You are seeing this message because your Web browser does not support basic Web standards. Find out more about why this message is appearing and what you can do to make your experience on this site better.


ABOUT ARCHIVES
Advanced Search

Welcome   | My Account | E-mail Alerts | Access Rights | Sign In


  Vol. 142 No. 6, June 1982 TABLE OF CONTENTS
  Archives
  •  Online Features
  REVIEW ARTICLES
 This Article
 •References
 •Full text PDF
 •Send to a friend
 • Save in My Folder
 •Save to citation manager
 •Permissions
 Citing Articles
 •Citation map
 •Citing articles on HighWire
 •Citing articles on Web of Science (146)
 •Contact me when this article is cited
 Related Content
 •Similar articles in this journal
 Social Bookmarking
  Add to CiteULike Add to Connotea Add to Del.icio.us Add to Digg Add to Reddit Add to Technorati Add to Twitter What's this?

The Neuroleptic Malignant Syndrome

Raymond A. Smego, Jr, MD; David T. Durack, MB, DPhil

Arch Intern Med. 1982;142(6):1183-1185.


Abstract

• The neuroleptic malignant syndrome (NMS) comprises hyperpyrexia, altered consciousness, muscular rigidity, and autonomic dysfunction. It is a rare idiosyncratic reaction to major tranquilizers, including the phenothiazines, butyrophenones, and thioxanthenes; haloperidol and fluphenazine enanthate or fluphenazine decanoate are the drugs most commonly incriminated. The syndrome occurs after therapeutic rather than toxic doses of neuroleptic drugs and is unrelated to the duration of therapy. The NMS is attributed to a disturbance of dopaminergic systems within the basal ganglia and hypothalamus. Associated laboratory abnormalities include leukocytosis, with elevated serum creatine phosphokinase (CPK) and liver enzyme concentrations. The NMS, which is known to some psychiatrists and neurologists but to few internists, probably is underdiagnosed; therefore, its true incidence is unknown. The NMS should be included in the differential diagnosis of any febrile patient with a history of neuroleptic treatment. Because the mortality of NMS is about 20%, early diagnosis and withdrawal of the neuroleptic drug therapy is crucial. Supportive treatment in a medical intensive care unit may be required.

(Arch Intern Med 1982;142:1183-1185)



Author Affiliations

From the Department of Medicine, Division of Infectious Diseases, Duke University Medical Center, Durham, NC.


Footnotes

Accepted for publication Feb 22, 1982.

Reprint requests to Duke University Medical Center, Box 31229, Durham, NC 27710 (Dr Smego).



Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter     What's this?

THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Neuroleptic Malignant Syndrome in a Multiple Trauma Patient
Boorse and Rhodes
Arch Surg 1990;125:274-275.
ABSTRACT  

Neuroleptic Malignant Syndrome in a Child Treated With Metoclopramide for Chemotherapy-Related Nausea
Brower et al.
J Child Neurol 1989;4:230-232.
 

Metoclopramide-Induced Neuroleptic Malignant Syndrome
Friedman et al.
Arch Intern Med 1987;147:1495-1497.
ABSTRACT  

Disorders of Temperature Control: Hyperthermia, Part II
Curley and Irwin
J Intensive Care Med 1986;1:91-100.
ABSTRACT  

A Neuroleptic Malignantlike Syndrome due to Levodopa Therapy Withdrawal
Friedman et al.
JAMA 1985;254:2792-2795.
ABSTRACT  

Neuroleptic Malignant Syndrome: Successful Treatment With Pancuronium
Sangal and Dimitrijevic
JAMA 1985;254:2795-2796.
ABSTRACT  

Myoglobinuria in Neuroleptic Malignant Syndrome
Fink
Arch Intern Med 1985;145:1736-1736.
ABSTRACT  

Hypercalcemia in the Neuroleptic Malignant Syndrome
Wang et al.
Arch Intern Med 1985;145:143-144.
ABSTRACT  

Neuroleptic Malignant Syndrome Complicated by Disseminated Intravascular Coagulation
Eles et al.
Arch Intern Med 1984;144:1296-1297.
ABSTRACT  

Neuroleptic Malignant Syndrome and Dopaminergic Blockade
Hashimoto et al.
Arch Intern Med 1984;144:629-630.
ABSTRACT  

Neuroleptic Malignant Syndrome: Successful Treatment With Bromocriptine
Mueller et al.
JAMA 1983;249:386-388.
ABSTRACT  





HOME | CURRENT ISSUE | PAST ISSUES | TOPIC COLLECTIONS | CME | SUBMIT | SUBSCRIBE | HELP
CONDITIONS OF USE | PRIVACY POLICY | CONTACT US | SITE MAP
 
© 1982 American Medical Association. All Rights Reserved.