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β-blockers did not decrease mortality in post-AMI patients without heart failure

onlinejacc.org
Literature - Dondo TB, Hall M, West RM, et al. - Journal of Am Coll Cardiol 2017; 69(22): 2710-20

Background

Existing evidence supports the use of β-blockers in acute myocardial infarction (AMI) patients with heart failure (HF), as well as in hospitalized patients who are hemodynamically stable [1,2]. However, data regarding the impact of β-blockers on the mortality of AMI patients without HF or left ventricular systolic dysfunction (LVSD) are contradicting and medical guidelines include different recommendations for β-blockers after AMI [3-5].

In this analysis of the MINAP registry, the impact of β-blockers on all-cause mortality at 1 year was evaluated in 170,475 survivors of hospitalized AMI without HF or LVSD.

Main results

  • Compared with those who did not receive β-blockers, patients who received β-blockers tended to be younger and male.
  • Compared with patients who received β-blockers, those who did not, were more frequently comorbid and of higher ischemic risk, including diabetic mellitus (15.4% vs. 11.6%), chronic renal failure (3.2% vs. 1.6%), asthma or COPD (20.6% vs. 7.8%), cardiovascular disease (7.0% vs. 3.8%), and they had more frequently an intermediate or high Global Registry of Acute Coronary Events risk score (76.5% vs. 69.8%).
  • The prescription of discharge medications, in-hospital procedures and enrolment into cardiac rehabilitation programmes was higher among those who received β-blockers.
  • For the entire cohort with >163,772 person-years of observation (maximum 1-year follow-up), there were 9,373 deaths (5.2%).
  • After propensity score matching, the unadjusted 1-year mortality was significantly lower for patients who received β-blockers compared with those who did not (4.9% vs. 11.2%, P<0.001).
  • After weighting and adjustment, there was no significant difference in mortality when comparing patients with β-blockers compared with those who did not use β-blockers (average treatment effects coefficient at 1 month 0.47, 95% CI -2.99 to 3.94, P=0.785; at 6 months 0.06, 95% CI -0.35 to 0.46, P=0.768; at 1 year 0.07, 95% CI -0.60 to 0.75, P=0.827), neither for ST-segment elevation myocardial infarction (STEMI) nor for non-STEMI patients.

Conclusion

The use of β-blockers was not associated with lower all-cause mortality at any time point up to 1 year, in STEMI and non-STEMI patients without HF or LVSD, who survived hospitalization in the MINAP registry. These results add to the increasing body of evidence that routine prescription of β-blockers in AMI patients without HF or LVSD should be might not be indicated, but needs further investigation.

Editorial comment

In their editorial article [6], Ibanez et al review briefly the history of β-blockers and note that opinions about their benefit in post-MI patients have changed dramatically, in the light of advances in the treatment of AMI patients. They recommend viewing the results of the study of Dondo et al with ‘’great caution’’ because of the following important limitations:

  • the cut-off LVEF level used was 30%, although there is an established benefit from the use of β-blockers for LVEFs between 30% and 40%
  • β-blockers were captured only at discharge and the treatment adherence during the follow-up year is unknown
  • statistical consideration: it is not clear whether the estimated effect of propensity score-matched sample is representative of the entire cohort

The authors conclude: ‘’Thus, as the authors acknowledge, the present study should be viewed as hypothesis-generating and should not change clinical practice. However, this important report highlights the need to reboot the system: the role of β-blockers in post-MI patients without LVSD (LVEF >40%) needs to be evaluated from scratch.’’

References

1. Capricorn Investigators. Effect of carvedilol on outcome after myocardial infarction in patients with left-ventricular dysfunction: the CAPRICORN randomised trial. Lancet 2001;357:1385–90.

2. Timolol-induced reduction in mortality and reinfarction in patients surviving acute myocardial infarction. N Engl J Med 1981;304:801–7.

3. Roffi M, Patrono C, Collet JP, et al. 2015 ESC guidelines for the management of acute coronary syndromes in patients presenting without persistent ST-segment elevation: Task Force for the Management of Acute Coronary Syndromes in Patients Presenting without Persistent ST Segment Elevation of the European Society of Cardiology (ESC). Eur Heart J 2016;37:267–315.

4. Amsterdam EA, Wenger NK, Brindis RG, et al. 2014 AHA/ACC guideline for the management of patients with non–ST-elevation acute coronary syndromes: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines. J Am Coll Cardiol 2014;64: e139–228.

5. Puymirat E, Riant E, Aissoui N, et al. b-Blockers and mortality after myocardial infarction in patients without heart failure: multicentre prospective cohort study. BMJ 2016;354:i4801.

6. Ibáñez B, Raposeiras-Roubin S, García-Ruiz JM. The Swing of b-blockers: Time for a System Reboot. Journal of Am Coll Cardiol 2017; 69(22):2721-4.

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Schedule18 May 2024