Department of Gastroenterology and Hepatology, Royal Adelaide Hospital, Adelaide, South Australia, Australia; Discipline of Medicine, University of Adelaide, Adelaide, South Australia, Australia.
Department of Gastroenterology and Hepatology, Royal Adelaide Hospital, Adelaide, South Australia, Australia.
Gastrointest Endosc. 2017 Jun;85(6):1212-1217. doi: 10.1016/j.gie.2016.11.019. Epub 2016 Nov 25.
This study aims to evaluate the role of unsedated, ultrathin disposable gastroscopy (TDG) against conventional gastroscopy (CG) in the screening and surveillance of gastroesophageal varices (GEVs) in patients with liver cirrhosis.
Forty-eight patients (56.4 ± 1.3 years; 38 male, 10 female) with liver cirrhosis referred for screening (n = 12) or surveillance (n = 36) of GEVs were prospectively enrolled. Unsedated gastroscopy was initially performed with TDG, followed by CG with conscious sedation. The 2 gastroscopies were performed by different endoscopists blinded to the results of the previous examination. Video recordings of both gastroscopies were validated by an independent investigator in a random, blinded fashion. Endpoints were accuracy and interobserver agreement of detecting GEVs, safety, and potential cost saving.
CG identified GEVs in 26 (54%) patients, 10 of whom (21%) had high-risk esophageal varices (HREV). Compared with CG, TDG had an accuracy of 92% for the detection of all GEVs, which increased to 100% for high-risk GEVs. The interobserver agreement for detecting all GEVs on TDG was 88% (κ = 0.74). This increased to 94% (κ = 0.82) for high-risk GEVs. There were no serious adverse events.
Unsedated TDG is safe and has high diagnostic accuracy and interobserver reliability for the detection of GEVs. The use of clinic-based TDG would allow immediate determination of a follow-up plan, making it attractive for variceal screening and surveillance programs. (Clinical trial (ANZCTR) registration number: ACTRN12616001103459.).
本研究旨在评估非镇静性超薄一次性胃镜(TDG)在肝硬化患者胃食管静脉曲张(GEV)筛查和监测中的作用。
前瞻性纳入 48 例(56.4±1.3 岁;38 名男性,10 名女性)因 GEV 筛查(n=12)或监测(n=36)而就诊的肝硬化患者。首先进行非镇静性胃镜检查,采用 TDG,然后在清醒镇静下进行 CG。由两名对前一次检查结果不知情的内镜医生进行这两种胃镜检查。由一名独立研究人员以随机、盲法的方式对这两种胃镜的视频记录进行验证。终点是检测 GEV 的准确性和观察者间一致性、安全性以及潜在的成本节约。
CG 在 26 名(54%)患者中发现了 GEV,其中 10 名(21%)有高危食管静脉曲张(HREV)。与 CG 相比,TDG 检测所有 GEV 的准确率为 92%,高危 GEV 的准确率为 100%。TDG 检测所有 GEV 的观察者间一致性为 88%(κ=0.74)。对于高危 GEV,这一比例增加到 94%(κ=0.82)。无严重不良事件。
非镇静性 TDG 安全,诊断准确性高,观察者间可靠性好,可用于检测 GEV。在临床中使用 TDG 可立即确定随访计划,因此对静脉曲张筛查和监测计划很有吸引力。(临床试验(ANZCTR)注册号:ACTRN12616001103459.)。