(Circulation. 2000;101:e46.)
© 2000 American Heart Association, Inc.
Circulation Electronic Pages |
Service de Cardiologie, Hôpital Broussais, Hôptial Lariboisiere, Paris, France
| Introduction |
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We have read with interest the article by Dr Berger and colleagues regarding safety and efficacy of ticlopidine for only 2 weeks after successful intracoronary stent placement.1 The authors conclude that "in patients receiving intracoronary stents, the discontinuation of ticlopidine therapy 14 days after stent placement is associated with a very low frequency of stent thrombosis and other adverse events." In our opinion, 3 major points need to be discussed regarding this conclusion.
First, the authors point out that intravascular ultrasound study (IVUS) was used "to facilitate stent placement in 73 patients (8.8%)." IVUS led to additional treatment (additional balloon inflation or placement of additional stents) in 36 patients. This point is crucial and needs to be discussed. Colombo and coworkers2 first demonstrated that optimization of stent implantation was a key issue in the prevention of subacute occlusion. Albiero et al3 demonstrated that stent thrombosis and other adverse events were not significantly different between the aspirin and the ticlopidine-plus-aspirin groups when stent expansion, controlled by IVUS, was adequate. The reasons that led to IVUS examination are not clearly defined in the article by Berger et al.1 We can hypothesize that IVUS was performed when the result was not satisfactory, eg, suboptimal final result, persistent slow flow or dissection, or persistent intraluminal defect. Therefore, several patients with a high risk of stent thrombosis before IVUS could be treated with aspirin alone after optimization.
Second, the rate of unstable coronary syndromes is not
clearly mentioned in the article by
Mayo Clinic, Rochester, Minn
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