Heit J A, Colwell C W, Francis C W, Ginsberg J S, Berkowitz S D, Whipple J, Peters G
Division of Cardiovascular Diseases, Hematology Research, Mayo Clinic, 200 First St SW, Rochester, MN 55905.
Arch Intern Med. 2001 Oct 8;161(18):2215-21. doi: 10.1001/archinte.161.18.2215.
Up to one third of patients who undergo total knee replacement develop deep vein thrombosis after surgery despite receiving low-molecular-weight heparin prophylaxis. Ximelagatran is a novel direct inhibitor of free and clot-bound thrombin.
We performed a randomized, parallel, dose-finding study of 600 adults undergoing elective total knee replacement at 68 North American hospitals to determine the optimum dose of ximelagatran to use as prophylaxis against venous thromboembolism after total knee replacement. Patients received either ximelagatran twice daily by mouth in blinded fixed doses of 8, 12, 18, or 24 mg or open-label enoxaparin sodium, 30 mg, subcutaneously twice daily, starting 12 to 24 hours after surgery and continuing for 6 to 12 days. We measured the 6- to 12-day cumulative incidence of symptomatic or venographic deep vein thrombosis, symptomatic pulmonary embolism, and bleeding.
A total of 594 patients received at least 1 dose of the study drug; 443 patients were evaluable for efficacy. Rates of overall venous thromboembolism (and proximal deep vein thrombosis or pulmonary embolism) for the 8-, 12-, 18-, and 24-mg doses of ximelagatran were 27% (6.6%), 19.8% (2.0%), 28.7% (5.8%), and 15.8% (3.2%), respectively. Rates of overall venous thromboembolism (22.7%) and proximal deep vein thrombosis or pulmonary embolism (3.1%) for enoxaparin did not differ significantly compared with 24-mg ximelagatran (overall difference, -6.9%; 95% confidence interval, -18.0% to 4.2%; P=.3). There was no major bleeding with administration of 24 mg of ximelagatran twice daily.
Fixed-dose, unmonitored ximelagatran, 24 mg twice daily, given after surgery appears to be safe and effective oral prophylaxis against venous thromboembolism after total knee replacement.
尽管接受了低分子量肝素预防治疗,但接受全膝关节置换术的患者中仍有高达三分之一在术后发生深静脉血栓形成。希美加群是一种新型的游离和结合于血栓的凝血酶直接抑制剂。
我们在北美68家医院对600例接受择期全膝关节置换术的成年人进行了一项随机、平行、剂量探索性研究,以确定用于预防全膝关节置换术后静脉血栓栓塞的希美加群最佳剂量。患者在术后12至24小时开始,以盲法固定剂量8、12、18或24毫克每日口服希美加群两次,或皮下注射开放标签的依诺肝素钠30毫克每日两次,持续6至12天。我们测量了有症状或静脉造影证实的深静脉血栓形成、有症状的肺栓塞和出血的6至12天累积发生率。
共有594例患者接受了至少1剂研究药物;443例患者可进行疗效评估。8毫克、12毫克、18毫克和24毫克剂量的希美加群的总体静脉血栓栓塞(以及近端深静脉血栓形成或肺栓塞)发生率分别为27%(6.6%)、19.8%(2.0%)、28.7%(5.8%)和15.8%(3.2%)。依诺肝素的总体静脉血栓栓塞发生率(22.7%)和近端深静脉血栓形成或肺栓塞发生率(3.1%)与24毫克希美加群相比无显著差异(总体差异,-6.9%;95%置信区间,-18.0%至4.2%;P = 0.3)。每日两次给予24毫克希美加群未发生大出血。
术后给予固定剂量、无需监测的希美加群每日两次,每次24毫克,似乎是全膝关节置换术后预防静脉血栓栓塞的安全有效的口服药物。