Evidence map›Paper›PMID 27891783›Full record

ArticleBirth defects research. Part A, Clinical and molecular teratology2016

Population-based microcephaly surveillance in the United States, 2009 to 2013: An analysis of potential sources of variation.

Janet D Cragan, Jennifer L Isenburg, Samantha E Parker, C J Alverson, Robert E Meyer, Erin B Stallings, Russell S Kirby, Philip J Lupo, Jennifer S Liu, Amanda Seagroves and 15 more

Abstract read
In one paragraph

Article in Birth defects research. Part A, Clinical and molecular teratology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 4 pooled it
–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

38 citing papers in PubMed, 4 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Review
  6. Article
  7. Article
  8. Article
  9. Microcephaly in Infants: A Retrospective Cohort Study from TurkeyJournal of clinical research in pediatric endocrinology · 2024
    Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Transcription factors in microcephaly.Frontiers in neuroscience · 2023
    Review
  15. Article
  16. Article
  17. Article
  18. Autosomal Recessive Primary Microcephaly: Not Just a Small Brain.Frontiers in cell and developmental biology · 2021
    Review
  19. Article
  20. 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

25 authors.

Janet D CraganDivision of Congenital and Developmental Disorders, National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, Georgia.
Jennifer L IsenburgDivision of Congenital and Developmental Disorders, National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, Georgia.
Samantha E ParkerDepartment of Epidemiology, Boston University School of Public Health, Boston, Massachusetts.
C J AlversonDivision of Congenital and Developmental Disorders, National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, Georgia.
Robert E MeyerState Center for Health Statistics, N.C. Division of Public Health, Raleigh, North Carolina.
Erin B StallingsDivision of Congenital and Developmental Disorders, National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, Georgia.
Russell S KirbyDepartment of Community and Family Health, College of Public Health, University of South Florida, Tampa, Florida.
Philip J LupoSection of Hematology-Oncology, Department of Pediatrics, Baylor College of Medicine, Houston, Texas.
Jennifer S LiuDivision of Congenital and Developmental Disorders, National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, Georgia.
Amanda SeagrovesDivision of Congenital and Developmental Disorders, National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, Georgia.
Mary K EthenBirth Defects Epidemiology and Surveillance Branch, Texas Department of State Health Services, Austin, Texas.
Sook Ja ChoDivision of Community and Family Health, Minnesota Department of Health, St. Paul, Minnesota.
MaryAnn EvansOregon Birth Anomalies Surveillance System, Oregon Public Health Division, Portland, Oregon.
Rebecca F LibermanCenter for Birth Defects Research and Prevention, Massachusetts Department of Public Health, Boston, Massachusetts.
Jane FornoffDivision of Epidemiologic Studies, Illinois Department of Public Health, Springfield, Illinois.
Marilyn L BrowneNew York State Department of Health, Albany, New York.ORCID http://orcid.org/0000-0002-1872-2787
Rachel E RutkowskiDepartment of Community and Family Health, College of Public Health, University of South Florida, Tampa, Florida.
Amy E NanceUtah Birth Defect Network, Division of Family Health and Preparedness, Utah Department of Health, Salt Lake City, Utah.
Marlene AnderkaNational Birth Defects Prevention Network, Houston, Texas.
Deborah J FoxNew York State Department of Health, Albany, New York.
Amy SteeleUtah Birth Defect Network, Division of Family Health and Preparedness, Utah Department of Health, Salt Lake City, Utah.
Glenn CopelandDivision for Vital Records and Health Statistics, Michigan Department of Health and Human Services, Lansing, Michigan.
Paul A RomittiCollege of Public Health, University of Iowa, Iowa City, Iowa.
Cara T MaiDivision of Congenital and Developmental Disorders, National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, Georgia.
National Birth Defects Prevention Network

Funding

Iowa CBDRP: Birth Defects Study To Evaluate Pregnancy exposureSU01DD001035 · DD · UNIVERSITY OF IOWA · PI ROMITTI, PAUL A · 2013 to 2017
$3.5M
Intramural CDC HHS CC999999NCBDD CDC HHS U01 DD001035
6 · The paper itself

Abstract

backgroundCongenital microcephaly has been linked to maternal Zika virus infection. However, ascertaining infants diagnosed with microcephaly can be challenging.

methodsThirty birth defects surveillance programs provided data on infants diagnosed with microcephaly born 2009 to 2013. The pooled prevalence of microcephaly per 10,000 live births was estimated overall and by maternal/infant characteristics. Variation in prevalence was examined across case finding methods. Nine programs provided data on head circumference and conditions potentially contributing to microcephaly.

resultsThe pooled prevalence of microcephaly was 8.7 per 10,000 live births. Median prevalence (per 10,000 live births) was similar among programs using active (6.7) and passive (6.6) methods; the interdecile range of prevalence estimates was wider among programs using passive methods for all race/ethnicity categories except Hispanic. Prevalence (per 10,000 live births) was lowest among non-Hispanic Whites (6.5) and highest among non-Hispanic Blacks and Hispanics (11.2 and 11.9, respectively); estimates followed a U-shaped distribution by maternal age with the highest prevalence among mothers <20 years (11.5) and ≥40 years (13.2). For gestational age and birth weight, the highest prevalence was among infants <32 weeks gestation and infants <1500 gm. Case definitions varied; 41.8% of cases had an HC ≥ the 10

conclusionDifferences in methods, population distribution of maternal/infant characteristics, and case definitions for microcephaly can contribute to the wide range of observed prevalence estimates across individual birth defects surveillance programs. Addressing these factors in the setting of Zika virus infection can improve the quality of prevalence estimates. Birth Defects Research (Part A) 106:972-982, 2016. © 2016 Wiley Periodicals, Inc.

Indexed as

Epidemiological MonitoringZika VirusFemaleHumansInfant, NewbornMaleMicrocephalyPrevalenceRetrospective StudiesUnited StatesZika Virus Infectionhead circumferencemicrocephalyprevalencesurveillance

Identifiers

PMID27891783
PMCPMC5485911

What OpenQuestion holds

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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.