Evidence map›Paper›PMID 36369700›Full record

ArticleBirth defects research2023

Validation of case definition algorithms for the ascertainment of congenital anomalies.

Yonabeth Nava de Escalante, Aanu Abayomi, Sylvie Langlois, Xibiao Ye, Anders Erickson, Henry Ngo, Rosemary Armour, Reiko Okamoto, Laura Arbour, Tanya Bedard and 5 more

Abstract read
In one paragraph

Article in Birth defects research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Innovation through collaboration: Identifying opportunities to improve congenital anomalies surveillance in Canada.Canadian journal of public health = Revue canadienne de sante publique · 2025
    Article
  4. 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

15 authors.

Yonabeth Nava de EscalanteBritish Columbia Ministry of Health, Victoria, British Columbia, Canada.ORCID 0000-0003-2843-2430
Aanu AbayomiBritish Columbia Ministry of Health, Victoria, British Columbia, Canada.
Sylvie LangloisDepartment of Medical Genetics, Faculty of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
Xibiao YeBritish Columbia Ministry of Health, Victoria, British Columbia, Canada.
Anders EricksonBritish Columbia Ministry of Health, Victoria, British Columbia, Canada.
Henry NgoBritish Columbia Ministry of Health, Victoria, British Columbia, Canada.
Rosemary ArmourBritish Columbia Vital Statistics Agency, Vancouver, British Columbia, Canada.
Reiko OkamotoBritish Columbia Ministry of Health, Victoria, British Columbia, Canada.
Laura ArbourDepartment of Medical Genetics, Faculty of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
Tanya BedardHealth Standards, Quality and Performance, Alberta Health, Edmonton, Alberta, Canada.
Kenny DerHealth Information Science, University of Victoria, Vancouver, British Columbia, Canada.
Margot Van AllenDepartment of Medical Genetics, Faculty of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
Erik SkarsgardDepartment of Surgery, British Columbia Children's Hospital, Vancouver, British Columbia, Canada.
Martin LavoieBritish Columbia Ministry of Health, Victoria, British Columbia, Canada.
Bonnie HenryBritish Columbia Ministry of Health, Victoria, British Columbia, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCongenital anomalies (CA) are one of the leading causes of infant mortality and long-term disability. Many jurisdictions rely on health administrative data to monitor these conditions. Case definition algorithms can be used to monitor CA; however, validation of these algorithms is needed to understand the strengths and limitations of the data. This study aimed to validate case definition algorithms used in a CA surveillance system in British Columbia (BC), Canada.

methodsA cohort of births between March 2000 and April 2002 in BC was linked to the Health Status Registry (HSR) and the BC Congenital Anomalies Surveillance System (BCCASS) to identify cases and non-cases of specific anomalies within each surveillance system. Measures of algorithm performance were calculated for each CA using the HSR as the reference standard. Agreement between both databases was calculated using kappa coefficient. The modified Standards for Reporting Diagnostic Accuracy guidelines were used to enhance the quality of the study.

resultsMeasures of algorithm performance varied by condition. Positive predictive value (PPV) ranged between approximately 73%-100%. Sensitivity was lower than PPV for most conditions. Internal congenital anomalies or conditions not easily identifiable at birth had the lowest sensitivity. Specificity and negative predictive value exceeded 99% for all algorithms.

conclusionCase definition algorithms may be used to monitor CA at the population level. Accuracy of algorithms is higher for conditions that are easily identified at birth. Jurisdictions with similar administrative data may benefit from using validated case definitions for CA surveillance as this facilitates cross-jurisdictional comparison.

Indexed as

AlgorithmsCanadaDatabases, FactualHumansInfantInfant, NewbornPredictive Value of TestsReference Standardsalgorithm validationcongenital anomalieshealth administrative datasurveillancevalidation study

Identifiers

PMID36369700
PMCPMC10099451

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.