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Comparative efficacy and safety of oral anticoagulants for the treatment of venous thromboembolism in the patients with different renal functions: a systematic review, pairwise and network meta-analysis

ObjectivesTo compare the efficacy and safety of direct oral anticoagulants (DOACs) in patients with venous thromboembolism (VTE) and different renal functions.DesignSystematic review containing pairwise and Bayesian network meta-analysis of randomised controlled trials (RCTs).Data sourcesMEDLINE, EM...

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Published in:BMJ open 2022-02, Vol.12 (2), p.e048619
Main Authors: Su, Xiaole, Yan, Bingjuan, Wang, Lihua, Cheng, Hong, Chen, Yipu
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Chen, Yipu
description ObjectivesTo compare the efficacy and safety of direct oral anticoagulants (DOACs) in patients with venous thromboembolism (VTE) and different renal functions.DesignSystematic review containing pairwise and Bayesian network meta-analysis of randomised controlled trials (RCTs).Data sourcesMEDLINE, EMBASE and Cochrane Library.Eligibility criteriaRCTs reporting the efficacy and safety outcomes of DOACs in different creatinine clearance (CrCl) subgroups.Data extraction and synthesisData extraction and quality assessment were undertaken by two independent reviewers. Data were pooled using the DerSimonian-Laird method in pairwise meta-analysis. Network meta-analysis within a Bayesian framework was conducted.ResultsData from 10 RCTs were included. In the treatment of acute VTE, DOACs did not significantly reduce recurrent VTE or VTE-related death (OR, 0.96; 95% CI, 0.82 to 1.11) but significantly reduced bleeding events (0.76, 0.68 to 0.90) compared with warfarin. In the extended treatment of VTE, DOACs produced significant benefits in recurrent VTE or VTE-related death (0.23, 0.16 to 0.29), but significantly increased bleeding events (1.86, 1.04 to 3.33) compared with placebo/aspirin. There were no significant differences in efficacy and safety of DOACs among the three CrCl stratified subgroups in acute and extended treatment of VTE (p for subgroup heterogeneity >0.1). Bayesian network meta-analysis suggested that apixaban 2.5 mg and 5 mg two times per day were associated with a lower risk of bleeding than dabigatran, rivaroxaban, warfarin and aspirin in the subgroup with CrCl >80 mL/min.ConclusionsFor the treatment of acute VTE, DOACs are similar to warfarin in reducing recurrent VTE and VTE-related death but are significantly superior to warfarin in reducing the risk of bleeding. For the efficacy and safety of DOACs across different CrCl stratifications (30–50, 50–80 and more than 80 mL/min), no significant difference was found. In light of minimal evidence, apixaban might be associated with a lower risk of bleeding in patients with VTE and CrCl >80 mL/min.PROSPERO registration numberCRD42018090896.
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Data were pooled using the DerSimonian-Laird method in pairwise meta-analysis. Network meta-analysis within a Bayesian framework was conducted.ResultsData from 10 RCTs were included. In the treatment of acute VTE, DOACs did not significantly reduce recurrent VTE or VTE-related death (OR, 0.96; 95% CI, 0.82 to 1.11) but significantly reduced bleeding events (0.76, 0.68 to 0.90) compared with warfarin. In the extended treatment of VTE, DOACs produced significant benefits in recurrent VTE or VTE-related death (0.23, 0.16 to 0.29), but significantly increased bleeding events (1.86, 1.04 to 3.33) compared with placebo/aspirin. There were no significant differences in efficacy and safety of DOACs among the three CrCl stratified subgroups in acute and extended treatment of VTE (p for subgroup heterogeneity &gt;0.1). Bayesian network meta-analysis suggested that apixaban 2.5 mg and 5 mg two times per day were associated with a lower risk of bleeding than dabigatran, rivaroxaban, warfarin and aspirin in the subgroup with CrCl &gt;80 mL/min.ConclusionsFor the treatment of acute VTE, DOACs are similar to warfarin in reducing recurrent VTE and VTE-related death but are significantly superior to warfarin in reducing the risk of bleeding. For the efficacy and safety of DOACs across different CrCl stratifications (30–50, 50–80 and more than 80 mL/min), no significant difference was found. In light of minimal evidence, apixaban might be associated with a lower risk of bleeding in patients with VTE and CrCl &gt;80 mL/min.PROSPERO registration numberCRD42018090896.</description><identifier>ISSN: 2044-6055</identifier><identifier>EISSN: 2044-6055</identifier><identifier>DOI: 10.1136/bmjopen-2021-048619</identifier><identifier>PMID: 35190410</identifier><language>eng</language><publisher>England: British Medical Journal Publishing Group</publisher><subject>Administration, Oral ; Anticoagulants ; Anticoagulants - adverse effects ; anticoagulation ; Humans ; Kidney - physiopathology ; Kidney diseases ; Meta-analysis ; nephrology ; Network Meta-Analysis ; Patient safety ; Side effects ; Systematic review ; Thromboembolism ; Urology ; Venous Thromboembolism - drug therapy ; Venous Thromboembolism - physiopathology</subject><ispartof>BMJ open, 2022-02, Vol.12 (2), p.e048619</ispartof><rights>Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.</rights><rights>2022 Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/ This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ . Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b539t-e4e218af174fcd4dfc68bffe04fdef32628a3e1d212ca338ba9127410716abaa3</citedby><cites>FETCH-LOGICAL-b539t-e4e218af174fcd4dfc68bffe04fdef32628a3e1d212ca338ba9127410716abaa3</cites><orcidid>0000-0002-5079-4334</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2632236912/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2632236912?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,3194,25753,27924,27925,37012,37013,44590,53791,53793,55341,55350,75126,77596,77597,77660,77686</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35190410$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Su, Xiaole</creatorcontrib><creatorcontrib>Yan, Bingjuan</creatorcontrib><creatorcontrib>Wang, Lihua</creatorcontrib><creatorcontrib>Cheng, Hong</creatorcontrib><creatorcontrib>Chen, Yipu</creatorcontrib><title>Comparative efficacy and safety of oral anticoagulants for the treatment of venous thromboembolism in the patients with different renal functions: a systematic review, pairwise and network meta-analysis</title><title>BMJ open</title><addtitle>BMJ Open</addtitle><addtitle>BMJ Open</addtitle><description>ObjectivesTo compare the efficacy and safety of direct oral anticoagulants (DOACs) in patients with venous thromboembolism (VTE) and different renal functions.DesignSystematic review containing pairwise and Bayesian network meta-analysis of randomised controlled trials (RCTs).Data sourcesMEDLINE, EMBASE and Cochrane Library.Eligibility criteriaRCTs reporting the efficacy and safety outcomes of DOACs in different creatinine clearance (CrCl) subgroups.Data extraction and synthesisData extraction and quality assessment were undertaken by two independent reviewers. Data were pooled using the DerSimonian-Laird method in pairwise meta-analysis. Network meta-analysis within a Bayesian framework was conducted.ResultsData from 10 RCTs were included. In the treatment of acute VTE, DOACs did not significantly reduce recurrent VTE or VTE-related death (OR, 0.96; 95% CI, 0.82 to 1.11) but significantly reduced bleeding events (0.76, 0.68 to 0.90) compared with warfarin. In the extended treatment of VTE, DOACs produced significant benefits in recurrent VTE or VTE-related death (0.23, 0.16 to 0.29), but significantly increased bleeding events (1.86, 1.04 to 3.33) compared with placebo/aspirin. There were no significant differences in efficacy and safety of DOACs among the three CrCl stratified subgroups in acute and extended treatment of VTE (p for subgroup heterogeneity &gt;0.1). Bayesian network meta-analysis suggested that apixaban 2.5 mg and 5 mg two times per day were associated with a lower risk of bleeding than dabigatran, rivaroxaban, warfarin and aspirin in the subgroup with CrCl &gt;80 mL/min.ConclusionsFor the treatment of acute VTE, DOACs are similar to warfarin in reducing recurrent VTE and VTE-related death but are significantly superior to warfarin in reducing the risk of bleeding. For the efficacy and safety of DOACs across different CrCl stratifications (30–50, 50–80 and more than 80 mL/min), no significant difference was found. In light of minimal evidence, apixaban might be associated with a lower risk of bleeding in patients with VTE and CrCl &gt;80 mL/min.PROSPERO registration numberCRD42018090896.</description><subject>Administration, Oral</subject><subject>Anticoagulants</subject><subject>Anticoagulants - adverse effects</subject><subject>anticoagulation</subject><subject>Humans</subject><subject>Kidney - physiopathology</subject><subject>Kidney diseases</subject><subject>Meta-analysis</subject><subject>nephrology</subject><subject>Network Meta-Analysis</subject><subject>Patient safety</subject><subject>Side effects</subject><subject>Systematic review</subject><subject>Thromboembolism</subject><subject>Urology</subject><subject>Venous Thromboembolism - drug therapy</subject><subject>Venous Thromboembolism - physiopathology</subject><issn>2044-6055</issn><issn>2044-6055</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>9YT</sourceid><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNp9kttu1DAQhiMEolXpEyAhS9xwQagPiTfLBVK14lCpEjdwbU2c8dZLEi-2s6t9RZ6K2QOl5QJLcazx9_8ej6coXgr-Tgilr9phFdY4lpJLUfKq0WL-pDiXvKpKzev66YP1WXGZ0orTqOp5XcvnxZmqxZxXgp8XvxZhWEOE7DfI0Dlvwe4YjB1L4DDvWHAsROgplL0NsJx6WiXmQmT5DlmOCHnAMe_BDY5hShSPYWgD0tf7NDA_HtA1HYJ77dbnO9Z55zDuhTSRv5tGm30Y03sGLO1SxoF4S7sbj9u3pPZx6xMechsxb0P8wQbMUALJd8mnF8UzB33Cy9P_ovj-6eO3xZfy9uvnm8X1bdnWap5LrFCKBpyYVc52VeesblrKhVeuQ6eklg0oFJ0U0oJSTQtzIWdUrJnQ0AKoi-Lm6NsFWJl19APEnQngzSEQ4tJApNR7NBYAocXO6m5GxddN3QnQAByt5U1tyevD0Ws9tQNxVA8q9iPTxzujvzPLsDFNo2VVN2Tw5mQQw88JUzaDTxZ7eiWktzBSK9HoSosZoa__QVdhilS8AyWl0nRRotSRsjGkFNHdJyO42beeObWe2beeObYeqV49vMe95k-jEXB1BEj999z_Wf4GjgTtqQ</recordid><startdate>20220221</startdate><enddate>20220221</enddate><creator>Su, Xiaole</creator><creator>Yan, Bingjuan</creator><creator>Wang, Lihua</creator><creator>Cheng, Hong</creator><creator>Chen, Yipu</creator><general>British Medical Journal Publishing Group</general><general>BMJ Publishing Group LTD</general><general>BMJ Publishing Group</general><scope>9YT</scope><scope>ACMMV</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>NAPCQ</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-5079-4334</orcidid></search><sort><creationdate>20220221</creationdate><title>Comparative efficacy and safety of oral anticoagulants for the treatment of venous thromboembolism in the patients with different renal functions: a systematic review, pairwise and network meta-analysis</title><author>Su, Xiaole ; 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Data were pooled using the DerSimonian-Laird method in pairwise meta-analysis. Network meta-analysis within a Bayesian framework was conducted.ResultsData from 10 RCTs were included. In the treatment of acute VTE, DOACs did not significantly reduce recurrent VTE or VTE-related death (OR, 0.96; 95% CI, 0.82 to 1.11) but significantly reduced bleeding events (0.76, 0.68 to 0.90) compared with warfarin. In the extended treatment of VTE, DOACs produced significant benefits in recurrent VTE or VTE-related death (0.23, 0.16 to 0.29), but significantly increased bleeding events (1.86, 1.04 to 3.33) compared with placebo/aspirin. There were no significant differences in efficacy and safety of DOACs among the three CrCl stratified subgroups in acute and extended treatment of VTE (p for subgroup heterogeneity &gt;0.1). Bayesian network meta-analysis suggested that apixaban 2.5 mg and 5 mg two times per day were associated with a lower risk of bleeding than dabigatran, rivaroxaban, warfarin and aspirin in the subgroup with CrCl &gt;80 mL/min.ConclusionsFor the treatment of acute VTE, DOACs are similar to warfarin in reducing recurrent VTE and VTE-related death but are significantly superior to warfarin in reducing the risk of bleeding. For the efficacy and safety of DOACs across different CrCl stratifications (30–50, 50–80 and more than 80 mL/min), no significant difference was found. In light of minimal evidence, apixaban might be associated with a lower risk of bleeding in patients with VTE and CrCl &gt;80 mL/min.PROSPERO registration numberCRD42018090896.</abstract><cop>England</cop><pub>British Medical Journal Publishing Group</pub><pmid>35190410</pmid><doi>10.1136/bmjopen-2021-048619</doi><orcidid>https://orcid.org/0000-0002-5079-4334</orcidid><oa>free_for_read</oa></addata></record>
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subjects Administration, Oral
Anticoagulants
Anticoagulants - adverse effects
anticoagulation
Humans
Kidney - physiopathology
Kidney diseases
Meta-analysis
nephrology
Network Meta-Analysis
Patient safety
Side effects
Systematic review
Thromboembolism
Urology
Venous Thromboembolism - drug therapy
Venous Thromboembolism - physiopathology
title Comparative efficacy and safety of oral anticoagulants for the treatment of venous thromboembolism in the patients with different renal functions: a systematic review, pairwise and network meta-analysis
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