Association of mechanical power during one-lung ventilation and post-operative pulmonary complications among patients undergoing lobectomy: a protocol for a prospective cohort study

• Published in: Updates in surgery 2023-12, Vol.75 (8), p.2365-2375
• Main Authors: Zhang, Ying-Ying, Zhang, Yu-Mei, Wu, Song-Lin, Wei, Min, Deng, Zhi-Peng, Lei, Xian-Ying, Bai, Yi-Ping, Wang, Xiao-Bin
• Format: Article
• Language: English
• Subjects: ChiCTR; ChiCTR2200062173; Humans; Lung; Lung Neoplasms - surgery; Medicine; Medicine & Public Health; Observational Studies as Topic; One-Lung Ventilation; Original Article; Postoperative Complications - epidemiology; Postoperative Complications - etiology; Prospective Studies; Surgery; Thoracic Surgery, Video-Assisted - adverse effects
• ISSN: 2038-131X; 2038-3312
• DOI: 10.1007/s13304-023-01595-4

The association of intra-operative mechanical power (MP) with post-operative pulmonary complications (PPCs) has been described before, but it is uncertain whether the potential inherent bias can limit the use of this parameter, particularly in the context of one-lung ventilation. This single-center study aims to investigate the effect of MP during one-lung ventilation (OLV), and the risks of PPCs in patients undergoing thoracoscopic lobectomy. This prospective observational study is being conducted in an academic tertiary hospital in mainland China. Participants diagnosed with lung cancer, and aged 50 to 80 years are eligible. Video-assisted thoracoscopic surgery (VATS) lobectomy is performed for all patients. The primary outcome is the occurrence of PPCs over 5 consecutive days after the surgery, or until discharge from the hospital. Secondary outcomes include the composite conditions of PPCs, in-hospital stay, systematic inflammation tested by blood samples, and changes in aeration compartments in the ventilated lung as assessed by CT scans. We aim to evaluate the association of mean MP and the temporal patterns in the trend of MP during OLV with the occurrence of PPCs. A total of 120 patients will be enrolled in this study. The study protocol has received approval from the Ethics Committee of the affiliated hospital of Southwest Medical University, China (Reference number: KY2022162). The findings will be made available to the funder and researchers via scientific conferences and peer-reviewed publications. This controlled trial was approved by the Ethics Committee of Southwest Medical University(ChiCTR2200062173), and registered in the Chinese Clinical Trial Register website ( http://www.chictr.org.cn/edit.aspx?pid=172533&htm=4 , ChiCTR2200062173). A written consent was obtained from each patient.