Canadian Psychiatric Association

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Editorial
Geriatric Psychiatry: Complex Challenges, Promising Treatments
Kenneth I Shulman
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In Review
Cognitive Pharmacotherapy of Alzheimer’s Disease and Other Dementias
Nathan Herrmann

(PDF)

Brief Screening Tests for Dementia
Wendy J Lorentz, James M Scanlan, Soo Borson

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Effective Use of Electroconvulsive Therapy in Late-Life Depression
Alastair J Flint, Nadine Gagnon

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Review Papers
Are Leptin and Cytokines Involved in Body Weight Gain During Treatment With Antipsychotic Drugs?

Trino Baptista, Serge Beaulieu

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Original Research
Strategies of Collaboration Between General Practitioners and Psychiatrists: A Survey of Practitioners’ Opinions and Characteristics

Ricardo J M Lucena, Alain Lesage, Robert Élie, Yves Lamontagne, Marc Corbière

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A Test of the Phase Model of Psychotherapy Change
Anthony S Joyce, John Ogrodniczuk, William E Piper, Mary McCallum

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Brief Communication
Lamotrigine Use in Geriatric Patients With Bipolar Depression

Matthew Robillard, David K Conn

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Dissolution Profile, Tolerability, and Acceptability of the Orally Disintegrating Olanzapine Tablet in Patients With Schizophrenia
Pierre Chue, Barry Jones, Cindy C Taylor, Ruth Dickson

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Progress Against Major Depression in Canada
Scott B Patten MD

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Book Reviews
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Obsessive–Compulsive Disorder: A Practical Guide
Reviewed by
Arun V. Ravindran

We Fly, We Cry: Our Lives With Manic Depression
Reviewed by
Paul Grof

Geriatric Consultation Liaison Psychiatry
Reviewed by
Ron Keren

Psychotherapy With Children and Adolescents
Reviewed by
Allan Frankland

The Early Stages of Schizophrenia
Reviewed by
Mary V. Seeman



Letters to the Editor
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Re: Atypical Antipsychotic Use in Treating Adolescents and Young Adults With Developmental Disabilities

Reply: Atypical Antipsychotic Use in Treating Adolescents and Young Adults With Developmental Disabilities

Evidence Supports Validity of Seasonal Affective Disorder

Reply: Evidence Supports Validity of Seasonal Affective Disorder

Seasonal Affective Disorder: The Latitude Hypothesis Revisited

Treatment Of Posttraumatic Stress Disorder With Tiagabine

Assessing Pain Tolerance in a Patient With Acute Psychosis

Musical Hallucinations During a Treatment With Benzodiazepine

Bupropion-Methylphenidate Combination and Grand Mal Seizures

The Association of Depressed Affect and Stroke in Institutionalized Canadians

Quetiapine and Neuroleptic Malignant Syndrome

Letters to the Editor

Quetiapine and Neuroleptic Malignant Syndrome

Dear Editor:

Neuroleptic malignant syndrome (NMS) is a reported complication of treatment with the atypical neuroleptics clozapine, risperidone, and olanzapine (1,2). I report a case of NMS associated with quetiapine as the sole neuroleptic.

Case Report

Mr AB is a reclusive, single, white man aged 44 years. His initial paranoid psychotic symptoms began 19 years previously, during multimodal therapy for stage 3A Hodgkin’s disease. For 3 years, he had been stable in the community on risperidone 4 mg daily, followed by olanzapine 20 mg daily for over 1 year prior to this episode. Six months before this admission, his olanzapine 20 mg daily was gradually tapered, with a view to his entering a ziprasidone trial. At 10 mg olanzapine his psychosis relapsed, and he was restabilized in hospital on quetiapine 400 mg and clonazepam 2.5 mg daily. Eight weeks after starting quetiapine, he suddenly and rapidly decompensated, displaying increased paranoia, loosened associations, and disorganized thinking and behaviour. On return to hospital, he had a temperature of 38.4ºC, a fluctuating blood pressure as high as 160/110, and a rapid, regular pulse rate of up to 140 beats per minute. He maintained postures, his muscle tone was only minimally increased, and his creatine phosphokinase (CPK) was elevated to 1613 IU/litre. His attention was impaired, and his sparse verbal output was grossly disordered, exhibiting grandiose and paranoid themes. He was extensively investigated for a fever of unknown origin. Aside from an elevated white cell count of 15.9 x 109/litre and CPK levels that peaked at 3485 IU/litre, the remaining results were all within the normal limits. He was treated for NMS with rehydration and dantrolene until his fever, pulse, blood pressure, and CPK settled 3 weeks later. His CPK fell to below 1000 IU/litre within 3 days of discontinuing quetiapine and took another 2 weeks to normalize.

Since he remained mute, disorganized, incontinent of urine, and severely psychotic, he was transferred back to psychiatry. When treated with a course of unilateral electroconvulsive therapy, he improved after the first treatment, becoming more communicative and organized. He recovered after 7 treatments and was restarted on olanzapine 10 mg daily. He was discharged for outpatient follow-up and 1 year later remains well and stable in the community.

NMS has been reported as a rare complication of treatment with clozapine, risperidone (1), and most recently, olanzapine (2). Quetiapine is a novel dibenzothiazepene clozapine–like neuroleptic with fewer D2-blocking properties than clozapine (3). It has a correspondingly low propensity to induce extrapyramidal side effects (EPS) (4). There are 3 reports of possible NMS associated with quetiapine, 1 case of which occurred with concomitant use of loxapine (5), 1 with concomitant use of sulpiride (6), and 1 in which quetiapine was the sole antipsychotic (7). The NMS picture that occurs with atypical antipsychotic agents may be milder than that which occurs with typical agents (8) and corresponds to 2 of the reported cases involving quetiapine (6,7). This patient had mild physical manifestations and more prominent mental status changes. Despite quetiapine’s low propensity to cause EPS, NMS needs to be considered in the differential of patients on quetiapine who present with NMS-like features.

References

1. Hasan S, Buckley P. Novel antipsychotics and the neuroleptic malignant syndrome: a review and critique. Am J Psychiatry 1998;155:1113–6.

2. Gheorghiu S, Knobler H, Drumer D. Recurrence of neuroleptic malignant syndrome with olanzapine treatment. Am J Psychiatry 1999;156:1836–7.

3. Gefvert O, Bergstrom M, Langstrom B, Lundberg T, Lindstrom L, Yates R. Time course of central nervous dopamine-D2 and 5HT2 receptor blockade and plasma concentrations after discontinuation of quetiapine (Seroquel) in patients with schizophrenia. Psychopharmacology 1998;135:119–26.

4. Targum SD, Arvantis LA. Quetiapine: efficacy, safety, and tolerability in elderly subject with psychotic disorders. Psychopharmacology Bulletin 1997;33:596.

5. Al-Waneen R. Neuroleptic malignant syndrome associated with quetiapine [letter]. Can J Psychiatry 2000;45:764.

6. Stanley AK, Hunter J. Possible neuroleptic malignant syndrome with quetiapine. Br J Psychiatry 2000;176:497.

7. Whalley N, Diaz P, Howard J. Neuroleptic malignant syndrome associated with the use of quetiapine. Can J Hospital Pharmacy 1999;52:112.

8. Sachdev P, Kruk J, Kneebone M, Kissane D. Clozapine-induced neuroleptic malignant syndrome: review and report of new cases. J Clin Psychopharmacol 1995;15:365–71.

Kevin Solomons, MD, FRCPC
Vancouver, British Columbia




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