Key result
An RV-GS/PASP ratio ≥-0.55 independently predicted 28-day mortality in sepsis patients (OR 6.026), and a nomogram incorporating this ratio and RV-FWS yielded excellent prognostic discrimination.
Why the study?
The RV plays a significant role in septic myocardial injury, but early identification of RVSD is needed and research on RVSD in sepsis remains limited.
Does a nomogram model incorporating right ventricular strain and RV-PA coupling predict 28-day mortality in adult sepsis patients?
Cohort (n=141)
No
Does a nomogram model incorporating right ventricular strain and RV-PA coupling predict 28-day mortality in adult sepsis patients?
A nomogram incorporating right ventricular strain and RV-PA coupling parameters alongside clinical variables accurately predicts 28-day mortality in sepsis patients.
RV strain nomogram may refine sepsis risk stratification; leaves open need for prospective validation before clinical adoption.
Background: The right ventricle (RV) plays a significant role in septic myocardial injury and associated organ dysfunction. Hence, identifying right ventricular systolic dysfunction (RVSD) early is crucial for improving outcomes in septic patients, yet current research on RVSD in sepsis remains limited. Objective: The study aims to identify risk factors for adverse outcomes in septic patients and construct a nomogram prediction model incorporating right ventricular strain and right ventricle-pulmonary artery coupling parameters. Methods: This single-center prospective study included 156 sepsis patients admitted from September 2021 to October 2024. General clinical, laboratory, and echocardiographic data were collected within 72 h of sepsis diagnosis. Prognosis was used to divide patients into two groups. Lasso regression was used to examine the baseline features of both groups. Multivariable logistic regression analysis and a nomogram were used to predict sepsis prognosis. The relationship between RVSD and 28-day mortality was examined. Multivariable logistic regression analysis identified age >67 years, SOFA score ≥7.5, procalcitonin ≥5.7 ng/ml, lactate ≥3.5 mmol/L, RV-FWS ≥-19.4%, and RV-GS/PASP ≥-0.55 as independent risk factors for poor sepsis outcomes. The prognostic model using these six risk factors had an area under the curve (AUC) of 0.907 (95% CI: 0.858-0.954). Internal validation showed strong nomogram calibration with a C-index of 0.88. Conclusion: The RV-GS/PASP ratio demonstrated significant prognostic utility for predicting clinical outcomes in sepsis patients. Furthermore, the nomogram model incorporating age, SOFA score, procalcitonin, lactate, and RV-FWS exhibited excellent discriminative ability, with an AUC of 0.907.
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Chen et al. (2025) conducted a cohort in Sepsis (n=141). Right ventricular-pulmonary artery coupling (RV-GS/PASP ratio ≥-0.55) vs. RV-GS/PASP ratio <-0.55 was evaluated on 28-day mortality (OR 6.026, 95% CI 2.023-17.95, p=0.001). An RV-GS/PASP ratio ≥-0.55 independently predicted 28-day mortality in sepsis patients (OR 6.026), and a nomogram incorporating this ratio and RV-FWS yielded excellent prognostic discrimination.
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