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Updated: Oct 9, 2026

Catheter Ablation in Combination With Left Atrial Appendage Closure for Atrial Fibrillation
Published on: February 26, 2013
[Effects of cilostazol in patients with bradycardiac atrial fibrillation]
M Kishida1, K Watanabe, T Tsuruoka
1Department of Internal Medicine, Ehime Prefectural Central Hospital, Ehime.
Insights
Cilostazol significantly improved heart rate and reduced pauses in patients with bradycardiac atrial fibrillation. This antithrombotic agent also demonstrated positive effects on cardiac structure and natriuretic peptide levels.
Area of Science:
- Cardiology
- Pharmacology
Background:
- Bradycardiac atrial fibrillation presents challenges in heart rate management.
- Cilostazol, an antithrombotic agent, is known to affect heart rate.
- Investigating cilostazol's chronotropic effects in cardiac failure is crucial.
Observation:
- Twelve patients with bradycardiac atrial fibrillation were studied.
- Patients received daily oral administration of 100-200 mg cilostazol for 6 months.
- Holter monitoring, echocardiography, and biomarker measurements were conducted before and after treatment.
Findings:
- Cilostazol increased 24-hour total heartbeat counts (mean heart rate from 48 to 60 bpm) and decreased pause frequency.
- Significant reductions were observed in cardiothoracic ratio and left ventricular end-diastolic diameter.
- Brain natriuretic peptide and atrial natriuretic peptide levels decreased significantly post-cilostazol treatment.
Implications:
- Cilostazol shows beneficial effects in patients with bradycardiac atrial fibrillation.
- The drug may improve atrioventricular nodal conductivity and coronary blood supply.
- Further research into cilostazol's role in managing bradycardiac arrhythmias is warranted.
Objectives:
Cilostazol, an antithrombotic agent, directly and indirectly increases the heart rate. This study investigated whether cilostazol increases the heart rate, and whether it has chronotropic effects on cardiac failure in patients with bradycardiac atrial fibrillation.
Methods:
Twelve patients (6 males and 6 females) with bradycardiac atrial fibrillation underwent Holter monitoring (24-hour total heartbeat counts and frequency of pause), echocardiography (left ventricular end-diastolic diameter, percentage fractional shortening), chest roentgenography (cardiothoracic ratio), and measurements of brain natriuretic peptide and atrial natriuretic peptide before and 6 months after daily oral administration of 100-200 mg cilostazol.
Results:
Cilostazol administration increased the 24-hour total heartbeat counts from 69,685 +/- 1,690 (mean +/- SE; mean heart rate: 48 beats/min) to 87,352 +/- 3,123 (60), and decreased the frequency of pause from 362.3 +/- 72.9 to 112.3 +/- 41.0. Cardiothoracic ratio decreased from 55.8 +/- 1.1% to 52.5 +/- 1.1%, left ventricular end-diastolic diameter from 56.1 +/- 0.9 to 52.9 +/- 0.8 mm, but percentage fractional shortening was not significantly changed (from 33.0 +/- 2.2% to 33.7 +/- 2.1%). Brain natriuretic peptide decreased from 97.9 +/- 20.5 to 33.5 +/- 4.8 pg/ml, and atrial natriuretic peptide from 69.5 +/- 12.1 to 46.7 +/- 8.3 pg/ml.
Conclusions:
Cilostazol has beneficial effects in patients with bradycardiac atrial fibrillation. The increase of heart rate may be mediated by improvement of conductivity in the atrioventricular node and increase of coronary blood supply caused by dilation of vessels.
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