Key result
Lower-dosage beta-blocker therapy after myocardial infarction was associated with a significant reduction in cardiovascular mortality compared to no therapy (HR 0.33; P=0.009).
Why the study?
Does lower-dosage beta-blocker therapy reduce cardiovascular mortality in patients who survived an acute myocardial infarction compared to no beta-blocker therapy?
Cohort (n=1,165)
Yes
Does lower-dosage beta-blocker therapy reduce cardiovascular mortality in patients who survived an acute myocardial infarction compared to no beta-blocker therapy?
Answers are grounded in this paper and cite their sources.
Lower dosages of beta-blockers after myocardial infarction are associated with a significant reduction in cardiovascular mortality, suggesting clinical benefit even when target doses from large trials are not achieved.
BACKGROUND: Although long-term beta-blocker therapy has been found beneficial in patients after an acute myocardial infarction, these drugs are greatly underused by clinicians. Moreover, the dosages of beta-blockers used in randomized controlled trials appear to be much larger than those routinely prescribed. OBJECTIVE: To determine whether an association exists between the dosage of beta-blockers prescribed after a myocardial infarction and cardiac mortality. METHODS: We performed a retrospective cohort study of 1165 patients who survived an acute myocardial infarction from January 1, 1990, through December 31, 1992. These patients represent a subgroup of the 6851 patients hospitalized at northern California Kaiser Permanente hospitals. RESULTS: Of the 37.7% of patients prescribed beta-blocker therapy, 48.1% were treated with dosages less than 50% of the dosage found to be effective in preventing cardiac death in large randomized clinical trials (lower-dosage therapy). Compared with patients not receiving beta-blockers, those treated with lower-dosage therapy appeared to have a greater reduction in cardiovascular mortality (hazard ratio, 0.33; P=.009) than patients treated with a higher dosage (hazard ratio, 0.82; P=0.51), after adjustment for age, sex, race, disease severity, and comorbidities. CONCLUSIONS: The dosages of beta-blockers shown to be effective in randomized trials are not commonly used in clinical practice, and treatment with lower dosages of beta-blockers was associated with at least as great a reduction in mortality as treatment with higher dosages. This suggests that physicians who are reluctant to prescribe beta-blockers because of the relatively large dosages used in the large prospective clinical trials should be encouraged to prescribe smaller dosages.
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Barron et al. (1998) conducted a cohort in acute myocardial infarction (n=1,165). Lower-dosage beta-blocker therapy vs. No beta-blockers was evaluated on cardiovascular mortality (HR 0.33, p=.009). Lower-dosage beta-blocker therapy after myocardial infarction was associated with a significant reduction in cardiovascular mortality compared to no therapy (HR 0.33; P=0.009).
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