The muscular Dystrophy Surveillance Tracking and Research Network (MD STARnet): surveillance methodology. Academic Article uri icon

Overview

abstract

  • BACKGROUND: This report focuses on the common protocol developed by the Muscular Dystrophy Surveillance Tracking and Research Network (MD STARnet) for population-based surveillance of Duchenne and Becker muscular dystrophy (DBMD) among 4 states (Arizona, Colorado, Iowa, and New York). METHODS: The network sites have developed a case definition and surveillance protocol along with software applications for medical record abstraction, clinical review, and pooled data. Neuromuscular specialists at each site review the pooled data to determine if a case meets the case criteria. Sources of potential cases of DBMD include neuromuscular specialty clinics, service sites for children with special healthcare needs, and hospital discharge databases. Each site also adheres to a common information assurance protocol. RESULTS: A population-based surveillance system for DBMD was created and implemented in participating states. CONCLUSIONS: The development and implementation of the population-based system will allow for the collection of information that is intended to provide a greater understanding of DBMD prevalence and health outcomes.

publication date

  • November 1, 2006

Research

keywords

  • Abstracting and Indexing
  • Clinical Protocols
  • Data Collection
  • Muscular Dystrophy, Duchenne
  • Population Surveillance

Identity

PubMed Central ID

  • PMC5863910

Scopus Document Identifier

  • 33751174484

Digital Object Identifier (DOI)

  • 10.1002/bdra.20279

PubMed ID

  • 17036307

Additional Document Info

volume

  • 76

issue

  • 11