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Survival in treated idiopathic normal pressure hydrocephalus
OBJECTIVE: To describe survival and causes of death in 979 treated iNPH patients from the Swedish Hydrocephalus Quality Registry (SHQR), and to examine the influence of comorbidities, symptom severity and postoperative outcome. METHODS: All 979 patients operated for iNPH 2004–2011 and registered in...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7035239/ https://www.ncbi.nlm.nih.gov/pubmed/31713102 http://dx.doi.org/10.1007/s00415-019-09598-1 |
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author | Andrén, Kerstin Wikkelsø, Carsten Sundström, Nina Israelsson, Hanna Agerskov, Simon Laurell, Katarina Hellström, Per Tullberg, Mats |
author_facet | Andrén, Kerstin Wikkelsø, Carsten Sundström, Nina Israelsson, Hanna Agerskov, Simon Laurell, Katarina Hellström, Per Tullberg, Mats |
author_sort | Andrén, Kerstin |
collection | PubMed |
description | OBJECTIVE: To describe survival and causes of death in 979 treated iNPH patients from the Swedish Hydrocephalus Quality Registry (SHQR), and to examine the influence of comorbidities, symptom severity and postoperative outcome. METHODS: All 979 patients operated for iNPH 2004–2011 and registered in the SHQR were included. A matched control group of 4890 persons from the general population was selected by Statistics Sweden. Data from the Swedish Cause of Death Registry was obtained for patients and controls. RESULTS: At a median 5.9 (IQR 4.2–8.1) year follow-up, 37% of the iNPH patients and 23% of the controls had died. Mortality was increased in iNPH patients by a hazard ratio of 1.81, 95% CI 1.61–2.04, p < 0.001. More pronounced symptoms in the preoperative ordinal gait scale and the Mini-mental State Examination were the most important independent predictors of mortality along with the prevalence of heart disease. Patients who improved in both the gait scale and in the modified Rankin Scale postoperatively (n = 144) had a similar survival as the general population (p = 0.391). Deaths due to cerebrovascular disease or dementia were more common in iNPH patients, while more controls died because of neoplasms or disorders of the circulatory system. CONCLUSIONS: Mortality in operated iNPH patients is 1.8 times increased compared to the general population, a lower figure than previously reported. The survival of iNPH patients who improve in gait and functional independence is similar to that of the general population, indicating that shunt surgery for iNPH, besides improving symptoms and signs, can normalize survival. |
format | Online Article Text |
id | pubmed-7035239 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-70352392020-03-06 Survival in treated idiopathic normal pressure hydrocephalus Andrén, Kerstin Wikkelsø, Carsten Sundström, Nina Israelsson, Hanna Agerskov, Simon Laurell, Katarina Hellström, Per Tullberg, Mats J Neurol Original Communication OBJECTIVE: To describe survival and causes of death in 979 treated iNPH patients from the Swedish Hydrocephalus Quality Registry (SHQR), and to examine the influence of comorbidities, symptom severity and postoperative outcome. METHODS: All 979 patients operated for iNPH 2004–2011 and registered in the SHQR were included. A matched control group of 4890 persons from the general population was selected by Statistics Sweden. Data from the Swedish Cause of Death Registry was obtained for patients and controls. RESULTS: At a median 5.9 (IQR 4.2–8.1) year follow-up, 37% of the iNPH patients and 23% of the controls had died. Mortality was increased in iNPH patients by a hazard ratio of 1.81, 95% CI 1.61–2.04, p < 0.001. More pronounced symptoms in the preoperative ordinal gait scale and the Mini-mental State Examination were the most important independent predictors of mortality along with the prevalence of heart disease. Patients who improved in both the gait scale and in the modified Rankin Scale postoperatively (n = 144) had a similar survival as the general population (p = 0.391). Deaths due to cerebrovascular disease or dementia were more common in iNPH patients, while more controls died because of neoplasms or disorders of the circulatory system. CONCLUSIONS: Mortality in operated iNPH patients is 1.8 times increased compared to the general population, a lower figure than previously reported. The survival of iNPH patients who improve in gait and functional independence is similar to that of the general population, indicating that shunt surgery for iNPH, besides improving symptoms and signs, can normalize survival. Springer Berlin Heidelberg 2019-11-11 2020 /pmc/articles/PMC7035239/ /pubmed/31713102 http://dx.doi.org/10.1007/s00415-019-09598-1 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. |
spellingShingle | Original Communication Andrén, Kerstin Wikkelsø, Carsten Sundström, Nina Israelsson, Hanna Agerskov, Simon Laurell, Katarina Hellström, Per Tullberg, Mats Survival in treated idiopathic normal pressure hydrocephalus |
title | Survival in treated idiopathic normal pressure hydrocephalus |
title_full | Survival in treated idiopathic normal pressure hydrocephalus |
title_fullStr | Survival in treated idiopathic normal pressure hydrocephalus |
title_full_unstemmed | Survival in treated idiopathic normal pressure hydrocephalus |
title_short | Survival in treated idiopathic normal pressure hydrocephalus |
title_sort | survival in treated idiopathic normal pressure hydrocephalus |
topic | Original Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7035239/ https://www.ncbi.nlm.nih.gov/pubmed/31713102 http://dx.doi.org/10.1007/s00415-019-09598-1 |
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