Length of stay following percutaneous left atrial appendage occlusion: Data from the prospective, multicenter Amplatzer Amulet Occluder Observational Study

dc.contributor.authorPiayda Kerstin
dc.contributor.authorAfzal Shazia
dc.contributor.authorNielsen-Kudsk Jens Erik
dc.contributor.authorSchmidt Boris
dc.contributor.authorMazzone Patrizio
dc.contributor.authorBerti Sergio
dc.contributor.authorFischer Sven
dc.contributor.authorLund Juha
dc.contributor.authorMontorfano Matteo
dc.contributor.authorHildick-Smith David
dc.contributor.authorGage Ryan
dc.contributor.authorZhao Hong
dc.contributor.authorZeus Tobias
dc.contributor.organizationfi=sisätautioppi|en=Internal Medicine|
dc.contributor.organizationfi=tyks, vsshp|en=tyks, varha|
dc.contributor.organization-code2607318
dc.converis.publication-id66884820
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/66884820
dc.date.accessioned2022-10-27T12:18:46Z
dc.date.available2022-10-27T12:18:46Z
dc.description.abstract<p><b>Aims</b> To evaluate factors influencing the length of stay in patients undergoing percutaneous left atrial appendage occlusion (LAAO). <br></p><p><b>Methods and results</b> Patient characteristics, procedural data and the occurrence of serious adverse events were analyzed from the Amplatzer Amulet Occluder Observational Study. Patients were divided into three groups: same day (S, 0day, n = 60, 5.6%) early (E, 1day, n = 526, 48.9%), regular (R, 2-3days, n = 338, 31.4%) and late (L, >= 4days, n = 152, 14.1%) discharge and followed up for 60 days. Procedure and device related SAE during the in-hospital stay (S: 0.0% vs. E: 1.0% vs. R: 2.1% vs. L: 23%, p<0.0001) were a major trigger for a prolonged in-hospital stay. Of the 37 subjects in the late discharge group with an SAE prior to discharge, cardiac or bleeding complications were the most common underlying conditions, occurring in 26 subjects. Multinomial logistic analysis only identified HAS-BLED score as an independent influencing factor (p = 0.04) for a late discharge. After 60 days, mortality tended to be greatest in the late discharge group (S: 0.0% vs. E: 1.0% vs. R: 1.2% vs. L: 3.3%, p = 0.1066). <br></p><p><b>Conclusion</b> Over half of the subjects receiving an Amplatzer Amulet occluder were discharged within 1 day of the implant procedure. Serious adverse events were a major trigger for a late discharge after LAAO. Increased HAS-BLED score was associated with a prolonged in-hospital stay.<br></p>
dc.identifier.eissn1932-6203
dc.identifier.jour-issn1932-6203
dc.identifier.olddbid174658
dc.identifier.oldhandle10024/157752
dc.identifier.urihttps://www.utupub.fi/handle/11111/34611
dc.identifier.urnURN:NBN:fi-fe2021093048101
dc.language.isoen
dc.okm.affiliatedauthorLund, Juha
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline3121 Internal medicineen_GB
dc.okm.discipline3121 Sisätauditfi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherPUBLIC LIBRARY SCIENCE
dc.publisher.countryUnited Statesen_GB
dc.publisher.countryYhdysvallat (USA)fi_FI
dc.publisher.country-codeUS
dc.relation.articlenumberARTN e0255721
dc.relation.doi10.1371/journal.pone.0255721
dc.relation.ispartofjournalPLoS ONE
dc.relation.issue8
dc.relation.volume16
dc.source.identifierhttps://www.utupub.fi/handle/10024/157752
dc.titleLength of stay following percutaneous left atrial appendage occlusion: Data from the prospective, multicenter Amplatzer Amulet Occluder Observational Study
dc.year.issued2021

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