!"#$%#&'()*$+,-.#/'.0"1!"0/"'2)3#",%.0")45'-.6)7#"-.6)8#99(,:;)))!! "#$$%&&'!"()%*+,-(.)!/0! Objective 1: Conduct population-based surveillance and research of Duchenne/Becker muscular dystrophy Activity 1.1. Examine data utility and quality of existing DBMD data set for public health practice. Participate with other MD STARnet sites through a new or existing committee to examine data quality issues associated with data collection, management and analysis of current MD STARnet data for DBMD. Activity 1.2. Provide information to CDC regarding site experiences with surveillance for DBMD as part of a CDC assessment of MD STARnet. Activity 1.3. Refine the number of clinical data variables collected on individuals who have DBMD to include a maximum of 75-100 variables that yield reliable, relevant information that informs public health practice. Activity 1.4. Conduct medical record abstraction of new and follow-up DBMD cases using the reduced number of variables during year 1 of the funding period. Activity 1.5. Design and conduct an interview to determine healthcare transition and other life stage issues affecting individuals with DBMD and their families. Objective 2: Design and implement population-based surveillance on seven additional muscular dystrophies (Myotonic, Congenital, Limb-Girdle, Emery-Dreifuss, Facioscapulohumeral, Distal, and Oculopharyngeal) Activity 2.1. Through assessment of the existing MD STARnet system, modify or develop: (a) Protocols for ascertaining cases;(b) Case definitions;(c) Data collection instruments to collect information on prevalence, demographics, healthcare coverage, and locations of care;(d) Comprehensive quality control procedures to address data quality issues associated with data collection, management and analysis. Activity 2.2. Develop or maintain partnerships with local clinics and stakeholders Activity 2.3. Conduct medical record abstraction for seven additional muscular dystrophies once during Y2-Y3 Objective 3: Assess methodology for conducting population-based surveillance for the nine muscular dystrophies Activity 3.1. Under the leadership of the national coordinating center, collaborate with other sites to produce a summary report assessing the expansion of surveillance to other muscular dystrophies. The summary should include: (a) Methods used;(b) Lessons learned;(c) Strengths;(d) Challenges;(e) Costs;(f) Barriers;(g) Recommendations for conducting muscular dystrophy and rare disease surveillance programs. Objective 4: Analyze data, publish articles, and disseminate reports using information collected on MD STARnet from 2002-2011 Activity 4.1. Propose and lead a minimum of three manuscripts;extensively collaborate on three other manuscripts. Activity 4.2. Participate in at least one PI meeting per year in Atlanta, for investigators to present study findings.

Public Health Relevance

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Agency
National Institute of Health (NIH)
Institute
Centers for Disease Control and Prevention (NCBDD)
Type
Research Project--Cooperative Agreements (U01)
Project #
5U01DD000830-02
Application #
8329374
Study Section
Special Emphasis Panel (ZDD1-CJM (07))
Project Start
2011-09-01
Project End
2014-08-31
Budget Start
2012-09-01
Budget End
2013-08-31
Support Year
2
Fiscal Year
2012
Total Cost
$550,000
Indirect Cost
$186,964
Name
University of Arizona
Department
Pediatrics
Type
Schools of Medicine
DUNS #
806345617
City
Tucson
State
AZ
Country
United States
Zip Code
85721