21st century patient registries Registries for evaluating patient outcomes: a user's guide: 3rd edition, addendum

This Addendum to the Third Edition of the Registries for Evaluating Patient Outcomes: A User's Guide was performed under a contract from the Agency for Healthcare Research and Quality (AHRQ) with the purpose of presenting new, emerging themes related to designing and conducting registries. Firs...

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Bibliographic Details
Corporate Authors: United States Agency for Healthcare Research and Quality, L&M Policy Research
Other Authors: Gliklich, Richard E. (Editor), Dreyer, Nancy A. (Editor), Leavy, Michelle B. (Editor), Christian, Jennifer (Editor)
Format: eBook
Language:English
Published: Rockville, MD Agency for Healthcare Research and Quality, U.S. Department of Health and Human Services 2018, February 2018
Series:AHRQ publication
Subjects:
Online Access:
Collection: National Center for Biotechnology Information - Collection details see MPG.ReNa
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520 |a This Addendum to the Third Edition of the Registries for Evaluating Patient Outcomes: A User's Guide was performed under a contract from the Agency for Healthcare Research and Quality (AHRQ) with the purpose of presenting new, emerging themes related to designing and conducting registries. First published in 2007, the User's Guide, with translations available in Chinese and Korean, serves as a reference for planning, developing, maintaining, and evaluating registries developed to collect data about patient outcomes. The second (2010) and third (2014) editions incorporated updates to existing topics and included new chapters on methodological and technological advances in registry science. We are pleased to present 5 new chapters that address emerging topics in registries, including increasing the focus on patients in registries including engaging with patients throughout the design and conduct of registries, methodological considerations for using digital health technologies, designing patient-centric studies, and building registry networks