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Published on: March 15, 2022
Safety of carotid endarterectomy in patients concurrently on clopidogrel
Mark D Fleming1, William M Stone, Paul Scott
1Department of Surgery, Mayo Clinic, Phoenix, AZ 85054, USA.
Insights
Patients on clopidogrel can safely undergo carotid endarterectomy (CEA). Continuing this antiplatelet medication during CEA does not increase risks of stroke, death, or hematoma.
Area of Science:
- Vascular Surgery
- Cardiology
- Pharmacology
Background:
- Increasing use of clopidogrel for cerebrovascular symptoms and drug-eluting stents.
- Patients on clopidogrel often require carotid endarterectomy (CEA).
- Discontinuation of clopidogrel increases coronary stent thrombosis risk.
Purpose of the Study:
- To evaluate the safety of performing carotid endarterectomy (CEA) while patients continue clopidogrel therapy.
- To determine if perioperative clopidogrel use impacts CEA outcomes.
Main Methods:
- Retrospective cohort study of 100 patients undergoing CEA over 24 months.
- Patients divided into two groups: perioperative clopidogrel users (n=19) and non-users (n=81).
- Comparison of preoperative demographics and postoperative results between groups.
Main Results:
- No significant difference in demographics between clopidogrel and control groups.
- No statistical differences in morbidity or mortality.
- Equivalent combined stroke/death rates (1.2% control vs. 0% clopidogrel).
- One non-operative hematoma in the control group.
Conclusions:
- Carotid endarterectomy (CEA) can be safely performed in patients concurrently on clopidogrel.
- Continuing clopidogrel during CEA does not elevate risks of hematoma or neurological complications.
- This approach is beneficial for managing patients at risk of adverse outcomes from clopidogrel discontinuation.
Background:
Clopidogrel (Plavix) usage is increasing, primarily for the management of patients with cerebrovascular symptoms and for those receiving drug-eluting coronary artery stents. A significant percentage of these patients will require carotid endarterectomy (CEA) while they are receiving clopidogrel. Recent data have demonstrated an increased incidence of coronary stent thrombosis when clopidogrel is discontinued. The objective of this study was to determine if CEA could be performed safely while patients are continued on clopidogrel therapy.
Methods:
A retrospective cohort design was employed to review consecutive patients who underwent CEA over a 24-month period ending March 2007. Patients were divided into two groups based on the perioperative use of clopidogrel. Preoperative demographics and postoperative results were compared between the two groups and statistically analyzed.
Results:
Of the 100 patients who underwent CEA, 19 were taking clopidogrel within 5 days of surgery. This comprised the study group. The control group consisted of the 81 patients who did not receive clopidogrel. Heparin anticoagulation was routinely utilized prior to clamping in both groups. Demographics were similar between the groups. There were no statistical differences in morbidity or mortality between the control group and the clopidogrel group. Combined stroke/death rates were equivalent between the two groups (1.2% control vs. 0% clopidogrel). One hematoma developed in the control group, which did not require operative intervention.
Conclusion:
In this series, our results suggest that patients concurrently on clopidogrel can safely undergo CEA without increased risk of hematoma or neurological complications. In view of recent data demonstrating adverse outcomes in patients discontinuing clopidogrel, this study is useful in optimally managing this group of patients.
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