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Blood pressure during long-term cilostazol-based dual antiplatelet therapy after stroke: a post hoc analysis of the
Kazunori Toyoda1, Masatoshi Koga2, Kenta Tanaka3
1Department of Cerebrovascular Medicine, National Cerebral and Cardiovascular Center, Suita, Japan. toyoda@ncvc.go.jp.
Insights
Lowering systolic blood pressure (SBP) after stroke reduces the risk of recurrent ischemic stroke. Dual antiplatelet therapy with cilostazol is effective for secondary stroke prevention across a broad SBP range.
Area of Science:
- Neurology
- Cardiology
- Clinical Trials
Background:
- Elevated blood pressure (BP) post-stroke is a risk factor for recurrence.
- Understanding the impact of BP on secondary stroke prevention strategies is crucial.
Purpose of the Study:
- To determine the association between follow-up blood pressure and subsequent ischemic stroke risk.
- To evaluate the effect of BP levels on dual antiplatelet therapy efficacy for secondary stroke prevention.
Main Methods:
- Sub-analysis of the randomized controlled trial (CSPS.com).
- Patients received aspirin, clopidogrel, or cilostazol plus aspirin/clopidogrel 8-180 days post-stroke.
- Follow-up BP changes and raw values were analyzed as time-dependent covariates.
Main Results:
- A 10% increase in systolic blood pressure (SBP) was associated with a 19% increased risk of ischemic stroke (HR 1.19).
- A 10 mmHg SBP increase correlated with a 14% higher stroke risk (HR 1.14).
- Dual therapy with cilostazol demonstrated uniform benefit across a wide SBP range (approx. 120-165 mmHg).
Conclusions:
- Lower long-term systolic BP levels post-stroke are linked to reduced risk of subsequent ischemic events.
- Dual antiplatelet therapy including cilostazol is effective for secondary stroke prevention across a broad SBP range.
Abstract:
We determined the associations of follow-up blood pressure (BP) after stroke as a time-dependent covariate with the risk of subsequent ischemic stroke, as well as those of BP levels with the difference in the impact of long-term clopidogrel or aspirin monotherapy versus additional cilostazol medication on secondary stroke prevention. In a sub-analysis of a randomized controlled trial (CSPS.com), patients between 8 and 180 days after stroke onset were randomly assigned to receive aspirin or clopidogrel alone, or a combination of cilostazol with aspirin or clopidogrel. The percent changes, differences, and raw values of follow-up BP were examined. The primary efficacy outcome was the first recurrence of ischemic stroke. In a total of 1657 patients (69.5 ± 9.3 years, female 29.1%) with median 1.5-year follow-up, ischemic stroke recurred in 74 patients. The adjusted hazard ratio for ischemic stroke of a 10% systolic BP (SBP) increase from baseline was 1.19 (95% CI 1.03-1.36), that of a 10 mmHg SBP increase was 1.14 (1.03-1.28), and that of SBP as the raw value with the baseline SBP as a fixed (time-independent) covariate was 1.14 (1.00-1.31). Such significant associations were not observed in diastolic BP-derived variables. The estimated adjusted hazard ratio curves for the outcome showed the benefit of dual therapy over a wide SBP range between ≈120 and ≈165 mmHg uniformly. Lower long-term SBP levels after ischemic stroke were associated with a lower risk of subsequent ischemic events. The efficacy of dual antiplatelet therapy including cilostazol for secondary stroke prevention was evident over a wide SBP range.
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Special considerations while measuring blood pressure
Monitoring Both Arms:
Monitoring BP in both arms during the initial assessment is advisable, as the systolic value may differ by five to ten mm Hg between arms. For subsequent BP assessments, use the arm with the higher reading.

