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Randomized Control of Sympathetic Drive With Continuous Intravenous Esmolol in Patients With Acute ST-Segment Elevation Myocardial Infarction: The BEtA-Blocker Therapy in Acute Myocardial Infarction (BEAT-AMI) Trial.
Er, Fikret; Dahlem, Kristina M; Nia, Amir M; Erdmann, Erland; Waltenberger, Johannes; Hellmich, Martin; Kuhr, Kathrin; Le, Minh Tam; Herrfurth, Tina; Taghiyev, Zulfugar; Biesenbach, Esther; Yüksel, Dilek; Eran-Ergöknil, Aslihan; Vanezi, Maria; Caglayan, Evren; Gassanov, Natig.
Afiliação
  • Er F; Klinikum Gütersloh, Department of Cardiology and Electrophysiology I, University Hospital Münster, Gütersloh, Germany. Electronic address: fikret.er@klinikum-guetersloh.de.
  • Dahlem KM; Department of Internal Medicine III, University of Cologne, Cologne, Germany.
  • Nia AM; Division of Cardiology, Pulmonology, and Vascular Medicine, Heinrich Heine University Medical Center Düsseldorf, Düsseldorf, Germany.
  • Erdmann E; Department of Internal Medicine III, University of Cologne, Cologne, Germany.
  • Waltenberger J; Department of Cardiovascular Medicine, University Hospital Münster, Münster, Germany.
  • Hellmich M; Institute of Medical Statistics, Informatics and Epidemiology, University of Cologne, Cologne, Germany.
  • Kuhr K; Institute of Medical Statistics, Informatics and Epidemiology, University of Cologne, Cologne, Germany.
  • Le MT; Department of Internal Medicine III, University of Cologne, Cologne, Germany.
  • Herrfurth T; Department of Internal Medicine III, University of Cologne, Cologne, Germany.
  • Taghiyev Z; Department of Cardiac and Thoracic Surgery, BG University Hospital Bergmannsheil, Bochum, Germany.
  • Biesenbach E; Department of Cardiology and Electrophysiology, University of Witten/Herdecke, Medical Center Porz am Rhein, Cologne, Germany.
  • Yüksel D; Klinikum Gütersloh, Department of Cardiology and Electrophysiology I, University Hospital Münster, Gütersloh, Germany.
  • Eran-Ergöknil A; Klinikum Gütersloh, Department of Cardiology and Electrophysiology I, University Hospital Münster, Gütersloh, Germany.
  • Vanezi M; Department of Internal Medicine III, University of Cologne, Cologne, Germany.
  • Caglayan E; Department of Internal Medicine III, University of Cologne, Cologne, Germany.
  • Gassanov N; Klinikum Gütersloh, Department of Cardiology and Electrophysiology I, University Hospital Münster, Gütersloh, Germany.
JACC Cardiovasc Interv ; 9(3): 231-240, 2016 Feb 08.
Article em En | MEDLINE | ID: mdl-26847114
OBJECTIVES: This study sought to evaluate the role of esmolol-induced tight sympathetic control in patients with ST-segment elevation myocardial infarction (STEMI). BACKGROUND: Elevated sympathetic drive has a detrimental effect on patients with acute STEMI. The effect of beta-blocker-induced heart rate mediated sympathetic control on myocardial damage is unknown. METHODS: The authors conducted a prospective, randomized, single-blind trial involving patients with STEMI and successful percutaneous intervention (Killip class I and II). Patients were randomly allocated to heart rate control with intravenous esmolol for 24 h or placebo. The primary outcome was the maximum change in troponin T release as a prognostic surrogate marker for myocardial damage. A total of 101 patients were enrolled in the study. RESULTS: There was a significant difference between patients allocated to placebo and those who received sympathetic control with esmolol in terms of maximum change in troponin T release: the median serum troponin T concentration increased from 0.2 ng/ml (interquartile range [IQR] 0.1 to 0.7 ng/ml) to 1.3 ng/ml (IQR: 0.6 to 4.7 ng/ml) in the esmolol group and from 0.3 ng/ml (IQR: 0.1 to 1.2 ng/ml) to 3.2 ng/ml (IQR: 1.5 to 5.3 ng/ml) in the placebo group (p = 0.010). The levels of peak creatine kinase (CK), CK subunit MB (CK-MB), and n-terminal brain natriuretic peptide (NT-proBNP) were lower in the esmolol group compared with placebo (CK 619 U/l [IQR: 250-1,701 U/l] vs. 1,308 U/l [IQR: 610 to 2,324 U/l]; p = 0.013; CKMB: 73.5 U/l [IQR: 30 to 192 U/l] vs. 158.5 U/l [IQR: 74 to 281 U/l]; p = 0.005; NT-proBNP: 1,048 pg/ml (IQR: 623 to 2,062 pg/ml] vs. 1,497 pg/ml [IQR: 739 to 3,318 pg/ml]; p = 0.059). Cardiogenic shock occurred in three patients in the placebo group and in none in the esmolol group. CONCLUSIONS: Esmolol treatment statistically significantly decreased troponin T, CK, CK-MB and NT-proBNP release as surrogate markers for myocardial injury in patients with STEMI. (Heart Rate Control After Acute Myocardial Infarction; DRKS00000766).
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Propanolaminas / Antagonistas de Receptores Adrenérgicos beta 1 / Infarto do Miocárdio Tipo de estudo: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Propanolaminas / Antagonistas de Receptores Adrenérgicos beta 1 / Infarto do Miocárdio Tipo de estudo: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Ano de publicação: 2016 Tipo de documento: Article