Paroxysmal Sympathetic Hyperactivity in Critically Ill Children with Encephalitis and Meningoencephalitis

Raquel Farias-Moeller1, Jessica L Carpenter1, Nathan Dean2

  • 1Department of Neurology, Children's National Medical Center, 111 Michigan Avenue NW, Washington, DC, 20010, USA.

Neurocritical Care
|March 1, 2015
PubMed

Insights

Paroxysmal Sympathetic Hyperactivity (PSH) affects 41% of critically ill children with encephalitis. Non-bacterial causes are linked to higher PSH incidence, with fever, seizures, and female gender as risk factors in this group.

Area of Science:

  • Pediatric critical care
  • Neurocritical care
  • Autonomic dysfunction

Background:

  • Autonomic dysfunction is common but understudied in pediatric acquired brain injury.
  • Paroxysmal Sympathetic Hyperactivity (PSH) is a significant concern in critically ill children.
  • Encephalitis and meningoencephalitis are key conditions associated with autonomic dysfunction.

Purpose of the Study:

  • To determine the incidence of PSH in pediatric patients with meningoencephalitis and encephalitis.
  • To identify risk factors associated with PSH in this population.
  • To evaluate the influence of PSH on patient outcomes.

Main Methods:

  • Retrospective review of a single-institution Neurocritical Care database.
  • Inclusion of pediatric patients diagnosed with meningoencephalitis and/or encephalitis.
  • Definition of PSH based on specific clinical signs (heart rate/blood pressure lability, hyperthermia, diaphoresis, etc.).

Main Results:

  • PSH was identified in 41% of the studied pediatric patients.
  • Higher PSH incidence was observed in non-bacterial encephalitis (51%) compared to bacterial causes (27%).
  • Fever, seizures on presentation, and female gender were associated with increased PSH in the non-bacterial group.

Conclusions:

  • PSH occurs frequently in critically ill children with encephalitis/meningoencephalitis.
  • Risk factors and outcomes for PSH vary significantly between bacterial and non-bacterial etiologies.
  • Further research is needed to understand and manage PSH in pediatric neurocritical care.
Abstract

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