Comparative analysis of the dorsopalmar (modified distal) and transradial access in primary percutaneous coronary interventions in patients with acute coronary syndrome

R. Akhramovich, S. P. Semitko, A. V. Azarov, A. I. Analeev, Ilya S. Melnichenko, I. E. Chernysheva, Andrey A. Tretyakov, David G. Iosseliani
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Abstract

Background: Primary percutaneous coronary interventions (PCI) in acute coronary syndrome (ACS) with transradial access (TRA) are associated with the risk of local complications, such as occlusion of the radial artery (ORA), hematomas, pseudoaneurysms, and arteriovenous fistulas. Aim: To perform comparative assessment of clinical efficacy and safety of the TRA and dorsopalmar (modified distal) radial access (DpRA) for primary percutaneous coronary intervention in in-patients with ACS. Materials and methods: This was a randomized, dynamic, single-center, prospective study in two parallel groups. The patients were randomized in a 1:1 ratio into two groups with different types of the radiation access: TRA (n = 100) or DpRA (n = 100). TRA was made at the distal third of the forearm and DpRA on the dorsal palm surface. After the access zone was evaluated by angiography, the pressure bandage was placed on the zone for 6 hours for hemostasis. The comfort of hemostasis was assessed by the Gaston-Johansson 10-point verbal-descriptive pain rating scale. On the 57th day after PCI, all patients were examined with palpation and ultrasound assessment of the access artery. Results: The number of attempts, average duration of the radial artery puncture, duration of the fluoroscopy procedure, and the conversion rate did not depend on the access type. The scoring of the subjective hemostasis comfort showed a significant advantage of DpRA over TRA (6.4 [4; 10] in the TRA group vs 1.7 [0; 6] in the DpRA group, p 0.001). The rate of EASY III hematomas was 15 (15%) in the TRA group vs 3 (3%) in the DpRA group (p = 0.004). There were no EASY IVV hematomas, occlusion of the radial artery of the forearm, pseudoaneurysms and arteriovenous fistulas in the DpRA group. The diameter of the forearm radial artery was significantly larger than the diameter on the dorsal palm surface in the patients of both groups, regardless of the type of access chosen (2.75 0.32 mm and 2.38 0.36 mm in the TRA group, p 0.001; 2.84 0.38 mm and 2.45 0.36 mm in the DpRA group, p 0.001). In the patients with access conversion in both groups, the diameter of the radial artery at both levels was less than the average one. Conclusion: DpRA for PCI in ACS patients is a safe alternative to conventional radiation access. Ultrasound examination of the radial artery diameter in its distal and forearm parts before PCI could reduce the conversion rate.
急性冠状动脉综合征患者经皮冠状动脉介入治疗中经背侧(改良远端)和经桡动脉通路的比较分析
背景:急性冠状动脉综合征(ACS)经桡动脉通路(TRA)的初步经皮冠状动脉介入治疗(PCI)与局部并发症的风险相关,如桡动脉闭塞(ORA)、血肿、假性动脉瘤和动静脉瘘。目的:比较评价经皮动脉介入治疗与经皮动脉介入治疗(经皮动脉介入治疗)的临床疗效和安全性。材料和方法:这是一项随机、动态、单中心、前瞻性研究,在两个平行组中进行。将患者按1:1的比例随机分为两组,分别采用不同类型的放射通路:TRA (n = 100)或DpRA (n = 100)。在前臂远端三分之一处进行TRA,在手掌背表面进行dpa。血管造影评估通路区后,在通路区放置压力绷带止血6小时。止血舒适度采用加斯顿-约翰逊10分言语描述性疼痛评定量表进行评估。PCI术后第57天,所有患者均行导管触诊及超声检查。结果:桡动脉穿刺次数、平均穿刺时间、透视时间和转换率与通道类型无关。主观止血舒适度评分显示dpa明显优于TRA(6.4分)[4;10] TRA组vs . 1.7 [0;[6] dpa组,p < 0.001)。TRA组EASY III型血肿发生率为15例(15%),而dpa组为3例(3%)(p = 0.004)。dpa组无EASY IVV血肿、前臂桡动脉闭塞、假性动脉瘤、动静脉瘘。两组患者前臂桡动脉直径均显著大于手掌背表面直径,与选择的通路类型无关(TRA组为2.75 0.32 mm, 2.38 0.36 mm, p 0.001;dpa组分别为2.84 0.38 mm和2.45 0.36 mm, p < 0.001)。两组通路转换患者,两段桡动脉直径均小于平均值。结论:急性冠脉综合征患者行PCI的dpa治疗是一种安全的替代方法。PCI前超声检查桡动脉远端及前臂桡动脉内径可降低转换率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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