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Published on: May 28, 2019
Prophylactic lidocaine for myocardial infarction
Arturo J Martí-Carvajal1, Daniel Simancas-Racines, Vidhu Anand
1Iberoamerican Cochrane Network, Valencia, Venezuela.
Prophylactic lidocaine shows little to no effect on mortality or ventricular fibrillation in myocardial infarction patients. Safety data is unclear, and trials had high bias, suggesting further research may not be needed.
Area of Science:
- Cardiology
- Clinical Trials
- Pharmacology
Background:
- Coronary artery disease (CAD) and acute coronary syndromes (ACS) are significant global health issues.
- Ventricular arrhythmia post-myocardial infarction (MI) poses a high mortality risk.
- Existing evidence on prophylactic lidocaine's efficacy and safety in MI is outdated and uncertain.
Purpose of the Study:
- To evaluate the clinical effectiveness and safety of prophylactic lidocaine in preventing death among myocardial infarction (MI) patients.
- To synthesize evidence from randomized controlled trials (RCTs) on lidocaine's impact on mortality and ventricular fibrillation.
Main Methods:
- Systematic review and meta-analysis of 37 RCTs involving 11,948 participants.
- Searched multiple databases (CENTRAL, MEDLINE, EMBASE, LILACS, Web of Science) with no language restrictions.
- Assessed risk of bias, performed duplicate data extraction, and used random-effects models with trial sequential analysis.
Main Results:
- Lidocaine showed no significant difference compared to placebo/no intervention for all-cause mortality (RR 1.02), cardiac mortality (RR 1.03), or ventricular fibrillation (RR 0.78).
- Evidence quality was low to very low for most outcomes.
- Lidocaine increased the risk of asystole (RR 2.32) and dizziness/drowsiness (RR 3.85), with poorly reported safety data.
Conclusions:
- Low-quality evidence suggests prophylactic lidocaine has minimal to no effect on mortality or ventricular fibrillation in acute MI.
- The safety profile of lidocaine remains unclear due to high risk of bias and poor reporting in included trials.
- Trial sequential analysis indicates further trials may not be necessary to rule out a 20% relative risk reduction.
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