The American Journal of Psychiatry
Journal Home Search Current Issue Past Issues Subscribe All APPI Journals Help Contact Us
 
Quicksearch
Advanced Search
Or Search All APPI Journals
This Article
* Full Text (PDF)
* Alert me when this article is cited
* Alert me if a correction is posted
Services
* Email this article to a Colleague
* Similar articles in this journal
* Similar articles in PubMed
* Alert me to new issues of the journal
* Add to My Articles & Searches
* Download to citation manager
* reprints & permissions
Citing Articles
* Citing Articles via HighWire
* Citing Articles via Google Scholar
Google Scholar
* Articles by DUGGAL, H. S.
* Articles by KITHAS, J.
* Search for Related Content
PubMed
* PubMed Citation
* Articles by DUGGAL, H. S.
* Articles by KITHAS, J.
Related Collections
* Depression
* Atypical Neuroleptics
* Antidepressants
Am J Psychiatry 162:397-398, February 2005
© 2005 American Psychiatric Association


Letter to the Editor

Possible Neuroleptic Malignant Syndrome With Aripiprazole and Fluoxetine

HARPREET S. DUGGAL, M.D., D.P.M., and JOSEPH KITHAS, M.D.
Pittsburgh, Pa.

To the Editor: There are rare reports of neuroleptic malignant syndrome occurring with a combination of atypical antipsychotics and selective serotonin reuptake inhibitors (1). We describe a similar case with a combination of aripiprazole and fluoxetine.

Mr. A, a 43-year-old man, was admitted to our hospital with severe depression and psychotic symptoms. Three weeks before, he had been admitted to a different hospital for similar symptoms and had been given bupropion and risperidone, titrated up to 150 mg/day and 1 mg/day, respectively. However, for unapparent reasons, these medications were discontinued abruptly after a week, and Mr. A was given aripiprazole, started at 30 mg/day, and fluoxetine, 20 mg/day. A week later, Mr. A was discharged from the hospital with the same regimen. Subsequently, after taking these medications for about 2 weeks, Mr. A came to us with complaints of muscle stiffness, restlessness, and fever of a week’s duration. In addition, he also had depressive and some psychotic symptoms, but his family’s predominant concern was his physical symptoms.

Upon examination, Mr. A exhibited marked psychomotor retardation, mask-like facies, and severe rigidity, with cog-wheeling, sialorrhea, tremors, and akathisia. He had fever (99.8°F), labile blood pressure (148/99–137/89 mm Hg), and tachycardia (110 bpm). He was fully oriented and did not display any cognitive deficits. Laboratory investigations revealed elevated creatine phosphokinase (248 IU/liter; normal range=0–200) and alanine aminotransferase (61 IU/liter; normal range=0–35) levels, whereas the results of renal function tests, a CBC, and a urine examination were normal. Although Mr. A had stopped taking aripiprazole 2 days before he came to visit us, his symptoms had shown little improvement. Fluoxetine was discontinued, and Mr. A was treated symptomatically with benztropine and acetaminophen and had an uneventful recovery within a week, with his creatine phosphokinase level returning to normal (138 IU/liter).

Although this patient had the core symptoms of neuroleptic malignant syndrome, including rigidity, fever, and autonomic instability and met the DSM-IV criteria for neuroleptic malignant syndrome, the symptoms of severe neuroleptic malignant syndrome, such as a marked creatine phosphokinase elevation, hyperthermia, and an altered sensorium, were absent. Early recognition of this condition, the use of an atypical antipsychotic (aripiprazole), and the patient’s discontinuation of aripiprazole may have contributed to his mild presentation of neuroleptic malignant syndrome. Serotonin syndrome, another differential in this case, cannot be ruled out, but the patient did not exhibit autonomic features, such as hyperhidrosis and diarrhea, or muscular signs, such as hyperreflexia and myoclonus, which are typical of this syndrome. The Physicians’ Desk Reference documents that two "possible" cases of neuroleptic malignant syndrome occurred during aripiprazole treatment in a premarketing worldwide clinical database, although we found no reports of neuroleptic malignant syndrome occurring with aripiprazole on PUBMED. Given that aripiprazole is a functional dopamine receptor agonist in a hypodopaminergic state (as occurs in neuroleptic malignant syndrome), the presentation of this syndrome may be different from other atypical antipsychotics. Serotonin 5-HT1A agonism, another hypothetical mechanism for neuroleptic malignant syndrome (2), can also be implicated in this case because aripiprazole is a partial agonist at this receptor. Of interest, this is also the mechanism underlying serotonin syndrome (3), and both neuroleptic malignant syndrome and serotonin syndrome have been considered under the rubric of catatonic syndromes (4). Although fluoxetine (an inhibitor of CYP2D6) alone has been associated with neuroleptic malignant syndrome (5), it may have further increased levels of aripiprazole (which is metabolized by CYP2D6). This, compounded with the altered dopamine balance due to abrupt withdrawal of risperidone, may have made the patient more vulnerable to neuroleptic malignant syndrome, as supported by reports of neuroleptic malignant syndrome after withdrawal of atypical antipsychotics (6).

References

  1. Kontaxakis VP, Havaki-Kontaxaki BJ, Pappa DA, Katritis DE, Christodoulou GN: Neuroleptic malignant syndrome after addition of paroxetine to olanzapine. J Clin Psychopharmacol 2003; 23:671–672[CrossRef][Medline]
  2. Carroll BT: The universal field hypothesis of catatonia and neuroleptic malignant syndrome. CNS Spectr 2000; 7:26–33
  3. Duggal HS, Fetchko J: Serotonin syndrome and atypical antipsychotics (letter). Am J Psychiatry 2002; 159:672–673[Free Full Text]
  4. Fink M, Taylor MA: The many varieties of catatonia. Eur Arch Psychiatry Clin Neurosci 2001; 251(suppl 1):8–13
  5. Halman M, Goldbloom DS: Fluoxetine and neuroleptic malignant syndrome. Biol Psychiatry 1990; 28:518–521[CrossRef][Medline]
  6. Caroff SN, Mann SC, Campbell EC: Atypical antipsychotics and neuroleptic syndrome. Psychiatr Annals 2000; 30:314–321



This article has been cited by other articles:


Home page
The Annals of PharmacotherapyHome page
D. L Stevens
Association Between Selective Serotonin-Reuptake Inhibitors, Second-Generation Antipsychotics, and Neuroleptic Malignant Syndrome
Ann. Pharmacother., September 1, 2008; 42(9): 1290 - 1297.
[Abstract] [Full Text] [PDF]


This Article
* Full Text (PDF)
* Alert me when this article is cited
* Alert me if a correction is posted
Services
* Email this article to a Colleague
* Similar articles in this journal
* Similar articles in PubMed
* Alert me to new issues of the journal
* Add to My Articles & Searches
* Download to citation manager
* reprints & permissions
Citing Articles
* Citing Articles via HighWire
* Citing Articles via Google Scholar
Google Scholar
* Articles by DUGGAL, H. S.
* Articles by KITHAS, J.
* Search for Related Content
PubMed
* PubMed Citation
* Articles by DUGGAL, H. S.
* Articles by KITHAS, J.
Related Collections
* Depression
* Atypical Neuroleptics
* Antidepressants


Get information about faster international access.

Privacy Policy

Copyright © 2005 American Psychiatric Association. All rights reserved.

Home | Search | Current Issue | Past Issues | Subscribe | All APPI Journals | Help | Contact Us

American Psychiatric Publishing, Inc. American Psychiatric Association
1000 Wilson Boulevard, Suite 1825, Arlington, VA 22209-3901 * 800-368-5777 * appi at psych.org