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胶囊内镜检测正常位置十二指肠乳头的能力有限。

Limited ability of capsule endoscopy to detect normally positioned duodenal papilla.

作者信息

Kong Hwi, Kim Yong Sik, Hyun Jong Jin, Cho Young Jig, Keum Bora, Jeen Yoon Tae, Lee Hong Sik, Chun Hoon Jai, Um Soon Ho, Lee Sang Woo, Choi Jai Hyun, Kim Chang Duck, Ryu Ho Sang, Hyun Jin Hai

机构信息

Department of Internal Medicine, Center for Digestive Disease, Korea University College of Medicine, Seoul, Korea.

出版信息

Gastrointest Endosc. 2006 Oct;64(4):538-41. doi: 10.1016/j.gie.2006.02.028.

DOI:10.1016/j.gie.2006.02.028
PMID:16996345
Abstract

BACKGROUND

The current power of capsule endoscopy (CE) to diagnose patients with obscure GI bleeding is 42% to 74.4%.

OBJECTIVE

The aim of this study was to evaluate the diagnostic power of CE through its ability to detect duodenal papilla.

DESIGN AND PATIENTS

A total of 112 consecutive CEs were retrospectively reviewed. All patients had undergone esophagogastroduodenoscopy and had their normal duodenal papilla confirmed.

SETTING AND INTERVENTIONS

The CE findings were reviewed separately at a rate of 15 images/second by 2 experienced and competent capsule readers.

MAIN OUTCOME MEASUREMENTS

The CE detection rate of duodenal papilla was calculated. In addition, the number of frames showing duodenal papilla was counted.

RESULTS

Among the total CEs, 2 cases were excluded because the capsule could not traverse the second portion of duodenum. The most common indication was obscure GI bleeding. CE only detected duodenal papilla in 48 cases (43.6%). The mean number of frames of the visualizing duodenal papilla was 3.5 +/- 2.5 (range 1-13).

LIMITATIONS

Choosing duodenal papilla as the reference may not be optimal because its position is difficult to identify.

CONCLUSIONS

Our study conveys an important message on the present power of CE; we should carefully review CE findings at a slower review rate to raise the detection ability of the current-powered CE, when it is passing through several "difficult to identify" locations such as second portion of the duodenum. In addition, to raise the power of CE, technologic improvements of CE, such as an extracorporeal-controllable device or a multiside viewing capsule, are needed.

摘要

背景

目前胶囊内镜(CE)诊断不明原因胃肠道出血患者的能力为42%至74.4%。

目的

本研究旨在通过胶囊内镜检测十二指肠乳头的能力来评估其诊断能力。

设计与患者

回顾性分析了连续112例胶囊内镜检查病例。所有患者均接受了食管胃十二指肠镜检查,且十二指肠乳头正常。

设置与干预

由2名经验丰富且资质合格的胶囊内镜阅片者以每秒15帧的速度分别查看胶囊内镜检查结果。

主要观察指标

计算十二指肠乳头的胶囊内镜检出率。此外,统计显示十二指肠乳头的帧数。

结果

在所有胶囊内镜检查病例中,2例因胶囊无法通过十二指肠第二部而被排除。最常见的适应证是不明原因胃肠道出血。胶囊内镜仅在48例(43.6%)中检测到十二指肠乳头。可视化十二指肠乳头的平均帧数为3.5±2.5(范围1 - 13)。

局限性

选择十二指肠乳头作为参考可能并非最佳,因为其位置难以确定。

结论

我们的研究传达了关于当前胶囊内镜能力的重要信息;当胶囊内镜通过十二指肠第二部等几个“难以识别”的部位时,我们应以较慢的阅片速度仔细查看检查结果,以提高现有胶囊内镜的检测能力。此外,为提高胶囊内镜的能力,需要对其进行技术改进,如体外可控装置或多视角胶囊。

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