Insufficient Nutrition and Mortality Risk in Septic Patients Admitted to ICU with a Focus on Immune Dysfunction

Nutrients. 2019 Feb 10;11(2):367. doi: 10.3390/nu11020367.

Abstract

Immune dysfunction is seen both in sepsis patients and in those with malnutrition. This study aimed to determine whether insufficient nutrition and immune dysfunction have a synergistic effect on mortality in critically ill septic patients. We conducted a prospective observational study from adult sepsis patients admitted to intensive care units (ICUs) between August 2013 and June 2016. Baseline characteristics including age, gender, body mass index, NUTRIC, Acute Physiology and Chronic Health Evaluation (APACHE) II and Sequential Organ Failure Assessment (SOFA) scores were recorded. Immune dysfunction, defined by human leukocyte antigen DR (HLA-DR) expression, was tested at days 1, 3, and 7 of ICU admission. The study included 151 patients with sepsis who were admitted to the ICU. The 28-day survivors had higher day 7 caloric intakes (89% vs 73%, p = 0.042) and higher day 1-HLA-DR expression (88.4 vs. 79.1, p = 0.045). The cut-off points of day 7 caloric intake and day 1-HLA-DR determined by operating characteristic curves were 65.1% and 87.2%, respectively. Immune dysfunction was defined as patients with day 1-HLA-DR < 87.2%. Insufficient nutrition had no influence on survival outcomes in patients with immune dysfunction. However, patients with insufficient nutrition had poor prognosis when they were immune competent. Insufficient nutrition and immune dysfunction did not have a synergistic effect on mortality in critically ill septic patients.

Keywords: HLA-DR; ICU; nutrition; sepsis.

Publication types

  • Observational Study

MeSH terms

  • Aged
  • Aged, 80 and over
  • Critical Care
  • Critical Illness
  • Female
  • Hospitalization
  • Humans
  • Immune System Diseases
  • Male
  • Malnutrition
  • Middle Aged
  • Nutritional Status / physiology*
  • Organ Dysfunction Scores
  • Prognosis
  • Prospective Studies
  • ROC Curve
  • Sepsis* / diagnosis
  • Sepsis* / immunology
  • Sepsis* / mortality
  • Sepsis* / physiopathology