Why the study?
Intracerebral hemorrhage risk is higher in elderly AF patients on antithrombotic therapy and in those with cerebral amyloid angiopathy, but whether underlying cerebral amyloid angiopathy influences mortality in this population was unknown.
Does the presence of cerebral amyloid angiopathy influence mortality in patients with atrial fibrillation on antithrombotic therapy who present with non-traumatic intracerebral hemorrhage?
Does the presence of cerebral amyloid angiopathy influence mortality in patients with atrial fibrillation on antithrombotic therapy who present with non-traumatic intracerebral hemorrhage?
In patients with atrial fibrillation on antithrombotic therapy who suffer a non-traumatic ICH, the presence of cerebral amyloid angiopathy does not significantly impact their already high mortality rate.
CAA does not modify post-ICH mortality in AF on antithrombotics; leaves open its role in secondary prevention decisions.
Background Intracerebral hemorrhage (ICH) risk is higher in elderly patients with atrial fibrillation on antithrombotic therapy as well as those with cerebral amyloid angiopathy (CAA). We investigated if mortality among patients with atrial fibrillation on antithrombotic therapy presenting with non‐traumatic ICH was influenced by underlying CAA. Methods and Results We used the Rochester Epidemiology Project to identify 6045 patients with atrial fibrillation aged >55 years on anticoagulation or antiplatelet therapy from 1995 to 2016. Seventy‐four patients in this cohort presented with non‐traumatic ICH. Medical records including imaging data were reviewed to identify those with CAA and record baseline variables and outcomes of interest; 38 of our 74 patients (51.4%) (mean age 81.5 years) met Modified Boston Criteria for possible or probable CAA. Twenty‐six of 74 patients (35%) died during the first 30 days while 56 of the 74 (76%) patients died by 10 years follow‐up after index ICH. Overall mortality was not significantly different between the CAA and non‐CAA groups at any point of time during follow‐up ( P =0.89) even amongst patients restarted on anticoagulation +/− antiplatelet (n=19) ( P =0.46) or those patients restarted only on antiplatelet therapy (n=22) ( P =0.66). Three of the 41 patients who restarted on antithrombotic therapy had a recurrent ICH; these 3 patients met criteria for possible or probable CAA. Conclusions Although more than half of our patients with atrial fibrillation on antithrombotic therapy and non‐traumatic ICH met Modified Boston Criteria for CAA, CAA did not significantly influence the high mortality seen in this cohort.
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Ponamgi et al. (2020) studied this question.
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