Information preferences of the general population when faced with life-limiting illness.

Background: Giving the public and the patients good information enables them to make effective choices about their care. This study describes public preferences for both themselves and their relatives on receiving information on end-of-life care topics when faced with a life-limiting illness and to...

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Publicado en:European Journal of Public Health Vol. 25; no. 3; pp. 532 - 539
Autores principales: Vleminck, Aline De, Pardon, Koen, Roelands, Marc, Houttekier, Dirk, Block, Lieve Van den, Stichele, Robert Vander, Deliens, Luc
Formato: research tables/charts Journal Article
Publicado: Oxford University Press / USA Jun2015
Acceso en línea:Ver este registro en EBSCOhost
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      dt: Jun2015
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        atl: Information preferences of the general population when faced with life-limiting illness.
      aug:
        au:
          Vleminck, Aline De
          Pardon, Koen
          Roelands, Marc
          Houttekier, Dirk
          Block, Lieve Van den
          Stichele, Robert Vander
          Deliens, Luc
        affil: Family Medicine and Chronic Care, End-of-Life Care Research group, Ghent University & Vrije Universiteit Brussel (VUB), Ghent, Belgium
      sug:
        subj:
          Information Seeking Behavior
          Health Information
          Truth Disclosure
          Terminally Ill Patients Psychosocial Factors
          Human
          Male
          Female
          Descriptive Statistics
          Data Analysis Software
          Confidence Intervals
          Odds Ratio
          Belgium
          Terminal Care
          Life Expectancy
          Aged
          Aged, 80 and Over
          Patient Attitudes
          Stratified Random Sample
          Cluster Sample
          Aged: 65+ years
          Aged, 80 & over
          Male
          Female
      ab: Background: Giving the public and the patients good information enables them to make effective choices about their care. This study describes public preferences for both themselves and their relatives on receiving information on end-of-life care topics when faced with a life-limiting illness and to identify associated factors. Method: This study used data from the cross-sectional Health Interview Study (HIS) 2008 that collected data from a representative sample (N= 9651) of the Belgian population. Results: Around 82% of respondents wanted to be informed always about diagnosis, chances of cure and available treatments, 77% wanted to be informed on life expectancy, 72% on options regarding palliative care and 67% on possibilities of prolonging or shortening life. Around 55%wanted their relative to be informed always about diagnosis, chances of cure, life expectancy and different treatments available, whereas 50% wanted this in relation to the options regarding palliative care and 46% on the possibilities of prolonging or shortening life. Younger adults, people with more education and people with a regular GP were more likely to want to be informed always. Younger adults and women were less likely to want their relatives to be informed always. Conclusion: The majority of the Belgian population wants to be informed always about end-of-life care topics when faced with a life-limiting illness. Physicians should be aware of the desired level of information and tailor information to individual patient preferences. Understanding population preferences may help to tailor patient education and health promotion programmes appropriately.
      pubtype: Academic Journal
      doctype:
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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