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Prevalence and Clinical Characteristics of Patients with Pause-Dependent Atrioventricular Block
Sok-Sithikun Bun1, Florian Asarisi1, Nathan Heme1
1Cardiology Department, Pasteur University Hospital, Côte-d'Azur University, 06000 Nice, France.
Insights
Pause-dependent atrioventricular block (PD-AVB) affects 14% of patients with complete atrioventricular block (AVB). PD-AVB is linked to a higher incidence of syncope, underscoring its clinical significance.
Area of Science:
- Cardiology
- Electrophysiology
- Internal Medicine
Background:
- Complete atrioventricular block (AVB) is a serious cardiac condition.
- The prevalence and characteristics of pause-dependent atrioventricular block (PD-AVB) in AVB patients remain unclear.
Purpose of the Study:
- To determine the prevalence of PD-AVB in patients with complete or high-grade AVB.
- To investigate the clinical characteristics associated with PD-AVB.
Main Methods:
- Prospective collection of electrocardiogram (ECG) and telemonitoring data from 100 patients with complete (or high-grade) AVB.
- ECG analysis by an electrophysiologist to identify PD-AVB mechanisms.
Main Results:
- 14% of patients (14 out of 100) were diagnosed with PD-AVB.
- PD-AVB patients had a significantly higher rate of syncope (86%) compared to non-PD-AVB patients (51%).
- Common triggers for PD-AVB included premature atrial contractions and premature ventricular contractions.
Conclusions:
- The prevalence of PD-AVB in complete AVB is approximately 14%, potentially underestimated.
- Syncope is a more frequent symptom in patients with PD-AVB.
Background:
In patients with complete atrioventricular block (AVB), the prevalence and clinical characteristics of patients with pause-dependent AVB (PD-AVB) is not known. Our objective was to assess the prevalence of PD-AVB in a population of patients with complete (or high-grade) AVB.
Methods:
Twelve-lead electrocardiogram (ECG) and/or telemonitoring from patients admitted (from September 2020 to November 2021) for complete (or high-degree) AVB were prospectively collected at the University Hospital of Nice. The ECG tracings were analyzed by an electrophysiologist to determine the underlying mechanism of PD-AVB.
Results:
100 patients were admitted for complete (or high-grade) AVB (men 55%; 82 ± 12 years). Arterial hypertension was present in 68% of the patients. Baseline QRS width was 117 ± 32 ms, and mean left ventricular ejection fraction was 56 ± 7%. Fourteen patients (14%) with PD-AVB were identified, and presented similar clinical characteristics in comparison with patients without PD-AVB, except for syncope (which was present in 86% versus 51% in the non-PD-AVB patients, p = 0.01). PD-AVB sequence was induced by: Premature atrial contraction (8/14), premature ventricular contraction (5/14), His extrasystole (1/14), conduction block in a branch (1/14), and atrial tachycardia termination (1/14). All patients with PD-AVB received a dual-chamber pacemaker during hospitalization.
Conclusion:
The prevalence of PD-AVB was 14%, and may be underestimated. PD-AVB episodes were more likely associated with syncope in comparison with patients without PD-AVB.
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