Ece Dilek, Keser Sevinç Hallaç, Çağlayan Benan, Salepçi Banu, Güler Gamze Babur, Sensu Sibel, Geçmen Gonca, Kökten Şermin
Department of Pathology, Dr. Lütfi Kırdar Kartal Training and Research Hospital, İstanbul, Turkey.
Department of Chest Diseases, Dr. Lütfi Kırdar Kartal Training and Research Hospital, İstanbul, Turkey.
Turk Gogus Kalp Damar Cerrahisi Derg. 2018 Jan 9;26(1):123-131. doi: 10.5606/tgkdc.dergisi.2018.14197. eCollection 2018 Jan.
This study aims to evaluate the factors influencing the adequacy of endobronchial ultrasound-guided transbronchial fine needle aspiration specimens.
A retrospective analysis of 1,700 endobronchial ultrasound-guided transbronchial fine needle aspiration samples obtained from 822 patients (500 males, 322 females; mean age 56±13 years; range 16 to 83 years) was performed between March 2011 and March 2014 at our center. Variables potentially associated with sampling adequacy, such as all cytological materials and procedure notes (lymph node and/or lesion size, localization, needle pass number, and slide number) were examined.
The overall specimen adequacy was 79.8%. The specimen adequacy was associated with needle pass number (p≤0.001). Adequacy rate was 66.9% for one needle pass and 85.8% for three needle passes. According to the sampling regions, adequacy rates showed a difference [69.2%-85.8%; (p≤0.005)]. In the multivariate logistic regression analysis of subcarinal (7) lymph node station, patient age (odds ratio, 0.983; 95% confidence interval, 0.966-1.000; p=0.049) and number of slides (odds ratio, 1.240; 95% confidence interval, 1.062-1.448; p=0.006) were independent determining factors of specimen adequacy. While independent determinants of specimen adequacy for the right paratracheal (4R) region were lymph node size (odds ratio, 1.486; 95% confidence interval, 0.973-2.268; p=0.067) and number of slides (odds ratio, 1.418; 95% confidence interval, 1.146-1.756; p=0.001), they were lymph node size (odds ratio, 1.594; 95% confidence interval, 0.960-2.645; p=0.071) and number of needle passes (odds ratio, 2.277; 95% confidence interval, 1.360-3.811; p=0.002) for the right interlobar (11R) region. Independent determinant of specimen adequacy for the left paratracheal (4L) lymph node station was the number of needle passes (odds ratio, 1.656; 95% confidence interval, 0.955-2.869; p=0.072).
During endobronchial ultrasound-guided transbronchial fine needle aspirations, particularly when rapid on site evaluation cannot be applied, consideration of factors affecting adequacy according to lymph node localizations may increase the chance for obtaining materials with suitable quality for cytologic evaluation.
本研究旨在评估影响支气管内超声引导下经支气管针吸活检标本充足性的因素。
2011年3月至2014年3月在本中心对822例患者(500例男性,322例女性;平均年龄56±13岁;年龄范围16至83岁)获取的1700份支气管内超声引导下经支气管针吸活检样本进行回顾性分析。检查了可能与采样充足性相关的变量,如所有细胞学材料和操作记录(淋巴结和/或病变大小、定位、穿刺针数和玻片数)。
总体标本充足率为79.8%。标本充足率与穿刺针数相关(p≤0.001)。单次穿刺的充足率为66.9%,三次穿刺的充足率为85.8%。根据采样区域,充足率存在差异[69.2%-85.8%;(p≤0.005)]。在隆突下(7)淋巴结站位的多因素逻辑回归分析中,患者年龄(比值比,0.983;95%置信区间,0.966-1.000;p=0.049)和玻片数(比值比,1.240;95%置信区间,1.062-1.448;p=0.006)是标本充足性的独立决定因素。而对于右主支气管旁(4R)区域,标本充足性的独立决定因素是淋巴结大小(比值比,1.486;95%置信区间,0.973-2.268;p=0.067)和玻片数(比值比,1.418;95%置信区间,1.146-1.756;p=0.001),对于右叶间(11R)区域则是淋巴结大小(比值比,1.594;95%置信区间,0.960-2.645;p=0.071)和穿刺针数(比值比,2.277;95%置信区间,1.360-3.811;p=0.002)。左主支气管旁(4L)淋巴结站位标本充足性的独立决定因素是穿刺针数(比值比,1.656;95%置信区间,0.955-2.869;p=0.072)。
在支气管内超声引导下经支气管针吸活检过程中,尤其是无法进行现场快速评估时,根据淋巴结定位考虑影响充足性的因素可能会增加获得适合细胞学评估质量材料的机会。