一项评估新型小容量结肠清洁程序用于胶囊结肠镜检查的初步研究。

A pilot study evaluating a new low-volume colon cleansing procedure for capsule colonoscopy.

机构信息

Department of Internal Medicine I, Sana Klinikum Lichtenberg, Berlin, Germany.

出版信息

Endoscopy. 2012 May;44(5):482-6. doi: 10.1055/s-0031-1291611. Epub 2012 Jan 24.

Abstract

BACKGROUND AND STUDY AIMS

Colon capsule endoscopy (CCE) offers an alternative approach for endoscopic visualization of the colon. Some of the current CCE bowel cleansing regimens use sodium phosphate, which has raised safety concerns. Therefore, the aim of the current study was to test the feasibility and efficacy of a new low-volume, sodium phosphate-free polyethylene glycol (PEG) bowel preparation.

METHODS

The first 26 patients (original cleansing procedure) received a colon cleansing regimen of PEG plus ascorbic acid: patients drank 1 L in the evening and 0.75 L in the morning before capsule ingestion. Patients also drank an additional 0.5 L PEG boost and an optional 0.25 L PEG boost during the capsule procedure. Following an interim analysis, the cleansing procedure of the subsequent 24 patients was modified, with the morning intake before capsule ingestion being increased to 1 L, as well as the second boost (0.25 L) being administered 1 - 2 hours earlier (modified cleansing procedure).

RESULTS

The overall colon cleanliness was considered to be good or excellent in 83 % (original cleansing procedure) and 82 % (modified cleansing procedure) of patients, without any significant difference between regimens (P > 0.05). In 37 /49 (76 %) of the CCE procedures, the hemorrhoidal plexus was identified and thus the examination was considered complete, with no significant differences between the two CCE cleansing procedures. The capsule sensitivity and specificity for detecting colonic polyps ≥ 6 mm were 91 % (95 %CI 70 % - 98 %) and 94 % (95 %CI 87 % - 97 %), respectively, compared with standard optical colonoscopy.

CONCLUSION

A colon cleansing procedure using PEG + ascorbic acid for capsule colonoscopy yielded an adequate cleansing level in > 80 % of patients, a completion rate of 76 %, and good accuracy for detecting polyps. This procedure may be considered as an alternative, particularly for patients in whom sodium phosphate-based preparations are contraindicated.

摘要

背景和研究目的

结肠胶囊内镜(CCE)为结肠内镜可视化提供了一种替代方法。目前一些 CCE 肠道清洁方案使用了磷酸钠,这引起了安全性方面的担忧。因此,本研究旨在测试一种新的低容量、无磷酸钠聚乙二醇(PEG)肠道准备的可行性和疗效。

方法

前 26 名患者(原始清洁程序)接受 PEG 加抗坏血酸的结肠清洁方案:患者在晚上喝 1 升,在胶囊摄入前的早上喝 0.75 升。患者在胶囊过程中还额外饮用 0.5 升 PEG 增强剂和可选的 0.25 升 PEG 增强剂。在中期分析后,随后 24 名患者的清洁程序进行了修改,胶囊摄入前的早上摄入量增加到 1 升,第二增强剂(0.25 升)在 1-2 小时前给药(改良清洁程序)。

结果

总体而言,83%(原始清洁程序)和 82%(改良清洁程序)的患者结肠清洁度被认为良好或优秀,两种方案之间无显著差异(P>0.05)。在 49 次 CCE 检查中的 37 次(76%)中,识别了痔丛,因此检查被认为是完整的,两种 CCE 清洁程序之间无显著差异。胶囊对检测 ≥ 6 毫米结肠息肉的敏感性和特异性分别为 91%(95%CI 70%-98%)和 94%(95%CI 87%-97%),与标准光学结肠镜检查相比。

结论

用于胶囊结肠镜检查的 PEG+抗坏血酸肠道清洁方案在>80%的患者中产生了足够的清洁水平,完成率为 76%,并且对检测息肉具有良好的准确性。该方案可被视为一种替代方案,特别是对于不能使用基于磷酸钠的制剂的患者。

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