SwePub
Sök i LIBRIS databas

  Utökad sökning

WFRF:(Wiss Johanna 1984 )
 

Sökning: WFRF:(Wiss Johanna 1984 ) > Prioritizing Rare D...

Prioritizing Rare Diseases: Psychological Effects Influencing Medical Decision Making

Wiss, Johanna, 1984- (författare)
Linköpings universitet,Avdelningen för hälso- och sjukvårdsanalys,Medicinska fakulteten
Levin, Lars-Åke, 1960- (författare)
Linköpings universitet,Avdelningen för hälso- och sjukvårdsanalys,Medicinska fakulteten
David, Andersson, 1985- (författare)
Linköpings universitet,Nationalekonomi,Filosofiska fakulteten,JEDIlab
visa fler...
Tinghög, Gustav, 1979- (författare)
Linköpings universitet,Nationalekonomi,Filosofiska fakulteten,Avdelningen för hälso- och sjukvårdsanalys,Medicinska fakulteten,JEDILab
visa färre...
 (creator_code:org_t)
Sage Publications, 2017
2017
Engelska.
Ingår i: Medical decision making. - : Sage Publications. - 0272-989X .- 1552-681X.
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Background. Measuring societal preferences for rarity has been proposed to determine whether paying pre- mium 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 treat- ment 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 present- ing 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 pre- ferences for rarity are expressed.  

Ämnesord

SAMHÄLLSVETENSKAP  -- Ekonomi och näringsliv -- Nationalekonomi (hsv//swe)
SOCIAL SCIENCES  -- Economics and Business -- Economics (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Hälsovetenskap -- Hälso- och sjukvårdsorganisation, hälsopolitik och hälsoekonomi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Health Sciences -- Health Care Service and Management, Health Policy and Services and Health Economy (hsv//eng)
SAMHÄLLSVETENSKAP  -- Psykologi -- Psykologi (hsv//swe)
SOCIAL SCIENCES  -- Psychology -- Psychology (hsv//eng)

Nyckelord

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

Publikations- och innehållstyp

ref (ämneskategori)
art (ämneskategori)

Hitta via bibliotek

Till lärosätets databas

Sök utanför SwePub

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Stäng

Kopiera och spara länken för att återkomma till aktuell vy