Effects of recombinant hirudin (lepirudin) compared with heparin on death, myocardial infarction, refractory angina, and revascularisation procedures in patients with acute myocardial ischaemia without ST elevation: a randomised trial. Organisation to Assess Strategies for Ischemic Syndromes (OASIS-2) Investigators
- PMID: 9989712
Effects of recombinant hirudin (lepirudin) compared with heparin on death, myocardial infarction, refractory angina, and revascularisation procedures in patients with acute myocardial ischaemia without ST elevation: a randomised trial. Organisation to Assess Strategies for Ischemic Syndromes (OASIS-2) Investigators
Abstract
Background: Despite the use of heparin and aspirin, 5-10% of patients with unstable angina develop myocardial infarction or refractory angina in hospital. We tested the hypothesis that recombinant hirudin (lepirudin), a direct thrombin inhibitor, would be superior to heparin, an indirect thrombin inhibitor, in patients with acute ischaemic syndromes who were receiving aspirin.
Methods: 10,141 patients with unstable angina or suspected acute myocardial infarction without ST elevation were randomly assigned heparin (5000 units bolus then 15 units kg(-1) h(-1); n=5058) or hirudin (0.4 mg/kg bolus then 0.15 mg kg(-1) h(-1) infusion; n=5083) for 72 h in a double-blind trial. The primary outcome measure was cardiovascular death or new myocardial infarction at 7 days. Analysis was by intention to treat.
Findings: At 7 days, 213 (4.2%) patients in the heparin group and 182 (3.6%) in the hirudin group had experienced cardiovascular death or new myocardial infarction (relative risk 0.84 [95% CI 0.69-1.02]; p=0.077). The numbers with cardiovascular death, new myocardial infarction, or refractory angina at 7 days were 340 (6.7%) with heparin and 284 (5.6%) with hirudin (0.82 [0.70-0.96]; p=0.0125). These differences were primarily observed during the 72 h treatment period (cardiovascular death or myocardial infarction relative risk 0.76 [0.59-0.99], p=0.039: cardiovascular death, myocardial infarction, or refractory angina 0.78 [0.63-0.96], p=0.019). Although there was an excess of major bleeding requiring transfusion with hirudin (59 [1.2%] vs 34 [0.7%] with heparin; p=0.01), there was no excess in life-threatening episodes (20 in each group) or strokes (14 in each group).
Interpretation: The data from OASIS-2 suggest that recombinant hirudin is superior to heparin in preventing cardiovascular death, myocardial infarction, and refractory angina with an acceptable safety profile in patients with unstable angina or acute myocardial infarction without ST elevation. Thus, a direct thrombin inhibitor is more effective than an indirect thrombin inhibitor.
Comment in
-
New antithrombotic treatment in unstable coronary syndrome--for whom?Lancet. 1999 Feb 6;353(9151):423-4. doi: 10.1016/S0140-6736(98)00362-6. Lancet. 1999. PMID: 9989707 No abstract available.
Similar articles
-
Design, baseline characteristics, and preliminary clinical results of the Organization to Assess Strategies for Ischemic Syndromes-2 (OASIS-2) trial.Am J Cardiol. 1999 Sep 2;84(5A):20M-25M. doi: 10.1016/s0002-9149(99)00549-4. Am J Cardiol. 1999. PMID: 10505539 Clinical Trial.
-
Comparison of the effects of two doses of recombinant hirudin compared with heparin in patients with acute myocardial ischemia without ST elevation: a pilot study. Organization to Assess Strategies for Ischemic Syndromes (OASIS) Investigators.Circulation. 1997 Aug 5;96(3):769-77. doi: 10.1161/01.cir.96.3.769. Circulation. 1997. PMID: 9264481 Clinical Trial.
-
Reactivation of coagulation after stopping infusions of recombinant hirudin and unfractionated heparin in unstable angina and myocardial infarction without ST elevation: results of a randomized trial. OASIS Pilot Study Investigators. Organization to Assess Strategies for Ischemic++ Syndromes.Eur Heart J. 2000 Sep;21(17):1473-81. doi: 10.1053/euhj.1999.2005. Eur Heart J. 2000. PMID: 10952840 Clinical Trial.
-
Bivalirudin: a review of its potential place in the management of acute coronary syndromes.Drugs. 2002;62(5):841-70. doi: 10.2165/00003495-200262050-00008. Drugs. 2002. PMID: 11929334 Review.
-
Anticoagulants in acute coronary syndromes.Am J Cardiol. 1999 Sep 2;84(5A):2M-6M. doi: 10.1016/s0002-9149(99)00490-7. Am J Cardiol. 1999. PMID: 10505536 Review.
Cited by
-
Anticoagulation for acute coronary syndromes and percutaneous coronary intervention in patients with heparin-induced thrombocytopenia.Curr Cardiol Rep. 2001 Sep;3(5):362-70. doi: 10.1007/s11886-001-0052-7. Curr Cardiol Rep. 2001. PMID: 11504572 Review.
-
Crystal structure of Enterobacter cloacae 908R class C beta-lactamase bound to iodo-acetamido-phenyl boronic acid, a transition-state analogue.Cell Mol Life Sci. 2003 Aug;60(8):1764-73. doi: 10.1007/s00018-003-3189-2. Cell Mol Life Sci. 2003. PMID: 14521155 Free PMC article.
-
Costs and cost effectiveness of low molecular weight heparins and platelet glycoprotein IIb/IIIa inhibitors: in the management of acute coronary syndromes.Pharmacoeconomics. 2003;21(16):1135-52. doi: 10.2165/00019053-200321160-00001. Pharmacoeconomics. 2003. PMID: 14594436 Review.
-
The risks of waiting for cardiac catheterization: a prospective study.CMAJ. 2002 Nov 26;167(11):1233-40. CMAJ. 2002. PMID: 12451076 Free PMC article.
-
Evolution of anticoagulant and antiplatelet therapy: benefits and risks of contemporary pharmacologic agents and their implications for myonecrosis and bleeding in percutaneous coronary intervention.Clin Cardiol. 2007 Oct;30(10 Suppl 2):II4-15. doi: 10.1002/clc.20237. Clin Cardiol. 2007. PMID: 18228647 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical