Disinvestment and Value-Based Purchasing Strategies for Pharmaceuticals: An International Review
Open accessAbstract
Pharmaceutical expenditure has increased rapidly across many Organisation for Economic Cooperation and Development (OECD) countries over the past three decades. This growth is an increasing concern for governments and other third-party payers seeking to provide equitable and comprehensive healthcare within sustainable budgets. In order to create headroom for increasing utilisation, and to fund new high-cost therapies, there is an active push to 'disinvest' from low-value drugs. The aim of this article is to review how reimbursement policy decision makers have sought to partially or completely disinvest from drugs in a range of OECD countries (UK, France, Canada, Australia and New Zealand) where they are publicly funded or subsidised. We employed a systematic literature search strategy and the incorporation of grey literature known to the authorship team. We canvass key policy instruments from each country to outline key approaches to the identification of candidate drugs for disinvestment assessment (passive approaches vs. more active approaches); methods of disinvestment and value-based purchasing (de-listing, restricting treatment, price or reimbursement rate reductions, encouraging generic prescribing); lessons learnt from the various approaches; the potential role of coverage with evidence development; and the need for careful stakeholder management. Dedicated sections are provided with detailed coverage of policy approaches (with drug examples) from each country. Historically, countries have relied on 'passive disinvestment'; however, due to (1) the availability of new cost-effectiveness evidence, or (2) 'leakage' in drug utilisation, or (3) market failure in terms of price competition, there is an increasing focus towards 'active disinvestment'. Isolating low-value drugs that would create headroom for innovative new products to enter the market is also motivating disinvestment efforts by multiple parties, including industry. Historically, disinvestment has mainly taken the form of price reductions, especially when market failures are perceived to exist, and restricting treatment to subpopulations, particularly when a drug is no longer considered value for money. There is considerable experimentation internationally in mechanisms for disinvestment and the opportunity for countries to learn from each other. Ongoing evaluation of disinvestment strategies is essential, and ought to be reported in the peer-reviewed literature.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Previous studies have described that obtaining support for disinvestment is very difficult because stakeholders often lack the will to support disinvestment due to limited perceived value and resistance to losing therapy options.
“it has also been described in previous studies that obtaining support for disinvestment is very difficult as stakeholders often lack the will to support disinvestment because of limited perceived value of disinvestment, which may take some time to realize, and their resistance to immediately “losing” therapy options [12, 35].”
From What influences the outcome of active disinvestment processes in healthcare? A qualitative interview study on five recent cases of active disinvestment (2021) · cites this paper as [12]
Conditional reimbursement has been described as creating a wedge effect, i.e. giving suppliers a "foot in the door" while creating challenges for decision-makers when the reversal of (conditional) reimbursement is warranted.
“conditional reimbursement has also been described as creating a wedge effect, i.e. giving suppliers a “foot in the door” while creating challenges for decision-makers when the reversal of (conditional) reimbursement is warranted [12].”
From What influences the outcome of active disinvestment processes in healthcare? A qualitative interview study on five recent cases of active disinvestment (2021) · cites this paper as [12]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
No references could be resolved yet.
Research works printed but not linked: 59
- Godman B, Malmstrom RE, Diogene E, Gray A, Jayathissa S, Timoney A et al. Are new models needed to optimize the utilization of new medicines to sustain healthcare systems? Expert review of clinical pharmacology. 2015;8(1):77-94.
- Garattini S, Bertele' V, Godman B, Haycox A, Wettermark B, Gustafsson LL et al. Enhancing the rational use of new medicines across European health care systems. European Journal of Clinical Pharmacology. 2008;64(12):1137-8.
- Cheema PK, Gavura S, Migus M, Godman B, Yeung L, Trudeau ME. International variability in the reimbursement of cancer drugs by publically funded drug programs. Current oncology. 2012;19(3):e165-76.
- MacKean G, Noseworthy T, Elshaug AG, Leggett L, Littlejohns P, Berezanski J et al. Health technology reassessment: the art of the possible. International journal of technology assessment in health care. 2013;29(4):418-23.
- Elshaug AG, Hiller JE, Tunis SR, Moss JR. Challenges in Australian policy processes for disinvestment from existing, ineffective health care practices. Australian and New Zealand Health Policy. 2007;4:23.
- Godman B AF, Guerra Júnior AA, Alvarez-Madrazo S , Faridah Aryani MY, Bishop I et al. Initiatives among Authorities to Improve the Quality and Efficiency of Prescribing and the Implications. Jn Pharma Care Health Sys. 2014;1(3):15.
- Wagner AK, Graves AJ, Reiss SK, Lecates R, Zhang F, Ross-Degnan D. Access to care and medicines, burden of health care expenditures, and risk protection: results from the World Health Survey. Health policy. 2011;100(2-3):151-8. doi:10.1016/j.healthpol.2010.08.004. · DOI
- Barber SL, Huang B, Santoso B, Laing R, Paris V, Wu C. The reform of the essential medicines system in China: a comprehensive approach to universal coverage. Journal of global health. 2013;3(1):010303. doi:10.7189/jogh.03.010303. · DOI
- Li X, Zhang W. The impacts of health insurance on health care utilization among the older people in China. Social science & medicine (1982). 2013;85:59-65. doi:10.1016/j.socscimed.2013.02.037. · DOI
- Van Minh H, Kim Phuong NT, Saksena P, James CD, Xu K. Financial burden of household out-of pocket health expenditure in Viet Nam: findings from the National Living Standard Survey 2002-2010. Social science & medicine (1982). 2013;96:258-63. doi:10.1016/j.socscimed.2012.11.028. · DOI
- Caires de Souza AL, de Assis Acurcio F, Guerra Junior AA, Rezende Macedo do Nascimento RC, Godman B, Diniz LM. Insulin glargine in a Brazilian state: should the government disinvest? An assessment based on a systematic review. Applied health economics and health policy. 2014;12(1):19-32. doi:10.1007/s40258-013- 0073-6. · DOI
- Sun Q, Santoro MA, Meng Q, Liu C, Eggleston K. Pharmaceutical policy in China. Health affairs (Project Hope). 2008;27(4):1042-50. doi:10.1377/hlthaff.27.4.1042. · DOI
- Li Y, Xu J, Wang F, Wang B, Liu L, Hou W et al. Overprescribing in China, driven by financial incentives, results in very high use of antibiotics, injections, and corticosteroids. Health affairs (Project Hope). 2012;31(5):1075-82. doi:10.1377/hlthaff.2010.0965. · DOI
- Tang S, Tao J, Bekedam H. Controlling cost escalation of healthcare: making universal health coverage sustainable in China. BMC public health. 2012;12 Suppl 1:S8. doi:10.1186/1471-2458-12-s1-s8. · DOI
- Mao W TS, Chen W. Does perverse economic incentive lead to the irrational uses of medicines? Expert Rev Pharmacoeconomics Outcomes Res 2013;13(6):693-96.
- Reynolds L, McKee M. Serve the people or close the sale? Profit-driven overuse of injections and infusions in China's market-based healthcare system. The International journal of health planning and management. 2011;26(4):449-70. doi:10.1002/hpm.1112. · DOI
- Zeng W, Finlayson AE, Shankar S, Bruyn W, Godman B. Prescribing efficiency of proton pump inhibitors in China: influence and future directions. BMC health services research. 2015;15(1):11. doi:10.1186/s12913- 014-0638-6. · DOI
- Zeng W, Zhen J, Feng M, Campbell SM, Finlayson AE, Godman B. Analysis of the influence of recent reforms in China: cardiovascular and cerebrovascular medicines as a case history to provide future direction. Journal of comparative effectiveness research. 2014;3(4):371-86. doi:10.2217/cer.14.28. · DOI
- Garner S, Littlejohns P. Disinvestment from low value clinical interventions: NICEly done? Bmj. 2011;343:d4519.
- Haas M, Hall J, Viney R, Gallego G. Breaking up is hard to do: why disinvestment in medical technology is harder than investment. Australian health review : a publication of the Australian Hospital Association. 2012;36(2):148-52.
- Polisena J, Clifford T, Elshaug A, Mitton C, Russell E, Skidmore B. Case studies that illustrate disinvestment and resource allocation decision-making processes in health care: a systematic review. International journal of technology assessment in health care. 2013;29(2):174-84.
- Elshaug AG, Moss JR, Littlejohns P, Karnon J, Merlin TL, Hiller JE. Identifying existing health care services that do not provide value for money. Medical Journal of Australia. 2009;190(5):269-73.
- Sermet C, Andrieu V, Godman B, Van Ganse E, Haycox A, Reynier JP. Ongoing pharmaceutical reforms in France: implications for key stakeholder groups. Applied health economics and health policy. 2010;8(1):7-24.
- Nova Scotia Canada. Nova Scotia Pharmacare. Nova Scotia Canada, Canada. 2015. http://novascotia.ca/dhw/pharmacare/atlantic-common-drug-review.asp#AEAC. Accessed 28 January 2015.
- Fisher ES, Wennberg DE, Stukel TA, Gottlieb DJ, Lucas FL, Pinder EL. The implications of regional variations in Medicare spending. Part 1: the content, quality, and accessibility of care. Annals of internal medicine. 2003;138(4):273-87.
- Pharmaceutical Benefits Advisory Committee. PBAC Recommendations from the Post-Market Review of Pharmaceutical Benefits Scheme anti-dementia drugs to treat Alzheimers Disease, Ratified Minutes of the December 2012 Special PBAC meeting, Item 4. Canberra: DoH; December 2012.
- Thornhill MH, Dayer MJ, Forde JM, Corey GR, Chu VH, Couper DJ et al. Impact of the NICE guideline recommending cessation of antibiotic prophylaxis for prevention of infective endocarditis: before and after study. British Medical Journal. 2011;342:d2392.
- Pichetti S, Sermet C, Godman B, Campbell SM, Gustafsson LL. Multilevel analysis of the influence of patients' and general practitioners' characteristics on patented versus multiple-sourced statin prescribing in France. Applied health economics and health policy. 2013;11(3):205-18.
- Garrison LP, Jr., Towse A, Briggs A, de Pouvourville G, Grueger J, Mohr PE et al. Performance-based risk- sharing arrangements-good practices for design, implementation, and evaluation: report of the ISPOR good practices for performance-based risk-sharing arrangements task force. Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research. 2013;16(5):703-19.
- Australian Government Department of Health and Ageing (DoHA). Review of Anticoagulation Therapies in Atrial Fibrillation. Canberra: DoHA; 2012.
- Godman B, Bishop I, Finlayson AE, Campbell S, Kwon HY, Bennie M. Reforms and initiatives in Scotland in recent years to encourage the prescribing of generic drugs, their influence and implications for other countries. Expert review of pharmacoeconomics & outcomes research. 2013;13(4):469-82.
- Pharmaceutical Benefits Advisory Committee. Public summary document: PBAC review of bDMARDs for the treatment of severe active rheumatoid athritis. Canberra: DoHA; December 2009.
- Clarke PM, Fitzgerald EM. Expiry of patent protection on statins: effects on pharmaceutical expenditure in Australia. Medical Journal of Australia. 2010;192(11):633-6.
- Bulfone L. High prices for generics in Australia -more competition might help. Australian Health Review. 2009;33(2):200-14.
- Morgan S, Hanley G, McMahon M, Barer M. Influencing Drug Prices through Formulary-Based Policies: Lessons from New Zealand. Healthcare policy = Politiques de sante. 2007;3(1):e121-40.
- Godman B, Wettermark B, van Woerkom M, Fraeyman J, Alvarez-Madrazo S, Berg C et al. Multiple policies to enhance prescribing efficiency for established medicines in Europe with a particular focus on demand-side measures: findings and future implications. Frontiers in pharmacology. 2014;5:106.
- Pichetti S, Sorasith C, Sermet C. Analysis of the impact of removing mucolytics and expectorants from the list of reimbursable drugs on prescription rates: a time-series analysis for France 1998-2010. Health policy. 2011;102(2-3):159-69.
- Riou Franca L, Vidal C, Bourechak N, Jeunne PL, Deville GS, Massol J. A cohort study of therapeutic prescriptions after the end of phytotherapy drug reimbursement by French Social Security. Pharmacoepidemiology and drug safety. 2013;22(7):760-8.
- Vitry A, Roughead E. Managed entry agreements for pharmaceuticals in Australia. Health policy. 2014;117(3):345-52.
- Carlson JJ, Sullivan SD, Garrison LP, Neumann PJ, Veenstra DL. Linking payment to health outcomes: a taxonomy and examination of performance-based reimbursement schemes between healthcare payers and manufacturers. Health policy. 2010;96(3):179-90.
- Stafinski T, McCabe CJ, Menon D. Funding the unfundable: mechanisms for managing uncertainty in decisions on the introduction of new and innovative technologies into healthcare systems. Pharmacoeconomics. 2010;28(2):113-42.
- Claxton K, Palmer S, Longworth L, Bojke L, Griffin S, McKenna C et al. Informing a decision framework for when NICE should recommend the use of health technologies only in the context of an appropriately designed programme of evidence development. Health technology assessment. 2012;16(46):1-323.
- Raftery J. Costly failure of a risk sharing scheme. British Medical Journal. 2010;340:1672.
- Boggild M, Palace J, Barton P, Ben-Shlomo Y, Bregenzer T, Dobson C et al. Multiple sclerosis risk sharing scheme: two year results of clinical cohort study with historical comparator. British Medical Journal. 2009;339:b4677.
- Hollingworth W, Chamberlain C. Re: Do NICE's recommendations for disinvestment add up? British Medical Journal. 2011;343:d4519.
- Chevreul K, Durand-Zaleski I, Bahrami S, Hernández-Quevedo C, Mladovsky P. France: health system review. Health Systems in Transition, European Observatory on Health Systems and Policies. 2010;12(6).
- Weill A, Paita M, Tuppin P, Fagot JP, Neumann A, Simon D et al. Benfluorex and valvular heart disease: a cohort study of a million people with diabetes mellitus. Pharmacoepidemiology and drug safety. 2010;19(12):1256-62. doi:10.1002/pds.2044. · DOI
- Harris CM, Scrivener G. Fundholders' prescribing costs: the first five years. British Medical Journal. 1996;313(7071):1531-4.
- Rawlins M. In pursuit of quality: the National Institute for Clinical Excellence. Lancet. 1999;353(9158):1079-82.
- Ford JA, Waugh N, Sharma P, Sculpher M, Walker A. NICE guidance: a comparative study of the introduction of the single technology appraisal process and comparison with guidance from Scottish Medicines Consortium. British Medical Journal Open. 2012;2(1):e000671.
- McGinn D, Godman B, Lonsdale J, Way R, Wettermark B, Haycox A. Initiatives to enhance the quality and efficiency of statin and PPI prescribing in the UK: impact and implications. Expert review of pharmacoeconomics & outcomes research. 2010;10(1):73-85.
- Martin A, Godman B, Miranda J, Tilstone J, Saleem N, Olsson E et al. Measures to improve angiotensin receptor blocker prescribing efficiency in the UK: findings and implications. Journal of comparative effectiveness research. 2014;3(1):41-51.
- Godman B, Shrank W, Andersen M, Berg C, Bishop I, Burkhardt T et al. Comparing policies to enhance prescribing efficiency in Europe through increasing generic utilization: changes seen and global implications. Expert review of pharmacoeconomics & outcomes research. 2010;10(6):707-22.
- Duerden MG, Hughes DA. Generic and therapeutic substitutions in the UK: are they a good thing? British journal of clinical pharmacology. 2010;70(3):335-41.
- Ferner RE, Lenney W, Marriott JF. Controversy over generic substitution. Bmj. 2010;340:c2548.
- Canadian Agency for Drugs and Technologies in Health (CADTH). About the Common Drug Review. CADTH, Canada. 2015. http://www.cadth.ca/en/products/cdr/cdr-overview. Accessed 28 January 2015.
- O'Donnell JC, Pham SV, Pashos CL, Miller DW, Smith MD. Health technology assessment: lessons learned from around the world -an overview. Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research. 2009;12 Suppl 2:S1-5. doi:10.1111/j.1524-4733.2009.00550.x. · DOI
- Gallego G, Haas M, Hall J, Viney R. Reducing the use of ineffective health care interventions: an Evidence Check rapid review brokered by the Sax Institute (www.saxinstitute.org.au), for the NSW Treasury. 2010.
- Australian Government Department of Health (DoH). Post-market Review of the Life Saving Drugs Programme (LSDP). DoH, Canberra. 2015. http://www.pbs.gov.au/info/reviews/life-saving-drugs. Accessed 20 January 2015. 100. Australian Government Department of Health (DoH). Schedule of Pharmaceutical Benefits, effective 1 January 2015 -31 January 2015. Canberra: DoH; 2015. 101. Australian Government Department of Health and Ageing (DoHA). The impact of PBS reform: report to parliament on the National Health Amendment (Pharmaceutical Benefits Scheme) Act 2007. Canberra: DoHA; 2010. 102. National Prescribing Service. Generic medicines are an equal choice, media release. NPS, Sydney. 2008. http://www.nps.org.au/__data/assets/pdf_file/0007/65527/Generic_medicines_are_an_equal_choice.pdf. Accessed 26 October 2011. 103. Medicare Australia. Practice incentives program: quality prescribing incentive guidelines. Canberra: Australian Department of Human Services; August 2011. 104. Pharmaceutical Benefits Pricing Authority. Policies, procedures and methods used in the recommendations for pricing of pharmaceutical products. Canberra: DoHA; 2009. 105. Australian Government Department of Health and Ageing (DoHA). Weighted Average Monthly Treatment Cost (WAMTC) users' manual. Canberra: DoHA; April 2009. 106. Duckett S, Willcox S. The Australian Health Care System. 4th ed. South Melbourne: Oxford University Press; 2011. 107. Australian Government Department of Health and Ageing (DoHA). Memorandum of Understanding between Medicines Australia and the Commonwealth of Australia. Canberra: DoHA; 6 May 2010. 108. Australian Government Department of Health and Ageing (DoHA). Pharmaceutical Benefits Scheme price disclosure: business rules. Canberra: DoHA; July 2007. 109. Australian Government Department of Health and Ageing (DoHA). Expanded and accelerated price disclosure: what's new? What's different? Canberra: DoHA; November 2010. 110. Medicare Australia. Bulletin Board, Autumn 2009. Canberra: Medicare Australia; 2009. 111. Viellaris R. Leftover drugs to be used on chemotherapy patients. The Courier-Mail. 2009. 112. Clinical Oncological Society of Australia and Medical Oncology Group of Australia and Haematology Society of Australia and New Zealand and Private Cancer Physicians of Australia. Joint position statement on intravenous chemotherapy supply program (ICSP) budget measure 2008. 2009. http://www.cosa.org.au/cosa_assets/files/About%20us%20- %20publications/Intravenous%20Chemotherapy%20Supply%20Program.pdf. 113. Department of Health and Ageing. Factsheet for the Efficient Funding of Chemotherapy Drugs. 2012. http://www.pbs.gov.au/info/publication/factsheets/shared/revised-arrangements-for-chemotherapy. Accessed 3 April 2012. 114. Ensor T. Transition to universal coverage in developing countries. In: Carrin G, Buse K, Heggenhougen K, Quah S, editors. Health Systems Policy, Finance and Organization. Oxford: Elsevier / Academic Press; 2009. 115. New Zealand Public Health and Disability Act 2000, (2000). 116. Pharmaceutical Management Agency (PHARMAC). Pharmaceutical Management Agency Annual Report for the year ended 30 June 2014. New Zealand: PHARMAC; 2014. 117. Grocott R. Applying Programme Budgeting Marginal Analysis in the health sector: 12 years of experience. Expert review of pharmacoeconomics & outcomes research. 2009;9(2):181-7. 118. Pharmaceutical Management Agency (PHARMAC). PHARMAC Annual Review 1995. New Zealand: PHARMAC; 1995. 119. Pharmaceutical Management Agency (PHARMAC). Notification: Proposal relating to sole supply of blood glucose meters and test strips approved. New Zealand: PHARMAC; 8 August 2012. 120. Allen + Clarke. Evaluation of the implementation of a decision to change the funding and supply of blood glucose meters and test strips. New Zealand: PHARMAC; September 2014.
Cited by
Sorted by citations
Rotteveel, A. H., Lambooij, M. S., van de Rijt, J. J. A., van Exel, J., Moons, K. G. M., & de Wit, G. A. (2021) · BMC Health Services Research · doi:10.1186/s12913-021-06298-3 · Cited by 16 · see citing works
- Authors
- Parkinson, B., Sermet, C., Clement, F., Crausaz, S., Godman, B., Garner, S., Choudhury, M., Pearson, S.-A., Viney, R., Lopert, R., & Elshaug, A. G.
- Affiliations
- University of Technology Sydney (AU)
- IRDES Institut de Recherche et Documentation en Économie de la Santé (FR)
- University of Calgary (CA)
- Pharmac (NZ)
- University of Strathclyde (GB)
- National Institute for Health and Care Excellence (GB)
- The University of Sydney (AU)
- George Washington University (US)
- Corresponding author
- Parkinson, Bonny
- Sermet, Catherine
- Clement, Fiona
- Crausaz, Steffan
- Godman, Brian
- Garner, Sarah
- Choudhury, Moni
- Pearson, Sallie-Anne
- Viney, Rosalie
- Lopert, Ruth
- Elshaug, Adam G.
- ORCID
- Venue
- PharmacoEconomics
- Published
- 2015-06-06
- Volume
- 33
- Issue
- 9
- Pages
- 905-924
- ISSN
- 1170-7690 (ISSN-L)
- 1179-2027
- OpenAlex
- W659344829
- Cited by
- 93
- References
- 0
- Citations by year
- 2026: 4 · 2025: 2 · 2024: 9 · 2023: 5 · 2022: 5 · 2021: 19 · 2020: 4 · 2019: 11 · 2018: 5 · 2017: 21 · 2016: 7 · 2015: 1
- FWCI
- 3.46
- Type
- journal article
- Language
- en
- Open access
- Licence
- www.springer.com/tdm (tdm)
- Locations
- PharmacoEconomics (publishedVersion)
- PubMed (publishedVersion)
- Strathprints: The University of Strathclyde institutional repository (University of Strathclyde) (acceptedVersion)
- RePEc: Research Papers in Economics (acceptedVersion)
- Funders
- National Health and Medical Research Council (627061, 571926, 1060407)
- HCF Research Foundation (Fellowship)
- Cancer Institute NSW (Harkness Fellowship)
- Topics
- Social Sciences › Economics, Econometrics and Finance › Economics and Econometrics › Pharmaceutical Economics and Policy
- Social Sciences › Economics, Econometrics and Finance › Economics and Econometrics › Health Systems, Economic Evaluations, Quality of Life
- Social Sciences › Economics, Econometrics and Finance › Finance › Healthcare Systems and Reforms
- Keywords
- value-based purchasing, pharmaceutical reimbursement policy, treatment limitations, discounts, generic prescribing, coverage with evidence development, market failure, pharmaceutical expenditure, stakeholder management, OECD countries
- MeSH terms
- Decision Making, Drug Utilization, Health Policy, Humans, Insurance, Health, Reimbursement, Drug Costs, Value-Based Purchasing, Organisation for Economic Co-Operation and Development
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review