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Learn about the efficient management of EHDI data and patient information to enhance services for infants with hearing loss and their families. Understand the importance of uniform state registries, national information databases, and tracking and follow-up systems. Discover how effective information management can contribute to measuring program quality and accountability.
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EHDI Information Management Les R. Schmeltz, MS, CCC-A Iowa
Looks like a simple, linear process: • Collect hospital information: • Identify hearing losses • Refer for early intervention services • Collect and report statistics
EHDI Data and Patient Information Management out Then a miracle occurs Start Good work, but I think we might need just a little more detail right here.
Joint Committee on Infant Hearing 2000 Position Statement • Uniform state registries and national information databases • Use of information generated
Uses of Information Management: • To improve services to infants and their families • To assess the quality of screening, evaluation and intervention • To facilitate collection of data on demographics of neonatal and infant hearing loss
Improving Services to Infants and Their Families • Multiple system components must be integrated • Each service provider participates • Tracking and follow-up • Monitoring of outcomes
Integrating Multiple System Components • Seamless system to infants and their families • Provider participation
Service Provider Participation • Hospitals and other birthing facilities • Primary care providers • Service providers • Early intervention and educational facilities
Tracking and Follow-Up • Timely and accurate description of services provided to each infant • Documents recommendations for follow-up and referral to other providers • Tracking
Monitoring of Outcomes • Effective information management used to promote program measurement and accountability • Factors contributing to delay in providing EHDI services • Measurement of quality indicators
Effective Information Management • Capable of aggregating data • Provides evaluation data • Centralized
Information Collection • Federal to state level • State to hospital & practitioner level • Hospital level
JCIH Quality Benchmarks & Quality Indicators • Benchmarks • Quality Indicators • Review process
CDC Pilot National Data Set • Number of live births • Number screened prior to discharge • Number screened before 1 month of age • Total number referred from initial or multiple screenings for audiologic evaluation
CDC Pilot National Data Set • Number with diagnostic audiological evaluation by 3 months of age • Number of children with permanent congenital hearing loss aged 0-7
CDC Pilot National Data Set • Hearing loss must be classified by type, degree and laterality • Average/median age in months of diagnosis of hearing loss • Number of infants receiving intervention by 6 months of age
Handouts: • JCIH Benchmarks and Quality Indicators • CDC Data Set Items