TY - JOUR
T1 - Spontaneous versus mechanical ventilation during video-assisted thoracoscopic surgery for spontaneous pneumothorax
T2 - A randomized trial
AU - International Tubeless-Video-Assisted Thoracoscopic Surgery Collaboration
AU - Liu, Jun
AU - Liang, Hengrui
AU - Cui, Fei
AU - Liu, Hui
AU - Zhu, Chengchu
AU - Liang, Wenhua
AU - He, Jianxing
AU - Wang, Wei
AU - Jiang, Shunjun
AU - Dong, Qinglong
AU - Liang, Lixia
AU - Yang, Hanyu
AU - Li, Yingfen
AU - Jin, Jiang
AU - Shen, Jianfei
AU - Dai, Tianyang
AU - He, Kaiming
AU - Cai, Kaican
AU - Feng, Siyang
AU - Wang, Haofei
AU - Zhang, Zhifeng
AU - Huang, Haoda
AU - Cheng, Chao
AU - Liu, Zhenguo
AU - Qiao, Kun
AU - Xia, Zhaohua
AU - Liu, Xiang
AU - Wang, Guangsuo
AU - Huang, Tonghai
AU - Xu, Shun
AU - Shen, Qiming
AU - Tan, Wenfei
AU - Ding, Jinfeng
AU - Liu, Yulin
AU - Ye, Jing
AU - Yu, Jiang
AU - Zhang, Huangkai
AU - Feng, Xia
AU - Ma, Mingfei
AU - Duan, Zhongxin
AU - Li, Yali
AU - Ma, Hong
AU - Ng, Calvin S.H.
AU - González-Rivas, Diego
AU - Pompeo, Eugenio
AU - Daley, Erlin
AU - Flores, Raja M.
AU - Shargall, Yaron
AU - Ismail, Mahmoud
AU - Ang, Keng Leong
N1 - Funding Information:
Supported by the Guangzhou Institute of Respiratory Disease .
Publisher Copyright:
© 2021
PY - 2022/5
Y1 - 2022/5
N2 - Objective: Spontaneous ventilation video-assisted thoracic surgery (SV-VATS) is reported to have superior or equal efficacy on postoperative recovery to mechanical ventilation VATS (MV-VATS). However, perioperative safety of the SV-VATS blebectomy is not entirely demonstrated. Methods: We performed a noninferiority, randomized controlled trial (No. NCT03016858) for primary spontaneous pneumothorax patients aged 16 to 50 years undergoing a SV-VATS and the MV-VATS procedure. The trial was conducted at 10 centers in China from April 2017 to January 2019. The primary outcome was the comparison of intra- and postoperative complications between SV-VATS and MV-VATS procedures. Secondary outcomes included total analgesia dose, change of vital sign during surgery, procedural duration, recovery time, postoperative visual analog pain scores, and hospitalization length. Results: In this study, 335 patients were included. There was no significant difference between the SV-VATS group and the MV-VATS group in the intra- and postoperative complication rates (17.90% vs 22.09%; relative risk, 0.81; 95% confidence interval, 0.52-1.26; P =.346). The SV-VATS group was associated with significantly decreased total dose of intraoperative opioid agents; that is, sufentanil (11.37 μg vs 20.92 μg; P <.001) and remifentanil (269.78 μg vs 404.96 μg; P <.001). The SV-VATS procedure was also associated with shorter extubation time (12.28 minutes vs 17.30 minutes; P <.001), postanesthesia care unit recovery time (25.43 minutes vs 30.67 minutes; P =.02) and food intake time (346.07 minute vs 404.02 minutes; P =.002). Moreover, the SV-VATS procedure deceased the anesthesia cost compared with the MV-VATS ($297.81 vs $399.81; P <.001). Conclusions: SV-VATS was shown to be noninferior to MV-VATS in term of complication rate and in selected patients undergoing blebectomy for primary spontaneous pneumothorax.
AB - Objective: Spontaneous ventilation video-assisted thoracic surgery (SV-VATS) is reported to have superior or equal efficacy on postoperative recovery to mechanical ventilation VATS (MV-VATS). However, perioperative safety of the SV-VATS blebectomy is not entirely demonstrated. Methods: We performed a noninferiority, randomized controlled trial (No. NCT03016858) for primary spontaneous pneumothorax patients aged 16 to 50 years undergoing a SV-VATS and the MV-VATS procedure. The trial was conducted at 10 centers in China from April 2017 to January 2019. The primary outcome was the comparison of intra- and postoperative complications between SV-VATS and MV-VATS procedures. Secondary outcomes included total analgesia dose, change of vital sign during surgery, procedural duration, recovery time, postoperative visual analog pain scores, and hospitalization length. Results: In this study, 335 patients were included. There was no significant difference between the SV-VATS group and the MV-VATS group in the intra- and postoperative complication rates (17.90% vs 22.09%; relative risk, 0.81; 95% confidence interval, 0.52-1.26; P =.346). The SV-VATS group was associated with significantly decreased total dose of intraoperative opioid agents; that is, sufentanil (11.37 μg vs 20.92 μg; P <.001) and remifentanil (269.78 μg vs 404.96 μg; P <.001). The SV-VATS procedure was also associated with shorter extubation time (12.28 minutes vs 17.30 minutes; P <.001), postanesthesia care unit recovery time (25.43 minutes vs 30.67 minutes; P =.02) and food intake time (346.07 minute vs 404.02 minutes; P =.002). Moreover, the SV-VATS procedure deceased the anesthesia cost compared with the MV-VATS ($297.81 vs $399.81; P <.001). Conclusions: SV-VATS was shown to be noninferior to MV-VATS in term of complication rate and in selected patients undergoing blebectomy for primary spontaneous pneumothorax.
KW - mechanical ventilation
KW - opioid anesthesia
KW - randomized controlled clinical trial
KW - spontaneous ventilation
KW - video-assisted thoracoscopic surgery
UR - http://www.scopus.com/inward/record.url?scp=85102005795&partnerID=8YFLogxK
U2 - 10.1016/j.jtcvs.2021.01.093
DO - 10.1016/j.jtcvs.2021.01.093
M3 - Article
C2 - 33785209
AN - SCOPUS:85102005795
VL - 163
SP - 1702-1714.e7
JO - Journal of Thoracic and Cardiovascular Surgery
JF - Journal of Thoracic and Cardiovascular Surgery
SN - 0022-5223
IS - 5
ER -