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Risk factors for repeated percutaneous transluminal angioplasty of hemodialysis vascular access after initial intervention.

作者信息

Tang Bin, Xiong Yuwan, Zhong Yingxue, Hao Guojun, Liu Yuanhao, He Wei, Wong Tak-Sui, Yu Zongchao, Hu Bo

机构信息

Department of Nephrology, Blood Purification Center, Zhongshan City People's Hospital, Zhongshan, China.

Department of Nephrology, The First Affiliated Hospital of Jinan University, Guangzhou, China.

出版信息

Vascular. 2025 Apr;33(2):342-348. doi: 10.1177/17085381241241362. Epub 2024 Mar 28.

DOI:10.1177/17085381241241362
PMID:38545905
Abstract

Background/AimsPercutaneous transluminal angioplasty (PTA) is a significant intervention to deal with occlusion and stenosis of vascular access. The study aimed to explore the risk factors of repeated PTA (re-PTA) after the initial intervention in patients undergoing hemodialysis.MethodsThis retrospective study included 180 patients who underwent successful PTA for the first time between March 2016 and December 2020. Information on demographic, clinical, anatomical, and medication variables was collected. Survival curves were plotted using Kaplan-Meier analysis and the risk factors associated with re-PTA were analyzed using univariate and multivariate Cox proportional hazards analyses.ResultsThe primary clinical patency rates at 6, 12, and 24 months after PTA were found to be 85.2%, 70.7%, and 58.6%, respectively. The univariate Cox proportion hazards analysis revealed the association of non-antiplatelet agents (HR 2.368 95% CI 1.351 to 4.150, = .003) and arteriovenous graft (AVG) (HR 2.096 95% CI 1.147 to 3.831, = .016) with re-PTA. However, only non-antiplatelet therapy showed statistical significance (HR 2.368 95% CI 1.351 to 4.150, = .003) in multivariate Cox proportional hazards analysis.ConclusionsAmong the patients undergoing hemodialysis, the use of antiplatelet agents was associated with a lower risk of re-PTA. Therefore, the use of antiplatelet drugs may reduce the rates of re-PTA and help in maintaining the patency of vascular access.

摘要

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