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1.
Medicina (Kaunas) ; 47(10): 536-43, 2011.
Article in English | MEDLINE | ID: mdl-22186117

ABSTRACT

BACKGROUND AND OBJECTIVE: Recent publications have demonstrated superior outcomes in unprotected left main patients after paclitaxel-eluting stent (PES) implantation. Long-term data in these patients are limited. The aim of this study was to evaluate if intravascular ultrasound (IVUS)-guided PES implantation is superior to bare metal stent (BMS) implantation in unprotected left main disease after lesion pretreatment with cutting balloon during long-term follow-up. MATERIAL AND METHODS: Unprotected left main patients were randomized to BMS (n=50) or PES implantation (n=53). All interventions were IVUS-guided and cutting balloon pretreatment before stenting was performed in all patients. All patients were scheduled for 6-month and 3-year follow-up. Subgroups of patients who underwend IVUS and OCT imaging at 3-year follow-up were analyzed. The primary endpoint was the major adverse cardiac events (MACEs) defined as death, Q-wave myocardial infarction, or target lesion revascularization. RESULTS: Baseline characteristics were similar in both the groups with a mean SYNTAX score of 31.4±14.5 in BMS and 32.6±11.7 in PES patients (P=0.718). At 3 years, MACEs occurred in 18 patients (36.0%) in the BMS and 7 patients (13.2%) in the PES group (P=0.011). By IVUS, percent neointimal volume obstruction at 3 years was reduced from 18.1%±8.7% with BMSs to 10.0%±5.4% with PESs (P<0.001). The total number of uncovered stent struts per OCT image and IVUS image was 0.4±0.8 and 1.2±1.5, respectively (P<0.001). CONCLUSIONS: The current study demonstrated that IVUS-guided PES implantation was superior to BMS implantation after cutting balloon pretreatment in unprotected left main disease at 3 years. If compared with IVUS, OCT was more precise in the assessment of stent endothelization.


Subject(s)
Coronary Artery Disease/diagnostic imaging , Coronary Artery Disease/drug therapy , Coronary Vessels/diagnostic imaging , Drug-Eluting Stents , Paclitaxel/administration & dosage , Tubulin Modulators/administration & dosage , Aged , Coronary Artery Bypass , Coronary Artery Disease/surgery , Female , Humans , Male , Middle Aged , Ultrasonography, Interventional
2.
J Am Coll Cardiol ; 50(6): 491-7, 2007 Aug 07.
Article in English | MEDLINE | ID: mdl-17678730

ABSTRACT

OBJECTIVES: To optimize percutaneous coronary intervention (PCI) strategy for unprotected left main (LM) disease, we performed a randomized study: intravascular ultrasound (IVUS)-guided bare-metal stent (BMS) or paclitaxel-eluting stent (PES) implantation after lesion pre-treatment with cutting balloon (CB) for unprotected LM lesions. BACKGROUND: Recent studies have shown promising results in terms of safety and feasibility for patients with LM disease who underwent PCI with stent implantation. However, comparison of BMS and PES for LM lesions has not yet been evaluated. METHODS: One hundred three patients were randomly assigned to receive BMS (n = 50) or PES (n = 53) implantation. All interventions were IVUS guided, and CB pre-treatment before stenting was performed in all patients. All patients were scheduled for 6-month follow-up. RESULTS: Baseline clinical characteristics were comparable in both cohorts. Stent implantation was successful in all lesions. Follow-up analysis showed binary restenosis in 11 (22%) BMS and in 3 (6%) PES patients (p = 0.021). By IVUS, percentage of neointimal volume obstruction at 6 months was reduced from 25.20 +/- 22.02% with BMS to 16.60 +/- 17.25% with PES (p = 0.02). At 6 months, the major adverse cardiac event-free survival rate was 70% in BMS and 87% in PES patients (p = 0.036). CONCLUSIONS: This study demonstrates that PCI of LM with IVUS guidance and CB pre-treatment is safe and effective. No serious procedure-related complications were observed, and clinical outcomes appeared to be good. Finally, the findings demonstrate that implantation of PES may be superior to BMS in the large-diameter LM vessel at 6 months, warranting the performance of a large-scale randomized trial.


Subject(s)
Antineoplastic Agents, Phytogenic/administration & dosage , Blood Vessel Prosthesis Implantation/instrumentation , Coronary Stenosis/therapy , Paclitaxel/administration & dosage , Stents , Aged , Angioplasty, Balloon, Coronary/instrumentation , Coronary Angiography , Coronary Restenosis/prevention & control , Coronary Stenosis/diagnostic imaging , Coronary Stenosis/pathology , Coronary Thrombosis/prevention & control , Coronary Vessels/pathology , Drug Delivery Systems , Female , Humans , Male , Middle Aged , Treatment Outcome , Ultrasonography, Interventional
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