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Timeliness of diagnosis in Motor Neurone Disease: a population-based study

Following the observation from our experience with the Northern Ireland Motor Neurone Disease (MND) register that excessive delays appeared to exist in the diagnosis of patients with MND, we performed a population-based study of the length and factors involved in the diagnostic process. In 73 patien...

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Detalles Bibliográficos
Autores principales: Donaghy, Colette, Dick, Alison, Hardiman, Orla, Patterson, Victor
Formato: Texto
Lenguaje:English
Publicado: The Ulster Medical Society 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2397016/
https://www.ncbi.nlm.nih.gov/pubmed/18269112
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author Donaghy, Colette
Dick, Alison
Hardiman, Orla
Patterson, Victor
author_facet Donaghy, Colette
Dick, Alison
Hardiman, Orla
Patterson, Victor
author_sort Donaghy, Colette
collection PubMed
description Following the observation from our experience with the Northern Ireland Motor Neurone Disease (MND) register that excessive delays appeared to exist in the diagnosis of patients with MND, we performed a population-based study of the length and factors involved in the diagnostic process. In 73 patients we found that the median time to diagnosis from symptom onset was 15.6 months, being shorter in bulbar onset patients and longer in females or those presenting with non-specific gait disturbance. We divided this interval into three time periods – symptom onset to first medical contact, first medical contact to neurology referral and neurology referral to diagnosis. The time period from first medical contact to neurology referral was the longest of the three periods studied indicating that appropriate timely referral of patients to neurologists was responsible for the greatest delay in making a diagnosis of MND. We propose that improving the accessibility of neurological services could potentially reduce the time to diagnosis by at least three months.
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spelling pubmed-23970162008-05-29 Timeliness of diagnosis in Motor Neurone Disease: a population-based study Donaghy, Colette Dick, Alison Hardiman, Orla Patterson, Victor Ulster Med J Paper Following the observation from our experience with the Northern Ireland Motor Neurone Disease (MND) register that excessive delays appeared to exist in the diagnosis of patients with MND, we performed a population-based study of the length and factors involved in the diagnostic process. In 73 patients we found that the median time to diagnosis from symptom onset was 15.6 months, being shorter in bulbar onset patients and longer in females or those presenting with non-specific gait disturbance. We divided this interval into three time periods – symptom onset to first medical contact, first medical contact to neurology referral and neurology referral to diagnosis. The time period from first medical contact to neurology referral was the longest of the three periods studied indicating that appropriate timely referral of patients to neurologists was responsible for the greatest delay in making a diagnosis of MND. We propose that improving the accessibility of neurological services could potentially reduce the time to diagnosis by at least three months. The Ulster Medical Society 2008-01 /pmc/articles/PMC2397016/ /pubmed/18269112 Text en © The Ulster Medical Society, 2008
spellingShingle Paper
Donaghy, Colette
Dick, Alison
Hardiman, Orla
Patterson, Victor
Timeliness of diagnosis in Motor Neurone Disease: a population-based study
title Timeliness of diagnosis in Motor Neurone Disease: a population-based study
title_full Timeliness of diagnosis in Motor Neurone Disease: a population-based study
title_fullStr Timeliness of diagnosis in Motor Neurone Disease: a population-based study
title_full_unstemmed Timeliness of diagnosis in Motor Neurone Disease: a population-based study
title_short Timeliness of diagnosis in Motor Neurone Disease: a population-based study
title_sort timeliness of diagnosis in motor neurone disease: a population-based study
topic Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2397016/
https://www.ncbi.nlm.nih.gov/pubmed/18269112
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