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partnering with patient in research is all about. Thromb Res [Internet]. 2017;150:113–20. Disponible en: http://dx.doi.org/10.1016/j. thromres.2016.10.029 30. Dugas M, Trottier MÈ, Chipenda Dansokho S, Vaisson G, Provencher T, Colquhoun H, et al. Involving members of vulnerable popula- tions in the development of patient decision aids: A mixed methods sequential explanatory study. BMC Med Inform Decis Mak [Internet]. 2017;17(1):1– 11. Disponible en: http://dx.doi.org/10.1186/ s12911-016-0399-8 31. Ward PR, Coffey C, Meyer S. Trust, choi- ce and obligation: A qualitative study of enablers of colorectal cancer screening in South Australia. Sociol Heal Illn. 2015;37(7):988–1006. 32. Dy SM, Purnell TS. Key concepts relevant to quality of complex and shared decision-making in health care: A literature review. Soc Sci Med [Internet]. 2012;74(4):582–7. Disponible en: http:// dx.doi.org/10.1016/j.socscimed.2011.11.015 33. Stone J. Race and healthcare disparities overcoming vulnerability. Theor Med Bioeth. 2002;23(6):499–518. 34. Robertson R, Dixon A, Le Grand J. Patient Choice in General Practice: The Implications of Patient Satisfaction Surveys. J Health Serv Res Policy [Internet]. 2008;13(2):67–72. Disponible en: http://journals.sagepub.com/doi/10.1258/ jhsrp.2007.007055 35. Ghadi V, Naiditch M. Comment construi- re la légitimité de la participation des usagers à des problématiques de santé? Sante Publique (Paris). 2006;18(2):171–86. 36. Ells C. Preventing and resolving ethical conflicts: more help for policy makers. Healthc Manage Forum [Internet]. 2001;14(1):22–4. Disponible en: http://dx.doi.org/10.1016/ S0840-4704(10)60388-2 37. Ko H. In science communication, why does the idea of a public deficit always return? Public Underst Sci. 2016;25(4):460–4. 38. Lopes E, Street J, Carter D, Merlin T. Involving patients in health technology funding decisions: Stakeholder perspectives on processes used in Australia. Heal Expect. 2016;19(2):331–44. 39. Goold SD. Allocating health care: cost-uti- lity analysis, informed democratic decision making, or the veil of ignorance? J Health Polit Policy Law [Internet]. 1996;21(1):69–98. Disponible en: http://www.ncbi.nlm.nih.gov/pubmed/8708343 40. Callahan R, Darzi A. Analysis & commen- tary: Five policy levers to meet the value challenge Astorga-Pinto S. in cancer care. Health Aff. 2015;34(9):1563–8. 41. Abraham J, Sheppard J. Democracy, Technocracy, and the Secret State of Medicines Control : Expert and Nonexpert Perspectives Author ( s ): John Abraham and Julie Sheppard. Sage Publications, Inc. 2017;22(2):139–67. 42. Facey K, Boivin A, Gracia J, Hansen HP, Lo Scalzo A, Mossman J, et al. Patients’ perspec- tives in health technology assessment: A route to robust evidence and fair deliberation. Int J Technol Assess Health Care. 2010;26(3):334–40. 43. Thomas R, Glasziou P, Rychetnik L, Mackenzie G, Gardiner R, Doust J. Deliberative democracy and cancer screening consent: A ran- domised control trial of the effect of a commu- nity jury on men’s knowledge about and inten- tions to participate in PSA screening. BMJ Open. 2014;4(12):1–8. 44. Carman KL, Maurer M, Mangrum R, Yang M, Ginsburg M, Sofaer S, et al. Understanding An Informed Public; Views On The Role Of Evidence In Making Health Care Decisions. Heal Aff [Internet]. 2016;35(4):566–74. Disponible en: http://dx.doi.org/10.1377/hlthaff.2015.1112 45. Hodgetts K, Hiller JE, Street JM, Carter D, Braunack-Mayer AJ, Watt AM, et al. Disinvestment policy and the public funding of assisted reproduc- tive technologies: Outcomes of deliberative enga- gements with three key stakeholder groups. BMC Health Serv Res. 2014;14(1). 46. Weeks WB, Kotzbauer GR, Weinstein JN. Using Publicly Available Data to Construct a Transparent Measure of Health Care Value: A Method and Initial Results. Milbank Q [Internet]. 2016;94(2):314–33. Disponible en: http://www. ncbi.nlm.nih.gov/pubmed/27265559%0Aht- tp://www.pubmedcentral.nih.gov/articlerender. fcgi?artid=PMC4911724%0Ahttp://doi.wiley. com/10.1111/1468-0009.12194 47. Williams A. Thinking about equity in heal- th care. J Nurs Manag. 2005;13(5):397–402. 48. Kolasa K, Dohnalik J, Borek E, Siemiatkowski M, Ścibiorski C. The paradox of public participation in the healthcare in Poland - What citizens want, and what they think. Health Policy (New York). 2014;118(2):159–65. 49. Douglas CMW, Wilcox E, Burgess M, Lynd LD. Why orphan drug coverage reimbur- sement decision-making needs patient and pu- blic involvement. Health Policy (New York). 2015;119(5):588–96. 68