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Intermittent ST depression and mortality after myocardial infarction
W Ruberman1, R Crow, C R Rosenberg
1Department of Environmental Medicine, New York University School of Medicine, NY 10010-2598.
Circulation
|April 1, 1992
Summary
Intermittent ST depression (STD) significantly increases mortality risk in untreated post-myocardial infarction patients. Propranolol may reduce this risk, suggesting an anti-ischemic protective effect.
Area of Science:
- Cardiology
- Clinical Research
- Morbidity and Mortality Studies
Background:
- Assessing the impact of intermittent ST depression (STD) on mortality in post-myocardial infarction (MI) patients.
- Utilizing data from the Beta Blocker Heart Attack Trial for a case-control analysis.
Purpose of the Study:
- To determine the contribution of intermittent ST depression to mortality.
- To investigate the potential protective effect of propranolol against STD-associated mortality.
Main Methods:
- Computer analysis of 24-hour ECG tapes to detect ST depression (>= 0.1 mV for >= 1 minute).
- Verification of computer-detected ST events by trained readers.
- Case-control analysis comparing 261 deaths with matched controls, adjusting for covariates.
Main Results:
- Intermittent ST depression (STD) was associated with a relative risk (RR) of 1.73 for mortality.
- In untreated patients, STD showed a higher RR of 2.56, while in propranolol-treated patients, the RR was 0.98.
- A dose-dependent relationship was observed in the placebo group, with >30 minutes of STD showing an RR of 4.33.
Conclusions:
- Transient ST depression on 24-hour monitoring significantly contributes to mortality in untreated early post-MI survivors.
- Propranolol's reduced effect suggests an anti-ischemic mechanism, potentially protecting against mortality.
- Further trials are warranted to explore if reducing STD improves survival outcomes.
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