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Remote monitoring of implantable loop recorders reduces time to diagnosis in patients with unexplained syncope: a multicenter propensity score-matched study

BACKGROUND: There are little data on remote monitoring (RM) of implantable loop recorders (ILRs) in patients with unexplained syncope and whether it confers enhanced diagnostic power. OBJECTIVE: To evaluate the effect of RM in ILR recipients for unexplained syncope for early detection of clinically...

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Detalles Bibliográficos
Autores principales: Russo, Vincenzo, Rago, Anna, Grimaldi, Nicola, Chianese, Raffaele, Viggiano, Aniello, D’Alterio, Giuliano, Colonna, Diego, Mattera Iacono, Agostino, Papa, Andrea Antonio, Spadaro Guerra, Andrea, Gargaro, Alessio, Rapacciuolo, Antonio, Sarubbi, Berardo, D’Onofrio, Antonio, Nigro, Gerardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10303931/
https://www.ncbi.nlm.nih.gov/pubmed/37388638
http://dx.doi.org/10.3389/fcvm.2023.1193805
Descripción
Sumario:BACKGROUND: There are little data on remote monitoring (RM) of implantable loop recorders (ILRs) in patients with unexplained syncope and whether it confers enhanced diagnostic power. OBJECTIVE: To evaluate the effect of RM in ILR recipients for unexplained syncope for early detection of clinically relevant arrhythmias by comparison with a historical cohort with no RM. METHODS: SyncRM is a propensity score (PS)-matched study prospectively including 133 consecutive patients with unexplained syncope and ILR followed up by RM (RM-ON group). A historical cohort of 108 consecutive ILR patients with biannual in-hospital follow-up visits was used as control group (RM-OFF group). The primary endpoint was the time to the clinician's evaluation of clinically relevant arrhythmias (types 1, 2, and 4 of the ISSUE classification). RESULTS: The primary endpoint of arrhythmia evaluation was reached in 38 patients (28.6%) of the RM-ON group after a median time of 46 days (interquartile range, 13–106) and in 22 patients (20.4%) of the RM-OFF group after 92 days (25–368). The PS-matched adjusted ratio of rates of arrhythmia evaluation was 2.53 (95% confidence interval, 1.32–4.86) in the RM-ON vs. RM-OFF group (p = 0.005). CONCLUSION: In our PS-matched comparison with a historical cohort, RM of ILR patients with unexplained syncope was associated with a 2.5-fold higher chance of evaluations of clinically relevant arrhythmias as compared with biannual in-office follow-up visits.