Key result
High Vasoactive-Inotropic Score linked to ~113% higher short-term mortality versus low scores.
Why the study?
The prognostic value of the Vasoactive-Inotropic Score (VIS) in patients admitted to the ICU after noncardiac surgery was unknown.
Does a higher Vasoactive-Inotropic Score (VIS) predict increased 28-day mortality in patients admitted to the ICU following noncardiac surgery?
Observational (n=3,365)
Yes
Does a higher Vasoactive-Inotropic Score (VIS) predict increased 28-day mortality in patients admitted to the ICU following noncardiac surgery?
The Vasoactive-Inotropic Score (VIS) is a robust, independent predictor of 28-day mortality in critically ill patients following noncardiac surgery, offering better short-term prognostic value than SOFA scores or serum lactate.
VIS >45 warrants heightened vigilance after noncardiac surgery; extends independent prognostic superiority over SOFA and lactate.
To explore the value of the Vasoactive-Inotropic Score (VIS) in evaluating the prognosis of patients admitted to the ICU after noncardiac surgical operations. A retrospective analysis was conducted on 3,365 post-noncardiac surgical patients admitted to the Department of Critical Care Medicine, The First Affiliated Hospital of Sun Yat-sen University, from January 2018 to June 2022. The VIS was calculated based on the maximum and average doses of vasoactive and inotropic agents administered within the first 24 h after noncardiac surgery. Patients were divided into five groups according to VIS levels: 0–5, 6–15, 16–30, 31–45, and > 45 points. The primary outcome was 28-day mortality. The mean 24-h maximum VIS of post-noncardiac surgical ICU patients was 1.2, with over half of the patients having a VIS below 5 points. Mortality in patients with higher VIS was significantly higher than in those with lower VIS, with the mortality rates of the five VIS groups being 7.5%, 9.4%, 12.1%, 17.2%, and 33.8%, respectively. Kaplan–Meier survival curves showed that patients with a VIS > 45 had poorer survival rates. The incidence of infection and sepsis increased with higher VIS. Multivariate logistic regression analysis identified a 24-h maximum VIS > 45 was an independent risk factor for 28-day mortality. VIS yielded an AUC of 0.744 for predicting ICU mortality and 0.683 for predicting 28-day mortality. In short-term prognosis assessment, the predictive value of VIS was better than the Sequential Organ Failure Assessment (SOFA) score and serum lactate level. Adult post-noncardiac surgical ICU patients have a high incidence of infection and poor outcomes. A higher VIS robustly predicts adverse postoperative outcomes, with independent prognostic value in this Chinese cohort. Though not supplanting established tools (e.g., Acute Physiology and Chronic Health Evaluation II [APACHE II], SOFA), VIS serves as a complementary indicator, providing additional real-time hemodynamic insights. Larger prospective studies are needed to verify whether VIS-guided interventions improve patient outcomes.
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Jiang et al. (2026) conducted an observational in Critical patients following noncardiac surgery (n=3,365). Vasoactive-Inotropic Score vs. No vasoactive support (VIS < 5) was evaluated on 28-day mortality (OR 2.126, 95% CI 1.536-2.941, p=<0.001). A Vasoactive-Inotropic Score greater than 45 points significantly increased the 28-day mortality rate to 33.8% compared to 7.5% in patients with a score less than 5 points.
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