Assessment of a randomized controlled trial on the safety of pre-placing bronchial balloons in transbronchial lung cryobiopsy for diagnosing interstitial lung disease

被引:1
|
作者
Bian, Yiding [1 ,2 ,3 ]
Zhou, Guowu [1 ,2 ]
Gao, Qian [1 ,2 ]
Deng, Mingming [1 ,2 ]
Tong, Run [1 ,2 ]
Xia, Yang [4 ]
Lin, Jieru [5 ]
Hou, Gang [1 ,2 ]
Dai, Huaping [1 ,2 ]
机构
[1] Inst Resp Med, Chinese Acad Med Sci, Natl Ctr Resp Med, Natl Clin Res Ctr Resp Dis,State Key Lab Resp Hlth, Beijing, Peoples R China
[2] China Japan Friendship Hosp, Ctr Resp Med, Dept Pulm & Crit Care Med, 2 Yinghuayuan East St, Beijing 100029, Peoples R China
[3] Chinese Acad Med Sci, Peking Union Med Coll, Beijing 100730, Peoples R China
[4] Zhejiang Univ, Affiliated Hosp 2, Sch Med, Dept Resp & Crit Care Med,Key Lab Resp Dis Zhejian, Hangzhou 310052, Zhejiang, Peoples R China
[5] Guizhou Prov Peoples Hosp, Dept Resp & Crit Care Med, Guiyang 550002, Peoples R China
关键词
Transbronchial lung cryobiopsy; Pre-placed bronchial balloon; Interstitial lung disease; IDIOPATHIC PULMONARY-FIBROSIS; BIOPSY; STATEMENT; SOCIETY; UPDATE; YIELD;
D O I
10.1186/s40001-024-01871-y
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Rationale and objectives Bleeding is a major complication of transbronchial lung cryobiopsy (TBLC), and pre-placing a bronchial balloon is one of the clinical practices used to prevent it, but with very weak evidence, which should be confirmed. This study aimed to conduct whether pre-placing a bronchial balloon in TBLC for diagnosing interstitial lung disease (ILD) is more safety. Materials and methods In this prospective, single-center, randomized controlled trial, patients with suspected ILD were enrolled and randomly assigned to pre-placed balloon and none-pre-placed balloon groups. The primary outcome was incidence of moderate bleeding in each group. The secondary endpoints were the incidence of severe bleeding, pneumothorax, and other procedural complications. Results Exactly 250 patients were enrolled between August 2019 and March 2022, with 125 in each group. There were no significant differences in severe bleeding between the none-pre-placed balloon group and pre-placed balloon group (1.6% vs. 0.8%; adjusted p = 0.520), while more moderate bleeding occurred in the none-pre-placed balloon group (26.4% vs. 6.4%, adjusted p = 0.001), as well as more use of hemostatic drug (28.0% vs. 6.4%, adjusted p = 0.001). Three patients in the none-pre-placed balloon group used the bronchial balloon. More samples could be acquired in the pre-placed balloon group than in the none-pre-placed balloon group (3.8 +/- 0.9 vs. 3.1 +/- 0.9, p < 0.001). There were no significant differences in multidisciplinary discussion (MDD) between the two groups (89.6% vs. 91.2%, adjusted p = 0.182). Conclusion A pre-placed bronchial balloon can reduce the incidence of moderate bleeding and increase the confidence of the bronchoscopists. However, it had no effect on increasing the diagnostic rate of MDD and reducing severe bleeding. Registration number: NCT04047667 (www.clinicaltrials.gov identifier).
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