Dual antiplatelet therapy after carotid artery stenting: trends and outcomes in a large national database
Eric S Sussman1, Michael Jin2, Arjun V Pendharkar2
1Neurosurgery, Stanford University School of Medicine, Stanford, California, USA esuss11@gmail.com.
Insights
Shorter dual antiplatelet therapy (dAPT) after carotid artery stenting (CAS) increases stroke risk, while longer durations raise bleeding risks, especially extracranial hemorrhage. Balancing these is crucial for patient outcomes.
Area of Science:
- Cardiovascular Medicine
- Neurology
- Vascular Surgery
Background:
- Dual antiplatelet therapy (dAPT) is standard post-carotid artery stenting (CAS).
- Optimal dAPT regimen and duration remain undefined.
- Carotid interventions include stenting (CAS) and endarterectomy (CEA).
Purpose of the Study:
- To evaluate the impact of dAPT duration on stroke-free survival after CAS.
- To assess the risk of hemorrhagic complications associated with dAPT post-CAS.
- To compare outcomes between CAS and CEA in a real-world setting.
Main Methods:
- Analysis of a large national database (IBM MarketScan) from 2007-2016.
- Inclusion of patients undergoing CAS or CEA for stroke or stenosis.
- Univariable and multivariable regression to assess stroke risk and bleeding complications related to dAPT duration.
Main Results:
- Shorter P2Y12-inhibition (<180 days) post-CAS increased stroke risk.
- Hemorrhagic complications, particularly extracranial hemorrhage, were significantly higher during dAPT.
- Extended dAPT showed a trend towards increased intracranial hemorrhage risk.
Conclusions:
- Prolonging dAPT post-CAS is linked to reduced stroke readmissions but elevated bleeding risks.
- The benefit of extended dAPT for ischemic prevention must be weighed against increased hemorrhagic risk.
- Extracranial hemorrhage is a significant concern with longer dAPT durations.
Background:
While dual antiplatelet therapy (dAPT) is standard of care following carotid artery stenting (CAS), the optimal dAPT regimen and duration has not been established.
Methods:
We canvassed a large national database (IBM MarketScan) to identify patients receiving carotid endarterectomy (CEA) or CAS for treatment of ischemic stroke or carotid artery stenosis from 2007 to 2016. We performed univariable and multivariable regression methods to evaluate the impact of covariates on post-CAS stroke-free survival, including post-discharge antiplatelet therapy.
Results:
A total of 79 084 patients diagnosed with ischemic stroke or carotid stenosis received CEA (71 178; 90.0%) or CAS (7906; 10.0%). After adjusting for covariates, <180 days prescribed post-CAS P2Y12-inhibition was associated with increased risk for stroke (<90 prescribed days HR=1.421, 95% CI 1.038 to 1.946; 90-179 prescribed days HR=1.484, 95% CI 1.045 to 2.106). The incidence of hemorrhagic complications was higher during the period of prescribed P2Y12-inhibition (1.16% per person-month vs 0.49% per person-month after discontinuation, P<0.001). The rate of extracranial hemorrhage was nearly six-fold higher while on dAPT (6.50% per patient-month vs 1.16% per patient-month, P<0.001), and there was a trend towards higher rate of intracranial hemorrhage that did not reach statistical significance (5.09% per patient-month vs 3.69% per patient-month, P=0.0556). Later hemorrhagic events beyond 30 days post-CAS were significantly more likely to be extracranial (P=0.028).
Conclusions:
Increased duration of post-CAS dAPT is associated with lower rates of readmissions for stroke, and with increased risk of hemorrhagic complications, particularly extracranial hemorrhage. The potential benefit of prolonging dAPT with regard to ischemic complications must be balanced with the corresponding increased risk of predominantly extracranial hemorrhagic complications.
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