Why the study?
Do different second-generation antipsychotics (risperidone, olanzapine, quetiapine, ziprasidone) differentially influence the QTc interval in adults acutely admitted for psychosis?
Do different second-generation antipsychotics (risperidone, olanzapine, quetiapine, ziprasidone) differentially influence the QTc interval in adults acutely admitted for psychosis?
In a pragmatic trial of acutely admitted patients with psychosis, none of the four second-generation antipsychotics (risperidone, olanzapine, quetiapine, ziprasidone) significantly prolonged the QTc interval, and no significant differences were found among them.
These antipsychotics show no differential QTc effects in acute psychosis; confirms comparable cardiac safety among risperidone, olanzapine, quetiapine, and ziprasidone.
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: = 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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Olsen et al. (2016) studied this question.
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