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Clozapine treatment following blood dyscrasia

Published online by Cambridge University Press:  02 January 2018

D. Esposito
Affiliation:
Department of Psychiatry, Bicêtre, Assistance Publique – Hôpitaux de Paris, Paris XI University, INSERM U 669, 8 rue du Général Leclerc, 94275 Le Kremlin-Bicêtre Cédex, France. Email: [email protected]
P. Hardy
Affiliation:
Department of Psychiatry, Bicêtre Hospital, Assistance Publique – Hôpitaux de Paris, Paris, France
E. Corruble
Affiliation:
Department of Psychiatry, Bicêtre Hospital, Assistance Publique – Hôpitaux de Paris, Paris, France
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Abstract

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Columns
Copyright
Copyright © 2006 The Royal College of Psychiatrists 

Dunk et al (Reference Dunk, Annan and Andrews2006) investigated 53 patients who were rechallenged with clozapine following leucopenia or neutropenia during previous therapy and found that 33 did not experience a second episode of blood dyscrasia and were able to continue drug treatment. This result is of considerable clinical relevance because it suggests that some patients with leucopenia or neutropenia may unnecessarily be denied effective clozapine treatment.

We agree that there may be two types of clozapine-associated neutropenia: an early sign of incipient agranulocytosis and a more common transient and harmless phenomenon, not necessitating the discontinuation of drug treatment. Transient neutropenia (defined as a return of the neutrophil count to normal values without changing the clozapine dosage) was found in 22% of 68 patients treated with clozapine for the first time (Reference Hummer, Kurz and BarnasHummer et al, 1994). Neutropenia of short duration (2-5 days) and weekly benign variations of the neutrophil count have been reported. Marked circadian variations in the number of circulating neutrophils (morning pseudoneutropenia) have also been described in several clozapine-treated patients (Reference Ahokas and ElonenAhokas & Elonen, 1999; Reference Esposito, Aouille and RouillonEsposito et al, 2004).

The actual issue might therefore not be which patients could be rechallenged with clozapine following drug-associated neutropenia but which could be maintained on clozapine despite this side-effect. Laboratory screening tests, including the use of a hydrocortisone test, are being devised to determine whether clozapine-associated neutropenia is transient or malignant (Reference Murry and LaurentMurry & Laurent, 2001). Until these tests become available for routine use, it is necessary to increase the frequency with which white blood cell counts are determined. As first suggested by Ahokas & Elonen (Reference Ahokas and Elonen1999), when the absolute neutrophil count is below the normal range in the morning, the test should be repeated in the afternoon of the same day before a decision to stop clozapine treatment is made. This might be the basis for further clarification of the significance of transient neutropenia.

References

Ahokas, A. & Elonen, E. (1999) Circadian rhythm of white blood cells during clozapine treatment. Psychopharmacology, 144, 301302.Google Scholar
Dunk, L. R., Annan, L. J. & Andrews, C. D. (2006) Rechallenge with clozapine following leucopenia or neutropenia during previous therapy. British Journal of Psychiatry, 188, 255263.Google Scholar
Esposito, D., Aouille, J., Rouillon, F., et al (2004) Two-year follow-up of a patient with successful continuation of clozapine treatment despite morning pseudoneutropenia. Journal of Clinical Psychiatry, 65, 1281.Google Scholar
Hummer, M., Kurz, M., Barnas, C., et al (1994) Clozapine-induced transient white blood count disorders. Journal of Clinical Psychiatry, 55, 429432.Google Scholar
Murry, P. & Laurent, A. (2001) Is it possible to distinguish between benign and malignant neutropenia in clozapine-treated patients by means of a hydrocortisone test? Psychopharmacology, 158, 329330.Google Scholar
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