Multiple organ dysfunction syndrome in critical surgical illness. Review uri icon

Overview

abstract

  • BACKGROUND: Multiple organ dysfunction syndrome (MODS) is the leading cause of death in surgical patients and in trauma patients who survive the first 24 h. First observed systematically among Vietnam War-era battle casualties who began to survive previously fatal injuries owing to improved evacuation, triage, and resuscitation, only to develop catastrophic manifestations of organ failure never before seen, the syndrome was recognized formally in 1975 as "multiple organ failure." Ensuing observations and investigations, undertaken in large part by surgeon-scientists, have refined our current understanding of MODS, yielding better outcomes. METHODS: Review and synthesis of pertinent literature with personal observations and recollections of the senior investigator. RESULTS: The MODS is now recognized as a continuum of physiologic derangements, rather than an all-or-nothing phenomenon. The most common precipitant appears to be ischemia-reperfusion injury, although severe sepsis also is commonplace. Descriptive biology has enhanced the understanding of the pathogenesis and outcomes of MODS, although the therapy is largely supportive, making prevention of paramount importance. Measures such as drotrecogin alfa (activated), intensive insulin therapy, corticosteroids, and low tidal volume ventilation may be effective. CONCLUSIONS: Although current treatment of MODS remains primarily supportive, the mortality rate appears to be decreasing. Appreciation of the interrelations between the inflammatory and coagulation systems provides hope in the battle against this frequent, elusive, deadly, and costly syndrome.

publication date

  • October 1, 2009

Research

keywords

  • Critical Illness
  • Multiple Organ Failure
  • Postoperative Complications

Identity

Scopus Document Identifier

  • 72449191275

Digital Object Identifier (DOI)

  • 10.1089/sur.2009.9935

PubMed ID

  • 19943773

Additional Document Info

volume

  • 10

issue

  • 5