Is the Oral Chemical Prophylaxis Necessary for the Prevention of Venous Thromboembolism after Joint Arthroplasty in a Korean Population?
- Author:
Kyoung Ho MOON
1
;
Joon Soon KANG
;
Yung Hun YOUN
Author Information
- Publication Type:Multicenter Study
- Keywords: Venous thromboembolism; Venous thrombosis; Hip replacement arthroplasty; Total knee arthroplasty; Rivaroxaban
- MeSH: Arthroplasty; Arthroplasty, Replacement, Hip; Arthroplasty, Replacement, Knee; Follow-Up Studies; Hip; Humans; Incidence; Joints; Knee; Odds Ratio; Orthopedics; Prevalence; Prospective Studies; Pulmonary Embolism; Rivaroxaban; Venous Thromboembolism; Venous Thrombosis
- From:Hip & Pelvis 2019;31(3):150-157
- CountryRepublic of Korea
- Language:English
- Abstract: PURPOSE: Venous thromboembolism (VTE) is a serious complication that may occur after a major orthopedic surgery. The aim of the present study was to determine the necessity of a chemical thromboprophylactic agent (rivaroxaban [RXB]) by analyzing the prevalence of VTE in Korean arthroplasty patients who received RXB for prophylaxis compared with those who did not receive RXB. MATERIALS AND METHODS: A total of 2,603 patients who underwent knee or hip arthroplasty between 1996 and 2017 were prospectively evaluated. Of these, 1,608 patients underwent surgery before January 2010 and were not administered any type of prophylaxis after surgery; the remaining 995 underwent surgery after 2010 and received oral RXB once daily for 5–13 days from the day after hemovac drain removal to postoperative day 14. RESULTS: The primary study outcome was the prevalence of VTE, pulmonary embolism or death during follow up. The overall incidence of VTE was 1.69% (n=44); of these, 12 occurred in the RXB group and 32 in the non-prophylactic group. The odds ratio of VTE in the RXB group was 0.61. However, the statistical power of the study was 0.313 due to the low incidence of VTE. CONCLUSION: Treatment with oral chemical prophylaxis decreased the incidence of VTE after knee or hip arthroplasty in a Korean population. Furthermore, no serious complications occurred after administering oral RXB, which, coupled with its convenience, suggests oral RXB offers an attractive alternative to other agents. However, we recommend that further studies, including a multicenter study, be conducted to achieve adequate statistical power.
