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   <subfield code="a">10.1007/s00701-015-2503-8</subfield>
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   <subfield code="a">Feasibility of radiological markers in idiopathic normal pressure hydrocephalus</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Maria Kojoukhova, Anne Koivisto, Riika Korhonen, Anne Remes, Ritva Vanninen, Hilkka Soininen, Juha Jääskeläinen, Anna Sutela, Ville Leinonen]</subfield>
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   <subfield code="a">Background: Various radiological markers have been proposed for diagnostics in idiopathic normal pressure hydrocephalus (iNPH). We examined the usefulness of radiological markers in the diagnostics and prediction of shunt response in iNPH. Method: In this retrospective cohort study, we evaluated brain CT or MRI scans of 390 patients with suspected iNPH. Based on a 24-h intraventricular pressure monitoring session, patients were classified into a non-NPH (n = 161) or probable iNPH (n = 229) group. Volumes of cerebrospinal fluid compartments (lateral ventricles, sylvian and suprasylvian subarachnoid spaces and basal cisterns) were visually assessed. Disproportionally enlarged subarachnoid spaces, flow void, white matter changes, medial temporal lobe atrophy and focally dilated sulci were evaluated. Moreover, we measured quantitative markers: Evans' index (EI), the modified cella media index, mean width of the temporal horns and callosal angle. Results: iNPH was more likely in patients with severe volumetric disproportion between the suprasylvian and sylvian subarachnoid spaces than in those without disproportion (OR 7.5, CI 95% 4.0-14.1, P &lt; 0.0001). Mild disproportion (OR 2.6, CI 95% 1.4-4.6, P = 0.001) and narrow temporal horns (OR per 1mm 0.91, CI 95% 0.84-0.98, P = 0.014) were also associated with an iNPH diagnosis. Other radiological markers had little association with the iNPH diagnosis in the final combined multivariate model. Interestingly, EI was higher in non-NPH than iNPH patients (0.40 vs. 0.38, P = 0.039). Preoperative radiological markers were not associated with shunt response. Conclusions: Visually evaluated disproportion was the most useful radiological marker in iNPH diagnostics. Narrower temporal horns also supported an iNPH diagnosis, possibly since atrophy was more pronounced in the non-NPH than iNPH group.</subfield>
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   <subfield code="a">Springer-Verlag Wien, 2015</subfield>
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   <subfield code="a">Idiopathic normal pressure hydrocephalus</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Radiology</subfield>
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   <subfield code="a">Marker</subfield>
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   <subfield code="a">Diagnosis</subfield>
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   <subfield code="a">Shunt response</subfield>
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   <subfield code="a">Disproportion</subfield>
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   <subfield code="a">AD : Alzheimer's disease</subfield>
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   <subfield code="a">CA : Callosal angle</subfield>
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   <subfield code="a">CSF : Cerebrospinal fluid</subfield>
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   <subfield code="a">CT : Computed tomography</subfield>
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   <subfield code="a">EI : Evans' index</subfield>
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   <subfield code="a">FDS : Focally dilated sulci</subfield>
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   <subfield code="a">iNPH : Idiopathic normal pressure hydrocephalus</subfield>
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   <subfield code="a">MRI : Magnetic resonance imaging</subfield>
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   <subfield code="a">mCMI : Modified cella media index</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">NPH : Normal pressure hydrocephalus</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">SA : Subarachnoid</subfield>
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   <subfield code="a">sNPH : Secondary normal pressure hydrocephalus</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">VD : Vascular dementia</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Kojoukhova</subfield>
   <subfield code="D">Maria</subfield>
   <subfield code="u">Neurosurgery of NeuroCenter, Kuopio University Hospital and University of Eastern Finland, P.O. Box 100, FIN-70029, Kuopio, Finland</subfield>
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   <subfield code="a">Koivisto</subfield>
   <subfield code="D">Anne</subfield>
   <subfield code="u">Unit of Neurology, Institute of Clinical Medicine, University of Eastern Finland, Kuopio, Finland</subfield>
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   <subfield code="a">Korhonen</subfield>
   <subfield code="D">Riika</subfield>
   <subfield code="u">Neurosurgery of NeuroCenter, Kuopio University Hospital and University of Eastern Finland, P.O. Box 100, FIN-70029, Kuopio, Finland</subfield>
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   <subfield code="a">Remes</subfield>
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   <subfield code="u">Unit of Neurology, Institute of Clinical Medicine, University of Eastern Finland, Kuopio, Finland</subfield>
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   <subfield code="a">Vanninen</subfield>
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   <subfield code="u">Department of Radiology, Kuopio University Hospital and University of Eastern Finland, Kuopio, Finland</subfield>
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   <subfield code="u">Unit of Neurology, Institute of Clinical Medicine, University of Eastern Finland, Kuopio, Finland</subfield>
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   <subfield code="u">Neurosurgery of NeuroCenter, Kuopio University Hospital and University of Eastern Finland, P.O. Box 100, FIN-70029, Kuopio, Finland</subfield>
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   <subfield code="a">Sutela</subfield>
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   <subfield code="u">Department of Radiology, Kuopio University Hospital and University of Eastern Finland, Kuopio, Finland</subfield>
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   <subfield code="u">Neurosurgery of NeuroCenter, Kuopio University Hospital and University of Eastern Finland, P.O. Box 100, FIN-70029, Kuopio, Finland</subfield>
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   <subfield code="t">Acta Neurochirurgica</subfield>
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   <subfield code="g">157/10(2015-10-01), 1709-1719</subfield>
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   <subfield code="a">Metadata rights reserved</subfield>
   <subfield code="b">Springer special CC-BY-NC licence</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="u">Neurosurgery of NeuroCenter, Kuopio University Hospital and University of Eastern Finland, P.O. Box 100, FIN-70029, Kuopio, Finland</subfield>
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