Key result
Dual-lead pacemakers are linked to ~15% more perioperative complications than single-lead devices.
Why the study?
Does dual-lead device implantation increase perioperative complications compared to single-lead devices in patients undergoing new pacemaker or ICD implantation?
Cohort (n=169,547)
Yes
Does dual-lead device implantation increase perioperative complications compared to single-lead devices in patients undergoing new pacemaker or ICD implantation?
Dual-lead pacemakers are associated with a higher risk of perioperative complications compared to single-lead pacemakers, primarily due to lead dislocations, a difference not observed in ICD implantations.
Answers are grounded in this paper and cite their sources.
Higher complications with dual-lead pacemakers warrant caution; hypothesis-generating and requires randomized confirmation.
Background/Objective: Previous studies have indicated a higher incidence of complications associated with dual-lead devices compared to single-lead devices. This retrospective study aimed to investigate the effect of lead count and other factors on peri/postoperative complications for new pacemaker (PM) or implantable cardioverter-defibrillator (ICD) implantations in a representative German cohort. Methods: In accordance with quality assurance (QS) requirements, all hospitals in Germany collect patient-specific data on cardiac device implantation. We utilized the QS database from North Rhine-Westphalia to analyze data from 169,547 patients who underwent PM (n = 137,208) or ICD (n = 32,339) implantation between 2010 and 2014. The primary endpoint was the incidence of perioperative complications in the PM and ICD groups, analyzed separately for single- and dual-lead systems. Regression analysis was performed to identify specific risk factors and the effect of lead number on complications. Results: In the PM group, patients with dual-lead devices experienced significantly more complications than those with single-lead devices (3.27% vs. 2.85%, p < 0.001), largely driven by lead dislocations. In the ICD group, no significant difference in complication rates was observed between single-lead and dual-lead devices (1.39% vs. 1.46%, p = 0.635). The risk of complications was over twice as high for PM implantation compared to ICD implantation (3.17% vs. 1.42%). Patients with intrahospital complications faced a significantly higher risk of mortality than those without complications (PM: 4.5% vs. 1.6%; ICD: 3.9% vs. 0.5%). Independent risk factors for complications and mortality were identified in both groups, with a notable increase in the risk of intrahospital mortality associated with complications. Conclusions: Complications of dual-lead PM implantations are higher than single-lead procedures, mostly due to lead dislocations. Such a difference, though, was not observed in ICD implantations. Our findings may help optimize procedural strategies to improve patient safety, especially in PM implantations.
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Scholten et al. (2025) conducted a cohort in Pacemaker or implantable cardioverter-defibrillator (ICD) implantation (n=169,547). Dual-lead devices vs. Single-lead devices was evaluated on Incidence of perioperative complications (p=<0.001). Dual-lead pacemaker implantations were associated with more perioperative complications than single-lead devices, while no significant difference was observed for ICDs.
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