Division of Gastroenterology and Hepatology, Department of Medicine, Stanford University School of Medicine, Stanford, California.
Critical Care Quality and Strategic Initiatives, Stanford Health Care, Stanford, California.
Clin Gastroenterol Hepatol. 2021 Sep;19(9):1873-1882. doi: 10.1016/j.cgh.2021.04.027. Epub 2021 Apr 22.
The adenoma detection rate at screening (ADR) predicts interval colorectal cancer. Monitoring other lesion detection rates and colonoscopy indications has been proposed. We developed a comprehensive, automated colonoscopy audit program based on standardized clinical documentation, explored detection rates across indications, and developed the Adenoma Detection Rate - Extended to all Screening / Surveillance (ADR-ESS) score.
In a prospective cohort study, we calculated overall and advanced adenoma and sessile serrated lesion (SSL) detection rates among 15,253 colonoscopies by 35 endoscopists from 4 endoscopy units across all colonoscopy indications. We explored correlations between detection rates, and the precision and stability of ADR-ESS versus ADR.
The overall "screening, first" ADR was 36.3% (95% confidence interval [CI], 34.5%-38.1%). The adenoma detection rate was lower for "screening, not first" (relative rate [RR], 0.80; 95% CI, 0.74-0.87) and "family history" (RR, 0.84; 95% CI, 0.74-0.96), and higher for "surveillance" (RR, 1.22; 95% CI, 1.15-1.31) and "follow-up, FIT" (RR, 1.21; 95% CI, 1.07-1.37). For "screening, first," the detection rates for advanced adenoma, SSL, and advanced SSL were 6.7% (95% CI, 5.7%-7.7%), 7.2% (95% CI, 6.2%-8.2%), and 2.6% (95% CI, 2.0%-3.2%), respectively. Adenoma and SSL detection were correlated (r = 0.44; P = .008). ADR-ESS had substantially narrower confidence intervals and less period-to-period variability than ADR, and was not improved by weighting for indication volume and correction for detection by indication.
Comprehensive, automated colonoscopy audit based on standardized clinical documentation is feasible. Adenoma detection is a fair but imperfect proxy for SSL detection. ADR-ESS increases the precision of adenoma detection assessments and emphasizes quality across colonoscopy indications.
筛查时的腺瘤检出率(ADR)可预测结直肠间隔期癌。有人提出监测其他病变检出率和结肠镜检查适应证。我们基于标准化临床文件开发了一种全面的、自动化的结肠镜检查审核程序,探讨了各种适应证下的检出率,并制定了腺瘤检出率-扩展至所有筛查/监测(ADR-ESS)评分。
在一项前瞻性队列研究中,我们对来自 4 个内镜科室的 35 名内镜医生进行的 15253 例结肠镜检查的总体和高级腺瘤及无蒂锯齿状病变(SSL)的检出率进行了计算。我们探讨了检出率之间的相关性,以及 ADR-ESS 与 ADR 的精确性和稳定性。
总体“筛查,首次”ADR 为 36.3%(95%置信区间[CI],34.5%-38.1%)。“筛查,非首次”(相对风险[RR],0.80;95%CI,0.74-0.87)和“家族史”(RR,0.84;95%CI,0.74-0.96)的腺瘤检出率较低,“监测”(RR,1.22;95%CI,1.15-1.31)和“随访,FIT”(RR,1.21;95%CI,1.07-1.37)的腺瘤检出率较高。对于“筛查,首次”,高级腺瘤、SSL 和高级 SSL 的检出率分别为 6.7%(95%CI,5.7%-7.7%)、7.2%(95%CI,6.2%-8.2%)和 2.6%(95%CI,2.0%-3.2%)。腺瘤和 SSL 的检出率相关(r=0.44;P=0.008)。ADR-ESS 的置信区间明显较窄,且较各期间的变异性小,并且通过按适应证体积加权和按适应证校正检出率,并没有得到改善。
基于标准化临床文件的全面、自动化结肠镜检查审核是可行的。腺瘤检出率是 SSL 检出率的一个公平但不完美的替代指标。ADR-ESS 提高了腺瘤检出评估的精确性,并强调了各种结肠镜检查适应证的质量。