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Published on: October 21, 2017
Clopidogrel-induced mixed hepatocellular and cholestatic liver injury
1Memorial Regional Hospital, Hollywood, Florida, USA.
Insights
An 81-year-old woman experienced liver disease after taking clopidogrel for a coronary stent. This case highlights potential liver injury from clopidogrel, emphasizing the need for careful monitoring in patients undergoing stenting.
Area of Science:
- Cardiology
- Pharmacology
- Hepatology
Background:
- Clopidogrel is a widely used antiplatelet medication for patients with coronary artery disease, particularly after stent implantation.
- Adjunctive antiplatelet therapy is crucial for preventing stent thrombosis but can be associated with adverse effects.
Observation:
- An 81-year-old female patient developed symptomatic liver disease three weeks after initiating clopidogrel therapy.
- The liver disease onset was temporally linked to the short-term, periprocedural use of clopidogrel following coronary stenting.
Findings:
- This case represents a rare instance of symptomatic liver disease associated with clopidogrel administration in the context of coronary stenting.
- The patient was also receiving other medications metabolized by cytochrome P450 2C9, raising questions about potential drug interactions.
Implications:
- The findings suggest that clopidogrel, even with short-term use, can potentially cause liver injury.
- Further investigation is warranted to understand the clinical significance and mechanisms of clopidogrel-induced liver injury, especially in patients with multiple drug therapies.
- Clinicians should maintain a high index of suspicion for drug-induced liver injury in patients presenting with liver dysfunction after clopidogrel initiation.
Abstract:
An 81-year-old woman developed symptomatic liver disease 3 weeks after beginning clopidogrel as adjunctive antiplatelet therapy for a coronary stent implantation. Symptomatic liver disease associated with short-term periprocedural administration of clopidogrel for coronary stenting has not been well described. The clinical significance of this event as well as a possible interaction between clopidogrel and other drugs metabolized by the cytochrome P450 2C9 pathways coadministered to this patient are discussed.
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