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210907 r ||| eng |
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|a Gliklich, Richard E.
|e [editor]
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|a Tools and technologies for registry interoperability
|h Elektronische Ressource
|b registries for evaluating patient outcomes : a user's guide, 3rd edition, addendum 2
|c editors, Richard E. Gliklich, Michelle B. Leavy, Nancy A. Dreyer
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|a a user's guide
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|a 3rd edition, addendum 2
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|a Rockville, MD
|b Agency for Healthcare Research and Quality, U.S. Department of Health and Human Services
|c October 2019, 2019
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|a 1 PDF file (various pagings)
|b illustrations
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|a Includes bibliographical references
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|a United States
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|a Outcome Assessment, Health Care
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|a Medical Informatics
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|a Registries
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|a Leavy, Michelle B.
|e [editor]
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|a Dreyer, Nancy A.
|e [editor]
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|a United States
|b Agency for Healthcare Research and Quality
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|a L&M Policy Research
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|a Registries for evaluating patient outcomes
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|a eng
|2 ISO 639-2
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|b NCBI
|a National Center for Biotechnology Information
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|a AHRQ publication
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|u http://www.ncbi.nlm.nih.gov/books/NBK551879
|3 Volltext
|n NLM Bookshelf Books
|3 Volltext
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|a 610
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|a Addendum II 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 designed 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. The first addendum to the Third Edition of the Registries for Evaluating Patient Outcomes, 21st Century Patient Registries, EBook addendum, was published in March 2018
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