Literature DB >> 27891786

A quality assessment of reporting sources for microcephaly in Utah, 2003 to 2013.

Amy Steele1, Jane Johnson2, Amy Nance2, Robert Satterfield1, C J Alverson3, Cara Mai3.   

Abstract

BACKGROUND: Obtaining accurate microcephaly prevalence is important given the recent association between microcephaly and Zika virus. Assessing the quality of data sources can guide surveillance programs as they focus their data collection efforts. The Utah Birth Defect Network (UBDN) has monitored microcephaly by data sources since 2003. The objective of this study was to examine the impact of reporting sources for microcephaly surveillance.
METHODS: All reported cases of microcephaly among Utah mothers from 2003 to 2013 were clinically reviewed and confirmed. The UBDN database was linked to state vital records and hospital discharge data for analysis. Reporting sources were analyzed for positive predictive value and sensitivity.
RESULTS: Of the 477 reported cases of microcephaly, 251 (52.6%) were confirmed as true cases. The UBDN identified 94 additional cases that were reported to the surveillance system as another birth defect, but were ultimately determined to be true microcephaly cases. The prevalence for microcephaly based on the UBDN medical record abstraction and clinical review was 8.2 per 10,000 live births. Data sources varied in the number and accuracy of reporting, but a case was more likely to be a true case if identified from multiple sources than from a single source.
CONCLUSION: While some reporting sources are more likely to identify possible and true microcephaly cases, maintaining a multiple source methodology allows for more complete case ascertainment. Surveillance programs should conduct periodic assessments of data sources to ensure their systems are capturing all possible birth defects cases. Birth Defects Research (Part A) 106:983-988, 2016.
© 2016 Wiley Periodicals, Inc. © 2016 Wiley Periodicals, Inc.

Entities:  

Keywords:  Utah; birth defects; hospital discharge data; microcephaly; quality assessment; reporting

Mesh:

Year:  2016        PMID: 27891786      PMCID: PMC5569316          DOI: 10.1002/bdra.23593

Source DB:  PubMed          Journal:  Birth Defects Res A Clin Mol Teratol        ISSN: 1542-0752


  9 in total

1.  Random error and undercounting in birth defects surveillance data: implications for inference.

Authors:  Adolfo Correa-Villaseñor; Glen A Satten; Henry Rolka; Peter Langlois; Owen Devine
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2003-09

2.  The surveillance of birth defects: the usefulness of the revised US standard birth certificate.

Authors:  M L Watkins; L Edmonds; A McClearn; L Mullins; J Mulinare; M Khoury
Journal:  Am J Public Health       Date:  1996-05       Impact factor: 9.308

3.  The methodology of the Utah Birth Defect Network: congenital heart defects as an illustration.

Authors:  Marcia Feldkamp; Lynne Macleod; Luciana Young; Kara Lecheminant; John C Carey
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2005-10

4.  Birth defects surveillance in Florida: infant death certificates as a case ascertainment source.

Authors:  Jean Paul Tanner; Jason L Salemi; Kimberlea W Hauser; Jane A Correia; Sharon M Watkins; Russell S Kirby
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2010-09-14

5.  Sensitivity of birth certificate reports of birth defects in Atlanta, 1995-2005: effects of maternal, infant, and hospital characteristics.

Authors:  Sheree L Boulet; Mikyong Shin; Russell S Kirby; David Goodman; Adolfo Correa
Journal:  Public Health Rep       Date:  2011 Mar-Apr       Impact factor: 2.792

6.  The influence of misclassification bias on the reported rates of congenital anomalies on the birth certificates for West Virginia--a consequence of an open-ended query.

Authors:  Ji Li; Shayhan Robbins; Steven H Lamm
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2013-03-01

7.  Bias in congenital malformations information from the birth certificate.

Authors:  A C Hexter; J A Harris
Journal:  Teratology       Date:  1991-08

8.  Evaluating false positives in two hospital discharge data sets of the Birth Defects Monitoring Program.

Authors:  F A Callif-Daley; C A Huether; L D Edmonds
Journal:  Public Health Rep       Date:  1995 Mar-Apr       Impact factor: 2.792

9.  Assessing the Practices of Population-Based Birth Defects Surveillance Programs Using the CDC Strategic Framework, 2012.

Authors:  Cara T Mai; Adolfo Correa; Russell S Kirby; Deborah Rosenberg; Michael Petros; Michael C Fagen
Journal:  Public Health Rep       Date:  2015 Nov-Dec       Impact factor: 2.792

  9 in total
  2 in total

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

Authors:  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; Mary K Ethen; Sook Ja Cho; MaryAnn Evans; Rebecca F Liberman; Jane Fornoff; Marilyn L Browne; Rachel E Rutkowski; Amy E Nance; Marlene Anderka; Deborah J Fox; Amy Steele; Glenn Copeland; Paul A Romitti; Cara T Mai
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2016-11

2.  EUROlinkCAT protocol for a European population-based data linkage study investigating the survival, morbidity and education of children with congenital anomalies.

Authors:  Joan K Morris; Ester Garne; Maria Loane; Ingeborg Barisic; James Densem; Anna Latos-Bieleńska; Amanda Neville; Anna Pierini; Judith Rankin; Anke Rissmann; Hermien de Walle; Joachim Tan; Joanne Emma Given; Hugh Claridge
Journal:  BMJ Open       Date:  2021-06-28       Impact factor: 2.692

  2 in total

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