Key result
Antipsychotic use in patients with schizophrenia showed varying rates of cardiovascular adverse events (13.1% to 63.5%) compared to controls, with heterogeneity precluding meta-analysis.
Why the study?
Does the use of antipsychotic agents increase the risk of cardiovascular adverse events in patients with schizophrenia?
Systematic Review (n=522,098)
Does the use of antipsychotic agents increase the risk of cardiovascular adverse events in patients with schizophrenia?
This systematic review suggests an association between antipsychotic use and cardiovascular adverse events in patients with schizophrenia, though high clinical heterogeneity precluded a quantitative meta-analysis.
OBJECTIVE:: Determine whether there is an association between the risk of cardiovascular adverse events and the use of antipsychotic agents. METHOD:: Analysis of original articles retrieved from the following databases: LILACS, PubMed, Cochrane Controlled Trials Clinical Data Bank (CENTRAL) and PsycINFO, without language restriction, dated until November 2015. After screening of 2,812 studies, three cohort original articles were selected for quality analysis. RESULTS:: 403,083 patients with schizophrenia and 119,015 participants in the control group data were analyzed. The occurrence of cardiovascular events observed in the articles was: 63.5% (article 1), 13.1% (article 2) and 24.95% (article 3) in the group of treated schizophrenic patients, and 46.2%, 86.9% and 24.9%, respectively, in the control groups. CONCLUSION:: Clinical heterogeneity among the studies led to a provisional response and made it impossible to perform the meta-analysis, although the articles demonstrate an association between cardiovascular adverse events and the use of antipsychotics. More quality clinical trials are needed to support this evidence.
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Silva et al. (2017) conducted a systematic review in Schizophrenia (n=522,098). Antipsychotic agents vs. Control group was evaluated on Cardiovascular adverse events. Antipsychotic use in patients with schizophrenia showed varying rates of cardiovascular adverse events (13.1% to 63.5%) compared to controls, with heterogeneity precluding meta-analysis.
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