Dual antiplatelet therapy did not significantly impact the long-term risk of stroke recurrence or mortality compared to single antiplatelet therapy in acute ischemic stroke patients.
Does dual antiplatelet therapy (aspirin plus clopidogrel) reduce net adverse clinical and cerebral events compared to single antiplatelet therapy in patients with acute ischemic stroke?
912 patients with acute ischemic stroke (AIS), mean age 65.21 years.
Dual antiplatelet therapy (DAPT) consisting of aspirin plus clopidogrel
Single antiplatelet therapy (SAPT) consisting of aspirin or clopidogrel alone
Incidence of net adverse clinical and cerebral events (NACCE), defined as the incidence of any hemorrhagic transformation within 30 days, stroke recurrence and/or all-cause mortality within 12 months of the index strokecomposite
Long-term use of dual antiplatelet therapy does not significantly improve 12-month clinical outcomes or reduce stroke recurrence compared to single antiplatelet therapy in patients with acute ischemic stroke.
Background: Short-term use of dual antiplatelet therapy (DAPT) has been shown to be superior to single antiplatelet therapy (SAPT) in improving outcomes in patients with acute ischemic stroke (AIS). However, the long-term effects following SAPT and DAPT remain unclear. This study aimed to investigate the long-term impact of DAPT and SAPT on clinical outcomes in AIS patients. Methods: A retrospective cohort study was conducted at King Abdulaziz Medical City (KAMC) facilities in Riyadh and Jeddah, and Prince Mohammed bin Abdulaziz Hospital (PMBAH) in Madinah, and included 912 AIS patients who received either DAPT (aspirin plus clopidogrel) or SAPT (aspirin or clopidogrel alone). The primary outcome was the incidence of net adverse clinical and cerebral events (NACCE), defined as the incidence of any hemorrhagic transformation within 30 days, stroke recurrence and/or all-cause mortality within 12 months of the index stroke. Results: Of 4043 patients screened, 912 met the inclusion criteria, with a mean age of 65.21 years. Among them, 582 patients (63.8%) received DAPT. There was no statistically significant difference in the incidence of the NACCE between the DAPT and SAPT groups over 12 months (p = 0.946). Although the DAPT group showed a higher rate of stroke recurrence after 50 days of the index stroke, this difference was not statistically significant (p = 0.107). Similarly, the SAPT group had a slightly higher incidence of mortality after six months and haemorrhagic transformation within 5 days, but these were also not statistically significant (p = 0.312 and 0.214, respectively). Conclusion: The addition of a second antiplatelet agent did not significantly affect the long-term risk of stroke recurrence or mortality in AIS patients over a 12-month period. Prospective studies are needed to clarify the long-term benefits and risks of DAPT compared to SAPT in different stroke subpopulations.
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Alamri et al. (Thu,) reported a other. Dual antiplatelet therapy did not significantly impact the long-term risk of stroke recurrence or mortality compared to single antiplatelet therapy in acute ischemic stroke patients.
www.synapsesocial.com/papers/6980fbf6c1c9540dea80dc38 — DOI: https://doi.org/10.1161/str.57.suppl_1.tp046
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:
Faisal Alamri
Eman A. Alraddadi
Yasser Alatawi
Stroke
King Abdulaziz University
King Saud bin Abdulaziz University for Health Sciences
University of Jeddah
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