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变应性食管炎成人内镜活动评估和内镜评分验证的差异。

Variation in Endoscopic Activity Assessment and Endoscopy Score Validation in Adults With Eosinophilic Esophagitis.

机构信息

Division of Gastroenterology and Hepatology, Centre Hospitalier Universitaire Vaudois/CHUV, Lausanne, Switzerland.

Division of Gastroenterology, Northwestern University Feinberg School of Medicine, Chicago, Illinois.

出版信息

Clin Gastroenterol Hepatol. 2019 Jul;17(8):1477-1488.e10. doi: 10.1016/j.cgh.2018.11.032. Epub 2018 Nov 23.

Abstract

BACKGROUND & AIMS: Eosinophilic esophagitis (EoE) is assessed endoscopically (endoscopic activity), based on grades of edema, rings, exudates, furrows, and strictures (EREFS). We examined variations in endoscopic assessments of severity, developed and validated 3 EREFS-based scoring systems, and assessed responsiveness of these systems using data from a randomized placebo-controlled trial of patients with EoE.

METHODS

For the development set, 5 gastroenterologists reviewed EREFS findings from 266 adults with EoE and provided endoscopist global assessment scores (EndoGA, scale of 0 to 10); variation (ΔEndoGA) was assessed using linear regression. We evaluated simple scores (features given arbitrary values from 0 to 3) and developed 2 scoring systems (adjusted score range, 0-100). We then fitted our linear regression model with mean EndoGA to data from 146 adults recruited in centers in Switzerland and the United States between April 2011 and December 2012. For the validation set, we collected data from 120 separate adults (recruited in centers in Switzerland and the United States between May 2013 and July 2014), assessing regression coefficient-based scores using Bland-Altman method. We assessed the responsiveness of our scoring systems using data from a randomized trial of patients with EoE given fluticasone (n=16) or placebo (n=8).

RESULTS

The distribution of EndoGA values differed among endoscopists (mean ΔEndoGA, 2.6±1.8; range 0-6.6). We developed 2 regression-based scoring systems to assess overall and proximal and distal esophageal findings; variation in endoscopic features accounted for more than 90% of the mean EndoGA variation. In the validation group, differences between mean EndoGA and regression-based scores were small (ranging from -4.70 to 2.03), indicating good agreement. In analyses of data from the randomized trial, the baseline to end of study change in patients given fluticasone was a reduction of 24.3 in simple score (reduction of 4.6 in patients given placebo, P=.052); a reduction of 23.5 in regression-based overall score (reduction of 6.56 in patients given placebo, P=.12), and a reduction of 23.8 (reduction of 8.44 in patients given placebo, P=.11).

CONCLUSION

Assessments of endoscopic activity in patients with EoE vary among endoscopists. In an analysis of data from a randomized controlled trial, we found that newly developed scoring systems are no better than simple scoring system in detecting changes in endoscopic activity. These results support the use of a simple scoring system in evaluation of endoscopic activity in patients with EoE. clinicaltrials.gov no: NCT00939263 and NCT01386112.

摘要

背景与目的

嗜酸性粒细胞性食管炎(EoE)通过内镜(内镜活动)进行评估,根据水肿、环、渗出物、皱纹和狭窄(EREFS)的程度进行分级。我们研究了严重程度内镜评估的变化,开发并验证了 3 种基于 EREFS 的评分系统,并使用来自 EoE 患者的随机安慰剂对照试验的数据评估了这些系统的反应性。

方法

在开发集方面,5 名胃肠病学家对 266 名 EoE 患者的 EREFS 发现进行了审查,并提供了内镜全球评估评分(EndoGA,范围为 0 至 10);使用线性回归评估了变化(ΔEndoGA)。我们评估了简单评分(特征被赋予 0 至 3 的任意值)并开发了 2 种评分系统(调整评分范围,0-100)。然后,我们使用来自 2011 年 4 月至 2012 年 12 月在美国和瑞士中心招募的 146 名成人的数据拟合了我们的平均 EndoGA 线性回归模型。在验证集中,我们从 2013 年 5 月至 2014 年 7 月在美国和瑞士的不同中心招募的 120 名成人(n=120)中收集数据,使用 Bland-Altman 方法评估基于回归系数的评分。我们使用来自接受氟替卡松(n=16)或安慰剂(n=8)的 EoE 患者随机试验的数据评估了我们评分系统的反应性。

结果

EndoGA 值在不同内镜医生之间存在差异(平均ΔEndoGA,2.6±1.8;范围 0-6.6)。我们开发了 2 种基于回归的评分系统来评估整个食管和食管近端和远端的发现;内镜特征的变化占平均 EndoGA 变化的 90%以上。在验证组中,平均 EndoGA 和基于回归的评分之间的差异较小(范围从-4.70 到 2.03),表明具有良好的一致性。在接受氟替卡松治疗的患者随机试验数据分析中,氟替卡松治疗组的基线至研究结束时的变化为简单评分降低 24.3(接受安慰剂治疗的患者降低 4.6,P=.052);基于回归的总体评分降低 23.5(接受安慰剂治疗的患者降低 6.56,P=.12),以及降低 23.8(接受安慰剂治疗的患者降低 8.44,P=.11)。

结论

在对 EoE 患者内镜活动的评估中,内镜医生之间存在差异。在对随机对照试验数据的分析中,我们发现新开发的评分系统在检测内镜活动变化方面并不优于简单评分系统。这些结果支持在评估 EoE 患者的内镜活动时使用简单的评分系统。临床试验.gov 号:NCT00939263 和 NCT01386112。

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