Right ventricular dysfunction is common in patients with early sepsis and serves as an independent risk factor for 30-day death.
Key Findings
Results
The majority of sepsis patients developed some form of ventricular dysfunction, with isolated right ventricular dysfunction being the most common subtype.
Among 196 patients with sepsis, 136 patients (69.4%) developed ventricular dysfunction.
Isolated right ventricular dysfunction occurred in 50 patients (25.5%).
Isolated left ventricular systolic dysfunction occurred in 33 patients (16.8%).
Combined left ventricular systolic dysfunction and right ventricular dysfunction occurred in 25 patients (12.8%).
Combined left ventricular systolic dysfunction, left ventricular diastolic dysfunction, and right ventricular dysfunction occurred in 20 patients (10.2%).
Results
Right ventricular dysfunction occurred in nearly half of all sepsis patients and was associated with worse clinical outcomes.
Right ventricular dysfunction occurred in 96 cases (49.0%) among 196 sepsis patients.
Patients with right ventricular dysfunction had higher 30-day mortality compared to those without: 40.6% (39/96) vs. 21.0% (21/100), P<0.05.
Patients with right ventricular dysfunction had higher incidence of acute renal failure: 63.5% (61/96) vs. 48.0% (48/100).
Patients with right ventricular dysfunction had higher Lac (mmol/L): 7.8±3.4 vs. 4.2±2.3, and higher fluid resuscitation volume (mL): 2032±225 vs. 1123±115.
Results
30-day mortality was highest in patients with isolated right ventricular dysfunction among all ventricular dysfunction subtypes.
30-day mortality was highest in patients with isolated right ventricular dysfunction at 36.0% (18/50).
Patients with biventricular dysfunction had 30-day mortality of 30.4% (14/46).
Patients with isolated left ventricular dysfunction had 30-day mortality of 22.5% (9/40).
Patients without ventricular dysfunction had the lowest 30-day mortality at 13.8% (8/60).
The difference across groups was statistically significant (P<0.05).
Results
Non-survivors had significantly worse echocardiographic parameters compared to survivors, including lower TAPSE, lower right ventricular fractional area change, and lower LVEF.
TAPSE (mm) was lower in non-survivors: 16.0±3.6 vs. 19.3±4.4, P<0.05.
Right ventricular fractional area change was lower in non-survivors: (30.23±8.14)% vs. (33.69±7.81)%, P<0.05.
LVEF was lower in non-survivors: 0.575±0.129 vs. 0.637±0.069, P<0.05.
Right ventricular end-systolic area (cm²) was higher in non-survivors: 15.75±4.45 vs. 14.27±3.39, P<0.05.
Left ventricular E/E' ratio was higher in non-survivors: 9.18±4.43 vs. 7.74±3.12, P<0.05.
Results
Multivariate logistic regression identified right ventricular dysfunction as an independent risk factor for 30-day death in sepsis patients.
Right ventricular dysfunction was independently associated with 30-day mortality: OR=2.34, 95%CI 1.21–3.78, P<0.05.
Left ventricular diastolic dysfunction was also an independent risk factor: OR=2.35, 95%CI 1.09–5.18, P<0.05.
Mechanical ventilation had the highest OR among independent risk factors: OR=92.45, 95%CI 34.67–369.45.
Higher vasoactive drug dose was independently associated with mortality: OR=65.45, 95%CI 19.88–195.83.
Higher Lac was independently associated with mortality: OR=13.44, 95%CI 6.15–25.35; higher APACHE II score: OR=1.35, 95%CI 1.21–1.65; and CRRT: OR=2.43, 95%CI 0.25–0.64.
Results
Non-survivors differed from survivors on multiple clinical parameters beyond echocardiographic measures.
Non-survivors had less urine output, higher proportion receiving CRRT, higher APACHE II scores, higher Lac levels, higher vasoactive drug doses, and higher proportion requiring mechanical ventilation compared to survivors.
The study was a retrospective cohort of 196 adult sepsis patients admitted to critical care medicine from January 2020 to December 2023.
Of 196 patients, 157 survived to 30 days and 39 died.
Xiong F, Yang H, Yan J, Wang C, Bai L, Du Q. (2026). [Association between right ventricular function and short-term death risk in patients with sepsis].. Zhonghua wei zhong bing ji jiu yi xue. https://doi.org/10.3760/cma.j.cn121430-20240426-00217