2015
DOI: 10.1016/j.acvd.2014.09.009
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SAfety of Fondaparinux in transoesophageal echocardiography-guided Electric cardioversion of Atrial Fibrillation (SAFE-AF) study: A pilot study

Abstract: In this pilot study in patients with TEE-guided cardioversion, the use of fondaparinux appeared to be well tolerated, with similar efficacy to UFH+VKA. Furthermore, a trend to greater thrombus resolution was observed.

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Cited by 8 publications
(6 citation statements)
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“…The flowchart of the systematic review is depicted in Figure . Of the 8,468 articles screened, 17 articles were selected for the final analyses . The initial and follow‐up data of the articles included in the final analyses are listed in Table and in Table , respectively.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…The flowchart of the systematic review is depicted in Figure . Of the 8,468 articles screened, 17 articles were selected for the final analyses . The initial and follow‐up data of the articles included in the final analyses are listed in Table and in Table , respectively.…”
Section: Resultsmentioning
confidence: 99%
“…There were no randomized controlled trials of OAC agents and/or doses. One randomized controlled trial compared subcutaneous fondaparinux to intravenous unfractionated heparin plus oral VKA in subjects with AF who had been diagnosed with LAT on TEE prior to anticipated cardioversion . Additional data with DOACs are needed before they may be considered first‐line alternatives to warfarin.…”
Section: Resultsmentioning
confidence: 99%
“…Fondaparinux appeared to be well tolerated and showed a similar efficacy to unfractionated heparin and vitamin K antagonist. A trend of greater thrombus resolution was also observed [ 32 ]. Fondaparinux also appears to be a safe alternative to heparin to prevent graft failure after CABG [ 33 ].…”
Section: Practical Recommendationsmentioning
confidence: 88%
“…The evidence for the use of parenteral anticoagulants with respect to AF is limited 3 . Fondaparinux has been successfully used as a single anticoagulant prior to transoesophageal echocardiography‐guided cardioversion (total treatment time of 28‐56 days), 4 and one study revealed the non‐inferiority of enoxaparin compared to UFH + warfarin in similar clinical settings 5 …”
Section: What Is Known and Objectivementioning
confidence: 99%