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Comparison of the Effect of a 6-French Glidesheath Slender and a Conventional Sheath on Distal Radial Artery Occlusion: A Randomized Controlled Trial

医学 桡动脉 随机对照试验 闭塞 桡骨骨折 外科 动脉 手腕
作者
Wei Lu,Tao Chen,Haibo Wang,Anni Yang,Lamei Li,Ganwei Shi,Sheliang Xue,Feng Li,Jianqiang Xiao,Jun Gu,Liuyan Zhang,Xiaofang Liang,Wenhua Li,Gaojun Cai
出处
期刊:Canadian Journal of Cardiology [Elsevier]
卷期号:40 (11): 2292-2300
标识
DOI:10.1016/j.cjca.2024.07.011
摘要

BackgroundThere is a lack of randomized clinical trials on whether the 6-French (Fr) Glidesheath Slender (GSS; Terumo, Tokyo, Japan) is superior to the 6-Fr conventional radial sheath (CS) with respect to the early-term incidence of distal radial artery occlusion (dRAO) in patients who have undergone coronary angiography (CAG) and/or percutaneous coronary intervention (PCI) via distal transradial access.MethodsThis was a prospective, single-centre trial of patients who were randomized to undergo CAG and/or PCI with either a 6-Fr GSS or a 6-Fr CS. The primary end point was the incidence of dRAO at 24 hours postoperatively, evaluated using Doppler ultrasound.ResultsA total of 620 patients were included in the study. The baseline patient and procedural characteristics were similar among the 2 groups. For the primary end point, the incidence of dRAO at 24 hours after the procedure was 1.0% (3/314) in the GSS group and 3.6% (11/306) in the CS group (risk ratio, 0.266; 95% confidence interval, 0.075-0.943; P = 0.027) according to the intention to treat analysis. For the secondary end points, the incidence of proximal radial artery occlusion was 0.3% (1/314) in the GSS group and 2.3% (7/306) in the CS group (P = 0.029). Other secondary end points, including the puncture success rate, procedural outcomes, other puncture-related outcomes, and access-related complications were not significantly different in the 2 groups.ConclusionsThe use of a thin-walled and hydrophilic coating sheath can reduce the incidence of early-term dRAO in patients who undergo CAG and/or PCI via the distal transradial access.Clinical Trial RegistrationNCT05501925.
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