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Updated: Jul 16, 2026

A Murine Model of Stent Implantation in the Carotid Artery for the Study of Restenosis
Published on: May 14, 2013
Benefits of clopidogrel in patients undergoing coronary stenting significantly depend on loading dose: evidence from
Giuseppe G L Biondi-Zoccai1, Marzia Lotrionte, Pierfrancesco Agostoni
1Interventional Cardiology, Division of Cardiology, University of Turin, Turin, Italy. gbiondizoccai@gmail.com
Insights
For patients undergoing coronary stenting, clopidogrel with an initial loading dose is superior to ticlopidine. This finding supports optimal initial dosing strategies for antiplatelet therapy after stenting.
Area of Science:
- Cardiology
- Pharmacology
- Clinical Trials
Background:
- Clopidogrel is a safer alternative to ticlopidine for patients post-coronary stenting.
- Optimal initial dosing of clopidogrel remains unclear.
Purpose of the Study:
- To systematically review and meta-regression analyze randomized clinical trials comparing clopidogrel and ticlopidine.
- To evaluate the impact of clopidogrel front-loading on patient outcomes.
Main Methods:
- Systematic review of randomized clinical trials updated to August 2006.
- Meta-regression analysis to assess the effect of clopidogrel loading doses.
Main Results:
- Seven trials involving 3382 patients were analyzed.
- Clopidogrel with a loading dose showed significantly better outcomes than ticlopidine (OR 0.60, P = .05).
- Meta-regression confirmed the significant interaction between clopidogrel loading and improved outcomes.
Conclusions:
- A clopidogrel regimen including an initial loading dose is superior to ticlopidine.
- This supports the use of loading doses for clopidogrel in patients undergoing coronary stenting.
Background:
Clopidogrel is an established alternative to ticlopidine in addition to aspirin after coronary stenting because of its safety, but its optimal initial dosing is unclear. We performed a systematic review and meta-regression of randomized clinical trials comparing clopidogrel versus ticlopidine, focusing on clopidogrel front-loading.
Methods:
PubMed was searched for pertinent studies (updated August 2006). Random-effect odds ratios (ORs) with 95% CIs were computed for death or nonfatal myocardial infarction, and weighted least squares random-effect meta-regression was performed to explore the impact of loading versus nonloading clopidogrel scheme.
Results:
We retrieved 7 trials (3382 patients, average follow-up of 7 months). In 5 studies, both clopidogrel and ticlopidine were started with a loading dose, in 1 trial clopidogrel was administered without loading, and in 1 trial clopidogrel could be administered with or without loading. Overall analysis (P for heterogeneity = .02) showed similar results for clopidogrel and ticlopidine (OR 0.90, 95% CI 0.44-1.84, P = .77). In studies administering clopidogrel with loading, this treatment was, however, significantly better than ticlopidine (OR 0.60, 95% CI 0.36-0.99, P = .05). This significant interaction between clopidogrel loading and its superiority in comparison with ticlopidine was also formally confirmed by meta-regression (beta = -0.64, P = .012).
Conclusions:
This work supports the superiority of a clopidogrel regimen including an initial loading dose in comparison with ticlopidine in patients undergoing coronary stenting.
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