Contribution of Novel Anticoagulants Fondaparinux and Dabigatran to Venous Thromboembolism Prevention

被引:2
作者
Antonijevic, Nebojsa [1 ,2 ]
Kanjuh, Vladimir [1 ,3 ]
Zivkovic, Ivana [2 ]
Jovanovic, Ljubica [2 ]
Vukcevic, Miodrag [1 ,4 ]
Apostolovic, Milan [1 ,5 ]
机构
[1] Univ Belgrade, Sch Med, Belgrade, Serbia
[2] KIin Ctr Srbije, Klin Kardiol, Beograd 11000, Serbia
[3] Serbian Acad Arts & Sci, Comm Cardiovasc Pathol, Belgrade, Serbia
[4] Med Ctr Bezanijska Kosa, Belgrade, Serbia
[5] Inst Orthoped Surg Banj, Belgrade, Serbia
关键词
prevention; venous thromoembolism; fondaparinux; dabigatran; RANDOMIZED DOUBLE-BLIND; HIP-REPLACEMENT SURGERY; POSTOPERATIVE FONDAPARINUX; ORTHOPEDIC-SURGERY; MEDICAL PATIENTS; ENOXAPARIN; EFFICACY; THERAPY; SAFETY; TRIAL;
D O I
10.2298/SARH1504230A
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
The data that episodes and sequels of venous thromboembolism (VTE) are recorded in a significant percentage of patients receiving standard anticoagulants as VTE prophylaxis (unfractionated, low-molecular-weight heparin and vitamin K inhibitors) as well as the fact that these drugs have significant limitations and that they may cause serious side-effects in some patients indicate the need for the introduction of new anticoagulant drugs. Fondaparinux, a selective inhibitor of Factor Xa, administered following major orthopedic surgeries having a high risk for the development of VIE, is more efficient than enoxaparin sodium used in European and North-American approved doses. The increased incidence of major bleeding (excluding fatal) due to fondaparinux could be perhaps lowered by dosage reduction in patients with a mildly decreased creatinine clearance. Dabigatran, a peroral direct thrombin inhibitor, administered for VIE prophylaxis in elective hip and knee surgery, showed in to date studies the efficacy comparable (if dabigat- ran is given in both dosage regimes of 150 mg and 220 mg daily) or superior (if dabigatran is given at a dose of 220 mg daily) to enoxaparin administered in European-approved doses, while North American-approved doses of enoxaparin were superior than dabigatran in VTE reduction. No significant differences in bleeding rates were determined in any of the study groups. We consider that the introduction of new anticoagulants, including fondaparinux and dabigatran, will contribute to the establishment of a better safety profile and efficacy, and will also enable adequate therapy individualization for each patient depending on his/hers clinical characteristics. The introduction of novel peroral anticoagulants will, inter alia, significantly contribute to improvement in the quality of life, release the patient from numerous limitations in nutrition, interreaction, frequent laboratory monitoring, and also significantly improve therapeutic predictability.
引用
收藏
页码:230 / 236
页数:7
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