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Prophylaxis of post-myocardial infarction dysrhythmias by long-term timolol therapy
N Ranganathan1, P M Rautaharju, G G Jablonsky
1St. Michael's Hospital, Department of Physiology and Biophysics, Dalhousie University, Halifax, Nova Scotia, Canada.
Insights
Timolol maleate showed no immediate antiarrhythmic effect in acute myocardial infarction patients. However, it significantly reduced early-cycle ventricular and supraventricular complexes after 7 days.
Area of Science:
- Cardiology
- Pharmacology
Background:
- Acute myocardial infarction (AMI) poses a significant risk of cardiac arrhythmias.
- Early identification and management of arrhythmias are crucial in AMI patients.
Purpose of the Study:
- To evaluate the antiarrhythmic efficacy of early timolol maleate treatment in patients with acute myocardial infarction.
- To assess the impact of timolol on ventricular premature complexes (VPCs), supraventricular complexes (SVCs), and QRS duration.
Main Methods:
- A randomized controlled trial involving 94 patients with acute myocardial infarction.
- Comparison of early timolol maleate treatment versus placebo.
- Monitoring of VPC rates, couplets, runs, and early-cycle VPCs/SVCs.
- Assessment of QRS duration and adverse effects.
Main Results:
- No significant differences in mean/peak hourly VPC rates, couplets, or runs between timolol and placebo groups early in treatment.
- A significant 66% reduction in early-cycle VPCs (p < 0.001) observed 7-9 days after timolol initiation.
- A significant 73% reduction in early-cycle SVCs (p < 0.001) persisted throughout the 28-day study period.
- Significantly longer mean QRS duration in placebo-treated patients (p = 0.008).
- No difference in adverse effects between groups.
Conclusions:
- Timolol maleate demonstrates a delayed antiarrhythmic effect in acute myocardial infarction, specifically reducing early-cycle VPCs and SVCs.
- The drug appears safe for early administration in this patient population.
- Further research may explore optimal timing and duration for timolol use in AMI management.
Abstract:
The antiarrhythmic efficacy of timolol maleate was assessed in 94 patients with acute myocardial infarction. No significant differences were noted between early treatment with timolol and placebo in the mean and peak hourly ventricular premature complex rates, ventricular premature complex couplets, or runs. However, compared to the placebo treatment, there was a significant (p less than 0.001) 66% reduction in the relative fraction of early-cycle ventricular premature complexes 7 to 9 days after initiation of timolol therapy and a more prolonged significant (p less than 0.001) 73% reduction in the fraction of early-cycle supraventricular complexes throughout the 28-day timolol and placebo comparison period. The frequency distribution of QRS duration was significantly different between the placebo- and timolol-treated patients, with the mean duration 8 msec longer in the placebo-treated patients (p = 0.008). Adverse effects from early administration of timolol did not differ from those in the placebo-treated patients.
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