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Published in: PharmacoEconomics 3/2016

Open Access 01-03-2016 | Original Research Article

Can the EVIDEM Framework Tackle Issues Raised by Evaluating Treatments for Rare Diseases: Analysis of Issues and Policies, and Context-Specific Adaptation

Authors: Monika Wagner, Hanane Khoury, Jacob Willet, Donna Rindress, Mireille Goetghebeur

Published in: PharmacoEconomics | Issue 3/2016

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Abstract

Background

The multiplicity of issues, including uncertainty and ethical dilemmas, and policies involved in appraising interventions for rare diseases suggests that multicriteria decision analysis (MCDA) based on a holistic definition of value is uniquely suited for this purpose. The objective of this study was to analyze and further develop a comprehensive MCDA framework (EVIDEM) to address rare disease issues and policies, while maintaining its applicability across disease areas.

Methods

Specific issues and policies for rare diseases were identified through literature review. Ethical and methodological foundations of the EVIDEM framework v3.0 were systematically analyzed from the perspective of these issues, and policies and modifications of the framework were performed accordingly to ensure their integration.

Results

Analysis showed that the framework integrates ethical dilemmas and issues inherent to appraising interventions for rare diseases but required further integration of specific aspects. Modification thus included the addition of subcriteria to further differentiate disease severity, disease-specific treatment outcomes, and economic consequences of interventions for rare diseases. Scoring scales were further developed to include negative scales for all comparative criteria. A methodology was established to incorporate context-specific population priorities and policies, such as those for rare diseases, into the quantitative part of the framework. This design allows making more explicit trade-offs between competing ethical positions of fairness (prioritization of those who are worst off), the goal of benefiting as many people as possible, the imperative to help, and wise use of knowledge and resources. It also allows addressing variability in institutional policies regarding prioritization of specific disease areas, in addition to existing uncertainty analysis available from EVIDEM.

Conclusion

The adapted framework measures value in its widest sense, while being responsive to rare disease issues and policies. It provides an operationalizable platform to integrate values, competing ethical dilemmas, and uncertainty in appraising healthcare interventions.
Appendix
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Literature
2.
3.
go back to reference Kole A, Faurisson F. Rare diseases social epidemiology: analysis of inequalities. Adv Exp Med Biol. 2010;686:223–50.CrossRefPubMed Kole A, Faurisson F. Rare diseases social epidemiology: analysis of inequalities. Adv Exp Med Biol. 2010;686:223–50.CrossRefPubMed
4.
go back to reference Beutler E. Lysosomal storage diseases: natural history and ethical and economic aspects. Mol Genet Metab. 2006;88(3):208–15.CrossRefPubMed Beutler E. Lysosomal storage diseases: natural history and ethical and economic aspects. Mol Genet Metab. 2006;88(3):208–15.CrossRefPubMed
5.
go back to reference Gomez-Rubio V, Lopez-Quilez A. Statistical methods for the geographical analysis of rare diseases. Adv Exp Med Biol. 2010;686:151–71.CrossRefPubMed Gomez-Rubio V, Lopez-Quilez A. Statistical methods for the geographical analysis of rare diseases. Adv Exp Med Biol. 2010;686:151–71.CrossRefPubMed
6.
go back to reference de la Paz MP, Villaverde-Hueso A, Alonso V, Janos S, Zurriaga O, Pollan M, et al. Rare diseases epidemiology research. Adv Exp Med Biol. 2010;686:17–39.CrossRefPubMed de la Paz MP, Villaverde-Hueso A, Alonso V, Janos S, Zurriaga O, Pollan M, et al. Rare diseases epidemiology research. Adv Exp Med Biol. 2010;686:17–39.CrossRefPubMed
7.
go back to reference Groft SC, de la Paz MP. Rare diseases—avoiding misperceptions and establishing realities: the need for reliable epidemiological data. Adv Exp Med Biol. 2010;686:3–14.CrossRefPubMed Groft SC, de la Paz MP. Rare diseases—avoiding misperceptions and establishing realities: the need for reliable epidemiological data. Adv Exp Med Biol. 2010;686:3–14.CrossRefPubMed
8.
go back to reference Fuller M, Meikle PJ, Hopwood JJ. Epidemiology of lysosomal storage diseases: an overview. In: Mehta A, Beck M, Sunder-Plassmann G, editors. Fabry disease: perspectives from 5 years of FOS. Oxford: Oxford PharmaGenesis; 2006. Fuller M, Meikle PJ, Hopwood JJ. Epidemiology of lysosomal storage diseases: an overview. In: Mehta A, Beck M, Sunder-Plassmann G, editors. Fabry disease: perspectives from 5 years of FOS. Oxford: Oxford PharmaGenesis; 2006.
9.
go back to reference Hughes DA, Tunnage B, Yeo ST. Drugs for exceptionally rare diseases: do they deserve special status for funding? QJM. 2005;98(11):829–36.CrossRefPubMed Hughes DA, Tunnage B, Yeo ST. Drugs for exceptionally rare diseases: do they deserve special status for funding? QJM. 2005;98(11):829–36.CrossRefPubMed
10.
go back to reference Kanters TA, de Sonneville-Koedoot C, Redekop WK, Hakkaart L. Systematic review of available evidence on 11 high-priced inpatient orphan drugs. Orphanet J Rare Dis. 2013;8(1):124.PubMedCentralCrossRefPubMed Kanters TA, de Sonneville-Koedoot C, Redekop WK, Hakkaart L. Systematic review of available evidence on 11 high-priced inpatient orphan drugs. Orphanet J Rare Dis. 2013;8(1):124.PubMedCentralCrossRefPubMed
11.
go back to reference Liu BC, He L, He G, He Y. A cross-national comparative study of orphan drug policies in the United States, the European Union, and Japan: towards a made-in-China orphan drug policy. J Public Health Policy. 2010;31(4):407–20.CrossRefPubMed Liu BC, He L, He G, He Y. A cross-national comparative study of orphan drug policies in the United States, the European Union, and Japan: towards a made-in-China orphan drug policy. J Public Health Policy. 2010;31(4):407–20.CrossRefPubMed
12.
go back to reference Loorand-Stiver L. Drugs for rare diseases: evolving trends in regulatory and health technology assessment perspectives. Environ Scan. 2013;2013(42):1–40. Loorand-Stiver L. Drugs for rare diseases: evolving trends in regulatory and health technology assessment perspectives. Environ Scan. 2013;2013(42):1–40.
13.
go back to reference Roll K, Stargardt T, Schreyogg J. Authorization and reimbursement of orphan drugs in an international comparison [in German]. Gesundheitswesen. 2011;73(8–9):504–14.CrossRefPubMed Roll K, Stargardt T, Schreyogg J. Authorization and reimbursement of orphan drugs in an international comparison [in German]. Gesundheitswesen. 2011;73(8–9):504–14.CrossRefPubMed
14.
go back to reference Tambuyzer E. Rare diseases, orphan drugs and their regulation: questions and misconceptions. Nat Rev Drug Discov. 2010;9(12):921–9.CrossRefPubMed Tambuyzer E. Rare diseases, orphan drugs and their regulation: questions and misconceptions. Nat Rev Drug Discov. 2010;9(12):921–9.CrossRefPubMed
15.
go back to reference Herder M. When everyone is an orphan: against adopting a U.S.-styled orphan drug policy in Canada. Acc Res. 2013;20(4):227–69.CrossRef Herder M. When everyone is an orphan: against adopting a U.S.-styled orphan drug policy in Canada. Acc Res. 2013;20(4):227–69.CrossRef
17.
go back to reference Winquist E, Bell CM, Clarke JT, Evans G, Martin J, Sabharwal M, et al. An evaluation framework for funding drugs for rare diseases. Value Health. 2012;15(6):982–6.CrossRefPubMed Winquist E, Bell CM, Clarke JT, Evans G, Martin J, Sabharwal M, et al. An evaluation framework for funding drugs for rare diseases. Value Health. 2012;15(6):982–6.CrossRefPubMed
18.
go back to reference Hughes-Wilson W, Palma A, Schuurman A, Simoens S. Paying for the Orphan Drug System: break or bend? Is it time for a new evaluation system for payers in Europe to take account of new rare disease treatments? Orphanet J Rare Dis. 2012;7:74.PubMedCentralCrossRefPubMed Hughes-Wilson W, Palma A, Schuurman A, Simoens S. Paying for the Orphan Drug System: break or bend? Is it time for a new evaluation system for payers in Europe to take account of new rare disease treatments? Orphanet J Rare Dis. 2012;7:74.PubMedCentralCrossRefPubMed
19.
go back to reference Paulden M, Stafinski T, Menon D, McCabe C. Value-based reimbursement decisions for orphan drugs: a scoping review and decision framework. Pharmacoeconomics. 2014;33(3):255–69.PubMedCentralCrossRef Paulden M, Stafinski T, Menon D, McCabe C. Value-based reimbursement decisions for orphan drugs: a scoping review and decision framework. Pharmacoeconomics. 2014;33(3):255–69.PubMedCentralCrossRef
20.
go back to reference Sussex J, Rollet P, Garau M, Schmitt C, Kent A, Hutchings A. A pilot study of multicriteria decision analysis for valuing orphan medicines. Value Health. 2013;16(8):1163–9.CrossRefPubMed Sussex J, Rollet P, Garau M, Schmitt C, Kent A, Hutchings A. A pilot study of multicriteria decision analysis for valuing orphan medicines. Value Health. 2013;16(8):1163–9.CrossRefPubMed
21.
go back to reference Clark S, Weale A. Social values in health priority setting: a conceptual framework. J Health Organ Manag. 2012;26(3):293–316.CrossRefPubMed Clark S, Weale A. Social values in health priority setting: a conceptual framework. J Health Organ Manag. 2012;26(3):293–316.CrossRefPubMed
22.
go back to reference Biron L, Rumbold B, Faden R. Social value judgments in healthcare: a philosophical critique. J Health Organ Manag. 2012;26(3):317–30.CrossRefPubMed Biron L, Rumbold B, Faden R. Social value judgments in healthcare: a philosophical critique. J Health Organ Manag. 2012;26(3):317–30.CrossRefPubMed
23.
go back to reference Daniels N, Sabin J. Limits to health care: fair procedures, democratic deliberation, and the legitimacy problem for insurers. Philos Public Aff. 1997;26(4):303–50.CrossRefPubMed Daniels N, Sabin J. Limits to health care: fair procedures, democratic deliberation, and the legitimacy problem for insurers. Philos Public Aff. 1997;26(4):303–50.CrossRefPubMed
25.
go back to reference Goetghebeur M, Wagner M, Khoury H, Levitt RJ, Erickson LJ, Rindress D. Evidence and value: impact on DEcisionMaking: the EVIDEM framework and potential applications. BMC Health Serv Res. 2008;8(1):270.PubMedCentralCrossRefPubMed Goetghebeur M, Wagner M, Khoury H, Levitt RJ, Erickson LJ, Rindress D. Evidence and value: impact on DEcisionMaking: the EVIDEM framework and potential applications. BMC Health Serv Res. 2008;8(1):270.PubMedCentralCrossRefPubMed
26.
go back to reference Goetghebeur M, Wagner M, Khoury H, Rindress D, Gregoire JP, Deal C. Combining multicriteria decision analysis, ethics and health technology assessment: applying the EVIDEM decision making framework to growth hormone for Turner syndrome patients. Cost Eff Resour Alloc. 2010;8(1):4.PubMedCentralCrossRefPubMed Goetghebeur M, Wagner M, Khoury H, Rindress D, Gregoire JP, Deal C. Combining multicriteria decision analysis, ethics and health technology assessment: applying the EVIDEM decision making framework to growth hormone for Turner syndrome patients. Cost Eff Resour Alloc. 2010;8(1):4.PubMedCentralCrossRefPubMed
27.
go back to reference Goetghebeur MM, Wagner M, Khoury H, Levitt RJ, Erickson LJ, Rindress D. Bridging health technology assessment (HTA) and efficient health care decision making with multicriteria decision analysis (MCDA): applying the EVIDEM framework to medicines appraisal. Med Decis Mak. 2012;32(2):376–88.CrossRef Goetghebeur MM, Wagner M, Khoury H, Levitt RJ, Erickson LJ, Rindress D. Bridging health technology assessment (HTA) and efficient health care decision making with multicriteria decision analysis (MCDA): applying the EVIDEM framework to medicines appraisal. Med Decis Mak. 2012;32(2):376–88.CrossRef
28.
go back to reference Tanios N, Wagner M, Tony M, Baltussen R, van Til J, Rindress D, et al. Which criteria are considered in healthcare decisions? Insights from an international survey of policy and clinical decision makers. Int J Technol Assess Health Care. 2013;29(4):456–65.CrossRefPubMed Tanios N, Wagner M, Tony M, Baltussen R, van Til J, Rindress D, et al. Which criteria are considered in healthcare decisions? Insights from an international survey of policy and clinical decision makers. Int J Technol Assess Health Care. 2013;29(4):456–65.CrossRefPubMed
29.
go back to reference Guindo LA, Wagner M, Baltussen R, Rindress D, van Til J, Kind P, et al. From efficacy to equity: review of decision criteria used in resource allocation and healthcare decisionmaking. Cost Eff Resour Alloc. 2012;10(1):9.PubMedCentralCrossRefPubMed Guindo LA, Wagner M, Baltussen R, Rindress D, van Til J, Kind P, et al. From efficacy to equity: review of decision criteria used in resource allocation and healthcare decisionmaking. Cost Eff Resour Alloc. 2012;10(1):9.PubMedCentralCrossRefPubMed
30.
go back to reference van Til J, Groothuis-Oudshoorn C, Lieferink M, Dolan J, Goetghebeur M. Does technique matter: a pilot study exploring weighting techniques for a multi-criteria decision support framework. Cost Eff Resour Alloc. 2014;12:22.PubMedCentralCrossRefPubMed van Til J, Groothuis-Oudshoorn C, Lieferink M, Dolan J, Goetghebeur M. Does technique matter: a pilot study exploring weighting techniques for a multi-criteria decision support framework. Cost Eff Resour Alloc. 2014;12:22.PubMedCentralCrossRefPubMed
32.
go back to reference Miot J, Wagner M, Khoury H, Anderson AN, Rindress D, Goetghebeur MM. Field testing of a framework for coverage of a diagnostic test for cervical cancer in South Africa. Cost Eff Resour Alloc. 2011;10(1):2.CrossRef Miot J, Wagner M, Khoury H, Anderson AN, Rindress D, Goetghebeur MM. Field testing of a framework for coverage of a diagnostic test for cervical cancer in South Africa. Cost Eff Resour Alloc. 2011;10(1):2.CrossRef
33.
go back to reference Tony M, Wagner M, Khoury H, Rindress D, Papastavros T, Oh P, et al. Bridging health technology assessment (HTA) with multicriteria decision analyses (MCDA): field testing of the EVIDEM framework for coverage decisions by a public payer in Canada. BMC Health Serv Res. 2011;11:329.PubMedCentralCrossRefPubMed Tony M, Wagner M, Khoury H, Rindress D, Papastavros T, Oh P, et al. Bridging health technology assessment (HTA) with multicriteria decision analyses (MCDA): field testing of the EVIDEM framework for coverage decisions by a public payer in Canada. BMC Health Serv Res. 2011;11:329.PubMedCentralCrossRefPubMed
34.
go back to reference Radaelli G, Lettieri E, Masella C, Merlino L, Strada A, Tringali M. Implementation of EUnetHTA Core Model(R) in Lombardia: the VTS framework. Int J Technol Assess Health Care. 2014;30(1):105–12.CrossRefPubMed Radaelli G, Lettieri E, Masella C, Merlino L, Strada A, Tringali M. Implementation of EUnetHTA Core Model(R) in Lombardia: the VTS framework. Int J Technol Assess Health Care. 2014;30(1):105–12.CrossRefPubMed
35.
go back to reference MCDA for HTA in action: leveraging experience from Europe and Latin America. Panel presented at the Health Technology Assessment International (HTAi) 12th Annual Conference, 15–17 June 2015: Oslo; 2015. MCDA for HTA in action: leveraging experience from Europe and Latin America. Panel presented at the Health Technology Assessment International (HTAi) 12th Annual Conference, 15–17 June 2015: Oslo; 2015.
36.
go back to reference Goetghebeur M, Wagner M. Defining value: the ethical foundations of MCDA in healthcare decision making. Manuscript in preparation. In: Marsh K, Thokala P, Goetghebeur M, Baltussen R, editors. Healthcare decisions supported by multi-criteria decision analysis. Cham: Springer International Publishing AG; 2015. Goetghebeur M, Wagner M. Defining value: the ethical foundations of MCDA in healthcare decision making. Manuscript in preparation. In: Marsh K, Thokala P, Goetghebeur M, Baltussen R, editors. Healthcare decisions supported by multi-criteria decision analysis. Cham: Springer International Publishing AG; 2015.
39.
go back to reference Beauchamp TL, Childress JF. Principles of biomedical ethics. Oxford; New York: Oxford University Press; 2001. Beauchamp TL, Childress JF. Principles of biomedical ethics. Oxford; New York: Oxford University Press; 2001.
40.
go back to reference Beauchamp TL. The ‘four principles’ approach. Principles of health care ethics. Chichester: Wiley; 1994. p. 3–12. Beauchamp TL. The ‘four principles’ approach. Principles of health care ethics. Chichester: Wiley; 1994. p. 3–12.
41.
go back to reference Lawrence DJ. The four principles of biomedical ethics: a foundation for current bioethical debate. J Chiropr Humanit. 2007;14:34–40.CrossRef Lawrence DJ. The four principles of biomedical ethics: a foundation for current bioethical debate. J Chiropr Humanit. 2007;14:34–40.CrossRef
44.
go back to reference Hoedemaekers R, Dekkers W. Justice and solidarity in priority setting in health care. Health Care Anal. 2003;11(4):325–43.CrossRefPubMed Hoedemaekers R, Dekkers W. Justice and solidarity in priority setting in health care. Health Care Anal. 2003;11(4):325–43.CrossRefPubMed
46.
go back to reference Department for Communities and Local Government. Multi-criteria analysis: a manual. London: Department for Communities and Local Government; 2009. Department for Communities and Local Government. Multi-criteria analysis: a manual. London: Department for Communities and Local Government; 2009.
47.
go back to reference Black AP, Baker M. The impact of parent advocacy groups, the Internet, and social networking on rare diseases: the IDEA League and IDEA League United Kingdom example. Epilepsia. 2011;52(Suppl 2):102–4.CrossRefPubMed Black AP, Baker M. The impact of parent advocacy groups, the Internet, and social networking on rare diseases: the IDEA League and IDEA League United Kingdom example. Epilepsia. 2011;52(Suppl 2):102–4.CrossRefPubMed
48.
go back to reference Boon W, Broekgaarden R. The role of patient advocacy organisations in neuromuscular disease R&D: the case of the Dutch neuromuscular disease association VSN. Neuromuscul Disord. 2010;20(2):148–51.CrossRefPubMed Boon W, Broekgaarden R. The role of patient advocacy organisations in neuromuscular disease R&D: the case of the Dutch neuromuscular disease association VSN. Neuromuscul Disord. 2010;20(2):148–51.CrossRefPubMed
49.
go back to reference Cornu C, Kassai B, Fisch R, Chiron C, Alberti C, Guerrini R, et al. Experimental designs for small randomised clinical trials: an algorithm for choice. Orphanet J Rare Dis. 2013;8:48.PubMedCentralCrossRefPubMed Cornu C, Kassai B, Fisch R, Chiron C, Alberti C, Guerrini R, et al. Experimental designs for small randomised clinical trials: an algorithm for choice. Orphanet J Rare Dis. 2013;8:48.PubMedCentralCrossRefPubMed
50.
go back to reference Denis A, Mergaert L, Fostier C, Cleemput I, Simoens S. Budget impact analysis of orphan drugs in Belgium: estimates from 2008 to 2013. J Med Econ. 2010;13(2):295–301.CrossRefPubMed Denis A, Mergaert L, Fostier C, Cleemput I, Simoens S. Budget impact analysis of orphan drugs in Belgium: estimates from 2008 to 2013. J Med Econ. 2010;13(2):295–301.CrossRefPubMed
51.
go back to reference Desser AS, Gyrd-Hansen D, Olsen JA, Grepperud S, Kristiansen IS. Societal views on orphan drugs: cross sectional survey of Norwegians aged 40 to 67. BMJ. 2010;341:c4715.PubMedCentralCrossRefPubMed Desser AS, Gyrd-Hansen D, Olsen JA, Grepperud S, Kristiansen IS. Societal views on orphan drugs: cross sectional survey of Norwegians aged 40 to 67. BMJ. 2010;341:c4715.PubMedCentralCrossRefPubMed
52.
go back to reference Desser AS. Prioritizing treatment of rare diseases: a survey of preferences of Norwegian doctors. Soc Sci Med. 2013;94:56–62.CrossRefPubMed Desser AS. Prioritizing treatment of rare diseases: a survey of preferences of Norwegian doctors. Soc Sci Med. 2013;94:56–62.CrossRefPubMed
53.
go back to reference Dimichele DM, Blanchette V, Berntorp E. Clinical trial design in haemophilia. Haemophilia. 2012;18(Suppl. 4):18–23.CrossRefPubMed Dimichele DM, Blanchette V, Berntorp E. Clinical trial design in haemophilia. Haemophilia. 2012;18(Suppl. 4):18–23.CrossRefPubMed
54.
go back to reference Dunkle M, Pines W, Saltonstall PL. Advocacy groups and their role in rare diseases research. Adv Exp Med Biol. 2010;686:515–25.CrossRefPubMed Dunkle M, Pines W, Saltonstall PL. Advocacy groups and their role in rare diseases research. Adv Exp Med Biol. 2010;686:515–25.CrossRefPubMed
57.
go back to reference Henderson SL, Packman W, Packman S. Psychosocial aspects of patients with Niemann-Pick disease, type B. Am J Med Genet A. 2009;149A(11):2430–6.CrossRefPubMed Henderson SL, Packman W, Packman S. Psychosocial aspects of patients with Niemann-Pick disease, type B. Am J Med Genet A. 2009;149A(11):2430–6.CrossRefPubMed
58.
go back to reference Hollak CE, Aerts JM, Ayme S, Manuel J. Limitations of drug registries to evaluate orphan medicinal products for the treatment of lysosomal storage disorders. Orphanet J Rare Dis. 2011;6:16.PubMedCentralCrossRefPubMed Hollak CE, Aerts JM, Ayme S, Manuel J. Limitations of drug registries to evaluate orphan medicinal products for the treatment of lysosomal storage disorders. Orphanet J Rare Dis. 2011;6:16.PubMedCentralCrossRefPubMed
59.
go back to reference Joppi R, Bertele’ V, Garattini S. Orphan drugs, orphan diseases. The first decade of orphan drug legislation in the EU. Eur J Clin Pharmacol. 2013;69(4):1009–24.CrossRefPubMed Joppi R, Bertele’ V, Garattini S. Orphan drugs, orphan diseases. The first decade of orphan drug legislation in the EU. Eur J Clin Pharmacol. 2013;69(4):1009–24.CrossRefPubMed
60.
61.
go back to reference Kesselheim AS, Myers JA, Avorn J. Characteristics of clinical trials to support approval of orphan vs nonorphan drugs for cancer. JAMA. 2011;305(22):2320–6.CrossRefPubMed Kesselheim AS, Myers JA, Avorn J. Characteristics of clinical trials to support approval of orphan vs nonorphan drugs for cancer. JAMA. 2011;305(22):2320–6.CrossRefPubMed
62.
go back to reference Lavery C. Role of patient support groups in lysosomal storage diseases. In: Mehta A, Beck M, Sunder-Plassmann G, editors. Fabry disease: perspectives from 5 years of FOS. Oxford: Oxford PharmaGenesis; 2006. Lavery C. Role of patient support groups in lysosomal storage diseases. In: Mehta A, Beck M, Sunder-Plassmann G, editors. Fabry disease: perspectives from 5 years of FOS. Oxford: Oxford PharmaGenesis; 2006.
63.
go back to reference Linley WG, Hughes DA. Societal views on NICE, cancer drugs fund and value-based pricing criteria for prioritising medicines: a cross-sectional survey of 4118 adults in Great Britain. Health Econ. 2013;22(8):948–64.CrossRefPubMed Linley WG, Hughes DA. Societal views on NICE, cancer drugs fund and value-based pricing criteria for prioritising medicines: a cross-sectional survey of 4118 adults in Great Britain. Health Econ. 2013;22(8):948–64.CrossRefPubMed
64.
go back to reference MacLeod S. Optimal therapy for rare disorders and genetic diseases: ethical and political challenges. Proc West Pharmacol Soc. 2007;50:21–3.PubMed MacLeod S. Optimal therapy for rare disorders and genetic diseases: ethical and political challenges. Proc West Pharmacol Soc. 2007;50:21–3.PubMed
65.
go back to reference Mavris M, Le CY. Involvement of patient organisations in research and development of orphan drugs for rare diseases in europe. Mol Syndromol. 2012;3(5):237–43.PubMedCentralPubMed Mavris M, Le CY. Involvement of patient organisations in research and development of orphan drugs for rare diseases in europe. Mol Syndromol. 2012;3(5):237–43.PubMedCentralPubMed
66.
go back to reference Mentzakis E, Stefanowska P, Hurley J. A discrete choice experiment investigating preferences for funding drugs used to treat orphan diseases: an exploratory study. Health Econ Policy Law. 2011;6(3):405–33.CrossRefPubMed Mentzakis E, Stefanowska P, Hurley J. A discrete choice experiment investigating preferences for funding drugs used to treat orphan diseases: an exploratory study. Health Econ Policy Law. 2011;6(3):405–33.CrossRefPubMed
67.
go back to reference Orofino J, Soto J, Casado MA, Oyaguez I. Global spending on orphan drugs in France, Germany, the UK, Italy and Spain during 2007. Appl Health Econ Health Policy. 2010;8(5):301–15.CrossRefPubMed Orofino J, Soto J, Casado MA, Oyaguez I. Global spending on orphan drugs in France, Germany, the UK, Italy and Spain during 2007. Appl Health Econ Health Policy. 2010;8(5):301–15.CrossRefPubMed
68.
go back to reference Pinxten W, Denier Y, Dooms M, Cassiman JJ, Dierickx K. A fair share for the orphans: ethical guidelines for a fair distribution of resources within the bounds of the 10-year-old European Orphan Drug Regulation. J Med Ethics. 2012;38(3):148–53.CrossRefPubMed Pinxten W, Denier Y, Dooms M, Cassiman JJ, Dierickx K. A fair share for the orphans: ethical guidelines for a fair distribution of resources within the bounds of the 10-year-old European Orphan Drug Regulation. J Med Ethics. 2012;38(3):148–53.CrossRefPubMed
69.
go back to reference Rajmil L, Perestelo-Perez L, Herdman M. Quality of life and rare diseases. Adv Exp Med Biol. 2010;686:251–72.CrossRefPubMed Rajmil L, Perestelo-Perez L, Herdman M. Quality of life and rare diseases. Adv Exp Med Biol. 2010;686:251–72.CrossRefPubMed
70.
go back to reference Rosselli D, Rueda JD, Solano M. Ethical and economic considerations of rare diseases in ethnic minorities: the case of mucopolysaccharidosis VI in Colombia. J Med Ethics. 2012;38(11):699–700.PubMedCentralCrossRefPubMed Rosselli D, Rueda JD, Solano M. Ethical and economic considerations of rare diseases in ethnic minorities: the case of mucopolysaccharidosis VI in Colombia. J Med Ethics. 2012;38(11):699–700.PubMedCentralCrossRefPubMed
72.
go back to reference van der Kloot WA, Hamdy NA, Hafkemeijer LC, den Dulk FM, Chotkan SA, van Emmerik AA, et al. The psychological burden of an initially unexplained illness: patients with sternocostoclavicular hyperostosis before and after delayed diagnosis. Health Qual Life Outcomes. 2010;8:97.PubMedCentralCrossRefPubMed van der Kloot WA, Hamdy NA, Hafkemeijer LC, den Dulk FM, Chotkan SA, van Emmerik AA, et al. The psychological burden of an initially unexplained illness: patients with sternocostoclavicular hyperostosis before and after delayed diagnosis. Health Qual Life Outcomes. 2010;8:97.PubMedCentralCrossRefPubMed
73.
go back to reference Wyatt K, Henley W, Anderson L, Anderson R, Nikolaou V, Stein K, et al. The effectiveness and cost-effectiveness of enzyme and substrate replacement therapies: a longitudinal cohort study of people with lysosomal storage disorders. Health Technol Assess. 2012;16(39):1–543.CrossRefPubMed Wyatt K, Henley W, Anderson L, Anderson R, Nikolaou V, Stein K, et al. The effectiveness and cost-effectiveness of enzyme and substrate replacement therapies: a longitudinal cohort study of people with lysosomal storage disorders. Health Technol Assess. 2012;16(39):1–543.CrossRefPubMed
74.
go back to reference Drummond M, Towse A. Orphan drugs policies: a suitable case for treatment. Eur J Health Econ. 2014;15(4):335–40.CrossRefPubMed Drummond M, Towse A. Orphan drugs policies: a suitable case for treatment. Eur J Health Econ. 2014;15(4):335–40.CrossRefPubMed
75.
go back to reference Dolan JG. Multi-criteria clinical decision support. A primer on the use of multiple-criteria decision-making methods to promote evidence-based, patient-centered healthcare. Patient. 2010;3(4):229–248. Dolan JG. Multi-criteria clinical decision support. A primer on the use of multiple-criteria decision-making methods to promote evidence-based, patient-centered healthcare. Patient. 2010;3(4):229–248.
77.
go back to reference Golan OG, Hansen P. Which health technologies should be funded? A prioritization framework based explicitly on value for money. Isr J Health Policy Res. 2012;1(1):44.PubMedCentralCrossRefPubMed Golan OG, Hansen P. Which health technologies should be funded? A prioritization framework based explicitly on value for money. Isr J Health Policy Res. 2012;1(1):44.PubMedCentralCrossRefPubMed
78.
go back to reference Brouwers MC, Kho ME, Browman GP, Burgers JS, Cluzeau F, Feder G, et al. AGREE II: advancing guideline development, reporting and evaluation in health care. CMAJ. 2010;182(18):E839–42.PubMedCentralCrossRefPubMed Brouwers MC, Kho ME, Browman GP, Burgers JS, Cluzeau F, Feder G, et al. AGREE II: advancing guideline development, reporting and evaluation in health care. CMAJ. 2010;182(18):E839–42.PubMedCentralCrossRefPubMed
81.
go back to reference Taruscio D, Vittozzi L, Stefanov R. National plans and strategies on rare diseases in Europe. Adv Exp Med Biol. 2010;686:475–91.CrossRefPubMed Taruscio D, Vittozzi L, Stefanov R. National plans and strategies on rare diseases in Europe. Adv Exp Med Biol. 2010;686:475–91.CrossRefPubMed
83.
go back to reference Molster C, Youngs L, Hammond E, Dawkins H. Key outcomes from stakeholder workshops at a symposium to inform the development of an Australian national plan for rare diseases. Orphanet J Rare Dis. 2012;7:50.PubMedCentralCrossRefPubMed Molster C, Youngs L, Hammond E, Dawkins H. Key outcomes from stakeholder workshops at a symposium to inform the development of an Australian national plan for rare diseases. Orphanet J Rare Dis. 2012;7:50.PubMedCentralCrossRefPubMed
85.
go back to reference Goetghebeur M, Wagner M, Bec M, Nikodem M, Zyla A, Micaleff A et al. IMI work package 6: report. Benefit-risk balance re-evaluation case study Raptiva® (efalizumab). European Medicines Agency. 2015. v.2.6:1–99.http://www.imi-protect.eu/. Accessed 23 Oct 2015. Goetghebeur M, Wagner M, Bec M, Nikodem M, Zyla A, Micaleff A et al. IMI work package 6: report. Benefit-risk balance re-evaluation case study Raptiva® (efalizumab). European Medicines Agency. 2015. v.2.6:1–99.http://​www.​imi-protect.​eu/​. Accessed 23 Oct 2015.
86.
go back to reference Cox R, Sanchez J, Revie CW. Multi-criteria decision analysis tools for prioritising emerging or re-emerging infectious diseases associated with climate change in Canada. PLoS One. 2013;8(8):e68338.PubMedCentralCrossRefPubMed Cox R, Sanchez J, Revie CW. Multi-criteria decision analysis tools for prioritising emerging or re-emerging infectious diseases associated with climate change in Canada. PLoS One. 2013;8(8):e68338.PubMedCentralCrossRefPubMed
87.
go back to reference Shrout PE, Fleiss JL. Intraclass correlations: uses in assessing rater reliability. Psychol Bull. 1979;86(2):420–8.CrossRefPubMed Shrout PE, Fleiss JL. Intraclass correlations: uses in assessing rater reliability. Psychol Bull. 1979;86(2):420–8.CrossRefPubMed
88.
go back to reference Denis A, Mergaert L, Fostier C, Cleemput I, Hulstaert F, Simoens S. Critical assessment of Belgian reimbursement dossiers of orphan drugs. Pharmacoeconomics. 2011;29(10):883–93.CrossRefPubMed Denis A, Mergaert L, Fostier C, Cleemput I, Hulstaert F, Simoens S. Critical assessment of Belgian reimbursement dossiers of orphan drugs. Pharmacoeconomics. 2011;29(10):883–93.CrossRefPubMed
89.
go back to reference Drummond M, Evans B, LeLorier J, Karakiewicz P, Martin D, Tugwell P, et al. Evidence and values: requirements for public reimbursement of drugs for rare diseases: a case study in oncology. Can J Clin Pharmacol. 2009;16(2):e273–81.PubMed Drummond M, Evans B, LeLorier J, Karakiewicz P, Martin D, Tugwell P, et al. Evidence and values: requirements for public reimbursement of drugs for rare diseases: a case study in oncology. Can J Clin Pharmacol. 2009;16(2):e273–81.PubMed
90.
go back to reference Bettinger TL, Shuler G, Jones DR, Wilson JP. Schizophrenia: multi-attribute utility theory approach to selection of atypical antipsychotics. Ann Pharmacother. 2007;41(2):201–7.CrossRefPubMed Bettinger TL, Shuler G, Jones DR, Wilson JP. Schizophrenia: multi-attribute utility theory approach to selection of atypical antipsychotics. Ann Pharmacother. 2007;41(2):201–7.CrossRefPubMed
91.
92.
go back to reference Aenishaenslin C, Hongoh V, Cisse HD, Hoen AG, Samoura K, Michel P, et al. Multi-criteria decision analysis as an innovative approach to managing zoonoses: results from a study on Lyme disease in Canada. BMC Public Health. 2013;13(1):897.PubMedCentralCrossRefPubMed Aenishaenslin C, Hongoh V, Cisse HD, Hoen AG, Samoura K, Michel P, et al. Multi-criteria decision analysis as an innovative approach to managing zoonoses: results from a study on Lyme disease in Canada. BMC Public Health. 2013;13(1):897.PubMedCentralCrossRefPubMed
93.
go back to reference Tromp N, Baltussen R. Mapping of multiple criteria for priority setting of health interventions: an aid for decision makers. BMC Health Serv Res. 2012;12:454.PubMedCentralCrossRefPubMed Tromp N, Baltussen R. Mapping of multiple criteria for priority setting of health interventions: an aid for decision makers. BMC Health Serv Res. 2012;12:454.PubMedCentralCrossRefPubMed
Metadata
Title
Can the EVIDEM Framework Tackle Issues Raised by Evaluating Treatments for Rare Diseases: Analysis of Issues and Policies, and Context-Specific Adaptation
Authors
Monika Wagner
Hanane Khoury
Jacob Willet
Donna Rindress
Mireille Goetghebeur
Publication date
01-03-2016
Publisher
Springer International Publishing
Published in
PharmacoEconomics / Issue 3/2016
Print ISSN: 1170-7690
Electronic ISSN: 1179-2027
DOI
https://doi.org/10.1007/s40273-015-0340-5

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