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Prevention of syncope through permanent cardiac pacing in patients with bifascicular block and syncope of unexplained
Massimo Santini1, Antonio Castro, Franco Giada
1Azienda Ospedaliera S. Filippo Neri, Roma, Italy. m.santini@rmnet.it
Insights
Permanent pacemaker programming with DDD60 significantly reduced syncope and symptoms in bifascicular block patients compared to DDI30. This study highlights effective pacing strategies for managing unexplained syncope in this population.
Area of Science:
- Cardiology
- Electrophysiology
- Medical Devices
Background:
- Syncope in patients with bifascicular block (BFB) presents diagnostic challenges.
- Identifying the cause of syncope in BFB is crucial for effective management.
Purpose of the Study:
- To evaluate the efficacy of permanent cardiac pacing in reducing symptomatic events in patients with BFB and syncope of undetermined origin.
- To compare two pacemaker programming modes: DDD with a lower rate of 60 bpm (DDD60) versus DDI with a lower rate of 30 bpm (DDI30).
Main Methods:
- A multicenter, prospective, randomized, single-blinded study (PRESS trial) enrolled 101 patients.
- Patients with BFB and syncope were randomized to DDD60 or DDI30 pacing.
- Primary endpoint events included syncope, symptomatic presyncope with device intervention, and symptomatic atrioventricular block.
Main Results:
- A significant reduction in primary endpoint events at 2 years was observed in the DDD60 group (HR, 0.32; P=0.042).
- Overall symptom reduction was superior in DDD60 compared to DDI30 (HR, 0.4; P=0.0053).
- 15% of patients developed new rhythm diseases requiring pacing within 2 years.
Conclusions:
- Dual-chamber pacing programmed to DDD60 significantly reduces syncope and cardioinhibitory symptoms in BFB patients compared to DDI30.
- New onset of rhythm diseases requiring pacing occurred in 15% of the study population over 2 years.
Background:
Syncope in patients with bifascicular block (BFB) is a common event whose causes might be difficult to assess.
Methods And Results:
Prevention of syncope through permanent cardiac pacing in patients with bifascicular block (PRESS) is a multicenter, prospective, randomized, single-blinded study designed to demonstrate a reduction in symptomatic events in patients with bifascicular block and syncope of undetermined origin implanted with permanent pacemaker. Device programming mode (NASPE/BPEG code) at DDD with a lower rate of 60 ppm is compared with backup pacing at DDI with a lower rate of 30 ppm. The end point consisted of (1) syncope, (2) symptomatic presyncopal episodes associated with a device intervention (ventricular pacing), and (3) symptomatic episodes associated with intermittent or permanent atrioventricular block (any degree). One hundred one patients were enrolled and randomized. Primary end point events at 2 years were observed in 23 patients, with a significant lower incidence in the study group (hazard ratio, 0.32; 95% confidence interval [CI], 0.10-0.96; P=0.042). Reduction of any symptoms, associated or not with device intervention, was superior in DDD60 compared with DDI30 (hazard ratio, 0.4; 95% confidence interval, 0.25-0.78; P=0.0053). Fourteen patients developed other rhythm diseases and met class I indication for pacing. The annual incidence of rhythm disease development was 7.4%.
Conclusions:
In patients with bifascicular block and syncope of undetermined origin, the use of a dual chamber pacemaker programmed to DDD60 led to a significant reduction of syncope or symptomatic events associated with a cardioinhibitory origin, compared with DDI30 programming. Symptoms associated with a new onset of rhythm disease were found in 15% of the population at 2 years.
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