Major adverse cardiac events with haloperidol: A meta-analysis
Michael Cristian Garcia1,2, Mason Anderson1, Michelle Li1
1Clinical Pharmacology and Toxicology Research Group, Research Institute of St Joe's Hamilton, Hamilton, Canada.
Insights
Haloperidol, a QT interval-prolonging medication, did not increase major adverse cardiac events or mortality in short-term trials. Further research is needed to clarify clinical outcomes for safe prescribing.
Area of Science:
- Cardiology
- Pharmacology
- Psychiatry
Background:
- Haloperidol is a widely used antipsychotic with known QT interval-prolonging risks.
- It is frequently flagged in medication safety alerts.
- This study investigates cardiac risks associated with haloperidol.
Purpose of the Study:
- To systematically review and summarize high-quality evidence on the frequency and nature of proarrhythmic major adverse cardiac events (MACE) linked to haloperidol.
- To assess the association between haloperidol use and cardiac safety outcomes.
Main Methods:
- Searched multiple databases (Medline, Embase, etc.) for randomized controlled trials (RCTs) comparing haloperidol to placebo in adults.
- Utilized an FDA-adapted MACE composite outcome (death, cardiac arrest, ventricular tachyarrhythmia, seizure, syncope).
- Performed random-effects meta-analyses, including corrections for zero-event studies.
Main Results:
- Analyzed 84 RCTs with 12,180 participants; 44% included patients with psychiatric diagnoses, and 59.5% collected ECG data.
- Over 1100 events were recorded, predominantly deaths (97.8%), with few ventricular arrhythmias or seizures/syncope.
- No significant difference in MACE was found between haloperidol and placebo groups (RR 0.93, 95% CI: 0.80-1.08), nor an increased risk of mortality with IV haloperidol.
Conclusions:
- Haloperidol was not found to be arrhythmogenic or increase mortality in the analyzed short-duration trials.
- Further research is essential to understand the real-world clinical outcomes associated with QT interval-prolonging medications (QTPmeds).
- Findings aim to inform safer prescribing practices for haloperidol.
Background:
Haloperidol is a commonly used antipsychotic drug and a frequent source of medication safety alerts because of its listing as a "known risk" QT interval-prolonging medication (QTPmed). We aimed to summarize the high-quality literature on the frequency and nature of proarrhythmic major adverse cardiac events (MACE) associated with haloperidol.
Methods:
We searched Medline, Embase, International Pharmaceutical Abstracts, and Cochrane Central for randomized controlled trials (RCTs) involving patients 18 years or older comparing haloperidol to placebo. The FDA-adapted MACE composite included death, non-fatal cardiac arrest, ventricular tachyarrhythmia including torsades de pointes, and seizure or syncope. Random-effects meta-analyses were performed with a treatment-arm continuity correction for single and double zero event studies.
Results:
84 RCTs (n = 12180, 46% female), 23.8% of trials reported mean or median ages of their participants to be older than 65 years with 37 (44.0%) involving participants with psychiatric diagnoses, and 50 (59.5%) including electrocardiograms. Median follow-up duration was 28.0 days (interquartile range [IQR]=51.0). There were 1144 events, of which 97.8% were deaths, with 22 ventricular arrhythmias and 3 seizures or syncope. There was no difference in MACE with exposure to haloperidol compared to placebo (risk ratio [RR] 0.93, 95% CI: 0.80-1.08; I2 = 0%). IV haloperidol was not associated with increased risk of mortality (n = 5873, RR: 0.88, 95%CI:0.72-1.08).
Conclusions:
We did not find that haloperidol was arrhythmogenic or increased mortality in these largely short-duration trials. Further research to clarify actual clinical outcomes related to QTPmeds is important to inform safe prescribing practices.
More Related Videos
09:12Three Laboratory Procedures for Assessing Different Manifestations of Impulsivity in Rats
Published on: March 17, 2019
08:28Methods for ECG Evaluation of Indicators of Cardiac Risk, and Susceptibility to Aconitine-induced Arrhythmias in Rats Following Status Epilepticus
Published on: April 5, 2011
Related Concept Videos
Adrenergic Antagonists: Pharmacological Actions of β-Receptor Blockers
Antiarrhythmic Drugs: Class II Agents as β-Adrenergic Blockers
Heart Failure Drugs: Inotropic Agents
Nonlinear Pharmacokinetics: Dependence of Elimination Half-Life and Dose Clearance
A study on guinea pigs examined the...
Skeletal Muscle Relaxants: Adverse Effects
Unlike...
Heart Failure Drugs: β-Blockers
