98%
921
2 minutes
20
Background & Aims: Terlipressin improves renal function in ∼40% of patients with hepatorenal syndrome-acute kidney injury (HRS-AKI). Nonetheless, the pathophysiological mechanisms of terlipressin remain unclear. Therefore, we investigated the cardiovascular changes that occur after terlipressin is given to patients with HRS-AKI.
Methods: Cardiac and phase-contrast magnetic resonance imaging were used to assess cardiac function, as well as renal, splanchnic, and peripheral blood flow changes after the first bolus of 2 mg terlipressin in 10 patients with HRS-AKI, six of whom also had acute-on-chronic liver failure. Hemodynamic changes were analyzed using the Wilcoxon matched-pairs signed-rank test. Patients were followed prospectively to investigate any associations between terlipressin-induced hemodynamic changes and clinical outcomes.
Results: Cardiac output (CO) decreased by 15% following terlipressin ( <0.01). Despite this decrease in CO, renal artery blood flow increased by 23% ( <0.01), and the renal artery blood flow percentage of CO increased by 49% ( = 0.01). Superior mesenteric artery blood flow and femoral artery blood flow decreased by 27% and 40%, respectively (both <0.01). Mean arterial pressure (MAP) and systemic vascular resistance increased by 13% and 32%, respectively (both <0.01). Baseline renal artery blood flow correlated with serum creatinine ( <0.01). By contrast, changes in renal artery blood flow and other cardiocirculatory variables did not correlate with changes in serum creatinine after terlipressin or with mortality.
Conclusions: Terlipressin increases renal artery blood flow, reduces CO, and alleviates splanchnic and peripheral vasodilatation. These effects, combined with an increase in MAP, appear to explain the therapeutic benefits of terlipressin in patients with HRS-AKI.
Impact And Implications: This study is the first to provide a detailed mapping of the hemodynamic changes following terlipressin treatment in patients critically ill with HRS-AKI. The results indicate that the beneficial effects of terlipressin are driven by selective peripheral and splanchnic vasoconstriction, which redistributes blood flow, normalizes MAP, and ultimately improves renal perfusion despite reduced cardiac output. This study also highlights the advantages of using magnetic resonance imaging as a non-invasive method to evaluate pharmacological interventions, with the potential to contribute to future advances in personalized medicine for patients with cirrhosis.
Clinical Trials Registration: NCT03483272.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12270624 | PMC |
http://dx.doi.org/10.1016/j.jhepr.2025.101452 | DOI Listing |
Clinicoecon Outcomes Res
August 2025
Mallinckrodt Pharmaceuticals, Bridgewater, NJ, USA.
Introduction: Terlipressin is the only Food and Drug Administration-approved medication for adults with hepatorenal syndrome-acute kidney injury (HRS-AKI) with rapid reduction in kidney function. Treatment with terlipressin, particularly in patients with lower serum creatinine (SCr) at diagnosis, improves outcomes. Despite evidence suggesting that treating HRS-AKI at lower SCr thresholds may improve clinical outcomes, the impact on healthcare resource utilization (HCRU) and medical costs of an earlier intervention strategy remains unquantified.
View Article and Find Full Text PDFGastroenterol Hepatol (N Y)
August 2025
Division of Gastroenterology and Hepatology, Department of Medicine, University of Toronto, Toronto, Ontario, Canada.
The use of terlipressin in the treatment of hepatorenal syndrome type 1 (HRS-1) in patients with advanced cirrhosis wait-listed for liver transplant (LT) has been controversial. Successful treatment lowers patients' Model for End-Stage Liver Disease (MELD) score and hence their LT priority. Terlipressin's potential ischemic side effects and risks for respiratory failure in susceptible patients lend support to directly proceed to LT.
View Article and Find Full Text PDFCureus
July 2025
Internal Medicine, Mayo Hospital, Lahore, PAK.
This systematic review evaluates and compares the clinical effectiveness of terlipressin and octreotide in the management of acute gastroesophageal variceal bleeding among cirrhotic patients. A comprehensive literature search was conducted across PubMed, Google Scholar, and clinical trial registries, identifying five randomized controlled trials that met predefined inclusion criteria. These studies assessed key outcomes, including bleeding control, mortality, hepatic venous pressure gradient (HVPG) reduction, hemodynamic stability, and safety profiles.
View Article and Find Full Text PDFCureus
June 2025
Internal Medicine, California Institute of Behavioral Neurosciences & Psychology, Fairfield, USA.
High pressure in the portal circulation is a key indicator of advanced liver disease. It has many harmful effects on patients with cirrhosis, such as promoting the growth of dilated esophageal vessels. As portal pressure rises, it creates serious risks for life-threatening bleeding problems from variceal sources, which leads to higher mortality and worse patient outcomes.
View Article and Find Full Text PDFAliment Pharmacol Ther
July 2025
Department of Medicine, University of Toronto, Toronto, Ontario, Canada.
Background: Terlipressin is the FDA-approved systemic vasoconstrictor therapy for hepatorenal syndrome-acute kidney injury (HRS-AKI)-a rapidly progressive renal failure occurring in patients with decompensated cirrhosis and ascites. Bradycardia, a known effect of terlipressin, as well as other arrhythmias, has previously been reported in terlipressin-treated patients.
Aim: To assess terlipressin-related cardiac adverse events (AEs) in patients with HRS-AKI.