Sarah Zeriouh
Vasileios Sousonis
Roberto Menè
Serge Boveda
Quentin Voglimacci-StephanopoliStéphane Combes*
- Heart Rhythm Management Department, Clinique Pasteur, Toulouse, France
Background: Cardiac Implantable Electronic Device infections increase short- and long-term mortality, along with healthcare costs. Leadless pacemakers (PM) were developed to overcome pocket- and minimize lead-related complications in selected high-risk patients. Recent advancements enable leadless devices to mechanically detect atrial activity, facilitating atrioventricular (AV) synchronous stimulation.
Case summary: A 90-year-old woman, implanted with a dual-chamber pacemaker eight years ago due to sinus node dysfunction, presented with syncope. A diagnosis of complete AV block, in the setting of ventricular lead dysfunction was made. Due to a high risk of infection, the patient was implanted with a leadless PM capable of maintaining AV synchrony in VDD mode (MICRA™ model MC1AVR1). The transvenous PM was programmed to AAI-R mode to drive the atria, which, in turn, triggered the leadless PM to stimulate the ventricles. At six month follow-up, the AV synchrony rate was 85%.
Conclusion: The combination of classic atrial pacing with leadless ventricular stimulation can be used in high-risk patients to reduce the risk of complications, in the setting of ventricular lead dysfunction. In this manner, AV synchrony can be maintained, improving hemodynamic parameters and quality of life. Low sinus rate variability at rest is essential to achieve a high AV synchrony rate in such cases.
1. Introduction
Cardiac Implantable Electronic Devices (CIEDs) reduce morbidity and mortality in appropriately selected patients. These benefits may be mitigated by complications such as infections, that increase short- and long-term mortality along with healthcare costs (1). Several risk factors for CIED-related infections have been identified and include: age, the lack of antibiotic prophylaxis, diabetes, renal impairment, the use of corticosteroids and early reinterventions (2). Leadless pacemakers (PM) were developed to overcome pocket- and minimize lead-related complications. In order to preserve atrioventricular (AV) synchrony, recent models are equipped with an accelerometer-based atrial sensing algorithm. In this case report, we present a patient at high risk of infection, with complete AV block due to dysfunction of a ventricular pacing lead, in whom AV synchrony was achieved with the combination of a MICRA AV and a transvenous dual-chamber PM.
2. Case description
A 90-year-old woman presented to the Emergency Department for syncope. Her past medical history included a moderate chronic kidney disease and the implantation of a dual-chamber PM for symptomatic sinus node dysfunction eight years prior to her presentation. Of note, PM implantation was complicated by an early displacement of the ventricular lead, necessitating a reintervention on the first day following the procedure. At her admission, the patient was confused and hypotensive with a blood pressure of 89/56 mmHg and a heart rate of 35 beats per minute. Physical examination revealed no signs of heart failure or heart murmurs. Laboratory results showed a potassium level of 5,6 mmol/L (normal ranges 3,5–5,0 mmol/L), a glomerular filtration rate of 38 ml/min and a C-reactive protein of 7,6 mg/L (normal ranges < 5 mg/L). The electrocardiogram revealed a complete AV block due to intermittent loss of capture of the ventricular lead (Figure 1). Echocardiography showed a preserved right and left ventricular systolic function, without significant heart valve disease. The interrogation of the PM revealed an elevation of the ventricular stimulation threshold (3,5 V at a pulse width of 0,5 ms), compared with 0,7 V at a pulse width of 0,5 ms three months ago, along with a ventricular sensing at 8 mV and a stable impedance of 480 ohms. Corresponding parameters for the atrial lead included a stimulation threshold of 0,6 Volts at a pulse width of 0,5 ms, a sensing of 0,4 mV and an impedance of 420 ohms. Battery's longevity was estimated at three years. Chest x-ray did not show any macroscopic lead fracture or displacement. Based on the above, the diagnosis of a syncope due to complete AV block in the setting of ventricular lead dysfunction was made.
Figure 1. Electrocardiogram showing spontaneous P wave activity followed by unipolar ventricular stimulation spikes that most of the times are ineffective (blue arrows) and rarely result in ventricular capture (green arrows).
As the risk of CIEDs-related infection was high, with a calculated PADIT score at 7, representing a subsequent rate of hospitalization for device infection of 2.82% at one year, the patient was implanted with a leadless PM capable of maintaining AV synchrony in VDD mode (MICRA™ AV model MC1AVR1, Medtronic, MN, USA). The device was implanted at the level of the lower interventricular septum, as shown in Figure 2, since the mid-septum was difficult to access. During the implantation procedure, while performing the leadless stimulation threshold testing, no atrial retrograde conduction was observed. The transvenous PM was programmed to an AAI-R mode. With these settings, the transvenous PM was responsible for rate-responsive atrial stimulation, while the leadless PM allowed for atrial triggered ventricular stimulation (Figure 3). At day one after implantation, a chest x-ray showed no signs of displacement (Figure 4) and the leadless PM interrogation revealed satisfying parameters: stimulation threshold of 0,25 volts at a pulse width of 0,24 ms and an impedance 870 ohms. The patient was discharged one day after implantation. During follow-up, the electrocardiogram and device interrogation revealed stable stimulation parameters with an AV synchrony rate of 88% at one month (Figure 5) and 85% at six months (Table 1). An AAI-R mode setting was maintained for the transvenous PM. The patient had no perioperative or short-terms complications.
Figure 2. Procedural fluoroscopy images showing leadless PM's position at the level of the lower interventricular septum, just before device deployment. RAO, right anterior oblique; LAO, left anterior oblique.
Figure 3. Electrocardiogram showing unipolar atrial stimulation by the transvenous pacemaker followed by a ventricular spike generated by the leadless pacemaker that leads to ventricular capture with a fixed atrioventricular delay, resulting in atrioventricular synchrony. One ventricular and one atrial ectopic beat are also present.
Figure 4. Post-procedural chest x-Ray showing a dual chamber transvenous pacemaker and a MICRA™ AV leadless pacemaker implanted at the interventricular septum.
Figure 5. MICRA™ AV window. Lead DI shows a sharp and high-amplitude signal that corresponds to the atrial pacing stimulus. An atrial mechanical event is sensed during the A3 (passive ventricular filling phase)/A4 (active ventricular filling) window, marked as AM on the stip. After the predefined atrioventricular delay, the pacing stimulus is delivered (VP). The amplitude of the recorded atrial signal has been automatically decreased to adapt to the sensing of the high amplitude far-field atrial pacing stimulus. Nevertheless, the atrial activity is well recognized by the accelerometer and the resulting atrioventricular synchrony is effective. VE, defines the end of the A3 window; AM, presumed atrial mechanical contraction (A4 signal/A-wave); VP, ventricular pacing.
3. Timeline
Table 1. Timeline.
4. Discussion
Infection is one of the most threatening CIEDs complications, significantly increasing morbidity, mortality and healthcare costs (3, 4). Infection rates are known to be higher with device replacement procedures (5). Among others risk factors, early reintervention is also associated with an increased risk of infection (OR15.04; 95% CI, 6.7 to 33.73) (2). Renal insufficiency, even when moderate (GFR ≤60 cc/min/1.73 m2), dramatically increases the risk of infection (6). Recent technological advances introduced the use of leadless PMs. Their main advantage is the absence of a subcutaneous pocket and transvenous leads, resulting in a very low rate of device-related infections (7). Originally, these devices where only able to sense and stimulate the right ventricle (i.e., VVI mode) (8). The potential benefits of atrial pacing in patients with sinus node dysfunction, as well as the recognized benefits of AV synchrony mandated further development of leadless PMs. Atrioventricular synchrony decreases the incidence of pacemaker syndrome, improves stroke volume and positively influences functional status and quality of life of patients with AV block (9–11). Recently, the second-generation of the most widely used leadless PM, the MICRATM AV model MC1AVR1 (Medtronic, MN, USA) was introduced to widen the spectrum of patients who qualify for leadless pacing. This device provides contactless atrial sensing and allows for AV synchronous ventricular stimulation in VDD mode. Atrial sensing relies on mechanical detection of the atrial contraction via an integrated accelerometer-based sensor. Atrioventricular synchrony in early short-term feasibility studies ranged from 60%–90%, even though it was heavily dependent on patient's activity level and intrinsic AV conduction (12, 13). A recent study showed that a high AV synchrony rate can be predicted by an E/A ratio < 0.94 and a low sinus rate variability at rest (standard deviation of successive differences of P-P intervals < 5 bpm) (14).
The patient presented in this case was a fragile 90-year-old woman, initially implanted with a dual chamber PM for sinus node dysfunction, who subsequently developed a complete AV block. She had several risk factors for device related infection: a history of early device reintervention, a ventricular lead dysfunction and renal impairment. We therefore decided to implant a leadless PM programmed in a VDD mode to minimize the risk of device infection while, at the same time, preserving AV synchrony. The AV synchrony rate was satisfying at 88% at one month follow-sup, and 85% at 6 months The relative stable atrial stimulation by the transvenous PM in AAI-R mode in a patient with a low level of physical activity seems to account for the observed high level of AV synchrony.
Data availability statement
The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author.
Ethics statement
Written informed consent was obtained from the individual(s) for the publication of any potentially identifiable images or data included in this article. Written informed consent was obtained from the participant/patient(s) for the publication of this case report.
Author contributions
SZ: Writing – original draft, Writing – review & editing. VS: Writing – review & editing. RM: Conceptualization, Writing – review & editing. SB: Resources, Supervision, Validation, Writing – review & editing. QV: Conceptualization, Data curation, Validation, Writing – original draft. SC: Writing – review & editing.
Funding
The author(s) declare that no financial support was received for the research, authorship, and/or publication of this article.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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Keywords: leadless pacemaker, endovascular pacemaker, atrioventricular synchrony, lead dysfunction, device infection
Citation: Zeriouh S, Sousonis V, Menè R, Boveda S, Voglimacci-Stephanopoli Q and Combes S (2023) Case Report: A leadless and endovascular pacemaker teamwork. Front. Cardiovasc. Med. 10:1287506. doi: 10.3389/fcvm.2023.1287506
Received: 1 September 2023; Accepted: 11 October 2023;
Published: 9 November 2023.
Edited by:
Simon Pecha, University Heart and Vascular Center, University Medical Center Hamburg-Eppendorf, GermanyReviewed by:
Weichieh Lee, Chi Mei Medical Center, TaiwanQun-Shan Wang, Shanghai Jiao Tong University, China
© 2023 Zeriouh, Sousonis, Menè, Boveda, Voglimacci-Stephanopoli and Combes. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Stéphane Combes scombes@cinique-pasteur.com