Systematic review on costs and resource use of randomized clinical trials shows a lack of transparent and comprehensive data
Autor: | Reem Alturki, Matthias Schwenkglenks, Christiane Pauli-Magnus, Neera Bhatnagar, Nadine Schur, Arnav Agarwal, Benjamin Kasenda, Benjamin Speich, Belinda von Niederhäusern, Matthias Briel, Lars G. Hemkens, Thomas Fürst |
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Přispěvatelé: | University of Zurich, Briel, Matthias |
Rok vydání: | 2018 |
Předmět: |
Empirical data
Epidemiology Cost-Benefit Analysis MEDLINE 610 Medicine & health Disclosure law.invention 03 medical and health sciences 0302 clinical medicine Resource (project management) Randomized controlled trial law Humans Medicine Operations management 030212 general & internal medicine Empirical evidence Randomized Controlled Trials as Topic Cost database business.industry Patient Selection 10060 Epidemiology Biostatistics and Prevention Institute (EBPI) Cost driver 030220 oncology & carcinogenesis Resource use business 2713 Epidemiology |
Zdroj: | Journal of Clinical Epidemiology. 96:1-11 |
ISSN: | 0895-4356 |
Popis: | Objectives Randomised clinical trials (RCTs) are costly. We aimed to provide a systematic overview of the available evidence on resource use and costs for RCTs to support budget planning. Study Design and Setting We systematically searched MEDLINE, EMBASE and HealthSTAR from inception until November 30, 2016 without language restrictions. We included any publication reporting empirical data on resource use and costs of RCTs and categorised them depending on whether they reported (i) resource and costs of all aspects at all study stages of an RCT (including conception, planning, preparation, conduct, and all tasks after the last patient has completed the RCT); (ii) on several aspects, (iii) on a single aspect (e.g. recruitment); or (iv) on overall costs for RCTs. Median costs of different recruitment strategies were calculated. Other results (e.g. overall costs) were listed descriptively. All cost data were converted into USD 2017. Results A total of 56 articles that reported on cost or resource use of RCTs were included. None of the articles provided empirical resource use and cost data for all aspects of an entire RCT. Eight articles presented resource use and cost data on several aspects (e.g. aggregated cost data of different drug development phases, site specific costs, selected cost components). Thirty-five articles assessed costs of one specific aspect of an RCT (i.e. 30 on recruitment; 5 others). The median costs per recruited patient were USD 409 (range: USD 41-6,990). Overall costs of an RCT, as provided in 16 articles, ranged from USD 43-103,254 per patient, and USD 0.2-611.5 Mio per RCT but the methodology of gathering these overall estimates remained unclear in 12 out of 16 articles (75%). Conclusion The usefulness of the available empirical evidence on resource use and costs of RCTs is limited. Transparent and comprehensive resource use and cost data are urgently needed to support budget planning for RCTs and help improve sustainability. |
Databáze: | OpenAIRE |
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