Halliday Edwin, Harrison Eleanor, Sansom Hugh, Ahsan Syed Farhan, Harrison Katherine
Department of ENT, Shrewsbury and Telford Hospital NHS Trust, Royal Shrewsbury Hospital, Shrewsbury, UK.
Department of Cellular Pathology, Shrewsbury and Telford Hospital NHS Trust, Royal Shrewsbury Hospital, Shrewsbury, UK.
Cytopathology. 2020 Nov;31(6):514-524. doi: 10.1111/cyt.12834. Epub 2020 May 20.
In the UK, guidelines from the Royal College of Pathologists (RCPath) facilitate consistent and reproducible reporting and classification of fine needle aspiration cytology (FNAC) thyroid specimens. The aim was to audit our department against RCPath guidelines to refine and improve our reporting process.
Two-cycle retrospective observational audit of all patients undergoing thyroid FNAC over a 2-year period (1 year for each cycle). Final histology was correlated. The positive predictive value (PPV) for malignant neoplastic lesions was calculated; for Thy1, Thy1c, Thy2 and Thy2c all cases without final histology were assumed to be benign, while for Thy3a, Thy3f, Thy4 and Thy5 samples the PPV calculation was based only on those cytology samples with corresponding histology. False positive and false negative cases were reviewed.
In total, 288 cytology samples were included in the first cycle; 96 (33.3%) had corresponding histology. There were 287 samples included in the second cycle; 119 (41.5%) had follow-up histology. The rate of non-diagnostic samples (Thy1/1c) decreased from 39.6% to 30.0%. The PPV for malignant neoplastic lesions was Thy1/1c 2.6%, Thy2/2c 0.0%, Thy3a 40.0%, Thy3f 19.4%, Thy4 75.0%, Thy5 100.0% (first cycle); Thy1/1c 4.7%, Thy2/2c 0.7%, Thy3a 13.3%, Thy3f, 7.7%, Thy4, 50.0%, Thy5 100.0% (second cycle).
Our department was able to reduce the rate of non-diagnostic FNAC samples and improve the diagnostic accuracy of FNAC. Auditing local outcomes helps refine and improve the reporting process. Review of false positive and false negative cases helps examine potential pitfalls of cytology.
在英国,皇家病理学家学会(RCPath)发布的指南有助于对甲状腺细针穿刺细胞学检查(FNAC)标本进行一致且可重复的报告和分类。目的是对照RCPath指南对我们科室进行审核,以完善和改进我们的报告流程。
对2年期间(每个周期1年)所有接受甲状腺FNAC检查的患者进行两周期回顾性观察审核。将最终组织学结果进行对比。计算恶性肿瘤性病变的阳性预测值(PPV);对于Thy1、Thy1c、Thy2和Thy2c,所有无最终组织学结果的病例均假定为良性,而对于Thy3a、Thy3f、Thy4和Thy5样本,PPV计算仅基于那些有相应组织学结果的细胞学样本。对假阳性和假阴性病例进行审查。
第一周期共纳入288份细胞学样本;96份(33.3%)有相应组织学结果。第二周期纳入287份样本;119份(41.5%)有随访组织学结果。非诊断性样本(Thy1/1c)的比例从39.6%降至30.0%。恶性肿瘤性病变的PPV为:Thy1/1c 2.6%,Thy2/2c 0.0%,Thy3a 40.0%,Thy3f 19.4%,Thy4 75.0%,Thy5 100.0%(第一周期);Thy1/1c 4.7%,Thy2/2c 0.7%,Thy3a 13.3%,Thy3f 7.7%,Thy4 50.0%,Thy5 100.0%(第二周期)。
我们科室能够降低非诊断性FNAC样本的比例,提高FNAC的诊断准确性。审核本地结果有助于完善和改进报告流程。审查假阳性和假阴性病例有助于检查细胞学的潜在缺陷。