How to Optimize Cardioversion of Atrial Fibrillation

dc.contributor.authorAiraksinen KE Juhani
dc.contributor.organizationfi=sisätautioppi|en=Internal Medicine|
dc.contributor.organizationfi=tyks, vsshp|en=tyks, varha|
dc.contributor.organization-code1.2.246.10.2458963.20.40502528769
dc.converis.publication-id175886892
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/175886892
dc.date.accessioned2022-10-28T13:39:58Z
dc.date.available2022-10-28T13:39:58Z
dc.description.abstractCardioversion (CV) is an essential component of rhythm control strategy in the treatment of atrial fibrillation (AF). Timing of CV is an important manageable factor in optimizing the safety and efficacy of CV. Based on observational studies, the success rate of CV seems to be best (approximate to 95%) at 12-48 h after the onset of arrhythmic symptoms compared with a lower success rate of approximate to 85% in later elective CV. Early AF recurrences are also less common after acute CV compared with later elective CV. CV causes a temporary increase in the risk of thromboembolic complications. Effective anticoagulation reduces this risk, especially during the first 2 weeks after successful CV. However, even during therapeutic anticoagulation, each elective CV increases the risk of stroke 4-fold (0.4% vs. 0.1%) during the first month after the procedure, compared with acute (<48 h) CV or avoiding CV. Spontaneous CVs are common during the early hours of AF. The short wait-and-see approach, up to 24-48 h, is a reasonable option for otherwise healthy but mildly symptomatic patients who are using therapeutic anticoagulation, since they are most likely to have spontaneous rhythm conversion and have no need for active CV. The probability of early treatment failure and antiarrhythmic treatment options should be evaluated before proceeding to CV to avoid the risks of futile CVs.
dc.identifier.eissn2077-0383
dc.identifier.olddbid183475
dc.identifier.oldhandle10024/166569
dc.identifier.urihttps://www.utupub.fi/handle/11111/29776
dc.identifier.urlhttps://doi.org/10.3390/jcm11123372
dc.identifier.urnURN:NBN:fi-fe2022081154597
dc.language.isoen
dc.okm.affiliatedauthorAiraksinen, Juhani
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline3121 Internal medicineen_GB
dc.okm.discipline3121 Sisätauditfi_FI
dc.okm.internationalcopublicationnot an international co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA2 Scientific Article
dc.publisherMDPI
dc.publisher.countrySwitzerlanden_GB
dc.publisher.countrySveitsifi_FI
dc.publisher.country-codeCH
dc.relation.articlenumber3372
dc.relation.doi10.3390/jcm11123372
dc.relation.ispartofjournalJournal of Clinical Medicine
dc.relation.issue12
dc.relation.volume11
dc.source.identifierhttps://www.utupub.fi/handle/10024/166569
dc.titleHow to Optimize Cardioversion of Atrial Fibrillation
dc.year.issued2022

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