Kerkhof M, Steyerberg E W, Kusters J G, Kuipers E J, Siersema P D
Department of Gastroenterology and Hepatology, Erasmus MC-University Medical Center Rotterdam, Rotterdam, The Netherlands.
Endoscopy. 2007 Sep;39(9):772-8. doi: 10.1055/s-2007-966737.
In patients with presumed Barrett esophagus we evaluated clinical risk factors that could predict the presence of intestinal metaplasia and dysplasia in biopsies of columnar-lined esophagus (CLE), independently of histological results.
In 908 patients with CLE of length > or = 2 cm, data on age, sex, reflux symptoms, tobacco and alcohol use, medication use, and upper gastrointestinal endoscopy findings were prospectively collected. Multivariate logistic regression analysis was performed, and a model for predicting the histological results was developed.
In 127/908 patients, biopsies of CLE did not contain intestinal metaplasia. Of the 781 patients with intestinal metaplasia, 663 patients (85%) had no dysplasia, and 118 (15%) had low grade dysplasia (LGD). The most important predictors for the presence of intestinal metaplasia were length of CLE, size of hiatal hernia, and male sex, while among those with intestinal metaplasia, age and male sex were most important for the presence of LGD. Multivariate combinations of these predictors yielded reliable models, which were able to discriminate intestinal metaplasia well from no intestinal metaplasia (area under receiver operating characteristic [ROC] curve 0.82), but only reasonably discriminated LGD from no dysplasia (area under ROC 0.65).
A simple model based on clinical findings can be used to predict the presence of intestinal metaplasia in biopsies from CLE. In contrast, predicting the presence of LGD versus no dysplasia in intestinal metaplasia is more difficult. Predictions from these models may aid decision making on whether a patient with CLE should have surveillance, in view of the known sampling error at endoscopy and interobserver variability at histology.
在疑似巴雷特食管患者中,我们评估了可独立于组织学结果预测柱状上皮化生食管(CLE)活检中肠化生及发育异常存在情况的临床风险因素。
前瞻性收集了908例CLE长度≥2 cm患者的年龄、性别、反流症状、吸烟与饮酒情况、用药情况以及上消化道内镜检查结果等数据。进行多因素逻辑回归分析,并建立预测组织学结果的模型。
127/908例患者的CLE活检未发现肠化生。在781例有肠化生的患者中,663例(85%)无发育异常,118例(15%)有低级别发育异常(LGD)。肠化生存在的最重要预测因素为CLE长度、食管裂孔疝大小及男性性别,而在有肠化生的患者中,年龄和男性性别对LGD的存在最为重要。这些预测因素的多因素组合产生了可靠的模型,能够很好地区分有肠化生与无肠化生情况(受试者操作特征曲线下面积[ROC]为0.82),但仅能合理地区分LGD与无发育异常情况(ROC下面积为0.65)。
基于临床发现的简单模型可用于预测CLE活检中肠化生的存在情况。相比之下,预测肠化生中LGD与无发育异常情况则更为困难。鉴于已知的内镜检查采样误差和组织学观察间的差异,这些模型的预测可能有助于决定CLE患者是否应接受监测。