Rivaroxaban versus nadroparin for preventing deep venous thrombosis after total hip arthroplasty following femoral neck fractures: A retrospective comparative study

被引:9
|
作者
Zhang, Chi [1 ]
Xu, Bo [2 ]
Liang, Guanzhao [3 ]
Zeng, Xianshang [4 ]
Yang, Chen [5 ]
Zhang, Fan [6 ]
Wan, Zi [7 ]
Yu, Weiguang [4 ]
Chen, Deng [8 ]
Ge, Zhe [9 ]
Zhang, Xinchao [9 ]
机构
[1] Guangzhou Med Univ, Dept Joint Surg, Affiliated Hosp 3, Guangzhou, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, Dept Thorac Surg, Affiliated Hosp 1, Guangzhou, Guangdong, Peoples R China
[3] Sun Yat Sen Univ, Emergency Dept, Affiliated Hosp 1, Guangzhou, Guangdong, Peoples R China
[4] Sun Yat Sen Univ, Dept Orthopaed, Affiliated Hosp 1, Guangzhou, Guangdong, Peoples R China
[5] Sun Yat Sen Univ, Dept Phys Examinat, Affiliated Hosp 1, Guangzhou, Guangdong, Peoples R China
[6] Sun Yat Sen Univ, Dept Radiol, Affiliated Hosp 1, Guangzhou, Guangdong, Peoples R China
[7] Sun Yat Sen Univ, Dept Urol, Affiliated Hosp 1, Guangzhou, Guangdong, Peoples R China
[8] First Peoples Hosp Jingmen, Dept Joint Surg, Jingmen, Hubei, Peoples R China
[9] Fudan Univ, Jinshan Hosp, Dept Orthopaed, Longhang Rd 1508, Shanghai 201508, Peoples R China
关键词
Rivaroxaban; nadroparin; deep venous thrombosis; total hip arthroplasty; femoral neck fracture; osteoporosis; MOLECULAR-WEIGHT HEPARIN; INTERTROCHANTERIC FEMUR FRACTURES; KNEE ARTHROPLASTY; IN-VITRO; THROMBOEMBOLISM; FRAXIPARINE; EFFICACY; SAFETY; RISK; THROMBOPROPHYLAXIS;
D O I
10.1177/0300060518762281
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Objective This study was performed to evaluate the efficacy of rivaroxaban versus nadroparin for preventing deep venous thrombosis (DVT) in elderly patients with osteoporosis undergoing initial total hip arthroplasty (THA) for femoral neck fractures. Methods Prospectively maintained databases were reviewed to retrospectively compare elderly patients with osteoporosis who underwent initial THA for femoral neck fractures from 2007 to 2015. The patients received peroral rivaroxaban at 10mg/day for 2 weeks or subcutaneous injections of nadroparin at 0.3 mL/day for 2 weeks until the primary analysis cut-off date. The time to first on-study DVT was the primary endpoint. Results In total, 399 patients were included (rivaroxaban group: n=200; mean age, 70.209.16 years and nadroparin group: n=199; mean age, 69.90 +/- 8.87 years), with a mean 3-year follow-up. The time to first on-study DVT was significantly longer in the rivaroxaban than nadroparin group (12 and 5 days, respectively). The incidence of DVT within the 2-week follow-up was significantly higher in the nadroparin than rivaroxaban group (6.8% and 19.7%, respectively), but this difference was no longer present at the final follow-up. Conclusion Rivaroxaban was associated with a significant reduction in the occurrence of first on-study DVT compared with nadroparin.
引用
收藏
页码:1936 / 1946
页数:11
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