Septic cardiomyopathy phenotype in the critically ill may depend on antimicrobial resistance

Background Sepsis is a life-threatening organ dysfunction, and septic cardiomyopathy (SCM) may complicate the course of the disease. Infection with multidrug-resistant (MDR) pathogens has been linked with worse outcomes. This study aims to evaluate SCM in patients with infections caused by different antimicrobial-resistant phenotypes. Method This retrospective study included patients with sepsis/septic shock, hospitalized, and intubated in the intensive care unit of the University Hospital of Larissa between January 2022 and September 2023 with echocardiographic data during the first two days after infection onset. The patients were divided into two groups: a non-MDR-SCM and an MDR-SCM. The cardiac function was compared between the two groups. Result A total of 62 patients were included in the study. Twenty-six patients (41.9%) presented with left ventricular (LV) systolic dysfunction, and ≤35% right ventricular fractional area change (RVFAC) was present in 56.4%. Forty-four patients comprised the MDR-SCM and 18 the non-MDR-SCM group. LV systolic function was more severely impaired in the non-MDR-SCM group (left ventricular ejection fraction, 35.8±4.9% vs. 45.6±2.4%, P=0.049; LV outflow tract velocity time integral, 10.1±1.4 cm vs. 15.3±0.74 cm, P=0.001; LV-Strain, -9.02±0.9% vs. -14.02±0.7%, P=0.001). The MDR-SCM group presented with more severe right ventricular (RV) dilatation (right ventricular end-diastolic area/left ventricular end-diastolic area, 0.81±0.03 vs. 0.7±0.05, P=0.042) and worse RV systolic function (RVFAC, 32.3±1.9% vs. 39.6±2.7%, P=0.035; tricuspid annular plane systolic excursion, 15.9±0.9 mm vs. 18.1±0.9 mm, P=0.165; systolic tissue Doppler velocity measured at the lateral tricuspid annulus, 9.9±0.5 cm/s vs. 13.1±0.8 cm/s, P=0.002; RV-strain, -11.1±0.7% vs. -15.1±0.9%, P=0.002). Conclusion SCM related to MDR infection presents with RV systolic dysfunction predominance, while non-MDR-SCM is mainly depicted with LV systolic dysfunction impairment.