Literature DB >> 21470087

Development of clinical-quality registries in Australia: the way forward.

Sue M Evans1, Ian A Scott, Niall P Johnson, Peter A Cameron, John J McNeil.   

Abstract

Australia is developing a national performance framework aimed at measuring health outcomes across the health system. Clinical registries provide a clinically credible means of monitoring health care processes and outcomes, yet only five Australian registries currently have national coverage. At a national level, clinical registry development should be prioritised to target conditions or procedures that are suspected of being associated with large variations in processes or outcomes of care and that impact significantly on health care costs and patient morbidity. Registries should also aim to capture information across care interfaces and to monitor the medium and long-term safety and effectiveness of specific devices, procedures and drugs. ©The Medical Journal of Australia 2011

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Year:  2011        PMID: 21470087     DOI: 10.5694/j.1326-5377.2011.tb03007.x

Source DB:  PubMed          Journal:  Med J Aust        ISSN: 0025-729X            Impact factor:   7.738


  22 in total

1.  Better outcomes for hospitalized patients with TIA when in stroke units: An observational study.

Authors:  Dominique A Cadilhac; Joosup Kim; Natasha A Lannin; Christopher R Levi; Helen M Dewey; Kelvin Hill; Steven Faux; Nadine E Andrew; Monique F Kilkenny; Rohan Grimley; Amanda G Thrift; Brenda Grabsch; Sandy Middleton; Craig S Anderson; Geoffrey A Donnan
Journal:  Neurology       Date:  2016-05-04       Impact factor: 9.910

2.  Clinical quality registries: engaging effectiveness data for quality improvement.

Authors:  Rob G Stirling
Journal:  Am J Public Health       Date:  2014-10-16       Impact factor: 9.308

3.  The Victorian Lung Cancer Registry pilot: improving the quality of lung cancer care through the use of a disease quality registry.

Authors:  Rob G Stirling; S M Evans; P McLaughlin; M Senthuren; J Millar; J Gooi; L Irving; P Mitchell; A Haydon; J Ruben; M Conron; T Leong; N Watkins; J J McNeil
Journal:  Lung       Date:  2014-06-08       Impact factor: 2.584

4.  In Defense of the International Collaboration of Breast Registry Activities (ICOBRA).

Authors:  Rod Cooter; Richard Barnett; Anand Deva; Mark R Magnusson; John McNeil; Graeme Perks; Hinne Rakhorst; Charles Verheyden
Journal:  Aesthet Surg J       Date:  2016-04-06       Impact factor: 4.283

5.  Improving outcomes for hospital patients with critical bleeding requiring massive transfusion: the Australian and New Zealand Massive Transfusion Registry study methodology.

Authors:  J C Oldroyd; K M Venardos; N J Aoki; A J Zatta; Z K McQuilten; L E Phillips; N Andrianopoulos; D J Cooper; P A Cameron; J P Isbister; E M Wood
Journal:  BMC Res Notes       Date:  2016-10-06

6.  Design and development of the Australian and New Zealand (ANZ) myeloma and related diseases registry.

Authors:  Krystal Bergin; Elizabeth Moore; Zoe McQuilten; Erica Wood; Bradley Augustson; Hilary Blacklock; Joy Ho; Noemi Horvath; Tracy King; John McNeil; Peter Mollee; Hang Quach; Christopher M Reid; Brian Rosengarten; Patricia Walker; Andrew Spencer
Journal:  BMC Med Res Methodol       Date:  2016-11-09       Impact factor: 4.615

7.  Electronic health records: a new tool to combat chronic kidney disease?

Authors:  Sankar D Navaneethan; Stacey E Jolly; John Sharp; Anil Jain; Jesse D Schold; Martin J Schreiber; Joseph V Nally
Journal:  Clin Nephrol       Date:  2013-03       Impact factor: 0.975

8.  Dispelling myths about rare disease registry system development.

Authors:  Matthew Bellgard; Christophe Beroud; Kay Parkinson; Tess Harris; Segolene Ayme; Gareth Baynam; Tarun Weeramanthri; Hugh Dawkins; Adam Hunter
Journal:  Source Code Biol Med       Date:  2013-10-16

9.  Impact of clinical registries on quality of patient care and health outcomes: protocol for a systematic review.

Authors:  Dewan Md Emdadul Hoque; Varuni Kumari; Rasa Ruseckaite; Lorena Romero; Sue M Evans
Journal:  BMJ Open       Date:  2016-04-26       Impact factor: 2.692

10.  Development of South Australian-Victorian Prostate Cancer Health Outcomes Research Dataset.

Authors:  Rasa Ruseckaite; Kerri Beckmann; Michael O'Callaghan; David Roder; Kim Moretti; John Zalcberg; Jeremy Millar; Sue Evans
Journal:  BMC Res Notes       Date:  2016-01-22
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