Hajelssedig Omer Eljyli, Zorron Cheng Tao Pu Leonardo, Thompson Jacqueline Y, Lord Anton, El Sayed Iman, Meyer Chase, Shaukat Ali Faisal, Abdulazeem Hebatullah M, Kheir Ammar O, Siepmann Timo, Singh Rajvinder
Master Program of Clinical Research, Dresden International University, Dresden, Germany.
DRESDEN INTERNATIONAL UNIVERSITAET (Freiberger Str. 37, 01067 Dresden, Germany).
J Gastroenterol Hepatol. 2021 Oct;36(10):2659-2671. doi: 10.1111/jgh.15577. Epub 2021 Jul 5.
BACKGROUND AND AIM: Endoscopic surveillance for dysplasia in Barrett's esophagus (BE) with random biopsies is the primary diagnostic tool for monitoring clinical progression into esophageal adenocarcinoma. As an alternative, narrow-band imaging (NBI) endoscopy offers targeted biopsies that can improve dysplasia detection. This study aimed to evaluate NBI-guided targeted biopsies' diagnostic accuracy for detecting dysplasia in patients undergoing endoscopic BE surveillance compared with the widely used Seattle protocol. METHODS: Cochrane DTA Register, MEDLINE/PubMed, EMBASE, OpenGrey, and bibliographies of identified papers were searched until 2018. Two independent investigators resolved discrepancies by consensus, study selection, data extraction, and quality assessment. Data on sensitivity, specificity, and predictive values were pooled and analyzed using a random-effects model. RESULTS: Of 9528 identified articles, six studies comprising 493 participants were eligible for quantitative synthesis. NBI-targeted biopsy showed high diagnostic accuracy in detection of dysplasia in BE with a sensitivity of 76% (95% confidence interval [CI]: 0.61-0.91), specificity of 99% (95% CI: 0.99-1.00), positive predictive value of 97% (95% CI: 0.96-0.99), and negative predictive value of 84% (95% CI: 0.69-0.99) for detection of all grades of dysplasia. The receiver-operating characteristic curve for NBI model performance was 0.8550 for detecting all dysplasia. CONCLUSION: Narrow-band imaging-guided biopsy demonstrated high diagnostic accuracy and might constitute a valid substitute for random biopsies during endoscopic surveillance for dysplasia in BE.
背景与目的:对巴雷特食管(BE)进行内镜监测并随机活检以筛查发育异常,是监测其进展为食管腺癌的主要诊断工具。作为一种替代方法,窄带成像(NBI)内镜检查可提供靶向活检,从而提高发育异常的检测率。本研究旨在评估与广泛使用的西雅图方案相比,NBI引导下的靶向活检在接受内镜BE监测的患者中检测发育异常的诊断准确性。 方法:检索Cochrane DTA Register、MEDLINE/PubMed、EMBASE、OpenGrey以及已识别论文的参考文献,检索时间截至2018年。由两名独立研究人员通过共识解决差异、进行研究选择、数据提取和质量评估。使用随机效应模型汇总并分析敏感性、特异性和预测值的数据。 结果:在9528篇已识别的文章中,有6项研究(共493名参与者)符合定量综合分析的条件。NBI靶向活检在检测BE发育异常方面显示出较高的诊断准确性,检测所有等级发育异常的敏感性为76%(95%置信区间[CI]:0.61 - 0.91),特异性为99%(95% CI:0.99 - 1.00),阳性预测值为97%(95% CI:0.9(6)- 0.99),阴性预测值为84%(95% CI:0.69 - 0.99)。NBI模型检测所有发育异常的受试者工作特征曲线为0.8550。 结论:窄带成像引导下的活检显示出较高的诊断准确性,可能成为BE发育异常内镜监测期间随机活检的有效替代方法。
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