Prediction of enzymatic infarct size in ST-segment elevation myocardial infarction


Autoria(s): Mills, James S.; Mahaffey, Kenneth W.; Lokhnygina, Yuliya; Nicolau, José C.; Ruzyllo, Witold; Adams, Peter X.; Todaro, Thomas G.; Armstrong, Paul W.; Granger, Christopher B.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

07/11/2013

07/11/2013

2012

Resumo

Objectives Predictors of adverse outcomes following myocardial infarction (MI) are well established; however, little is known about what predicts enzymatically estimated infarct size in patients with acute ST-elevation MI. The Complement And Reduction of INfarct size after Angioplasty or Lytics trials of pexelizumab used creatine kinase (CK)-MB area under the curve to determine infarct size in patients treated with primary percutaneous coronary intervention (PCI) or fibrinolysis. Methods Prediction of infarct size was carried out by measuring CK-MB area under the curve in patients with ST-segment elevation MI treated with reperfusion therapy from January 2000 to April 2002. Infarct size was calculated in 1622 patients (PCI=817; fibrinolysis=805). Logistic regression was used to examine the relationship between baseline demographics, total ST-segment elevation, index angiographic findings (PCI group), and binary outcome of CK-MB area under the curve greater than 3000 ng/ml. Results Large infarcts occurred in 63% (515) of the PCI group and 69% (554) of the fibrinolysis group. Independent predictors of large infarcts differed depending on mode of reperfusion. In PCI, male sex, no prior coronary revascularization and diabetes, decreased systolic blood pressure, sum of ST-segment elevation, total (angiographic) occlusion, and nonright coronary artery culprit artery were independent predictors of larger infarcts (C index=0.73). In fibrinolysis, younger age, decreased heart rate, white race, no history of arrhythmia, increased time to fibrinolytic therapy in patients treated up to 2 h after symptom onset, and sum of ST-segment elevation were independently associated with a larger infarct size (C index=0.68). Conclusion Clinical and patient data can be used to predict larger infarcts on the basis of CK-MB quantification. These models may be helpful in designing future trials and in guiding the use of novel pharmacotherapies aimed at limiting infarct size in clinical practice. Coron Artery Dis 23:118-125 (C) 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins.

Procter & Gamble Pharmaceuticals

Alexion Pharmaceuticals Inc.

Identificador

CORONARY ARTERY DISEASE, PHILADELPHIA, v. 23, n. 2, pp. 118-125, MAR, 2012

0954-6928

http://www.producao.usp.br/handle/BDPI/42896

10.1097/MCA.0b013e32834e4f8f

http://dx.doi.org/10.1097/MCA.0b013e32834e4f8f

Idioma(s)

eng

Publicador

LIPPINCOTT WILLIAMS & WILKINS

PHILADELPHIA

Relação

CORONARY ARTERY DISEASE

Direitos

closedAccess

Copyright LIPPINCOTT WILLIAMS & WILKINS

Palavras-Chave #CARDIAC BIOMARKERS #CREATINE KINASE #INFARCT SIZE #MYOCARDIAL INFARCTION #ST-SEGMENT ELEVATION MYOCARDIAL INFARCTION #CREATINE-KINASE-MB #ACUTE CORONARY SYNDROMES #TISSUE-PLASMINOGEN ACTIVATOR #ANTI-C5 COMPLEMENT ANTIBODY #THROMBOLYTIC THERAPY #INTRAVENOUS STREPTOKINASE #INTERNATIONAL TRIAL #ADJUNCTIVE THERAPY #ANGIOPLASTY #REPERFUSION #PERIPHERAL VASCULAR DISEASE
Tipo

article

original article

publishedVersion