Eventos adversos associados ao marcapasso cardíaco leadless AveirTM: um estudo da base de dados MAUDE da Food and Drug Administration.
PMID: 37209414 ·
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Resumo
Leadless pacemaker (LP) offers an innovative approach for treating bradyarrhythmia, thus avoiding pacemaker pocket and lead-related complications. The Food and Drug Administration (FDA) has recently approved the Aveir™ leadless pacing system (screw-in type LP). We queried the FDA MAUDE database to study the safety profile and assess the types of complications with this relatively novel device technology. A MAUDE database search was conducted on January 20, 2023, for reports received post-FDA app
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