2005
DOI: 10.1016/s0140-6736(05)67222-4
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5-year outcome of an interventional strategy in non-ST-elevation acute coronary syndrome: the British Heart Foundation RITA 3 randomised trial

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Cited by 321 publications
(206 citation statements)
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“…This is a high value when compared to data from higher-risk randomized controlled trials, but it was a similar value to that observed in the RITA 3 (Randomized Intervention Trial on unstable Angina) trial, where in a lower risk population, 28% of patients allocated for an invasive strategy had a normal coronary angiogram 14 .…”
Section: Baseline Datasupporting
confidence: 76%
“…This is a high value when compared to data from higher-risk randomized controlled trials, but it was a similar value to that observed in the RITA 3 (Randomized Intervention Trial on unstable Angina) trial, where in a lower risk population, 28% of patients allocated for an invasive strategy had a normal coronary angiogram 14 .…”
Section: Baseline Datasupporting
confidence: 76%
“…With these developments, recurrent ischemic complications have been substantially reduced (21,22) and long-term survival has improved (23). However, the improved outcomes came with an increased risk of major hemorrhage.…”
Section: Management Strategy and Bleedingmentioning
confidence: 99%
“…Several meta-analyses that included contemporary randomized, controlled trials (RCTs) have shown a substantial risk reduction in all-cause mortality and myocardial infarction (MI) at 1 to 2 years after an early invasive strategy, 1,2 particularly in patients with the highest risk profile. 3 The treatment of choice, whether percutaneous coronary intervention (PCI) or coronary artery bypass grafting (CABG), is based on the same considerations used for patients with stable coronary artery disease. 4 Approximately 7% to 13% of patients hospitalized with NSTEMI undergo in-hospital CABG, 5,6 about a third performed within 48 hours of hospital admission.…”
mentioning
confidence: 99%