支气管超声引导下取样:针活检和低温活检除针吸外的诊断率。

IF 5.4
Jason Beattie, Hamad Nasim, Jacqueline Chen, Annika Bharwani, Juan Lara, Raymond Parrish, Kai Swenson, Mihir Parikh, Kirill Karlin, Paul A VanderLaan, Adnan Majid
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引用次数: 0

摘要

背景:支气管内超声(EBUS)引导取样评估良性状况和淋巴瘤是不规范的。随着新工具的出现,抽样方法仍在研究中。方法:我们进行了一项单中心研究,采用协议化的采样和处理来评估经支气管针穿刺(TBNA)、Franseen针活检(TBNB)和低温活检在纵隔和肺门异常患者中诊断结节状、淋巴瘤或未分化淋巴结病的有效性。在TBNA之后,进行探索性抽样。用TBNB针穿刺术建立一个通道,然后进行冷冻活检。随后,每个工具交替取样3次。主要结果是诊断产率,采用最新ATS/ACCP指南的严格标准。次要结果包括手术结果和TBNB和冷冻活检样本的病理评估。结果:2024年1月至12月,51例患者共采集56个淋巴结。每个淋巴结的总诊断率为86%(48/56)。就单个工具而言,TBNA的产量为50%,TBNB的产量为73%,低温活检的产量为82% (p=0.0001 TBNA vs低温活检;p=0.006 TBNA vs TBNB; p=0.13 TBNB vs低温活检)。在亚组分析中,TBNB和低温活检提高了良性疾病的诊断率(TBNA- 59%, TBNB-88%,低温活检-100%;p=0.002 TBNA vs低温活检,p=0.01 TBNA vs TBNB, p=0.11 TBNB vs低温活检)。对于淋巴瘤,每个淋巴结的诊断率TBNA为3/10,TBNB为5/10,低温活检为6/10 (p= 0.001)TBNA vs冷冻活检,p=0.1 TBNA vs TBNB, p=0.1 TBNB vs冷冻活检)。经病理检查,与冷冻活检相比,TBNB提供了更大的样本,但TBNB样本含有更大比例的血液;这些差异转化为两种工具相似的诊断组织的结果区域。冷冻活检中免疫组织化学和特殊染色的样本使用率(61%)高于TBNB(33%)。在所有并发症发生率为2%(1例气胸)的患者中,研究抽样是可行的。结论:TBNB和低温活检都能提供完整的组织学样本,提高EBUS TBNA在良性情况下的诊断率。使用三种活检工具对单个淋巴结进行多次检查是安全可行的。相对于TBNB,低温活检在淋巴瘤中提供了更好的样品质量和更高的产量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Endobronchial Ultrasound Guided Sampling: Diagnostic Yield of Needle Biopsy and Cryobiopsy in Addition to Needle Aspiration.

Background: Endobronchial ultrasound (EBUS) guided sampling for evaluation of benign conditions and lymphoma is not standardized. Sampling methods remain under study as new tools become available.

Methods: We performed a single center study with protocolized sampling and processing to evaluate the diagnostic utility of transbronchial needle aspiration (TBNA), Franseen needle biopsy (TBNB), and cryobiopsy in patients with mediastinal and hilar abnormality with concern for sarcoid, lymphoma, or undifferentiated lymphadenopathy. Following TBNA, exploratory sampling was performed. A tract was created with a TBNB needle pass followed by cryobiopsy. Sampling was subsequently alternated for a total of 3 passes per tool. The primary outcome was diagnostic yield-using a strict criterion modeled from recent ATS/ACCP guidelines. Secondary outcomes included procedural outcomes and pathologic assessment of TBNB and cryobiopsy samples.

Results: Between January and December 2024, 56 nodes were sampled in 51 patients. The overall diagnostic yield per node was 86% (48/56). Regarding individual tools, the yield was 50% for TBNA, 73% for TBNB, and 82% for cryobiopsy (p=0.0001 TBNA vs cryobiopsy; p=0.006 TBNA vs TBNB; p=0.13 TBNB vs cryobiopsy). In subgroup analysis, TBNB and cryobiopsy enhanced diagnostic yield in benign conditions (TBNA- 59%, TBNB-88%, and cryobiopsy-100%; p=0.002 TBNA vs cryobiopsy, p=0.01 TBNA vs TBNB, p=0.11 TBNB vs cryobiopsy). For lymphoma, the diagnostic yield per node was 3/10 for TBNA, 5/10 for TBNB, and 6/10 for cryobiopsy (p=.001 TBNA vs cryobiopsy, p=0.1 TBNA vs TBNB, p=0.1 TBNB vs cryobiopsy). Upon pathology review, TBNB provided larger samples compared to cryobiopsy however TBNB samples contained a larger proportion of blood; these differences translated to similar resultant areas of diagnostic tissue for both tools. Sample usage for immunohistochemistry and special staining was higher for cryobiopsy (61%) vs TBNB (33%). Study sampling was feasible in all patients with a 2% complication rate (1 pneumothorax).

Conclusion: Both TBNB and cryobiopsy provide intact histologic sampling that enhance the diagnostic yield of EBUS TBNA in benign conditions. Multiple passes with three biopsy tools at an individual lymph node is safe and feasible. Cryobiopsy provides superior sample quality relative to TBNB and superior yield vs TBNA in lymphoma.

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