2022
DOI: 10.1016/j.recesp.2021.10.025
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Guía ESC 2021 sobre estimulación cardiaca y terapia de resincronización

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Cited by 18 publications
(11 citation statements)
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References 800 publications
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“…Although the two previously mentioned population-based studies were unable to control for all relevant SCD risk factors, such as left ventricular function, they corroborate our observations. Previous studies and pacing guidelines have defined non-specific IVCD as either a QRS duration of ≥ 110 ms (13,31,33) or a QRS duration of ≥120 ms (19,32,34) without meeting the criteria for LBBB or RBBB. Thus, we decided to include QRS duration of 110-119 ms as a covariate in our study.…”
Section: Conduction Disorders and Scdmentioning
confidence: 99%
“…Although the two previously mentioned population-based studies were unable to control for all relevant SCD risk factors, such as left ventricular function, they corroborate our observations. Previous studies and pacing guidelines have defined non-specific IVCD as either a QRS duration of ≥ 110 ms (13,31,33) or a QRS duration of ≥120 ms (19,32,34) without meeting the criteria for LBBB or RBBB. Thus, we decided to include QRS duration of 110-119 ms as a covariate in our study.…”
Section: Conduction Disorders and Scdmentioning
confidence: 99%
“…According to current guidelines, the patients were addressed for implantation when affected by symptomatic HFrEF (New York Heart Association class II to ambulatory class IV) despite optimal medical therapy, LV systolic dysfunction with ejection fraction ≤35%, and QRS width ≥130 ms together with LBBB morphology (8). The presence of a LBBB was defined in case of QRS ≥ 130 ms; QS or rS complex in V1 to V2; monophasic and notched or slurred R waves in I, aVL, V5, or V6; and absent Q waves in leads V5 and V6 (9). A three pacing-lead device was implanted in each patient and was programmed to obtain the highest percentage of biventricular stimulation (≥90% of total beats).…”
Section: Study Design and Participantsmentioning
confidence: 99%
“…In 2013, European guidelines recommend that a 7-day monitor to be used as a threshold for whether to install PPM (9), while in the 2021 European guidelines, permanent pacemaker can be used in patients with HAVB that persists for 24-48 h after TAVR (10), the new recommendation was based on an observational study of only 50 patients (11). Prospective trials to investigate surveillance and management of HAVB after TAVR are lacking and current guidelines are based mostly on expert opinions (12).…”
Section: Introductionmentioning
confidence: 99%