Xu Shan, Yin Qianlong, Zhang Jisong, Xu Xiaoling, Chen Enguo, Ying Kejing
Respiratory and Critical Care Medicine, Regional Medical Center for National Institute of Respiratory Disease, Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University, Hangzhou, People's Republic of China.
Cancer Center, Zhejiang University, Hangzhou, People's Republic of China.
Int J Gen Med. 2025 Apr 24;18:2237-2245. doi: 10.2147/IJGM.S513395. eCollection 2025.
Currently, Endobronchial ultrasound (EBUS) and rapid on-site evaluation (ROSE) are extensively utilized in the clinical practice of respiratory medicine. The combined diagnostic approach has been shown to enhance the clinical diagnostic accuracy; however, certain controversies remain.
This study included 200 patients who underwent endobronchial ultrasound combined with transbronchial lung biopsy with a guide sheath (EBUS-GS-TBLB) or endobronchial ultrasound combined with transbronchial needle aspiration (EBUS-TBNA) and received histopathological diagnoses at the Bronchoscopy Department, from January 2021 to January 2022. Of these, 168 patients were assigned to the ROSE group and 32 to the non-ROSE group. The diagnosis rates of EBUS-GS-TBLB and EBUS-TBNA, both with and without ROSE, along with the secondary biopsy rate, complication probability, and mean number of biopsies, were compared to analyze the differences between tumors and non-tumors. The safety of EBUS-GS-TBLB and EBUS-TBNA was also evaluated.
The overall diagnostic accuracy was 85.71% in the ROSE group and 65.62% in the non-ROSE group. The diagnostic accuracy of the ROSE group was significantly higher than that of the non-ROSE group (P < 0.05). Compared to the non-ROSE group, the rate of secondary biopsy in the ROSE group was significantly reduced (P < 0.05), particularly in non-tumor cases. However, there was no significant difference in the incidence of complications and the average number of biopsies between the two groups (P > 0.05). Compared to the EBUS-GS-TBLB group, the EBUS-TBNA group showed a significantly lower incidence of complications and fewer biopsies (P < 0.05).
The integration of ROSE with EBUS enhanced the diagnostic rate and reduced the need for secondary examinations in the biopsy diagnosis of lung lesions, particularly in the definitive diagnosis of non-neoplastic lesions. The combination of ROSE technology appears to be more advantageous. Compared to EBUS-GS-TBLB, EBUS-TBNA demonstrated a lower incidence of complications and fewer biopsies.
目前,支气管内超声(EBUS)和快速现场评估(ROSE)在呼吸医学临床实践中被广泛应用。联合诊断方法已被证明可提高临床诊断准确性;然而,仍存在一些争议。
本研究纳入了200例于2021年1月至2022年1月期间在支气管镜科接受支气管内超声联合带鞘支气管肺活检(EBUS-GS-TBLB)或支气管内超声联合经支气管针吸活检(EBUS-TBNA)并获得组织病理学诊断的患者。其中,168例患者被分配至ROSE组,32例被分配至非ROSE组。比较了有ROSE和无ROSE情况下EBUS-GS-TBLB和EBUS-TBNA的诊断率,以及二次活检率、并发症概率和平均活检次数,以分析肿瘤与非肿瘤之间的差异。还评估了EBUS-GS-TBLB和EBUS-TBNA的安全性。
ROSE组的总体诊断准确率为85.71%,非ROSE组为65.62%。ROSE组的诊断准确率显著高于非ROSE组(P < 0.05)。与非ROSE组相比,ROSE组的二次活检率显著降低(P < 0.05),尤其是在非肿瘤病例中。然而,两组之间的并发症发生率和平均活检次数无显著差异(P > 0.05)。与EBUS-GS-TBLB组相比,EBUS-TBNA组的并发症发生率显著更低,活检次数更少(P < 0.05)。
ROSE与EBUS相结合提高了肺病变活检诊断的诊断率,减少了二次检查的需求,特别是在非肿瘤性病变的明确诊断中。ROSE技术的联合应用似乎更具优势。与EBUS-GS-TBLB相比,EBUS-TBNA的并发症发生率更低,活检次数更少。