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Ultrasound-guided fine-needle aspiration biopsy of the thyroid: Methods to decrease the rate of unsatisfactory biopsies in the absence of an on-site pathologist

机译:甲状腺超声引导下细针穿刺活检:在没有现场病理学家的情况下降低不满意的活检率的方法

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Purpose: The rate of unsatisfactory samples from ultrasound-guided fine-needle aspirations of thyroid nodules varies widely in the literature. We aimed to evaluate our thyroid ultrasound-guided fine-needle aspiration biopsy technique in the absence of on-site microscopic examination by a pathologist; determine factors that affect the adequacy rate, such as the number of needle passes and needle size; compare our results with the literature; and establish an optimal technique. Materials and Methods: We performed a retrospective review of cytopathology reports from 252 consecutive thyroid ultrasound-guided fine-needle aspiration biopsies performed by a radiologist between 2005 and 2010 in our hospital's radiology department. Sample adequacy, the number of needle passes, and needle size were determined. There was an on-site cytologist who prepared slides immediately after fine-needle aspiration but no on-site microscopic assessment of sample adequacy to guide the number of needle passes that should be performed. Cytopathology biopsy reports were classified as either unsatisfactory or satisfactory samples for diagnosis; the latter consisted of benign, malignant, and undetermined diagnoses. Results: Seventy-seven biopsies were performed with 1 needle pass, 124 with 2 needle passes, and 51 with 3 needle passes. The rates of unsatisfactory biopsies were 33.8%, 23.4% (odds ratio [OR] 0.599 [95% confidence interval {CI}, 0.319-1.123]; P =.110), and 13.7% (OR 0.312 [95% CI, 0.124-0.788]; P =.014), respectively. Conclusion: In a hospital in which there is no on-site pathologist, a 3-pass method increases the specimen satisfactory rate by 20% compared with 1 pass, achieves similar rates to the literature, and provides a basis for further improvement of our practice.
机译:目的:甲状腺结节的超声引导下细针穿刺抽吸不合格样品的比率在文献中有很大差异。我们的目标是在没有病理学家现场显微镜检查的情况下评估甲状腺超声引导下的细针穿刺活检技术。确定影响合格率的因素,例如针的通过次数和针的大小;将我们的结果与文献进行比较;并建立最佳技术。材料和方法:我们对2005年至2010年间在我院放射科进行的252次连续的甲状腺超声引导下的细针穿刺活检进行了细胞病理学报告的回顾性研究。确定样品的充足性,针的通过次数和针的尺寸。有一位现场细胞学家在细针抽吸后立即准备了载玻片,但没有现场对样品的适当性进行显微镜评估以指导应进行的穿针次数。细胞病理学活检报告被分类为不能令人满意的样本或令人满意的诊断样本;后者由良性,恶性和不确定的诊断组成。结果:1针通过了77次活检,2针通过了124次活检,3针通过了51次活检。活检不合格率分别为33.8%,23.4%(赔率[OR] 0.599 [95%置信区间{CI},0.319-1.123]; P = .110)和13.7%(OR 0.312 [95%CI,0.124] -0.788]; P = .014)。结论:在没有现场病理学家的医院中,3次通过方法与1次通过相比将标本满意率提高了20%,达到了与文献相似的比率,并为进一步改进我们的实践提供了基础。

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