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The Kuopio idiopathic normal pressure hydrocephalus protocol: initial outcome of 175 patients

BACKGROUND: The Kuopio University Hospital (KUH) idiopathic normal pressure hydrocephalus (iNPH) cerebrospinal fluid (CSF) shunting protocol is described together with the initial outcomes of 175 patients with probable iNPH treated according to this protocol from a defined population. Our secondary...

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Autores principales: Junkkari, A., Luikku, A. J., Danner, N., Jyrkkänen, H. K., Rauramaa, T., Korhonen, V. E., Koivisto, A. M., Nerg, O., Kojoukhova, M., Huttunen, T. J., Jääskeläinen, J. E., Leinonen, V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6657079/
https://www.ncbi.nlm.nih.gov/pubmed/31340831
http://dx.doi.org/10.1186/s12987-019-0142-9
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author Junkkari, A.
Luikku, A. J.
Danner, N.
Jyrkkänen, H. K.
Rauramaa, T.
Korhonen, V. E.
Koivisto, A. M.
Nerg, O.
Kojoukhova, M.
Huttunen, T. J.
Jääskeläinen, J. E.
Leinonen, V.
author_facet Junkkari, A.
Luikku, A. J.
Danner, N.
Jyrkkänen, H. K.
Rauramaa, T.
Korhonen, V. E.
Koivisto, A. M.
Nerg, O.
Kojoukhova, M.
Huttunen, T. J.
Jääskeläinen, J. E.
Leinonen, V.
author_sort Junkkari, A.
collection PubMed
description BACKGROUND: The Kuopio University Hospital (KUH) idiopathic normal pressure hydrocephalus (iNPH) cerebrospinal fluid (CSF) shunting protocol is described together with the initial outcomes of 175 patients with probable iNPH treated according to this protocol from a defined population. Our secondary aim was to display the variety of differential diagnoses referred to the KUH iNPH outpatient clinic from 2010 until 2017. METHODS: Patients were divided into four groups according to the prognostic tests: tap test (positive or negative) and infusion test (positive or negative). The short-term outcome was compared between groups. The 3-month outcome following shunt surgery was assessed by measuring gait speed improvement, using a 12-point iNPH grading scale (iNPHGS) and the 15D instrument. RESULTS: From 341 patients suspected of iNPH, 88 patients were excluded from further research mostly due to deviation from the protocol’s gait assessment guidelines. Hence 253 patients with suspected iNPH were included in the study, 177/253 (70%) of whom were treated with a CSF shunt. A favorable clinical outcome following surgery was observed in 79–93% of patients depending on the prognostic group. A moderate association (Cramer’s V = 0.32) was found between the gait speed improvement rate and the prognostic group (X(2), p = 0.003). Patients with a positive tap test had the highest gait speed improvement rate (75%). In addition, an improvement in walking speed was observed in 4/11 patients who had both a negative tap test and a negative infusion test. Other outcome measures did not differ between the prognostic groups. Conditions other than iNPH were found in 25% of the patients referred to iNPH outpatient clinic, with the most prevalent being Alzheimer’s disease. CONCLUSIONS: Our results emphasize the importance of a systematic diagnostic and prognostic workup especially in cases with an atypical presentation of iNPH. Additional diagnostic testing may be required, but should not delay adequate care. Active surgical treatment is recommended in patients with a high clinical probability of iNPH. Other neurological conditions contributed to most of the non iNPH diagnoses. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12987-019-0142-9) contains supplementary material, which is available to authorized users.
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spelling pubmed-66570792019-07-31 The Kuopio idiopathic normal pressure hydrocephalus protocol: initial outcome of 175 patients Junkkari, A. Luikku, A. J. Danner, N. Jyrkkänen, H. K. Rauramaa, T. Korhonen, V. E. Koivisto, A. M. Nerg, O. Kojoukhova, M. Huttunen, T. J. Jääskeläinen, J. E. Leinonen, V. Fluids Barriers CNS Research BACKGROUND: The Kuopio University Hospital (KUH) idiopathic normal pressure hydrocephalus (iNPH) cerebrospinal fluid (CSF) shunting protocol is described together with the initial outcomes of 175 patients with probable iNPH treated according to this protocol from a defined population. Our secondary aim was to display the variety of differential diagnoses referred to the KUH iNPH outpatient clinic from 2010 until 2017. METHODS: Patients were divided into four groups according to the prognostic tests: tap test (positive or negative) and infusion test (positive or negative). The short-term outcome was compared between groups. The 3-month outcome following shunt surgery was assessed by measuring gait speed improvement, using a 12-point iNPH grading scale (iNPHGS) and the 15D instrument. RESULTS: From 341 patients suspected of iNPH, 88 patients were excluded from further research mostly due to deviation from the protocol’s gait assessment guidelines. Hence 253 patients with suspected iNPH were included in the study, 177/253 (70%) of whom were treated with a CSF shunt. A favorable clinical outcome following surgery was observed in 79–93% of patients depending on the prognostic group. A moderate association (Cramer’s V = 0.32) was found between the gait speed improvement rate and the prognostic group (X(2), p = 0.003). Patients with a positive tap test had the highest gait speed improvement rate (75%). In addition, an improvement in walking speed was observed in 4/11 patients who had both a negative tap test and a negative infusion test. Other outcome measures did not differ between the prognostic groups. Conditions other than iNPH were found in 25% of the patients referred to iNPH outpatient clinic, with the most prevalent being Alzheimer’s disease. CONCLUSIONS: Our results emphasize the importance of a systematic diagnostic and prognostic workup especially in cases with an atypical presentation of iNPH. Additional diagnostic testing may be required, but should not delay adequate care. Active surgical treatment is recommended in patients with a high clinical probability of iNPH. Other neurological conditions contributed to most of the non iNPH diagnoses. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12987-019-0142-9) contains supplementary material, which is available to authorized users. BioMed Central 2019-07-25 /pmc/articles/PMC6657079/ /pubmed/31340831 http://dx.doi.org/10.1186/s12987-019-0142-9 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Junkkari, A.
Luikku, A. J.
Danner, N.
Jyrkkänen, H. K.
Rauramaa, T.
Korhonen, V. E.
Koivisto, A. M.
Nerg, O.
Kojoukhova, M.
Huttunen, T. J.
Jääskeläinen, J. E.
Leinonen, V.
The Kuopio idiopathic normal pressure hydrocephalus protocol: initial outcome of 175 patients
title The Kuopio idiopathic normal pressure hydrocephalus protocol: initial outcome of 175 patients
title_full The Kuopio idiopathic normal pressure hydrocephalus protocol: initial outcome of 175 patients
title_fullStr The Kuopio idiopathic normal pressure hydrocephalus protocol: initial outcome of 175 patients
title_full_unstemmed The Kuopio idiopathic normal pressure hydrocephalus protocol: initial outcome of 175 patients
title_short The Kuopio idiopathic normal pressure hydrocephalus protocol: initial outcome of 175 patients
title_sort kuopio idiopathic normal pressure hydrocephalus protocol: initial outcome of 175 patients
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6657079/
https://www.ncbi.nlm.nih.gov/pubmed/31340831
http://dx.doi.org/10.1186/s12987-019-0142-9
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