Study on the potential clinical significance of subclinical stent edge effects after drug-eluting stent implantation.

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Tác giả: Hai-Bo Jia, Xiao-Han Kong, Bin Liu, Pei-Na Meng, Yi-Fei Wang, Xiang-Qi Wu, Zhi-Ming Wu, Tian Xu, Yi Xu, Fei Ye, De-Lu Yin, Wei You, Mei-En Zhan, Meng-Yao Zhao

Ngôn ngữ: eng

Ký hiệu phân loại:

Thông tin xuất bản: England : Scientific reports , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 686139

UNLABELLED: The edge effect (EE) of isolated restenosis at one or both ends of a stent is not reduced by drug-eluting stent (DES). The purpose of the study was to investigate the long-term outcome of 1-year subclinical DES-EE (sDES-EE), which was defined as any reduction in the minimal lumen area (MLA) at stent edge without any evidence of clinical ischemia. A total of 252 patients were enrolled from one of our previous randomized controlled studies, who were detected by optical coherence tomography (OCT) immediately after DES implantation and 1 year later. The primary endpoint was EE-related target lesion failure (EE-TLF) at 5 years. Secondary endpoints were the changes of morphologies and composition of stent edge plaque, and each component of EE-TLF. sDES-EE at 1 year was significantly correlated with EE-TLF at 5 years by binary logistic regression analysis after propensity scoring. The most valuable cutoff value of sDES-EE at 1 year was a 25% MLA reduction at the stent edge, according to receiver operating characteristic analysis, which showed a major increase in lipid normalized total volume (0.99 ± 0.25 mm TRIAL REGISTRATION: ClinicalTrials.gov. Number NCT02140801. STUDY REGISTRATION: http://www. CLINICALTRIALS: gov . identifier: NCT02140801.
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