In patients with ST-segment elevation myocardial infarction (STEMI), early subcutaneous administration of zalunfiban significantly improved coronary artery patency and reduced the risk of adverse 30-day clinical outcomes without increasing severe bleeding. In an international, double-blind, placebo-controlled trial of 2,467 patients randomly assigned to receive zalunfiban (0.11 mg/kg or 0.13 mg/kg) or placebo at first medical contact, zalunfiban significantly improved the primary 30-day hierarchical efficacy end point—a composite ranking of death, stroke, recurrent myocardial infarction, acute stent thrombosis, heart failure, infarct size, and absence of events—compared with placebo (adjusted odds ratio, 0.79). Angiography demonstrated faster coronary blood flow with zalunfiban (median corrected frame count, 109 vs. 176). Severe or life-threatening bleeding was similar between groups (1.2% vs. 0.8%), though mild to moderate bleeding was more frequent with zalunfiban (6.4% vs. 2.5%). These findings suggest that early and fast glycoprotein IIb/IIIa inhibition with zalunfiban could enhance preintervention reperfusion and clinical outcomes in STEMI, with an acceptable safety profile. Source: https://evidence.nejm.org/
A circadian subtype of depression is associated with earlier disease onset, more severe clinical features,…
A longitudinal study of 995 U.S. older adults found that frequent and unintentional daytime napping…
A multicohort genetic association study found that the ancestry-enriched CD36 Y325* variant accounted for a…
An American College of Cardiology scientific statement emphasizes that exercise should be prescribed as a…
A 16-week low-fat vegan diet was associated with significant reductions in body weight, visceral fat,…
A systematic review and meta-analysis of 27 studies involving 88,830 participants found that intensive blood…
This website uses cookies.