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Effect of β-Blockers on the Risk of Atrial Fibrillation in Patients with Acute Myocardial Infarction

INTRODUCTION: Oral β-blockers improve the prognosis of patients with acute myocardial infarction, while atrial fibrillation worsens the prognosis of this population. The reduction of atrial fibrillation incidence in patients treated with β-blockers could at least in part explain the benefits of this...

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Autores principales: Pesaro, Antonio Eduardo, de Matos Soeiro, Alexandre, Serrano, Carlos Vicente, Giraldez, Roberto Rocha, Ladeira, Renata Teixeira, Nicolau, José Carlos
Formato: Texto
Lenguaje:English
Publicado: Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2845766/
https://www.ncbi.nlm.nih.gov/pubmed/20360916
http://dx.doi.org/10.1590/S1807-59322010000300005
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author Pesaro, Antonio Eduardo
de Matos Soeiro, Alexandre
Serrano, Carlos Vicente
Giraldez, Roberto Rocha
Ladeira, Renata Teixeira
Nicolau, José Carlos
author_facet Pesaro, Antonio Eduardo
de Matos Soeiro, Alexandre
Serrano, Carlos Vicente
Giraldez, Roberto Rocha
Ladeira, Renata Teixeira
Nicolau, José Carlos
author_sort Pesaro, Antonio Eduardo
collection PubMed
description INTRODUCTION: Oral β-blockers improve the prognosis of patients with acute myocardial infarction, while atrial fibrillation worsens the prognosis of this population. The reduction of atrial fibrillation incidence in patients treated with β-blockers could at least in part explain the benefits of this drug. OBJECTIVE: To investigate the effect of β-blockers on the incidence of atrial fibrillation in patients with acute myocardial infarction. METHODS: We analyzed 1401 patients with acute myocardial infarction and evaluated the occurrence or absence of atrial fibrillation, the use of oral β-blockers and mortality during the first 24 hours. RESULTS: a) The use of β-blockers was inversely correlated with the presence of atrial fibrillation (ρ = 0.004; OR = 0.54). b) Correlations with mortality were as follows: 31.5% in patients with atrial fibrillation, 9.2% in those without atrial fibrillation (ρ < 0.001; Odds Ratio = 4.52), and 17.5% in patients not treated with β-blockers and 6.7% in those who received the drug (ρ < 0.001; OR = 0.34). c) Adjusted Models: The presence of atrial fibrillation was independently correlated with mortality (OR = 2.48, ρ = 0.002). The use of β-blockers was inversely and independently correlated with mortality (OR = 0.53; ρ = 0.002). The patients who used β-blockers showed a lower risk of atrial fibrillation (OR = 0.59; ρ = 0.029) in the adjusted model. CONCLUSION: The presence of atrial fibrillation and the absence of oral β-blockers increased in-hospital mortality in patients with acute myocardial infarction. Oral β-blockers reduced the incidence of atrial fibrillation, which might be at least partially responsible for the drug’s benefit.
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spelling pubmed-28457662010-04-01 Effect of β-Blockers on the Risk of Atrial Fibrillation in Patients with Acute Myocardial Infarction Pesaro, Antonio Eduardo de Matos Soeiro, Alexandre Serrano, Carlos Vicente Giraldez, Roberto Rocha Ladeira, Renata Teixeira Nicolau, José Carlos Clinics (Sao Paulo) Clinical Science INTRODUCTION: Oral β-blockers improve the prognosis of patients with acute myocardial infarction, while atrial fibrillation worsens the prognosis of this population. The reduction of atrial fibrillation incidence in patients treated with β-blockers could at least in part explain the benefits of this drug. OBJECTIVE: To investigate the effect of β-blockers on the incidence of atrial fibrillation in patients with acute myocardial infarction. METHODS: We analyzed 1401 patients with acute myocardial infarction and evaluated the occurrence or absence of atrial fibrillation, the use of oral β-blockers and mortality during the first 24 hours. RESULTS: a) The use of β-blockers was inversely correlated with the presence of atrial fibrillation (ρ = 0.004; OR = 0.54). b) Correlations with mortality were as follows: 31.5% in patients with atrial fibrillation, 9.2% in those without atrial fibrillation (ρ < 0.001; Odds Ratio = 4.52), and 17.5% in patients not treated with β-blockers and 6.7% in those who received the drug (ρ < 0.001; OR = 0.34). c) Adjusted Models: The presence of atrial fibrillation was independently correlated with mortality (OR = 2.48, ρ = 0.002). The use of β-blockers was inversely and independently correlated with mortality (OR = 0.53; ρ = 0.002). The patients who used β-blockers showed a lower risk of atrial fibrillation (OR = 0.59; ρ = 0.029) in the adjusted model. CONCLUSION: The presence of atrial fibrillation and the absence of oral β-blockers increased in-hospital mortality in patients with acute myocardial infarction. Oral β-blockers reduced the incidence of atrial fibrillation, which might be at least partially responsible for the drug’s benefit. Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo 2010-03 /pmc/articles/PMC2845766/ /pubmed/20360916 http://dx.doi.org/10.1590/S1807-59322010000300005 Text en Copyright © 2010 Hospital das Clínicas da FMUSP
spellingShingle Clinical Science
Pesaro, Antonio Eduardo
de Matos Soeiro, Alexandre
Serrano, Carlos Vicente
Giraldez, Roberto Rocha
Ladeira, Renata Teixeira
Nicolau, José Carlos
Effect of β-Blockers on the Risk of Atrial Fibrillation in Patients with Acute Myocardial Infarction
title Effect of β-Blockers on the Risk of Atrial Fibrillation in Patients with Acute Myocardial Infarction
title_full Effect of β-Blockers on the Risk of Atrial Fibrillation in Patients with Acute Myocardial Infarction
title_fullStr Effect of β-Blockers on the Risk of Atrial Fibrillation in Patients with Acute Myocardial Infarction
title_full_unstemmed Effect of β-Blockers on the Risk of Atrial Fibrillation in Patients with Acute Myocardial Infarction
title_short Effect of β-Blockers on the Risk of Atrial Fibrillation in Patients with Acute Myocardial Infarction
title_sort effect of β-blockers on the risk of atrial fibrillation in patients with acute myocardial infarction
topic Clinical Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2845766/
https://www.ncbi.nlm.nih.gov/pubmed/20360916
http://dx.doi.org/10.1590/S1807-59322010000300005
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