Back to Search Start Over

Spontaneous Ventilation versus Mechanical Ventilation During Video-Assisted Thoracoscopic Surgery for Spontaneous Pneumothorax: A Multicenter Randomized Controlled Trial

Authors :
Wenfei Tan
Jing Ye
Mingfei Ma
Qinglong Dong
Kaiming He
Wenhua Liang
Zhongxin Duan
Haofei Wang
Cui Fei
Hui Liu
Tonghai Huang
Yali Li
Hengrui Liang
Nanshan Zhong
Huankai Zhang
Chengchu Zhu
Wang Wei
Kaican Cai
Xiang Liu
Shun Xu
Jianfei Shen
Haoda Huang
Qiming Shen
Jianxing He
Chao Cheng
Guangsuo Wang
Jinfeng Ding
Hong Ma
Kun Qiao
Tianyang Dai
Xia Feng
Jiang Jin
Zhenguo Liu
Yulin Liu
Yu Jiang
Lixia Liang
Yingfen Li
Siyang Feng
Zhaohua Xia
Shunjun Jiang
Zhifeng Zhang
Jun Liu
Hanyu Yang
Source :
SSRN Electronic Journal.
Publication Year :
2019
Publisher :
Elsevier BV, 2019.

Abstract

Background: Spontaneous ventilation VATS (SV-VATS) is reported to be associated with faster recovery and fewer complications than mechanical ventilation video-assisted thoracic surgery (MV-VATS). This study aimed to evaluate the effect of SV-VATS for patients with spontaneous pneumothorax. Methods: We performed a randomized controlled trial at 10 medical centers by recruiting primary pneumothorax patients undergoing SV-VATS and MV-VATS. Participants were randomly assigned (1:1), to receive non-intubated spontaneous ventilation (SV-VATS) or intubated mechanical one lung ventilation (MV-VATS). The primary outcome was the intraoperative surgery/anesthesia related accident rate, which was assessed according to incedences of intraoperative hypoxia, conversion to open surgery, conversion to intubation and other intraoperative adverse events that could happen in both groups. Other study outcomes included changes of vital signs, total analgesic dose, recovery time, post-operative complication rates, cost-effectiveness evaluation, etc. Findings: The trial began on Apr 10, 2017, and ended on Jan 03, 2019. During this time, 355 patients were assessed. After evaluation and randomization, 325 eligible patients were assigned to receive an SV-VATS (n=162) or MV-VATS (n=163) procedure. In the intention-to-treat analysis, there was no difference between the intraoperative accident rate of the SV-VATS (1.23%) and MV-VATS (1.23%) group (P=0.995). The SV-VATS group was associated with significantly decreased total dosage of both sufentanil (11.37 μg vs 20.92 μg; p

Details

ISSN :
15565068
Database :
OpenAIRE
Journal :
SSRN Electronic Journal
Accession number :
edsair.doi...........7756ae0bb879abb01deafcaf9c37fc17