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The Elephant in the Room Series Four: DSM-V: What do we know so far?

Posted by meagenda on December 16, 2009

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Keywords

APA    DSM    DSM-IV    DSM-V    DSM-5   WHO    ICD    ICD-10    ICD-11    American Psychiatric Association    Diagnostic and Statistical Manual of Mental Disorders    World Health Organization    Classifications    DSM Revision Process    DSM-V Task Force    DSM-V Somatic Distress Disorders Work Group    Somatic Symptom Disorders Work Group    DSM-ICD Harmonization Coordination Group    International Advisory Group    Revision of ICD Mental and Behavioural Disorders    Global Scientific Partnership Coordination Group    ICD Update and Revision Platform    WHO Collaborating Centre    CISSD Project    MUPSS Project    Somatoform    Somatisation    Somatization    Functional Somatic Syndromes    FSS    MUS    Myalgic encephalomyelitis    ME    Chronic fatigue syndrome    CFS    Fibromyalgia    FM    IBS    CS    CI    GWS

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The Elephant in the Room Series Four: DSM-V: What do we know so far?

A copy of this material has been sent to:

Sir Peter Spencer, Heather Walker, Tristana Rodriguez (Action for M.E.); Dr Charles Shepherd, Neil Riley, Tony Britton (ME Association); Jane Colby (The Young ME Sufferers Trust); Mary Jane Willows (AYME); ME Research UK; Simon Lawrence (25% M.E. Group); Trustees Invest in ME; BRAME; RiME; The Countess of Mar; Dr Ellen Goudsmit; Professor Malcolm Hooper. Five documents have been also been provided, including WHO ICD Revision: Content Model Style Guide; WHO ICD Revision: Content Model Blank; WHO ICD Revision: Morbidity Reference Group Discussion paper: ICD-11 rules, conventions and structure available from:
https://sites.google.com/site/icd11revision/home/documents

Part One

DSM-V draft proposals

In the UK, the Diagnostic and Statistical Manual of Mental Disorders (DSM), published by the American Psychiatric Association (APA), does not have as much relevance for us as the WHO’s ICD. But the revision of DSM-IV will shape international research and literature in the fields of liaison psychiatry and psychosomatics for many years to come.

Until the APA publishes its alpha draft, we won’t know what the most recent proposals are. But if our corner needs fighting, then according to UK health psychologist, Dr Ellen Goudsmit C.Psychol. FBPsS, we can rely on US psychologists, Jason and Friedberg, to fight our corner for us. Who else might we rely on?

In his commentary Alert to the Research Community—Be Prepared to Weigh in on DSM-V, Psychiatric Times, 3 December, Allen Francis MD, who had chaired the DSM-IV revision Task Force, wrote:

The research community has a central role and a great responsibility in taking advantage of this precious opportunity to carefully review and identify the problems in the DSM-V drafts and to suggest solutions…

Will our own professional advocates – our researchers, clinicians and patient organisations be reviewing and commenting on these draft proposals when they are published, early next year?

According to a PowerPoint presentation delivered Dr B Üstün at the WHO’s September ICD-11 iCAMP meeting:

“ICD will be about 15 thousand Diseases, disorders…”

and will involve

“Between 5000 – 50,000 contributors”

We are just one patient constituency amongst thousands of diseases, disorders and syndromes. But because of the means through which ICD is being revised this time round, there will be opportunity for input from a far wider range of sources into the ICD-11 development process. Again, our interests will need to be effectively represented and it should not be left entirely to the patient community. Our researchers and clinicians will need to be encouraged to input into the ICD revision process, too.

The “H” word

The APA participates with the WHO in the International Advisory Group (AG) for the Revision of ICD-10 Mental and Behavioural Disorders and a DSM-ICD Harmonization Coordination Group.

The DSM-V Task Force and ICD-11 Revision Steering Group have committed as far as possible “to facilitate the achievement of the highest possible extent of uniformity and harmonization between ICD-11 mental and behavioural disorders and DSM-V disorders and their diagnostic criteria” with the objective that “the WHO and APA should make all attempts to ensure that in their core versions, the category names, glossary descriptions and criteria are identical for ICD and DSM.”

The forthcoming shift, scheduled for October 2013, to a US modification of ICD-10 (ICD-10 CM*) and the disparity between the proposed ICD-10 CM classifications and the current ICD-10 codings for Postviral fatigue syndrome, (Benign) myalgic encephalomyelitis and chronic fatigue syndrome may account for an apparent lack of interest in the US in the development of ICD-11. But the proposed structure of ICD-11 may have implications for the US patient population, even though the US might not anticipate moving on to ICD-11 for many years.

From the APA’s 10 December press release:

APA will continue to work with the WHO to harmonize the DSM-5 with the mental and behavioral disorders section of the ICD-11. Given the timing of the release of both DSM-5 and ICD-11 in relation to the ICD-10-CM, the APA will also work with the CDC and CMS to propose a structure for the U.S. ICD-10 CM that is reflective of the DSM-5 and ICD-11 harmonization efforts. This will be done prior to the time when the ICD-10-CM revisions are “frozen” for CMS and insurance companies to prepare for the October 1, 2013, adoption.

It was reported, in August (DSM-V Field Trials Set to Begin Elsevier Global Medical News), that the APA planned to launch some field trials for DSM-V in October, with all field trials scheduled for completion by the end of 2010, for a previously anticipated publication date of May 2012.

According to Christopher Lane, author of Shyness: How Normal Behavior Became a Sickness, most of the field trials have yet to begin because the Work Groups can’t agree on their criteria (Psychology Today).

*For current proposals for US modification ICD-10 CM see: 
http://en.wikipedia.org/wiki/History_of_chronic_fatigue_syndrome#ICD-10-CM   

**Postviral fatigue syndrome and (Benign) myalgic encephalomyelitis are classified in Chapter VI of ICD-10: Volume 2: The Tabular List at G93.3; Chronic fatigue syndrome is indexed at G93.3 in ICD-10: Volume 3: The Alphabetical Index.

See:  http://apps.who.int/classifications/apps/icd/icd10online/?gg90.htm+g933 
See:  http://www.scribd.com/doc/7350978/ICD10-2006-Alphabetical-Index-Volume-3  (Page 528, top right hand column)

 

Somatic Distress Disorders

The DSM-V Work Group that has relevance for us is the Work Group for “Somatic Distress Disorders” (aka “Somatic Symptom Disorders”).

This group has responsibility for the revision of the DSM classifications currently listed under “Somatoform Disorders”. The equivalent section in ICD-10 is “Somatoform Disorders” classified in Chapter V: Mental and Behavioural Disorders between codes F45 – F48.0.

Go here: http://meagenda.wordpress.com/dsm-v-directory/

scroll down to the heading “Related documents” and open Document [6] DSM-IV ICD-10 Classifications

This document sets out how the two classification systems currently correspond for “Somatoform Disorders”. You will also find links in Document [6] for ICD Chapter V classifications for “Somatoform Disorders” codings at F45 – F48.0, and for G93.3 (ICD Chapter VI, the Neurological chapter).

The members of the Somatic Distress Disorders Work Group (SDD WG) are published on the APA’s website here:

http://www.psych.org/MainMenu/Research/DSMIV/DSMV/WorkGroups/SomaticDistress.aspx

This document also includes biosketches and disclosure information for each Work Group member. The group is chaired by Professor Joel E. Dimsdale, MD. The nine members of the DSM-V Somatic Distress Disorders Work Group are:

Arthur J. Barsky, MD*; Francis Creed, MD*; Nancy Frasure-Smith, PhD; Michael R. Irwin, MD; Francis J. Keefe, PhD; Sing Lee, MD; James L. Levenson, MD*; Michael Sharpe, MD*; Lawson R. Wulsin, MD.

DSM-V Task Force member, Javier Escobar, MD, serves as Task Force liaison to the DSM-V Somatic Distress Disorders Work Group and works closely with this group.

Four out of the ten members of the DSM-V Somatic Distress Disorders Work Group (asterisked) were also members of the CISSD Project workgroup; Prof Michael Sharpe served as the CISSD Project’s UK Chair. The CISSD Project’s International Chair was Prof Kurt Kroenke, MD.

We have no information on how closely the ICD Topic Advisory Group for the revision of Mental and Behavioural Disorders (TAG MH) is collaborating with the DSM-V SDD Work Group over the revisions of their respective “Somatoform Disorders” sections. Until the iCAT platform is launched, it is not apparent what changes TAG MH might be proposing for the structure and content of its corresponding Chapter V: F45 – F48.0 codes or to what extent ICD Revision intends that any changes to its own “Somatoform Disorders” will mirror Task Force proposals for DSM-V.

If the DSM-V Task Force were to approve radical changes to its “Somatoform Disorders” category, will ICD Revision still aim for “harmonization”?

Earlier this year, I called publicly on the ME Association to publish an analysis and commentary on the aims, objectives and recommendations of the CISSD Project in the context of the ICD and DSM revision processes and to inform its members, generally, around the forthcoming revisions of these two classification systems, which have been in progress since 2007 and 1999.

To date, apart from trumping Action for M.E. by publishing a summary report on the CISSD Project, provided by Dr Richard Sykes (in response to which the ME Association has expressed no comment or opinion whatsoever), this organisation has done nothing to inform its membership and the wider ME community around the forthcoming ICD revision, or that of DSM.

Nor has the ME Association clarified whether it intends to participate in draft consultations or in the submission of proposals to ICD, and if so, whether its membership will be given an opportunity to inform its position.

I have provided the ME Association board members with key information and documents: not a flicker of interest.

Stephen Ralph, who maintains the ME Action UK website, reports that when he approached Dr Charles Shepherd, recently, to ask what the ME Association was doing in relation to DSM and ICD, Dr Shepherd’s response had been that this was not an issue he had time for or was interested in.

An extraordinary response from an Honorary Medical Adviser given:

  The influential membership of the CISSD Project workgroup and the positions that some of its members now hold on the DSM Task Force and Somatic Distress Disorders Work Group.

•  The potential for review and revision of the current ICD-10 classifications and codings for Postviral fatigue syndrome, (Benign) myalgic encephalomyelitis (both currently classified in Chapter VI at G93.3) and chronic fatigue syndrome (currently indexed in Volume 3 at G93.3, only);

•  The means through which ICD-11 will be developed (the iCAT electronic multi-authoring platform) enabling a wide range of input from many sources;

•  The potential for, and implications of a radical revision of the DSM-IV category currently known as “Somatoform Disorders”;

•  The commitment of ICD and DSM to “harmonization” and congruency between the two systems;

•  The potential for considerably more content to be included in ICD-11 than in previous versions of ICD*.

*See: Key documents, particularly: Content Model Style Guide on the ICD-11 Revision site at: https://sites.google.com/site/icd11revision/home/documents 

The ME Association has adopted and promotes the use of the term “myalgic encephalopathy”. Is this at the root of Dr Shepherd’s disinclination to become drawn into debate around the forthcoming ICD revision, since “myalgic encephalopathy” has no classification or coding within ICD-10, at all?

Given the views expressed by Jane Colby, Executive Director of The Young ME Sufferers Trust, it would be useful if Ms Colby would also set out her organisation’s position in relation to PVFS, ME, CFS in the context of ICD-11.

Part Two

The 10 December APA press release noted that draft changes to the DSM will be posted on the DSM-V website in January 2010 and that comments will be accepted for two months and reviewed by the relevant DSM-V Work Groups in each diagnostic category.

That’s not very long for consultation for a patient community like ours.

A number of patient communities and interest groups have already been engaging for some time with DSM-V Work Groups. For one category (schizophrenia), quite detailed proposals have been made available for discussion and posted online. But for the DSM-V Work Group that has relevance for us – the “Somatic Distress Disorders” aka the “Somatic Symptom Disorders” Work Group, very little has emerged to date, and what has been published is lacking in detail.

What do we know so far?

Since the DSM-V Work Groups were announced in May 2008, each group has published just two progress reports.

The November 2008 report of the Somatic Distress Disorders Work Group can be read here:

http://tinyurl.com/DSMSDDWGNov08

The April ‘09 progress report of the Work Group can be read here:

http://tinyurl.com/DSMSDDWGApril09

Since April, no further updates have been issued by any of the DSM-V Work Groups. So until a draft for DSM revision proposals is released we are forced to glean what we can from journals.

In April ‘09, the Somatic Distress Disorders Work Group reported that they were exploring the potential for eliminating criteria such as “medically unexplained symptoms”:

…More controversial is a proposal the group has been examining, which would combine somatization disorder, hypochondriasis, pain disorder and undifferentiated somatoform disorder into one overarching disorder (tentatively entitled, “complex somatic symptom disorder”). The hallmark of this disorder would be somatic symptoms associated with significant distress and disability. In some cases the patient’s response is disproportionate and maladaptive. Our group is exploring the potential for eliminating criteria such as “medically unexplained symptoms” as a marker of this disorder because such considerations are commonly unreliable, divisive between doctor and patient and lead to mind-body dualism…

This was followed, in June, by an Editorial co-authored by DSM-V Work Group Chair, Joel Dimsdale, and fellow Work Group member, Francis Creed, which expanded on the themes in the April ‘09 update. This Editorial was published as free access, so at least those without access to journal papers were able to read it – assuming they were aware of it.

The Editorial: “The proposed diagnosis of somatic symptom disorders in DSM-V to replace somatoform disorders in DSM-IV – a preliminary report” was published on behalf of the Somatic Symptom Disorders Work Group in the June ‘09 issue of the Journal of Psychosomatic Research, for which Francis Creed is a co-editor. Several Letters to the editor in response to this Editorial have been published in the January ‘10 edition of this journal, but these are not free access.

Free full text and PDF versions of the June ‘09 Editorial here:

http://www.jpsychores.com/article/S0022-3999(09)00088-9/fulltext

The relevant section is “Psychological factor affecting a general medical condition” – towards the end of the document.

Under this section, Dimsdale and Creed wrote that some authors have recommended wider use of this existing DSM-IV category as “a diagnosis that encompasses the interface between psychiatric and general medical disorders”, citing the 2005 paper by Mayou R, Kirmayer LJ, Simon G, Kroenke K, Sharpe M: Somatoform disorders: time for a new approach in DSM-V. Am J Psychiat. 2005;162:847–855.

Free full text: http://ajp.psychiatryonline.org/cgi/content/full/162/5/847 

The Editorial reports that the [Psychological factors affecting a general medical condition] diagnosis “has been underused because of the dichotomy, inherent in the ‘Somatoform’ section of DSM-IV, between disorders based on medically unexplained symptoms and patients with organic disease”, and that by doing away with the “controversial concept of medically unexplained”, the proposed classification might diminish the problem.

The conceptual framework the Work Group were proposing, at that point:

…will allow a diagnosis of somatic symptom disorder in addition to a general medical condition, whether the latter is a well-recognized organic disease or a functional somatic syndrome such as irritable bowel syndrome or chronic fatigue syndrome.

The Editorial goes on to list a variety of different subtypes included within the diagnosis of “Psychological factors affecting a general medical condition” including a specific psychiatric disorder which affects a general medical condition; psychological distress in the wake of a general medical condition and personality traits or poor coping that contribute to worsening of a medical condition.

It suggests that these might be considered in the rubric “adjustment disorders” but that the location of this type of adjustment disorder had yet to be settled within the draft of DSM-V and that the text and placement for these different variants of the interface between psychiatric and general medical disorders was still under review.

(The current use of the diagnosis “Psychological Factors Affecting Medical Condition” in DSM-IV is set out here: http://www.behavenet.com/capsules/disorders/psyfactorsmedcon.htm )

The recently published Editorial: Is there a better term than “Medically unexplained symptoms”? Creed F, Guthrie E, Fink P, Henningsen P, Rief W, Sharpe M and White P (Journal of Psychosomatic Research: Volume 68, Issue 1, Pages 5-8 January 2010) discusses the deliberations of the EACLPP study group* on which I have previously reported. The Editorial also includes references to the DSM and ICD revision processes.

* http://meagenda.wordpress.com/2009/05/18/the-elephant-in-the-room-series-two-more-on-mups/
* http://www.eaclpp.org/documents/Patientswithmedicallyunexplainedsymptomsandsomatisation.doc

References to DSM and ICD revision in:

Is there a better term than “Medically unexplained symptoms”? Creed F, Guthrie E, Fink P, Henningsen P, Rief W, Sharpe M and White P. J Psychoso Res: Volume 68, Issue 1, Pages 5-8.

[Extract]

Introduction

The European Association of Consultation Liaison Psychiatry and Psychosomatics (EACLPP) is preparing a document aimed at improving the quality of care received by patients who have “medically unexplained symptoms” or “somatisation” [1]. Part of this document identifies barriers to improved care and it has become apparent that the term “medically unexplained symptoms” is itself a barrier to improved care…

…The authors of this paper met in Manchester in May 2009 to review thoroughly this problem of terminology and make recommendations for a better term….The deliberations of the group form the basis of this paper…

[...]

Our priority was to identify a term or terms that would facilitate management – that is it would encourage joint medical psychiatric/psychological assessment and treatment and be acceptable to physicians, patients, psychiatrists and psychologists.

Criteria to judge the value of alternative terms for “medically unexplained symptoms”

Ten criteria were developed in order to judge the value of potential terms which might be used to describe the group of symptoms currently referred to as medically unexplained symptoms. Obviously, this list of criteria does not claim to be exhaustive, but we believe that it captures the most important aspects. The criteria are that the term:

1. is acceptable to patients
2. is acceptable and usable by doctors and other health care professionals, making it likely that they will use it in daily practice.
3. does not reinforce unhelpful dualistic thinking.
4. can be used readily in patients who also have pathologically established disease
5. can be adequate as a stand alone diagnosis
6. has a clear core theoretical concept
7. will facilitate the possibility of multi-disciplinary (medical and psychological) treatment
8. has similar meaning in different cultures
9. is neutral with regard to aetiology and pathology
10. has a satisfactory acronym.

Terms suggested as alternatives for “medically unexplained symptoms”

The group reviewed terms which are used currently or have been proposed for the future. An extensive list was abbreviated to the following 8 terms or categories: The terms we reviewed were:

1. Medically unexplained symptoms or medically unexplained physical symptoms
2. Functional disorder or functional somatic syndromes
3. Bodily distress syndrome/disorder or bodily stress syndrome/disorder
4. Somatic symptom disorder
5. Psychophysical / psychophysiological disorder
6. Psychosomatic disorder
7. Symptom defined illness or syndrome
8. Somatoform disorder

[...]

Implications for DSM-V and ICD-11

There is overlap between the discussion reported here and the discussion currently under way towards the creation of DSM-V. Two of the authors (FC, MS) are also members of the working group on Somatic Distress Disorders of the American Psychiatric Association (APA), which is proposing a new classification to replace the DSM-IV “somatoform” and related disorders. In this working group, similar concerns about the use of the term and concept of “medically unexplained symptoms” have been raised [12]. The current suggestion by the DSM-V work group to use the term “Complex somatic symptom disorder” must be seen as step in a process and not as a final proposal. Unfortunately this term does not appear to meet many of the criteria listed above.

[...]

One major problem for reforming the classification relates to the fact that the DSM system includes only “mental” disorders whereas what we have described above is the necessity of not trying to force these disorders into either a “mental” or “physical” classification. The ICD-10 system has a similar problem as it has mental disorders separated from the rest of medical disorders.

The solution of “interface disorders”, suggested by DSM IV, is a compromise but it is unsatisfactory as it is based on the dualistic separation of organic and psychological disorders and prevents the integration of the disorders with which we are concerned here. This lack of integration affects the ICD classification also. For example functional somatic syndromes (e.g. irritable bowel syndrome) would be classified within the “physical” classification of ICD or Axis III in DSM (gastrointestinal disorders) and omitted from the mental and behavioural chapter entirely [13].

[End Extract]

Peter Denton White, Professor of Psychological Medicine, Barts and the London Medical School, has had quite a lot to say, recently, about ICD-10. In December 2008, Prof White gave a workshop presentation titled “Chronic fatigue syndrome: neurological, psychological or both?” at a Neurology and Psychiatry SpRs Teaching Weekend held in Oxford and sponsored by UCB Pharma and Biogen Idec UK. In the workshop handbook, Prof White talks about the taxonomy of CFS as being “a mess”.

Prof White writes:

My personal view is that it is high time that all mental health disorders and neurological diseases affecting the brain were classified within the same chapter, simply called diseases/disorders of the brain and nervous system.

(Workshop Handbook: Prof Peter White: Pages 46 – 50 http://bnpa.org.uk/doc/HANDBOOK.pdf  )

During his Royal Society of Medicine “CFS” Conference presentation, in April 2008, Prof White had told the conference:

…So ICD-10 is not helpful and I would not suggest, as clinicians, you use ICD-10 criteria. They really need sorting out; and they will be in due course, God willing.

See: Document [5] Extract, transcript, RSM CFS Conference presentation: Prof Peter White discouraging Conference from using ICD:  http://meagenda.wordpress.com/dsm-v-directory/  

In the paper: “Risk markers for both chronic fatigue and irritable bowel syndromes: a prospective case-control study of primary care” Psychological Medicine, Nov 2009, co-authored by Prof White, the authors propose a change to current ICD-10 codings ( http://www.ncbi.nlm.nih.gov/pubmed/19366500 ).

In the section “Implications for Further Research” the authors state that because the paper finds, “These data also suggest that fatigue syndromes are heterogeneous (Vollmer-Conna et al. 2006), and that CFS/ME and PVFS should be considered as separate conditions, with CFS/ME having more in common with IBS than PVFS does (Aggarwal et al. 2006). This requires revision of the ICD-10 taxonomy, which classifies PVFS with ME (WHO, 1992).”

According to DSM-V Task Force member, Javier Escobar, who works closely with the Somatic Distress Disorders Work Group, the so-called “Functional Somatic Syndromes (FSS)”, or “Medically Unexplained Symptoms (MUS)” include a long list of medical conditions:

Irritable bowel syndrome, Chronic fatigue syndrome, Fibromyalgia, Multiple chemical sensitivity, Nonspecific chest pain, Premenstrual disorder, Non-ulcer dyspepsia, Repetitive strain injury, Tension headache, Temporomandibular joint disorder, Atypical facial pain, Hyperventilation syndrome, Globus syndrome, Sick building syndrome, Chronic pelvic pain, Chronic whiplash syndrome, Chronic Lyme disease, Silicone breast implant effects, Candidiasis hypersensivity, Food allergy, Gulf War syndrome, Mitral valve prolapse, Hypoglycemia, Chronic low back pain, Dizziness, Interstitial cystitis, Tinnitus, Pseudoseizures, Insomnia, Systemic yeast infection, Total allergy syndrome [1]

[1] PSYCHIATRY AND MEDICAL ILLNESS Special Report
Unexplained Physical Symptoms What’s a Psychiatrist to Do? Humberto Marin, MD and Javier I. Escobar, MD,  Psychiatric Times. Vol. 25 No. 9, 01 August 2008.
http://www.psychiatrictimes.com/display/article/10168/1171223

——————

Over the past four or five years, dozens of journal reviews, papers and editorials have been published to inform the DSM revision process (with a very few papers specifically ICD-centric). Research planning conferences, symposia and monographs have further generated dialogue within the field around the taxonomy of the so-called “somatoform disorders” - it’s been quite an industry for liaison psychiatry and psychosomatics.

The CISSD Project, initiated in 2002 by Dr Richard Sykes, PhD, and administered by Action for M.E., between 2003 and 2007, is one project that has fed into both the DSM and the ICD revisions. Dr Sykes describes his project’s objective “to stimulate a multidisciplinary dialogue about the taxonomy of somatoform disorders and the medical diagnoses of functional somatic syndromes (e.g., irritable bowel syndrome, chronic fatigue syndrome, fibromyalgia)” and that the three CISSD Project workshops “brought together American and European experts to further consider the key questions and potential changes to be addressed in any revision of the Somatoform Disorders category, with the explicit aim of informing the development of DSM–V.”

The members of the CISSD Project workgroup were drawn almost exclusively from the fields of liaison psychiatry and psychosomatics. There were no patient organisation representatives on board and the only patient rep had co-authored a book on CFS with Prof Michael Sharpe, the project’s UK Chair.  Little wonder that Action for M.E. sought to keep a lid on this project for so long.

Understand that this unofficial project, initiated by Dr Richard Sykes and administered by Action for M.E. as part of the “merger” deal between Action for M.E. and Westcare UK, in mid 2002, does not have the authority of either the WHO or the APA, but that a number of influential CISSD Project workgroup members now serve on DSM-V Task Force and DSM-V Work Group committees – including Sharpe, Creed, Barsky, Levenson, Escobar and Dimsdale.

The first two tranches of funding paid to Dr Sykes for his co-ordination of the CISSD Project (£24,000 and £18,750) had been recorded in Action for M.E.’s year end accounts for 2006, and 2007, as a grant administered for the WHO Somatisation Project This grant is provided to help lobby the World Health Organisation for the recognition of M.E. and its re-categorisation as a physical illness.”

But the review paper resulting out of the CISSD Project, published by project leads Kroenke K, Sharpe M, Sykes R: Revising the Classification of Somatoform Disorders: Key Questions and Preliminary Recommendations. Psychosomatics 2007 Jul-Aug;48(4):277-285, was DSM-centric.

(Full free text: http://psy.psychiatryonline.org/cgi/content/full/48/4/277  )

A single reference to ICD appears in Table 2: Recommendations for Revising Somatoform Disorders in DSM-V at point VII. under “Other Recommendations: 3. The APA and WHO should work together to make DSM-V and ICD-11 compatible with respect to the categories, disorders, and criteria for mental disorders…”

Chronic fatigue syndrome is mentioned twice: in the introduction, and under Key Questions 5. How should functional somatic syndromes be classified? These so-called functional somatic syndromes include conditions such as irritable bowel syndrome, fibromyalgia, chronic fatigue syndrome, interstitial cystitis, and others. These syndromes are overlapping and frequently coexist…”

There is no reference in the review to Postviral fatigue syndrome or to (Benign) myalgic encephalomyelitis; the paper does not set out what its authors understand by the term “chronic fatigue syndrome” or their understanding of its relationship to Postviral fatigue syndrome or to (Benign) myalgic encephalomyelitis nor does it set out existing ICD-10 classifications and codings for any of these terms.

The paper fails to acknowledge that in ICD-10, Chronic fatigue syndrome is indexed in Volume 3 at G93.3. In fact, Dr Sykes had undertaken his project under the misapprehension that Chronic fatigue syndrome was not included anywhere in ICD-10 – a point he has since conceded.

The review paper has informed both the DSM and ICD revision processes and its recommendations have been submitted to the ICD Update and Revision Platform by Dr Sykes, in 2008, on behalf of the CISSD Project workgroup.

Note that the journal review paper, published in Psychosomatics 2007 Jul-Aug, by CISSD Project leads, Kroenke K, Sharpe M and Sykes R, is an entirely different document to the “CISSD Project and CFS/ME Report on the CISSD Project for Action for ME” which was an internal document handed to the project administrators, Action for M.E., in December 2007, by project co-ordinator, Dr Sykes, and not intended for publication. A copy of Dr Sykes’ Report for Action for M.E. and an accompanying “Co-ordinator’s Report” are now in the public domain.

( http://www.afme.org.uk/res/img/resources/CISSD%20project%20report%201.pdf  )
( http://www.afme.org.uk/res/img/resources/CISSD%20project%20report%202.pdf  )

In addition to its 13 Work Groups, DSM-V also uses external advisers whose names are not being disclosed. ICD Revision Topic Advisory Group Managing Editors (TAGMEs) will be networking for external peer reviewers for revision proposals and content.

( http://whoicd11.blogspot.com/2009/09/who-icd-11-googlesite.html#comments  )

One of the questions I raised, in October, with the WHO’s Dr Robert Jakob [Medical Officer (ICD) Classifications, Terminologies, and Standards] is whether those acting as independent peer reviewers to the various TAGs, and also external sources from whom input/opinion might otherwise be being sought, would be identified via iCAT to users outside the ICD revision process; whether the evaluations undertaken by external reviewers and input from external sources would be visible to those outside ICD revision and whether COI disclosures would be required of external reviewers.

——————

This represents about all that is available to me at the moment on the deliberations of the DSM-V Work Group – other than the Letters to the editor in response to “The proposed diagnosis of somatic symptom disorders in DSM-V to replace somatoform disorders in DSM-IV – a preliminary report”.

According to the APA, we can anticipate DSM-V draft proposals published in the New Year.

ICD-11 Alpha Draft is timelined for May 2010. We have no ETA yet for the launch of iCAT, the wiki-like electronic authoring platform through which ICD-11 will be developed so it is not yet evident what content will form the “Start-up list” for those categories of relevance to us.*

*Each Chapter of ICD-11 will have a “Start-up list” which, according to ICD Revision documentation, will include current ICD-10 content, input from ICD clinical modifications and WHO affiliate organisations, proposals already received via the ICD Update and Revision Platform.

——————

For information, commentary and updates on the development of ICD-11 and DSM-V on ME agenda: http://meagenda.wordpress.com/dsm-v-directory/

For detailed information on the proposed structure of ICD-11, the Content Model and operation of iCAT, the collaborative authoring platform through which the WHO will be revising ICD-10, please scrutinise key documents on the WHO’s ICD-11 Revision Google site:

https://sites.google.com/site/icd11revision/
https://sites.google.com/site/icd11revision/home/documents

For ICD Revision iCamp YouTube videos:  http://www.youtube.com/user/WHOICD11

For DSM-V pages on the website of the American Psychiatric Association (APA): http://www.psych.org/MainMenu/Research/DSMIV/DSMV.aspx

Psychiatric Times for updates, articles and commentary on DSM-V:  http://www.psychiatrictimes.com/dsm-v

Posted in AfME, Action for M.E., CISSD Project, Consultations, Criticism of DSM-V, DSM-5, DSM revision process, DSM-5, Elephant Series DSM-V, ICD revision process, ICD-11, MUS, Professor Peter White, WHO (World Health Organization) | Comments Off

American Psychiatry Is Facing “Civil War” over Its Diagnostic Manual What’s the real reason DSM-V has been delayed? Christopher Lane

Posted by meagenda on December 14, 2009

Shortlink: http://wp.me/p5foE-2wt

See also previous postings: 

Press Release: DSM-5 Publication Date Moved to May 2013  

Opinion on DSM-V (DSM-5) revision on Psychiatric Times site and in this week’s New Scientist, 9 December

PDF of press release here:  http://DSM5toMay2013.notlong.com

The American Psychiatric Association (APA) has yet to update its website to reflect last Thursday’s predicted announcement that the publication date for DSM-V is being shifted from May 2012 to May 2013. According to the press release, draft changes to DSM are to be posted on the DSM-V website in January 2010. Comments will be accepted for two months for review by the relevant DSM-V Work Groups for each diagnostic category. Field trials for testing proposed changes will be conducted in three phases.

DSM-V pages herehttp://www.psych.org/MainMenu/Research/DSMIV/DSMV.aspx

DSM-V Timeline page here:  http://www.psych.org/MainMenu/Research/DSMIV/DSMV/Timeline.aspx

——————–

Interesting piece on 12 December from Christopher Lane:

Christopher Lane is the Pearce Miller Research Professor of Literature at Northwestern University and the author of Shyness: How Normal Behavior Became a Sickness.

Psychology Today

Blogs
Side Effects
From quirky to serious, trends in psychology and psychiatry.

by Christopher Lane, Ph.D.

http://www.psychologytoday.com/blog/side-effects/200912/american-psychiatry-is-facing-civil-war-over-its-diagnostic-manual

December 12, 2009, Psychiatry

American Psychiatry Is Facing “Civil War” over Its Diagnostic Manual What’s the real reason DSM-V has been delayed?

What’s the real reason DSM-V has been delayed?

Yesterday, the American Psychiatric Association announced that it is pushing back the publication of DSM-V until 2013. The APA tried to put a good face on this rather embarrassing admission—embarrassing, because several spokespeople for the organization had insisted, quite recently, that they were on-track for publication in 2012 and that nothing would deter them. They maintained that position even as an increasingly acrimonious quarrel between current and former editors of the manual spilled onto the pages of Psychiatric News…Read on

The original dissemination date for ICD-11 had also been 2012, with the timelines for ICD-11 and DSM-V running more or less in parallel ( http://www.apa.org/international/s08agenda25-Exhibit1.pdf  ). ICD-11 has since slipped by two years.

The most recent timeline I can provide was included in the June 2009 PowerPoint presentation by Robert Jakob (Medical Officer, Classifications and Terminologies, WHO Geneva), download here: ICD Revision Process [PDF format 1.33 MB]

ICD Revision Process
ICD-11 June 2009

Presentation: Robert Jakob / Bedirhan Üstün

See Slide 9 for “Tentative Timeline” (for overall revision process)

Tentative Timeline

2010 : Alpha version ( ICD 10+ → ICD 11 draft)
– +1 YR : Commentaries and consultations
2011 : Beta version & Field Trials Version
– +2 YR : Field trials
2013 : Final version for public viewing
– 2014 : WHA Approval
2015+ : Implementation

See Slide 38 for “ICD-11 Alpha Drafting Timeline” (to May 2010)

See Slide 39 for “ICD-11 Alpha Draft Calendar” (to May 2010)

Alpha Draft Calendar

Preparations will finish before 31 August 2009
Overall Drafting Period: 14 September 2009 – 15 April 2010
Phase 1: 14 Sept – 11 Dec 2009 (10 WORKING WEEKS)
Provisional Interim Review: 15 Dec – 15 Jan
Phase 2: 18 Jan – 16 April 2010 (10 WORKING WEEKS)
Prefinal Review by WHOFIC: 15 April – Council
Submission for Systematic ALPHA TESTS: May 2010

According to “ICD Revision” on Facebook:

http://www.facebook.com/pages/ICD-Revision/117942832025

ICD-11 alpha draft will be ready by 10 May 2010
ICD-11 beta draft will be ready by 10 May 2011
ICD final draft will be submitted to WHA by 2014

It was reported, in August (DSM-V Field Trials Set to Begin, Elsevier Global Medical News), that the APA had planned to launch some field trials for DSM-V in October, with all field trials scheduled for completion by the end of 2010, for a previously anticipated publication date of May 2012. Lane claims that most of the field trials have yet to begin because the Work Groups can’t agree on their criteria.

The recently published Editorial: Is there a better term than “Medically unexplained symptoms”? Creed F, Guthrie E, Fink P, Henningsen P, Rief W, Sharpe M and White P (J Psychosoma Res:Volume 68, Issue 1, Pages 5-8, Jan 2010) discusses the deliberations of the EACLPP study group and includes references to the DSM and ICD revision processes which suggest that the progress of  the DSM-V “Somatic Distress Disorders” Work Group is in chaos.

In Advice To DSM V…Change Deadlines And Text, Keep Criteria Stable , (Psychiatric Times, 26 August), Allen Frances MD, who had chaired the revision of DSM-IV, raised the issue of non parallel timelines and the forthcoming shift from ICD-9-CM to ICD-10-CM in the US – a transition now scheduled for October 2013:

Frances wrote:

“Under normal circumstances, it would make sense to continue the tradition of publishing DSM-V and ICD-11 simultaneously, whenever ICD-11 is ready—probably in 2014. But there is also a problem with a 2014 deadline caused by a coding change that will go into effect before then. ICD-9-CM is now the official method of diagnostic coding used to specify all medical encounters in the United States. It will be replaced in October 2013 by a completely revamped ICD-10-CM. Publishing DSM-V much before October 2013 would result in great confusion and force a choice between 2 equally undesirable options: publish DSM-V in 2012 with the current ICD-9-CM codes, which would be usable only for 18 months; or else, publish DSM-V with the new ICD-10-CM codes even though DSM users would still have to use the ICD-9-CM codes for the next 18 months. Only by delaying publication of DSM-V until just before October 2013 would this problem be solved.”

On 09 July, in Dr Frances Responds to Dr Carpenter: A Sharp Difference of Opinion, Frances had called for the posting of all the suggested wordings for DSM-V criteria sets well before considering field trials:

“Will [Dr William Carpenter, MD] seems to think that his presentations at professional meetings in front of relatively small audiences provide a sufficiently open DSM-V process…We, the field, still know almost nothing about the content of what is being considered for DSM-V or how the options still in play are justified by the literature reviews and data reanalyses…We should have every wording of every proposed criteria set or dimension. Why not post these now to allow for the widest review well before field trials are started? I cannot imagine going to the trouble and expense of field testing before there is confidence that the diagnostic concepts make sense and that they are appropriately worded. Equally puzzling is the lack of posting of the literature reviews and of the methods of the proposed field trials. The DSM-V leadership has made the truly bizarre claim that they have provided the “most open process” of all the previous DSM revisions, but they have not posted any explicit or detailed indication of what they are doing and why…If the real reason for not posting is that the material is not yet in a presentable form, admit this and postpone the field trials until everything can be posted and fully vetted.”

We have no information on how closely ICD Revision and DSM have been collaborating on the revision of their respective “Somatoform Disorders” sections, what changes ICD Revision might be proposing for its corresponding Chapter V: F45 – F48 codes, or to what extent WHO intends that any changes to this section of Chapter V will mirror Task Force proposals for DSM-V. If DSM Task Force has approved radical changes to the categories currently classified under “Somatoform Disorders”, will ICD Revision still aim for “harmonisation”?

Despite the ICD Revision iCAMP meeting YouTubes, the ICD Revision blog and its Facebook site, we have no ETA for the launch of iCAT, the electronic platform through which ICD-11 will be developed. Is iCAT on schedule and will ICD-11 Alpha Draft be ready for May 2010 or is the WHO revision of ICD slipping, too?

Posted in CISSD Project, Consultations, Criticism of DSM-V, DSM-5, DSM revision process, Elephant Series DSM-V, ICD revision process, ICD-11, MUPSS Project, MUS, WHO (World Health Organization) | Comments Off

Opinion on DSM-V revision: Psychiatric Times and New Scientist, 9 December

Posted by meagenda on December 11, 2009

Opinion on DSM-V (DSM-5) revision on Psychiatric Times site and in this week’s New Scientist, 9 December

Shortlink: http://wp.me/p5foE-2v4

Note: The APA Press Release announcing the extension of the timeline for the publication of DSM-V from May 2012 to an anticpated release date of May 2013 uses “DSM-5″ rather than “DSM-V”. Unless the APA adopts the use of “DSM-5″ on new documents, I will continue to use “DSM-V”. According to the Style Guide for ICD-11, it is proposed that chapters in ICD-11 will no longer use Roman numerals – so we might anticipate, for example, “Chapter 5″ and “Chapter 6″.

http://www.psychiatrictimes.com/display/article/10168/1493263  

03 December 2009
Psychiatric Times

COMMENTARY
Alert to the Research Community—Be Prepared to Weigh in on DSM-V
Allen Frances, MD

Dr Frances was the chair of the DSM-IV Task Force and of the department of psychiatry at Duke University School of Medicine, Durham, NC. He is currently professor emeritus at Duke.

“This commentary will suggest how the research community can be instrumental in improving DSM-V and helping it avoid unintended consequences. According to several converging, anonymous (but I think quite reliable) sources to which I have had access, the draft options for DSM-V will finally be posted between mid-January and mid-February 2010. There will then be just one additional month until mid-March for collecting comments. The good news is that the products of a previously closed process will finally be available for wide review and correction. The bad news is that there will be only a very brief period allotted for this absolutely crucial input from the field.

“The research community has a central role and a great responsibility in taking advantage of this precious opportunity to carefully review and identify the problems in the DSM-V drafts and to suggest solutions…”  Read on

—————————-

http://www.psychiatrictimes.com/display/article/10168/1494481

08 December 2009
Psychiatric Times

A Call to DSM-V to Focus on the Designation of Borderline Intellectual Functioning
Jerrold Pollak, PhD
Program in Medical and Forensic Neuropsychology

John J. Miller, MD
Department of Psychiatry, Seacoast Mental Health Center, Portsmouth, New Hampshire

—————————-

http://www.psychiatrictimes.com/display/article/10168/1494500

08 December 2009
Psychiatric Times

DSM-V and Pain
Steven A. King, MD, MS
Dr King is in the private practice of pain medicine in New York and he is also clinical professor of psychiatry at the New York University School of Medicine.

—————————-

Articles on DSM-V revision process in this week’s New Scientist:

http://www.newscientist.com/article/mg20427382.400-times-up-for-psychiatrys-bible.html

Editorial:

Time’s up for psychiatry’s bible
09 December 2009

“Proponents of some of the changes are being accused of running ahead of the science, and there are warnings that the APA is risking “disastrous unintended consequences” if it goes ahead with plans to publish DSM-V, as the new manual will be known, in 2012.*

“It doesn’t have to be this way. With the advent of the internet, there is no longer any compelling need to rewrite the diagnostic criteria for the whole of psychiatry in one go. Yes, diagnoses should be revised as new scientific findings come in. But for this, specialists can be assembled when necessary to address specific areas that have become outmoded. Their suggestions can be posted on the web for comment. More research can be commissioned, if necessary. And when consensus is reached, new diagnostic criteria can be posted online…”  Read full article

*Ed: Article to press prior to APA announcement on 10 December.

http://www.newscientist.com/article/mg20427381.300-psychiatrys-civil-war.html

Article:

Psychiatry’s civil war
09 December 2009 by Peter Aldhous

“…The wording used in the DSM has a significance that goes far beyond questions of semantics. The diagnoses it enshrines affect what treatments people receive, and whether health insurers will fund them. They can also exacerbate social stigmas and may even be used to deem an individual such a grave danger to society that they are locked up.”

“…Attention has also turned to the financial interests of those working on DSM-V. The APA has ruled that members of the task force and work groups may not receive more than $10,000 per year from industry while working on DSM-V, and must keep their stock holdings below $50,000. This doesn’t satisfy Lisa Cosgrove of the University of Massachusetts, Boston, who studies financial conflicts in psychiatry (New Scientist, 29 April 2006, p 14). She notes that the APA’s ruling places no limit on industry research grants, and has found that the proportion of DSM-V panel members who have industry links is exactly the same as it was for DSM-IV, at 56 per cent (The New England Journal of Medicine, vol 360, p 2035).”  Read full article

—————————-

Short link for PDF of APA Press Release  | 10 December  2009
Press Release No. 09-65:

http://DSM5toMay2013.notlong.com

or copy on ME agenda at: http://wp.me/p5foE-2uO

Posted in CISSD Project, Consultations, Criticism of DSM-V, DSM-5, DSM revision process, Elephant Series DSM-V, ICD revision process, ICD-11, MUPSS Project, MUS, WHO (World Health Organization) | Comments Off

Press Release: DSM-5 Publication Date Moved to May 2013

Posted by meagenda on December 10, 2009

I am not at all surprised by this announcement, today, by the American Psychiatric Association (APA):

Shortlink: http://wp.me/p5foE-2uO

PDF Press Release: DSM-5 Publication Date Moved Press Release

http://DSM5toMay2013.notlong.com

Press Release

For Information Contact:

Beth Casteel 703-907-8640 December 10, 2009
press@psych.org Release No. 09-65

Jaime Valora 703-907-8562
jvalora@psych.org

For Immediate Release:

December 10, 2009
Release No. 09-65

DSM-5 Publication Date Moved to May 2013

ARLINGTON, Va. (Dec. 10, 2009) – The American Psychiatric Association revised the timeline for publishing the fifth edition of the Diagnostic and Statistical Manual of Mental Disorders, moving the anticipated release date to May 2013.

“Extending the timeline will allow more time for public review, field trials and revisions,” said APA President Alan Schatzberg, M.D.” The APA is committed to developing a manual that is based on the best science available and useful to clinicians and researchers.”

The extension will also permit the DSM-5 to better link with the U.S. implementation of the ICD-10-CM codes for all Medicare/Medicaid claims reporting, scheduled for October 1, 2013.

Although ICD-10 was published by the WHO in 1990, the “Clinical Modification” version (ICD-10-CM) authorized by the U.S. Centers for Medicare and Medicaid Services (CMS) and the Centers for Disease Control (CDC) is not being implemented in the U.S. until 23 years later.

The ICD-10-CM includes disorder names, logical groupings of disorders and code numbers but not explicit diagnostic criteria. The APA has already worked with CMS and CDC to develop a common structure for the currently in-use DSM-IV and the mental disorders section of the ICD-10-CM.

The International Classification of Diseases (ICD) is published by the WHO for all member countries to classify diseases and medical conditions for international health care, public health, and statistical use. The WHO plans to release its next version of the ICD, the ICD-11, in 2014.

APA will continue to work with the WHO to harmonize the DSM-5 with the mental and behavioral disorders section of the ICD-11. Given the timing of the release of both DSM-5 and ICD-11 in relation to the ICD-10-CM, the APA will also work with the CDC and CMS to propose a structure for the U.S. ICD-10 CM that is reflective of the DSM-5 and ICD-11 harmonization efforts. This will be done prior to the time when the ICD-10-CM revisions are “frozen” for CMS and insurance companies to prepare for the October 1, 2013, adoption.

The Timeline

David Kupfer, M.D., chair of the DSM-5 Task Force, which is in charge of the DSM revision process, noted that draft changes to the DSM will be posted on the DSM-5 Web site in January 2010. Comments will be accepted for two months and reviewed by the relevant DSM-5 Work Groups in each diagnostic category. Field trials for testing proposed changes will be conducted in three phases.

The process for developing the DSM-5 began a decade ago, with an initial research planning conference under the joint sponsorship of the APA and the National Institute of Mental Health.

Additional global research planning conferences, under the auspices of the American Psychiatric Institute for Research and Education (APIRE), the World Health Organization, and three institutes of the National Institutes of Health produced a series of monographs, which helped lay the groundwork for the revisions. The APA’s DSM-5 Task Force and Work Group members were identified in 2007; they are tasked with reviewing scientific advances and research to develop draft diagnostic criteria in diagnostic categories of psychiatric disorders. Information about the revision process is available online at http://www.DSM5.org .

The American Psychiatric Association is a national medical specialty society whose physician members specialize in the diagnosis, treatment, prevention and research of mental illnesses, including substance use disorders. Visit the APA at http://www.psych.org  and http://www.healthyminds.org .

Posted in CBT, CBT/GET, CFS Research, CISSD Project, Criticism of DSM-V, DSM-5, DSM revision process, Elephant Series DSM-V, ICD revision process, ICD-11, MUPSS Project, MUS, WHO (World Health Organization), WHO Somatisation Project | Comments Off

The Elephant in the Room Series Four: New papers in Jan 10 Journal of Psychosomatic Research

Posted by meagenda on December 10, 2009

Image | belgianchocolate | Creative Commons

Keywords

APA    DSM    DSM-IV    DSM-V    WHO    ICD    ICD-10    ICD-11    American Psychiatric Association    Diagnostic and Statistical Manual of Mental Disorders    World Health Organization    Classifications    DSM Revision Process    DSM-V Task Force    DSM-V Somatic Distress Disorders Work Group    Somatic Symptom Disorders Work Group    DSM-ICD Harmonization Coordination Group    International Advisory Group    Revision of ICD Mental and Behavioural Disorders    Global Scientific Partnership Coordination Group    ICD Update and Revision Platform    WHO Collaborating Centre    CISSD Project    MUPSS Project    Somatoform    Somatisation    Somatization    Functional Somatic Syndromes    FSS    MUS    Myalgic encephalomyelitis    ME    Chronic fatigue syndrome    CFS    Fibromyalgia    FM    IBS    CS    CI    GWS

The Elephant in the Room Series Four:

New papers in the January 2010 edition of the Journal of Psychosomatic Research

Shortlink: http://wp.me/p5foE-2uH
 

For DSM-V watchers (and I’m sure I can’t be the only one) – new papers in the January 2010 edition of the Journal of Psychosomatic Research.

In Letter to the editor: The proposed diagnosis of somatic symptom disorders in DSM-V to replace somatoform disorders in DSM-IV-A preliminary report: Joel E. Dimsdale, Francis H. Creed, the authors write:

“We are pleased that the authors of these letters appreciate our efforts to be open regarding the proposed changes to the diagnostic criteria of the Somatoform Disorders chapter of DSM-V.”

Note there have been no updates published by the APA DSM-V revision Task Force since the March 09 Task Force report and April 09 updates from the 13 DSM-V Work Groups.

So much for APA (American Psychiatric Association) transparency!

http://www.psych.org/MainMenu/Research/DSMIV/DSMV/DSMRevisionActivities.aspx

—————-

Journal of Psychosomatic Research, Editors: Creed F, Shapiro C.

http://www.journals.elsevierhealth.com/periodicals/psr/home

http://www.journals.elsevierhealth.com/periodicals/psr/current

Current Issue

January 2010 | Vol. 68, No. 1

Editorials

Painting the picture of distressing somatic symptoms
Winfried Rief
pages 1-3

Is there a better term than “Medically unexplained symptoms”?, 19 October 2009
Francis Creed, Elspeth Guthrie, Per Fink, Peter Henningsen, Winfried Rief, Michael Sharpe, Peter White
pages 5-8

Original articles

Causal symptom attributions in somatoform disorder and chronic pain, 05 October 2009
Wolfgang Hiller, Marian Cebulla, Hans-Jürgen Korn, Rolf Leibbrand, Bodo Röers, Paul Nilges
pages 9-19

http://www.jpsychores.com/article/S0022-3999(09)00262-1/abstract

Letters to the editor

The proposed diagnosis of somatic symptom disorders in DSM-V: Two steps forward and one step backward?
Andreas Schröder, Per Fink
pages 95-96

The concept of comorbidity in somatoform disorder-a DSM-V alternative for the DSM-IV classification of Somatoform disorder
Christina M. van der Feltz-Cornelis, Anton J.L.M. van Balkom
pages 97-99

The proposed diagnosis of somatic symptom disorders in DSM-V to replace somatoform disorders in DSM-IV-A preliminary report, 04 November 2009
Joel E. Dimsdale, Francis H. Creed
pages 99-100

—————-

New documents on the WHO ICD-11 Revision Google site:

https://sites.google.com/site/icd11revision/home/documents

iSUMMARY of iCAMP

Summary of iCAMP and TAG [Topic Advisory Group] Meetings
Draft Summary and Action items

(Uploaded 2 December)

also

iCamp Content Model Style – Updated Style Guide from Discussions

WHO House Style

WHO House Style Spelling List

(All three uploaded on 30 October)

https://sites.google.com/site/icd11revision/home/face-to-face-meetings/tag-internal-medicine

There are also some PowerPoint presentations at the page above.

———————

DSM-V and ICD-11 have committed as far as possible “to facilitate the achievement of the highest possible extent of uniformity and harmonization between ICD-11 mental and behavioural disorders and DSM-V disorders and their diagnostic criteria” with the objective that “the WHO and APA should make all attempts to ensure that in their core versions, the category names, glossary descriptions and criteria are identical for ICD and DSM.”

The International Advisory Group for the Revision of ICD-10 Mental and Behavioural Disorders most recent meeting took place on 28 – 29 September. It is anticipated that a Summary Report of the meeting will be available in December.

For detailed information on the proposed structure of ICD-11, the Content Model and operation of iCAT, the collaborative authoring platform through which the WHO will be revising ICD-10, please scrutinise key documents on the ICD-11 Revision Google site:

https://sites.google.com/site/icd11revision/
https://sites.google.com/site/icd11revision/home/documents

For information around the DSM and ICD revision processes see DSM-V and ICD-11 Directory page: http://meagenda.wordpress.com/dsm-v-directory/

Posted in CBT, CBT/GET, CFS Research, CISSD Project, Criticism of DSM-V, DSM-5, DSM revision process, Elephant Series DSM-V, ICD revision process, ICD-11, MUPSS Project, MUS, Professor Peter White, WHO (World Health Organization), WHO Somatisation Project | Comments Off

Prof Peter D White: Neurology and Psychiatry SpRs Teaching Weekend

Posted by meagenda on November 15, 2009

Prof PD White: Neurology and Psychiatry SpRs Teaching Weekend

Shortlink for this posting: http://wp.me/p5foE-2p0

14 November 2009

THE BRITISH NEUROPSYCHIATRY ASSOCIATION

http://www.bnpa.org.uk

http://bnpa.org.uk/doc/HANDBOOK.pdf

Neurology and Psychiatry SpRs Teaching Weekend

12 to 14 December 2008 St Anne’s College – Oxford

THE ESSENTIALS OF NEUROPSYCHIATRY

Presentations:

[...]

09:50 Chronic fatigue syndrome: neurological, psychological or both?

Peter White, Professor of Psychological Medicine, Barts and the London Medical School

The extract I am appending is a summary of Professor Peter Denton White’s presentation (Page 46 of PDF) in which he talks about the taxonomy of CFS “being a mess”.

During his Royal Society of Medicine “CFS” Conference presentation, in April 2008, White had said, ominously:

“…So ICD-10 is not helpful and I would not suggest, as clinicians, you use ICD-10 criteria. They really need sorting out; and they will be in due course, God willing.”

See unofficial transcript of part of White’s RSM presentation, here, in which he presents his thoughts on current ICD taxonomy:

Prof Peter White discouraging RSM Conference from using ICD-10: http://tinyurl.com/PDW-RSM-ICD-10

In an April 2009 paper, co-authored by White, the authors propose a change to current ICD-10 codings:

http://www.ncbi.nlm.nih.gov/pubmed/19366500

Psychological Medicine Preprint “Risk markers for both chronic fatigue and irritable bowel syndromes: a prospective case-control study of primary care”

In the section “Implications for Further Research” the authors state that because the paper finds that:

“These data also suggest that fatigue syndromes are heterogeneous (Vollmer-Conna et al. 2006), and that CFS/ME and PVFS should be considered as separate conditions, with CFS/ME having more in common with IBS than PVFS does (Aggarwal et al. 2006). This requires revision of the ICD-10 taxonomy, which classifies PVFS with ME (WHO, 1992)”

 Presentation given at Neurology and Psychiatry SpRs Teaching Weekend

http://bnpa.org.uk/doc/HANDBOOK.pdf

[Extract]

Presentation:

Chronic fatigue syndrome: neurological, psychological or both?

Peter White, Professor of Psychological Medicine, Barts and the London Medical School

Epidemiology of fatigue and CFS

Fatigue is a common symptom in both the community and primary care. When asked, between 10 and 20 per cent of people in the community will report feeling abnormally tired at any one time.

At the same time, fatigue is continuously distributed within the community, with no point of rarity.

Therefore any cut-off is arbitrary and the prevalence will vary by how the question is asked, the symptom volunteered, and its context. Between 1.5 % and 6.5 % of European patients will consult their general practitioner with a primary complaint of fatigue every year, the incidence varying by age and population. Fatigue is more commonly reported and presented to general practitioners by women and the middle-aged, and is most closely associated with mood disorders and reported stress. It does not seem to vary by ethnicity in the UK, but there is an intriguing paradox in that it is reported more commonly by those in high income countries, yet is presented to medical care more often in low income countries.

Prolonged or chronic fatigue is significantly less common than the symptom of fatigue and it is only in the last 10 years that consensus has emerged about the existence of a chronic fatigue syndrome (CFS), also called myalgic encephalomyelitis (ME). CFS is now accepted as a valid diagnosis by medical authorities in the UK, in the United States of America, as well as internationally. About one third of patients presenting to their doctor with six months of fatigue will meet criteria for a chronic fatigue syndrome. The other two thirds have fatigue secondary to another condition, most commonly mood and primary sleep disorders. Its primary symptom is fatigue, both physical and mental, which particularly follows exertion. Other symptoms agreed in consensual guidelines include poor concentration and memory, sleep disturbance, headache, sore throat, tender lymph glands, muscle and joint pain.

There are several criterion based definitions of CFS. These definitions were derived by consensus and have not been supported by empirical studies, and continue to be refined. Their utility stems from providing reliable criteria for research studies, rather than clinical use. The prevalence of CFS is between 2.5 % and 0.4 % depending on the definition used and whether comorbid mood disorders are excluded (that is mood disorders that are not thought to be the primary diagnoses). It is most common in women, the middle-aged, and ethnic minorities (unlike fatigue) – at least in English speaking countries.

The diagnosis and classification of CFS

The clinical taxonomy for CFS is a mess. The ICD-10 classification defines CFS within both the neurology chapter and mental health chapters. Myalgic encephalomyelitis, the alternative name for CFS, is classified as a neurological disease (G93.3) (a.k.a. post-viral CFS), whereas neurasthenia (a.k.a. CFS not otherwise specified) is classified within mental health (F48).

[Ed: Note that White does not mention, here, that Chronic fatigue syndrome is listed in ICD-10: Volume 3, The Alphabetical Index* at G93.3, the same coding as for Benign myalgic encephalomyelitis, and for Postviral fatigue syndrome (ICD-10: Volume 1: The Tabular List).]

*ICD-10: Volume 3, The Alphabetical Index:
http://www.scribd.com/doc/7350978/ICD10-2006-Alphabetical-Index-Volume-3

[Back to PDW]

(Incidentally, this mess is not specific to CFS, since there are several conditions within the neurology chapter of ICD-10 that are also classified in the mental and behavioural disorders chapter. For instance, Alzheimer’s disease is classified within neurology, whereas dementia due to Alzheimer’s disease is classified under mental health. My personal view is that it is high time that all mental health disorders and neurological diseases affecting the brain were classified within the same chapter, simply called diseases/disorders of the brain and nervous system.)

[Ed: The WHO Department of Mental Health and Substance Abuse, which is overseeing the revision of Chapter V (Mental and Behavioural Disorders), is also managing the technical part of the revision of Chapter VI (Diseases of the Nervous System). According to Dr Geoffrey Reed, Senior Project Officer, WHO Department of Mental Health and Substance Abuse, Proposal forms for ICD Chapter V and Chapter VI are in preparation and expected to be released shortly.]

[Back to PDW]

There is also a current debate between “lumpers” and “splitters” about the nosology of “functional” somatic syndromes (symptom defined conditions), such as CFS, IBS and “fibromyalgia”. Some argue that the close associations between the syndromes (those with CFS are also more likely to have fibromyalgia and/or IBS) argues in favour of their being different manifestations of one over-arching functional somatic syndrome (the “lumpers”). Others argue that these syndromes are best understood by exploring their heterogeneity (the “splitters”). There is evidence to support both arguments, but two large and recent epidemiological studies suggest that chronic unexplained fatigue, for one, is both associated with and separate from other “functional” somatic syndromes. In particular, predisposing risk factors are shared whereas triggering factors are different.

CFS is not an easy diagnosis to make, since misdiagnosis is common in patients diagnosed as having CFS. A recent audit of my CFS clinic revealed that 4 out of 10 new patients (n = 250) assessed did not have CFS, and that was after a third of referrals had already been rejected as not being CFS.

The most common misdiagnoses were mood disorders, especially depressive disorders, and primary sleep disorders, particularly sleep apnoea. Other misdiagnoses included coeliac disease and autoimmune conditions. Alternative neurological diagnoses were made in 2%.

Aetiology and pathophysiology

The aetiology of CFS is unknown, but there is evidence that different risk markers are associated with predisposition, triggering, and maintenance of the illness. Predisposing risk markers include female sex, middle age, mood disorders (especially depressive disorders), other symptom defined syndromes, such as irritable bowel syndrome, and possibly either sedentary behaviour or excessive activity. As might be expected CFS patients are more likely to have attended their GP, than healthy matched controls, even up to 15 years before onset, but recent work shows that those with IBS (and no CFS) have the same tendency.

Triggering risk markers are less well established, but there is sufficient evidence to support certain infections as aetiological factors not only for fatigue but also CFS, with the best replicated evidence supporting a role for Epstein-Barr virus infection, which triggers CFS in 10% of those infected.

Maintaining or perpetuating risk markers are most important in determining treatment programmes, since reversing maintaining factors should lead to improvement. Reasonably well established factors include mood disorders, such as dysthymia, illness beliefs such as believing the whole condition is physical, pervasive inactivity, avoidant coping, membership of a patient support group, and being in receipt of or dispute about financial benefits.

Few pathophysiological findings in CFS have been replicated in independent studies. Those that have been include down-regulated hypothalamic pituitary-adrenal axis, physical deconditioning, and discrepant reports between perception of symptoms and disability and their objective tests.

The latter finding is now supported by functional brain scanning studies suggesting altered brain activity with specific tasks. The discrepancy between subjective states and objective tests has been found before in other symptom defined syndromes, such as “fibromyalgia”, and may be related to enhanced interoception (the perception of visceral phenomena), a concept first described by Charles Sherrington in 1904. One hypothesis currently being tested is that the common predisposition to “functional” somatic syndromes is caused by enhanced interoception.

Recent work suggests that these factors may be reversed by rehabilitation.

Prognosis

Without treatment the prognosis of CFS is poor with a systematic review of outcomes finding the median full recovery rate was 5 % (range 0-31%) and the median proportion of patients who improved of 39.5% (range 8-63%). Being younger, having less fatigue baseline, a sense of control over symptoms and not attributing illness to a physical cause were all associated with a better outcome. The prognosis is considerably better after treatment.

Treatment

The NICE guidelines, published in 2007, were based on an updated systematic review. The essence of specialist care is rehabilitation, provided on an individual basis with an appropriately qualified and trained therapist. The two approaches with the greatest evidence of efficacy are cognitive behaviour therapy (CBT) and graded exercise therapy (GET). Approximately 60% of patients report significant improvement with these approaches and about 25%report full recovery, which lasts. No pharmacological treatments are recommended (antidepressants are ineffective), but symptomatic pharmacotherapy for specific symptoms (such as pain) or comorbid conditions such as depressive illness) can be helpful complementary treatments.

These rehabilitation approaches have not received universal approval from patient charities, with concerns that patients may be harmed by exercise therapies or that CBT implying that the condition is psychological.

Is CFS neurological or psychological?

This is a nonsensical question when one considers the neuroscience of consciousness and recent advances in functional brain physiology. The philosopher, John Searle, stated the answer to this Cartesian dualism that still bedevils western medicine. “Conscious states are caused by neurophysiological mechanisms, and are realised in neurophysiological systems.” Therefore it is not possible to have a psychological process or event without a neurological mediating process. It is neither of the mind or body; it is both.

Fatigue secondary to neurological diseases

Fatigue is commonly associated with chronic medical disorders, but it should be differentiated from fatiguability. Fatiguability is the onset of a physical sensation of fatigue and weakness after exertion and is commonly reported with neurological diseases such as multiple sclerosis and myopathies.

Apart from measures of disease activity, other associations of secondary fatigue in general that have been repeatedly found include sleep disturbance, mood disorders, inactivity and physical deconditioning. Studies of fatigue associated with multiple sclerosis are instructive and exemplary. As in all studies of secondary fatigue, measures of the severity or pathophysiology of the disease itself are associated with fatigue. Some cytokines are associated, but others are not.

Associations vary depending on the fatigue measure, confirming the multidimensional nature of fatigue, but all measures are associated with depression. Objectively confirmed sleep disturbance is also associated with fatigue. Fatigue associated with MS therefore requires biopsychosocial management.

There have been a number of studies of various treatments aimed at reversing the associations of secondary fatigue in general, in the hope they would help fatigue directly, with variable results. As with CFS, the most consistent evidence of efficacy has been with graded exercise programmes and CBT.

Attarian HP, Brown KM, Duntley SP, et al. The relationship of sleep disturbances and fatigue in multiple sclerosis. Arch. Neurol. 61 (2004), 525-8.

Baker R, Shaw EJ. Diagnosis and management of chronic fatigue syndrome or myalgic encephalomyelitis (or encephalopathy): summary of NICE guidance. BMJ 2007 doi: 10.1136/bmj.39302.509005. AE

Chambers D, Bagnall A-M, Hempel S, Forbes C. Interventions for the treatment, management and rehabilitation of patients with chronic fatigue syndrome/myalgic encephalomyelitis: an updated systematic review. J R Soc Med 2006;99:506-20.

Cleare AJ. The neuroendocrinology of chronic fatigue syndrome. Endocr. Rev. 24 (2003), 236-52.

Flachenecker P, Bihler I, Weber F, et al., Cytokine mRNA expression in patients with multiple sclerosis and fatigue. Mult. Scler. 10 (2004), 165-9.

Fulcher KY, White PD. Strength and physiological response to exercise in patients with the chronic fatigue syndrome. J. Neurol. Neurosurg. Psychiatry 69 (2000), 302-7.

Joyce J, Hotopf M, Wessely S. The prognosis of chronic fatigue and chronic fatigue syndrome: a systematic review. Q. J. Med. 90 (1997), 223-33.

Kroencke DC, Lynch SG, Denney DR. Fatigue in multiple sclerosis: relationship to depression, disability, and disease pattern. Mult. Scler. 6 (2000), 131-6.

Lyall M, Peakman M, Wessely S. A systematic review and critical evaluation of the immunology of chronic fatigue syndrome. J. Psychosom. Res. 55 2003), 79-90.

National Institute for Health and Clinical Excellence. Clinical guideline CG53. Chronic fatigue syndrome/myalgic encephalomyelitis (or encephalopathy): diagnosis and management. London, NICE, 2007. http://guidance.nice.org.uk/CG53.

Reeves WC et al. Identification of ambiguities in the 1994 chronic fatigue syndrome research case definition and recommendations for resolution.BMC Health Serv Res 3 (2003), 25.

Romani A, Bergamaschi R, Candeloro E, et al., Fatigue inmultiple sclerosis: multidimensional assessment and response to symptomatic treatment. Mult. Scler. 10 (2004), 462-8.

M. C. Tartaglia, S. Narayanan, S. J. Francis, et al., The relationship between diffuse axonal damage and fatigue in multiple sclerosis. Arch. Neurol. 61 (2004), 201-7.

Wessely SC, Hotopf M, Sharpe M. Chronic Fatigue and its Syndromes (Oxford: Oxford University Press, 1998).

Wessely S, Nimnuan C, Sharpe M. Functional somatic syndromes: one or many? Lancet 354 (1999), 936-9.

Wessely S, White PD. In debate: there is only one functional somatic syndrome. Br. J. Psychiatry 185 (2004), 95-6.

White PD, Thomas JM, Kangro HO, et al., Predictions and associations of fatigue syndromes and mood disorders that occur after infectious mononucleosis. Lancet 358 (2001), 1946-54.

White PD, Sharpe MC, Chalder T, DeCesare JC, Walwyn R; on behalf of the PACE trial group. Protocol for the PACE trial: a randomised controlled trial of adaptive pacing, cognitive behaviour therapy, and graded exercise, as supplements to standardised specialist medical care versus standardised specialist medical care alone for patients with the chronic fatigue syndrome/myalgic encephalomyelitis or encephalopathy. BMC Neurol 2007;7:6.

[ Extract ends, doc: http://bnpa.org.uk/doc/HANDBOOK.pdf ]

For detailed information on the proposed structure of ICD-11, the Content Model and operation of iCAT, the collaborative authoring platform through which the WHO will be revising ICD-10, please scrutinise key documents on the ICD-11 Revision Google site:
https://sites.google.com/site/icd11revision/
https://sites.google.com/site/icd11revision/home/documents

For information around the DSM and ICD revision processes see DSM-V and ICD-11 Directory page: http://meagenda.wordpress.com/dsm-v-directory/

Suzy Chapman
http://meagenda.wordpress.com
http://twitter.com/MEagenda

Posted in CBT, CBT/GET, CFS Clinics, CFS Research, CISSD Project, ICD revision process, ICD-11, ME Research, ME in children, MUPSS Project, Professor Peter White, WHO (World Health Organization), WHO Somatisation Project | Comments Off

Correspondence between Stephen Ralph and Dr Charles Shepherd

Posted by meagenda on November 6, 2009

Correspondence between Stephen Ralph and Dr Charles Shepherd

WordPress Shortlink: http://wp.me/p5foE-2jm

The opinion piece below, which includes extracts from recent correspondence with Dr Charles Shepherd is authored and published by Stephen Ralph; the views and opinions expressed are the views and opinions of Mr Ralph and any comments or queries resulting out of this opinion piece should be addressed to Mr Ralph and not to ME agenda.

Stephen Ralph maintains a website at  www.meactionuk.org.uk 

Dr Charles Shepherd is an Honorary Medical Advisor and a Trustee/Director of the ME Association http://www.meassociation.org.uk/

A copy of the statement which Stephen Ralph quotes from is here:

 XMRV and ME/CFS: WHAT DO WE KNOW SO FAR? AND WHAT DON’T WE KNOW? (VERSION 3) (04.11.09)  http://wp.me/p5foE-2kq

—————–

By Stephen Ralph  ME Action UK

Permission to Repost

06 November 2009

Like many of you, I was alarmed when I read the recent MEA XMRV Statement No.3 particularly because of one telling sentence.

I decided to ask Dr Shepherd a series of questions and although I had several answers, I had no answer at all to one important question that I asked several times.

I asked Dr Shepherd about this statement.

“Demonstrating a link between a retrovirus and ME/CFS does not, by itself, resolve the physical vs psychological debate.

Research studies have demonstrated links between retroviruses and diseases as diverse as autoimmune disorders (which could be relevant to ME/CFS), immunodeficiency diseases, multiple sclerosis, tumours, anaemias and even schizophrenia.”

In reply I got the following from Dr Shepherd.

“I don’t think this comment will have any effect whatsoever on psychiatry.

Psychiatrists already know that viruses and psychiatric illness can sometimes be linked.

I put this info into version 3 because some people are wrongly assuming that having a viral link in an illness means that it must be physical rather than psychological. And that the physical vs psychological battle in ME/CFS is now almost over. I only wish…..

Retroviruses may be involved in schizophrenia and it is being said the up to 40% of people with autism have XMRV.”

I then asked Dr Shepherd what he would do if he found he was XMRV negative and how this might impact on his judgment.

In reply I had the following from Dr Shepherd…

“I don’t know my XMRV status. I obviously could have access to XMRV testing facilities. But as knowing my XMRV result isn’t going to affect either my diagnosis of ME or the management of my illness at this stage I don’t see any point in being tested.”

Lastly, I asked Dr Shepherd if he did or did not support the views of Professors Simon Wessely, Michael Sharpe and Peter White.

I asked this question twice for the sake of clarification.

Dr Shepherd has decided not to answer that question.

I asked the question because on numerous occasions the MEA have released hedge betting, sitting-on-the-fence statements or cheek turning Statements that effectively support the agenda of Somatoform Psychiatry or completely ignore the agenda of Somatoform Psychiatry.

The statement regarding XMRV not ending the debate on mental v physical is for my eyes indicating that yet again the MEA and Dr Shepherd are entertaining the possibility that Wessely White and Sharpe are right.

Dr Shepherd – you should be actively ending the involvement of Professors Wessely, White and Sharpe and you should be representing the total “State of Science” from across the Atlantic as is the case with the ESME – see their website for example…

http://esme-eu.com/news/category7.html

…instead of selectively picking what you want to feed your members and back peddling on the profound implications of XMRV and what was said at the CFSAC last week.

As we all know, the liaison faction of psychiatry firmly and militantly assert that CFS is a functional psychosomatic syndrome and that ME does not exist at all.

We know that the likes of Wessely, White and Sharpe are trying to get CFS into the next edition of the DSM – DSM-V and reclassified in ICD-11.

Both Action for ME and the ME Association are doing nothing to stop this agenda.

I asked Dr Shepherd some time ago if he or the MEA were going to do anything about the CSSID DSM-V ICD-11 agenda and Dr Shepherd said he was too busy and it wasn’t on his list of things to do.

In my view, the ME Association is not a lot more than the Public Relations arm of Action for ME.

Yes they seem approachable and yes they seem to press all the buttons that please some of their members.

But as soon as you ask anything considered “controversial” or important – then Dr Shepherd and/or the MEA goes silent and refuses to answer the question as is the case by default with Action for ME.

It seems to me that here in the UK and for many years, the ME population are being held hostage by the mental health movement who seem to have castrated both Action for ME and the ME Association who between them dominate the arena yet lay silent and do nothing to counter the mental health agenda…

So it seems to me that neither charity actually give a damn about the concerns of the ME community unless those views accord with their agenda that they will not discuss when challenged in ANY detail.

They say the devil is in the detail but we do not know what the detail is because when we ask we get nothing back.

Under these circumstances we need those over in the USA and those in the UK with Independence of mind and purposes such as ME Research UK, the 25% ME Group and Invest in ME – to come to the rescue of the UK ME patient population.

If people are not happy with this e-mail I have written and you think I am being unfair then you should ask Dr Shepherd and the MEA yourselves and get the answers he would not give to me or the many others who have asked similar questions over the years that never get answered.

Why does the MEA turn the other cheek and choose not to robustly challenge the views of Professor Wessely and his colleagues and instead state that “they already know” so that these individuals are therefore beyond challenging…

How exactly does liaison psychiatry “already know” that retro-viruses cause mental illness and does the MEA believe that XMRV potentially causes functional mental illness in people with ME? If not then why stay silent – creating a space for the opposition to occupy.

Why does the MEA put out neutered statements that reflect the views of liaison psychiatry instead of using all the evidence available to robustly and technically challenge those views?

Why is the ME Association calling for the use of the CDC Fukuda Criteria in UK XMRV research when the Fukuda criteria has been and is still being exploited by Wessely et al due to its well known ability to produce a heterogeneous patient group and therefore research results that are by default inconclusive and “mixed” and challengeable by those with a mental health agenda?

Why does the ME Association not firmly call for the use the Canadian criteria or use both Fukuda and the Canadian criteria in parallel research to make the research outcomes more meaningful and less open to exploitative deconstruction when the ME Association at one time adopted the Canadian Criteria by a democratic vote and then quietly swept that democratic vote under their carpet?

This is all about accountability. We should be given full answers to all of the above questions.

What is wrong in asking?  Why does that make us bad?

Yours sincerely,

Stephen Ralph

www.meactionuk.org.uk

Posted in AfME, Action for M.E., CBT/GET, CFS Clinics, CFS Research, CFS in the media, CFSAC, CISSD Project, Canadian Criteria, Criticism of DSM-V, DSM-5, ICD revision process, ICD-11, Institute of Psychiatry, ME Association, ME Research, ME in journals, ME in the media, Professor Peter White, Simon Wessely, WHO (World Health Organization), XMRV, XMRV Retrovirus | Comments Off

Action for M.E. and Facebook; CISSD Final Report finally published

Posted by meagenda on October 30, 2009

Action for M.E. and Facebook; CISSD Final Report finally published

WordPress Shortlink: http://wp.me/p5foE-2gi

Action for M.E. maintains a Facebook site at: http://www.facebook.com/actionforme

Over the past few weeks, questions and criticism around Action for M.E.’s governance, the way in which it relates to its membership, its policies and operation and its relationship with government have been raised by various users on its Facebook “Wall”.

Action for M.E. has chosen not to respond to these questions individually, on the Wall, itself, but by issuing a set of responses in a PDF document. The first document was this one: Facebook responses 20.10.09

A second, updated, set of responses was issued yesterday. It’s not clear whether these responses have been compiled by Action for M.E.’s new Policy Manager or by another member of staff, as the document is unsigned, but it’s interesting to see how the organisation has fielded these questions and concerns.

[To clarify - none of the questions for which responses were provided had been raised by me. I prefer to liaise directly with organisations for information, documents or for policy and position statements or, where applicable, obtain information via the Freedom of Information Act.]

Action for M.E. is becoming rather discomforted that its Facebook site is being used by some as a vehicle for raising political issues but you cannot take the politics out of ME. Users are already asking how the organisation intends to define “political”.

Those of us who were members, in 2003, of the joint charities’ message board “MEssage-UK” will recall how rapidly first Action for M.E., then AYME pulled out of this venture when faced with too many awkward questions; how the message board was then set for pre-moderation by the ME Association; how the moderator, Tony Britton, vetoed posts of a “political nature” without ever setting out how he was going to define what came under the heading of “political” and what did not; how the archives were sifted through for “contentious” messages by senior ME Association staff and then quietly excised without the authors being informed; how the board was closed down suddenly just days before the critical December 03 AGM in which Dr Shepherd was standing as a candidate in the Trustee elections…

When will our patient organisations learn that if they are going to place themselves on public platforms they first need to develop policies for the fielding of questions?

This latest set of responses can be opened in PDF format here:

PDF file: ONGOING FB Q and A document. 29.10.09

Answers to questions raised on the Action for M.E. facebook page, October 2009. Updated

or from Action for M.E’s website, here: http://tinyurl.com/ongoingFB-responses291009

—————-

One of the responses is for a question raised (note, not by me) around the CISSD Project, for which Action for M.E. had acted as principal administrators throughout the project’s life (2003 to 2007).

In response to this question, on Page 23:

Question: “What was your involvement in the CISSD project Conceptual Issues in Somatoform and Similar Disorders for which you received a grant of 67k and why was this project kept so secretive from your members? Only information about it was released when freedom of information act requests were made that pushed you in to a corner where you had to confirm you were involved in it. Was this CISSD project set up with the purpose as suggested by other sources with the intent to look at changing the ME/CFS ICD-10 coding* to that of a Somatoform disorder?”

Action for M.E prefaces its reply with, “As a charity, Action for M.E. is not obliged to answer questions under the Freedom of Information Act but provides information of its free will, as resources allow.”

I should like to clarify that the Freedom of Information requests submitted by me in relation to the CISSD Project had been submitted to the Institute of Psychiatry. Information resulting out of these requests under the FOIA is available here: http://meagenda.wordpress.com/dsm-v-directory/information-obtained-under-foi-act/

One of my requests to the Institute of Psychiatry had been for a copy of the December 2007 “CISSD Final Report” from Dr Richard Sykes to Action for M.E. I had suggested to the Institute of Psychiatry’s Legal Compliance Office that the report ought to be provided with a erratum note, by Dr Sykes, addressing a number of errors he had made in the document that had come to light in June 09, when an unauthorised copy of the text had been placed in the public domain.

Unfortunately, what the Institute of Psychiatry were provided with by Dr Sykes, in order to fulfil the request, is evidently an earlier draft of the December 2007 text. It is missing the Contents page, and there are other disparities between the text that I was provided with and the Final version. No erratum note had been attached, either.

However, as part of its response to the Facebook question, Action for M.E. has now elected to publish two files. The first is a copy of the December 2007 CISSD “Final Report” to Action for M.E., the second, a copy of the “Co-ordinator’s Report”, with a covering letter and summary.

Action for M.E. has finally put these documents in the public domain!

Open PDF files here:

CISSD project report 1

The CISSD Project and CFS/ME Report on the CISSD Project for Action for ME 

Conceptual Issues in Somatoform and Similar Disorders

Report to be read in conjunction with Co-ordinator’s Final Report

Richard Sykes December 2007

CISSD project report 2

Covering letter

The CISSD Project 2003-2007

(Conceptual Issues in Somatoform and Similar Disorders)

Summary

FINAL REPORT OF CO-ORDINATOR   Richard Sykes PhD, CQSW

or from Action for M.E’s website, here:

http://www.afme.org.uk/res/img/resources/CISSD%20project%20report%201.pdf
http://www.afme.org.uk/res/img/resources/CISSD%20project%20report%202.pdf

 

In August, Action for M.E. had published an article titled “Classification conundrum” on pages 16 and 17 of Issue 69 of its membership magazine, InterAction.

You can read a copy of the article here, in an ME agenda posting dated 25 August 2009:

“Action for M.E. stuffs the elephant back into the cupboard”

Note that although the Project had been initiated by Dr Richard Sykes, Dr Sykes does not appear to have contributed to this article – basically an apologia piece authored by Dr Derek Pheby.

In fact, Dr Sykes and his role as instigator and co-ordinator of the Project is not mentioned in the article at all. Nor is the Project’s source of funding – the charitable Trust run by Dr Sykes’ brother, Sir Hugh Sykes, a non-executive director of A4e, the largest European provider of Welfare to Work programmes. 

The December 2007 “Final Report” document has historical significance.  It also contains material (including an entire Appendix) which was omitted from the “CISSD Summary Report” that the ME Association published in June, this year, having negotiated with Dr Sykes for an article. (But having trumped Action for M.E., the MEA has made no comment whatsoever on the implications of the CISSD Project nor provided its membership with an analysis of the various papers and documents that came out of it.  Nor has the MEA made any comment or published any information on the progress of the ICD-10 and DSM revision processes for which the CISSD Project was initiated and has fed into.)

The document sets out Dr Sykes’ views, opinions and perceptions (and misperceptions) that had not previously been publicly available. It would have been appropriate for Action for M.E. to have negotiated with Dr Sykes for this document to have been published in 2007.  Instead, it kept the lid on this project –  a project that had been chaired by Professors Michael Sharpe and Kurt Kroenke and had involved many influential, international researchers and clinicians from the field of liaison psychiatry and psychosomatics – several of whom are now directly involved in the revision of the American Psychiatric Association’s DSM-IV.

In August, I called publicly on Action for M.E. to publish a copy of the CISSD “Final Report” on its website and to preface it with an erratum note addressing both the errors of coding within “Appendix B” of the document and also Dr Sykes’ misconception that “Chronic fatigue syndrome” does not appear in ICD-10.

Chronic fatigue syndrome is listed in the International Statistical Classification of Diseases and Related Health Problems: 10th Revision Version for 2006, Volume 3, the Alphabetical Index (ICD-10 Volume 3).

For the entry in question, see page 528, top right hand column:

http://www.scribd.com/doc/7350978/ICD10-2006-Alphabetical-Index-Volume-3

Since no erratum note has been published with these documents please be aware that where Dr Sykes has written “G33.3″ and “G33.4″ on Pages 12 and 13 of document:

http://www.afme.org.uk/res/img/resources/CISSD%20project%20report%201.pdf

this should read “G93.3″ and “G93.4″.

Why has Action for M.E. published these documents without negotiating with Dr Sykes for an Erratum?

Why did Action for M.E. not publish these documents in August to accompany the article in InterAction?

 

*There is no coding for “ME/CFS” in ICD-10. 
Postviral fatigue syndrome is classified in Chapter VI of ICD-10 Volume 1: The Tabular List at G93.3.
(Benign) myalgic encephalomyelitis is classified in Chapter VI of ICD-10 Volume 1: The Tabular List at G93.3.
Chronic fatigue syndrome is listed in ICD-10 Volume 3: The Alphabetical Index under G93.3.

—————–

Text version of December 2007 CISSD “Final Report” here: CISSD Final Report to AfME 2007

Text version of December 2007 CISSD “Co-ordinator’s Report” here: CISSD PROJECT Coordinators Final Report

June 2009 Summary Report on CISSD as published by the ME Association

The Editorial: The proposed diagnosis of somatic symptom disorders in DSM-V to replace somatoform disorders in DSM-IV – a preliminary report by DSM-V Work Group members, Joel Dimsdale and Francis Creed was published in the June issue of the Journal of Psychosomatic Research:

Free access to both text and PDF versions of this Editorial at: http://www.jpsychores.com/article/S0022-3999(09)00088-9/fulltext

For detailed information on the proposed structure of ICD-11, the Content Model and operation of iCAT, the collaborative authoring platform through which the WHO will be revising ICD-10, please scrutinise key documents on the ICD-11 Revision Google site:

https://sites.google.com/site/icd11revision/
https://sites.google.com/site/icd11revision/home/documents

For information around the DSM and ICD revision processes see DSM-V and ICD-11 Directory page: http://meagenda.wordpress.com/dsm-v-directory/

Posted in A4e, AfME, Action for M.E., CISSD Project, DSM revision process, Elephant Series DSM-V, Freedom of Information, ICD revision process, ICD-11, MUPSS Project, NICE Judicial Review, PACE Trials, Professor Peter White, WHO (World Health Organization), WHO Collaborating Centre, WHO Somatisation Project, XMRV Retrovirus | Comments Off

Journal of Psychosomatic Research: In Press: Is there a better term than “Medically unexplained symptoms”?

Posted by meagenda on October 24, 2009

elephant3

Image | belgianchocolate | Creative Commons

Keywords

APA    DSM    DSM-IV    DSM-V    WHO    ICD    ICD-10    ICD-11    American Psychiatric Association    Diagnostic and Statistical Manual of Mental Disorders    World Health Organization    Classifications    DSM Revision Process    DSM-V Task Force    DSM-V Somatic Distress Disorders Work Group    Somatic Symptom Disorders Work Group    DSM-ICD Harmonization Coordination Group    International Advisory Group    Revision of ICD Mental and Behavioural Disorders    Global Scientific Partnership Coordination Group    ICD Update and Revision Platform    WHO Collaborating Centre    CISSD Project    MUPSS Project    Somatoform    Somatisation    Somatization    Functional Somatic Syndromes    FSS    MUS    Myalgic encephalomyelitis    ME    Chronic fatigue syndrome    CFS    Fibromyalgia    FM    IBS    CS    CI    GWS

The Elephant in the Room Series Three:

Journal of Psychosomatic Research In Press: Is there a better term than “Medically unexplained symptoms”?

WordPress Shortlink for this posting: http://wp.me/p5foE-2d6

24 October 2009

 

An In Press version of the Editorial: Is there a better term than “Medically unexplained symptoms”?, to be published in a forthcoming issue of the Journal of Psychosomatic Research, is already available online (purchase required). The Editorial needs to be read in conjunction with a white paper from:

The European Association for Consultation-Liaison Psychiatry and Psychosomatics (EACLPP) http://www.eaclpp.org/

A white paper of the EACLPP Medically Unexplained Symptoms study group

Patients with medically unexplained symptoms and somatisation – a challenge for European health care systems  (Gillian.D.Dunkerley@manchester.ac.uk )

The White Paper can be downloaded from the EACLPP site here: http://www.eaclpp.org/working_groups.html

The document is approx 76 pages long, including tables and charts.  I had considerable difficulty opening this document, in May, due to a corrupted table and I note that the file on the EACLPP site is still glitchy. A copy of the document was therefore obtained directly from the EACLPP and can be opened by clicking the link below.  Note that there may have been revisions to the document as supplied on 19 May, but it will serve as reference for those who might also experience difficulties opening the file from the EACLPP website. If you would like a copy of the file sent to you as a Word.doc, email ME agenda with “EACLPP MUS DOC” in the subject line and I will forward a copy [600 KB].  The tables and charts are slow to load.

Draft – prepared by: Peter Henningsen and Francis Creed January 2009

EACLPP Working group on MUS version 16 Jan 2009

The current issue of the Journal of Psychosomatic Research is Volume 67, Issue 5, Pages A1-A4, 367-466 (November 2009)  http://www.sciencedirect.com/science/journal/00223999

Journal of Psychosomatic Research

In Press

Editorial
Is there a better term than “Medically unexplained symptoms”?

Abstract: http://tinyurl.com/jpsychoresMUS

doi:10.1016/j.jpsychores.2009.09.004

References and further reading may be available for this article. To view references and further reading you must purchase this article.

Editorial

Francis Creed a, Elspeth Guthrie a, Per Fink b, Peter Henningsen c, Winfried Rief d, Michael Sharpe e and Peter White f

a University of Manchester, Manchester, UK 
b University Hospital Aarhus, Denmark
c Technical University, Munich Germany
d University of Marburg, Germany
e University of Edinburgh, UK
f Queen Mary University of London, UK

Received 24 August 2009; revised 24 August 2009; accepted 7 September 2009. Available online 17 October 2009.

Article Outline

Introduction

“Medically unexplained symptoms” – one advantage, but many reasons to discontinue use of the term

Criteria to judge the value of alternative terms for “medically unexplained symptoms”

Terms suggested as alternatives for “medically unexplained symptoms”

Implications for treatment

Implications for DSM-V and ICD-11

Conclusion

References

Note:

Francis Creed is Co-Editor of the Journal of Psychosomatic Research.

Francis Creed, Per Fink, Peter Henningsen and Winfried Rief were all members of the international CISSD Project, (Principal Administrators: Action for M.E.; Co-ordinator: Dr Richard Sykes. Dr Sykes is now engaged in the “London MUPSS Project” in association with the Institute of Psychiatry).

Michael Sharpe was UK Chair for the CISSD Project.

Michael Sharpe and Francis Creed have been members of the APA’s DSM-V Somatic Distress Disorders Work Group since 2007.

Francis Creed (UK), Peter Henningsen (Germany) and Per Fink (Denmark) are the co-ordinators of European EACLPP MUS Work Group.

Francis Creed and Peter Henningsen were the authors of “A white paper of the EACLPP Medically Unexplained Symptoms study group – Patients with medically unexplained symptoms and somatisation – a challenge for European health care systems”, January 2009.

Draft white paper here: http://www.eaclpp.org/working_groups.html

Per Fink is a member of the Danish Working Group on Chronic Fatigue Syndrome, established in August 2008 and expected to complete its work in spring 2009.

 

An Editorial: The proposed diagnosis of somatic symptom disorders in DSM-V to replace somatoform disorders in DSM-IV – a preliminary report by DSM-V Work Group members, Joel Dimsdale and Francis Creed on behalf of the DSM-V Workgroup on Somatic Symptom Disorders was published in the June 2009 issue of the Journal of Psychosomatic Research.

Full text of the June 2009 DSM-V SSD Work Group preliminary report can be accessed here:

http://www.jpsychores.com/article/S0022-3999(09)00088-9/fulltext

See section: Psychological factor affecting general medical condition 

“…The conceptual framework that we propose will allow a diagnosis of somatic symptom disorder in addition to a general medical condition, whether the latter is a well-recognized organic disease or a functional somatic syndrome such as irritable bowel syndrome or chronic fatigue syndrome…”

No updates or reports have been published on the APA’s website by DSM-V Task Force or Work Groups since brief reports issued in April 2009. DSM-V is anticipated to be finalised in May 2012 with field trials expected to start this October. No detailed Timeline for DSM-V is available.

Previous DSM Task Force chairs, Robert L Spitzer and Allen Frances, have been two of the most vocal critics of the current Task Force’s oversight of the revision process. Read their joint letter to the APA Board of Trustees here:  Letter to APA Board of Trustees July 09. In Dr Frances Responds to Dr Carpenter: A Sharp Difference of Opinion, Psychiatric Times, 9 July, Frances called for the posting of all the suggested wordings for DSM-V criteria sets well before considering field trials.

 

Javier Escobar, co-author of the Special Report: Unexplained Physical Symptoms: What’s a Psychiatrist to Do? Psychiatric Times, Aug 2008, was also a member of the Work Group for the “Conceptual Issues in Somatoform and Similar Disorders (CISSD) Project.

Javier Escobar is a member of the DSM-V Task Force, serves as a Task Force liaison to the Somatic Symptom Disorders Work Group and said to work closely with this work group.

http://www.psychiatrictimes.com/display/article/10168/1171223

01 August 2008
Psychiatric Times. Vol. 25 No. 9
Special Report

PSYCHIATRY AND MEDICAL ILLNESS
Unexplained Physical Symptoms What’s a Psychiatrist to Do?

Humberto Marin, MD and Javier I. Escobar, MD

According to Escobar and Marin:

“The list of somatoform disorders kept expanding with the addition of vague categories, such as “undifferentiated somatoform disorder” or “somatoform disorder NOS [not otherwise specified],” which, unfortunately, are the most common diagnoses within the somatoform genre. These terms failed to transcend specialty boundaries. Perhaps as a corollary of turf issues, general medicine and medical specialties started carving these syndromes with their own tools. The resulting list of “medicalized,” specialty-driven labels that continues to expand includes fibromyalgia, chronic fatigue syndome, multiple chemical sensitivity, and many others (Table 1).

Table 1

Functional somatic syndromes

Irritable bowel syndrome
Chronic fatigue syndrome
Fibromyalgia
Multiple chemical sensitivity
Nonspecific chest pain
Premenstrual disorder
Non-ulcer dyspepsia
Repetitive strain injury
Tension headache
Temporomandibular joint disorder
Atypical facial pain
Hyperventilation syndrome
Globus syndrome
Sick building syndrome
Chronic pelvic pain
Chronic whiplash syndrome
Chronic Lyme disease
Silicone breast implant effects
Candidiasis hypersensivity
Food allergy
Gulf War syndrome
Mitral valve prolapse
Hypoglycemia
Chronic low back pain
Dizziness
Interstitial cystitis
Tinnitus
Pseudoseizures
Insomnia
Systemic yeast infection
Total allergy syndrome”

These labels fall under the general category of functional somatic syndromes and seem more acceptable to patients because they may be perceived as less stigmatizing than psychiatric ones. However, using DSM criteria, virtually all these functional syndromes would fall into the somatoform disorders category given their phenomenology, unknown physical causes, absence of reliable markers, and the frequent coexistence of somatic and psychiatric symptoms.”

DSM-V and ICD-11 have committed as far as possible “to facilitate the achievement of the highest possible extent of uniformity and harmonization between ICD-11 mental and behavioural disorders and DSM-V disorders and their diagnostic criteria” with the objective that “the WHO and APA should make all attempts to ensure that in their core versions, the category names, glossary descriptions and criteria are identical for ICD and DSM.”

The International Advisory Group for the Revision of ICD-10 Mental and Behavioural Disorders most recent meeting took place on 28 – 29 September. It is anticipated that a Summary Report of the meeting will be available in late November/December.

For detailed information on the proposed structure of ICD-11, the Content Model and operation of iCAT, the collaborative authoring platform through which the WHO will be revising ICD-10, please scrutinise key documents on the ICD-11 Revision Google site:

https://sites.google.com/site/icd11revision/
https://sites.google.com/site/icd11revision/home/documents

For information around the DSM and ICD revision processes see DSM-V and ICD-11 Directory page: http://meagenda.wordpress.com/dsm-v-directory/

Posted in CBT, CBT/GET, CISSD Project, Criticism of DSM-V, DSM-5, DSM revision process, Elephant Series DSM-V, ICD revision process, ICD-11, Institute of Psychiatry, MUPSS Project, MUS, Professor Peter White, WHO (World Health Organization), WHO Collaborating Centre, WHO Somatisation Project | Comments Off

ICD Revision Advisory Groups: Mental and Behavioural Disorders and TAG Neurology

Posted by meagenda on October 2, 2009

Information on the new International Advisory Group for the Revision of ICD-10 Mental and Behavioural Disorders and the Topic Advisory Group (TAG) for Neurology

WordPress Shortlink for this posting: http://wp.me/p5foE-25M

The text below has been compiled using information provided by the Senior Project Officer, Department of Mental Health and Substance Abuse, WHO, Geneva, and is published with permission. The text may be reposted provided it is published unedited, in full and http://meagenda.wordpress.com is credited as the source.  

The International Advisory Group for the Revision of ICD-10 Mental and Behavioural Disorders was constituted by the WHO for a period of two years (2007 – 2008) with the primary task of advising the WHO on all steps leading to the revision of the mental and behavioural disorders classification in ICD-10, in line with the overall ICD revision process.

The initial period of operation has now expired and the group has been reconstituted and reappointed for the next two year period. The appointment of the Harmonization Group and other working groups reporting to the Advisory Group has also now expired, and new working groups will be appointed based on the current needs of the revision.

The Advisory Group is co-ordinated by Senior Project Officer, Dr Geoffrey M Reed, PhD, who is seconded to the Department of Mental Health and Substance Abuse, WHO, Geneva, through the IUPsyS (International Union for Psychological Science). The Department of Mental Health and Substance Abuse will also be managing the technical part of the revision of Diseases of the Nervous System (currently Chapter VI), as it is doing for Chapter V.

The new Advisory Group expands and makes some changes to its composition in order to obtain better geographical representation and also based on the nature of the tasks of the next period of the revision process.

The members of the new International Advisory Group for the Revision of ICD-10 Mental and Behavioural Disorders are:

Steven Hyman (Chair), Harvard University, Cambridge, Massachusetts, USA
José Luís Ayuso-Mateos, Universidad Autónoma de Madrid, Madrid, Spain
Alan Flisher, University of Cape Town, Rondebosch, South Africa
Wolfgang Gaebel, Heinrich-Heine University, Düsseldorf, Germany
Oye Gureje, University College Hospital, Ibadan, Nigeria
Assen Jablensky, University of Western Australia, Crawley, Australia
Brigitte Khoury, American University of Beirut Medical Center, Beirut, Lebanon
Anne Lovell, Institute National de la Santé et de la Recherche Médicale, Paris, France
Maria Elena Medina-Mora, Instituto Nacional de Psiquiatria Ramon de la Fuente, México, D.F., Mexico.
Afarin Rahimi, Tehran University of Medical Sciences, Tehran, Iran
Norman Sartorius, Geneva, Switzerland
Pratap Sharan, All India Institute of Medical Sciences, New Delhi, India
Pichet Udomratn, Prince Songkha University, Hat Yai, Thailand
Xiao Zeping, Shanghai Mental Health Center, Shanghai, China

The professional and scientific organisations that have been asked to appoint representatives to the International Advisory Group for Mental and Behavioural Disorders, and the names of their representatives, are:

International Association of Child and Adolescent Psychiatry and Allied Professions (IACAPAP):
Per-anders Rydelius, Karolinska Institutet, Stockholm, Sweden

International Council of Nurses (ICN):
Tesfamicael Ghebrehiwet, International Council of Nurses, Geneva, Switzerland

International Federation of Social Workers (IFSW):
Dr Sabine Bährer- Kohler, Psychiatric University Clinic, Basel, Switzerland

International Union of Psychological Science (IUPsyS):
Ann D. Watts, Entabeni Hospital, Durban, South Africa

World Organization of National Colleges, Academies, and Academic Associations of General Practitioners/Family Physicians (WONCA):
Michael Klinkman, University of Michigan, Ann Arbor, Michigan, USA

World Psychiatric Association (WPA):
Mario Maj, University of Naples, Naples, Italy

All of these organisations were also represented on the previous Advisory Group with the exception of IACAPAP.

The first meeting of the reconstituted Advisory Group took place on 28 – 29 September 2009, in Geneva. There have been no other meetings since the December 2008 meeting of the former group. It is anticipated that a Summary Report of the meeting held last month, 28 – 29 September will be available within two months.

The report of the meeting held on 1 – 2 December 2008 can be read here: http://www.who.int/mental_health/evidence/icd_advisory_group_december_08_summary.pdf

—————–

Topic Advisory Group for Neurology

Lead WHO Secretariat for TAG Neurology is Dr Tarun Dua, Management of Mental and Brain Disorders, Department of Mental Health and Substance Abuse, WHO. Email: duat@who.int.

Dr Dua, a neurologist, co-ordinated the Atlas Multiple Sclerosis Resources in the World 2008, a collaboration between the World Health Organization and the Multiple Sclerosis International Federation and was a co-author of the World Health Organization publication, Neurological Disorders: Public Health Challenges, 2006 or download by chapters in PDF format at: http://www.who.int/mental_health/neurology/neurodiso/en/index.html

The members of the Topic Advisory Group (TAG) for Neurology are:

Raad Shakir (Chair), Imperial College London, London, UK
Donna Bergen, Rush University Medical Center, Chicago, Illinois, USA
Pierre Bill, Inkosi Ambert Luthuli Central Hospital, Durban, South Africa
Mandaville Gourie-Devi, Institute of Human Behaviour and Allied Sciences, New Delhi, India
Mitsuru Kawamua, School of Medicine, Showa University, Tokyo, Japan
Marco Medina, National Autonomos University of Honduras, Tegucigalpa, Honduras
Mohamad Mikati, American University of Beirut Medical Center, Beirut, Lebanon

The professional and scientific organisations that have been asked to appoint representatives to the Topic Advisory Group for Neurology, and the names of their representatives, are:

Alzheimer’s Disease International:
Murat Emre, Istanbul Faculty of Medicine, Istanbul, Turkey

International Brain Research Organization:
Krister Kristensson, Karolinska Institutet, Stockholm, Sweden

International Child Neurology Association
Marc Patterson, Mayo Clinic, Rochester, Minnesota, USA

International Headache Society:
Jes Olesen, University of Copenhagen, Copenhagen, Denmark

International League Against Epilepsy:
Ettore Beghi, Istituto “Mario Negri”, Milan, Italy

International Neuropsychological Society:
Andreas Monsch, University Hospital Basel, Basel, Switzerland

Movement Disorders Society:
Kapil D Sethi, Medical College of Georgia, Augusta, Georgia, USA

Multiple Sclerosis International Federation:
Alan J. Thompson, Director, National Hospital for Neurology & Neurosurgery, London, UK

World Federation of Neurosurgical Societies:
Marc Levivier, Centre Romand de Neurochirurgie, Lausanne, Switzerland

World Federation of Neurology:
Johan Aarli, University of Bergen, Bergen, Norway

World Stroke Organization:
Bo Norrving, Lund University, Lund, Sweden

1 October 2009

—————————–

Daily iCAMP YouTubes on the WHOICD11 Channel: http://www.youtube.com/user/WHOICD11

Transcripts of YouTube narrations on the ICD11 blog: http://whoicd11.blogspot.com/

For further information on the proposed structure of ICD-11, the Content Model and iCAT, the collaborative authoring platform the WHO will be using to revise ICD-10:

https://sites.google.com/site/icd11revision/
https://sites.google.com/site/icd11revision/home/documents

Agenda for the 22 September – 2 October iCAMP Alpha Draft Training Meeting [MS Word]

Content Model Style Guide document [MS Word]

Morbidity Reference Group Discussion papers:
        ICD-11 rules, conventions and structure [MS Word]
        Revision topics for topic advisory groups [MS Word]

Content Model Blank document [Excel]

Content Model Myocardial infarction example document [Excel]

Content Model Hypertension Category example document [Excel]

ICD 11 Alpha Draft presentation by Dr B. Ustun [MS pptx slides]

Start-Up List presentation by Dr R. Jakob [MS pptx slides]

Myocardial infarction Content Model presentation [MS ppt slides]

[Note that some of these documents are "works in progress" and subject to ongoing review and revision.]

Posted in CISSD Project, DSM revision process, Elephant Series DSM-V, ICD revision process, ICD-11, WHO (World Health Organization), WHO Collaborating Centre, WHO Somatisation Project | Comments Off