Efficacy of tranexamic acid on blood loss after primary cementless total hip replacement with rivaroxaban thromboprophylaxis: A case-control study in 70 patients

被引:56
作者
Clave, A. [1 ,2 ]
Fazilleau, F. [1 ,2 ]
Dumser, D. [3 ]
Lacroix, J. [4 ]
机构
[1] Western Britany Univ, Fac Med, F-29285 Brest, France
[2] La Cavale Blanche Univ Hosp Ctr, Orthoped & Traumatol Surg Dept, F-29200 Brest, France
[3] Les Pays Morlaix Hosp Ctr, Anesthesia & Intens Care Dept, F-29600 Morlaix, France
[4] Les Pays Morlaix Hosp Ctr, Orthoped & Traumatol Surg Dept, F-29600 Morlaix, France
关键词
Total hip replacement; Blood loss; Tranexamic acid; Rivaroxaban; ORTHOPEDIC-SURGERY; RANDOMIZED-TRIALS; ARTHROPLASTY; TRANSFUSION; CONSERVATION; METAANALYSIS; MANAGEMENT; MORTALITY; KNEE;
D O I
10.1016/j.otsr.2011.12.005
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Introduction: Perioperative blood loss is a frequent cause of complications in total hip replacement (THR). The present prospective study assessed the efficacy of tranexamic acid (Exacyl (R)) in reducing blood loss in primary THR associated to rivaroxaban (Xarelto (R)) thromboprophylaxis. Hypothesis: Tranexamic acid associated to rivaroxaban reduces blood loss. Material and method: A prospective case-control study included 70 primary cementless THRs performed by a single surgeon on a standardized technique, between September 2009 and September 2010. Thirty-seven patients received perioperative tranexamic acid; all patients received rivaroxaban thromboprophylaxis. Results: There was no significant difference between the two groups in terms of peroperative blood-loss volume or rates of thromboembolic or ischemic events or hematoma. Postoperative blood loss, D0-5 differential hemoglobinemia and real blood loss (in mL 100% hematocrit) were significantly lower in the tranexamic acid group. No transfusions were required in the tranexamic acid group, versus four in the control group. Discussion: Tranexamic acid associated to direct anti-Xa (antithrombin-independent) oral anticoagulants was effective in reducing postoperative blood loss, improving hemoglobinemia at 5 days and reducing transfusion rates. The results also confirmed the efficacy of and tolerance for rivaroxaban thromboprophylaxis in primary THR, with no clinical thrombotic events induced by the association of tranexamic acid with rivaroxaban. Conclusions: Tranexamic acid is a simple means of reducing postoperative blood loss in THR, without increased risk of thromboembolism when associated to rivaroxaban thromboprophylaxis. Level of evidence: Level III prospective case-control study. (C) 2012 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:484 / 490
页数:7
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