The validity of broadly defined hysteria and DSM-III conversion disorder: outcome, family history, and mortality

Insights

Patients diagnosed with conversion disorder, previously labeled hysteria, show higher mortality rates similar to those with primary depression. This suggests conversion disorder may be a distinct diagnostic category needing further validation.

Area of Science:

  • Psychiatry
  • Clinical Psychology
  • Medical Sociology

Background:

  • Patients diagnosed with hysteria often do not meet criteria for Briquet's syndrome (somatization disorder).
  • Previous research indicated familial psychopathology similarities between these patients and those with primary depression.
  • The diagnostic validity and clinical outcomes of conversion disorder require further investigation.

Purpose of the Study:

  • To investigate the familial psychopathology and mortality rates in patients with conversion disorder.
  • To compare the outcomes of conversion disorder patients with those diagnosed with Briquet's syndrome.
  • To assess the diagnostic heterogeneity within conversion disorder.

Main Methods:

  • Retrospective analysis of patient records with chart diagnoses of hysteria.
  • Comparison of familial psychopathology and mortality data between diagnostic groups.
  • Application of DSM-III criteria for conversion disorder and Briquet's syndrome.

Main Results:

  • Patients meeting DSM-III criteria for conversion disorder exhibited excess mortality, mirroring primary depression.
  • Outcome and mortality data differentiated conversion disorder from Briquet's syndrome.
  • Family history data indicated significant heterogeneity within the conversion disorder diagnosis.

Conclusions:

  • Conversion disorder patients share mortality patterns with primary depression, suggesting a distinct clinical entity.
  • The current diagnostic criteria for conversion disorder may encompass heterogeneous patient groups.
  • The label "conversion disorder" is proposed as a descriptive alternative to "undiagnosed" pending further diagnostic validation.

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