AI Article Synopsis

  • - The study highlights that septic patients with cirrhosis have a worse prognosis than those without cirrhosis, emphasizing the need for early and accurate prognosis determination to inform treatment choices.
  • - Researchers analyzed data from the MIMIC-IV database, including 1,340 septic cirrhotic patients, and found that a higher albumin-corrected anion gap (ACAG) is significantly associated with increased 28-day mortality.
  • - The findings suggest that ACAG could be a useful indicator for clinicians, offering insights that may help guide treatment decisions in this high-risk patient group.

Article Abstract

The prognosis of septic patients with cirrhosis is worse compared to septic patients without cirrhosis. Early and accurate prognosis determination in patients with cirrhosis and sepsis is pivotal for guiding treatment decisions. The aim of this study was to investigate the association between albumin-corrected anion gap (ACAG) and clinical prognosis of patients with sepsis and cirrhosis. This study extracted data of patients with sepsis and cirrhosis from the Medical Information Mart for Intensive Care (MIMIC-IV) database. A total of 1340 patients (64.6% male) were enrolled. After confounders adjusting, elevated ACAG had a significant association with 28-day mortality (HR1.604; 95% CI 1.258-2.048; P < 0.001). Restricted cubic spline revealed that a linear relationship between ACAG and 28-day mortality (P-nonlinear = 0.089, P-overall = 0.001). According to the ROC curve analysis, the ACAG demonstrated a higher area under the curve (AUC) of 0.703 compared to AG (0.675). Kaplan-Meier analysis revealed higher 28-day mortality in high ACAG group (log-rank test, χ^2 = 175.638, P < 0.001). Furthermore, subgroup analysis showed a significant interaction between ACAG and etiology of cirrhosis (P for interaction = 0.014). Therefore, ACAG could provide clinicians with valuable insights for guiding interventions in this high-risk population.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11401841PMC
http://dx.doi.org/10.1038/s41598-024-72703-6DOI Listing

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