Pharmacopsychiatry 2007; 40(3): 89-92
DOI: 10.1055/s-2007-973835
Original Paper

© Georg Thieme Verlag KG · Stuttgart · New York

Ziprasidone Outcome and Tolerability: A Practical Clinical Trial With Plasma Drug Levels

M. C. Mauri 1 , A. Colasanti 1 , M. Rossattini 1 , L. S. Volonteri 1 , F. Dragogna 1 , A. Fiorentini 1 , A. Fiorentini 1 , A. Valli 2 , P. Papa 2
  • 1Clinical Neuropsychopharmacology Unit, Department of Internal Medicine, Clinical Psychiatry, University of Milan, Fondazione IRCCS Ospedale Maggiore Policlinico, Via F. Sforza 35, Milano, Italy
  • 2Department of Clinical Chemistry, Laboratory of Analytical Toxicology, Foundation IRCCS Policlinico S. Matteo, Pavia, Italy
Further Information

Publication History

received 02. 06. 2006 revised 02. 02. 2007

accepted 13. 03. 2007

Publication Date:
01 June 2007 (online)

Abstract

Introduction: The aim of this study was to evaluate clinical outcomes and the tolerability of ziprasidone in relation to its plasma levels.

Methods: Thirteen inpatients affected by schizophrenia were included in the study after an acute exacerbation phase. Ziprasidone monotherapy was administered for a period of eight weeks at a mean dose of 123.07±30.38 mg/day. Plasma concentrations were measured by high-performance liquid chromatography.

Results: Nine patients completed the study. A significant clinical improvement was observed, especially in negative symptoms (P<0.05), and there was a significant improvement in extrapyramidal symptoms (P<0.01). Clinical laboratory tests, such as ECG and weight, did not significantly change from baseline. Plasma ziprasidone levels ranged from 20 ng/mL to 160 ng/mL (mean: 75.8 ng/mL) and were significantly related to the improvement in negative symptoms.

Discussion: The study showed that ziprasidone was effective and tolerable, that use of ziprasidone was characterized by an absence of extrapyramidal symptoms and weight gain, and that no alterations in clinical laboratory tests occurred. The findings suggest a relationship between plasma levels and the clinical response to negative symptoms of schizophrenia.

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Correspondence

M. C. MauriMD, PhD 

Clinical Neuropsychopharmacology Unit

Clinical Psychiatry

Guardia II

IRCCS Ospedale Maggiore Policlinico

Via F. Sforza 35

20122 Milano

Italy

Phone: 02/55/03 59 15

Fax: 02/50/32 03 10

Email: maurimc@policlinico.mi.it

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