Key result
Cilostazol is associated with ~13-ms shorter total atrial conduction time in peripheral artery disease.
Why the study?
Total atrial conduction time is a key predictor of new-onset atrial fibrillation, and the effect of cilostazol on this parameter in peripheral artery disease patients was unknown.
Observational (n=30)
Absolute Event Rate: 109.1% vs 121.8%
p-value: p=<0.001
Cilostazol was associated with shorter TACT in PAD; hypothesis-generating for AF prevention, needs randomized confirmation.
OBJECTIVE: Total atrial conduction time (TACT) is the most important parameter in predicting the development of new-onset atrial fibrillation. We investigated the effect of cilostazol therapy on TACT in patients with peripheral artery disease. METHODS: Thirty patients with peripheral artery disease were treated with cilostazol (200 mg/day) for 6 months. The baseline echocardiographic total atrial conduction time parameter was compared with the 6-month follow-up. RESULTS: The TACT duration was decreased in all patients compared with the baseline after therapy (121.8 ± 19.3 vs. 109.1 ± 15.9 milliseconds, p<0.001). However, left atrial (LA) diameter was not changed with the therapy. The reduction of TACT duration was correlated with the increase in mitral E wave velocity/mitral A wave velocity ratio (r=-0.48, p<0.003). CONCLUSION: Our results showed that 200 mg cilostazol treatment decreased TACT duration in patients with peripheral artery disease, which may also prevent the development and/or recurrence of atrial fibrillation (AF).
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Alızade et al. (2013) conducted an observational in Peripheral artery disease (n=30). Cilostazol vs. Baseline was evaluated on Total atrial conduction time (TACT) (p=<0.001). Cilostazol treatment (200 mg/day) significantly decreased total atrial conduction time from 121.8 to 109.1 milliseconds over 6 months in patients with peripheral artery disease.
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