Thromboembolism and bleeding risk in atrial fibrillation ablation with uninterrupted anticoagulation between new oral anticoagulants and vitamin K antagonists: insights from an updated meta-analysis

Cumulative reports comparing the efficacy and safety outcomes between uninterrupted NOACs and vitamin K antagonists (VKA) in AF ablation had been freshly published. This meta-analysis aimed at offering a more comprehensive evaluation between these two anticoagulants in uninterrupted strategy. We sea...

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Veröffentlicht in:Journal of thrombosis and thrombolysis 2020-07, Vol.50 (1), p.201-210
Hauptverfasser: Liu, Xiao-Hua, Gao, Xiao-Fei, Chen, Chao-Feng, Chen, Bin, Xu, Yi-Zhou
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container_issue 1
container_start_page 201
container_title Journal of thrombosis and thrombolysis
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creator Liu, Xiao-Hua
Gao, Xiao-Fei
Chen, Chao-Feng
Chen, Bin
Xu, Yi-Zhou
description Cumulative reports comparing the efficacy and safety outcomes between uninterrupted NOACs and vitamin K antagonists (VKA) in AF ablation had been freshly published. This meta-analysis aimed at offering a more comprehensive evaluation between these two anticoagulants in uninterrupted strategy. We searched in PUBMED, EMBASE, and Cochrane Library (inception to June 10, 2019) for eligible studies. Fixed-effects model was preferred in pooled analysis if I 2   300 s. In conclusions, uninterrupted NOACs was more effective than uninterrupted VKA in reducing major bleeding and pericardial effusion risk without increasing thromboembolism risk, and the benefits of uninterrupted NOACs on major bleeding complication could be more pronounced if CHA 2 DS 2 -VASc score ≥ 2 or target ACT > 300 s.
doi_str_mv 10.1007/s11239-019-01989-5
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This meta-analysis aimed at offering a more comprehensive evaluation between these two anticoagulants in uninterrupted strategy. We searched in PUBMED, EMBASE, and Cochrane Library (inception to June 10, 2019) for eligible studies. Fixed-effects model was preferred in pooled analysis if I 2  &lt; 50%. Publication bias was also evaluated. A total of 23 studies involving 12,725 individuals were analyzed in this literature. There were no difference between uninterrupted NOACs and VKA groups in incidence of Stroke/TIA (RR 0.98, 95% CI 0.54–1.77, P = 0.93, I 2  = 0%), silent cerebral embolism (RR 1.09, 95% CI 0.82–1.43, P = 0.56, I 2  = 0%), minor bleeding complication (RR 0.97, 95% CI 0.83–1.14, P = 0.73, I 2  = 0%), cardiac tamponade (RR 0.95, 95% CI 0.63–1.42, P = 0.80, I 2  = 0%). Uninterrupted NOACs was associated with significantly lower major bleeding incidence (RR 0.67, 95% CI 0.49–0.92, P = 0.01, I 2  = 0%), pericardial effusion (RR 0.75, 95% CI 0.56–1.00, P = 0.048, I 2  = 9%). In sub-analysis, no difference was found in all sub-analyses for Stroke/TIA while significant major bleeding risk reduction in uninterrupted NOACs was identified in the subgroup of CHA 2 DS 2 -VASc score ≥ 2 and target activated clotting time (ACT) &gt; 300 s. In conclusions, uninterrupted NOACs was more effective than uninterrupted VKA in reducing major bleeding and pericardial effusion risk without increasing thromboembolism risk, and the benefits of uninterrupted NOACs on major bleeding complication could be more pronounced if CHA 2 DS 2 -VASc score ≥ 2 or target ACT &gt; 300 s.</description><identifier>ISSN: 0929-5305</identifier><identifier>EISSN: 1573-742X</identifier><identifier>DOI: 10.1007/s11239-019-01989-5</identifier><identifier>PMID: 31686297</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Ablation ; Antagonists ; Anticoagulants ; Anticoagulants - administration &amp; dosage ; Anticoagulants - adverse effects ; Anticoagulants - classification ; Atrial Fibrillation - therapy ; Bleeding ; Cardiology ; Catheter Ablation - adverse effects ; Catheter Ablation - methods ; Clotting ; Effusion ; Embolism ; Fibrillation ; Hematology ; Hemorrhage - chemically induced ; Hemorrhage - prevention &amp; control ; Humans ; Medicine ; Medicine &amp; Public Health ; Meta-analysis ; Risk Adjustment ; Tamponade ; Thromboembolism ; Thromboembolism - etiology ; Thromboembolism - prevention &amp; control ; Vitamin K</subject><ispartof>Journal of thrombosis and thrombolysis, 2020-07, Vol.50 (1), p.201-210</ispartof><rights>Springer Science+Business Media, LLC, part of Springer Nature 2019</rights><rights>Springer Science+Business Media, LLC, part of Springer Nature 2019.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c375t-304ccd1fe90108f7ad140be2dc19c0dbde58917fb17825b5b42259dc4ac65c153</citedby><cites>FETCH-LOGICAL-c375t-304ccd1fe90108f7ad140be2dc19c0dbde58917fb17825b5b42259dc4ac65c153</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s11239-019-01989-5$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11239-019-01989-5$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31686297$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Liu, Xiao-Hua</creatorcontrib><creatorcontrib>Gao, Xiao-Fei</creatorcontrib><creatorcontrib>Chen, Chao-Feng</creatorcontrib><creatorcontrib>Chen, Bin</creatorcontrib><creatorcontrib>Xu, Yi-Zhou</creatorcontrib><title>Thromboembolism and bleeding risk in atrial fibrillation ablation with uninterrupted anticoagulation between new oral anticoagulants and vitamin K antagonists: insights from an updated meta-analysis</title><title>Journal of thrombosis and thrombolysis</title><addtitle>J Thromb Thrombolysis</addtitle><addtitle>J Thromb Thrombolysis</addtitle><description>Cumulative reports comparing the efficacy and safety outcomes between uninterrupted NOACs and vitamin K antagonists (VKA) in AF ablation had been freshly published. This meta-analysis aimed at offering a more comprehensive evaluation between these two anticoagulants in uninterrupted strategy. We searched in PUBMED, EMBASE, and Cochrane Library (inception to June 10, 2019) for eligible studies. Fixed-effects model was preferred in pooled analysis if I 2  &lt; 50%. Publication bias was also evaluated. A total of 23 studies involving 12,725 individuals were analyzed in this literature. There were no difference between uninterrupted NOACs and VKA groups in incidence of Stroke/TIA (RR 0.98, 95% CI 0.54–1.77, P = 0.93, I 2  = 0%), silent cerebral embolism (RR 1.09, 95% CI 0.82–1.43, P = 0.56, I 2  = 0%), minor bleeding complication (RR 0.97, 95% CI 0.83–1.14, P = 0.73, I 2  = 0%), cardiac tamponade (RR 0.95, 95% CI 0.63–1.42, P = 0.80, I 2  = 0%). Uninterrupted NOACs was associated with significantly lower major bleeding incidence (RR 0.67, 95% CI 0.49–0.92, P = 0.01, I 2  = 0%), pericardial effusion (RR 0.75, 95% CI 0.56–1.00, P = 0.048, I 2  = 9%). 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This meta-analysis aimed at offering a more comprehensive evaluation between these two anticoagulants in uninterrupted strategy. We searched in PUBMED, EMBASE, and Cochrane Library (inception to June 10, 2019) for eligible studies. Fixed-effects model was preferred in pooled analysis if I 2  &lt; 50%. Publication bias was also evaluated. A total of 23 studies involving 12,725 individuals were analyzed in this literature. There were no difference between uninterrupted NOACs and VKA groups in incidence of Stroke/TIA (RR 0.98, 95% CI 0.54–1.77, P = 0.93, I 2  = 0%), silent cerebral embolism (RR 1.09, 95% CI 0.82–1.43, P = 0.56, I 2  = 0%), minor bleeding complication (RR 0.97, 95% CI 0.83–1.14, P = 0.73, I 2  = 0%), cardiac tamponade (RR 0.95, 95% CI 0.63–1.42, P = 0.80, I 2  = 0%). Uninterrupted NOACs was associated with significantly lower major bleeding incidence (RR 0.67, 95% CI 0.49–0.92, P = 0.01, I 2  = 0%), pericardial effusion (RR 0.75, 95% CI 0.56–1.00, P = 0.048, I 2  = 9%). In sub-analysis, no difference was found in all sub-analyses for Stroke/TIA while significant major bleeding risk reduction in uninterrupted NOACs was identified in the subgroup of CHA 2 DS 2 -VASc score ≥ 2 and target activated clotting time (ACT) &gt; 300 s. In conclusions, uninterrupted NOACs was more effective than uninterrupted VKA in reducing major bleeding and pericardial effusion risk without increasing thromboembolism risk, and the benefits of uninterrupted NOACs on major bleeding complication could be more pronounced if CHA 2 DS 2 -VASc score ≥ 2 or target ACT &gt; 300 s.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>31686297</pmid><doi>10.1007/s11239-019-01989-5</doi><tpages>10</tpages></addata></record>
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subjects Ablation
Antagonists
Anticoagulants
Anticoagulants - administration & dosage
Anticoagulants - adverse effects
Anticoagulants - classification
Atrial Fibrillation - therapy
Bleeding
Cardiology
Catheter Ablation - adverse effects
Catheter Ablation - methods
Clotting
Effusion
Embolism
Fibrillation
Hematology
Hemorrhage - chemically induced
Hemorrhage - prevention & control
Humans
Medicine
Medicine & Public Health
Meta-analysis
Risk Adjustment
Tamponade
Thromboembolism
Thromboembolism - etiology
Thromboembolism - prevention & control
Vitamin K
title Thromboembolism and bleeding risk in atrial fibrillation ablation with uninterrupted anticoagulation between new oral anticoagulants and vitamin K antagonists: insights from an updated meta-analysis
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