Title |
Do different clinical evidence bases lead to discordant health-technology assessment decisions? An in-depth case series across three jurisdictions
|
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Published in |
ClinicoEconomics and Outcomes Research: CEOR, January 2013
|
DOI | 10.2147/ceor.s39624 |
Pubmed ID | |
Authors |
Daryl S Spinner, Julie Birt, Jeffrey W Walter, Lee Bowman, Josephine Mauskopf, Michael F Drummond, Catherine Copley-Merriman |
Abstract |
Health-technology assessment (HTA) plays an important role in informing drug-reimbursement decision-making in many countries. HTA processes for the Pharmaceutical Benefits Advisory Committee (PBAC) in Australia, the Common Drug Review (CDR) in Canada, and the National Institute for Health and Clinical Excellence (NICE) in England and Wales are among the most established in the world. In this study, we performed nine in-depth case studies to assess whether different clinical evidence bases may have influenced listing recommendations made by PBAC, CDR, and NICE. |
X Demographics
Geographical breakdown
Country | Count | As % |
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Canada | 1 | 100% |
Demographic breakdown
Type | Count | As % |
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Scientists | 1 | 100% |
Mendeley readers
Geographical breakdown
Country | Count | As % |
---|---|---|
Japan | 1 | 1% |
Canada | 1 | 1% |
Unknown | 69 | 97% |
Demographic breakdown
Readers by professional status | Count | As % |
---|---|---|
Student > Master | 16 | 23% |
Student > Ph. D. Student | 10 | 14% |
Researcher | 9 | 13% |
Student > Bachelor | 7 | 10% |
Student > Postgraduate | 5 | 7% |
Other | 13 | 18% |
Unknown | 11 | 15% |
Readers by discipline | Count | As % |
---|---|---|
Medicine and Dentistry | 25 | 35% |
Pharmacology, Toxicology and Pharmaceutical Science | 8 | 11% |
Social Sciences | 6 | 8% |
Economics, Econometrics and Finance | 6 | 8% |
Psychology | 2 | 3% |
Other | 8 | 11% |
Unknown | 16 | 23% |