A139 EARLY VIDEO CAPSULE ENDOSCOPY VERSUS COLONOSCOPY FOLLOWING NEGATIVE ESOPHAGOGASTRODUDENOSCOPY IN PATIENTS WITH SUSPECTED UPPER GASTROINTESTINAL BLEEDING: PRELIMINARY DATA FROM A RANDOMIZED CONTROLLED TRIAL

K Patel, D. Yang, T. Krahn, S. Wesilenko, B. Halloran, S. Zepeda-Gomez
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Abstract

Abstract Background Esophagogastroduodenoscopy (EGD) is recommended for initial endoscopic evaluation of patients with suspected upper gastrointestinal bleeding (UGIB). When this is negative, the standard recommendation is to perform a colonoscopy, despite low diagnostic yield of less than 5%. In these patients, the question remains as to whether small bowel investigations would be of higher yield prior to colonoscopy. Aims To compare the diagnostic yield between early video capsule endoscopy (VCE) versus colonoscopy after a negative EGD in patients with suspected UGIB. Methods This is preliminary data from a prospective randomized control trial (RCT) of adult patients with suspected UGIB (melena and hemoglobin drop of more than 20 g/L within 48 hours of admission). Patients at a single centre were enrolled prior to initial EGD; those with negative EGD were included and randomized to either colonoscopy (next day) or early VCE (immediately after EGD). Patients with a confirmed source of bleeding in their group required no further testing, but those without underwent further testing with the alternative (VCE or colonoscopy). We evaluated patient outcomes, including bleeding localization time, hospitalization duration, procedure count, complications and rebleeding rates. Results A total of 19 adult patients have been enrolled, of which 12 had negative EGD and were randomized to either VCE or colonoscopy, with six patients in each arm (Figure 1). In the VCE group, 100% (6/6) of patients had bleeding sources detected by early VCE, with 50% (3/6) of them undergoing endoscopic treatment. In the colonoscopy group, only one patient had a positive finding (1/6), the rest underwent subsequent VCE. The VCE identified the bleeding source in 80% (4/5) of patients with negative colonoscopy. Patient are outlined in Table 1. Conclusions Based on our preliminary data, the diagnostic yield of early and subsequent VCE was higher when compared to colonoscopy after initial negative EGD in patients with suspected UGIB. Table 1. Summary of findings and patient outcomes OUTCOMES Early VCE Arm Colonoscopy Arm All participants Bleeding localized after first test, % (n) 100 (6/6) 17 (1/6) 58 (7/12) Average time to localization of bleed (days) ± standard deviation 5.33 ±2.46 6 ±2.31 5.67 ±1.62 Average length of hospital stay (days) ± standard deviation 5.33 ±0.97 5.17 ±1.55 5.25 ±0.874 Average number of procedures 2.67 3.17 2.92 Etiology of bleeding -Actively bleeding AVMs in small bowel – 33% (2/6) -Non-bleeding AVMs – 50% (3/6) -Active bleeding in right colon – 17% (1/6) -Clean based longitudinal ulcer in transverse colon – 17% (1/6) Funding Agencies Medtronic Canada (Brampton, ON, CA) will provide the video capsule in the treatment group. This is the only equipment funding required in this study.
A139 疑似上消化道出血患者在食管胃肠镜检查阴性后进行早期视频胶囊内镜检查与结肠镜检查的比较:随机对照试验的初步数据
摘要 背景 建议对疑似上消化道出血(UGIB)患者进行食管胃十二指肠镜(EGD)初步内镜评估。如果检查结果为阴性,标准建议是进行结肠镜检查,尽管结肠镜检查的诊断率很低,不到 5%。对于这些患者,在进行结肠镜检查前进行小肠检查是否能获得更高的诊断率仍是一个问题。目的 比较疑似 UGIB 患者在 EGD 阴性后进行早期视频胶囊内镜检查 (VCE) 和结肠镜检查的诊断率。方法 这是一项前瞻性随机对照试验(RCT)的初步数据,研究对象为疑似 UGIB(入院 48 小时内出现血便和血红蛋白下降超过 20 g/L)的成年患者。一个中心的患者在最初的胃肠造影检查之前就已被纳入;胃肠造影检查阴性的患者被纳入并随机接受结肠镜检查(次日)或早期 VCE(胃肠造影检查后立即)。本组中确诊出血源的患者无需接受进一步检查,但未确诊出血源的患者则需接受替代检查(VCE 或结肠镜检查)。我们对患者的结果进行了评估,包括出血定位时间、住院时间、手术次数、并发症和再出血率。结果 共招募了 19 名成年患者,其中 12 名患者的胃肠造影检查结果为阴性,他们被随机分配到 VCE 或结肠镜检查组,每组 6 名患者(图 1)。在 VCE 组中,100%(6/6)的患者通过早期 VCE 发现出血源,其中 50%(3/6)的患者接受了内镜治疗。在结肠镜检查组中,只有一名患者(1/6)有阳性发现,其余患者随后接受了 VCE 检查。在结肠镜检查阴性的患者中,80%(4/5)的患者通过 VCE 确定了出血源。患者情况见表 1。结论 根据我们的初步数据,与结肠镜检查相比,在最初胃食管造影阴性的疑似 UGIB 患者中,早期和后续 VCE 的诊断率更高。表 1.早期 VCE 手臂 结肠镜手臂 所有参与者 首次检查后出血定位,% (n) 100 (6/6) 17 (1/6) 58 (7/12) 平均出血定位时间(天)± 标准偏差 5.33 ±2.46 6 ±2.31 5.67 ±1.62 平均住院时间(天)± 标准偏差 5.33 ±0.97 5.17 ±1.55 5.25 ±0.874 平均手术次数 2.67 3.17 2.92 出血病因 -小肠动静脉畸形主动出血 -33%(2/6) -非出血动静脉畸形 -50%(3/6) -右结肠主动出血 -17%(1/6) -横结肠清洁型纵向溃疡 -17%(1/6) 资助机构 加拿大美敦力公司(加利福尼亚州安大略省布兰普顿市)将为治疗组提供视频胶囊。这是本研究唯一需要的设备资助。
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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