Current Directions in Biomedical Engineering (Sep 2016)

Determination of regional lung function in cystic fibrosis using electrical impedance tomography

  • Krueger-Ziolek Sabine,
  • Schullcke Benjamin,
  • Zhao Zhanqi,
  • Gong Bo,
  • Moeller Knut

DOI
https://doi.org/10.1515/cdbme-2016-0139
Journal volume & issue
Vol. 2, no. 1
pp. 633 – 636

Abstract

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Electrical impedance tomography (EIT) can be used to monitor regional lung ventilation. Due to its relatively high temporal resolution, EIT has already been applied during lung function tests in spontaneously breathing subjects with obstructive lung diseases like chronic obstructive pulmonary disease (COPD) or cystic fibrosis (CF). In our study, ratios of the maximal volume exhaled in 1 s during forced expiration and forced vital capacity (FEV1/FVC) were calculated in predefined lung regions for five CF patients and five lung healthy subjects. The degree of FEV1/FVC homogeneity was assessed by using a slightly modified version of the global inhomogeneity index (GIFEV1/FVC). CF patients showed a higher degree of inhomogeneity in pixel FEV1/FVC than lung healthy subjects. Since EIT is able to deliver regional information to assess airway obstruction in CF patients, it might represent a promising supplement to existing methods like spirometry providing global lung parameters.

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