Psychiatric Drug Facts via breggin.com :

“Most psychiatric drugs can cause withdrawal reactions, sometimes including life-threatening emotional and physical withdrawal problems… Withdrawal from psychiatric drugs should be done carefully under experienced clinical supervision.” Dr. Peter Breggin
Showing posts with label Allen Frances. Show all posts
Showing posts with label Allen Frances. Show all posts

Sep 17, 2013

Recovery and Psychiatry: Dirk Corstens, Chair of Intervoice responds to Allen Frances



Allen Frances responded to the open letter by writing, "Reconciling Recovery and Psychiatry: Response to Open Letter" for his blog in Psychology Today.  I find Allen Frances' criticism of those harmed by psychiatry insulting; frankly, I find his professional posturing in this instance, resembles juvenile bullying. Frances claims his criticism is motivated by concern for people with psychiatric diagnoses; apparently, he is afraid people may believe and be inspired by the hearing voices movement. Why is the idea that people with a diagnosis of schizophrenia may feel hopeful for recovery is something to fear? Frances states he is concerned that "trying to follow Ms Longdon's path might help some, but may harm others." 

I, on the other hand, am concerned that Frances did not "cover the waterfront of possibilities" accurately or ethically in his response. The hearing voices method, "could not possibly serve as a model for everyone who hears voices," so Frances claims he wants to prevent people from thinking Eleanor Longden's personal story is "a blanket condemnation of all psychiatric treatment"?!  I'm skeptical of the veracity of this claim since Frances is promoting the medical model as "essential," while decrying the harm done by "Big Pharma and the physicians who over prescribe. My skepticism arises from Allen Frances's failure to disclose his collaboration with Big Pharma, the widely disseminated Expert Consensus Guidelines; which are still marketed as treatment standards meant to inform pediatricians, GPs, Internists, etc. to guide how they treat people using current psychiatric standards of care.  There's no concern about patients being disabled and killed as a direct result of being diagnosed and treated according to a consensus of expert opinions...

Doctors rely on guidelines to inform treatment decisions believing the guidelines are based on valid evidence of treatment safety and effectiveness; not a drug marketing strategy! 

I want to share the comment left by psychiatrist, Dirk Corstens, the Chair of Intervoice, in response to Allen Frances's blog post answering Intervoice's Open Letter:

Recovery and Psychiatry
Submitted by Dirk Corstens on September 17, 2013 - 12:41am.


Dear Professor Frances,

Thank you for your prompt response to the open letter sent to you from Intervoice. I would like to take this opportunity to continue the dialogue by offering some of my own reflections on your recent article.

You reiterate that people diagnosed with schizophrenia need medication, because you witnessed "dozens of lives ruined" by people coming off it. That is what I also learned during my psychiatric training, something that was systematically confirmed by colleagues. Proceeding with that mind-set, I also saw dozens of people struggling to come off medication, often unsuccessfully - but mostly due to lack of support (e.g., "when you don't take your medication we stop treatment").

After more than 25 years of experience working in clinical and social psychiatry, much reading, and much meeting and collaborating with many voice hearers, like Eleanor, who bravely took their own roads to recovery, I have definitively changed my mind and practice.

My present mind-set - my most accurate and honest conclusion about psychosis and medication - is that I really don't know who needs medication and who does not. I now believe it is better to prevent prescribing medication whenever possible.
Modern psychiatric practice tends to endorse that people with psychotic experiences - or what psychiatrists believe are psychotic experiences - rarely get access to psychological therapies, and almost never as a first-response treatment (despite robust evidence that it works). Without much communication, and almost automatically, antipsychotics are prescribed. As you may know, in some European countries young patients are even prescribed three different medications at a time. Modern psychiatric practice is ruled by a fundamental fear of psychotic experiences and the objectively false premise that antipsychotics eliminate it. There is abundant reason to change this mind-set: communicate, care, and support. Wait, create a safe environment. Wait and listen. Try to make sense of experiences. Only prescribe low doses when necessary and stop when possible.

The most important reasons:
- The diagnosis of schizophrenia is scientifically unreliable (see for example Richard Bentall and Mary Boyle - not anti-psychiatrists, but research-psychologists who think in a scientific way) and more stigmatising than helpful. And of course, there are no specific symptoms nor tests that confirm if the diagnosis is accurate or not.
- It is more and more uncertain that antipsychotics improve the long-term prognosis of psychosis. Many colleagues now state that the prognosis is not better or worse than before chlorpromazine was administered to patients. Functional recovery seems better when people don't take antipsychotics or only in low doses (e.g., Harrow, Wunderink, Mosher, Ciompi).
- There is good reason to believe that antipsychotics often do more harm than good (e.g., Breggin, Whitaker, Healy, Moncrieff, Lehmann).
- There are a lot of promising alternatives: Open Dialogue, Soteria, CBT, psychosocial therapies, hearing voices networks, self-help groups, trauma-informed therapies. These alternatives have existed a long time; are well documented; propagate the cautious and sparse use of medication - and give good results.
- More and more people who utilise psychiatric services openly state that they prefer a personal approach and need a say in their treatment and choice.
It is really exciting and rewarding to operate as a psychiatrist from this alternative mind-set with people who report subjective experiences that overwhelm them.

Eleanor's story tells us professionals that meeting the person behind the symptoms, communicating about the real personal story, creating a safe environment, and supporting family members and other allies are the most fundamental ingredients of good psychiatric care and cure. She didn't say what other people should do or not. It is not a story about medication at all - she only tells it didn't help her, and after taking it for a while came off it. It is a story of struggle and hope. A real and personal story.

I really don't understand why you feel the need to censor her.

Dirk Corstens, consultant psychiatrist
Chair of Intervoice
www.intervoiceonline.org


photo credit here

May 26, 2013

Allen Frances, M.D. "We shouldn't think of the DSM definitions as being diseases."


via Science Magazine Videos:

During a google hangout chat called, "ScienceLIVE: Does Psychiatry's 'Bible' Need to Be Rewritten?;" the host, Emily Underwood, asks, "How do you define "normal" behavior when you're looking across cultures?" Allen Frances, outspoken critic of DSM5, answers by stating in part, "We shouldn't think of the DSM definitions as being diseases." Watch the entire chat here on youtube.









May 24, 2013

Redefining mental illness


"[The DSM] it's not really a bible, it shouldn't be worshipped.  It's a guide, it's mostly a guide to clinical care to help in deciding who has what disorder, and what's the best treatment for it. Unfortunately [it] has been taken out of context, and used in many real life decisions often beyond the competence of the manual … so it's moved out of the clinical arena ... and now it has all sort of society influences often beyond its competence." Allen Francis, M.D.

via ALJAZEERA Inside Story Americas:

Redefining mental illness

As the new edition of an influential US psychiatry manual is released, we analyse its impact beyond clinical diagnosis.

 Last Modified: 23 May 2013 09:37
Inside Story Americas, with presenter Shihab Rattansi, discusses with guests: Dr. Allen Frances, former chair of the psychiatry department at Duke University and author of the book Saving Normal; and Robert Whitaker, a journalist and author of the book Anatomy of an Epidemic.  Read the article here 


hat tip: Kermit Cole at madinamerica.com

May 6, 2013

Insel's assumptions are biased beliefs predicated on a hypothetical etiology that is reminiscent of eugenics

via NIMH The Director's Blog
Transforming Diagnosis
an excerpt: 

NIMH has launched the Research Domain Criteria (RDoC) project to transform diagnosis by incorporating genetics, imaging, cognitive science, and other levels of information to lay the foundation for a new classification system. Through a series of workshops over the past 18 months, we have tried to define several major categories for a new nosology (see below). This approach began with several assumptions:

A diagnostic approach based on the biology as well as the symptoms must not be constrained by the current DSM categories,

Mental disorders are biological disorders involving brain circuits that implicate specific domains of cognition, emotion, or behavior, (emphasis mine)

Each level of analysis needs to be understood across a dimension of function,

Mapping the cognitive, circuit, and genetic aspects of mental disorders will yield new and better targets for treatment.

Apparently, Thomas Insel is unaware that in order to ethically determine the direction and the focus of scientific research requires an open mind; not a pre-determined agenda. Insel's announcement that the NIMH will no longer use the DSM is a political decision. Insel acknowledges the NIMH adopted a biological research focus based on assumptions; instead of using ethical scientific principles, and allowing the existing empirical data to guide the direction of psychiatric research; he says, "because we lack the data"!? What a crock! Insel knows there is little to no scientific basis in his assertion that "Mental disorders are biological disorders."

It is an assumption that is and has been embedded in the language of psychiatric diagnosis and treatment, an assumption that was entrenched along with the eugenic theories that spawned it. Eugenic theories which are still used in an attempt to justify the inhumane "standards of care" that are without empirical support, standards without empirical support should not be considered "standards of care" since by definition, standards are theoretically to be derived from the evidence base; instead, psychiatry validated their standards of care by consensus,  a quasi-democratic political process, not using ethical medical judgement and empirical data from psychiatric research.  By consensus, psychiatry effectively determined that some people with certain  psychiatric diagnoses don't need their Human Rights protected; people of all ages are effectively stripped of their Human Rights by psychiatry, based on a belief that a diagnosis of mental illness is evidence the person has an incurable brain disease, that requires life-long treatment with teratogenic drugs. Without any definitive evidence to validate the brain disease hypothesis, it's simply a hope-filled belief in a hypothesis that is still seeking validation; it's not even a theory...let alone an actual disease.

Insel's assumptions are beliefs reminiscent of eugenics.  The eugenics movement in this country also proceeded without any empirical evidence to validate it's ignorant assumptions. 

The NIMH will assume that the brain disease hypothesis is a brain disorder or disease in the absence of  empirical evidence that would validate the hypothesis. According to Thomas Insel, the NIMH is going to proceed as if an assumption, i.e."Mental disorders are biological disorders," is a sufficient substitute for using critical thinking skills, and for relying on the existing research data on "mental disorders" exercising sound judgment to determine what the focus and direction for psychiatric research should be. I wonder, if the best interests of those who experience cognitive, emotional and behavioral symptoms were even considered? Is there empirical data that supports Insel's use of biased assumptions that are without empirical support to justify this biased and myopic focus on brain biology for psychiatric research? Insel's announcement that the NIMH will focus on seeking evidence that "mental illness" is caused by a brain disease is not 'news;' the NIMH has been focused on seeking the evidence which would validate the brain disease hypothesis for decades...Insel's announcement that research funded by NIMH will no longer be guided by the DSM, due to it's lack of validity; is long overdue. The irony is, in the same blog post, Insel uses biased assumptions as if bigotry-based assumptions are a sufficient substitute for valid information when making mental health research policy decisions (theoretically) in the public interest. There is no ethical justification for the NIMH to continue to fund research looking for the still illusive genetic defects, brain diseases and bio-markers as it's  main agenda. The pre-occupation with proving schizophrenia and/or any other psychiatric diagnosis, is caused by a biological defect or disease seems to purposely exclude research on known and suspected social and environmental risk factors that cause cognitive and emotional difficulties; worse it neglects the cognitive/behavioral/psycho/social/ therapeutic treatments that can help people right now in real world practice, if the treatments were actually available...

In effect, Insel is announcing all cognitive and emotional symptoms of distress, including undesirable, or disapproved of behavior, is caused by a yet to be identified, biological disorder or disease process---while simultaneously ignoring the overwhelming evidence of environmental causal factors such as  sexual, physical, and emotional abuse and neglect, poverty, malnutrition, environmental violence, socio-economic-political status and intra- and inter-personal conflicts are highly correlated with, and known to exacerbate (if not cause) what Insel 'assumes' are biological disorders...

Allen Frances, had a OP-Ed published in New Scientist, which concludes with the statement, "Anything that goes into the manual should already have passed rigorous research testing; the manuals are far too important to include untested hypotheses. DSM-5 is not, and cannot be, an appropriate guide to future research." 

I agree. I would add that assumptions about the scientific validity of a hypothetical, neuro-biological cause for any psychiatric diagnoses (or anything else) is also inappropriate. An assumption is not an ethical scientific basis for psychiatric research; it is not an ethical foundation for a new nosology either.  

I wonder if Insel can explain why dangerous neuroleptic, or "antipsychotic" drugs that are minimally effective for a minority of people diagnosed with schizophrenia, are prescribed off label, to children? 

Human Experimentation is "effective psychiatric treatment." 
It's the standard of care used in psychiatric practice. 

via National Advisory Mental Health Council 219th Meeting September 18-19, 2008 
NIMH Director's Report: 
an excerpt:
"Results from the NIMH-funded 6-year multisite Treatment of Early Onset Schizophrenia Study (TEOSS) found no significant differences in outcomes with first- or second-generation antipsychotic medications. There was a striking difference in side effects, but there was no evidence that any of the medications was the best choice for the entire group of people being treated. Similar results were obtained in the Clinical Antipsychotic Trials of Intervention Effectiveness (CATIE) trial, the Cost Utility of The Latest Antipsychotics in Severe Schizophrenia (CUtLASS) trial from the United Kingdom, and the large-scale Veterans Administration trial. Despite the lack of a clear superiority in overall effectiveness of the second-generation drugs, they account for more than 90 percent of the market and cost about 20 times more than the first-generation compounds." Thomas Insel 

via National Institutes of Health:
The NIH Public Access Policy ensures that the public has access to the published results of NIH funded research. It requires scientists to submit final peer-reviewed journal manuscripts that arise from NIH funds to the digital archive PubMed Central upon acceptance for publication. To help advance science and improve human health, the Policy requires that these papers are accessible to the public on PubMed Central no later than 12 months after publication.

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