Prevention of one-year vein-graft occlusion after aortocoronary-bypass surgery: a comparison of low-dose aspirin, low-dose aspirin plus dipyridamole, and oral anticoagulants. The CABADAS Research Group of the Interuniversity Cardiology Institute of The Netherlands
- PMID: 8101300
- DOI: 10.1016/0140-6736(93)91815-4
Prevention of one-year vein-graft occlusion after aortocoronary-bypass surgery: a comparison of low-dose aspirin, low-dose aspirin plus dipyridamole, and oral anticoagulants. The CABADAS Research Group of the Interuniversity Cardiology Institute of The Netherlands
Erratum in
- Lancet 1993 Sep 11;342(8872):690
Abstract
Aspirin, alone or in combination with dipyridamole, is known to prevent occlusion of aortocoronary vein grafts. The benefit of dipyridamole in addition to aspirin remains controversial, and the efficacy and safety of oral anticoagulants for prevention of vein-graft occlusion have not been established. We assessed one-year angiographic vein-graft patency after aortocoronary-bypass surgery in 948 patients assigned to receive aspirin, aspirin plus dipyridamole, or oral anticoagulants in a prospective, randomised trial. The design was double-blind and placebo-controlled for the aspirin groups, but open for oral anticoagulant treatment. Dipyridamole (5 mg/kg per 24 h intravenously for 28 h, followed by 200 mg twice daily) and oral anticoagulants (desired prothrombin time range 2.8-4.8 international normalised ratio) were started before surgery, and aspirin (50 mg per day) was started after surgery. Clinical outcome was assessed by the incidence of myocardial infarction, thrombosis, major bleeding, or death. Occlusion rate of distal anastomoses was 11% in the aspirin plus dipyridamole group versus 15% in the aspirin group (relative risk 0.76, 95% CI 0.54-1.05) and 13% in the oral anticoagulants group. Clinical events occurred in 20.3% of patients receiving aspirin plus dipyridamole compared with 13.9% of the aspirin group (relative risk 1.46, 95% CI 1.02-2.08) and 16.9% of the oral anticoagulants group. Our data provide no convincing evidence that addition of dipyridamole to 50 mg aspirin per day improves aortocoronary vein-graft patency. Moreover, there is evidence that the combination increases the overall clinical-event rate. Compared with aspirin, oral anticoagulants provided no benefit.
Comment in
- ACP J Club. 1994 Jan-Feb;120 Suppl 1:7
-
Prevention of graft occlusion by aspirin, dipyridamole, and oral anticoagulants.Lancet. 1993 Sep 25;342(8874):806; author reply 807. Lancet. 1993. PMID: 8103893 No abstract available.
-
Prevention of graft occlusion by aspirin, dipyridamole, and oral anticoagulants.Lancet. 1993 Sep 25;342(8874):806-7. Lancet. 1993. PMID: 8103894 No abstract available.
Similar articles
-
Effects of low dose aspirin (50 mg/day), low dose aspirin plus dipyridamole, and oral anticoagulant agents after internal mammary artery bypass grafting: patency and clinical outcome at 1 year. CABADAS Research Group of the Interuniversity Cardiology Institute of The Netherlands. Prevention of Coronary Artery Bypass Graft Occlusion by Aspirin, Dipyridamole and Acenocoumarol/Phenprocoumon Study.J Am Coll Cardiol. 1994 Nov 1;24(5):1181-8. doi: 10.1016/0735-1097(94)90096-5. J Am Coll Cardiol. 1994. PMID: 7930237 Clinical Trial.
-
Effect of various antithrombotic regimens (aspirin, aspirin plus dipyridamole, anticoagulants) on the functional status of patients and grafts one year after coronary artery bypass grafting.Eur Heart J. 1994 Aug;15(8):1129-34. doi: 10.1093/oxfordjournals.eurheartj.a060639. Eur Heart J. 1994. PMID: 7988607 Clinical Trial.
-
Trial of low-dose aspirin plus dipyridamole versus anticoagulants for prevention of aortocoronary vein graft occlusion.Lancet. 1989 Jul 1;2(8653):1-7. doi: 10.1016/s0140-6736(89)90253-5. Lancet. 1989. PMID: 2567792 Clinical Trial.
-
Systematic review of randomized controlled trials of aspirin and oral anticoagulants in the prevention of graft occlusion and ischemic events after infrainguinal bypass surgery.J Vasc Surg. 1999 Oct;30(4):701-9. doi: 10.1016/s0741-5214(99)70109-6. J Vasc Surg. 1999. PMID: 10514209
-
Clinical trials evaluating platelet-modifying drugs in patients with atherosclerotic cardiovascular disease and thrombosis.Circulation. 1986 Feb;73(2):206-23. doi: 10.1161/01.cir.73.2.206. Circulation. 1986. PMID: 3510760 Review.
Cited by
-
Collaborative overview of randomised trials of antiplatelet therapy--II: Maintenance of vascular graft or arterial patency by antiplatelet therapy. Antiplatelet Trialists' Collaboration.BMJ. 1994 Jan 15;308(6922):159-68. BMJ. 1994. PMID: 8312766 Free PMC article. Review.
-
Role of patient compliance in clinical pharmacokinetics. A review of recent research.Clin Pharmacokinet. 1994 Sep;27(3):202-15. doi: 10.2165/00003088-199427030-00004. Clin Pharmacokinet. 1994. PMID: 7988102 Review.
-
Vein graft failure: from pathophysiology to clinical outcomes.Nat Rev Cardiol. 2016 Aug;13(8):451-70. doi: 10.1038/nrcardio.2016.76. Epub 2016 May 19. Nat Rev Cardiol. 2016. PMID: 27194091 Review.
-
Collaborative overview of randomised trials of antiplatelet therapy--I: Prevention of death, myocardial infarction, and stroke by prolonged antiplatelet therapy in various categories of patients. Antiplatelet Trialists' Collaboration.BMJ. 1994 Jan 8;308(6921):81-106. BMJ. 1994. PMID: 8298418 Free PMC article.
-
Antiplatelet therapy with CABG: chaos in the Netherlands.Neth Heart J. 2017 Sep;25(9):479-480. doi: 10.1007/s12471-017-1022-z. Neth Heart J. 2017. PMID: 28707229 Free PMC article. No abstract available.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical