Observational study to determine the optimal timing for surgery following SARS-CoV-2 infection and assess key global surgery indicators.
* Prospective, observational international cohort study. * Any hospital worldwide can participate (including hospitals that have not admitted SARS-CoV-2 infected patients). * All patients undergoing a surgical procedure in an operating theatre will be included. All consecutive eligible patients should be included. * 7-day data collection period, with follow-up at 30 days after surgery for each patient. However, no changes should be made to normal patient care/ follow-up pathways * Primary outcome is 30-day mortality. * All collaborators will be included as PubMed-citable co-authors on resulting publications.
Study Type
OBSERVATIONAL
Enrollment
1,000
Post-operative mortality
Mortality at 30 days after surgery
Time frame: 30 days after surgery
In-patient mortality
Mortality while the patient is admitted to hospital
Time frame: 30 days after surgery
Post-operative pulmonary complications
30-day postoperative pulmonary complications (pneumonia \[CDC definition\], ARDS, unexpected ventilation)
Time frame: 30 days after surgery
Post-operative venous thromboembolism
30-day venous thromboembolism (deep vein thrombosis/ pulmonary embolism)
Time frame: 30 days after surgery
Post-operative complications
30-day Clavien-Dindo grade
Time frame: 30 days after surgery
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.