Published in Clinical Trials Week, June 27th, 2005
According to researchers in Canada, "We sought to characterize the outcomes of patients with a prior percutaneous coronary intervention (PCI) who presented with a non-ST-segment elevation acute coronary syndrome (ACS). We analyzed the 30 and 180 day outcomes of 3012 patients with prior PCI and 21,154 patients without prior PCI enrolled in three randomized ACS trials (GUSTO IIb, PURSUIT, and PARAGON-B)."
M. Labinaz and colleagues of the University of Ottawa explained, "The median (25th, 75th percentile) interval between...
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Source: Clinical Trials Week (2005-06-27)
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