机器人辅助支气管镜检查周围肺病变:离子平台的单中心体验

Azeem Rathore, Cameron Kahn, Sawyer J. Bawek, A. Bajwa
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摘要

理由:电磁导航支气管镜对肺部病变的诊断率仍然很低。多中心导航研究显示,3厘米以下病变的诊断率为71%,2厘米以下病变的诊断率为67%。机器人辅助导航平台的引入可能会克服以前方法遇到的一些传统障碍。我们的目标是评估Ion™腔内系统(Intuitive Surgical, Inc., Sunnyvale, California)对以前无法使用传统白光支气管镜进行活检的肺病变的导航和诊断效果。方法:我们回顾性回顾和分析了2020年3月11日至2020年11月25日在我们的单一中心由一名程序医生连续进行的76例机器人辅助导航支气管镜(RAB)病例的数据。次要终点包括平台的安全性,如气胸和重大出血事件的发生率。结果:使用形状传感技术定位病变的能力为100% (n=76)。通过桡骨支气管内超声确认病变显像,导航成功率为76% (n=58)。额外使用二维透视进行病灶穿刺指导和快速现场评估,以评估是否有足够的组织采样,诊断率为92% (n=70)。气胸并发症发生率为0%,术后出血发生率明显。结论:我们的研究支持了目前关于离子™RAB用于周围肺病变活检的安全性和有效性的文献。根据导航成功的定义,根据我们的结果,Ion™RAB与柔性支气管镜检查相当或更好。诊断率与柔性支气管镜相当或更好,但略低于金标准计算机断层扫描引导下的经胸活检(CTTB)周围肺病变。然而,与CTTB相比,Ion™RAB在气胸和大出血方面的并发症发生率较低。需要进一步的研究来直接比较目前的两种机器人系统与第三种系统,Noah Medical的Galaxy system™,正在等待FDA的批准。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Robotic-assisted bronchoscopy for peripheral pulmonary lesions: A single-center experience of the Ion platform
Rationale: The diagnostic yield of electromagnetic navigational bronchoscopy to access lung lesions remains low. The multicenter NAVIGATE study showed the diagnostic yield to be 71% for lesions up to 3 cm and 67% for lesions up to 2 cm. The introduction of robotic-assisted navigational platforms may overcome some of the traditional barriers encountered with previous approaches. We aim to assess the navigational and diagnostic yield of the Ion™ endoluminal system (Intuitive Surgical, Inc., Sunnyvale, California) regarding pulmonary lesions that could not previously be biopsied using conventional white light bronchoscopy. Methods: We retrospectively reviewed and analyzed data from our first 76 consecutive robotic-assisted navigational bronchoscopy (RAB) cases performed by a single proceduralist at our single center between March 11, 2020, to November 25, 2020. Secondary endpoints included the safety of the platform, such as incidences of pneumothoraces and significant bleeding events. Results: The ability to localize the lesion using the shape sensing technology was 100% (n=76). Navigational success, as determined by lesion visualization using radial endobronchial ultrasound confirmation, was 76% (n=58) of the nodules. The additional use of 2D-fluoroscopy for needle-in-lesion guidance and Rapid Onsite Evaluation to assess for adequate tissue sampling resulted in a diagnostic yield of 92% (n=70). There was a 0% complication rate for pneumothorax and significant bleeding events in the postoperative phase. Conclusions: Our study supports the current literature regarding the safety and efficacy of the Ion™ RAB for use in obtaining biopsy of peripheral lung lesions. Depending on the definition of navigational success, based on our results, the Ion™ RAB is comparable to or better than flexible bronchoscopy. The diagnostic yield is comparable to or better than flexible bronchoscopy but slightly lower than the gold standard computed tomography-guided transthoracic biopsy (CTTB) for peripheral lung lesions. However, in contrast to CTTB, the Ion™ RAB has lower complication rates for pneumothoraces and major bleeding. Further studies are needed to directly compare the current two robotic systems with a third system, Galaxy System™ by Noah Medical that is pending FDA approval.
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