Why the study?
It was hypothesized that intracranial hemorrhage risk in patients with cardioembolic ischemic stroke treated with oral anticoagulants can be predicted by baseline MRI markers of hemorrhagic-prone cerebral angiopathies.
Do baseline MRI markers of cerebral small vessel disease predict intracranial hemorrhage in older patients with cardioembolic stroke starting oral anticoagulants?
Do baseline MRI markers of cerebral small vessel disease predict intracranial hemorrhage in older patients with cardioembolic stroke starting oral anticoagulants?
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Baseline MRI evidence of advanced cerebral small vessel disease strongly predicts the risk of intracranial hemorrhage in older patients starting oral anticoagulation for cardioembolic stroke.
Objective We tested the hypothesis that the risk of intracranial hemorrhage (ICH) in patients with cardioembolic ischemic stroke who are treated with oral anticoagulants (OAs) can be predicted by evaluating surrogate markers of hemorrhagic-prone cerebral angiopathies using a baseline MRI. Methods Patients were participants in a multicenter and prospective observational study. They were older than 64 years, had a recent cardioembolic ischemic stroke, and were new users of OAs. They underwent a baseline MRI analysis to evaluate microbleeds, white matter hyperintensities, and cortical superficial siderosis. We collected demographic variables, clinical characteristics, risk scores, and therapeutic data. The primary endpoint was ICH that occurred during follow-up. We performed bivariate and multivariate Cox regression analyses. Results We recruited 937 patients (aged 77.6 ± 6.5 years; 47.9% were men). Microbleeds were detected in 207 patients (22.5%), moderate/severe white matter hyperintensities in 419 (45.1%), and superficial siderosis in 28 patients (3%). After a mean follow-up of 23.1 ± 6.8 months, 18 patients (1.9%) experienced an ICH. In multivariable analysis, microbleeds (hazard ratio 2.7, 95% confidence interval [CI] 1.1–7, p = 0.034) and moderate/severe white matter hyperintensities (hazard ratio 5.7, 95% CI 1.6–20, p = 0.006) were associated with ICH (C index 0.76, 95% CI 0.66–0.85). Rate of ICH was highest in patients with both microbleed and moderate/severe WMH (3.76 per 100 patient-years, 95% CI 1.62–7.4). Conclusion Patients taking OAs who have advanced cerebral small vessel disease, evidenced by microbleeds and moderate to severe white matter hyperintensities, had an increased risk of ICH. Our results should help to determine the risk of prescribing OA for a patient with cardioembolic stroke. ClinicalTrials.gov identifier NCT02238470.
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Martí‐Fábregas et al. (2019) studied this question.
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