Surgery and invasive procedures in patients on long term treatment with oral direct thrombin or factor Xa inhibitors (update 2012)

被引:1
作者
Sie, Pierre [1 ]
Samama, Charles Marc [2 ]
Godier, Anne [2 ]
Rosencher, Nadia [3 ]
Steib, Annick [4 ]
Llau, Juan V. [5 ]
van der Linden, Philippe [6 ]
Pernod, Gilles [7 ]
Lecompte, Thomas [8 ]
Gouin-Thibault, Isabelle [9 ]
Albaladejo, Pierre
机构
[1] CHU Toulouse, Hop Rangueil, Lab Hematol, F-31059 Toulouse, France
[2] Hop Hotel Dieu, Serv Anesthesie Reanimat, F-75181 Paris 04, France
[3] Hop Cochin, Dept Anesthesie Reanimat, F-75014 Paris, France
[4] Hop Civil, Dept Anesthesiol, F-37091 Strasbourg, France
[5] Serv Anesthesie Reanimat, Valencia, Spain
[6] CHU Brugmann, Serv Anesthesie Reanimat, HUDERF, B-1020 Brussels, Belgium
[7] CHU Grenoble, Serv Med Vasc, F-38043 Grenoble 09, France
[8] Serv Hematol, Geneva, Switzerland
[9] IGT, F-94200 Ivry, France
来源
SANG THROMBOSE VAISSEAUX | 2012年 / 24卷 / 06期
关键词
surgery; bleeding; thrombosis; oral anticoagulants; thrombin; factor Xa inhibitors; PROTHROMBIN COMPLEX CONCENTRATE; RECOMBINANT FACTOR VIIA; ACTIVATED FACTOR-VII; ANTICOAGULANTS DABIGATRAN; COAGULATION ASSAYS; BLEEDING-TIME; RIVAROXABAN; REVERSAL; WARFARIN; SAFETY;
D O I
10.1684/stv.2012.0716
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Surgery and invasive procedures in patients on long term treatment with oral direct thrombin or factor Xa inhibitors (update 2012) Direct Oral Anticoagulants (DOAs), inhibitors of factor Ila or Xa, are expected to replace vitamin K antagonists in most of their indications. It is likely that patients on long-term treatment with DOAs will be exposed to elective or emergency surgery or invasive procedures. Due to the present lack of experience in such conditions, we cannot make recommendations, but only propose perioperative management for optimal safety as regards the risk of bleeding and thrombosis. DOAs may increase surgical bleeding, they have no validated antagonists, they cannot be monitored by simple, standardised laboratory assays, and their pharmacokinetics vary significantly from patient to patient. Although DOAs differ in many respects, the proposals in the perioperative setting need not be specific to each. For procedures with low risk of haemorrhage, a therapeutic window of 48h is proposed. For procedures with medium or high haemorrhagic risk, we suggest stopping DOAs 5 days before surgery to ensure complete elimination of the drug in all patients. The treatment should be resumed only when the risk of bleeding has been controlled. In patients with a high risk of thrombosis (e.g. those in atrial fibrillation with an antecedent of stroke or recent venous thromboembolic event), bridging with heparin (low molecular weight, or unfractionated if the former is contraindicated) is proposed. In emergency, the procedure should be postponed for as long as possible (minimum 1-2 half-lives) and non-specific anti-haemorrhagic agents, such as recombinant human activated factor Vila, or prothrombin concentrates, should not be given for prophylactic reversal, due to their uncertain benefit-risk.
引用
收藏
页码:269 / 278
页数:10
相关论文
共 35 条
[1]  
[Anonymous], BLOOD
[2]   Oral Rivaroxaban for Symptomatic Venous Thromboembolism. [J].
Bauersachs, Rupert ;
Berkowitz, Scott D. ;
Brenner, Benjamin ;
Buller, Harry R. ;
Decousus, Herve ;
Gallus, Alex S. ;
Lensing, Anthonie W. ;
Misselwitz, Frank ;
Prins, Martin H. ;
Raskob, Gary E. ;
Segers, Annelise ;
Verhamme, Peter ;
Wells, Phil ;
Agnelli, Giancarlo ;
Bounameaux, Henri ;
Cohen, Alexander ;
Davidson, Bruce L. ;
Piovella, Franco ;
Schellong, Sebastian .
NEW ENGLAND JOURNAL OF MEDICINE, 2010, 363 (26) :2499-2510
[3]   Reversal of the inhibitory effect of Fondaparinux on Thrombin generation by rFVIIa, aCCP and PCC [J].
Desmurs-Clavel, H. ;
Huchon, C. ;
Chatard, B. ;
Negrier, C. ;
Dargaud, Y. .
THROMBOSIS RESEARCH, 2009, 123 (05) :796-798
[4]   Perioperative Management of Antithrombotic Therapy Antithrombotic Therapy and Prevention of Thrombosis, 9th ed: American College of Chest Physicians Evidence- Based Clinical Practice Guidelines [J].
Douketis, James D. ;
Spyropoulos, Alex C. ;
Spencer, Frederick A. ;
Mayr, Michael ;
Jaffer, Amir K. ;
Eckman, Mark H. ;
Dunn, Andrew S. ;
Kunz, Regina .
CHEST, 2012, 141 (02) :E326S-E350S
[5]   Impact of dabigatran on a large panel of routine or specific coagulation assays Laboratory recommendations for monitoring of dabigatran etexilate [J].
Douxfils, Jonathan ;
Mullier, Francois ;
Robert, Severine ;
Chatelain, Christian ;
Chatelain, Bernard ;
Dogne, Jean-Michel .
THROMBOSIS AND HAEMOSTASIS, 2012, 107 (05) :985-997
[6]   Reversal of Rivaroxaban and Dabigatran by Prothrombin Complex Concentrate A Randomized, Placebo-Controlled, Crossover Study in Healthy Subjects [J].
Eerenberg, Elise S. ;
Kamphuisen, Pieter W. ;
Sijpkens, Meertien K. ;
Meijers, Joost C. ;
Buller, Harry R. ;
Levi, Marcel .
CIRCULATION, 2011, 124 (14) :1573-1579
[7]   Effects of agents, used to treat bleeding disorders, on bleeding time prolonged by a very high dose of a direct thrombin inhibitor in anesthesized rats and rabbits [J].
Elg, M ;
Carlsson, S ;
Gustafsson, D .
THROMBOSIS RESEARCH, 2001, 101 (03) :159-170
[8]   Effect of activated prothrombin complex concentrate or recombinant factor VIIa on the bleeding time and thrombus formation during anticoagulation with a direct thrombin inhibitor [J].
Elg, M ;
Carlsson, S ;
Gustafsson, D .
THROMBOSIS RESEARCH, 2001, 101 (03) :145-157
[9]   Dose escalating safety study of a new oral direct thrombin inhibitor, dabigatran etexilate, in patients undergoing total hip replacement:: BISTRO I [J].
Eriksson, BI ;
Dahl, OE ;
Ahnfelt, L ;
Kälebo, P ;
Stangier, J ;
Nehmiz, G ;
Hermansson, K ;
Kohlbrenner, V .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2004, 2 (09) :1573-1580
[10]   Dabigatran with or without concomitant Aspirin compared with Warfarin alone in patients with nonvalvular atrial fibrillation (PETRO study) [J].
Ezekowitz, Michael D. ;
Reilly, Paul A. ;
Nehmiz, Gerhard ;
Simmers, Timothy A. ;
Nagarakanti, Rangadham ;
Parcham-Azad, Kambiz ;
Pedersen, K. Erik ;
Lionetti, Dominick A. ;
Stangier, Joachim ;
Wallentin, Lars .
AMERICAN JOURNAL OF CARDIOLOGY, 2007, 100 (09) :1419-1426