Testing the feasibility of a National Spina Bifida Patient Registry

Birth Defects Res A Clin Mol Teratol. 2013 Jan;97(1):36-41. doi: 10.1002/bdra.23094. Epub 2012 Nov 2.

Abstract

Background: The purpose of this study was to describe the development and early implementation of a national spina bifida (SB) patient registry, the goal of which is to monitor the health status, clinical care, and outcomes of people with SB by collecting and analyzing patient data from comprehensive SB clinics.

Methods: Using a web-based, SB-specific electronic medical record, 10 SB clinics collected health-related information for patients diagnosed with myelomeningocele, lipomyelomeningocele, fatty filum, or meningocele. This information was compiled and de-identified for transmission to the Centers for Disease Control and Prevention (CDC) for quality control and analysis.

Results: A total of 2070 patients were enrolled from 2009 through 2011: 84.9% were younger than 18 years of age; 1095 were women; 64.2% were non-Hispanic white; 6.5% were non-Hispanic black or African American; and 24.2% were Hispanic or Latino. Myelomeningocele was the most common diagnosis (81.5%).

Conclusions: The creation of a National Spina Bifida Patient Registry partnership between the CDC and SB clinics has been feasible. Through planned longitudinal data collection and the inclusion of additional clinics, the data generated by the registry will become more robust and representative of the population of patients attending SB clinics in the United States and will allow for the investigation of patient outcomes.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adolescent
  • Centers for Disease Control and Prevention, U.S.
  • Child
  • Child, Preschool
  • Databases, Factual
  • Demography
  • Electronic Health Records
  • Feasibility Studies
  • Female
  • Health Status
  • Humans
  • Longitudinal Studies
  • Male
  • Meningomyelocele / diagnosis
  • Meningomyelocele / epidemiology*
  • Meningomyelocele / physiopathology
  • Population Surveillance / methods*
  • Registries*
  • Spinal Dysraphism / diagnosis
  • Spinal Dysraphism / epidemiology*
  • Spinal Dysraphism / physiopathology
  • United States
  • Young Adult

Supplementary concepts

  • Lipomyelomeningocele