Potential of acetaminophen on the sublingual microcirculation and peripheral tissue perfusion of febrile septic patients: prospective observational study

• Published in: Annals of intensive care Vol. 14; no. 1; pp. 23 - 11
• Main Authors: Domizi, R., Damiani, E., Carsetti, A., Graciotti, L., Procopio, A. D., Scorcella, C., Casarotta, E., Giaccaglia, P., Donati, A., Adrario, E.
• Format: Journal Article
• Language: English
• Published: Cham Springer International Publishing 10.02.2024; Springer Nature B.V; SpringerOpen
• Subjects: Acetaminophen; Analgesics; Anesthesiology; Critical Care Medicine; Emergency Medicine; Fever; Hemodynamic; Intensive; Intensive care; Medicine; Medicine & Public Health; Microcirculation; Observational studies; Oxygen saturation; Sepsis; Septic shock; Tissue perfusion; Microcirculation; Sepsis; Septic shock; Tissue perfusion; Acetaminophen; Hemodynamic
• ISSN: 2110-5820; 2110-5820
• DOI: 10.1186/s13613-024-01251-z

Background Acetaminophen (ACT) has been studied in septic patients with detectable plasmatic levels of cell-free hemoglobin (Hb), where it demonstrated to inhibit the hemoprotein-mediated lipid peroxidation and oxidative injury, with a potential of beneficial effect on the endothelium. On the basis of this background, the aim of this study was to evaluate the sublingual microcirculation and the peripheral tissue perfusion before-and-after administration of ACT on clinical judgment in a cohort of febrile septic and septic shock patients. Methods Prospective observational study. 50 adult septic and septic shocks treated with ACT for pyrexia, where the sublingual microcirculation and the peripheral tissue perfusion with Near Infrared Spectroscopy (NIRS) and vascular occlusion test (VOT) were evaluated before ACT (t0), after 30 min (t1) and after 2 h (t2). Cell-free Hb and the markers of oxidative stress and endothelial damage were measured at t0 and t2. Results The study showed a significant increase of the density of the perfused small and total vessels of the sublingual microcirculation 30 min after the infusion of ACT; it also showed an increase of the Microvascular Flow Index (MFI) and a decrease in the heterogeneity of the flow. At a peripheral muscular level, we found an acceleration in the reperfusion curve after VOT at t1, expression of a higher reactivity of the microvasculature. Conclusions ACT infusion did not show a clear correlation with cell-free Hb; however, it exhibited protective effect toward the microcirculation that was evident in particular in septic patients. This correlation merits further exploration.