Search engine for discovering works of Art, research articles, and books related to Art and Culture
ShareThis
Javascript must be enabled to continue!

Abstract 4367732: Leadless Pacemaker Implantation in the Region of Bachmann’s Bundle: Initial Results

View through CrossRef
Background: Leadless pacemakers are an emerging technology offering a less invasive alternative to traditional transvenous systems. Bachmann bundle (BB) pacing is a novel atrial pacing strategy that may promote more physiologic atrial activation. However, data on the feasibility, safety, and procedural characteristics of leadless pacemaker implantation targeting the Bachmann bundle remains limited. Methods: This retrospective case series was conducted at a tertiary center in Iowa City, USA. We included consecutive patients who underwent attempted BB targeted leadless pacemaker implantation between April 2024 and May 2025. Eligibility for the procedure was determined by the implanting physician. Outcomes included procedural success, procedure time, fluoroscopy duration, radiation dose (mGy), device parameters, EKG parameters, and complications. BB targeting was guided by fluoroscopic landmarks. Descriptive statistics summarized baseline characteristics and outcomes. Results: 17 patients (mean age 67.2 ± 15.5 years; 53% male; 94% white) were included. Of those, 13 (76.5%) had successful BB region leadless pacemaker implantation. Most common indications were sinus node dysfunction (46.2%) and complete heart block (38.5%). The mean procedure time was 72.7 ± 35.1 minutes, fluoroscopy time 10 ± 6.1 minutes, and mean radiation dose was 56.6 ± 47.2 mGy. Initial device parameters (n=13) showed a mean capture threshold of 2.0 ± 0.8 V at 0.6 ± 0.3 ms, sensing amplitude of 1.9 ± 0.9 mV, and impedance of 308.5 ± 67.3 ohms. Follow-up device interrogation, available for 10 patients, showed a mean capture threshold decreased to 0.9 ± 0.5 V at 0.5 ± 0.3 ms, sensing amplitude increased to 3.5 ± 1.4 mV, and impedance decreased to 279 ± 35.7 ohms. P wave duration decreased post-implant (140.3 ± 21.5 ms) vs. pre-implant (154.9 ± 33.5 ms). No procedural complications were reported. Conclusions: Leadless pacemaker implantation targeting the Bachmann’s Bundle is feasible and safe, with a high success rate and encouraging early electrical outcomes. These findings support further investigation of physiologic atrial pacing using leadless technology.
Title: Abstract 4367732: Leadless Pacemaker Implantation in the Region of Bachmann’s Bundle: Initial Results
Description:
Background: Leadless pacemakers are an emerging technology offering a less invasive alternative to traditional transvenous systems.
Bachmann bundle (BB) pacing is a novel atrial pacing strategy that may promote more physiologic atrial activation.
However, data on the feasibility, safety, and procedural characteristics of leadless pacemaker implantation targeting the Bachmann bundle remains limited.
Methods: This retrospective case series was conducted at a tertiary center in Iowa City, USA.
We included consecutive patients who underwent attempted BB targeted leadless pacemaker implantation between April 2024 and May 2025.
Eligibility for the procedure was determined by the implanting physician.
Outcomes included procedural success, procedure time, fluoroscopy duration, radiation dose (mGy), device parameters, EKG parameters, and complications.
BB targeting was guided by fluoroscopic landmarks.
Descriptive statistics summarized baseline characteristics and outcomes.
Results: 17 patients (mean age 67.
2 ± 15.
5 years; 53% male; 94% white) were included.
Of those, 13 (76.
5%) had successful BB region leadless pacemaker implantation.
Most common indications were sinus node dysfunction (46.
2%) and complete heart block (38.
5%).
The mean procedure time was 72.
7 ± 35.
1 minutes, fluoroscopy time 10 ± 6.
1 minutes, and mean radiation dose was 56.
6 ± 47.
2 mGy.
Initial device parameters (n=13) showed a mean capture threshold of 2.
0 ± 0.
8 V at 0.
6 ± 0.
3 ms, sensing amplitude of 1.
9 ± 0.
9 mV, and impedance of 308.
5 ± 67.
3 ohms.
Follow-up device interrogation, available for 10 patients, showed a mean capture threshold decreased to 0.
9 ± 0.
5 V at 0.
5 ± 0.
3 ms, sensing amplitude increased to 3.
5 ± 1.
4 mV, and impedance decreased to 279 ± 35.
7 ohms.
P wave duration decreased post-implant (140.
3 ± 21.
5 ms) vs.
pre-implant (154.
9 ± 33.
5 ms).
No procedural complications were reported.
Conclusions: Leadless pacemaker implantation targeting the Bachmann’s Bundle is feasible and safe, with a high success rate and encouraging early electrical outcomes.
These findings support further investigation of physiologic atrial pacing using leadless technology.

Related Results

Aveir Leadless Pacemaker implantation in pediatric population: a case series
Aveir Leadless Pacemaker implantation in pediatric population: a case series
Abstract Background While the Medtronic Micra pacemaker provided a small device for leadless pacemaker implantation, the Aveir d...
Leadless Pacemaker tine fracture and dislocation: two case reports
Leadless Pacemaker tine fracture and dislocation: two case reports
Abstract The rate of leadless pacemaker implantation is increasing worldwide. To date, there have been few reports of leadless pacemaker dislocation and extraction. This ar...
P185 FOLLOW–UP OF PATIENTS UNDERGOING POST–EXTRACTION LEADLESS PACEMAKER IMPLANTATION
P185 FOLLOW–UP OF PATIENTS UNDERGOING POST–EXTRACTION LEADLESS PACEMAKER IMPLANTATION
Abstract Introduction The implantation of traditional stimulation devices involves numerous complications, in the short and long...
Leadless pacemaker implantation sites confirmed by computed tomography and their parameters and complication rates
Leadless pacemaker implantation sites confirmed by computed tomography and their parameters and complication rates
AbstractBackgroundImplantations of leadless pacemakers in the septum lower the risk of cardiac perforation. However, the relationship between the implantation site and the success ...
Improving outcomes in single chamber leadless pacemakers: strategies for minimizing vascular complications
Improving outcomes in single chamber leadless pacemakers: strategies for minimizing vascular complications
Abstract Background Leadless pacemaker therapy is associated with a significant reduction in lead-related complication rate compared to conventional...
The angle of the tines before the pull and hold test predicts engagement of the tines in Micra leadless pacemaker implantation
The angle of the tines before the pull and hold test predicts engagement of the tines in Micra leadless pacemaker implantation
AbstractBackgroundMicra leadless pacemaker is secured to the myocardium by engagement of at least 2/4 tines confirmed with pull and hold test. However, the pull and hold test is so...
Bacteraemia after leadless pacemaker implantation
Bacteraemia after leadless pacemaker implantation
Background: Transvenous permanent pacemaker related infection is a severe condition associated with significant morbidity and mortality. Leadless pacemakers may be more resistant t...

Back to Top