Tarantini Giuseppe, Favaretto Enrico, Napodano Massimo, Perazzolo Marra Martina, Cacciavillani Luisa, Babuin Luciano, Giovagnoni Andrea, Renda Pietro, De Biasio Valeria, Plebani Mario, Mion Monica, Zaninotto Martina, Mistrorigo Flavio, Panfili Marco, Isabella Giambattista, Bilato Claudio, Iliceto Sabino
Department of Cardiac, Thoracic and Vascular Sciences, University of Padua, Padua, Italy.
Cardiology. 2010;116(2):110-6. doi: 10.1159/000316967. Epub 2010 Jun 29.
Reperfusion remains the definitive treatment for acute myocardial infarction (AMI), but restoring blood flow carries the potential to exacerbate the ischemia-related injury. Postconditioning might modify reperfusion-induced adverse events.
The POSTconditioning during Coronary Angioplasty in Acute Myocardial Infarction (POST-AMI) trial is a single-center, prospective, randomized study, with a planned inclusion of 78 patients with ST-elevation AMI. Patients will be randomly assigned to the postconditioning arm [primary angioplasty (PA) and stenting followed by brief episodes of ischemia-reperfusion early after recanalization] or non-postconditioning arm. All patients will be treated medically according to current international guidelines, including glycoprotein IIb/IIIa inhibitors before PA. The primary end point is to evaluate whether postconditioning, compared to plain PA, reduces infarct size estimated by cardiac magnetic resonance (CMR) at 30 +/- 10 days after the AMI. Secondary end points are microvascular obstruction observed at CMR, ST-segment resolution, angiographic myocardial blush grade <2, non-sustained/sustained ventricular tachycardia in the 48 h following PA, left ventricular remodeling and function at follow-up CMR, and the reduction of major adverse cardiac events at 30 days and 6 months.
The POST-AMI trial will evaluate the usefulness of postconditioning in limiting infarct size during the early and late phases after AMI.
