Cargando…
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...
Autores principales: | , , , , |
---|---|
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 |
_version_ | 1783230634063298560 |
---|---|
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. |
format | Online Article Text |
id | pubmed-5399384 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT smithmichaelg capturerecapturemethodologytostudyrareconditionsusingsurveillancedataforfragilexsyndromeandmusculardystrophy AT royerjulie capturerecapturemethodologytostudyrareconditionsusingsurveillancedataforfragilexsyndromeandmusculardystrophy AT mannjoshua capturerecapturemethodologytostudyrareconditionsusingsurveillancedataforfragilexsyndromeandmusculardystrophy AT mcdermottsuzanne capturerecapturemethodologytostudyrareconditionsusingsurveillancedataforfragilexsyndromeandmusculardystrophy AT valdezrodolfo capturerecapturemethodologytostudyrareconditionsusingsurveillancedataforfragilexsyndromeandmusculardystrophy |