Left atrial appendage closure followed by 6 weeks of antithrombotic therapy: A prospective single-center experience
Background Currently, 2 different left atrial appendage (LAA) closure systems are available for stroke prevention in nonvalvular atrial fibrillation but comparative data are lacking. Objectives To prospectively compare procedural data and patient outcome for 2 contemporary LAA closure systems and to...
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Veröffentlicht in: | Heart rhythm 2013-12, Vol.10 (12), p.1792-1799 |
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creator | Chun, KR Julian, MD Bordignon, Stefano, MD Urban, Verena, MD Perrotta, Laura, MD Dugo, Daniela, MD Fürnkranz, Alexander, MD Nowak, Bernd, MD Schmidt, Boris, MD, FHRS |
description | Background Currently, 2 different left atrial appendage (LAA) closure systems are available for stroke prevention in nonvalvular atrial fibrillation but comparative data are lacking. Objectives To prospectively compare procedural data and patient outcome for 2 contemporary LAA closure systems and to investigate an alternative antithrombotic treatment regimen in high-risk patients. Methods Patients with nonvalvular atrial fibrillation, with high risk for stroke, and who either had contraindication or were not willing to accept oral anticoagulation were prospectively enrolled. Watchman (Boston Scientific, Natick, MA; group A) or Amplatzer Cardiac Plug (St Jude Medical, Minneapolis, MN; group B) devices were implanted. All patients received antithrombotic therapy for 6 weeks. After repeat transesophageal echocardiography, patients were switched to aspirin. Results Eighty patients were enrolled. There was no statistical difference in patient characteristics in groups A and B: CHA2 DS2 VASC score: 4.1 ± 1.5 versus 4.5 ± 1.8; HASBLED score: 3.1 ± 1.1 versus 3.1 ± 1.1, respectively. LAA closure was achieved in 78 of 80 patients (98%) (group A: 38 of 40 [95%] vs group B: 40 of 40 [100%]). There was no difference in procedure time (group A: 48 ± 16 minutes vs group B: 47 ± 15 minutes; P = .69) and fluoroscopy time (group A: 6.0 ± 4.7 minutes vs group B: 7.3 ± 4.4 minutes; P = .25). Major complications included 1 air embolism and delayed tamponade in each group. After 6 weeks, 1 device dislodgment and 4 device-related thrombi were detected. Ninety-four percent of the patients (73 of 77) were switched to aspirin after 6 weeks. During a median follow-up of 364 days (Q1–Q3: 283–539 days), no systemic embolism occurred, but 3 patients died (heart failure: n = 2; bleeding: n = 1). Conclusions Implantation of both LAA closure devices can be performed with high success rates in high-risk patients. Postprocedural 6 weeks antithrombotic therapy followed by aspirin therapy needs to be confirmed in a larger study. |
doi_str_mv | 10.1016/j.hrthm.2013.08.025 |
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Objectives To prospectively compare procedural data and patient outcome for 2 contemporary LAA closure systems and to investigate an alternative antithrombotic treatment regimen in high-risk patients. Methods Patients with nonvalvular atrial fibrillation, with high risk for stroke, and who either had contraindication or were not willing to accept oral anticoagulation were prospectively enrolled. Watchman (Boston Scientific, Natick, MA; group A) or Amplatzer Cardiac Plug (St Jude Medical, Minneapolis, MN; group B) devices were implanted. All patients received antithrombotic therapy for 6 weeks. After repeat transesophageal echocardiography, patients were switched to aspirin. Results Eighty patients were enrolled. There was no statistical difference in patient characteristics in groups A and B: CHA2 DS2 VASC score: 4.1 ± 1.5 versus 4.5 ± 1.8; HASBLED score: 3.1 ± 1.1 versus 3.1 ± 1.1, respectively. LAA closure was achieved in 78 of 80 patients (98%) (group A: 38 of 40 [95%] vs group B: 40 of 40 [100%]). There was no difference in procedure time (group A: 48 ± 16 minutes vs group B: 47 ± 15 minutes; P = .69) and fluoroscopy time (group A: 6.0 ± 4.7 minutes vs group B: 7.3 ± 4.4 minutes; P = .25). Major complications included 1 air embolism and delayed tamponade in each group. After 6 weeks, 1 device dislodgment and 4 device-related thrombi were detected. Ninety-four percent of the patients (73 of 77) were switched to aspirin after 6 weeks. During a median follow-up of 364 days (Q1–Q3: 283–539 days), no systemic embolism occurred, but 3 patients died (heart failure: n = 2; bleeding: n = 1). Conclusions Implantation of both LAA closure devices can be performed with high success rates in high-risk patients. Postprocedural 6 weeks antithrombotic therapy followed by aspirin therapy needs to be confirmed in a larger study.</description><identifier>ISSN: 1547-5271</identifier><identifier>EISSN: 1556-3871</identifier><identifier>DOI: 10.1016/j.hrthm.2013.08.025</identifier><identifier>PMID: 23973952</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Aged ; Atrial Appendage - diagnostic imaging ; Atrial fibrillation ; Atrial Fibrillation - complications ; Atrial Fibrillation - physiopathology ; Atrial Fibrillation - therapy ; Cardiovascular ; Echocardiography, Transesophageal ; Female ; Fibrinolytic Agents - therapeutic use ; Follow-Up Studies ; Humans ; Left atrial appendage closure ; Male ; Prospective Studies ; Stroke ; Stroke - etiology ; Stroke - prevention & control ; Thrombosis - complications ; Thrombosis - drug therapy ; Time Factors ; Treatment Outcome</subject><ispartof>Heart rhythm, 2013-12, Vol.10 (12), p.1792-1799</ispartof><rights>Heart Rhythm Society</rights><rights>2013 Heart Rhythm Society</rights><rights>Copyright © 2013 Heart Rhythm Society. Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c480t-d5716fa3c6feb1780919a30251a8788a6355f566e782f4adcd4f4868e7f476f03</citedby><cites>FETCH-LOGICAL-c480t-d5716fa3c6feb1780919a30251a8788a6355f566e782f4adcd4f4868e7f476f03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1547527113009004$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23973952$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chun, KR Julian, MD</creatorcontrib><creatorcontrib>Bordignon, Stefano, MD</creatorcontrib><creatorcontrib>Urban, Verena, MD</creatorcontrib><creatorcontrib>Perrotta, Laura, MD</creatorcontrib><creatorcontrib>Dugo, Daniela, MD</creatorcontrib><creatorcontrib>Fürnkranz, Alexander, MD</creatorcontrib><creatorcontrib>Nowak, Bernd, MD</creatorcontrib><creatorcontrib>Schmidt, Boris, MD, FHRS</creatorcontrib><title>Left atrial appendage closure followed by 6 weeks of antithrombotic therapy: A prospective single-center experience</title><title>Heart rhythm</title><addtitle>Heart Rhythm</addtitle><description>Background Currently, 2 different left atrial appendage (LAA) closure systems are available for stroke prevention in nonvalvular atrial fibrillation but comparative data are lacking. Objectives To prospectively compare procedural data and patient outcome for 2 contemporary LAA closure systems and to investigate an alternative antithrombotic treatment regimen in high-risk patients. Methods Patients with nonvalvular atrial fibrillation, with high risk for stroke, and who either had contraindication or were not willing to accept oral anticoagulation were prospectively enrolled. Watchman (Boston Scientific, Natick, MA; group A) or Amplatzer Cardiac Plug (St Jude Medical, Minneapolis, MN; group B) devices were implanted. All patients received antithrombotic therapy for 6 weeks. After repeat transesophageal echocardiography, patients were switched to aspirin. Results Eighty patients were enrolled. There was no statistical difference in patient characteristics in groups A and B: CHA2 DS2 VASC score: 4.1 ± 1.5 versus 4.5 ± 1.8; HASBLED score: 3.1 ± 1.1 versus 3.1 ± 1.1, respectively. LAA closure was achieved in 78 of 80 patients (98%) (group A: 38 of 40 [95%] vs group B: 40 of 40 [100%]). There was no difference in procedure time (group A: 48 ± 16 minutes vs group B: 47 ± 15 minutes; P = .69) and fluoroscopy time (group A: 6.0 ± 4.7 minutes vs group B: 7.3 ± 4.4 minutes; P = .25). Major complications included 1 air embolism and delayed tamponade in each group. After 6 weeks, 1 device dislodgment and 4 device-related thrombi were detected. Ninety-four percent of the patients (73 of 77) were switched to aspirin after 6 weeks. During a median follow-up of 364 days (Q1–Q3: 283–539 days), no systemic embolism occurred, but 3 patients died (heart failure: n = 2; bleeding: n = 1). Conclusions Implantation of both LAA closure devices can be performed with high success rates in high-risk patients. Postprocedural 6 weeks antithrombotic therapy followed by aspirin therapy needs to be confirmed in a larger study.</description><subject>Aged</subject><subject>Atrial Appendage - diagnostic imaging</subject><subject>Atrial fibrillation</subject><subject>Atrial Fibrillation - complications</subject><subject>Atrial Fibrillation - physiopathology</subject><subject>Atrial Fibrillation - therapy</subject><subject>Cardiovascular</subject><subject>Echocardiography, Transesophageal</subject><subject>Female</subject><subject>Fibrinolytic Agents - therapeutic use</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>Left atrial appendage closure</subject><subject>Male</subject><subject>Prospective Studies</subject><subject>Stroke</subject><subject>Stroke - etiology</subject><subject>Stroke - prevention & control</subject><subject>Thrombosis - complications</subject><subject>Thrombosis - drug therapy</subject><subject>Time Factors</subject><subject>Treatment Outcome</subject><issn>1547-5271</issn><issn>1556-3871</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1v1DAQhiMEoh_wC5CQj1wS_JHYDhJIVUWh0kocgLPldcZdb5042E7L_nucbuHQC6eZw_vOvPNMVb0huCGY8Pf7ZhfzbmwoJqzBssG0e1adkq7jNZOCPF_7VtQdFeSkOktpjzHtOWYvqxPKesH6jp5WaQM2I52j0x7peYZp0DeAjA9piYBs8D7cw4C2B8TRPcBtQsEiPWWXdzGM25CdQXkHUc-HD-gCzTGkGUx2d4CSm2481AamDBHB7xmig8nAq-qF1T7B68d6Xv28-vzj8mu9-fbl-vJiU5tW4lwPnSDcama4hS0REvek16xcSbQUUmrOus52nIOQ1LZ6MENrW8klCNsKbjE7r94d55ZQvxZIWY0uGfBeTxCWpEjLW9lTLmiRsqPUlPwpglVzdKOOB0WwWmmrvXqgrVbaCktVchTX28cFy3aE4Z_nL94i-HgUQDnzzkFUyTwgGFwskNQQ3H8WfHriN95Nzmh_CwdI-7DEqRBURCWqsPq-Pnz9N2EY9xi37A8Yy6fS</recordid><startdate>20131201</startdate><enddate>20131201</enddate><creator>Chun, KR Julian, MD</creator><creator>Bordignon, Stefano, MD</creator><creator>Urban, Verena, MD</creator><creator>Perrotta, Laura, MD</creator><creator>Dugo, Daniela, MD</creator><creator>Fürnkranz, Alexander, MD</creator><creator>Nowak, Bernd, MD</creator><creator>Schmidt, Boris, MD, FHRS</creator><general>Elsevier Inc</general><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>7X8</scope></search><sort><creationdate>20131201</creationdate><title>Left atrial appendage closure followed by 6 weeks of antithrombotic therapy: A prospective single-center experience</title><author>Chun, KR Julian, MD ; Bordignon, Stefano, MD ; Urban, Verena, MD ; Perrotta, Laura, MD ; Dugo, Daniela, MD ; Fürnkranz, Alexander, MD ; Nowak, Bernd, MD ; Schmidt, Boris, MD, FHRS</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c480t-d5716fa3c6feb1780919a30251a8788a6355f566e782f4adcd4f4868e7f476f03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Aged</topic><topic>Atrial Appendage - diagnostic imaging</topic><topic>Atrial fibrillation</topic><topic>Atrial Fibrillation - complications</topic><topic>Atrial Fibrillation - physiopathology</topic><topic>Atrial Fibrillation - therapy</topic><topic>Cardiovascular</topic><topic>Echocardiography, Transesophageal</topic><topic>Female</topic><topic>Fibrinolytic Agents - therapeutic use</topic><topic>Follow-Up Studies</topic><topic>Humans</topic><topic>Left atrial appendage closure</topic><topic>Male</topic><topic>Prospective Studies</topic><topic>Stroke</topic><topic>Stroke - etiology</topic><topic>Stroke - prevention & control</topic><topic>Thrombosis - complications</topic><topic>Thrombosis - drug therapy</topic><topic>Time Factors</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chun, KR Julian, MD</creatorcontrib><creatorcontrib>Bordignon, Stefano, MD</creatorcontrib><creatorcontrib>Urban, Verena, MD</creatorcontrib><creatorcontrib>Perrotta, Laura, MD</creatorcontrib><creatorcontrib>Dugo, Daniela, MD</creatorcontrib><creatorcontrib>Fürnkranz, Alexander, MD</creatorcontrib><creatorcontrib>Nowak, Bernd, MD</creatorcontrib><creatorcontrib>Schmidt, Boris, MD, FHRS</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Heart rhythm</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chun, KR Julian, MD</au><au>Bordignon, Stefano, MD</au><au>Urban, Verena, MD</au><au>Perrotta, Laura, MD</au><au>Dugo, Daniela, MD</au><au>Fürnkranz, Alexander, MD</au><au>Nowak, Bernd, MD</au><au>Schmidt, Boris, MD, FHRS</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Left atrial appendage closure followed by 6 weeks of antithrombotic therapy: A prospective single-center experience</atitle><jtitle>Heart rhythm</jtitle><addtitle>Heart Rhythm</addtitle><date>2013-12-01</date><risdate>2013</risdate><volume>10</volume><issue>12</issue><spage>1792</spage><epage>1799</epage><pages>1792-1799</pages><issn>1547-5271</issn><eissn>1556-3871</eissn><abstract>Background Currently, 2 different left atrial appendage (LAA) closure systems are available for stroke prevention in nonvalvular atrial fibrillation but comparative data are lacking. Objectives To prospectively compare procedural data and patient outcome for 2 contemporary LAA closure systems and to investigate an alternative antithrombotic treatment regimen in high-risk patients. Methods Patients with nonvalvular atrial fibrillation, with high risk for stroke, and who either had contraindication or were not willing to accept oral anticoagulation were prospectively enrolled. Watchman (Boston Scientific, Natick, MA; group A) or Amplatzer Cardiac Plug (St Jude Medical, Minneapolis, MN; group B) devices were implanted. All patients received antithrombotic therapy for 6 weeks. After repeat transesophageal echocardiography, patients were switched to aspirin. Results Eighty patients were enrolled. There was no statistical difference in patient characteristics in groups A and B: CHA2 DS2 VASC score: 4.1 ± 1.5 versus 4.5 ± 1.8; HASBLED score: 3.1 ± 1.1 versus 3.1 ± 1.1, respectively. LAA closure was achieved in 78 of 80 patients (98%) (group A: 38 of 40 [95%] vs group B: 40 of 40 [100%]). There was no difference in procedure time (group A: 48 ± 16 minutes vs group B: 47 ± 15 minutes; P = .69) and fluoroscopy time (group A: 6.0 ± 4.7 minutes vs group B: 7.3 ± 4.4 minutes; P = .25). Major complications included 1 air embolism and delayed tamponade in each group. After 6 weeks, 1 device dislodgment and 4 device-related thrombi were detected. Ninety-four percent of the patients (73 of 77) were switched to aspirin after 6 weeks. During a median follow-up of 364 days (Q1–Q3: 283–539 days), no systemic embolism occurred, but 3 patients died (heart failure: n = 2; bleeding: n = 1). Conclusions Implantation of both LAA closure devices can be performed with high success rates in high-risk patients. Postprocedural 6 weeks antithrombotic therapy followed by aspirin therapy needs to be confirmed in a larger study.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>23973952</pmid><doi>10.1016/j.hrthm.2013.08.025</doi><tpages>8</tpages></addata></record> |
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subjects | Aged Atrial Appendage - diagnostic imaging Atrial fibrillation Atrial Fibrillation - complications Atrial Fibrillation - physiopathology Atrial Fibrillation - therapy Cardiovascular Echocardiography, Transesophageal Female Fibrinolytic Agents - therapeutic use Follow-Up Studies Humans Left atrial appendage closure Male Prospective Studies Stroke Stroke - etiology Stroke - prevention & control Thrombosis - complications Thrombosis - drug therapy Time Factors Treatment Outcome |
title | Left atrial appendage closure followed by 6 weeks of antithrombotic therapy: A prospective single-center experience |
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