Editorial Note: This is the start of a series that will likely run through to the End of the Year. For those of you who like Murder Mysteries, this is one. Please comment, speculate and help put a new source of harassment and intimidation properly on the map.
This post accompanies a talk I gave at the Hay on Wye HowTheLightGetsIn Festival this May, called The Persecution of Heretics. The talk can be seen here and an accompanying article, a variation on this post, is here.
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Behind the apparent Biblical Authority of the Clinical Trial Literature in medicine lies an Inquisitional like apparatus run by company PR agencies and agencies whose job it is to manage the perception of science, linking in academics, aimed at silencing dissent and ensuring that prescribing doctors continue to prescribe. It focusses most clearly on anyone who suggests that a Brand name drug might have significant adverse events.
Such a person will be harassed in a range of ways, including being referred to the General Medical Council (GMC). There is a need for the full details of the many ways harassment can be carried out to see the light of day.
At the time the talk was being given, unknown to me, I was again being referred to the GMC.
The stake at which the heretic ends up is in the broad light of day but the persecutor hides in the shadows. In this case is it the local Health Board, clinical colleagues, the relevant Royal College, the GMC itself, one of the major pharmaceutical companies or the Government? Watch this space.
For millennia we have struggled with death and disease. In the 1950s, there was a huge increase in the number of truly effective medicines and this has played a part in improving life-spans and quality of life, in particular among children. These new drugs supported the creation of the National Health Service as treatments that work will make populations healthier and more effective at work and the provision of services offering treatments that work will pay for themselves and will make a country better able to compete with others.
Although almost all new treatments emerged without a clinical trial in sight, following the thalidomide crisis in 1962, clinical trials were put in place as a way to evaluate treatments. The established wisdom now is that clinical trials reveal the truth about medicines – they are the gold standard method of evaluation – and that once a trial confirms that a drug works, doctors should give them, and guidelines should enforce the giving, and health systems should make these treatments available at whatever cost as if effective they essentially pay for themselves.
Another safeguard put in place was that even though prescription only was a status for medicines invented to control addicts, all new drugs would be made available on prescription only. This puts doctors very clearly centre stage.
The view that medicine should be evidence based and that doctors should adhere to the evidence has become increasingly solidified in recent years. Linked to this an ever increasing proportion of the population is on an ever greater number of medicines for ever longer periods of time.
Meanwhile, treatment induced death has become one of the three leading causes of death and it now takes decades before doctors recognize a link between serious life threatening adverse events and treatment where such recognition used to be much quicker.
The medical literature has become ghost-written with close to the entire literature stemming from clinical trials of on-patent drugs ghost-written and the raw data from those trials is inaccessible. Nobody – not even the regulators – gets to see it.
In the face of this, the standard response from medicine has been that the problems lie within the pharmaceutical industry and that the only issue for doctors is one of conflicts of interest and this problem can be solved if doctors declare any conflicts they have.
Whatever about the pharmaceutical industry, doctors are good people who are trained to make sure you get the right treatment and the General Medical Council (GMC) takes care of those few doctors who might pose a risk to your health.
Latterly with the realization that clinical trial data has been concealed, there has been more of a push for access to Clinical Study Reports – the written in the company account of what its study shows. Doctors and medical researchers apparently don’t want to or can’t be trusted to have access to patient level data for reasons of confidentiality.
While there are some things we are not happy about happening within the pharmaceutical industry, medical journals and individual doctors have the belief that they are effectively drawing attention to problems and that individual doctors attempting to raise issues will find their colleagues supportive.
In fact adverse events now take 10-20 years from the time they are reported first to the point where it is accepted they can happen. Randomized controlled trials have become the Gold Standard way to Hide adverse events and the blind adoption of trials is a mistake of historic proportions. The National Health Service meanwhile is on its way to being transformed into a system to deliver clinical trial patients to pharmaceutical companies.
It is extraordinarily easy to intimidate doctors. One simple clinical misstep can provide an opportunity for a complaint against a doctor. And clinical practice inevitably gives rise to missteps. Once it does, the GMC can be used as a weapon to persecute heretics.
Wonderful though the GMC can be, its role is asymmetric. It will not take action against doctors working for pharmaceutical companies who put out grossly misleading information about the lethal hazards of the latest blockbuster drug. It won’t take an action based on its own Good Prescribing Practice against doctors who without seeing the data put their names to ghost written articles that are part of a marketing strategy to encourage doctors to prescribe drugs that are ineffective and dangerous.
Far from being trained in one of the major determinants of clinical practice, doctors have no training in how pharmaceutical companies market drugs, no knowledge of how to investigate adverse events and they are becoming ever less able to hear awkward messages coming from patients.
The pressure on doctors is vastly greater than they are aware and this can distort well-meaning people into not very nice people. Faced with a patient or a colleague questioning whether treatment is likely to have caused an adverse event or not, from cognitive failures on statins to suicidality on antidepressants, doctors feel threatened and are liable to turn nasty. Try it and see.Share this: