Abstract
Clozapine is mainly metabolized by the cytochrome P450 1A2 (CYP1A2), which may be inhibited by serious respiratory infections. This case report supports that a serious respiratory infection may increase clozapine levels and contribute to side effects. Plasma clozapine and norclozapine levels were monitored 17 times during 1 year. The concentration-to-dose ratio (C/D), an index of metabolic activity, was obtained by dividing the sum of plasma clozapine and norclozapine concentration (total clozapine concentration) by clozapine dose. The coefficient of variation (CV) of the total clozapine concentrations was calculated at different doses to provide a measure of the noise associated with determining clozapine concentrations in clinical practice. During a respiratory infection, the patient was taking 600 mg/day of clozapine. Clozapine levels were 1245 ng/ml (norclozapine 472 ng/ml), reflecting a decrease in clozapine metabolism by approximately a factor of 2. The high clozapine levels were associated with side effects (myoclonus and increased sedation). The C/D during the infection was 2.9, while the rest of C/Ds ranged between 1.0 and 1.6. CVs before and after the infection, at different doses, were always lower than 20%. When the level during the infection was included to calculate the CV on 600 mg/day, the CV increased to 54%. The theophylline literature, a prior case report and this case all suggest that if a clozapine patient develops a severe respiratory infection with fever, the psychiatrist must pay particular attention to any signs suggestive of major clozapine toxicity associated to a decrease in clozapine metabolism. If any of these signs appear, the psychiatrist may need to consider cutting the clozapine dose in half until the patient has recovered from the infection.
Original language | English |
---|---|
Pages (from-to) | 1059-1063 |
Number of pages | 5 |
Journal | Progress in Neuro-Psychopharmacology and Biological Psychiatry |
Volume | 27 |
Issue number | 6 |
DOIs | |
State | Published - Sep 2003 |
Bibliographical note
Funding Information:A grant from the Office of Mental Health and Mental Retardation from the Commonwealth of Kentucky supported Dr. Diaz's salary and part of Dr. de Leon's salary. The first author is grateful to the staff of Gragg-2 at Eastern State Hospital who provided excellent care for this very difficult patient and to the hospital laboratory staff and its director Kay Marshall who helped in collecting all the samples for plasma levels. Margaret T. Susce, RN MLT assisted with editing. The collaboration and trust by the patient's mother (and guardian) and the patient made this clozapine trial possible.
Keywords
- Clozapine
- Cytochrome P450 1A2
- Infections
- Metabolism
ASJC Scopus subject areas
- Pharmacology
- Biological Psychiatry