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Use Of 13 Disease Registries In 5 Countries Demonstrates The Potential To Use Outcome Data To Improve Health Care's Value
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Medical Sciences. Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Medicinska och farmaceutiska vetenskapsområdet, centrumbildningar mm , UCR-Uppsala Clinical Research Center. (Kardiologi)
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2012 (English)In: Health Affairs, ISSN 1535-3702, E-ISSN 1535-3699, Vol. 31, no 1, 220-227 p.Article in journal (Refereed) Published
Abstract [en]

As health care systems worldwide struggle with rising costs, a consensus is emerging to refocus reform efforts on value, as determined by the evaluation of patient outcomes relative to costs. One method of using outcome data to improve health care value is the disease registry. An international study of thirteen registries in five countries (Australia, Denmark, Sweden, the United Kingdom, and the United States) suggests that by making outcome data transparent to both practitioners and the public, well-managed registries enable medical professionals to engage in continuous learning and to identify and share best clinical practices. The apparent result: improved health outcomes, often at lower cost. For example, we calculate that if the United States had a registry for hip replacement surgery comparable to one in Sweden that enabled reductions in the rates at which these surgeries are performed a second time to replace or repair hip prostheses, the United States would avoid $2 billion of an expected $24 billion in total costs for these surgeries in 2015.

Place, publisher, year, edition, pages
2012. Vol. 31, no 1, 220-227 p.
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Cardiac and Cardiovascular Systems
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URN: urn:nbn:se:uu:diva-166061DOI: 10.1377/hlthaff.2011.0762ISI: 000299309000027PubMedID: 22155485OAI: oai:DiVA.org:uu-166061DiVA: diva2:475240
Available from: 2012-01-10 Created: 2012-01-10 Last updated: 2017-12-08Bibliographically approved

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Lindahl, Bertil

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