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Progressive multifocal leukoencephalopathy in Finland: a cross-sectional registry study

OBJECTIVE: To investigate if progressive multifocal leucoencephalopathy (PML) incidence has increased in Finland like in the neighbouring Sweden. METHODS: National administrative registries were searched for all PML admissions aged 16 years or more in 2004–2014 on all neurological and internal medic...

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Autores principales: Sipilä, Jussi O. T., Soilu-Hänninen, Merja, Rautava, Päivi, Kytö, Ville
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6373365/
https://www.ncbi.nlm.nih.gov/pubmed/30612143
http://dx.doi.org/10.1007/s00415-018-09167-y
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author Sipilä, Jussi O. T.
Soilu-Hänninen, Merja
Rautava, Päivi
Kytö, Ville
author_facet Sipilä, Jussi O. T.
Soilu-Hänninen, Merja
Rautava, Päivi
Kytö, Ville
author_sort Sipilä, Jussi O. T.
collection PubMed
description OBJECTIVE: To investigate if progressive multifocal leucoencephalopathy (PML) incidence has increased in Finland like in the neighbouring Sweden. METHODS: National administrative registries were searched for all PML admissions aged 16 years or more in 2004–2014 on all neurological and internal medicine wards in Finland. The mortality data of the patients was extracted from the national causes of death registry. National level data on annual predisposing drug use was obtained from the national pharmaceutical authority. RESULTS: We identified 35 PML cases (57% male) with a peak in 2010–2011 that amounted to 49% of all cases. The annual incidence for the entire study period was 0.072/100,000 person-years (95% CI 0.050–0.10) with no temporal trend (p = 0.18). Mean age was 57 years (22–88 years) with no sex difference (p = 0.42). Neoplasms (60%), HIV infection (17%) and systemic connective tissue disorders (CTD, 14%) were the most common predisposing conditions. MS was recorded in three cases (9%). The national level use of drugs that predispose to PML increased during the study period, with the exceptions of alemtuzumab and fludarabine. Overall survival was 85% at 90 days, 79% at 1 year, and 66% at 5 years. Survival was worst in patients with malignancy and best in patients with CTD. CONCLUSIONS: PML most often occurs in patients with malignancies and patients with HIV or CTD cover a third. PML incidence in Finland is lower than in Sweden and shows no temporal trend despite increasing use of predisposing drugs. Mortality after PML varies according to the predisposing condition. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00415-018-09167-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-63733652019-03-01 Progressive multifocal leukoencephalopathy in Finland: a cross-sectional registry study Sipilä, Jussi O. T. Soilu-Hänninen, Merja Rautava, Päivi Kytö, Ville J Neurol Original Communication OBJECTIVE: To investigate if progressive multifocal leucoencephalopathy (PML) incidence has increased in Finland like in the neighbouring Sweden. METHODS: National administrative registries were searched for all PML admissions aged 16 years or more in 2004–2014 on all neurological and internal medicine wards in Finland. The mortality data of the patients was extracted from the national causes of death registry. National level data on annual predisposing drug use was obtained from the national pharmaceutical authority. RESULTS: We identified 35 PML cases (57% male) with a peak in 2010–2011 that amounted to 49% of all cases. The annual incidence for the entire study period was 0.072/100,000 person-years (95% CI 0.050–0.10) with no temporal trend (p = 0.18). Mean age was 57 years (22–88 years) with no sex difference (p = 0.42). Neoplasms (60%), HIV infection (17%) and systemic connective tissue disorders (CTD, 14%) were the most common predisposing conditions. MS was recorded in three cases (9%). The national level use of drugs that predispose to PML increased during the study period, with the exceptions of alemtuzumab and fludarabine. Overall survival was 85% at 90 days, 79% at 1 year, and 66% at 5 years. Survival was worst in patients with malignancy and best in patients with CTD. CONCLUSIONS: PML most often occurs in patients with malignancies and patients with HIV or CTD cover a third. PML incidence in Finland is lower than in Sweden and shows no temporal trend despite increasing use of predisposing drugs. Mortality after PML varies according to the predisposing condition. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00415-018-09167-y) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2019-01-05 2019 /pmc/articles/PMC6373365/ /pubmed/30612143 http://dx.doi.org/10.1007/s00415-018-09167-y Text en © The Author(s) 2019 OpenAccessThis 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
Sipilä, Jussi O. T.
Soilu-Hänninen, Merja
Rautava, Päivi
Kytö, Ville
Progressive multifocal leukoencephalopathy in Finland: a cross-sectional registry study
title Progressive multifocal leukoencephalopathy in Finland: a cross-sectional registry study
title_full Progressive multifocal leukoencephalopathy in Finland: a cross-sectional registry study
title_fullStr Progressive multifocal leukoencephalopathy in Finland: a cross-sectional registry study
title_full_unstemmed Progressive multifocal leukoencephalopathy in Finland: a cross-sectional registry study
title_short Progressive multifocal leukoencephalopathy in Finland: a cross-sectional registry study
title_sort progressive multifocal leukoencephalopathy in finland: a cross-sectional registry study
topic Original Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6373365/
https://www.ncbi.nlm.nih.gov/pubmed/30612143
http://dx.doi.org/10.1007/s00415-018-09167-y
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