PMID- 12714021 OWN - NLM STAT- MEDLINE DCOM- 20030626 LR - 20190513 IS - 0195-668X (Print) IS - 0195-668X (Linking) VI - 24 IP - 10 DP - 2003 May TI - Low molecular weight heparin (dalteparin) compared to unfractionated heparin as an adjunct to rt-PA (alteplase) for improvement of coronary artery patency in acute myocardial infarction-the ASSENT Plus study. PG - 897-908 AB - BACKGROUND: Current thrombolytic-antithrombotic regimens in acute myocardialinfarction (AMI) are limited by incomplete early coronary reperfusion and by reocclusion and reinfarction. We compared the effects of low molecular weight heparin (LMWH) versus unfractionated heparin (UFH) as an adjunct to recombinant tissue-plasminogen activator (alteplase) on coronary artery patency and clinical outcomes in AMI. METHODS: Patients with AMI treated with alteplase (n=439) were randomised to either subcutaneous dalteparin (120 IU/kg every 12h) for 4-7 days or intravenous infusion of UFH for 48 h. Coronary angiography was performed between day 4 and hospital discharge. Clinical events and safety were evaluated until day 30. RESULTS: Overall there were higher thrombolysis in myocardial infarction (TIMI) flows in the infarct related coronary artery in the dalteparin group (p=0.016). The predefined primary end-point, TIMI grade 3 flow, did not reach statistical significance (dalteparin 69.3% versus heparin 62.5%; p=0.163). However, TIMI 0-1 flow (13.4 versus 24.4%; p=0.006) and its combination with intraluminal thrombus (27.9 versus 42.0%; p=0.003) were less common in the dalteparin group. During the period of randomised treatment there were less myocardial reinfarctions in the dalteparin group(p=0.010) but after cessation of dalteparin there were more reinfarctions resulting in no difference in death or MI at 30 days. There were no significant differences in major bleeding or stroke after 30 days. CONCLUSIONS: In alteplase treated AMI adjunctive dalteparin for 4-7 days seems to reduce the risk of early coronary artery occlusion and reinfarction. However, early after cessation of treatment there is a raised risk of events, which might eliminate any long-term gains. FAU - Wallentin, Lars AU - Wallentin L AD - Department of Medical Sciences, Cardiology, University Hospital, S-751 85, Uppsala, Sweden. lars.wallentin@thorax.uas.lul.se FAU - Bergstrand, Lott AU - Bergstrand L FAU - Dellborg, Mikael AU - Dellborg M FAU - Fellenius, Carin AU - Fellenius C FAU - Granger, Christopher B AU - Granger CB FAU - Lindahl, Bertil AU - Lindahl B FAU - Lins, Lars Eric AU - Lins LE FAU - Nilsson, Tage AU - Nilsson T FAU - Pehrsson, Kenneth AU - Pehrsson K FAU - Siegbahn, Agneta AU - Siegbahn A FAU - Swahn, Eva AU - Swahn E LA - eng PT - Clinical Trial PT - Comparative Study PT - Journal Article PT - Multicenter Study PT - Randomized Controlled Trial PT - Research Support, Non-U.S. Gov't PL - England TA - Eur Heart J JT - European heart journal JID - 8006263 RN - 0 (Antibodies, Monoclonal) RN - 0 (Anticoagulants) RN - 0 (Heparin, Low-Molecular-Weight) RN - 0 (Immunoglobulin Fab Fragments) RN - 0 (Platelet Aggregation Inhibitors) RN - 9005-49-6 (Heparin) RN - EC 3.4.21.68 (Tissue Plasminogen Activator) RN - R16CO5Y76E (Aspirin) RN - S79O08V79F (Dalteparin) RN - X85G7936GV (Abciximab) SB - IM MH - Abciximab MH - Administration, Cutaneous MH - Aged MH - Antibodies, Monoclonal/administration & dosage MH - Anticoagulants/*administration & dosage MH - Aspirin/administration & dosage MH - Blood Flow Velocity MH - Chemotherapy, Adjuvant MH - Coronary Angiography MH - Dalteparin/administration & dosage MH - Drug Therapy, Combination MH - Female MH - Heparin/*administration & dosage MH - Heparin, Low-Molecular-Weight/administration & dosage MH - Humans MH - Immunoglobulin Fab Fragments/administration & dosage MH - Infusions, Intravenous MH - Male MH - Myocardial Infarction/*drug therapy MH - Myocardial Revascularization MH - Platelet Aggregation Inhibitors/administration & dosage MH - Recurrence MH - Tissue Plasminogen Activator/*administration & dosage MH - Treatment Outcome MH - Vascular Patency EDAT- 2003/04/26 05:00 MHDA- 2003/06/27 05:00 CRDT- 2003/04/26 05:00 PHST- 2003/04/26 05:00 [pubmed] PHST- 2003/06/27 05:00 [medline] PHST- 2003/04/26 05:00 [entrez] AID - S0195668X0300006X [pii] AID - 10.1016/s0195-668x(03)00006-x [doi] PST - ppublish SO - Eur Heart J. 2003 May;24(10):897-908. doi: 10.1016/s0195-668x(03)00006-x.