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									<identifier>oai:www.peertechzpublications.org:10.17352/ac.000019</identifier>
									<datestamp>2022-12-31</datestamp>
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									<oai_dc:dc xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:mml="http://www.w3.org/1998/Math/MathML" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
										<dc:title>
										Comparison of complication and success rates of perclose proglide device with surgical cut down in patients undergoing TAVI and TEVAR/EVAR Procedures
										</dc:title><dc:creator>Jamal Moosavi</dc:creator><dc:creator> Somaye Ahmadi</dc:creator><dc:creator> Parham Sadeghipour</dc:creator><dc:creator> Ata Firoozi</dc:creator><dc:creator> Bahram Mohebbi</dc:creator><dc:creator> Omid Shafe</dc:creator><dc:creator> Hooman Bakhshandeh Abkenar</dc:creator><dc:creator>Ahoura Salehi Nobandegani</dc:creator><dc:description>&lt;p&gt;Background: The Common Femoral Artery (CFA) is the most frequently used peripheral artery for Trans-catheter aortic valve implantation (TAVI) and Endovascular Aortic Repair (EVAR)/ Thoracic Endovascular Aortic Repair (TEVAR) procedures. CFA access hemostasis could be obtained by manual compression, surgical cut-down, or using arteriotomy closure devices, including ProGlide.&lt;/p&gt;&lt;p&gt;Method: During a retrospective cohort study we compared ProGlide with surgical cut-down hemostasis in 225 patients who underwent TAVI or EVAR/TEVAR, including 290 access sites, during a 10 years period in terms of access site complications, procedure length and post-procedural hospitalization duration.&lt;/p&gt;&lt;p&gt;Results: The success rate of hemostasis was 100% in the PP device group and 98.3% in the SCD group. The mean Procedure length was significantly shorter in ProGlide device hemostasis and the mean post-procedural hospitalization length had a non-significant difference between the two groups. Access site complications occurred in 21.1% of the ProGlide group and 26% of the SCD group.&amp;nbsp;&lt;/p&gt;&lt;p&gt;Conclusion: Perclose ProGlide device is safe and effective for access site closure in procedures that need large sheaths and it is non-inferior to standard surgical cut-down. Training, experience and careful application of the device have significant importance in ensuring successful hemostasis.&lt;/p&gt;</dc:description>
										<dc:publisher>Annals of Circulation - Peertechz Publications</dc:publisher>
										<dc:date>2022-12-31</dc:date>
										<dc:type>Case Report</dc:type>
										<dc:identifier>https://doi.org/10.17352/ac.000019</dc:identifier>
										<dc:language>en</dc:language>
										<dc:rights>Copyright © Jamal Moosavi et al.</dc:rights>
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