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Published on: December 11, 2017
Possible survival benefit from concomitant beta-but not calcium-antagonist therapy during reperfusion for acute
S G Ellis1, D W Muller, E J Topol
1Department of Internal Medicine, University of Michigan Hospital, Ann Arbor.
Insights
Long-term beta-blocker therapy before myocardial infarction improved in-hospital survival compared to reperfusion alone. Calcium-antagonist therapy showed no survival benefit in this study of acute myocardial infarction patients.
Area of Science:
- Cardiology
- Pharmacology
Background:
- Long-term beta- or calcium-antagonist therapy may impact survival after myocardial infarction (MI) and reperfusion.
- Investigating pre-infarction medication effects on in-hospital survival is crucial for patient outcomes.
Purpose of the Study:
- To test if long-term beta- or calcium-antagonist therapy before myocardial infarction improves in-hospital survival compared to reperfusion alone.
Main Methods:
- Retrospective analysis of 424 patients undergoing coronary angioplasty within 12 hours of MI symptom onset.
- Stepwise logistic regression identified independent predictors of in-hospital death.
- Compared survival rates between patients on beta-blockers, calcium antagonists, and no pre-infarction medication.
Main Results:
- Beta-blocker use was independently correlated with improved in-hospital survival (0% vs 8% mortality).
- Calcium-antagonist therapy did not significantly affect survival rates.
- Patients on beta-blockers had lower heart rate and left ventricular end-diastolic pressure.
Conclusions:
- Pre-infarction beta-blocker therapy may improve early survival in acute myocardial infarction patients undergoing reperfusion.
- Calcium-antagonist therapy did not demonstrate a survival benefit in this cohort.
- Further research is needed to confirm these findings on beta-blocker efficacy.
Abstract:
To test the hypothesis that long-term beta- or calcium-antagonist therapy begun before the time of myocardial infarction and coronary reperfusion might improve patient in-hospital survival compared with reperfusion alone, 424 consecutive patients successfully reperfused with coronary angioplasty within 12 hours of infarct symptom onset were carefully and retrospectively characterized. Forty-seven patients (11%) were taking beta antagonists and 74 patients (17%) were taking calcium antagonists at the time of infarction. Patients receiving beta antagonists had a more frequent history of hypertension (p less than or equal to 0.001) and prior infarction (p less than or equal to 0.01) than those not so treated and patients receiving calcium antagonists had a more frequent history of prior infarction, prior angina, hypertension and diabetes (all p less than or equal to 0.001) than their nontreated counterparts. Stepwise logistic regression analysis found significant independent correlations between in-hospital death and the following variables: recurrent ischemia (p less than or equal to 0.001); proximal left anterior descending coronary infarct (p less than or equal to 0.001); 3-vessel disease (p = 0.002); patient age (p = 0.004); and initial total occlusion of the infarct artery (p = 0.022). After adjustment for these factors, beta antagonist use (mortality = 0 vs 8% without treatment) was still significantly correlated with improved survival (p = 0.048), whereas calcium-antagonist therapy made no difference in survival. Heart rate and left ventricular end-diastolic pressure upon presentation were significantly lower in patients treated with beta antagonists. Thus, beta-antagonists therapy, but probably not calcium-antagonist therapy, taken before reperfusion for acute myocardial infarction, may improve early survival compared to reperfusion alone. Larger studies will be required to confirm or refute these observations.
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