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150223 r ||| eng |
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|a Medical tests
|h Elektronische Ressource
|b white paper series
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260 |
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|a Rockville, MD
|b Agency for Healthcare Research and Quality
|c 2009, 2009
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300 |
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|a 1 online resource
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|a Decision-analytic modeling to evaluate benefits and harms of medical tests : uses and limitations / Thomas A. Trikalinos, Uwe Siebert, and Joseph Lau -- Using the principles of randomized controlled trial design to guide test evaluation / Sarah J. Lord, Les Irwig, and Patrick M.M. Bossuyt -- Proposals for a phased evaluation of medical tests / Jeroen G. Lijmer, Mariska Leeflang, and Patrick M.M. Bossuyt -- Additional patient outcomes and pathways in evaluations of testing / Patrick M.M. Bossuyt and Kirsten McCaffery
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505 |
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|a Includes bibliographical references
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653 |
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|a Clinical Laboratory Techniques
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653 |
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|a Evaluation Studies as Topic
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710 |
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|a United States
|b Agency for Healthcare Research and Quality
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740 |
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|a Medical decision making
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|a eng
|2 ISO 639-2
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989 |
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|b NCBI
|a National Center for Biotechnology Information
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|a Title from Bookshelf document home page
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|u https://www.ncbi.nlm.nih.gov/books/NBK49465
|3 Volltext
|n NLM Bookshelf Books
|3 Volltext
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|a 610
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|a On May 28-29, 2008, AHRQ hosted a working meeting to discuss particularly challenging methodological issues in assessing medical tests. This working meeting included a group of investigators from the Evidence-based Practice Centers (EPCs), other experts in government, industry, and academia and also marked the launch of a Medical Test Evaluation Work Group within the EPC program. This Work Group was charged with developing guidance for conducting comparative effectiveness reviews of medical test technologies for the AHRQ Effective Health Care Program. A series of scientific publications (white papers) were commissioned for the meeting. These white papers have been published in Medical Decision Making and were intended to serve as background papers for the Work Group, which is expected to complete their draft guidance in the first part of 2010
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