Hostname: page-component-586b7cd67f-2brh9 Total loading time: 0 Render date: 2024-11-28T19:57:20.943Z Has data issue: false hasContentIssue false

Lethal Catatonia and Neuroleptic Malignant Syndrome

A Dopamine Receptor Shut-down Hypothesis

Published online by Cambridge University Press:  02 January 2018

Abdelkarim A. Osman*
Affiliation:
King Fahd Hospital, Jeddah, Saudi Arabia
Mohamed H. Khurasani
Affiliation:
King Fahd Hospital, Jeddah, Saudi Arabia
*
Dr Osman, PO Box 50505 (176), King Fahd Hospital, Jeddah, Saudi Arabia

Abstract

Background

Lethal catatonia and neuroleptic malignant syndrome (NMS) have been suggested to have a common neurochemical cause. We hypothesise that both conditions may be due to a sudden and massive blockade of dopamine neurotransmitters.

Method

NMS was diagnosed in psychotic in-patients treated with neuroleptics if four features were present: diffuse severe rigidity, altered level of consciousness, hyperpyrexia and autonomic instability.

Results

Over three years, five NMS cases were diagnosed. Two presented with catatonic features and were diagnosed as acute reactive psychosis. Their neuroleptic doses were small, arguing for a particular sensitivity in these two cases.

Conclusion

The sensitivity of two patients with catatonic features who developed NMS with small doses of neuroleptics supports a common neurochemical basis for the two conditions.

Type
Research Article
Copyright
Copyright © Royal College of Psychiatrists, 1994 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Addonizio, G., Susman, V. L. & Roth, S. D. (1986) Symptoms of neuroleptic malignant syndrome in 82 consecutive inpatients. American Journal of Psychiatry, 143, 15871590.Google Scholar
Adityanjee, , Singh, S., Singh, G., et al (1988) Spectrum concept of neuroleptic malignant syndrome. British Journal of Psychiatry, 153, 107111.CrossRefGoogle ScholarPubMed
Caroff, S. N. (1980) The neuroleptic malignant syndrome. Journal of Clinical Psychiatry, 41, 7983.Google Scholar
Fujitake, J., Kuno, S. & Nishitani, H. (1984) Neuroleptic malignant syndrome-like state in eight patients with Parkinsonism. Rinsho Shinkeigaku, 24, 371378.Google Scholar
Kellam, A. M. P. (1987) The neuroleptic malignant syndrome, so-called: a survey of the world literature. British Journal of Psychiatry, 150, 752759.Google Scholar
Kellam, A. M. P. (1990) The (frequently) neuroleptic malignant syndrome. Current Opinion in Psychiatry, 4, 3437.Google Scholar
Levenson, J. L. (1985) Neuroleptic malignant syndrome. American Journal of Psychiatry, 142, 11371145.Google Scholar
Mann, S. C., Caroff, S. N., Bleier, H. R., et al (1986) Lethal catatonia. American Journal of Psychiatry, 143, 13741381.Google Scholar
Osman, A., Al Khateeb, S. & Ali, A. (1993) The pattern of admission to Jeddah Psychiatric Hospital. Saudi Medical Journal, 14, 334339.Google Scholar
Rosebush, P. & Stewart, T. (1989) A prospective analysis of 24 episodes of neuroleptic malignant syndrome. American Journal of Psychiatry, 146, 717725.Google Scholar
Shalev, A. & Munitz, H. (1986) The neuroleptic malignant syndrome agent and host interaction. Acta Psychiatrica Scandinavica, 73, 337347.Google Scholar
White, D. & Robins, A. H. (1991) Catatonia: harbinger of the neuroleptic malignant syndrome. British Journal of Psychiatry, 158, 419421.Google Scholar
Submit a response

eLetters

No eLetters have been published for this article.