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Long‐term outcomes after stent implantation in very small vessel coronary artery disease

BACKGROUND: Percutaneous coronary interventions (PCI) in very small vessel lesions represent an intriguing aspect of coronary artery disease (CAD). Uncertainty still exists in stent implantation in very small caliber vessels. This study aimed to evaluate the long‐term outcomes of patients treated wi...

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Autores principales: Liu, En‐Shao, Yang, Tse‐Hsuan, Tai, Ta‐Hsin, Chiang, Cheng‐Hung, Cheng, Chin‐Chang, Huang, Wei‐Chun, Mar, Guang‐Yuan, Kuo, Feng‐Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10106663/
https://www.ncbi.nlm.nih.gov/pubmed/36824027
http://dx.doi.org/10.1002/clc.24000
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author Liu, En‐Shao
Yang, Tse‐Hsuan
Tai, Ta‐Hsin
Chiang, Cheng‐Hung
Cheng, Chin‐Chang
Huang, Wei‐Chun
Mar, Guang‐Yuan
Kuo, Feng‐Yu
author_facet Liu, En‐Shao
Yang, Tse‐Hsuan
Tai, Ta‐Hsin
Chiang, Cheng‐Hung
Cheng, Chin‐Chang
Huang, Wei‐Chun
Mar, Guang‐Yuan
Kuo, Feng‐Yu
author_sort Liu, En‐Shao
collection PubMed
description BACKGROUND: Percutaneous coronary interventions (PCI) in very small vessel lesions represent an intriguing aspect of coronary artery disease (CAD). Uncertainty still exists in stent implantation in very small caliber vessels. This study aimed to evaluate the long‐term outcomes of patients treated with 2.0‐mm drug‐eluting stent (DES). METHOD: This retrospective observational study included 134 patients undergoing PCI with 2.0‐mm zotarolimus DES from December 2016 to May 2020. The primary endpoint was major adverse cardiovascular events (MACE) at 2‐year follow‐up, which was composed of all‐cause mortality, target vessel myocardial infarction, and ischemia‐driven target lesion revascularization. Multiple logistic regression analysis was used to identify the independent predictors of MACE, and odds ratios (OR) and 95% confidence intervals (CI) were calculated. RESULT: The lesions were diffuse (mean length 20.9 ± 5.51 mm) and belong to type B2/C lesions (90.3%). On follow‐up, the MACE rate was 20.1% and mostly driven by late lumen loss demanding revascularization (11.9%). In multivariable analysis, chronic kidney disease (CKD) (OR: 4.291, 95% CI: 1.574−11.704, p = 0.004) and calcified lesions (OR: 3.688, 95% CI: 1.311−10.371, p = 0.013) were the independent predictors of subsequent cardiovascular events, whereas statin was associated with better outcomes (OR: 0.335, 95% CI: 0.119−0.949, p = 0.040). CONCLUSION: 2.0‐mm DES is a feasible option for treating very small vessel CAD in complex lesions. Patients with CKD and calcified lesions carry the hazard of worse outcomes, and careful consideration should be taken before stenting in this high‐risk population.
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spelling pubmed-101066632023-04-18 Long‐term outcomes after stent implantation in very small vessel coronary artery disease Liu, En‐Shao Yang, Tse‐Hsuan Tai, Ta‐Hsin Chiang, Cheng‐Hung Cheng, Chin‐Chang Huang, Wei‐Chun Mar, Guang‐Yuan Kuo, Feng‐Yu Clin Cardiol Clinical Investigations BACKGROUND: Percutaneous coronary interventions (PCI) in very small vessel lesions represent an intriguing aspect of coronary artery disease (CAD). Uncertainty still exists in stent implantation in very small caliber vessels. This study aimed to evaluate the long‐term outcomes of patients treated with 2.0‐mm drug‐eluting stent (DES). METHOD: This retrospective observational study included 134 patients undergoing PCI with 2.0‐mm zotarolimus DES from December 2016 to May 2020. The primary endpoint was major adverse cardiovascular events (MACE) at 2‐year follow‐up, which was composed of all‐cause mortality, target vessel myocardial infarction, and ischemia‐driven target lesion revascularization. Multiple logistic regression analysis was used to identify the independent predictors of MACE, and odds ratios (OR) and 95% confidence intervals (CI) were calculated. RESULT: The lesions were diffuse (mean length 20.9 ± 5.51 mm) and belong to type B2/C lesions (90.3%). On follow‐up, the MACE rate was 20.1% and mostly driven by late lumen loss demanding revascularization (11.9%). In multivariable analysis, chronic kidney disease (CKD) (OR: 4.291, 95% CI: 1.574−11.704, p = 0.004) and calcified lesions (OR: 3.688, 95% CI: 1.311−10.371, p = 0.013) were the independent predictors of subsequent cardiovascular events, whereas statin was associated with better outcomes (OR: 0.335, 95% CI: 0.119−0.949, p = 0.040). CONCLUSION: 2.0‐mm DES is a feasible option for treating very small vessel CAD in complex lesions. Patients with CKD and calcified lesions carry the hazard of worse outcomes, and careful consideration should be taken before stenting in this high‐risk population. John Wiley and Sons Inc. 2023-02-23 /pmc/articles/PMC10106663/ /pubmed/36824027 http://dx.doi.org/10.1002/clc.24000 Text en © 2023 The Authors. Clinical Cardiology published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Investigations
Liu, En‐Shao
Yang, Tse‐Hsuan
Tai, Ta‐Hsin
Chiang, Cheng‐Hung
Cheng, Chin‐Chang
Huang, Wei‐Chun
Mar, Guang‐Yuan
Kuo, Feng‐Yu
Long‐term outcomes after stent implantation in very small vessel coronary artery disease
title Long‐term outcomes after stent implantation in very small vessel coronary artery disease
title_full Long‐term outcomes after stent implantation in very small vessel coronary artery disease
title_fullStr Long‐term outcomes after stent implantation in very small vessel coronary artery disease
title_full_unstemmed Long‐term outcomes after stent implantation in very small vessel coronary artery disease
title_short Long‐term outcomes after stent implantation in very small vessel coronary artery disease
title_sort long‐term outcomes after stent implantation in very small vessel coronary artery disease
topic Clinical Investigations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10106663/
https://www.ncbi.nlm.nih.gov/pubmed/36824027
http://dx.doi.org/10.1002/clc.24000
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