred Friedberg, Staci Stevens,  Steve Krafchick, and Jon Kaiser — noted: “Some tests might not be suitable for clinical use but might provide a gold standard test for research purposes [and] may also provide clues to the pathophysiology of this disease and even to future treatments.”

“They identified 9 key areas of investigation requiring urgent need of government support and funding.”

Read more about these key areas of investigation into testing for ME and CFS.

  • LOW NATURAL KILLER CELL ACTIVITY
  • 2-DAY REPEATED CARDIOPULMONARY EXERCISE TESTING
  • NEUROPSYCHOLOGICAL TESTING RELATED TO INFORMATION PROCESSING
  • TILT TABLE TESTING
  • NEUROINFLAMMATION
  • UNREFRESHING SLEEP, HEART RATE VARIABILITY, AND SYMPATHETIC PREDOMINANCE
  • FAMILIAL STUDIES
  • ENERGY METABOLISM ISSUES AND LACTATE PROCESSING IN MUSCLE AND BRAIN
  • POST-INFECTIOUS TRIGGERS
Posted in News | Tagged , , , , | 1 Comment

US report says there’s (almost) no evidence CBT/GET work in ME/CFS

Health rising blog, by Cort Johnson, 18 August 2016: Federal Report Says There’s (Almost) No Evidence CBT/GET Work in Chronic Fatigue Syndrome (ME/CFS)

This has a been good week for advocacy.  It’s shown that smart advocacy works. Twice advocates went straight back into “the system” looking for results and twice – once with the PACE trial and here with AHRQ report in the U.S. – they got them.

Spearheaded by Mary Dimmock who for years has lead the fight to secure a better definition, advocates asked the AHRQ to reanalyze it’s finding regarding CBT and GET.

The AHRQ agreed to test definition against definition
As part of the Pathways to Prevention (P2P) project, the AHRQ had been tasked determined with determining which treatments were effective for chronic fatigue syndrome (ME/CFS).  The group applied tough, tough standards – so tough that it rejected 90% of ME/CFS studies, and only 30 treatment studies made it to the analysis stage.  Of those only four studies were deemed “high quality”.

Since most of the trials that made to the final analysis were small, unreplicated studies the AHRQ deemed the evidence insufficient to say anything about any treatments other than CBT/GET.

That lead to some strong outcries from some advocates, including some of the same advocates requesting another analysis secondary analysis. The AHRQ was too tough, some said, for such an underfunded field. It made ME/CFS researchers and the chronic fatigue syndrome (ME/CFS) field look bad. That same rigor the AHRQ applied to its first analysis, however, paid dividends this time.

CBT and GET didn’t fare so well in the initial report. The AHRQ stated it  had only “moderate” confidence that CBT was able to reduce fatigue or produce “global improvement”, and had low confidence it was able to improve overall functioning, enhance quality of life, increase working hours, or reduce work impairment in the ME/CFS.

Mary Dimmock noted the conclusions had a flaw.  The P2P report stated that the Oxford definition was so broad – only requiring that unexplained fatigue be present – that any study using it was likely to include people who did not have ME/CFS.

The Oxford definition is an anomalous definition used mostly by a small group of CBT/GET researchers based mostly in the U.K. and the Netherlands. The vast majority of researchers have always used the Fukuda definition for research but in the CBT/GET field the Oxford definition has dominated. The P2P report recommended that the Oxford definition be trashed.

In their CBT and GET analyses, though, the AHRQ treated the Oxford definition like it was valid, lumping studies using it and the Fukuda definition studies together.  When that logical inconsistency was pointed out they agreed to reanalyze the CBT and GET studies, comparing studies using the Oxford definition to those using Fukuda definition.

The expectation was that studies using the Oxford definition would fare better than those using the stricter (but still not particularly strict) Fukuda definition, and, indeed, the AHRQ’s conclusions regarding the effectiveness of CBT/GET in ME/CFS changed dramatically once the analysis was done.

Results

For the first time the AHRQ panel asked these questions”

Does CBT Increase Functioning In Fukuda Patients?

In the original report the AHRQ found “low evidence” that CBT does not improve functioning at all. When studies using the Oxford definition were removed the four studies left found that two studies produced benefit and two did not The AHRQ downgraded their evaluation of CBT stating that given the inconsistent results, the imprecise nature of the results and the mixed quality of the studies made it impossible for them to determine if CBT was effective or not in Fukuda patient.

Does CBT Reduce Fatigue in Fukuda Patients?

When studies using the Oxford case definition were removed, the AHRQ was left with four fair-quality studies, three of which found benefit (n=327), one which found no benefit (n=65), and one poor-quality study finding no benefit (n=58).  In general the trend was upwards but the quality of the studies was only fair: the AHRQ determined that this body of work provided a “low strength of evidence that CBT improves fatigue”.

Does CBT Improve the Employment Status of Fukuda Patients?

A starker difference was found in the effects of CBT/GET on employment. Once the AHRQ removed the Oxford definition studies they found that CBT had no impact at all on employment.

Does CBT Improve Quality of Life in Fukuda Patients?

Because all three studies measuring quality of life already used the Fukuda criteria, the AHRQ’s assessment remained the same. Two of the three found no effects on quality of life leading the AHRQ to conclude that the strength of evidence that CBT/GET did not affect quality of life was low.

Does CBT Result in Global Improvement in Fukuda Patients?

Only two studies (but containing 540 people) assessed global improvement.  Both the Oxford and CDC definition studies found improvement in global improvement but the authors deemed the evidence insufficient to make a recommendation.

Does Graded Exercise Therapy Improve Outcomes in Fukuda Patients?

Four trials, three using the Oxford Definition and one using the CDC definition were included in the original analysis.  The results from all the trials were consistent; there was moderate strength of evidence that GET improved functioning (4 trials, n=607) and global improvement (3 trials, n=539), low strength of evidence that it reduced fatigue (4 trials, n=607) or decreased work impairment (1 trial, n=480).

When they removed the Oxford trials from the analysis, the one study left showed improvement but it alone provided insufficient evidence that GET was successful in Fukuda patients.

Conclusions

The AHRQ re-analysis of the CBT and GET trials resulted in it downgrading its recommendations significantly. In two cases (CBT’s effects on functioning and employment) the  reanalysis suggested that CBT was less effective in Fukuda patients than in Oxford criteria patients.

In other cases (CBT – Global Improvement; GET – functioning, global improvement, fatigue) the Fukuda studies suggested that some improvements did occur but too few studies were done for the AHRQ to  make a recommendation.

In the end the only mildly positive statement the AHRQ could make was that there was low strength of evidence that CBT improved fatigue in  ME/CFS. Otherwise it found no evidentiary basis for the use of CBT/GET in ME/CFS. It didn’t state that these techniques are helpful or not helpful; it simply stated that they are unproven.

Check out Mary Dimmock’s and Jennie Spotila’s blog on the AHRQ finding here.
Meanwhile we should note that the Fukuda definition, which has been the gold standard definition ME/CFS research for over 20 years is nothing to shout about either.  It’s more than past time for a new, statistically based research definition for ME/CFS. What better way to start the NIH’s new era of ME/CFS research than with a definition that works?

Now What?

The AHRQ has spoken. Now that they have basically demolished the idea that anything positive can be said with certainty regarding the effectiveness of CBT/GET in ME/CFS where do we do go from here?

The AHRQ, we should note, applies the most rigorous standards of any review body.

One might assume that the more rigorous reports might be authoritative in the field. The AHRQ is highly respected but it’s competing with the Cochrane Reports which are less rigorous and probably more used.

The Cochrane Reports probably include many studies that AHRQ rejected in their reports and are cited frequently.

A look at major medical websites indicates that the idea that CBT/GET is not just an effective treatment but is the only effective treatment for ME/CFS is deeply embedded in some.

These websites tend to provide  rudimentary, imprecise analyses of treatments.  They don’t get into the niceties regarding different definitions. Time will tell but it may be difficult to get them to change their ways. Let’s look at what four prominent medical websites say about CBT/GET and ME/CFS

UpToDate
Up to Date may be the most critical website since it’s commonly used by physicians seeking to get up to date information on treatments. A pay to play website, UpToDate probably provides the most comprehensive overviews of treatments on the web. It’s CBT/GET section starts off with some proviso’s:

“a systematic review of 35 randomized trials evaluating therapies for SEID/CFS concluded that counseling therapies and graded exercise therapy may have benefits for some patients with SEID/CFS [5]. However, neither of these modalities is curative.”

But then goes on to state that

“Cognitive behavioral therapy (CBT) has been effective in patients with SEID/CFS”.

The first CBT and GET trial UpToDate cites is the PACE trial. It notes that the trial involved 600 plus patients – thus providing automatic validation for many practitioners – but provides no hint that any  issues exist with this trial. It then provides the kind of imprecise summary so common in medical websites. UpToDate states that

“CBT in combination with specialist medical care  (in the PACE trial) was associated with less fatigue and better physical function compared with specialist medical care alone”

without noting that the effects weren’t considered clinically significant. UpToDate does the same thing with the GET arm of the PACE trial stating that

“GET in combination with specialist medical care was associated with less fatigue and better physical function compared with specialist medical care alone”

without noting that the step test results indicated that the participants were still severely disabled.

In another study UpToDate stated that CBT in combination with managed care  was more effective than managed care without saying how more effective it was

Each of the vague statements UpToDate makes could be and probably are often interpreted to suggest that CBT/GET is really helpful in ME/CFS.

UpToDate then cherry-picked studies to cite one indicating no cardiopulmonary problems exist in ME/CFS and that exercise does not increase symptoms. It could have easily cited studies showing the opposite but chose to cite studies that reflected its conclusion – that exercise therapy is effective in ME/CFS.

The American Family Physician
The American Family Physician states

“There is substantial evidence for two treatments for CFS: cognitive behavior therapy (CBT) and graded exercise therapy.”

Unless you’re doing the kind of analysis that the AHRQ does, that is probably a true statement. It goes on to say that:

“Persons diagnosed with chronic fatigue syndrome should be treated with cognitive behavior therapy, graded exercise therapy, or both. Cognitive behavior therapy and graded exercise therapy have been shown to improve fatigue, work and social adjustment, anxiety, and postexertional malaise.”

AFP obviously goes far, far beyond the AHRQ’s conclusions, and even goes far beyond the Cochrane Report’s conclusion. It hardly attempts to produce a balanced report of CBT or GET’s limitations or their very moderate effects.

WebMD
WebMD is a bit more enlightened. CBT is not presented as a cure but as a coping mechanism that can help some people.

“(CBT) is a type of counseling that has been shown to help some people who have CFS feel less tired” that “teaches you how to change the way you think and do things. These changes can help you better cope with fatigue and other symptoms.”

With regard to GET, WebMD states that it may help some people but suggests that those who are severely ill stay away.

“Unless your CFS is severe, try a graded exercise program, starting out with gentle and easy movement. Start with as little as 1 minute, and slowly add more over days or weeks. Studies have shown that a carefully planned graded exercise program can help some people with CFS regain their strength and energy and feel better. “

The Centers For Disease Control
The CDC has muted  its recommendations for CBT and GET considerably in recent years. The CBT section is now posted in the Improving Health and Quality of Life section (not the Treatment section). No mention of a cure is made. The CDC contextualizes CBT as a way to effectively pace and reduce stress.

For CFS patients, CBT can be useful by helping them pace themselves and avoid the push-crash cycle in which a person does too much, crashes, rests, starts to feel a little better, and then does too much once again. Often, CBT is prescribed along with other therapies to help CFS patients manage activity levels, stress, and symptoms. CBT can help CFS patients better adapt to the impact of CFS and improve their ability to function and their quality of life.

The GET  section is now posted in the management (not the treatment) section. The stated goal is not cure ME/CFS but to improve fitness and contains many qualifiers: GET can help “some” patients “manage” their illness, and exercise should stop before patients get tired and ME/CFS is reactivated. It has a separate section for the severely ill.

Gradual, guided physical activity can help some CFS patients manage the illness. Appropriate rest is an important element of GET, and patients should learn to stop activity before illness and fatigue are worsened.

The end point of each GET session….. should be reached before the patient becomes tired….Appropriate goals are to prevent tiredness, to avoid activating the syndrome, and to increase overall fitness.

The CDC has been thought of as a leader that other websites will follow but this short analysis suggests this is not so. The CDC has the mildest recommendations regarding CBT and GET but its recommendations should indicate there is now almost no evidentiary base to conclude that CBT/GET are effective in ME/CFS.

Conclusions

Hopefully the AHRQ’s reanalysis will help the blunt the emphasis given to CBT/GET in this field. What this field really, really, really needs,though, is to end the dominance of European government funded behavior based trials. No two entities should be able, simply by pouring money into a field, to dictate its treatment options, but that’s essentially what’s happened in ME/CFS.

See The Chokehold Behavioral Treatments Have on Chronic Fatigue Syndrome (ME/CFS)

The major medical websites will shift their emphasis when good treatment trials provide evidence that other treatments are effective in ME/CFS. The NIH can begin this  process by funding Ampligen and Rituximab trials.

One successful Ampligen trial – which could be set up quickly and easily – would be enough to get FDA approval.  Rituxmab would take longer but the NIH has a great deal of experience running Rituximab trials.

With the AHRQ re-analysis in hand, approvals for  Ampligen and Rituximab, if they should occur, could go a long way to blunting the effects that years of over emphasis on CBT/GET have had. The NIH has said it’s serious about ME/CFS; funding these two trials would indicate that it is.  It’s time for the U.S. to step up.

Posted in News | Tagged , , , , , , , , , , , , | Comments Off on US report says there’s (almost) no evidence CBT/GET work in ME/CFS

More PACE trial tribunal comments

PACE trial ruling: Respondent Alem Mathees main response

The essential daily briefing, 19 August 2016: Chronic Fatigue Syndrome sufferers have just had a small victory

Health Rising discussion, 17 August 2016: The PACE Trial’s Big Stumble: UK Tribunal Orders Release of PACE Data

Centre for Welfare Reform blog post, 19 august 2016: Major breakthrough on PACE trial

Retraction watch blog post, 17 August 2016: UK tribunal orders release of data from controversial chronic fatigue syndrome study

Applied clinical trials blog post, by Philip Ward, 19 August 2016: Tribunal Orders Release of Withheld Data from London Trial

Quick thoughts blog post, by James Coyne, 17 August 2016: QMUL responds to UK Tribunal ordering release of PACE chronic fatigue syndrome trial data

Quick thoughts blog post, by James Coyne, 18 August 2016: Release the PACE trial data: My submission to the UK Tribunal

The Feed blog post, by Naomi Chainey, 29  August: Do you suffer from Chronic Fatigue Syndrome? There’s some good news for you

PACE Trial : Le tribunal ordonne la divulgation des données

PACE and the interests of trial participants, by Calrk Ellis, 29 August 2016

 

 

Posted in News | Tagged , , , | Comments Off on More PACE trial tribunal comments

ME Association challenges Pulse Learning’s classification of ME/CFS as a mental health disorder

ME Association blog post, by Dr Charles Shepherd, 21 August 2016: ME Association challenges Pulse Learning’s classification of ME/CFS as a mental health disorder 

The ME Association has today asked the medical education website Pulse Learning to remove Chronic Fatigue Syndrome (CFS) from its classification as a mental health disorder. Pulse Learning has just published a new learning module on CFS and listed it in its mental health section.

Our medical adviser, Dr Charles Shepherd, has sent this email to Pulse Learning:
Dear Pulse Learning

Re Case based learning on CFS: http://pulse-learning.co.uk/clinical-modules/mental-health/cfs-case-based

I am not currently registered with PULSE to do your CPD learning modules and have not therefore gone through this new learning module on ME/CFS.

I am, however, very concerned to see that this module has been incorrectly inserted into the ‘mental health’ section of your learning modules.

As I am sure the authors of the module are aware, ME is classified as a neurological disease by the World Health Organisation (WHO) in their International Classification of Diseases (>> ICD10 section G93:3) and that this WHO neurological classification is accepted by the Department of Health, NHS etc. CFS is linked to this ME classification in ICD10.

In addition, the most recent report – Beyond Myalgic Encephalomyelitis/Chronic Fatigue Syndrome – on ME/CFS from the Institute of Medicine in America states quite clearly that ME/CFS (or systemic exertion intolerance disease/SEID – as they have recommended as a new name for ME/CFS) is not a psychological or psychiatric condition. It is a complex multisystem medical disease.

IoM Report: http://www.nationalacademies.org/hmd/~/media/Files/Report%20Files/2015/MECFS/MECFScliniciansguide.pdf

There are obviously disagreements and uncertainties surrounding many aspects of ME/CFS.

However, if GPs are going to immediately start off by working on the incorrect basis that they are dealing with a mental health/psychiatric condition, this will not only lead to conflict with patients. It will also lead to inappropriate and possibly harmful advice on management.

I will try and look at the module during the coming week.

In the meantime, please could it be inserted into a section covering neurological and/or immunological disease – where it belongs.

Posted in News | Tagged , , , , | Comments Off on ME Association challenges Pulse Learning’s classification of ME/CFS as a mental health disorder