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type=\u0022text\/css\u0022 rel=\u0022stylesheet\u0022 href=\u0022\/\/d282kpwvnogo5m.cloudfront.net\/sites\/default\/files\/advagg_css\/css__ce2QY63WIanKyr8eSq7eavr1XQRRmFD6ZSmwpyJi8lM__zXwFqpqmxrZOXXcd_TpBQpjuELbmIP9wBR5UuTDWAO4__YJWWMMdfCJuAFm5cUEp88OsodhO3ZA-2lzRfoBsSlk4.css\u0022 media=\u0022all\u0022 \/\u003E\n\u003Clink rel=\u0027stylesheet\u0027 type=\u0027text\/css\u0027 href=\u0027\/sites\/all\/modules\/contrib\/panels\/plugins\/layouts\/onecol\/onecol.css\u0027 \/\u003E\u003C\/head\u003E\u003Cbody\u003E\u003Cdiv class=\u0022panels-ajax-tab-panel panels-ajax-tab-panel-sageoa-tab-art\u0022\u003E\u003Cdiv class=\u0022panel-display panel-1col clearfix\u0022 \u003E\n  \u003Cdiv class=\u0022panel-panel panel-col\u0022\u003E\n    \u003Cdiv\u003E\u003Cdiv class=\u0022panel-pane pane-highwire-markup\u0022 \u003E\n  \n      \n  \n  \u003Cdiv class=\u0022pane-content\u0022\u003E\n    \u003Cdiv class=\u0022highwire-markup\u0022\u003E\u003Cdiv xmlns=\u0022http:\/\/www.w3.org\/1999\/xhtml\u0022 id=\u0022content-block-markup\u0022 xmlns:xhtml=\u0022http:\/\/www.w3.org\/1999\/xhtml\u0022\u003E\u003Cdiv class=\u0022article fulltext-view \u0022\u003E\u003Cspan class=\u0022highwire-journal-article-marker-start\u0022\u003E\u003C\/span\u003E\u003Cdiv class=\u0022section abstract\u0022 id=\u0022abstract-1\u0022\u003E\u003Ch2\u003ESummary\u003C\/h2\u003E\u003Cp id=\u0022p-1\u0022\u003EIn the BRIDGE trial, bridging with low molecular weight heparin in patients with atrial fibrillation who underwent surgery or an invasive procedure that required warfarin interruption resulted in similar rates of arterial thromboembolism but significantly higher rates of minor and major bleeding.\u003C\/p\u003E\u003C\/div\u003E\u003Cul class=\u0022kwd-group\u0022\u003E\u003Cli class=\u0022kwd\u0022\u003EBRIDGE\u003C\/li\u003E\u003Cli class=\u0022kwd\u0022\u003ENCT00786474\u003C\/li\u003E\u003Cli class=\u0022kwd\u0022\u003Eatrial fibrillation\u003C\/li\u003E\u003Cli class=\u0022kwd\u0022\u003Ewarfarin\u003C\/li\u003E\u003Cli class=\u0022kwd\u0022\u003Elow molecular weight heparin\u003C\/li\u003E\u003Cli class=\u0022kwd\u0022\u003ELMWH\u003C\/li\u003E\u003Cli class=\u0022kwd\u0022\u003Ebridging\u003C\/li\u003E\u003Cli class=\u0022kwd\u0022\u003Eperiprocedural\u003C\/li\u003E\u003Cli class=\u0022kwd\u0022\u003Earrhythmias\u003C\/li\u003E\u003Cli class=\u0022kwd\u0022\u003Ecardiology \u0026amp; cardiovascular medicine clinical trials\u003C\/li\u003E\u003C\/ul\u003E\u003Cdiv class=\u0022section\u0022 id=\u0022sec-1\u0022\u003E\u003Cp id=\u0022p-2\u0022\u003EBridging warfarin interruption with low molecular weight heparin (LMWH) around the time of surgery or invasive procedures in patients with atrial fibrillation (AF) resulted in similar rates of arterial thromboembolism but significantly greater rates of minor and major bleeding. Thomas L. Ortel, MD, PhD, Duke University Medical Center, Durham, North Carolina, USA, presented data from the BRIDGE trial [Douketis JD et al. \u003Cem\u003EN Engl J Med\u003C\/em\u003E. 2015].\u003C\/p\u003E\u003Cp id=\u0022p-3\u0022\u003EIt is uncertain whether bridging with LMWH is optimal practice to reduce the risk of thromboembolism during the perioperative interruption of warfarin. The purpose of the BRIDGE trial was to determine the safety and efficacy of bridging with LMWH in patients with AF who required interruption of warfarin for surgery or an invasive procedure. The investigators hypothesized that a strategy of foregoing bridging would be noninferior to bridging for the prevention of arterial thromboembolism and would be superior to bridging for major bleeding.\u003C\/p\u003E\u003Cp id=\u0022p-4\u0022\u003EThe double-blind, phase 3 BRIDGE trial randomly assigned 1884 patients with AF to receive bridging with LMWH or matched placebo 3 days prior to and for 5 to 10 days after surgery or a procedure. Warfarin was stopped 5 days prior to the surgery or procedure and was restarted within 24 hours afterward. The study drug was stopped when patients achieved a therapeutic INR. Patients were followed for 30 days after the initial surgery or procedure. The primary outcomes were arterial thromboembolism or major bleeding. The secondary outcomes were acute myocardial infarction, venous thromboembolism, or death, and minor bleeding.\u003C\/p\u003E\u003Cp id=\u0022p-5\u0022\u003EAll patients had nonvalvular or valvular AF or atrial flutter, were receiving warfarin for \u2265\u20053 months with a target INR of 2.0 to 3.0, and had a CHADS\u003Csub\u003E2\u003C\/sub\u003E score of \u2265\u20051. Exclusion criteria included presence of a mechanical heart valve, major bleeding within the past 6 weeks, venous thromboembolism within the past 12 weeks, creatinine clearance \u0026lt;\u200530 mL\/min, and platelet count \u0026lt;\u2005100 \u00d7 10\u003Csup\u003E3\u003C\/sup\u003E\/m\u003Csup\u003E3\u003C\/sup\u003E, as well as a stroke, systemic embolism, or transient ischemic attack (TIA) within the past 12 weeks or planned cardiac, intracranial, or intraspinal surgery.\u003C\/p\u003E\u003Cp id=\u0022p-6\u0022\u003EThe mean age was 71.7 years and the mean CHADS\u003Csub\u003E2\u003C\/sub\u003E score was 2.35, with about 23%, 39%, 24%, and 11% of patients having a score of 1, 2, 3, or 4, respectively. At baseline, the mean INR was 2.4, about 87% of patients had hypertension, about 31% had chronic heart failure or left ventricular dysfunction, 41% had diabetes mellitus, 8% had a history of TIA, and 16% had mitral valve disease.\u003C\/p\u003E\u003Cp id=\u0022p-7\u0022\u003EBridging with LMWH was noninferior, but not superior, to no bridging (\u003Cem\u003EP\u003C\/em\u003E\u003Csub\u003ENoninferiority\u003C\/sub\u003E\u2005=\u2005.01). However, there was significantly more major bleeding in the bridging arm (3.2%) compared with the no-bridging arm (1.3%; \u003Cem\u003EP\u003C\/em\u003E\u003Csub\u003ESuperiority\u003C\/sub\u003E\u2005=\u2005.005). In addition, minor bleeding was also significantly greater with LMWH bridging (20.9%) compared with no bridging (12.0%; \u003Cem\u003EP\u003C\/em\u003E\u003Csub\u003ESuperiority\u003C\/sub\u003E\u2005\u0026lt;\u2005.001). There was no significant difference among the other secondary outcomes.\u003C\/p\u003E\u003Cp id=\u0022p-8\u0022\u003EDr Ortel commented that the study was limited by the low mean CHADS\u003Csub\u003E2\u003C\/sub\u003E score and that most patients underwent low-risk procedures. In addition, he stated that these results are not applicable to patients who are receiving a nonwarfarin oral anticoagulant instead of warfarin.\u003C\/p\u003E\u003C\/div\u003E\u003Cul class=\u0022copyright-statement\u0022\u003E\u003Cli class=\u0022fn\u0022 id=\u0022copyright-statement-1\u0022\u003E\u00a9 2015 SAGE Publications\u003C\/li\u003E\u003C\/ul\u003E\u003Cspan class=\u0022highwire-journal-article-marker-end\u0022\u003E\u003C\/span\u003E\u003C\/div\u003E\u003Cspan id=\u0022related-urls\u0022\u003E\u003C\/span\u003E\u003C\/div\u003E\u003Ca href=\u0022http:\/\/mdc.sagepub.com\/content\/15\/21\/6.1.abstract\u0022 class=\u0022hw-link hw-link-article-abstract\u0022 data-icon-position=\u0022\u0022 data-hide-link-title=\u00220\u0022\u003EView Summary\u003C\/a\u003E\u003C\/div\u003E  \u003C\/div\u003E\n\n  \n  \u003C\/div\u003E\n\u003C\/div\u003E\n  \u003C\/div\u003E\n\u003C\/div\u003E\n\u003C\/div\u003E\u003Cscript type=\u0022text\/javascript\u0022 src=\u0022http:\/\/mdc.sagepub.com\/sites\/all\/modules\/highwire\/highwire\/plugins\/highwire_markup_process\/js\/highwire_openurl.js?nzlga1\u0022\u003E\u003C\/script\u003E\n\u003C\/body\u003E\u003C\/html\u003E"}