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Influence of different second generation antipsychotics on the QTc interval: A pragmatic study

AIM: To investigate whether differential influence on the QTc interval exists among four second generation antipsychotics (SGAs) in psychosis. METHODS: Data were drawn from a pragmatic, randomized head-to-head trial of the SGAs risperidone, olanzapine, quetiapine, and ziprasidone in acute admissions...

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Autores principales: Olsen, Roy E, Kroken, Rune A, Bjørhovde, Sigmund, Aanesen, Kristina, Jørgensen, Hugo A, Løberg, Else-Marie, Johnsen, Erik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5183996/
https://www.ncbi.nlm.nih.gov/pubmed/28078208
http://dx.doi.org/10.5498/wjp.v6.i4.442
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author Olsen, Roy E
Kroken, Rune A
Bjørhovde, Sigmund
Aanesen, Kristina
Jørgensen, Hugo A
Løberg, Else-Marie
Johnsen, Erik
author_facet Olsen, Roy E
Kroken, Rune A
Bjørhovde, Sigmund
Aanesen, Kristina
Jørgensen, Hugo A
Løberg, Else-Marie
Johnsen, Erik
author_sort Olsen, Roy E
collection PubMed
description AIM: To investigate whether differential influence on the QTc interval exists among four second generation antipsychotics (SGAs) in psychosis. METHODS: Data were drawn from a pragmatic, randomized head-to-head trial of the SGAs risperidone, olanzapine, quetiapine, and ziprasidone in acute admissions patients with psychosis, and with follow-up visits at discharge or maximally 6-9 wk, 3, 6, 12 and 24 mo. Electrocardiograms were recorded on all visits. To mimic clinical shared decision-making, the patients were randomized not to a single drug, but to a sequence of the SGAs under investigation. The first drug in the sequence defined the randomization group, but the patient and/or clinician could choose an SGA later in the sequence if prior negative experiences with the first one(s) in the sequence had occurred. The study focuses on the time of, and actual use of the SGAs under investigation, that is until treatment discontinuation or change, in order to capture the direct medication effects on the QTc interval. Secondary intention-to-treat (ITT) analyses were also performed. RESULTS: A total of 173 patients, with even distribution among the treatment groups, underwent ECG assessments. About 70% were males and 43% had never used antipsychotic drugs before the study. The mean antipsychotic doses in milligrams per day with standard deviations (SD) were 3.4 (1.2) for risperidone, 13.9 (4.6) for olanzapine, 325.9 (185.8) for quetiapine, and 97.2 (42.8) for ziprasidone treated groups. The time until discontinuation of the antipsychotic drug used did not differ in a statistically significant way among the groups (Log-Rank test: P = 0.171). The maximum QTc interval recorded during follow-up was 462 ms. Based on linear mixed effects analyses, the QTc interval change per day with standard error was -0.0030 (0.0280) for risperidone; -0.0099 (0.0108) for olanzapine; -0.0027 (0.0170) for quetiapine, and -0.0081 (0.0229) for ziprasidone. There were no statistically significant differences among the groups in this regard. LME analyses based on ITT groups (the randomization groups), revealed almost identical slopes with -0.0063 (0.0160) for risperidone, -0.0130 (0.0126) for olanzapine, -0.0034 (0.0168) for quetiapine, and -0.0045 (0.0225) for ziprasidone. CONCLUSION: None of the SGAs under investigation led to statistically significant QTc prolongation. No statistically significant differences among the SGAs were found.
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spelling pubmed-51839962017-01-11 Influence of different second generation antipsychotics on the QTc interval: A pragmatic study Olsen, Roy E Kroken, Rune A Bjørhovde, Sigmund Aanesen, Kristina Jørgensen, Hugo A Løberg, Else-Marie Johnsen, Erik World J Psychiatry Randomized Clinical Trial AIM: To investigate whether differential influence on the QTc interval exists among four second generation antipsychotics (SGAs) in psychosis. METHODS: Data were drawn from a pragmatic, randomized head-to-head trial of the SGAs risperidone, olanzapine, quetiapine, and ziprasidone in acute admissions patients with psychosis, and with follow-up visits at discharge or maximally 6-9 wk, 3, 6, 12 and 24 mo. Electrocardiograms were recorded on all visits. To mimic clinical shared decision-making, the patients were randomized not to a single drug, but to a sequence of the SGAs under investigation. The first drug in the sequence defined the randomization group, but the patient and/or clinician could choose an SGA later in the sequence if prior negative experiences with the first one(s) in the sequence had occurred. The study focuses on the time of, and actual use of the SGAs under investigation, that is until treatment discontinuation or change, in order to capture the direct medication effects on the QTc interval. Secondary intention-to-treat (ITT) analyses were also performed. RESULTS: A total of 173 patients, with even distribution among the treatment groups, underwent ECG assessments. About 70% were males and 43% had never used antipsychotic drugs before the study. The mean antipsychotic doses in milligrams per day with standard deviations (SD) were 3.4 (1.2) for risperidone, 13.9 (4.6) for olanzapine, 325.9 (185.8) for quetiapine, and 97.2 (42.8) for ziprasidone treated groups. The time until discontinuation of the antipsychotic drug used did not differ in a statistically significant way among the groups (Log-Rank test: P = 0.171). The maximum QTc interval recorded during follow-up was 462 ms. Based on linear mixed effects analyses, the QTc interval change per day with standard error was -0.0030 (0.0280) for risperidone; -0.0099 (0.0108) for olanzapine; -0.0027 (0.0170) for quetiapine, and -0.0081 (0.0229) for ziprasidone. There were no statistically significant differences among the groups in this regard. LME analyses based on ITT groups (the randomization groups), revealed almost identical slopes with -0.0063 (0.0160) for risperidone, -0.0130 (0.0126) for olanzapine, -0.0034 (0.0168) for quetiapine, and -0.0045 (0.0225) for ziprasidone. CONCLUSION: None of the SGAs under investigation led to statistically significant QTc prolongation. No statistically significant differences among the SGAs were found. Baishideng Publishing Group Inc 2016-12-22 /pmc/articles/PMC5183996/ /pubmed/28078208 http://dx.doi.org/10.5498/wjp.v6.i4.442 Text en ©The Author(s) 2016. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ Open-Access: This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Randomized Clinical Trial
Olsen, Roy E
Kroken, Rune A
Bjørhovde, Sigmund
Aanesen, Kristina
Jørgensen, Hugo A
Løberg, Else-Marie
Johnsen, Erik
Influence of different second generation antipsychotics on the QTc interval: A pragmatic study
title Influence of different second generation antipsychotics on the QTc interval: A pragmatic study
title_full Influence of different second generation antipsychotics on the QTc interval: A pragmatic study
title_fullStr Influence of different second generation antipsychotics on the QTc interval: A pragmatic study
title_full_unstemmed Influence of different second generation antipsychotics on the QTc interval: A pragmatic study
title_short Influence of different second generation antipsychotics on the QTc interval: A pragmatic study
title_sort influence of different second generation antipsychotics on the qtc interval: a pragmatic study
topic Randomized Clinical Trial
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5183996/
https://www.ncbi.nlm.nih.gov/pubmed/28078208
http://dx.doi.org/10.5498/wjp.v6.i4.442
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