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Stroke prevention by cilostazol in patients with atherothrombosis: meta-analysis of placebo-controlled randomized
Shinichiro Uchiyama1, Bart M Demaerschalk, Shinya Goto
1Department of Neurology, Tokyo Women's Medical University School of Medicine, Shinjuku-ku, Tokyo, Japan. suchiyam@nij.twmu.ac.jp
Insights
Cilostazol significantly reduces cerebrovascular events in atherothrombosis patients, according to this meta-analysis. The antiplatelet drug showed no increased risk of bleeding complications.
Area of Science:
- Cardiovascular Medicine
- Neurology
- Pharmacology
Background:
- Cilostazol is an antiplatelet agent inhibiting phosphodiesterase III.
- Previous trials on cilostazol for cerebrovascular event prevention yielded mixed results.
Purpose of the Study:
- To systematically review and meta-analyze randomized clinical trials.
- To determine cilostazol's effects on cerebrovascular, cardiac, and vascular events, and major bleeding in atherothrombosis patients.
Main Methods:
- Systematic review and meta-analysis of 12 randomized controlled trials.
- Involved 5674 patients with peripheral arterial disease, cerebrovascular disease, or coronary stenting.
- Data analyzed for cerebrovascular, cardiac, and major bleeding events.
Main Results:
- Cilostazol significantly reduced total vascular events (RR, 0.86; P=.038).
- Cerebrovascular event incidence significantly decreased with cilostazol (RR, 0.58; P < .001).
- No significant difference in cardiac events or major bleeding.
Conclusions:
- Cilostazol significantly reduces cerebrovascular event risk in atherothrombosis.
- This meta-analysis shows no increased bleeding risk associated with cilostazol.
Background:
Cilostazol is an antiplatelet agent that inhibits phosphodiesterase III in platelets and vascular endothelium. Previous randomized controlled trials of cilostazol for prevention of cerebrovascular events have garnered mixed results. We performed a systematic review and meta-analysis of the randomized clinical trials in patients with atherothrombotic diseases to determine the effects of cilostazol on cerebrovascular, cardiac, and all vascular events, and on all major hemorrhagic events.
Methods:
Relevant trials were identified by searching MEDLINE, EMBASE, and the Cochrane Controlled Trial Registry for titles and abstracts. Data from 12 randomized controlled trials, involving 5674 patients, were analyzed for end points of cerebrovascular, cardiac, and major bleeding events. Searching, determination of eligibility, data extraction, and meta-analyses were conducted by multiple independent investigators.
Results:
Data were available in 3782, 1187, and 705 patients with peripheral arterial disease, cerebrovascular disease, and coronary stenting, respectively. Incidence of total vascular events was significantly lower in the cilostazol group compared with the placebo group (relative risk [RR], 0.86; 95% confidence interval [CI], 0.74-0.99; P=.038). This was particularly influenced by a significant decrease of incidence of cerebrovascular events in the cilostazol group (RR, 0.58; 95% CI, 0.43-0.78; P < .001). There was no significant intergroup difference in incidence of cardiac events (RR, 0.99; 95% CI, 0.83-1.17; P=.908) and serious bleeding complications (RR, 1.00; 95% CI, 0.66-1.51; P=.996).
Conclusions:
This first meta-analysis of cilostazol in patients with atherothrombosis demonstrated a significant risk reduction for cerebrovascular events, with no associated increase of bleeding risk.
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