Characteristics of intracranial pressure (ICP) waves and ICP in children with treatment-responsive hydrocephalus

Terje Sæhle1, Per Kristian Eide

  • 1Department of Neurosurgery, Oslo University Hospital - Rikshospitalet, PB 4950 Nydalen, 0424, Oslo, Norway.

Acta Neurochirurgica
|April 15, 2015
PubMed

Insights

Pediatric hydrocephalus patients who improved after surgery showed higher intracranial pressure (ICP) wave amplitudes and mean ICP. These findings suggest improved intracranial compliance is key to shunt effectiveness in children.

Area of Science:

  • Pediatric Neurosurgery
  • Neurology
  • Medical Engineering

Background:

  • Pediatric hydrocephalus treatment aims to normalize intracranial pressure (ICP) and optimize brain development.
  • Understanding ICP wave characteristics in hydrocephalus offers insights into treatment mechanisms.

Purpose of the Study:

  • To characterize ICP waves in pediatric hydrocephalus patients who improved after surgery.
  • To compare ICP characteristics between surgically treated and non-surgically managed hydrocephalus patients.

Main Methods:

  • Retrospective analysis of ICP monitoring data from 2002-2011 in pediatric hydrocephalus patients.
  • Determination of ICP wave amplitude, rise time, rise time coefficient, and mean ICP.
  • Comparison of ICP parameters between surgically treated and reference (non-surgically managed) groups.

Main Results:

  • 58 patients included; 31 underwent surgery and showed clinical improvement.
  • Surgically treated patients exhibited increased mean ICP and elevated ICP wave amplitudes (MWA) compared to reference patients.
  • ICP alterations were similar in communicating and non-communicating hydrocephalus, with no correlation to symptoms, ventricular size, or age.

Conclusions:

  • Clinically improved pediatric hydrocephalus patients present with elevated MWA and mean ICP.
  • Elevated MWA suggests impaired intracranial compliance, a state reversible by shunting.
  • Improved intracranial compliance is a likely mechanism for shunt efficacy in pediatric hydrocephalus.
Abstract