Abstract
The global spread of coronavirus disease 2019 (COVID-19) has had a profound public health impact, particularly on perioperative management, rendering the optimization of timing for post-infection thoracic oncologic surgery a pressing clinical concern. This multicenter retrospective cohort study included adult patients who underwent elective video-assisted thoracic oncologic surgery in February 2023 with confirmed COVID-19 infection ≥ 4 weeks prior. A matched historical control cohort from February 2019 was used for comparison. Propensity score matching (PSM) and inverse probability of treatment weighting (IPTW) were applied to adjust for confounders. Subgroup analyses were conducted based on clinical variables, and logistic regression was used to assess the association between infection-to-surgery interval and PPCs. A total of 846 patients were included. After PSM and IPTW, the incidence of PPCs remained comparable between the COVID-19 and no-COVID-19 groups (PSM: 26.1% vs. 31.8%, p = 0.784; IPTW: 28.0% vs. 29.7%, p = 0.615). No significant differences in PPC rates were observed across infection-to-surgery intervals (4–6, 6–8, and 8–12 weeks; p = 0.953). Prior COVID-19 infection was associated with higher postoperative WBC counts and lower lymphocyte levels, but not with increased PPCs risk. Smoking history was an independent predictor of PPCs (OR: 2.503, p = 0.005), while infection timing was not. Thoracic oncologic surgery may be considered ≥ 4 weeks after COVID-19 recovery in carefully selected patients. Further prospective studies are needed to assess safety in earlier postoperative intervals and among patients recovering from severe infection.
Data availability
Data are available from the corresponding author upon reasonable request.
References
WHO. WHO (2024) Number of COVID-19 Cases Reported to WHO (Cumulative Total), https://data.who.int/dashboards/covid19/cases?n=c (2024).
Lei, S. et al. Clinical characteristics and outcomes of patients undergoing surgeries during the incubation period of COVID-19 infection. EClinicalMedicine 21, 100331. https://doi.org/10.1016/j.eclinm.2020.100331 (2020).
O’Glasser, A. Y. & Schenning, K. J. COVID-19 in the perioperative setting: A review of the literature and the clinical landscape. Perioper Care Oper. Room Manag. 28, 100272. https://doi.org/10.1016/j.pcorm.2022.100272 (2022).
Mortality Pulmonary complications in patients undergoing surgery with perioperative SARS-CoV-2 infection: an international cohort study. Lancet (London England). 396, 27–38. https://doi.org/10.1016/s0140-6736(20)31182-x (2020).
Fernandez-Bustamante, A. et al. Postoperative pulmonary Complications, early Mortality, and hospital stay following noncardiothoracic surgery: A multicenter study by the perioperative research network investigators. JAMA Surg. 152, 157–166. https://doi.org/10.1001/jamasurg.2016.4065 (2017).
Leonardi, B. et al. Outcomes of thoracoscopic lobectomy after recent COVID-19 infection. Pathogens 12 https://doi.org/10.3390/pathogens12020257 (2023).
Foundation, A. S. o. A. a. A. P. S. ASA and APSF Joint Statement on Elective Surgery Procedures and Anesthesia for Patients After COVID-19 Infection, https://www.asahq.org/about-asa/newsroom/news-releases/2023/06/asa-and-apsf-joint-statement-on-elective-surgery-procedures-and-anesthesia-for-patients-after-covid-19-infection (2023).
Leeds, I. L. et al. Postoperative outcomes associated with the timing of surgery after SARS-CoV-2 infection. Ann. Surg. 280, 241–247. https://doi.org/10.1097/sla.0000000000006227 (2024).
Verhagen, N. B. et al. Severity of prior coronavirus disease 2019 is associated with postoperative outcomes after major inpatient surgery. Ann. Surg. 278, e949–e956. https://doi.org/10.1097/sla.0000000000006035 (2023).
Li, X. F. et al. Comparative effect of Propofol and volatile anesthetics on postoperative pulmonary complications after lung resection surgery: A randomized clinical trial. Anesth. Analg. 133, 949–957. https://doi.org/10.1213/ANE.0000000000005334 (2021).
Zhang, Y. et al. Unveiling the protective role of Sevoflurane in video-assisted thoracoscopic surgery associated-acute lung injury: Inhibition of ferroptosis. Pulm. Pharmacol. Ther. 86, 102312. https://doi.org/10.1016/j.pupt.2024.102312 (2024).
Shewale, J. B. et al. Time trends of perioperative outcomes in early stage Non-Small cell lung cancer resection patients. Ann. Thorac. Surg. 109, 404–411. https://doi.org/10.1016/j.athoracsur.2019.08.018 (2020).
Bang, H. T. et al. Effectiveness of the enhanced recovery after surgery (ERAS) program after lobectomy for lung cancer: a single-center observational study using propensity score matching in Vietnam. J. Thorac. Dis. 16, 7686–7696. https://doi.org/10.21037/jtd-24-1053 (2024).
El-Boghdadly, K. et al. SARS-CoV-2 infection, COVID-19 and timing of elective surgery. Anaesthesia 76, 940–946. https://doi.org/10.1111/anae.15464 (2021).
Quinn, K. L. et al. Complications following elective major noncardiac surgery among patients with prior SARS-CoV-2 infection. JAMA Netw. Open. 5, e2247341. https://doi.org/10.1001/jamanetworkopen.2022.47341 (2022).
Canet, J. et al. Prediction of postoperative pulmonary complications in a population-based surgical cohort. Anesthesiology 113, 1338–1350. https://doi.org/10.1097/ALN.0b013e3181fc6e0a (2010).
Bryant, J. M. et al. Association of Time to Surgery After COVID-19 Infection With Risk of Postoperative Cardiovascular Morbidity. JAMA Netw. open. 5, e2246922 https://doi.org/10.1001/jamanetworkopen.2022.46922 (2022).
Aziz, M. F. et al. Perioperative mortality of the COVID-19 recovered patient compared to a matched control: A multicenter retrospective cohort study. Anesthesiology 140, 195–206. https://doi.org/10.1097/aln.0000000000004809 (2024).
You, J., Chen, D., Liu, X., Zhang, H. & Zheng, Z. Postoperative pneumonia in patients with non-small cell lung cancer undergoing thoracoscopic surgery: what should we care about? Front. Oncol. 15, 1564042. https://doi.org/10.3389/fonc.2025.1564042 (2025).
He, X. et al. Prediction models for postoperative pulmonary complications in intensive care unit patients after noncardiac thoracic surgery. BMC Pulm Med. 24, 420. https://doi.org/10.1186/s12890-024-03153-z (2024).
Huang, C. et al. Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China. Lancet (London England). 395, 497–506. https://doi.org/10.1016/s0140-6736(20)30183-5 (2020).
Guan, W. J. et al. Clinical characteristics of coronavirus disease 2019 in China. N. Engl. J. Med. 382, 1708–1720. https://doi.org/10.1056/NEJMoa2002032 (2020).
Cheng, L. L. et al. Effect of Recombinant human granulocyte Colony-Stimulating factor for patients with coronavirus disease 2019 (COVID-19) and lymphopenia: A randomized clinical trial. JAMA Intern. Med. 181, 71–78. https://doi.org/10.1001/jamainternmed.2020.5503 (2021).
Miskovic, A. & Lumb, A. B. Postoperative pulmonary complications. Br. J. Anaesth. 118, 317–334. https://doi.org/10.1093/bja/aex002 (2017).
Myers, K., Hajek, P., Hinds, C. & McRobbie, H. Stopping smoking shortly before surgery and postoperative complications: a systematic review and meta-analysis. Arch. Intern. Med. 171, 983–989. https://doi.org/10.1001/archinternmed.2011.97 (2011).
Acknowledgements
Thank Professor Jin Liu of the First Affiliated Hospital with Nanjing Medical University for the guidance of statistics in this study.
Funding
No external funding was procured for this clinical trial.
Author information
Authors and Affiliations
Contributions
Y.Z. and Y.L. performed the formal analysis and investigation, and drafted the original manuscript. H.X. contributed to the formal analysis, investigation, methodology, and visualization. L.Y. and Y.W. were responsible for data curation and visualization. X.Z., H.L., and B.G. contributed to study conceptualization and supervision, and critically reviewed the manuscript. B.G. also acquired the funding. All authors reviewed and approved the final manuscript.
Corresponding authors
Ethics declarations
Ethics approval and consent to participate
Ethical approval for this multicenter study was obtained from the Institutional Review Boards of all three participating hospitals, and the requirement for informed consent was waived.
Competing interests
The authors declare no competing interests.
Additional information
Publisher’s note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary Information
Below is the link to the electronic supplementary material.
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc-nd/4.0/.
About this article
Cite this article
Zhang, Y., Liu, Y., Xu, H. et al. Elective thoracic oncologic resections in selected patients appear safe beyond four weeks after COVID-19 infection. Sci Rep (2026). https://doi.org/10.1038/s41598-026-39978-3
Received:
Accepted:
Published:
DOI: https://doi.org/10.1038/s41598-026-39978-3