Five-year safety and efficacy of leadless pacemakers in a Dutch cohort

BACKGROUND: Adequate real-world safety and efficacy of leadless pacemakers (LPs) have been demonstrated up to 3 years after implantation. Longer-term data are warranted to assess the net clinical benefit of leadless pacing. OBJECTIVE: The purpose of this study was to evaluate the long-term safety and efficacy of LP therapy in a real-world cohort. METHODS: In this retrospective cohort study, all consecutive patients with a first LP implantation from December 21, 2012, to December 13, 2016, in 6 Dutch high-volume centers were included. The primary safety endpoint was the rate of major procedure-... Mehr ...

Verfasser: Breeman, Karel T N
Oosterwerff, Erik F J
de Graaf, Michiel A
Juffer, Albert
Saleem-Talib, Shmaila
Maass, Alexander H
Wilde, Arthur A M
Boersma, Lucas V A
Ramanna, Hemanth
van Dijk, Vincent F
van Erven, Lieselot
Delnoy, Peter-Paul H M
Tjong, Fleur V Y
Knops, Reinoud E
Dokumenttyp: Artikel
Erscheinungsdatum: 2023
Reihe/Periodikum: Breeman , K T N , Oosterwerff , E F J , de Graaf , M A , Juffer , A , Saleem-Talib , S , Maass , A H , Wilde , A A M , Boersma , L V A , Ramanna , H , van Dijk , V F , van Erven , L , Delnoy , P-P H M , Tjong , F V Y & Knops , R E 2023 , ' Five-year safety and efficacy of leadless pacemakers in a Dutch cohort ' , Heart Rhythm , vol. 20 , no. 8 , pp. 1128-1135 . https://doi.org/10.1016/j.hrthm.2023.05.031
Sprache: Englisch
Permalink: https://search.fid-benelux.de/Record/base-27445635
Datenquelle: BASE; Originalkatalog
Powered By: BASE
Link(s) : https://hdl.handle.net/11370/278ddd25-7069-4545-bb08-e34362f2365e

BACKGROUND: Adequate real-world safety and efficacy of leadless pacemakers (LPs) have been demonstrated up to 3 years after implantation. Longer-term data are warranted to assess the net clinical benefit of leadless pacing. OBJECTIVE: The purpose of this study was to evaluate the long-term safety and efficacy of LP therapy in a real-world cohort. METHODS: In this retrospective cohort study, all consecutive patients with a first LP implantation from December 21, 2012, to December 13, 2016, in 6 Dutch high-volume centers were included. The primary safety endpoint was the rate of major procedure- or device-related complications (ie, requiring surgery) at 5-year follow-up. Analyses were performed with and without Nanostim battery advisory-related complications. The primary efficacy endpoint was the percentage of patients with a pacing capture threshold ≤2.0 V at implantation and without ≥1.5-V increase at the last follow-up visit. RESULTS: A total of 179 patients were included (mean age 79 ± 9 years), 93 (52%) with a Nanostim and 86 (48%) with a Micra VR LP. Mean follow-up duration was 44 ± 26 months. Forty-one major complications occurred, of which 7 were not advisory related. The 5-year major complication rate was 4% without advisory-related complications and 27% including advisory-related complications. No advisory-related major complications occurred a median 10 days (range 0-88 days) postimplantation. The pacing capture threshold was low in 163 of 167 patients (98%) and stable in 157 of 160 (98%). CONCLUSION: The long-term major complication rate without advisory-related complications was low with LPs. No complications occurred after the acute phase and no infections occurred, which may be a specific benefit of LPs. The performance was adequate with a stable pacing capture threshold.