Severe syncope and sudden death in children with inborn salt-losing hypokalaemic tubulopathies

Nephrol Dial Transplant. 2005 Sep;20(9):1981-3. doi: 10.1093/ndt/gfh893. Epub 2005 Jun 28.

Abstract

Background: Potassium deficiency may cause cardiac arrhythmias culminating in syncope or sudden death.

Methods: An inquiry performed among physicians caring for a total of 249 patients with inborn salt-losing tubulopathies revealed that acute cardiac complications occurred in seven children.

Results: Four patients died suddenly and three had severe syncope. These episodes occurred in the context of severe chronic hypokalaemia (< or =2.5 mmol/l) or were precipitated by acute diseases, which exacerbated hypokalaemia (< or =2.0 mmol/l).

Conclusions: In conclusion, severe chronic or acute hypokalaemia is hazardous in inborn salt-losing tubulopathies.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Child
  • Death, Sudden*
  • Female
  • Humans
  • Infant
  • Kidney Tubular Necrosis, Acute / mortality*
  • Male
  • Metabolism, Inborn Errors / complications*
  • Metabolism, Inborn Errors / mortality
  • Potassium Deficiency / complications*
  • Survival Analysis
  • Syncope / epidemiology*