Surgery and invasive procedures in patients on long-term treatment with oral direct thrombin or factor Xa inhibitors

被引:24
作者
Sie, P. [1 ]
Samama, C. -M. [2 ]
Godier, A. [2 ]
Rosencher, N. [3 ]
Steib, A. [4 ]
Llau, J. -V. [5 ]
van der Linden, P. [6 ]
Pernod, G. [7 ]
Lecompte, T. [8 ]
Gouin-Thibault, I. [9 ]
Albaladejo, P. [7 ]
机构
[1] CHU Toulouse, Hop Rangueil, Hematol Lab, F-31059 Toulouse, France
[2] Hop Hotel Dieu, AP HP, Serv Anesthesie Reanimat, F-75181 Paris 04, France
[3] Hop Cochin, AP HP, 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, HUDERF, Anesthesiol Serv, B-1020 Brussels, Belgium
[7] CHU Grenoble, F-38043 Grenoble 09, France
[8] Hop Cent, Lab Hematol Biol, F-54035 Nancy, France
[9] AP HP, IGT, F-94200 Ivry, France
来源
ANNALES FRANCAISES D ANESTHESIE ET DE REANIMATION | 2011年 / 30卷 / 09期
关键词
Surgery; Bleeding; Thrombosis; Oral anticoagulants; Thrombin; Factor Xa; inhibitors; RECOMBINANT FACTOR VIIA; DABIGATRAN ETEXILATE; BLEEDING-TIME; RIVAROXABAN; WARFARIN; SAFETY; ANTICOAGULATION; GENERATION; PREVENTION; REVERSAL;
D O I
10.1016/j.annfar.2011.06.018
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Direct oral anticoagulants (DOAs), inhibitors of factor IIa 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 48 h (last administration 24 h before surgery, restart 24 h after) 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), 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. (C) 2011 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:645 / 650
页数:6
相关论文
共 26 条
[1]   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
[2]  
BULLER HR, 2009, BLOOD, P114
[3]   Dabigatran versus Warfarin in Patients with Atrial Fibrillation. [J].
Connolly, Stuart J. ;
Ezekowitz, Michael D. ;
Yusuf, Salim ;
Eikelboom, John ;
Oldgren, Jonas ;
Parekh, Amit ;
Pogue, Janice ;
Reilly, Paul A. ;
Themeles, Ellison ;
Varrone, Jeanne ;
Wang, Susan ;
Alings, Marco ;
Xavier, Denis ;
Zhu, Jun ;
Diaz, Rafael ;
Lewis, Basil S. ;
Darius, Harald ;
Diener, Hans-Christoph ;
Joyner, Campbell D. ;
Wallentin, Lars .
NEW ENGLAND JOURNAL OF MEDICINE, 2009, 361 (12) :1139-1151
[4]   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
[5]   Perioperative anticoagulation management in patients who are receiving oral anticoagulant therapy: a practical guide for clinicians [J].
Douketis, JD .
THROMBOSIS RESEARCH, 2002, 108 (01) :3-13
[6]   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
[7]   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
[8]   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
[9]   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
[10]   Coagulation parameters in patients receiving dabigatran etexilate or rivaroxaban: Two observational studies in patients undergoing total hip or total knee replacement [J].
Freyburger, Genevieve ;
Macouillard, Gerard ;
Labrouche, Sylvie ;
Sztark, Francois .
THROMBOSIS RESEARCH, 2011, 127 (05) :457-465