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Published on: October 15, 2021
P2Y12 Inhibitors and Mortality in Patients Hospitalized With Intracerebral Hemorrhage
Chen Jin1, Ying Song1, Brian Mac Grory2,3
1Department of Cardiology, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
P2Y12 inhibitors, used for cardiovascular disease, increase risks of severe stroke, in-hospital death, and poor functional recovery in patients experiencing intracerebral hemorrhage (ICH). Aspirin monotherapy showed comparable outcomes to no antiplatelet therapy.
Area of Science:
- Neurology
- Cardiology
- Pharmacology
Background:
- P2Y12 inhibitors are common for atherosclerotic cardiovascular disease.
- Limited data exist on their association with intracerebral hemorrhage (ICH).
Purpose of the Study:
- To compare stroke severity, in-hospital mortality, and functional outcomes in ICH patients based on pre-ICH antiplatelet therapy.
- Investigate outcomes for P2Y12 inhibitor monotherapy, dual antiplatelet therapy (DAPT), aspirin monotherapy, and no antiplatelet therapy.
Main Methods:
- Retrospective cohort study using the Get With The Guidelines-Stroke registry (2013-2021).
- Included 252,691 patients hospitalized with spontaneous ICH.
- Analyzed outcomes including stroke severity (NIHSS), in-hospital mortality, and functional status (mRS).
Main Results:
- P2Y12 inhibitor use (mono or DAPT) was associated with higher rates of severe ICH (NIHSS ≥21) and in-hospital mortality compared to aspirin monotherapy or no antiplatelet therapy.
- Patients on P2Y12 inhibitors had worse functional outcomes at discharge, including lower rates of home discharge and independent ambulation.
- No significant outcome differences were observed between aspirin monotherapy and no antiplatelet therapy groups.
Conclusions:
- Pre-ICH P2Y12 inhibitor use is linked to more severe strokes, increased mortality, and poorer functional recovery.
- Aspirin monotherapy appears safer regarding ICH outcomes compared to P2Y12 inhibitor-based regimens.
- Further research is needed to optimize antiplatelet strategies in patients with ICH risk.
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