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Evaluation of insertable cardiac monitor placement and safety in the LUX-Dx PERFORM study

FUNDING ACKNOWLEDGEMENTS: Type of funding sources: Private company. Main funding source(s): Boston Scientific Corporation BACKGROUND: The LUX-Dx PERFORM Study is designed to evaluate safety and performance of the LUX-Dx insertable cardiac monitor (ICM) in a general patient population. Enrollment and...

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Detalles Bibliográficos
Autores principales: Richards, M, Stolen, C, Simon, T, Stoltz, T, Manyam, H, Dukes, J W, Bavikati, V, Rosman, J, Rogers, J D, Garner, J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10207579/
http://dx.doi.org/10.1093/europace/euad122.654
Descripción
Sumario:FUNDING ACKNOWLEDGEMENTS: Type of funding sources: Private company. Main funding source(s): Boston Scientific Corporation BACKGROUND: The LUX-Dx PERFORM Study is designed to evaluate safety and performance of the LUX-Dx insertable cardiac monitor (ICM) in a general patient population. Enrollment and device insertions are complete, and all patients have completed 30 days of follow-up. This abstract describes the study population, characterizes device insertion, and reports on preliminary data for ICM system-related complications. METHODS: The LUX-Dx PERFORM study is a prospective, multi-center, single arm, post-market, observational study. The ICM system-related complication-free rate (CFR) at 30 days post-insertion was calculated using Kaplan-Meier methodology and the 97.5% one-side lower confidence limit (LCL) was compared to the prespecified performance target of 94%. All ICM system-related adverse events were adjudicated by independent physician reviewers. RESULTS: 727 patients were enrolled at 24 centers in the United States from March 2021 to May 2022. The study population was 49% male, 91% white and 66+/-14 years old. 717 patients had device insertions and were successfully registered in the LATITUDE Clarity data management system. There were 9 withdrawals prior to insertion and 1 aborted procedure due to deployment difficulty. ICM insertion was performed in-hospital 76% of the time (N=547) and in-clinic 24% of the time (N=171). 96% were de novo device insertions. A variety of closure techniques were used including surgical glue (62%), adhesive strips (45%), sutures (42%), and staples (9%). Median procedure time was 4 minutes (range 1 - 37). There were 4 ICM system-related complications in the first 30 days (CFR 99%, LCL 99%) which meets the acute safety performance goal. The system-related complications include 1 case of ICM deployment difficulty, 1 case of device expulsion three days post insertion, and 2 infections that were treated with oral antibiotics and resolved without further mitigation. CONCLUSION: The LUX-Dx ICM can be inserted quickly, in both hospital and clinic settings, with a very low complication rate. [Figure: see text]