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Optical coherence tomography for the diagnosis and monitoring of idiopathic intracranial hypertension

Item Type:Article
Title:Optical coherence tomography for the diagnosis and monitoring of idiopathic intracranial hypertension
Creators Name:Albrecht, P., Blasberg, C., Ringelstein, M., Mueller, A.K., Finis, D., Guthoff, R., Kadas, E.M., Lagreze, W., Aktas, O., Hartung, H.P., Paul, F., Brandt, A.U. and Methner, A.
Abstract:The objectives of the study were to investigate the value of optical coherence tomography in detecting papilledema in patients with idiopathic intracranial hypertension (IIH), a disease which is difficult to monitor and which can lead to permanent visual deficits; to analyze retinal changes over time. In this non-interventional case-control study, spectral-domain optical coherence tomography (SD-OCT) was used to analyze the retinal and optic nerve head (ONH) morphology of 21 patients with IIH and 27 age- and sex-matched healthy controls over time. We analyzed the ONH volume using a custom-made algorithm and employed semi-automated segmentation of macular volume scans to assess the macular retinal nerve fiber layer (RNFL) and ganglion cell layer and inner plexiform layer complex as well as the total macular volume. In IIH patients, the ONH volume was increased and correlated with cerebrospinal fluid (CSF) pressure. The ONH volume decreased after the initiation of treatment with acetazolamide. The macular RNFL volume decreased by 5% in 3.5 months, and a stepwise multivariate regression analysis identified CSF pressure as the main influence on macular RNFL volume at diagnosis. The only factor predicting macular RNFL volume loss over time was ONH volume. SD-OCT can non-invasively monitor changes in retinal and ONH morphology in patients with IIH. Increased ONH volume leads to retinal atrophy in the form of macular RNFL volume loss, presumably due to mechanic jamming of the optic nerve at the disc and subsequent axonal loss.
Keywords:Idiopathic Intracranial Hypertension, Optical Coherence Tomography
Source:Journal of Neurology
ISSN:0340-5354
Publisher:Springer
Volume:264
Number:7
Page Range:1370-1380
Date:July 2017
Official Publication:https://doi.org/10.1007/s00415-017-8532-x
PubMed:View item in PubMed

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