Computer‐Aided Diagnosis of Colorectal Polyps: Clinical Usefulness and Limitations

医学 疾病 叙述性评论 重症监护医学 集合(抽象数据类型) 临床实习 结直肠癌 梅德林 临床决策支持系统 医学物理学 诊断试验 医疗保健系统 放射科 诊断准确性 试验预测值 医学诊断 病理 临床诊断 临床决策 预测值
作者
Kenneth Weicong Lin,Kwong‐Ming Fock,James Weiquan Li,Kenneth Weicong Lin,Kwong‐Ming Fock,James Weiquan Li
出处
期刊:Digestive Endoscopy [Wiley]
标识
DOI:10.1111/den.70056
摘要

ABSTRACT Computer‐aided diagnosis (CADx) systems have emerged as promising tools to support real‐time optical characterization of colorectal polyps during colonoscopy. This narrative review critically evaluates their clinical utility and limitations, focusing on two key strategies: “resect and discard” and “leave in situ.” While CADx offers potential benefits, such as cost reduction, increased diagnostic consistency, and support for nonexpert endoscopists, its performance in clinical settings remains variable and often below established thresholds by societies like ESGE and ASGE. Key metrics such as positive predictive value, negative predictive value, sensitivity, and specificity fluctuate widely across studies and CADx platforms, influenced by system training data, disease prevalence, and human–AI interactions. Importantly, trust and explainability issues hinder adoption, with studies revealing underutilization of accurate CADx predictions due to clinician skepticism. Additionally, CADx systems struggle to reliably differentiate sessile serrated lesions from hyperplastic polyps, partly due to limitations in histopathological ground truth and data set representation. Cost‐effectiveness analyses show promise, but practical implementation is challenged by equipment, regulatory, and training costs. Finally, emerging applications of CADx in predicting invasion depth in colorectal cancer show potential but require more robust validation. Overall, while CADx technologies may enhance diagnostic confidence and aid decision‐making, especially for less experienced endoscopists, their widespread clinical integration depends on addressing human–AI interaction challenges, improving system transparency, and refining models to include underrepresented lesion types.

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