Evidence map›Paper›PMID 27574026›Full record

ArticleJMIR public health and surveillance2016

Testing the Feasibility of a Passive and Active Case Ascertainment System for Multiple Rare Conditions Simultaneously: The Experience in Three US States.

Amanda Reichard, Suzanne McDermott, Margaret Ruttenber, Joshua Mann, Michael G Smith, Julie Royer, Rodolfo Valdez

Abstract read
In one paragraph

Article in JMIR public health and surveillance, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Impact of data sources and ascertainment methods on reporting paediatric genetic condition prevalence: A scoping review.Health information management : journal of the Health Information Management Association of Australia · 2026
    Article
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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

7 authors.

Amanda Reichard *Institute on DisabilityUniversity of New HampshireDurham, NHUnited States.ORCID 0000-0002-7431-1333
Suzanne McDermottDepartment of Epidemiology and BiostatisticsUniversity of South CarolinaColumbia, SCUnited States.ORCID 0000-0003-1517-5033
Margaret RuttenberSpecial Health Care NeedsColorado Department of Public Health and EnvironmentDenver, COUnited States.ORCID 0000-0002-1378-3724
Joshua MannDepartment of Preventive MedicineUniversity of Mississippi Medical CenterJackson, MSUnited States.ORCID 0000-0002-3716-3642
Michael G SmithSouth Carolina Department of Health and Environmental ControlColumbia, SCUnited States.ORCID 0000-0002-8297-2203
Julie RoyerRevenue and Fiscal Affairs OfficeSouth Carolina Budget and ControlColumbia, SCUnited States.ORCID 0000-0001-5323-1986
Rodolfo ValdezNational Center for Birth Defects and Developmental DisabilitiesCenters for Disease Control and PreventionAtlanta, GAUnited States.ORCID 0000-0001-9979-3140

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 DD000927
6 · The paper itself

Abstract

backgroundOwing to their low prevalence, single rare conditions are difficult to monitor through current state passive and active case ascertainment systems. However, such monitoring is important because, as a group, rare conditions have great impact on the health of affected individuals and the well-being of their caregivers. A viable approach could be to conduct passive and active case ascertainment of several rare conditions simultaneously. This is a report about the feasibility of such an approach.

objectiveTo test the feasibility of a case ascertainment system with passive and active components aimed at monitoring 3 rare conditions simultaneously in 3 states of the United States (Colorado, Kansas, and South Carolina). The 3 conditions are spina bifida, muscular dystrophy, and fragile X syndrome.

methodsTeams from each state evaluated the possibility of using current or modified versions of their local passive and active case ascertainment systems and datasets to monitor the 3 conditions. Together, these teams established the case definitions and selected the variables and the abstraction tools for the active case ascertainment approach. After testing the ability of their local passive and active case ascertainment system to capture all 3 conditions, the next steps were to report the number of cases detected actively and passively for each condition, to list the local barriers against the combined passive and active case ascertainment system, and to describe the experiences in trying to overcome these barriers.

resultsDuring the test period, the team from South Carolina was able to collect data on all 3 conditions simultaneously for all ages. The Colorado team was also able to collect data on all 3 conditions but, because of age restrictions in its passive and active case ascertainment system, it was able to report few cases of fragile X syndrome. The team from Kansas was able to collect data only on spina bifida. For all states, the implementation of an active component of the ascertainment system was problematic. The passive component appears viable with minor modifications.

conclusionsDespite evident barriers, the joint passive and active case ascertainment of rare disorders using modified existing surveillance systems and datasets seems feasible, especially for systems that rely on passive case ascertainment.

Indexed as

fragile X syndromemuscular dystrophyspina bifidasurveillance

Identifiers

PMID27574026
PMCPMC5020310

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Registered trials

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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.