The changing pattern of acute kidney injury: from one to multiple organ failure

Contrib Nephrol. 2010:165:153-158. doi: 10.1159/000313754. Epub 2010 Apr 20.

Abstract

Acute kidney injury (AKI) is frequently encountered in the intensive care unit, and from its inception, morbidity and mortality increase in these patients compared to those without AKI. Despite numerous clinical trials and newer pharmacological agents, very little progress has been made to reduce the deaths that occur in this population. An important emerging concept is that AKI does not occur in isolation and it frequently involves other organs. Clinical conditions such as shock, trauma, and sepsis lead to an increase in fluid volume, cytokines/chemokines, uremic toxins and other soluble mediators that are known to affect distant organs. This critical loss of balance of these mediators appears to be due both to a reduction in clearance and increase in production as demonstrated by experimental studies of bilateral nephrectomy and ischemia-reperfusion, respectively. The evidence and mechanisms for distant organ injury following AKI will be discussed.

MeSH terms

  • Acute Kidney Injury / complications
  • Acute Kidney Injury / mortality
  • Acute Kidney Injury / physiopathology*
  • Animals
  • Central Nervous System Diseases / etiology
  • Central Nervous System Diseases / physiopathology
  • Heart Diseases / etiology
  • Heart Diseases / physiopathology
  • Humans
  • Inflammation / complications
  • Inflammation / etiology
  • Inflammation / physiopathology
  • Intercellular Adhesion Molecule-1 / genetics
  • Interleukin-1 / genetics
  • Kidney / injuries*
  • Lung Diseases / etiology
  • Lung Diseases / physiopathology
  • Mice
  • Multiple Organ Failure / etiology
  • Multiple Organ Failure / physiopathology*
  • Nephrectomy
  • RNA, Messenger / genetics
  • Reperfusion Injury / physiopathology
  • Sepsis / etiology
  • Tumor Necrosis Factor-alpha / genetics

Substances

  • Interleukin-1
  • RNA, Messenger
  • Tumor Necrosis Factor-alpha
  • Intercellular Adhesion Molecule-1