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This project evaluated the effects of providing caregivers of older adults proxy access to electronic patient portals and found that information exchange between caregivers and providers increased.
This project compared high and low intensity support for implementation of clinical decision support (CDS) and found that the low intensity support may be sufficient to help community health centers improve their use of CDS over a relatively short time period.
This project implemented clinical decision support and clinical messaging to improve clinician reporting of notifiable conditions to public health agencies.
This project evaluated the feasibility of implementing The Symptom Monitoring & Systematic Assessment in Young Survivors (SyMon-SAYS) in pediatric oncology clinics.
This project evaluated the CancerHelp® Talking Touchscreen, a low-literacy, multimedia information technology system that provides patient education on cancer diagnoses, treatment, support, side effects, prevention, and screening.
This project investigated and validated the prevalence and patterns of exception reporting among physicians participating in the Cardio-HIT collaborative, a practice-based research network. The overall objectives of this study were to assess the prevalence of exception reporting, document specific reasons for exceptions, evaluate the relative accuracy of reported exceptions, and identify the location of exception data in electronic health records.
The aim of this project is to understand how health IT can improve access to and management of laboratory information for patients with HIV and/or in need of cervical cancer screening.
Implements an emergency medical records system that will provide shared access to patient records across various community health care providers and incorporates electronic tools for prescription distribution and management.
Implemented an electronic health records system in a network of community health centers and developed a data warehouse to monitor, aggregate, and provide data for quality improvement.
The Indiana Network for Patient Care, an operational health information exchange (HIE) in central Indiana, is one of six AHRQ sponsored State and Regional demonstration projects begun in late 2004 and early 2005 to create State or regional HIEs.