Defibrotide versus heparin in the prevention of coronary reocclusion after thrombolysis in acute myocardial infarction
- PMID: 8110625
- DOI: 10.1007/BF00878935
Defibrotide versus heparin in the prevention of coronary reocclusion after thrombolysis in acute myocardial infarction
Abstract
A multicenter controlled study versus heparin was conducted to explore the activity of defibrotide, a polydesoxyribonucleotide drug, in preventing reocclusion after urokinase thrombolysis in patients with acute myocardial infarction (AMI). The study involved 137 consecutive patients with AMI and a time from the onset of symptoms < or = 6 hours, treated with urokinase (1,000,000 U intravenous bolus followed by 1,000,000 U slow-drip infusion over 12 hours). Immediately after thrombolysis, patients were allocated to treatment with defibrotide (group D: day 0, 3.6 g by intravenous infusion in 12 hours; days +1 to +6, 800 mg tid intravenously; days +7 to +10/+12, 400 mg tid intramuscularly), or heparin (group H: day 0, 1000 IU/hour infused over 12 hours; days +1 to +10/+12, 5000 IU tid subcutaneously). Coronary angiography was done, whenever possible, at +10/+12 days. The following parameters were assessed: (a) noninvasive estimate of myocardial reperfusion, through the analysis of CPK time-activity curves; (b) incidence of infarct-related artery (IRA) patency (TIMI scores 2-3) at coronary angiography. A total of 125 patients had a complete enzymatic curve (63 in group D and 62 in group H) and 106 had coronary angiography as well. IRA patency (the main end point) was observed in 63% of group D versus 43% of group H patients (p = 0.07). No statistically significant differences were found in the proportion of patients with indirect signs of early reperfusion (63% in group D versus 52% in group H patients).(ABSTRACT TRUNCATED AT 250 WORDS)
Similar articles
-
Thrombolysis with recombinant unglycosylated single-chain urokinase-type plasminogen activator (saruplase) in acute myocardial infarction: influence of heparin on early patency rate (LIMITS study). Liquemin in Myocardial Infarction During Thrombolysis With Saruplase.J Am Coll Cardiol. 1995 Aug;26(2):365-73. doi: 10.1016/0735-1097(95)80008-5. J Am Coll Cardiol. 1995. PMID: 7608436 Clinical Trial.
-
A pilot trial of recombinant desulfatohirudin compared with heparin in conjunction with tissue-type plasminogen activator and aspirin for acute myocardial infarction: results of the Thrombolysis in Myocardial Infarction (TIMI) 5 trial.J Am Coll Cardiol. 1994 Apr;23(5):993-1003. doi: 10.1016/0735-1097(94)90581-9. J Am Coll Cardiol. 1994. PMID: 8144799 Clinical Trial.
-
High dose bolus heparin as initial therapy before primary angioplasty for acute myocardial infarction: results of the Heparin in Early Patency (HEAP) pilot study.J Am Coll Cardiol. 1998 Feb;31(2):289-93. doi: 10.1016/s0735-1097(97)00495-6. J Am Coll Cardiol. 1998. PMID: 9462569
-
Adjunctive use of direct thrombin inhibitors in patients receiving fibrinolytic therapy for acute myocardial infarction.Am J Cardiovasc Drugs. 2004;4(2):107-15. doi: 10.2165/00129784-200404020-00004. Am J Cardiovasc Drugs. 2004. PMID: 15049722 Review.
-
Reocclusion: the flip side of coronary thrombolysis.J Am Coll Cardiol. 1996 Mar 15;27(4):766-73. doi: 10.1016/0735-1097(95)00492-0. J Am Coll Cardiol. 1996. PMID: 8613601 Review.
Cited by
-
The use of defibrotide in blood and marrow transplantation.Blood Adv. 2018 Jun 26;2(12):1495-1509. doi: 10.1182/bloodadvances.2017008375. Blood Adv. 2018. PMID: 29945939 Free PMC article. Review.
-
Diagnosis and Treatment of VOD/SOS After Allogeneic Hematopoietic Stem Cell Transplantation.Front Immunol. 2020 Apr 3;11:489. doi: 10.3389/fimmu.2020.00489. eCollection 2020. Front Immunol. 2020. PMID: 32318059 Free PMC article. Review.
-
A Meta-Analysis Evaluating the Incidence of Bleeding Events With Intravenous Defibrotide Treatment Outside the Veno-Occlusive Disease/Sinusoidal Obstruction Syndrome Setting.Clin Appl Thromb Hemost. 2020 Jan-Dec;26:1076029620935202. doi: 10.1177/1076029620935202. Clin Appl Thromb Hemost. 2020. PMID: 32687402 Free PMC article.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Medical