甲状腺结节ACR-TIRADS与ATA指南的比较:颈部与颈部的比较

J. Qiang,, Carrie Betel, K. Hack, Z. Ghorab, J. Gilmour, M. Mohammadi, K. Burton, K. Higgins, I. Halperin
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引用次数: 1

摘要

简介:本研究的目的是比较美国放射学会甲状腺影像报告和数据系统(ACR-TIRADS)和美国甲状腺协会(ATA)系统在识别恶性甲状腺结节方面的表现特点。方法:回顾性分析2014- 2015年在加拿大某学术中心活检的所有甲状腺结节的超声图像,由两名放射科医生进行分析。将甲状腺结节的超声特征与细胞学或病理学结果进行比较,确定TIRADS和ATA预测癌风险的阳性预测值(PPV)、阴性预测值(NPV)、敏感性和特异性。根据ACR-TIRADS描述了不需要随访或干预的结节的临床病程。在ACR-TIRADS中加入血运情况,以确定TIRADS的敏感性是否得到改善。结果:共回顾417例甲状腺结节,82%为良性(Bethesda II)。ATA和TIRADS的敏感性、特异性、PPV和NPV分别为97%、11%、9%、98%和70%、29%、18%和81%。在10例根据TIRADS标准不需要超声随访的结节中,2例为恶性结节,其余为流感。如果在TIRADS (TIRADS- vasc)中增加血管分布,则遗漏的恶性病例数量可能减少43%(从7例减少到4例)。结论:TIRADS的特异性较ATA高,但敏感性较ATA低,漏检少量恶性结节。临床医生需要根据自己的判断来决定哪些结节需要活检,因为单独使用TIRADS会遗漏一些恶性病例。
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Comparison of ACR-TIRADS to the ATA Guidelines for Thyroid Nodules: A Neck to Neck Comparison
Introduction: The goal of this study was to compare the performance characteristics of the American College of Radiology Thyroid Imaging Reporting and Data System (ACR-TIRADS) and the American Thyroid Association (ATA) systems in identifying malignant thyroid nodules. Methods: In a retrospective chart review, ultrasound images of all thyroid nodules biopsied in 2014- 2015 at a Canadian academic centre were reviewed by two radiologists. The ultrasound characteristics of thyroid nodules were compared with cytologic or pathologic results to determine the positive predictive value (PPV), negative predictive value (NPV), sensitivity and specificity for TIRADS and ATA in predicting cancer risk. Clinical course of nodules not requiring follow up or intervention according to ACR-TIRADS was described. Vascularity was added to ACR-TIRADS to determine whether sensitivity of TIRADS improves. Results: A total of 417 thyroid nodules were reviewed, 82% were benign (Bethesda II). The sensitivity, specificity, PPV, and NPV were 97%, 11%, 9%, 98%, and 70%, 29%, 18%, and 81% for ATA and TIRADS, respectively. Of the 10 nodules that did not need ultrasound follow up based on TIRADS criteria, 2 were malignant, the rest were FLUS. If vascularity was added to TIRADS (TIRADS-Vasc), the number of malignant cases missed could have been reduced by 43% (from 7 to 4 cases). Conclusions: TIRADS is more specific but less sensitive than ATA, and misses a small number of malignant nodules. Clinicians need to use their judgement to decide which nodules require biopsy as some malignant cases will be missed using TIRADS alone.
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