Persistent Inflammation, Immunosuppression and Catabolism Syndrome

Crit Care Clin. 2017 Apr;33(2):245-258. doi: 10.1016/j.ccc.2016.12.001.

Abstract

Following advances in critical care, in-hospital multiple organ failure-related mortality is declining. Consequently, incidence of chronic critical illness is increasing. These patients linger in the intensive care unit, have high resource utilization, and poor long-term outcomes. Within this population, the authors propose that a substantial subset of patients have a new phenotype: persistent inflammation, immunosuppression, and catabolism syndrome. There is evidence that myelodysplasia with expansion of myeloid-derived suppressor cells, innate and adaptive immune suppression, and protein catabolism with malnutrition are major contributors. Optimal care of these patients will require novel multimodality interventions.

Keywords: Cachexia; Chronic critical illness; Multiple organ failure; Myeloid-derived suppressor cells; PICS; Sepsis; Shock; Trauma.

Publication types

  • Review

MeSH terms

  • Critical Illness* / therapy
  • Humans
  • Immune Tolerance* / physiology
  • Inflammation / complications*
  • Inflammation / physiopathology
  • Metabolism* / physiology
  • Multiple Organ Failure / therapy
  • Syndrome