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in patients initially not reperfused, the incidence of severe haemorrhage was 1.2% for fondaparinux vs 1.5% for controls.
bij patiënten die in eerste instantie geen reperfusie ondergingen was de incidentie van ernstige hemorragie 1,2 % in de fondaparinux versus 1,5 % in de controlegroep.
Last Update: 2017-04-26
Usage Frequency: 3
Quality:
among patients initially not reperfused, the incidence of death/ re-mi at day 30 was significantly reduced from 15% for the control group to 12.1% for the fondaparinux group (hazard ratio 0.79, 95% ci, 0.65; 0.97, p = 0.023).
van 15% voor de controlegroep tot 12,1% (risicoratio 0,79, 95% bi, 0,65; 0,97, p=0,023).
Last Update: 2011-10-23
Usage Frequency: 1
Quality:
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