Key result
Prior antiplatelet therapy linked to ~51% higher 30-day mortality after first-ever ICH.
Why the study?
Antiplatelet therapy is widely used in the general population, sometimes without clear indications, prompting an evaluation of the incidence, prognosis, and appropriateness of prescription in first-ever intracerebral hemorrhage.
Does prior antiplatelet therapy increase mortality and hematoma expansion in patients experiencing first-ever intracerebral hemorrhage?
Cohort (n=606)
None
Yes
Does prior antiplatelet therapy increase mortality and hematoma expansion in patients experiencing first-ever intracerebral hemorrhage?
Effect estimate: HR 1.51 (95% CI 1.03-2.14)
Absolute Event Rate: 44.7% vs 25.6%
p-value: p=0.023
Prior antiplatelet therapy is associated with increased 30-day mortality and larger hematoma volumes in patients with first-ever intracerebral hemorrhage, highlighting the danger of inappropriate antiplatelet prescribing.
Prior antiplatelet exposure signals higher ICH fatality risk; leaves open whether avoidance or reversal improves outcomes.
The use of antiplatelet therapy (APT) is prevalent among the general population, sometimes without clear indications. We provided updated figures on the incidence and prognosis of first-ever intracerebral hemorrhage occurring on APT (APT-ICH) over 10 years in a population-based stroke registry and investigated the rates of inappropriate APT prescription. We included all cases of first-ever ICH not on anticoagulants from January 2011 to December 2020 in the district of L'Aquila (Southern Italy). Indication to APT was adjudicated according to 2021 European Society of Cardiology (ESC) guidelines for cardiovascular prevention. We included 606 first-ever ICHs, of whom 251 (41.4%) were APT-related. One-hundred-forty-two APT-ICHs (56.6%) occurred in patients without clear indications to APT. While the incidence of non-APT-ICH decreased over time, the incidence of APT-ICH was stable. APT-ICH showed higher 30-day and 1-year case-fatality rates versus non-APT-ICH (44.7% versus 25.6%, 50.6% versus 34.4%; p < 0.001). APT intake was independently associated with higher 30-day case-fatality (HR 1.51, 95%CI 1.03-2.14; p = 0.023). Our findings suggest that APT-ICH exhibits sustained incidence over time and elevated mortality. Urgent initiatives are needed to enhance adherence to established guidelines for APT use. This effort has the potential to mitigate the risk of ICH and to reduce the associated mortality.
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Foschi et al. (2024) conducted a cohort in First-ever intracerebral hemorrhage (n=606). Antiplatelet therapy (APT) vs. No antiplatelet therapy was evaluated on 30-day case-fatality (HR 1.51, 95% CI 1.03-2.14, p=0.023). Prior antiplatelet therapy in patients with first-ever intracerebral hemorrhage was independently associated with higher 30-day case-fatality (HR 1.51) compared to no antiplatelet therapy.
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