Digestive and Liver Disease Unit, University La Sapienza, Sant'Andrea Hospital, Rome, Italy.
Dig Liver Dis. 2010 Feb;42(2):122-6. doi: 10.1016/j.dld.2009.04.019. Epub 2009 Jun 3.
Application of appropriate indications for upper endoscopy (EGD) should conserve limited endoscopic resources. To perform a systematic review and meta-analysis to assess the efficacy of American Society for Gastrointestinal Endoscopy and European Panel on the Appropriateness of Gastrointestinal Endoscopy guidelines in selecting patients referred for an upper endoscopy relative to the detection of gastro-oesophageal cancer.
Studies comparing the appropriateness of EGD indication according to American Society for Gastrointestinal Endoscopy or European Panel on the Appropriateness of Gastrointestinal Endoscopy guidelines and the detection of relevant endoscopic findings and cancer were identified by searching the Medline (1982 to September 2008). Pre-defined outputs of the meta-analysis were sensitivity, specificity, and positive and negative likelihood ratios (LR+, LR-).
We included eight cohort studies comprising 13,856 patients; 10,643 EGD indications were categorized as appropriate, and 3010 (22%) as inappropriate. For relevant findings, the adjusted sensitivity, specificity, LR+, and LR- were 85% (95% CI, 84-86%), 28% (95% CI, 27-29%), 1.18 (95% CI, 1.1-1.3) and 0.6 (95% CI, 0.5-0.7), respectively. For cancer detection, the adjusted sensitivity, specificity, LR+, and LR- were 97% (95% CI, 94-98%), 22% (95% CI, 22-23%), 1.2 (95% CI, 1.1-1.4), and 0.2 (95% CI, 0.05-0.9), respectively.
For inappropriate EGD, the very low likelihood of cancer argues against endoscopic referral, whereas the low specificity substantially reduces the predictive value of an appropriate indication for both cancer and relevant endoscopic findings.
适当应用上消化道内镜(EGD)可以节省有限的内镜资源。我们进行了系统回顾和荟萃分析,以评估美国胃肠内镜学会和欧洲胃肠内镜适宜性专家组指南在选择接受上消化道内镜检查患者方面的效果,该指南与胃食管癌症的检出率相关。
通过检索 Medline(1982 年至 2008 年 9 月),我们确定了比较美国胃肠内镜学会或欧洲胃肠内镜适宜性专家组指南的内镜适应证与相关内镜发现和癌症检出率的对照研究。荟萃分析的预定义结果为敏感性、特异性、阳性和阴性似然比(LR+、LR-)。
我们纳入了 8 项队列研究,共 13856 例患者;10643 例 EGD 适应证被归类为适当,3010 例(22%)为不适当。对于相关发现,调整后的敏感性、特异性、LR+和 LR-分别为 85%(95%CI,84-86%)、28%(95%CI,27-29%)、1.18(95%CI,1.1-1.3)和 0.6(95%CI,0.5-0.7)。对于癌症检出率,调整后的敏感性、特异性、LR+和 LR-分别为 97%(95%CI,94-98%)、22%(95%CI,22-23%)、1.2(95%CI,1.1-1.4)和 0.2(95%CI,0.05-0.9)。
对于不适当的 EGD,癌症的可能性非常低,因此不需要进行内镜转诊,而特异性低则大大降低了适当适应证对癌症和相关内镜发现的预测价值。