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使用无线动力胶囊和视频胶囊内镜对已知或疑似克罗恩病患者的小肠进行形态功能评估:初步研究

Morpho-functional evaluation of small bowel using wireless motility capsule and video capsule endoscopy in patients with known or suspected Crohn's disease: pilot study.

作者信息

Yung Diana, Douglas Sarah, Hobson Anthony R, Giannakou Andry, Plevris John N, Koulaouzidis Anastasios

机构信息

Royal Infirmary of Edinburgh - Centre of Liver & Digestive Disorders, Edinburgh, UK.

The Functional Gut Clinic - The Functional Gut Clinic, London, UK.

出版信息

Endosc Int Open. 2016 Apr;4(4):E480-6. doi: 10.1055/s-0042-100718. Epub 2016 Mar 22.

DOI:10.1055/s-0042-100718
PMID:27092333
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4831924/
Abstract

BACKGROUND AND STUDY AIMS

SmartPill(®) (Given Imaging Corp.,Yoqneam,Israel) is an ingestible, non-imaging capsule that records physiological data including contractions and pH throughout the gastrointestinal tract. There are scarce data looking at SmartPill(®) assessment of patients with known/suspected small-bowel Crohn's Disease (CD). This pilot study aims to investigate feasibility and safety of SmartPill(®) to assess gut motility in this group.

PATIENTS AND METHODS

Over 1 year, patients with known/suspected CD, referred for small-bowel capsule endoscopy (SBCE), were invited to participate and 12 were recruited (7 female, 5 male, mean age 44.2 ± 16.6 years). They underwent hydrogen breath test to exclude small-bowel bacterial overgrowth, patency capsule (Agile(®)), and provided stool samples for fecal calprotectin (FC). Patients ingested PillCam(®)SB2 and SmartPill(®) 4 hours apart. Using unpublished data, 33 healthy controls also were identified for the study. P < 0.05 was considered statistically significant.

RESULTS

Of the 12 patients enrolled, 10 underwent complete Smartpill(®) examination (1 stomach retention, 1 dropout). Pillcam(®) was complete in 10 (1 dropout, 1 stomach retention). Mean fecal calprotectin was 340 ± 307.71 mcg/g. The study group had longer transit times and lower gut motility index than did the controls. The difference in motility appears to be statistically significant (P < 0.05). Longer transit times for SmartPill(®) (not statistically significant) may have been due to different specifications between the capsules. Limitations included transient Smartpill(®) signal loss (5/10 studies).

CONCLUSIONS

This is the first pilot to attempt combining SBCE and SmartPill(®) to assess small-bowel CD. Data on motility in CD are scarce. Multimodal information can provide a clearer clinical picture. Despite concerns about capsule retention in CD patients, SmartPill(®) seems safe for use if a patency capsule is employed beforehand.

摘要

背景与研究目的

SmartPill(®)(以色列约纳姆的Given Imaging公司)是一种可吞咽的非成像胶囊,可记录整个胃肠道的生理数据,包括收缩和pH值。关于SmartPill(®)对已知/疑似小肠克罗恩病(CD)患者评估的数据很少。这项初步研究旨在调查SmartPill(®)评估该组患者肠道动力的可行性和安全性。

患者与方法

在1年多的时间里,邀请因小肠胶囊内镜检查(SBCE)前来就诊的已知/疑似CD患者参与研究,招募了12名患者(7名女性,5名男性,平均年龄44.2±16.6岁)。他们接受了氢呼气试验以排除小肠细菌过度生长,吞服了通畅胶囊(Agile(®)),并提供粪便样本用于检测粪便钙卫蛋白(FC)。患者在相隔4小时的时间分别吞服PillCam(®)SB2和SmartPill(®)。利用未发表的数据,还确定了33名健康对照者参与该研究。P<0.05被认为具有统计学意义。

结果

在纳入的12名患者中,10名完成了Smartpill(®)检查(1例胃潴留,1例退出)。10名患者完成了Pillcam(®)检查(1例退出,1例胃潴留)。粪便钙卫蛋白平均水平为340±307.71 mcg/g。研究组的转运时间比对照组更长,肠道动力指数更低。动力方面的差异似乎具有统计学意义(P<0.05)。SmartPill(®)转运时间较长(无统计学意义)可能是由于胶囊之间的规格不同。局限性包括Smartpill(®)信号短暂丢失(10项研究中有5项)。

结论

这是首次尝试将SBCE和SmartPill(®)结合起来评估小肠CD的初步研究。关于CD患者肠道动力的数据很少。多模式信息可以提供更清晰的临床情况。尽管担心CD患者会出现胶囊滞留,但如果事先使用通畅胶囊,SmartPill(®)似乎可以安全使用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2910/4831924/95ff26a39715/10-1055-s-0042-100718-i394ei6c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2910/4831924/9fa6eccbff38/10-1055-s-0042-100718-i394ei1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2910/4831924/8b584a3c4658/10-1055-s-0042-100718-i394ei2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2910/4831924/06696cf7d19f/10-1055-s-0042-100718-i394ei3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2910/4831924/4fd4f10f7969/10-1055-s-0042-100718-i394ei4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2910/4831924/03a6b42ab3b0/10-1055-s-0042-100718-i394ei5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2910/4831924/2ce618273e13/10-1055-s-0042-100718-i394ei6a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2910/4831924/6f37a07f408c/10-1055-s-0042-100718-i394ei6b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2910/4831924/95ff26a39715/10-1055-s-0042-100718-i394ei6c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2910/4831924/9fa6eccbff38/10-1055-s-0042-100718-i394ei1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2910/4831924/8b584a3c4658/10-1055-s-0042-100718-i394ei2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2910/4831924/06696cf7d19f/10-1055-s-0042-100718-i394ei3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2910/4831924/4fd4f10f7969/10-1055-s-0042-100718-i394ei4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2910/4831924/03a6b42ab3b0/10-1055-s-0042-100718-i394ei5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2910/4831924/2ce618273e13/10-1055-s-0042-100718-i394ei6a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2910/4831924/6f37a07f408c/10-1055-s-0042-100718-i394ei6b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2910/4831924/95ff26a39715/10-1055-s-0042-100718-i394ei6c.jpg

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