AI Article Synopsis

  • Acute hyperammonemia can lead to serious neurological issues, including coma and death, with key risk factors being the duration of coma and peak ammonia levels.
  • In children, causes primarily include severe liver failure and genetic metabolic disorders, and measuring ammonia levels can be tricky due to preanalytical issues.
  • Treatment involves addressing the underlying causes, reducing protein intake, using medications for ammonia removal, and in severe cases, employing methods like extracorporeal therapies or transcranial Doppler ultrasound for monitoring.

Article Abstract

Acute hyperammonemia may induce a neurologic impairment leading to an acute life-threatening condition. Coma duration, ammonia peak level, and hyperammonemia duration are the main risk factors of hyperammonemia-related neurologic deficits and death. In children, hyperammonemia is mainly caused by severe liver failure and inborn errors of metabolism. In an acute setting, obtaining reliable plasma ammonia levels can be challenging because of the preanalytical difficulties that need to be addressed carefully. The management of hyperammonemia includes 1) identification of precipitating factors and cerebral edema presence, 2) a decrease in ammonia production by reducing protein intake and reversing catabolism, and 3) ammonia removal with pharmacologic treatment and, in the most severe cases, with extracorporeal therapies. In case of severe coma, transcranial Doppler ultrasound could be the method of choice to noninvasively monitor cerebral blood flow and titrate therapies.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6140721PMC
http://dx.doi.org/10.2147/HMER.S140711DOI Listing

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