Literature DB >> 28195755

Prioritizing Rare Diseases: Psychological Effects Influencing Medical Decision Making.

Johanna Wiss1, Lars-Ake Levin2,3, David Andersson3, Gustav Tinghög1,3.   

Abstract

BACKGROUND: Measuring societal preferences for rarity has been proposed to determine whether paying premium prices for orphan drugs is acceptable.
OBJECTIVE: To investigate societal preferences for rarity and how psychological factors affect such preferences.
METHOD: A postal survey containing resource allocation dilemmas involving patients with a rare disease and patients with a common disease, equal in severity, was sent out to a randomly selected sample of the population in Sweden (return rate 42.3%, n = 1270).
RESULTS: Overall, we found no evidence of a general preference for prioritizing treatment of patients with rare disease patients over those with common diseases. When treatment costs were equal, most respondents (42.7%) were indifferent between the choice options. Preferences for prioritizing patients with common diseases over those with rare diseases were more frequently displayed (33.3% v. 23.9%). This tendency was, as expected, amplified when the rare disease was costlier to treat. The share of respondents choosing to treat patients with rare diseases increased when presenting the patients in need of treatment in relative rather than absolute terms (proportion dominance). Surprisingly, identifiability did not increase preferences for rarity. Instead, identifying the patient with a rare disease made respondents more willing to prioritize the patients with common diseases. Respondents' levels of education were significantly associated with choice-the lower the level of education, the more likely they were to choose the rare option.
CONCLUSIONS: We find no support for the existence of a general preference for rarity when setting health care priorities. Psychological effects, especially proportion dominance, are likely to play an important role when preferences for rarity are expressed.

Entities:  

Keywords:  identifiability; orphan drugs; priority setting; proportion dominance; rare diseases; resource allocation; societal preferences; survey

Mesh:

Year:  2017        PMID: 28195755     DOI: 10.1177/0272989X17691744

Source DB:  PubMed          Journal:  Med Decis Making        ISSN: 0272-989X            Impact factor:   2.583


  5 in total

Review 1.  A systematic review of moral reasons on orphan drug reimbursement.

Authors:  Bettina M Zimmermann; Johanna Eichinger; Matthias R Baumgartner
Journal:  Orphanet J Rare Dis       Date:  2021-06-30       Impact factor: 4.123

2.  Cost-effectiveness of enzyme replacement therapy with alglucosidase alfa in adult patients with Pompe disease.

Authors:  Tim A Kanters; Ans T van der Ploeg; Michelle E Kruijshaar; Dimitris Rizopoulos; W Ken Redekop; Maureen P M H Rutten-van Mӧlken; Leona Hakkaart-van Roijen
Journal:  Orphanet J Rare Dis       Date:  2017-12-13       Impact factor: 4.123

3.  Moving Towards Accountability for Reasonableness - A Systematic Exploration of the Features of Legitimate Healthcare Coverage Decision-Making Processes Using Rare Diseases and Regenerative Therapies as a Case Study.

Authors:  Monika Wagner; Dima Samaha; Roman Casciano; Matthew Brougham; Payam Abrishami; Charles Petrie; Bernard Avouac; Lorenzo Mantovani; Antonio Sarría-Santamera; Paul Kind; Michael Schlander; Michele Tringali
Journal:  Int J Health Policy Manag       Date:  2019-07-01

Review 4.  Value judgment of health interventions from different perspectives: arguments and criteria.

Authors:  Karin M Vermeulen; Paul F M Krabbe
Journal:  Cost Eff Resour Alloc       Date:  2018-04-17

5.  A novel method for predicting the budget impact of innovative medicines: validation study for oncolytics.

Authors:  Joost W Geenen; Svetlana V Belitser; Rick A Vreman; Martijn van Bloois; Olaf H Klungel; Cornelis Boersma; Anke M Hövels
Journal:  Eur J Health Econ       Date:  2020-04-04
  5 in total

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