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Health literacy

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Title: Health literacy


1
Health literacy
  • Angela Coulter
  • Picker Institute Europe
  • www.pickereurope.org

2
Topics
  • About health literacy
  • Uses of health literacy
  • What works?
  • Understanding illness, treatment and services
  • Selecting appropriate treatment / support
  • Managing long-term conditions
  • Preventing illness, reducing inequalities

3
About health literacy
4
What is it?
  • The ability to read, understand and act upon
    health information.
  • Reading understanding competence to make
    health decisions
  • Essential for patient engagement - relevant to
    whole population
  • Critically important in tackling health
    inequalities requires targeted approach

5
Levels of health literacy
  • Functional
  • Basic skills in reading and writing for
    understanding health information
  • Interactive
  • More advanced skills to enable active
    participation in healthcare choices
  • Critical
  • The ability to critically analyse information
    about health and healthcare and make effective
    use of it
  • Nutbeam 2000

6
People with low health literacy
  • Have poorer health status
  • Undergo more hospital admissions
  • Are less likely to adhere to treatment
    recommendations
  • Experience more drug and treatment errors
  • Make less use of preventive services
  • Institute of Medicine 2004

7
Low literacy in the UK
  • TOFHLA tests reading, numeracy and
    comprehension (e.g. instructions for taking
    medicines, exemption from prescription charges)
  • 11 of UK adults had marginal or inadequate
    literacy
  • Lowest levels among those who were
  • Older
  • Male
  • Lower educational attainment
  • Lower income
  • Worse diet
  • Less exercise
  • Smokers
  • Worse self-rated health
  • Von Wagner et al J Epid Com Health 2007

8
Understanding illness and treatment
9
What patients want
  • To understand what is wrong
  • To gain a realistic idea of prognosis
  • To make the most of consultations
  • To understand tests and treatments
  • To assist in self-care
  • To find services and sources of help
  • To find reassurance and help to cope
  • To help others understand
  • To learn how to prevent further illness
  • To find the best healthcare providers

10
Some patient information is not helpful
  • Topics of relevance to patients omitted
  • Failure to recognise patients decision-making
    role
  • Incomplete coverage of treatment options
  • Inaccurate and out-of-date
  • Biased more about benefits than risks
  • Uncertainties ignored or glossed over
  • Coulter et al. BMJ 1999 318 318-322

11
Information to support decision-making (IPDAS
criteria)
  • Starts with a clear statement of aims
  • Provides unbiased information about options
  • Presents outcome probabilities clearly
  • Contains accurate information
  • Helps people make decisions
  • Discloses conflicts of interest
  • Has a clear structure and layout
  • Helps the reader judge its reliability

12
Understanding illness, treatment and services
13
Health information sources (UK pop over 45)
14
Doctor gave clear goals and treatment plan
15
Doctor explained medication side-effects
16
Use of health websites and telephone helplines by
social group
17
Accessing information about health and social
care services
  • Professionals do not systematically or
    proactively provide information about local
    services
  • Lack of coordination between information
    providers
  • Lack of effective signposting
  • Telephone information not always useful or
    appropriate
  • Some websites are poorly designed
  • Information is often out-of-date
  • Information not always accessible to all

18
Understanding illness and treatment
  • Best Buys
  • Communications training for health professionals
  • Longer consultations in primary care
  • Personalised patient information
  • Pre-operative and pre-discharge information
  • Telephone helplines, telehealth

19
Selecting appropriate treatment
20
Would have liked more involvement in treatment
decisions (NHS patient surveys, England 2004/7)
21
Doctor always gives information about treatment
choices and elicits patients preferences
Commonwealth Fund survey 2005
22
Patient decision aids
23
BPH treatment options
  • Prostatectomy (open/TURP)
  • TUNA/TUMT/TUIP
  • Alpha blockers
  • Reductase inhibitors
  • Watchful waiting

24
BPH appraising the options
25
Selecting appropriate treatment
  • Best Buys
  • Decision aids for patients
  • Patient access to records
  • Patient-reported outcome measures (PROMs)

26
Managing long-term conditions
27
Care planning
  • We are committed to ensuring that by 2010 all
    people (of all ages) with a long-term condition,
    including people with mental health problems, are
    offered their own personalised care plan. Care
    plans will be signed off by individuals and their
    lead professionals to provide a record of what
    has been agreed. This will help people take
    greater control of their care, on a more equal
    partnership with the health and social care teams
    that support this care.
  • NHS Next Stage Review Our Vision for Primary and
    Community Care July 2008

28
Patients with chronic conditions given a
self-management plan
Commonwealth Fund survey 2005
29
Care planning for diabetes a process not a
piece of paper (Year of Care)
30
Managing long-term conditions
  • Best Buys
  • Integrated disease-specific self-management
    education and support
  • Lay-led self-management education
  • Health coaching, telehealth

31
Promoting health, reducing inequalities
32
Advice received on weight, diet or exercise
33
Promoting health, reducing inequalities
  • Best Buys
  • Opportunistic advice from health professionals
  • Reminders and motivational phone calls
  • Parenting programmes and home visits
  • Dietary education and motivation
  • Self-help information (print and electronic)
  • Mass media campaigns

34
Conclusions
  • Health literacy matters
  • People need information to help them make
    decisions
  • Professionals underestimate information needs
  • Staff training can be helpful
  • Personalised information is best
  • Self-care education and support should be
    integrated into care systems
  • Websites and the telephone can be effective
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