PMID- 27584567 OWN - NLM STAT- MEDLINE DCOM- 20171009 LR - 20190327 IS - 1874-1754 (Electronic) IS - 0167-5273 (Linking) VI - 223 DP - 2016 Nov 15 TI - Intravenous beta-blockers for patients undergoing primary percutaneous coronary intervention: A meta-analysis of randomized trials. PG - 891-897 LID - S0167-5273(16)32012-5 [pii] LID - 10.1016/j.ijcard.2016.08.293 [doi] AB - BACKGROUND: The efficacy and safety of intravenous beta-blockers in patients with ST elevation myocardial infarction (STEMI) undergoing primary percutaneous coronary intervention (PCI) are not well known. METHODS: Electronic databases were searched for randomized trials that compared intravenous beta-blocker use with routine care or placebo in patients with STEMI undergoing primary PCI. Summary estimates risk ratios (RR) were constructed using DerSimonian and Laird model. RESULTS: Four randomized trials with 1149 Killip class I or II STEMI patients were included. Intravenous beta-blockers were associated with a reduction in the risk of ventricular arrhythmias during hospitalization (RR 0.42, 95% confidence interval [CI] 0.26-0.69, P=0.001). The risk of cardiogenic shock (RR 0.78, 95% CI 0.31-1.97, P=0.61), bradycardia (RR 1.54, 95% CI 0.35-6.81, P=0.57), all-cause mortality (RR 0.71, 95% CI 0.19-3.17, P=0.72), and cardiovascular mortality (RR 0.93, 95% CI 0.35-2.48, P=0.88) during hospitalization was similar in both groups. There was a trend towards a lower risk of future heart failure hospitalizations with intravenous beta-blockers (RR 0.32, 95% CI 0.10-1.05, P=0.06). CONCLUSION: Intravenous beta-blockers, in STEMI patients (Killip class I or II) undergoing primary PCI, appear to be safe. Intravenous beta-blockers were associated with a reduced risk of ventricular arrhythmias. Due to the small number of patients, the impact on other outcomes could not be determined. Therefore, future trials are recommended to establish the efficacy of intravenous beta-blockers in primary PCI. CI - Copyright (c) 2016 Elsevier Ireland Ltd. All rights reserved. FAU - Elgendy, Islam Y AU - Elgendy IY AD - Department of Medicine, University of Florida, Gainesville, FL, USA. Electronic address: Islam.elgendy@medicine.ufl.edu. FAU - Elgendy, Akram Y AU - Elgendy AY AD - Department of Medicine, University of Florida, Gainesville, FL, USA. FAU - Mahmoud, Ahmed N AU - Mahmoud AN AD - Department of Medicine, University of Florida, Gainesville, FL, USA. FAU - Mansoor, Hend AU - Mansoor H AD - Department of Pharmaceutical Outcomes and Policy, University of Florida, Gainesville, FL, USA. FAU - Mojadidi, Mohammad K AU - Mojadidi MK AD - Department of Medicine, University of Florida, Gainesville, FL, USA. FAU - Bavry, Anthony A AU - Bavry AA AD - Department of Medicine, University of Florida, Gainesville, FL, USA; North Florida/South, Georgia Veterans Health System, Gainesville, FL, USA. LA - eng PT - Journal Article PT - Review DEP - 20160821 PL - Netherlands TA - Int J Cardiol JT - International journal of cardiology JID - 8200291 RN - 0 (Adrenergic beta-Antagonists) SB - IM MH - Administration, Intravenous MH - Adrenergic beta-Antagonists/*pharmacology MH - Arrhythmias, Cardiac/etiology/prevention & control MH - Humans MH - Percutaneous Coronary Intervention/*methods MH - Randomized Controlled Trials as Topic MH - *ST Elevation Myocardial Infarction/complications/drug therapy/surgery MH - Treatment Outcome OTO - NOTNLM OT - Adrenergic beta-antagonists OT - Meta-analysis OT - Myocardial infarction OT - Percutaneous coronary intervention EDAT- 2016/09/02 06:00 MHDA- 2017/10/11 06:00 CRDT- 2016/09/02 06:00 PHST- 2016/08/01 00:00 [received] PHST- 2016/08/18 00:00 [accepted] PHST- 2016/09/02 06:00 [pubmed] PHST- 2017/10/11 06:00 [medline] PHST- 2016/09/02 06:00 [entrez] AID - S0167-5273(16)32012-5 [pii] AID - 10.1016/j.ijcard.2016.08.293 [doi] PST - ppublish SO - Int J Cardiol. 2016 Nov 15;223:891-897. doi: 10.1016/j.ijcard.2016.08.293. Epub 2016 Aug 21.