Cargando…

Results of Florida's Amyotrophic Lateral Sclerosis Surveillance Project, 2009–2011

OBJECTIVE: Studies to determine the incidence and prevalence of amyotrophic lateral sclerosis (ALS) in defined geographic areas in the USA are needed. The Florida Department of Health received funding from the federal Agency for Toxic Substances and Disease Registry to implement a state-wide ALS Sur...

Descripción completa

Detalles Bibliográficos
Autores principales: Freer, Cecilia, Hylton, Tara, Jordan, Heather M, Kaye, Wendy E, Singh, Sabrina, Huang, Youjie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4410133/
https://www.ncbi.nlm.nih.gov/pubmed/25900464
http://dx.doi.org/10.1136/bmjopen-2014-007359
_version_ 1782368277410873344
author Freer, Cecilia
Hylton, Tara
Jordan, Heather M
Kaye, Wendy E
Singh, Sabrina
Huang, Youjie
author_facet Freer, Cecilia
Hylton, Tara
Jordan, Heather M
Kaye, Wendy E
Singh, Sabrina
Huang, Youjie
author_sort Freer, Cecilia
collection PubMed
description OBJECTIVE: Studies to determine the incidence and prevalence of amyotrophic lateral sclerosis (ALS) in defined geographic areas in the USA are needed. The Florida Department of Health received funding from the federal Agency for Toxic Substances and Disease Registry to implement a state-wide ALS Surveillance Project. The objectives of the project were to describe the demographic characteristics of ALS cases and to calculate the incidence and prevalence of ALS in Florida. SETTING/PARTICIPANTS: All neurologists were asked to submit case reports for persons with ALS diagnosed and/or under their care during 1 January 2009 through 31 December 2011. A medical record verification form and an electromyogram (EMG) report were requested for a sample of cases and reviewed by an independent consulting neurologist to confirm ALS diagnosis. Death data were used to aid with case report collection. PRIMARY AND SECONDARY OUTCOME MEASURES: Demographics, relevant history and clinical characteristics, El Escorial classifications, time from symptom onset to diagnosis, crude annual incidence rates and 2009 period prevalence are presented. RESULTS: The 1450 reported ALS cases were more likely to be older, male, white and non-Hispanic. Slightly more than 4% of cases were reported as also having dementia, and 4.8% were reported to have an immediate family member diagnosed with ALS. Incidence rates ranged from 1.7 to 1.9 per 100 000 person-years during the project period and the 2009 period prevalence was 4.0 per 100 000 persons. CONCLUSIONS: Project findings are generally consistent with findings of population-based studies in Europe, as well as geographically limited studies in the USA. Our findings add to the growing body of epidemiological literature about ALS in the USA. Future epidemiological studies in the USA should focus on identifying cases from minority groups and those that may have limited access to healthcare, and should consider conducting capture–recapture analysis to assess case ascertainment.
format Online
Article
Text
id pubmed-4410133
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher BMJ Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-44101332015-05-01 Results of Florida's Amyotrophic Lateral Sclerosis Surveillance Project, 2009–2011 Freer, Cecilia Hylton, Tara Jordan, Heather M Kaye, Wendy E Singh, Sabrina Huang, Youjie BMJ Open Epidemiology OBJECTIVE: Studies to determine the incidence and prevalence of amyotrophic lateral sclerosis (ALS) in defined geographic areas in the USA are needed. The Florida Department of Health received funding from the federal Agency for Toxic Substances and Disease Registry to implement a state-wide ALS Surveillance Project. The objectives of the project were to describe the demographic characteristics of ALS cases and to calculate the incidence and prevalence of ALS in Florida. SETTING/PARTICIPANTS: All neurologists were asked to submit case reports for persons with ALS diagnosed and/or under their care during 1 January 2009 through 31 December 2011. A medical record verification form and an electromyogram (EMG) report were requested for a sample of cases and reviewed by an independent consulting neurologist to confirm ALS diagnosis. Death data were used to aid with case report collection. PRIMARY AND SECONDARY OUTCOME MEASURES: Demographics, relevant history and clinical characteristics, El Escorial classifications, time from symptom onset to diagnosis, crude annual incidence rates and 2009 period prevalence are presented. RESULTS: The 1450 reported ALS cases were more likely to be older, male, white and non-Hispanic. Slightly more than 4% of cases were reported as also having dementia, and 4.8% were reported to have an immediate family member diagnosed with ALS. Incidence rates ranged from 1.7 to 1.9 per 100 000 person-years during the project period and the 2009 period prevalence was 4.0 per 100 000 persons. CONCLUSIONS: Project findings are generally consistent with findings of population-based studies in Europe, as well as geographically limited studies in the USA. Our findings add to the growing body of epidemiological literature about ALS in the USA. Future epidemiological studies in the USA should focus on identifying cases from minority groups and those that may have limited access to healthcare, and should consider conducting capture–recapture analysis to assess case ascertainment. BMJ Publishing Group 2015-04-21 /pmc/articles/PMC4410133/ /pubmed/25900464 http://dx.doi.org/10.1136/bmjopen-2014-007359 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Epidemiology
Freer, Cecilia
Hylton, Tara
Jordan, Heather M
Kaye, Wendy E
Singh, Sabrina
Huang, Youjie
Results of Florida's Amyotrophic Lateral Sclerosis Surveillance Project, 2009–2011
title Results of Florida's Amyotrophic Lateral Sclerosis Surveillance Project, 2009–2011
title_full Results of Florida's Amyotrophic Lateral Sclerosis Surveillance Project, 2009–2011
title_fullStr Results of Florida's Amyotrophic Lateral Sclerosis Surveillance Project, 2009–2011
title_full_unstemmed Results of Florida's Amyotrophic Lateral Sclerosis Surveillance Project, 2009–2011
title_short Results of Florida's Amyotrophic Lateral Sclerosis Surveillance Project, 2009–2011
title_sort results of florida's amyotrophic lateral sclerosis surveillance project, 2009–2011
topic Epidemiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4410133/
https://www.ncbi.nlm.nih.gov/pubmed/25900464
http://dx.doi.org/10.1136/bmjopen-2014-007359
work_keys_str_mv AT freercecilia resultsoffloridasamyotrophiclateralsclerosissurveillanceproject20092011
AT hyltontara resultsoffloridasamyotrophiclateralsclerosissurveillanceproject20092011
AT jordanheatherm resultsoffloridasamyotrophiclateralsclerosissurveillanceproject20092011
AT kayewendye resultsoffloridasamyotrophiclateralsclerosissurveillanceproject20092011
AT singhsabrina resultsoffloridasamyotrophiclateralsclerosissurveillanceproject20092011
AT huangyoujie resultsoffloridasamyotrophiclateralsclerosissurveillanceproject20092011