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Conversion disorder as defined in DSM-IV describes symptoms such as weakness, seizures, or abnormal movements that are not attributable to a general medical condition or to feigning and that are judged to be associated with psychological factors. As somatoform disorders are overhauled in DSM-5 (1), it is a good time to reconsider both the name and criteria for this diagnosis.
The name "conversion disorder" refers to a hypothesis based on psychoanalytic etiology. Although long dominant, the conversion hypothesis is now just one of many competing etiological hypotheses and has little supportive empirical evidence. Even the notion that the etiology of these symptoms is wholly psychological may be scientifically incorrect. For example, functional brain imaging studies showing findings such as contralateral thalamic hypoactivity in hemisensory conversion encourage us to understand conversion symptoms from a brain as well as mind perspective (2). Furthermore, the name "conversion disorder" has not been widely accepted by either nonpsychiatrists or patients (3, 4). We therefore need a name that sidesteps an unhelpful brain/mind dichotomy, will be more widely used clinically, and will be more accepted by patients (5). We suggest that the term "functional neurological disorder," as a diagnosis for symptoms such as "functional weakness," would be practically and theoretically more useful (6). This would be a return to an older terminology that is in keeping with the concept of functional somatic symptoms (7).
The current DSM-IV criteria require the positive exclusion of feigning. Proving feigning is difficult enough; proving the absence of feigning is arguably impossible. They also require the identification of psychological factors associated with symptom onset. Although the diagnostic stability of the neurological symptoms has been confirmed (8), these "psychological" criteria have not been shown to be either diagnostically reliable or predictive of outcome (9). For the majority of patients psychological factors can be identified, but not for all. Even when psychological factors are identified, there are no clear methods for determining whether they are etiologically relevant.
In practice, conversion disorder is usually diagnosed after a neurologist has identified a symptom as "nonorganic" because of clinical findings of incongruity with disease or internal inconsistency (6). For example, functional leg weakness can be demonstrated objectively when weakness of hip extension disappears during contralateral hip flexion against resistance (Hoover's sign). Functional arm tremor is suspected when a tremor disappears during voluntary rhythmical movement of the unaffected arm. A final example is a seizure-like event with simultaneous normal video EEG. The DSM-IV criteria currently require the exclusion of disease but do not refer to these useful diagnostic procedures. We suggest that incorporating physical diagnostic features observed in conversion disorder in the criteria would improve psychiatric understanding and confidence in the diagnosis.
In summary, we suggest that conversion disorder be renamed "functional neurological disorder" and that the requirement for the exclusion of feigning and identification of associated psychological factors be relegated to the accompanying text. We suggest that discriminating clinical features be given greater prominence (Figure 1). Together these changes have the potential to foster collaboration between psychiatrists and neurologists, which is critical to improving both the understanding and care of this neglected group of patients.
Figure 1. Proposed Criteria for "Functional Neurological Disorder" (Previously "Conversion Disorder") in DSM-5

References

1.
Dimsdale J, Creed F: The proposed diagnosis of somatic symptom disorders in DSM-V to replace somatoform disorders in DSM-IV—a preliminary report. J Psychosom Res 2009; 66:473–476
2.
Vuilleumier P, Chicherio C, Assal F, Schwartz S, Skusman D, Landis T: Functional neuroanatomical correlates of hysterical sensorimotor loss. Brain 2001; 124:1077–1090
3.
Espay AJ, Goldenhar LM, Voon V, Schrag A, Burton N, Lang AE: Opinions and clinical practices related to diagnosing and managing patients with psychogenic movement disorders: an international survey of movement disorder society members. Mov Disord 2009; 24:1366–1374
4.
Friedman J, LaFrance WC: Psychogenic disorders: the need to speak plainly. Arch Neurol (in press)
5.
Creed F, Guthrie E, Fink P, Henningsen P, Rief W, Sharpe M, White P: Is there a better term than "medically unexplained symptoms"? J Psychosom Res 2010; 68:5–8
6.
Stone J: The bare essentials: functional symptoms in neurology. Pract Neurol 2009; 9:179–189
7.
Wessely S, Nimnuan C, Sharpe M: Functional somatic syndromes: one or many? Lancet 1999; 354:936–939
8.
Stone J, Smyth R, Carson A, Lewis S, Prescott R, Warlow C, Sharpe M: Systematic review of misdiagnosis of conversion symptoms and "hysteria." BMJ 2005; 331:989
9.
Roelofs K, Spinhoven P, Sandijck P, Moene FC, Hoogduin KA: The impact of early trauma and recent life-events on symptom severity in patients with conversion disorder. J Nerv Ment Dis 2005; 193:508–514

Information & Authors

Information

Published In

Go to American Journal of Psychiatry
Go to American Journal of Psychiatry
American Journal of Psychiatry
Pages: 626 - 627
PubMed: 20516161

History

Accepted: January 2010
Published online: 1 June 2010
Published in print: June 2010

Authors

Details

Jon Stone, M.B., Ch.B, M.R.C.P., Ph.D.
W. Curt LaFrance, Jr., M.D., M.P.H.
James L. Levenson, M.D.

Notes

Address correspondence and reprint requests to Dr. Stone, Department of Clinical Neurosciences, Western General Hospital, Edinburgh, Scotland EH4 2XU, United Kingdom; [email protected] (e-mail). Editorial accepted for publication January 2010.

Competing Interests

Drs. Levenson and Sharpe are members of the DSM-5 Somatoform Disorders Work Group. Drs. Stone, LaFrance, and Sharpe are advisers on conversion disorder to the group. However, this article reflects the views of the authors and not necessarily those of the DSM-5 Somatoform Disorders Work Group.
Dr. LaFrance has received research funding from the National Institute of Neurological Disorders and Stroke, the American Epilepsy Society, the Epilepsy Foundation, and the Siravo Foundation, and he receives book royalties from Cambridge University Press. Dr. Freedman has reviewed this editorial and found no evidence of influence from these relationships. The other authors report no financial relationships with commercial interests.

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