Khan Usman, Abunassar Michael, Chatterjee Avijit, James Paul D
Faculty of Medicine, University of Ottawa, Ottawa, Ontario, Canada.
Division of Gastroenterology, Department of Medicine, St. Michael's Hospital, University of Toronto, Toronto, Ontario, Canada.
J Can Assoc Gastroenterol. 2020 Apr;3(2):83-90. doi: 10.1093/jcag/gwy066. Epub 2018 Dec 12.
The quality of endoscopic ultrasound (EUS) involving advanced endoscopy trainees (AETs) is not well understood. In this study, we aimed to examine adverse events (AE) risk and diagnostic yield of EUS procedures involving AETs.
We conducted a retrospective single-centre review from September 2009 to August 2015. Clinical, procedural, cytological, and hospital visit data within 30 days of the EUS procedure was collected. Primary outcomes were occurrence of an AE and a diagnostic specimen on cytopathology. Each AE was classified as "definitely related," "possibly related," or "not related to the EUS procedure based on a previously defined consensus approach. Advanced endoscopy trainee involvement was established through the operative report.
Our study included 1657 EUS procedures, of which 27% (451 of 1657) involved AETs. Endoscopic ultrasound was most commonly performed to evaluate pancreatic pathology (46% of cases). Overall AE incidence was 3.4%; it was 4.9% when an AET was involved and 2.8% when the EUS was performed without an AET ( = 0.04). The risk of an AE when AETs were involved was greatest in the first three months of training (7.9% versus 2.7%, = 0.04). Multivariate analysis limited to the first three months of training demonstrated AET involvement to be associated with an increased AE risk after adjusting for patient and procedural factors (adjusted OR 3.2; 95% CI, 1.1-8.7; = 0.03). The overall diagnostic yield was 76%. This was not compromised by AET involvement for any quartile of training.
We observed an increased risk of EUS-related AEs when procedures involved AETs during the first three months of training.
涉及高级内镜培训学员(AETs)的内镜超声检查(EUS)质量尚未得到充分了解。在本研究中,我们旨在检查涉及AETs的EUS检查的不良事件(AE)风险和诊断率。
我们对2009年9月至2015年8月进行了一项回顾性单中心研究。收集了EUS检查后30天内的临床、操作、细胞学和医院就诊数据。主要结局是AE的发生和细胞病理学诊断标本。根据先前定义的共识方法,将每个AE分类为“肯定相关”、“可能相关”或“与EUS检查无关”。通过手术报告确定高级内镜培训学员的参与情况。
我们的研究包括1657例EUS检查,其中27%(1657例中的451例)涉及AETs。内镜超声检查最常用于评估胰腺病变(46%的病例)。总体AE发生率为3.4%;当有AET参与时为4.9%,无AET进行EUS检查时为2.8%(P = 0.04)。AET参与时AE的风险在培训的前三个月最大(7.9%对2.7%,P = 0.04)。仅限于培训前三个月的多变量分析表明,在调整患者和操作因素后,AET参与与AE风险增加相关(调整后的OR 3.2;95%CI,1.1 - 8.7;P = 0.03)。总体诊断率为76%。在任何培训四分位数中,AET的参与都不会影响诊断率。
我们观察到,在培训的前三个月,当检查涉及AETs时,EUS相关AE的风险增加。