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High clopidogrel dose in patients with chronic kidney disease having clopidogrel resistance after percutaneous
Jing Liang1, Zhijian Wang1, Dongmei Shi1
1Department of Cardiology, Anzhen Hospital, Capital Medical University, Beijing, China.
Insights
Higher dose clopidogrel (150 mg/d) effectively reduced stent thrombosis and major adverse cardiac events in patients with chronic kidney disease and clopidogrel resistance after PCI, without increasing bleeding risk.
Area of Science:
- Cardiology
- Pharmacology
- Nephrology
Background:
- Patients with chronic kidney disease (CKD) often exhibit clopidogrel resistance (CR) after percutaneous coronary intervention (PCI).
- Standard clopidogrel dosing may be insufficient in CKD patients with CR, increasing risks of adverse cardiovascular events.
- Optimizing antiplatelet therapy is crucial for improving outcomes in this high-risk population.
Purpose of the Study:
- To evaluate the efficacy and safety of a higher dose of clopidogrel (150 mg/d) compared to standard dose (75 mg/d) in CKD patients with CR post-PCI.
- To assess the impact of 150 mg/d clopidogrel on maximal platelet aggregation (MPA), stent thrombosis (ST), major adverse cardiac events (MACEs), and bleeding.
Main Methods:
- A randomized controlled trial involving 370 CKD patients with CR after PCI.
- Patients received either clopidogrel 75 mg/d or 150 mg/d for 30 days post-PCI.
- Outcomes including MPA, ST, MACEs, and bleeding were assessed at 1-month follow-up.
Main Results:
- The 150 mg/d clopidogrel group showed significantly lower rates of ST and MACE compared to the 75 mg/d group.
- Patients receiving 150 mg/d clopidogrel exhibited lower MPA and greater platelet aggregation inhibition.
- No significant difference in major or minor bleeding events was observed between the two groups.
Conclusions:
- One-month administration of 150 mg/d clopidogrel is effective in reducing ST and MACE in CKD patients with CR after PCI.
- This higher dose regimen improves antiplatelet effect without increasing bleeding complications.
- Higher-dose clopidogrel represents a viable therapeutic option for managing high-risk CKD patients with clopidogrel resistance.
Abstract:
We evaluated the impact of clopidogrel 150 mg/d in patients with chronic kidney disease (CKD) having clopidogrel resistance (CR) after percutaneous coronary intervention (PCI); 1076 consecutive patients with coronary artery disease (CAD) having CKD were enrolled. Maximal platelet aggregation (MPA) was assessed before, 24 hours, and 30 days after a 300-mg loading dose of clopidogrel prior to PCI. After PCI, 370 patients with CR were randomized to receive clopidogrel 75 mg/d (n = 184) or 150 mg/d (n = 186) for 30 days. Stent thrombosis (ST), major adverse cardiac events (MACEs), and bleeding were analyzed after 1 month. Patients in the 150 mg group had significant lower rates of ST and MACE. There was no significant difference in major or minor bleeding. Patients in the 150 mg group had lower MPA and greater inhibition of platelet aggregation. One-month administration of 150 mg/d of clopidogrel decreases the rate of ST and MACE without increasing bleeding in patients with CKD having CR after PCI.
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