Key result
A low postoperative dose of aprotinin in patients receiving clopidogrel before CABG is safe, with comparable 30-day mortality (0.5% vs 2%, P=0.22) and bleeding compared to a high dose.
Why the study?
Does a low postoperative dose of aprotinin reduce bleeding and improve safety compared to a high intra- and postoperative dose in patients receiving clopidogrel before CABG?
RCT (n=399)
prospectively randomized
Does a low postoperative dose of aprotinin reduce bleeding and improve safety compared to a high intra- and postoperative dose in patients receiving clopidogrel before CABG?
Absolute Event Rate: 0.5% vs 2%
p-value: p=0.22
A low postoperative dose of aprotinin is as effective as a high dose for managing bleeding in patients on clopidogrel undergoing CABG, while avoiding the increased risk of renal impairment associated with high doses.
Low-dose aprotinin may be preferred in clopidogrel-treated CABG to limit renal impairment; confirms equivalent hemostasis with a safer profile.
Clopidogrel (Plavix) given before the operation increases bleeding complications following coronary artery bypass grafting (CABG). High perioperative doses of aprotinin (Trasylol) are known to reduce bleeding and transfusions after cardiac surgery, but may increase the risk of thrombosis, renal impairment, and mortality. The aim of the study was to evaluate the clinical effects of aprotinin given in high doses intra- and postoperatively vs. a low postoperative dose in patients on clopidogrel. Patients admitted for first-time CABG and receiving clopidogrel with or without aspirin, were prospectively randomized either to receive a total of 75,000 kallikrein inhibitor unit (KIU)/kg aprotinin given intra- and postoperatively or 25,000 KIU/kg aprotinin after the operation. Three hundred and ninety-nine patients aged 32-87 years (median 67 years) were included. Postoperative bleeding was slightly different, but moderate in both groups. The transfusion rate was similar, as were the incidences of postoperative neurological disturbances and myocardial infarction. Renal impairment and need for inotropic drugs were more frequent in the high dose group. Thirty-day mortality was similar (high dose 2%, low dose 0.5%, P=0.22). A low postoperative dose of aprotinin in patients receiving clopidogrel is safe and has comparable effects regarding postoperative bleeding complications as a high dose.
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Øvrum et al. (2010) conducted an RCT in Coronary artery bypass grafting (CABG) in patients receiving clopidogrel (n=399). Aprotinin vs. 75,000 KIU/kg intra- and postoperatively was evaluated on 30-day mortality (p=0.22). A low postoperative dose of aprotinin in patients receiving clopidogrel before CABG is safe, with comparable 30-day mortality (0.5% vs 2%, P=0.22) and bleeding compared to a high dose.
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