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Prevalence and incidence of neuromuscular conditions in the UK between 2000 and 2019: A retrospective study using primary care data

BACKGROUND: In the UK, large-scale electronic primary care datasets can provide up-to-date, accurate epidemiological information on rarer diseases, where specialist diagnoses from hospital discharges and clinic letters are generally well recorded and electronically searchable. Current estimates of t...

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Autores principales: Carey, Iain M., Banchoff, Emma, Nirmalananthan, Niranjanan, Harris, Tess, DeWilde, Stephen, Chaudhry, Umar A. R., Cook, Derek G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8719665/
https://www.ncbi.nlm.nih.gov/pubmed/34972157
http://dx.doi.org/10.1371/journal.pone.0261983
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author Carey, Iain M.
Banchoff, Emma
Nirmalananthan, Niranjanan
Harris, Tess
DeWilde, Stephen
Chaudhry, Umar A. R.
Cook, Derek G.
author_facet Carey, Iain M.
Banchoff, Emma
Nirmalananthan, Niranjanan
Harris, Tess
DeWilde, Stephen
Chaudhry, Umar A. R.
Cook, Derek G.
author_sort Carey, Iain M.
collection PubMed
description BACKGROUND: In the UK, large-scale electronic primary care datasets can provide up-to-date, accurate epidemiological information on rarer diseases, where specialist diagnoses from hospital discharges and clinic letters are generally well recorded and electronically searchable. Current estimates of the number of people living with neuromuscular disease (NMD) have largely been based on secondary care data sources and lacked direct denominators. OBJECTIVE: To estimate trends in the recording of neuromuscular disease in UK primary care between 2000–2019. METHODS: The Clinical Practice Research Datalink (CPRD) database was searched electronically to estimate incidence and prevalence rates (per 100,000) for a range of NMDs in each year. To compare trends over time, rates were age standardised to the most recent CPRD population (2019). RESULTS: Approximately 13 million patients were actively registered in each year. By 2019, 28,230 active patients had ever received a NMD diagnosis (223.6), which was higher among males (239.0) than females (208.3). The most common classifications were Guillain-Barre syndrome (40.1), myasthenia gravis (33.7), muscular dystrophy (29.5), Charcot-Marie-Tooth (29.5) and inflammatory myopathies (25.0). Since 2000, overall prevalence grew by 63%, with the largest increases seen at older ages (≥65-years). However, overall incidence remained constant, though myasthenia gravis incidence has risen steadily since 2008, while new cases of muscular dystrophy fell over the same period. CONCLUSIONS: Lifetime recording of many NMDs on primary care records exceed current estimates of people living with these conditions; these are important data for health service and care planning. Temporal trends suggest this number is steadily increasing, and while this may partially be due to better recording, it cannot be simply explained by new cases, as incidence remained constant. The increase in prevalence among older ages suggests increases in life expectancy among those living with NMDs may have occurred.
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spelling pubmed-87196652022-01-01 Prevalence and incidence of neuromuscular conditions in the UK between 2000 and 2019: A retrospective study using primary care data Carey, Iain M. Banchoff, Emma Nirmalananthan, Niranjanan Harris, Tess DeWilde, Stephen Chaudhry, Umar A. R. Cook, Derek G. PLoS One Research Article BACKGROUND: In the UK, large-scale electronic primary care datasets can provide up-to-date, accurate epidemiological information on rarer diseases, where specialist diagnoses from hospital discharges and clinic letters are generally well recorded and electronically searchable. Current estimates of the number of people living with neuromuscular disease (NMD) have largely been based on secondary care data sources and lacked direct denominators. OBJECTIVE: To estimate trends in the recording of neuromuscular disease in UK primary care between 2000–2019. METHODS: The Clinical Practice Research Datalink (CPRD) database was searched electronically to estimate incidence and prevalence rates (per 100,000) for a range of NMDs in each year. To compare trends over time, rates were age standardised to the most recent CPRD population (2019). RESULTS: Approximately 13 million patients were actively registered in each year. By 2019, 28,230 active patients had ever received a NMD diagnosis (223.6), which was higher among males (239.0) than females (208.3). The most common classifications were Guillain-Barre syndrome (40.1), myasthenia gravis (33.7), muscular dystrophy (29.5), Charcot-Marie-Tooth (29.5) and inflammatory myopathies (25.0). Since 2000, overall prevalence grew by 63%, with the largest increases seen at older ages (≥65-years). However, overall incidence remained constant, though myasthenia gravis incidence has risen steadily since 2008, while new cases of muscular dystrophy fell over the same period. CONCLUSIONS: Lifetime recording of many NMDs on primary care records exceed current estimates of people living with these conditions; these are important data for health service and care planning. Temporal trends suggest this number is steadily increasing, and while this may partially be due to better recording, it cannot be simply explained by new cases, as incidence remained constant. The increase in prevalence among older ages suggests increases in life expectancy among those living with NMDs may have occurred. Public Library of Science 2021-12-31 /pmc/articles/PMC8719665/ /pubmed/34972157 http://dx.doi.org/10.1371/journal.pone.0261983 Text en © 2021 Carey et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Carey, Iain M.
Banchoff, Emma
Nirmalananthan, Niranjanan
Harris, Tess
DeWilde, Stephen
Chaudhry, Umar A. R.
Cook, Derek G.
Prevalence and incidence of neuromuscular conditions in the UK between 2000 and 2019: A retrospective study using primary care data
title Prevalence and incidence of neuromuscular conditions in the UK between 2000 and 2019: A retrospective study using primary care data
title_full Prevalence and incidence of neuromuscular conditions in the UK between 2000 and 2019: A retrospective study using primary care data
title_fullStr Prevalence and incidence of neuromuscular conditions in the UK between 2000 and 2019: A retrospective study using primary care data
title_full_unstemmed Prevalence and incidence of neuromuscular conditions in the UK between 2000 and 2019: A retrospective study using primary care data
title_short Prevalence and incidence of neuromuscular conditions in the UK between 2000 and 2019: A retrospective study using primary care data
title_sort prevalence and incidence of neuromuscular conditions in the uk between 2000 and 2019: a retrospective study using primary care data
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8719665/
https://www.ncbi.nlm.nih.gov/pubmed/34972157
http://dx.doi.org/10.1371/journal.pone.0261983
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