Burks Allen Cole, Akulian Jason, MacRosty Christina R, Ghosh Sohini, Belanger Adam, Sakthivel Muthu, Benefield Thad S, Inscoe Christina R, Zhou Otto, Lu Jianping, Lee Yueh Z
Division of Pulmonary and Critical Care Medicine, University of North Carolina at Chapel Hill, NC, USA.
Division of Pulmonary and Critical Care, Allegheny Health Network, Pittsburgh, PA, USA.
J Thorac Dis. 2022 Feb;14(2):257-268. doi: 10.21037/jtd-21-1381.
Screen detected and incidental pulmonary nodules are increasingly common. Current guidelines recommend tissue sampling of solid nodules >8 mm. Bronchoscopic biopsy poses the lowest risk but is paired with the lowest diagnostic yield when compared to CT-guided biopsy or surgery. A need exists for a safe, mobile, low radiation dose, intra-procedural method to localize biopsy instruments within target nodules. This retrospective cross sectional reader feasibility study evaluates the ability of clinicians to identify pulmonary nodules using a prototype carbon nanotube radiation enabled stationary digital chest tomosynthesis system.
Patients with pulmonary nodules on prior CT imaging were recruited and consented for imaging with stationary digital chest tomosynthesis. Five pulmonologists of varying training levels participated as readers. Following review of patient CT and a thoracic radiologist's interpretation of nodule size and location the readers were tasked with interpreting the corresponding tomosynthesis scan to identify the same nodule found on CT.
Fifty-five patients were scanned with stationary digital chest tomosynthesis. The median nodule size was 6 mm (IQR =4-13 mm). Twenty nodules (37%) were greater than 8 mm. The radiation entrance dose for s-DCT was 0.6 mGy. A significant difference in identification of nodules using s-DCT was seen for nodules <8 ≥8 mm in size (57.7% 90.9%, CI: -0.375, -0.024; P<0.001). Inter-reader agreement was fair, and better for nodules ≥8 mm [0.278 (SE =0.043)].
With system and carbon nanotube array optimization, we hypothesize the detection rate for nodules will improve. Additional study is needed to evaluate its use in target and tool co-localization and target biopsy.
筛查发现和偶然发现的肺结节越来越常见。当前指南建议对直径大于8mm的实性结节进行组织采样。与CT引导下活检或手术相比,支气管镜活检风险最低,但诊断率也最低。需要一种安全、可移动、低辐射剂量的术中方法来将活检器械定位在目标结节内。这项回顾性横断面读者可行性研究评估了临床医生使用原型碳纳米管辐射固定式数字胸部断层合成系统识别肺结节的能力。
招募先前CT成像显示有肺结节的患者,并征得其同意进行固定式数字胸部断层合成成像。五名不同培训水平的肺科医生作为阅片者参与。在回顾患者CT以及胸科放射科医生对结节大小和位置的解读后,要求阅片者解读相应的断层合成扫描,以识别在CT上发现的同一结节。
对55名患者进行了固定式数字胸部断层合成扫描。结节的中位大小为6mm(四分位间距=4-13mm)。20个结节(37%)大于8mm。s-DCT的辐射入射剂量为0.6mGy。对于大小<8mm和≥8mm的结节,使用s-DCT识别结节存在显著差异(57.7%对90.9%,CI:-0.375,-0.024;P<0.001)。阅片者间的一致性一般,对于≥8mm的结节一致性更好[0.278(标准误=0.043)]。
通过系统和碳纳米管阵列优化,我们推测结节的检测率将会提高。需要进一步研究以评估其在目标与工具共定位及目标活检中的应用。