Evidence map›Paper›PMID 28427448›Full record

ArticleOrphanet journal of rare diseases2017

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

Michael G Smith, Julie Royer, Joshua Mann, Suzanne McDermott, Rodolfo Valdez

Open access · goldAbstract read
In one paragraph

Article in Orphanet journal of rare diseases, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 35% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Observational
  2. Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 4 institutions in 1 country.

Michael G SmithDepartment of Health Services Management and Policy, East Tennessee State University, Johnson City, TN, USA. smithmg1@etsu.edu.
Julie RoyerRevenue and Fiscal Affairs Office, Health and Demographics Section, Columbia, SC, USA.
Joshua MannDepartment of Preventive Medicine, University of Mississippi Medical Center, Jackson, MS, USA.
Suzanne McDermottDepartment of Epidemiology and Biostatistics, University of South Carolina, Columbia, SC, USA.
Rodolfo ValdezCenters for Disease Control and Prevention, National Center for Birth Defects and Developmental Disabilities, Atlanta, GA, USA.
Centers for Disease Control and Prevention · USEast Tennessee State University · USUniversity of Mississippi Medical Center · USUniversity of South Carolina · US

Funding

Three State Rare Conditions Surveillance ProjectU01DD000927 · DD · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI MCDERMOTT, SUZANNE W, SELASSIE, ANBESAW W. · 2012 to 2013
$796k
NCBDD CDC HHS U01 DD000927NCBDD CDC HHS U01 DD001117
6 · The paper itself

Abstract

backgroundRare 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.

methodsTwo 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.

resultsThere 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.

conclusionsApplying 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.

Indexed as

Population SurveillanceAdolescentAdultChildChild, PreschoolEpidemiologic MethodsFragile X SyndromeHumansInfantInternational Classification of DiseasesMaleMiddle AgedMuscular DystrophiesSouth CarolinaYoung AdultCapture-recaptureFragile X syndromeMuscular dystrophyPassive surveillance

Identifiers

PMID28427448
PMCPMC5399384
OpenAlexW2605723634

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.