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Systematic literature review of burden of illness in chronic inflammatory demyelinating polyneuropathy (CIDP)
BACKGROUND: Chronic inflammatory demyelinating polyneuropathy (CIDP) is a rare neurological disorder characterised by muscle weakness and impaired sensory function. The present study provides a comprehensive literature review of the burden of illness of CIDP. METHODS: Systematic literature search of...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8463372/ https://www.ncbi.nlm.nih.gov/pubmed/32583051 http://dx.doi.org/10.1007/s00415-020-09998-8 |
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author | Querol, Luis Crabtree, M. Herepath, M. Priedane, E. Viejo Viejo, I. Agush, S. Sommerer, P. |
author_facet | Querol, Luis Crabtree, M. Herepath, M. Priedane, E. Viejo Viejo, I. Agush, S. Sommerer, P. |
author_sort | Querol, Luis |
collection | PubMed |
description | BACKGROUND: Chronic inflammatory demyelinating polyneuropathy (CIDP) is a rare neurological disorder characterised by muscle weakness and impaired sensory function. The present study provides a comprehensive literature review of the burden of illness of CIDP. METHODS: Systematic literature search of PubMed, Embase, and key conferences in May 2019. Search terms identified studies on the epidemiology, humanistic burden, current treatment, and economic burden of CIDP published since 2009 in English. RESULTS: Forty-five full texts and nineteen conference proceedings were identified on the epidemiology (n = 9), humanistic burden (n = 7), current treatment (n = 40), and economic burden (n = 8) of CIDP. Epidemiological studies showed incidence and prevalence of 0.2–1.6 and 0.8–8.9 per 100,000, respectively, depending on geography and diagnostic criteria. Humanistic burden studies revealed that patients experienced physical and psychosocial burden, including impaired physical function, pain and depression. Publications on current treatments reported on six main types of therapy: intravenous immunoglobulins, subcutaneous immunoglobulins, corticosteroids, plasma exchange, immunosuppressants, and immunomodulators. Treatments may be burdensome, due to adverse events and reduced independence caused by treatment administration setting. In Germany, UK, France, and the US, CIDP economic burden was driven by direct costs of treatment and hospitalisation. CIDP was associated with indirect costs driven by impaired productivity. CONCLUSIONS: This first systematic review of CIDP burden of illness demonstrates the high physical and psychosocial burden of this rare disease. Future research is required to fully characterise the burden of CIDP, and to understand how appropriate treatment can mitigate burden for patients and healthcare systems. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00415-020-09998-8) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-8463372 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-84633722021-10-08 Systematic literature review of burden of illness in chronic inflammatory demyelinating polyneuropathy (CIDP) Querol, Luis Crabtree, M. Herepath, M. Priedane, E. Viejo Viejo, I. Agush, S. Sommerer, P. J Neurol Review BACKGROUND: Chronic inflammatory demyelinating polyneuropathy (CIDP) is a rare neurological disorder characterised by muscle weakness and impaired sensory function. The present study provides a comprehensive literature review of the burden of illness of CIDP. METHODS: Systematic literature search of PubMed, Embase, and key conferences in May 2019. Search terms identified studies on the epidemiology, humanistic burden, current treatment, and economic burden of CIDP published since 2009 in English. RESULTS: Forty-five full texts and nineteen conference proceedings were identified on the epidemiology (n = 9), humanistic burden (n = 7), current treatment (n = 40), and economic burden (n = 8) of CIDP. Epidemiological studies showed incidence and prevalence of 0.2–1.6 and 0.8–8.9 per 100,000, respectively, depending on geography and diagnostic criteria. Humanistic burden studies revealed that patients experienced physical and psychosocial burden, including impaired physical function, pain and depression. Publications on current treatments reported on six main types of therapy: intravenous immunoglobulins, subcutaneous immunoglobulins, corticosteroids, plasma exchange, immunosuppressants, and immunomodulators. Treatments may be burdensome, due to adverse events and reduced independence caused by treatment administration setting. In Germany, UK, France, and the US, CIDP economic burden was driven by direct costs of treatment and hospitalisation. CIDP was associated with indirect costs driven by impaired productivity. CONCLUSIONS: This first systematic review of CIDP burden of illness demonstrates the high physical and psychosocial burden of this rare disease. Future research is required to fully characterise the burden of CIDP, and to understand how appropriate treatment can mitigate burden for patients and healthcare systems. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00415-020-09998-8) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2020-06-24 2021 /pmc/articles/PMC8463372/ /pubmed/32583051 http://dx.doi.org/10.1007/s00415-020-09998-8 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Review Querol, Luis Crabtree, M. Herepath, M. Priedane, E. Viejo Viejo, I. Agush, S. Sommerer, P. Systematic literature review of burden of illness in chronic inflammatory demyelinating polyneuropathy (CIDP) |
title | Systematic literature review of burden of illness in chronic inflammatory demyelinating polyneuropathy (CIDP) |
title_full | Systematic literature review of burden of illness in chronic inflammatory demyelinating polyneuropathy (CIDP) |
title_fullStr | Systematic literature review of burden of illness in chronic inflammatory demyelinating polyneuropathy (CIDP) |
title_full_unstemmed | Systematic literature review of burden of illness in chronic inflammatory demyelinating polyneuropathy (CIDP) |
title_short | Systematic literature review of burden of illness in chronic inflammatory demyelinating polyneuropathy (CIDP) |
title_sort | systematic literature review of burden of illness in chronic inflammatory demyelinating polyneuropathy (cidp) |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8463372/ https://www.ncbi.nlm.nih.gov/pubmed/32583051 http://dx.doi.org/10.1007/s00415-020-09998-8 |
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