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Article: Potential Risk Factors Contributing to Development of Venous Thromboembolism for Total Knee Replacements Patients Prophylaxed With Rivaroxaban: A Retrospective Case-Control Study
Title | Potential Risk Factors Contributing to Development of Venous Thromboembolism for Total Knee Replacements Patients Prophylaxed With Rivaroxaban: A Retrospective Case-Control Study |
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Authors | |
Keywords | venous thromboembolism orthopedic surgery tourniquet body mass index rivaroxaban thromboprophylaxis |
Issue Date | 2020 |
Publisher | Sage Publications, Inc. The Journal's web site is located at http://cat.sagepub.com |
Citation | Clinical and Applied Thrombosis/Hemostasis, 2020, Epub 2020-10-16, v. 26 How to Cite? |
Abstract | Rivaroxaban after total knee arthroplasty (TKA) is used to prevent postoperative venous thromboembolism (VTE); however, despite thromboprophylaxis, some patients still develop postoperative VTE. To determine whether tourniquet time, time to initiate rivaroxaban (TTIRIV), or Body Mass Index (BMI) was associated with postoperative VTE. A retrospective case-control study was conducted. Those patients that developed VTE despite prophylaxis (cases) were compared to controls (no VTE). A univariate analysis was conducted (p < 0.05 statistically significant). Seven VTE cases were identified from 234 TKA-patients. Patients with and without VTE had BMI of 40.1+ 9.1 and 32.8 + 7.5, respectively (p = 0.064). TTIRIV in VTE and control group was 28.2+4.7 hours and 26.4+4.2 hours, respectively (p = 0.39). Mean tourniquet time in VTE and control group was 65.0+ 8.7 minutes and 49 + 8.8 minutes, respectively (p = 0.0007). Statistically significant differences in tourniquet times were noted between VTE and non-VTE group but not for TTIRIV and BMI. Prolonged tourniquet use could pose a potential risk factor for postoperative VTE. Thromboprophylaxis management may need to be adjusted, based on patient-specific factors that could include increasing doses of oral anticoagulants and/or mechanical prophylaxis. However, further large-scale studies are required to establish pathophysiology. |
Persistent Identifier | http://hdl.handle.net/10722/290525 |
ISSN | 2023 Impact Factor: 2.3 2023 SCImago Journal Rankings: 0.633 |
PubMed Central ID | |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Mian, O | - |
dc.contributor.author | Matino, D | - |
dc.contributor.author | Roberts, R | - |
dc.contributor.author | McDonald, E | - |
dc.contributor.author | Chan, AKC | - |
dc.contributor.author | Chan, HHW | - |
dc.date.accessioned | 2020-11-02T05:43:29Z | - |
dc.date.available | 2020-11-02T05:43:29Z | - |
dc.date.issued | 2020 | - |
dc.identifier.citation | Clinical and Applied Thrombosis/Hemostasis, 2020, Epub 2020-10-16, v. 26 | - |
dc.identifier.issn | 1076-0296 | - |
dc.identifier.uri | http://hdl.handle.net/10722/290525 | - |
dc.description.abstract | Rivaroxaban after total knee arthroplasty (TKA) is used to prevent postoperative venous thromboembolism (VTE); however, despite thromboprophylaxis, some patients still develop postoperative VTE. To determine whether tourniquet time, time to initiate rivaroxaban (TTIRIV), or Body Mass Index (BMI) was associated with postoperative VTE. A retrospective case-control study was conducted. Those patients that developed VTE despite prophylaxis (cases) were compared to controls (no VTE). A univariate analysis was conducted (p < 0.05 statistically significant). Seven VTE cases were identified from 234 TKA-patients. Patients with and without VTE had BMI of 40.1+ 9.1 and 32.8 + 7.5, respectively (p = 0.064). TTIRIV in VTE and control group was 28.2+4.7 hours and 26.4+4.2 hours, respectively (p = 0.39). Mean tourniquet time in VTE and control group was 65.0+ 8.7 minutes and 49 + 8.8 minutes, respectively (p = 0.0007). Statistically significant differences in tourniquet times were noted between VTE and non-VTE group but not for TTIRIV and BMI. Prolonged tourniquet use could pose a potential risk factor for postoperative VTE. Thromboprophylaxis management may need to be adjusted, based on patient-specific factors that could include increasing doses of oral anticoagulants and/or mechanical prophylaxis. However, further large-scale studies are required to establish pathophysiology. | - |
dc.language | eng | - |
dc.publisher | Sage Publications, Inc. The Journal's web site is located at http://cat.sagepub.com | - |
dc.relation.ispartof | Clinical and Applied Thrombosis/Hemostasis | - |
dc.rights | Author(s), Contribution Title, Journal Title (Clinical and Applied Thrombosis/Hemostasis, 2020, Epub 2020-10-16, v. 26) pp. xx-xx. Copyright © [2020] (Copyright Holder). DOI: [10.1177/1076029620962226]. | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.subject | venous thromboembolism | - |
dc.subject | orthopedic surgery | - |
dc.subject | tourniquet | - |
dc.subject | body mass index | - |
dc.subject | rivaroxaban thromboprophylaxis | - |
dc.title | Potential Risk Factors Contributing to Development of Venous Thromboembolism for Total Knee Replacements Patients Prophylaxed With Rivaroxaban: A Retrospective Case-Control Study | - |
dc.type | Article | - |
dc.identifier.email | Chan, HHW: hwhoward@hku.hk | - |
dc.description.nature | published_or_final_version | - |
dc.identifier.doi | 10.1177/1076029620962226 | - |
dc.identifier.pmid | 33064561 | - |
dc.identifier.pmcid | PMC7573710 | - |
dc.identifier.scopus | eid_2-s2.0-85092786658 | - |
dc.identifier.hkuros | 318045 | - |
dc.identifier.volume | Epub 2020-10-16, v. 26 | - |
dc.identifier.spage | 1 | - |
dc.identifier.epage | 8 | - |
dc.identifier.isi | WOS:000582166600001 | - |
dc.publisher.place | United States | - |
dc.identifier.issnl | 1076-0296 | - |