Computed Tomography–guided Percutaneous Lung Biopsy With Electromagnetic Navigation Compared With Conventional Approaches

Author:

Liu Qin1,Guo Xiaoxia1,Wang Ziyin1,Xu Hao12,Huang Wei1,Liu Jingjing1,Wang Zhongmin1,Yan Fuhua3,Wu Zhiyuan1,Ding Xiaoyi1

Affiliation:

1. Interventional Radiology

2. Department of Vascular Surgery and Interventional Radiology, Suzhou DuShu Lake Hospital, Soochow University, Suzhou, China

3. Radiology, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai

Abstract

Purpose: The purpose of this study was to assess the efficiency and safety of computed tomography (CT)-guided percutaneous biopsy of lung lesions with electromagnetic (EM) navigation and compare them with those of conventional approaches. Materials and Methods: Seventy-nine patients with lung or liver lesions who needed biopsies were enrolled in this trial. All patients were randomly assigned to the E group underwent CT-guided percutaneous biopsies with the EM navigation system or to the C group treated with conventional approaches. Results: In total, 27 patients with lung lesions were assigned to the E group, and 20 patients were assigned to the C group. The diagnostic success rate was 92.6% and 95% in both groups, respectively (P>0.9999). The median number of needle repositions in the E group was less than that in the C group (2.0 vs. 2.5, P=0.03). The positioning success rate with 1 or 2 needle repositions for the E group was significantly higher than the C group (81.5% vs. 50%, P=0.03). The median accuracy of the puncture location in the E group was better than that in the C group (2.0 vs. 6.6 mm, P<0.0001). The total procedure time lengthened in the E group compared with the C group (30.5±1.6 vs. 18.3±1.7 min, P<0.0001), but the number of CT acquisitions was not significantly different (P=0.08). There was no significant difference in complication incidence between the 2 groups (P=0.44). Conclusion: The EM navigation system is an effective and safe auxiliary tool for CT-guided percutaneous lung biopsy, but lengthen the procedure time. Trial Registration: ChiCTR2100043361, registered February 9, 2021—retrospectively registered (http://www.medresman.org.cn/uc/project/projectedit.aspx?proj=7591).

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Pulmonary and Respiratory Medicine,Radiology, Nuclear Medicine and imaging

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