Enokiya Tomoyuki, Muraki Yuichi, Iwamoto Takuya, Kawase Ryosuke, Hasegawa Masahiro, Sudo Akihiro, Uchida Atsumasa, Okuda Masahiro
Department of Pharmacy, Mie University Hospital, Tsu, Japan.
Yakugaku Zasshi. 2012;132(5):683-7. doi: 10.1248/yakushi.132.683.
Deep venous thrombosis (DVT) is a life-threatening postoperative complication and occurs frequently after total-knee-replacement arthroplasty (TKA) and total-hip-replacement arthroplasty (THA). Fondaparinux (FPX) has been used to treat and prevent DVT, however interindividual difference of the drug efficacy exists. Therefore, this chart review was retrospectively conducted to research risk factors for a residual DVT after FPX treatment. Total of 112 patients undergone TKA or THA were treated with 2.5 mg FPX once a day between postoperative day (POD) 1 and 14 from July 2007 through December 2008. Among these patients, 30 patients who were detected DVT on POD 4 were enrolled in this study. Thirty patients were divided into two groups according to the presence (n=11) or absence (n=19) of DVT on POD14. The DVT (-) group had a significantly longer activated partial thromboplastin time (APTT, median 31.4 s) on POD 1 than the DVT (+) group (28.5 s) (p<0.02). Multivariate logistic regression analysis revealed that APTT lower than 28.5 seconds on POD1 was considered to be independent risk factor significantly contributing to residual DVT (odds ratio 17.5, 95% confidential interval 2.0-295.4, p=0.02). These findings should provide useful information for understanding the interindividual difference of the efficacy of FPX after TKA or THA.
深静脉血栓形成(DVT)是一种危及生命的术后并发症,全膝关节置换术(TKA)和全髋关节置换术(THA)后经常发生。磺达肝癸钠(FPX)已被用于治疗和预防DVT,然而药物疗效存在个体差异。因此,本图表回顾性研究旨在探究FPX治疗后残留DVT的危险因素。2007年7月至2008年12月期间,共有112例行TKA或THA的患者在术后第1天(POD)至第14天每天接受2.5mg FPX治疗。在这些患者中,30例在POD 4时被检测出DVT的患者被纳入本研究。30例患者根据POD14时DVT的存在与否(n = 11)或不存在(n = 19)分为两组。DVT(-)组在POD 1时的活化部分凝血活酶时间(APTT,中位数31.4秒)明显长于DVT(+)组(28.5秒)(p<0.02)。多因素逻辑回归分析显示,POD1时APTT低于28.5秒被认为是导致残留DVT的独立危险因素(优势比17.5,95%置信区间2.0 - 295.4,p = 0.02)。这些发现应为理解TKA或THA后FPX疗效的个体差异提供有用信息。