Literature DB >> 20399985

Effects of high-dose ziprasidone and haloperidol on the QTc interval after intramuscular administration: a randomized, single-blind, parallel-group study in patients with schizophrenia or schizoaffective disorder.

Jeffrey J Miceli1, Thomas G Tensfeldt, Thomas Shiovitz, Richard J Anziano, Cedric O'Gorman, Rachel H Harrigan.   

Abstract

BACKGROUND: Antipsychotic agents have been associated with a prolonged QT interval. Data on the effects of ziprasidone and haloperidol on the QTc interval are lacking.
OBJECTIVE: This study aimed to characterize the effects of 2 high-dose intramuscular injections of ziprasidone and haloperidol on the QTc interval at T(max).
METHODS: This randomized, single-blind study enrolled patients with schizophrenia or schizoaffective disorder in whom long-term antipsychotic therapy was indicated. Patients were randomized to receive 2 high-dose intramuscular injections of ziprasidone (20 and 30 mg) or haloperidol (7.5 and 10 mg) separated by 4 hours. The primary outcome measure was the mean change from baseline in QTc at the T(max) of each injection. Each dose administration was followed by serial ECG and blood sampling for pharmacokinetic determinations. Twelve-lead ECG data were obtained immediately before and at predetermined times after injections. ECG tracings were read by a blinded central reader. Blood samples were obtained immediately before and after injections. Point estimates and 95% CIs for mean QTc and changes from baseline in QTc were estimated. No between-group hypothesis tests were conducted. For the assessments of tolerability and safety profile, patients underwent physical examination, including measurement of vital signs, clinical laboratory evaluation, and monitoring for adverse events (AEs) using spontaneous reporting.
RESULTS: A total of 59 patients were assigned to treatment, and 58 received study medication (ziprasidone, 31 patients; haloperidol, 27; age range, 21-72 years; 79% male). After the first injection, mean (95% CI) changes from baseline were 4.6 msec (0.4-8.9) with ziprasidone (n = 25) and 6.0 msec (1.4-10.5) with haloperidol (n = 24). After the second injection, these values were 12.8 msec (6.7-18.8) and 14.7 msec (10.2-19.2), respectively. Mild and transient changes in heart rate and blood pressure were observed with both treatments. None of the patients had a QTc interval >480 msec. Two patients in the ziprasidone group experienced QTc prolongation >450 msec (457 and 454 msec) and QTc changes that exceeded 60 msec (62 and 76 msec) relative to the time-matched baseline values. With haloperidol, QTc interval values were <450 msec with no changes >60 msec. Treatment-emergent AEs were reported in 29 of 31 patients (93.5%) in the ziprasidone group and 25 of 27 patients (92.6%) in the haloperidol group; most events were of mild or moderate severity. Frequently reported AEs were somnolence (90.3% and 81.5%, respectively), dizziness (22.6% and 7.4%), anxiety (16.1% and 7.4%), extrapyramidal symptoms (6.5% and 33.3%), agitation (6.5% and 18.5%), and insomnia (0% and 14.8%).
CONCLUSIONS: In this study of the effects of high-dose ziprasidone and haloperidol in patients with schizophrenic disorder, none of the patients had a QTc interval >480 msec, and changes from baseline QTc interval were clinically modest with both drugs. Both drugs were generally well tolerated. Copyright 2010 Excerpta Medica Inc. All rights reserved.

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Year:  2010        PMID: 20399985     DOI: 10.1016/j.clinthera.2010.03.003

Source DB:  PubMed          Journal:  Clin Ther        ISSN: 0149-2918            Impact factor:   3.393


  8 in total

1.  Improved ziprasidone formulations with enhanced bioavailability in the fasted state and a reduced food effect.

Authors:  Avinash G Thombre; Scott M Herbig; Jeffrey A Alderman
Journal:  Pharm Res       Date:  2011-06-15       Impact factor: 4.200

2.  Ziprasidone and the corrected QT interval: a comprehensive summary of clinical data.

Authors:  A John Camm; Onur N Karayal; Herbert Meltzer; Sheela Kolluri; Cedric O'Gorman; Jeffrey Miceli; Thomas Tensfeldt; John M Kane
Journal:  CNS Drugs       Date:  2012-04-01       Impact factor: 5.749

3.  Risk management of QTc-prolongation in patients receiving haloperidol: an epidemiological study in a University hospital in Belgium.

Authors:  Eline Vandael; Bert Vandenberk; Joris Vandenberghe; Isabel Spriet; Rik Willems; Veerle Foulon
Journal:  Int J Clin Pharm       Date:  2016-01-09

Review 4.  QTc interval prolongation and torsade de pointes associated with second-generation antipsychotics and antidepressants: a comprehensive review.

Authors:  Mehrul Hasnain; W Victor R Vieweg
Journal:  CNS Drugs       Date:  2014-10       Impact factor: 5.749

Review 5.  Efficacy of Atypical Antipsychotics in the Management of Acute Agitation and Aggression in Hospitalized Patients with Schizophrenia or Bipolar Disorder: Results from a Systematic Review.

Authors:  Xin Yu; Christoph U Correll; Yu-Tao Xiang; Yifeng Xu; Jizhong Huang; Fude Yang; Gang Wang; Tianmei Si; John M Kane; Prakash Masand
Journal:  Shanghai Arch Psychiatry       Date:  2016-10-25

6.  Ziprasidone hydrocloride: what role in the management of schizophrenia?

Authors:  Chiara Mattei; Maria Paola Rapagnani; Stephen M Stahl
Journal:  J Cent Nerv Syst Dis       Date:  2011-02-15

7.  QT Interval Prolongation Associated with Intramuscular Ziprasidone in Chinese Patients: A Case Report and a Comprehensive Literature Review with Meta-Analysis.

Authors:  Xian-Bin Li; Yi-Lang Tang; Wei Zheng; Chuan-Yue Wang; Jose de Leon
Journal:  Case Rep Psychiatry       Date:  2014-11-04

Review 8.  Antipsychotic Polypharmacy-Related Cardiovascular Morbidity and Mortality: A Comprehensive Review.

Authors:  Amber N Edinoff; Emily D Ellis; Laura M Nussdorf; Taylor W Hill; Elyse M Cornett; Adam M Kaye; Alan D Kaye
Journal:  Neurol Int       Date:  2022-03-17
  8 in total

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