Wang Sheng, Guo Jintao, Liu Xiang, Ge Nan, Wang Guoxin, Hu Jinlong, Zhang Kai, Sun Siyu
Department of Gastroenterology, Shengjing Hospital of China Medical University, Shenyang, Liaoning Province, China.
Endosc Ultrasound. 2021 Nov-Dec;10(6):431-439. doi: 10.4103/EUS-D-21-00100.
EUS is widely used in the clinical practice. This study aimed to evaluate the efficacy of a novel echoendoscope regarding image quality, maneuverability, stability of the entire machine system, and safety.
We conducted this open-label, multicenter, randomized, parallel-group, noninferiority clinical trial in three tertiary hospitals between November 2018 and April 2019.
One hundred and thirty patients were included. The stratified segment randomization method was employed. Sixty-five patients in the test group received an EUS examination using the new material radial echoendoscope, and 65 patients in the control group received an EUS examination using the existing endoscope. We recorded the image quality, maneuverability, stability of the entire machine system, and safety. For the main outcome, comprehensive image quality, the groups were compared with the noninferiority test, using the confidence interval method and 10% as the noninferiority threshold. The Pearson Chi-square test was used to compare the incidence of adverse events between the groups.
Sixty-five patients in the test group and 63 patients in the control group were analyzed. Two patients in control group did not complete an EUS examination due to machine problems. There were no significant differences in image quality, maneuverability of the echoendoscope, stability of the entire machine system, and safety between the groups.
This new material radial echoendoscope showed good capabilities for image quality, maneuverability, stability of the entire machine system, and safety. Our data suggest that the new echoendoscope may provide an additional option for endoscopic physicians.
超声内镜在临床实践中被广泛应用。本研究旨在评估一种新型超声内镜在图像质量、可操作性、整机系统稳定性及安全性方面的效能。
2018年11月至2019年4月期间,我们在三家三级医院开展了这项开放标签、多中心、随机、平行组、非劣效性临床试验。
纳入130例患者。采用分层分段随机化方法。试验组65例患者使用新型材料径向超声内镜进行超声内镜检查,对照组65例患者使用现有内镜进行超声内镜检查。我们记录了图像质量、可操作性、整机系统稳定性及安全性。对于主要结局指标综合图像质量,采用置信区间法并以10%作为非劣效性界值,通过非劣效性检验对两组进行比较。采用Pearson卡方检验比较两组不良事件的发生率。
试验组65例患者和对照组63例患者纳入分析。对照组有2例患者因机器问题未完成超声内镜检查。两组在图像质量、超声内镜可操作性、整机系统稳定性及安全性方面均无显著差异。
这种新型材料径向超声内镜在图像质量、可操作性、整机系统稳定性及安全性方面表现良好。我们的数据表明,这种新型超声内镜可能为内镜医师提供了一种额外的选择。