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Capture-recapture methodology to study rare conditions using surveillance data for fragile X syndrome and muscular dystrophy

BACKGROUND: Rare conditions can be catastrophic for families and the implications for public health can be substantial. Our study compared basic surveillance through active medical record review with a linked administrative data file to assess the number of cases of two rare conditions, fragile X sy...

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Autores principales: Smith, Michael G., Royer, Julie, Mann, Joshua, McDermott, Suzanne, Valdez, Rodolfo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5399384/
https://www.ncbi.nlm.nih.gov/pubmed/28427448
http://dx.doi.org/10.1186/s13023-017-0628-y
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author Smith, Michael G.
Royer, Julie
Mann, Joshua
McDermott, Suzanne
Valdez, Rodolfo
author_facet Smith, Michael G.
Royer, Julie
Mann, Joshua
McDermott, Suzanne
Valdez, Rodolfo
author_sort Smith, Michael G.
collection PubMed
description BACKGROUND: Rare conditions can be catastrophic for families and the implications for public health can be substantial. Our study compared basic surveillance through active medical record review with a linked administrative data file to assess the number of cases of two rare conditions, fragile X syndrome (FXS) and muscular dystrophy (MD) in a population. METHODS: Two methods of data collection were used to collect information from five counties comprising two standard metropolitan statistical areas of South Carolina. The passive system relied mostly on health claims data using ICD-9 CM diagnostic codes. The active system relied on a nurse abstracting records from a list of all licensed physicians with specialties in neurology, orthopedics, and genetics. RESULTS: There were 141 FXS cases and 348 MD cases that met the case definitions using active surveillance. Additional cases were found for both conditions but they were determined to not be true cases. After linking the actively collected MD and FXS cases to passive datasets, we found that the estimated total numbers of cases were similar to using capture-recapture analysis; the positive predictive values for cases identified in the passive system were 56.6% for MD and 75.7% for FXS. CONCLUSIONS: Applying capture-recapture methods to passively collected surveillance data for rare health conditions produced an estimate of the number of true cases that was similar to that obtained through active data collection.
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spelling pubmed-53993842017-04-24 Capture-recapture methodology to study rare conditions using surveillance data for fragile X syndrome and muscular dystrophy Smith, Michael G. Royer, Julie Mann, Joshua McDermott, Suzanne Valdez, Rodolfo Orphanet J Rare Dis Research BACKGROUND: Rare conditions can be catastrophic for families and the implications for public health can be substantial. Our study compared basic surveillance through active medical record review with a linked administrative data file to assess the number of cases of two rare conditions, fragile X syndrome (FXS) and muscular dystrophy (MD) in a population. METHODS: Two methods of data collection were used to collect information from five counties comprising two standard metropolitan statistical areas of South Carolina. The passive system relied mostly on health claims data using ICD-9 CM diagnostic codes. The active system relied on a nurse abstracting records from a list of all licensed physicians with specialties in neurology, orthopedics, and genetics. RESULTS: There were 141 FXS cases and 348 MD cases that met the case definitions using active surveillance. Additional cases were found for both conditions but they were determined to not be true cases. After linking the actively collected MD and FXS cases to passive datasets, we found that the estimated total numbers of cases were similar to using capture-recapture analysis; the positive predictive values for cases identified in the passive system were 56.6% for MD and 75.7% for FXS. CONCLUSIONS: Applying capture-recapture methods to passively collected surveillance data for rare health conditions produced an estimate of the number of true cases that was similar to that obtained through active data collection. BioMed Central 2017-04-21 /pmc/articles/PMC5399384/ /pubmed/28427448 http://dx.doi.org/10.1186/s13023-017-0628-y Text en © The Author(s). 2017 Open AccessThis 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Smith, Michael G.
Royer, Julie
Mann, Joshua
McDermott, Suzanne
Valdez, Rodolfo
Capture-recapture methodology to study rare conditions using surveillance data for fragile X syndrome and muscular dystrophy
title Capture-recapture methodology to study rare conditions using surveillance data for fragile X syndrome and muscular dystrophy
title_full Capture-recapture methodology to study rare conditions using surveillance data for fragile X syndrome and muscular dystrophy
title_fullStr Capture-recapture methodology to study rare conditions using surveillance data for fragile X syndrome and muscular dystrophy
title_full_unstemmed Capture-recapture methodology to study rare conditions using surveillance data for fragile X syndrome and muscular dystrophy
title_short Capture-recapture methodology to study rare conditions using surveillance data for fragile X syndrome and muscular dystrophy
title_sort capture-recapture methodology to study rare conditions using surveillance data for fragile x syndrome and muscular dystrophy
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5399384/
https://www.ncbi.nlm.nih.gov/pubmed/28427448
http://dx.doi.org/10.1186/s13023-017-0628-y
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