Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/31811
Title: A Randomized Comparison of Paclitaxel-Eluting Stents Versus Bare-Metal Stents for Treatment of Unprotected Left Main Coronary Artery Stenosis.
Authors: Saltups A.;Zakke I.;Erglis A.;Narbute I.;Kumsars I.;Jegere S.;Mintale I.;Strazdins U.
Institution: (Erglis, Narbute, Kumsars, Jegere, Mintale, Zakke, Strazdins) Latvian Center of Cardiology, Pauls Stradins Clinical University Hospital, Riga, Latvia (Saltups) Cabrini Medical Centre, Monash Medical Centre, Melbourne, Australia
Issue Date: 17-Oct-2012
Copyright year: 2007
Publisher: Elsevier USA (6277 Sea Harbor Drive, Orlando FL 32862 8239, United States)
Place of publication: United States
Publication information: Journal of the American College of Cardiology. 50 (6) (pp 491-497), 2007. Date of Publication: 07 Aug 2007.
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(s): 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. Method(s): 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. Result(s): 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). Conclusion(s): 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. © 2007 American College of Cardiology Foundation.
DOI: http://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1016/j.jacc.2007.03.055
PubMed URL: 17678730 [http://www.ncbi.nlm.nih.gov/pubmed/?term=17678730]
ISSN: 0735-1097
URI: https://repository.monashhealth.org/monashhealthjspui/handle/1/31811
Type: Article
Subjects: artery diameter
artery intima proliferation
article
clinical trial
controlled clinical trial
controlled study
*coronary artery obstruction/dt [Drug Therapy]
*coronary artery obstruction/th [Therapy]
*coronary stent
drug eluting stent
female
follow up
heart infarction/co [Complication]
human
intermethod comparison
intravascular ultrasound
left coronary artery
major clinical study
male
*percutaneous coronary intervention
priority journal
randomized controlled trial
risk assessment
safety
stent
survival rate
technical aid
clopidogrel/dt [Drug Therapy]
clopidogrel/pd [Pharmacology]
fibrinogen receptor antagonist/dt [Drug Therapy]
fibrinogen receptor antagonist/pd [Pharmacology]
heparin/dt [Drug Therapy]
heparin/pd [Pharmacology]
low molecular weight heparin/dt [Drug Therapy]
low molecular weight heparin/pd [Pharmacology]
*paclitaxel/ct [Clinical Trial]
*paclitaxel/pd [Pharmacology]
*rapamycin/ct [Clinical Trial]
*rapamycin/pd [Pharmacology]
bare metal stent
cutting balloon
paclitaxel eluting stent
outcomes research
adult
aged
female
follow up
heart infarction / complication
human
intermethod comparison
intravascular ultrasound
left coronary artery
major clinical study
male
outcomes research
*percutaneous coronary intervention
priority journal
randomized controlled trial
risk assessment
safety
stent
survival rate
artery diameter
aged
technical aid
artery intima proliferation
article
clinical trial
controlled clinical trial
controlled study
*coronary artery obstruction / *drug therapy / *therapy
*coronary stent
drug eluting stent
adult
Type of Clinical Study or Trial: Randomised controlled trial
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