Why the study?
To evaluate the impact of cerebral microbleeds presence, burden, and location on MACCE risk in acute ischemic stroke patients with AF on oral anticoagulants, and whether effects differ by oral anticoagulant type.
Does the presence and burden of cerebral microbleeds increase the risk of MACCE in patients with acute ischemic stroke and atrial fibrillation taking oral anticoagulants?
Does the presence and burden of cerebral microbleeds increase the risk of MACCE in patients with acute ischemic stroke and atrial fibrillation taking oral anticoagulants?
The presence of multiple cerebral microbleeds increases the risk of MACCE in patients with acute ischemic stroke and atrial fibrillation on oral anticoagulants, particularly those taking warfarin.
Higher CMB burden was associated with increased MACCE risk on OACs after AIS with AF; leaves open whether OAC type or CMB-guided decisions warrant trials.
Background and Purpose: We investigated the impact of the presence, burden, and location of cerebral microbleeds (CMBs) on the risk of major adverse cerebrovascular and cardiovascular events (MACCE) in patients with acute ischemic stroke and atrial fibrillation treated with oral anticoagulants (OACs). We also examined whether the clinical effect of CMBs differs according to the type of OACs. Methods: A total of 1742 patients with acute ischemic stroke and atrial fibrillation treated with OACs were enrolled in this cohort study. The primary composite outcome was the occurrence of MACCE (a composite of stroke, acute myocardial infarction, or vascular death) over a 2-year period according to CMB status. Results: CMB presence was significantly associated with the risk of future MACCE (hazard ratio, 1.89 [95% CI, 1.23–2.88]; P =0.003) after adjustment for confounders in patients with acute ischemic stroke and atrial fibrillation taking OACs. Patients with exactly 1 CMB had a similar rate of MACCE compared with those without CMBs ( P =0.461). However, patients with multiple CMBs (≥2), particularly high burden CMBs (≥5), had a significantly higher proportion of MACCE. Both CMB-positive groups with lobar and deep CMB had more frequent MACCE than the CMB-negative group, and the rate of MACCE was not different according to CMB location. In patients treated with warfarin, CMB was significantly associated with a risk of MACCE ( P =0.002), but not in patients treated with direct OACs ( P =0.517). Conclusions: The study results indicate that the risk of future MACCE increased with increasing CMB burden in patients with AIS and atrial fibrillation taking OACs, while the anatomic location of CMBs did not influence the risk of future MACCE. This risk seemed to be more apparent in patients taking warfarin.
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Choi et al. (2020) studied this question.
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