Department of Surgery, Institute of Clinical Sciences, Sahlgrenska University Hospital, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Department of Radiology, Institute of Clinical Sciences, Sahlgrenska University Hospital, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Endocr Pract. 2024 Sep;30(9):830-836. doi: 10.1016/j.eprac.2024.05.011. Epub 2024 May 28.
The European Thyroid Imaging Reporting and Data System (EU-TIRADS) allows for selective fine needle aspiration cytology (FNAC). In 2017, EU-TIRADS was implemented as part of a nationwide standardized care bundle for thyroid cancer in Western Sweden with a population of approximately 1.7 million. The objective of this study was to investigate the clinical value of EU-TIRADS attempting to reduce the number of unnecessary FNACs in referred patients with thyroid nodules.
The study cohort consisted of all patients referred to Sahlgrenska University Hospital due to a palpable, newly detected or growing thyroid nodules or a positron emission tomography-positive finding for examination with thyroid ultrasound and selective cytology between 2018 and 2022. Medical records on EU-TIRADS classification, corresponding FNAC results, and histopathologic diagnosis were retrospectively collected. Adherence to the EU-TIRADS guidelines, use of selective FNAC, and rate of malignancy in patients who underwent surgery were assessed.
In total, 1246 thyroid nodules in 990 patients were evaluated. The distributions of EU-TIRADS 2 to 5 (number [percentage]) for all examined nodules were 63 (5%), 462 (37%), 443 (36%), and 278 (22%), respectively. FNAC was omitted in 7% of the investigated patients. FNAC was performed in 124 nodules (10%) despite not fulfilling the EU-TIRADS criteria or absence of positron emission tomography-positive findings. The rate of malignancy was 33% and 1/50 in patients who underwent "unnecessary" FNAC.
Implementation of EU-TIRADS in routine management of thyroid nodules led to the selective use of FNAC; however, the clinical impact was limited. This study provides real-world data on the value and magnitude of diagnostic improvement by implementing EU-TIRADS in clinical practice.
欧洲甲状腺影像报告和数据系统(EU-TIRADS)允许进行选择性细针抽吸细胞学检查(FNAC)。2017 年,EU-TIRADS 作为瑞典西部全国性甲状腺癌标准化护理包的一部分得到实施,该地区的人口约为 170 万。本研究的目的是调查 EU-TIRADS 在减少转诊甲状腺结节患者中不必要的 FNAC 数量方面的临床价值。
研究队列包括 2018 年至 2022 年期间因可触及、新发现或增大的甲状腺结节或正电子发射断层扫描(PET)阳性发现而到萨赫勒格兰纳大学医院就诊,接受甲状腺超声和选择性细胞学检查的所有患者。回顾性收集 EU-TIRADS 分类、相应 FNAC 结果和组织病理学诊断的病历。评估了对 EU-TIRADS 指南的依从性、选择性 FNAC 的使用以及接受手术治疗的患者的恶性肿瘤发生率。
共评估了 990 例患者的 1246 个甲状腺结节。所有检查结节的 EU-TIRADS 2 至 5 分布(数量[百分比])分别为 63(5%)、462(37%)、443(36%)和 278(22%)。7%的研究患者 FNAC 被忽略。尽管不符合 EU-TIRADS 标准或 PET 阳性结果不存在,仍对 124 个结节进行了 FNAC。行“不必要”FNAC 的患者恶性肿瘤发生率为 33%和 1/50。
EU-TIRADS 在甲状腺结节常规管理中的实施导致了 FNAC 的选择性使用;然而,临床影响有限。本研究提供了在临床实践中实施 EU-TIRADS 对诊断改善的价值和程度的真实世界数据。