2005
DOI: 10.1002/bjs.5154
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Randomized clinical trial of postoperative fondaparinux versus perioperative dalteparin for prevention of venous thromboembolism in high-risk abdominal surgery

Abstract: Postoperative fondaparinux was at least as effective as perioperative dalteparin in patients undergoing high-risk abdominal surgery.

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Cited by 325 publications
(190 citation statements)
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“…1), supporting the adequacy of the prophylactic dose of 2.5 mg of fondaparinux and in accord with the substantial efficacy data already available with respect to a dose of 2.5 mg of fondaparinux in various clinical settings. [20][21][22][23] We chose a 45-day duration of treatment with the specific objective of avoiding the "catch-up" phenomenon observed with shorter (up to 30-day) courses of low-molecular-weight heparin. 6,17 This objective was met, since the efficacy of fondaparinux efficacy was maintained through day 77.…”
Section: By Day 47mentioning
confidence: 99%
“…1), supporting the adequacy of the prophylactic dose of 2.5 mg of fondaparinux and in accord with the substantial efficacy data already available with respect to a dose of 2.5 mg of fondaparinux in various clinical settings. [20][21][22][23] We chose a 45-day duration of treatment with the specific objective of avoiding the "catch-up" phenomenon observed with shorter (up to 30-day) courses of low-molecular-weight heparin. 6,17 This objective was met, since the efficacy of fondaparinux efficacy was maintained through day 77.…”
Section: By Day 47mentioning
confidence: 99%
“…Guidelines have been established on the necessity, intensity and duration of postoperative antithrombotic prophylaxis. 1 While the optimal postoperative antithrombotic management has been well defined 2 for most types of abdominal surgery, the postoperative risk and antithrombotic prophylaxis after splenectomy have not been studied systematically, although the risk may be considerable in some groups of patients.…”
Section: Introductionmentioning
confidence: 99%
“…Th is could lead to a conclusion that patients on fondaparinux have less need for postoperative allotransfusion due to the less intraoperative and early postoperative bleeding. A recent study by Hosaka et al 10 confi rmed the opinions from previous studies that excessive bleeding can be expected in patients undergoing surgery and receiving fondaparinux 5,12,[15][16][17] . In their study, Hosaka et al assessed the safety of fondaparinux versus enoxaparin after TKA in Japanese patients and concluded that thigh swelling and subcutaneous hematomas were greater in the fondaparinux group.…”
Section: Discussionmentioning
confidence: 71%