PMID- 20659761 OWN - NLM STAT- MEDLINE DCOM- 20101228 LR - 20151119 IS - 1879-2472 (Electronic) IS - 0049-3848 (Linking) VI - 126 IP - 3 DP - 2010 Sep TI - In vitro comparison of dabigatran, unfractionated heparin, and low-molecular-weight heparin in preventing thrombus formation on mechanical heart valves. PG - e196-200 LID - 10.1016/j.thromres.2010.06.011 [doi] AB - INTRODUCTION: Lifelong oral anticoagulation (OAC) therapy is required for the prevention of thromboembolic events after implantation of an artificial heart valve. Thromboembolism and anticoagulant-related bleedings account for approximately 75% of all complications experienced by heart valve recipients (2-9% of patients per year). The present study investigated the efficacy of dabigatran, a new direct thrombin inhibitor for oral use, as compared to unfractionated heparin (UFH) and low-molecular-weight heparin (LMWH) in preventing thrombus formation on mechanical heart valves in vitro. MATERIAL AND METHODS: Blood (230 ml) from healthy young male volunteers was anticoagulated either by dabigatran (1 micromol/l), UFH (150 IU), or LMWH (100 IU). Mechanical heart valve prostheses were placed in an in vitro thrombosis tester and exposed to the anticoagulated blood samples under continuous circulation at a rate of 75 beats per minute. RESULTS: In whole blood with no anticoagulant, the apparatus completely clotted in 15-20 minutes. When blood was treated with dabigatran, the mean thrombus weight was 164+/-55 mg, in the UFH group 159+/-69 mg, and in the LMWH group 182+/-82 mg (p-value: 0.704). Electron microscopy showed no significant difference in thrombus formation in any group. CONCLUSIONS: Dabigatran was as effective as UFH and LMWH in preventing thrombus formation on mechanical heart valves in our in vitro investigation. Thus, we hypothesize that dabigatran etexilate might potentially be a useful and competitive orally administered alternative to UFH and LMWH for recipients of alloplastic heart valve prostheses. CI - Copyright (c) 2010 Elsevier Ltd. All rights reserved. FAU - Maegdefessel, Lars AU - Maegdefessel L AD - Department of Medicine III at the University Hospital Haale (Saale), Martin-Luther-University Halle-Wittenberg, Germany. maegdefessel@stanford.edu FAU - Linde, Torsten AU - Linde T FAU - Krapiec, Franziska AU - Krapiec F FAU - Hamilton, Kathrin AU - Hamilton K FAU - Steinseifer, Ulrich AU - Steinseifer U FAU - van Ryn, Joanne AU - van Ryn J FAU - Raaz, Uwe AU - Raaz U FAU - Buerke, Michael AU - Buerke M FAU - Werdan, Karl AU - Werdan K FAU - Schlitt, Axel AU - Schlitt A LA - eng PT - Comparative Study PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20100724 PL - United States TA - Thromb Res JT - Thrombosis research JID - 0326377 RN - 0 (Anticoagulants) RN - 0 (Benzimidazoles) RN - 0 (Fibrinolytic Agents) RN - 0 (Heparin, Low-Molecular-Weight) RN - 0 (Pyridines) RN - 9005-49-6 (Heparin) RN - I0VM4M70GC (Dabigatran) SB - IM MH - Administration, Oral MH - Anticoagulants/administration & dosage/*pharmacology MH - Benzimidazoles/administration & dosage/*pharmacology MH - Blood Coagulation/*drug effects MH - Dabigatran MH - Fibrinolytic Agents/administration & dosage/*pharmacology MH - Heart Valve Prosthesis/*adverse effects MH - Heparin/administration & dosage/*pharmacology MH - Heparin, Low-Molecular-Weight/administration & dosage/*pharmacology MH - Humans MH - Male MH - Prosthesis Design MH - Pyridines/administration & dosage/*pharmacology MH - Thrombosis/blood/etiology/*prevention & control MH - Time Factors EDAT- 2010/07/28 06:00 MHDA- 2010/12/29 06:00 CRDT- 2010/07/28 06:00 PHST- 2010/03/08 00:00 [received] PHST- 2010/06/15 00:00 [revised] PHST- 2010/06/16 00:00 [accepted] PHST- 2010/07/28 06:00 [entrez] PHST- 2010/07/28 06:00 [pubmed] PHST- 2010/12/29 06:00 [medline] AID - S0049-3848(10)00350-6 [pii] AID - 10.1016/j.thromres.2010.06.011 [doi] PST - ppublish SO - Thromb Res. 2010 Sep;126(3):e196-200. doi: 10.1016/j.thromres.2010.06.011. Epub 2010 Jul 24.