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Do We Need a Patients Bill of Rights

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Title: Do We Need a Patients Bill of Rights


1
Do We Need a Patients Bill of Rights
Responsibilities?
  • Kidney Foundation Symposium
  • Saturday, November 2, 2002
  • Dr. Carolyn Bennett, M.P.

2
Rights ?
  • Or Rights
  • AND
  • Responsibilities

3
Right
  • a thing one may morally or legally claim the
    state of being entitled to a privilege or
    immunity or authority to act Concise Oxford

4
Responsibility
  • liable to be called to account for ones
    actions Concise Oxford

5
Presumption
  • Health care in Canada may not be an actual
    right but is the duty and obligation of a
    caring society. Sister Nuala Kenny

6
Quiz
  • Which of the following is NOT a principle of the
    Canada Health Act?
  • A) Portability
  • B) Accessibility
  • C) Comprehensive
  • D) High Quality Care
  • E) Publicly Funded
  • F) Universality

7
Measuring Quality
  • Accountability
  • Transparency

8
Process for Protecting Rights
  • Complaints based eg. Human Rights Commission
  • Audit CPSO, New Zealand

9
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10
Vision statement for Health CareKill or Cure ?
  • Emphasize that patients expect to be treated with
    respect
  • Health care providers must be able to do their
    jobs with pride knowing that they are
    participating in a world-class system that is
    constantly improved as it responds to the
    evolving need of Canadians
  • Providers must be appreciated and properly
    remunerated

11
Vision statement for Health CareKill or Cure ?
  • The ability to function to my full physical and
    mental capacity
  • A long-term commitment to health promotion and
    disease prevention health research
  • Guaranteed access to high-quality care in a
    timely fashion
  • A real say in setting, evaluating, and monitoring
    National Health Service Standards

12
Patients Rights in New ZealandRon Paterson,
Health Disability Commissioner
  • Background Report of the Cervical Cancer
    Inquiry 1988
  • Shift in public attitudes challenged
    traditional approach of beneficence and
    paternalism
  • Led to reforms of the medical disciplinary
    process
  • 1994 independent statutory Ombudsman created
    the Health Disability Commissioner
  • Develop enforce a Code of Consumers Rights
  • Designed to promote and protect the rights of
    health consumers facilitate the fair, simple,
    speedy and efficient resolution of complaints
  • The Code of Health and Disability Services
    Consumers Rights came into force in 1996 and
    sets out legally enforceable rights of consumers
    and corresponding duties of providers

13
The Code of Health Disability Services
Consumers Rights (N.Z.)
  • Clause 1
  • This establishes the duties and obligations of
    providers to comply with the Code, to ensure they
    promote awareness of it to consumers and enable
    consumers to exercise their rights.

14
The Code of Health Disability Services
Consumers Rights (N.Z.)
  • Clause 2
  • This details the 10 rights of consumers and
    duties of providers.

15
The Code of Health Disability Services
Consumers Rights (N.Z.)
  • Right 1 the right to be treated with respect
  • Right 2 the right to freedom from
    discrimination, coercion, harassment, and
    exploitation
  • Right 3 the right to dignity and independence
  • Right 4 the right to services of an appropriate
    standard
  • Right 5 the right to effective communication

16
The Code of Health Disability Services
Consumers Rights (N.Z.)
  • Right 6 the right to be fully informed
  • Right 7 the right to make an informed choice
    and give informed consent
  • Right 8 the right to support
  • Right 9 rights in respect of teaching or
    research
  • Right 10 the right to complain

17
The Code of Health Disability Services
Consumers Rights (N.Z.)
  • Clause 3
  • Sets out provider compliance requirements and
    states that where the rights cannot be met then
    the onus is on the provider to show that it was
    reasonable in the circumstances not to have done
    so.

18
The Code of Health Disability Services
Consumers Rights (N.Z.)
  • Clause 3 (contd)
  • This reasonableness test will be applied and
    developed over time. It is expected that over
    time, greater compliance will be demanded of
    providers. This clause gives some flexibility in
    terms of a gradual implementation of these
    rights.

19
The Code of Health Disability Services
Consumers Rights (N.Z.)
  • Clause 4
  • Establishes certain definitions where these are
    appropriate and elaborates on some of the
    definitions in the Act.

20
The Code of Health Disability Services
Consumers Rights (N.Z.)
  • Clause 5
  • Notes that in meeting the rights no provider is
    required to break any other New Zealand law.

21
The Code of Health Disability Services
Consumers Rights (N.Z.)
  • Clause 6
  • Ensures that all existing rights outside of the
    regulation still apply.

22
The Code of Health Disability Services
Consumers Rights (N.Z.)
  • The Code therefore covers all registered health
    professionals, such as doctors, nurses, dentists,
    etc, and in addition brings a level of
    accountability to all those who might be
    considered outside the mainstream of medical
    practice, e.g. naturopaths, homeopaths,
    acupuncturists etc.
  • As well as applying to individual providers, it
    also applies to hospitals and other health and
    disability institutions and allows the
    Commissioner to enquire into systems issues
    across professional boundaries.

23
The Code of Health Disability Services
Consumers Rights (N.Z.)
  • The obligation under the Code is to take
    "reasonable actions in the circumstances to give
    effect to the rights, and comply with the duties"
    in the Code.
  • The onus is on providers to show that such action
    has been taken.
  • The Code does not override other legislation and
    nothing in the Code requires providers to act in
    breach of a duty or obligation imposed by any
    enactment..

24
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25
Summary of Bill of Rights
  • Timely and accurate diagnosis
  • Timely access to specialty care
  • Information about arthritis and about their
    arthritis care
  • Informed consent regarding treatment decisions
  • Access to medications and other treatments
  • Participate fully in society (including
    self-care, leisure and work pursuits)
  • Research
  • Representation

26
Summary of Bill of Rights
  • Pursue healthy lifestyles
  • Become knowledgeable about their arthritis
    treatment plans
  • Actively participate in decisions about their
    arthritis care
  • Cooperate fully with mutually accepted courses of
    treatment


27
CMA A Prescription for Sustainability
  • June of 2002 called for a Canadian Health
    Charter that
  • articulates a shared vision of Canadas health
    system
  • Commits governments to plan and coordinate their
    efforts to ensure that Canadians have timely
    access to a common basket of core health services
    regardless of where they live

28
CMA A Prescription for Sustainability (contd)
  • sets out the roles, rights and responsibilities
    of patients, health care providers and governments

29
CMA - Canadian Health Charter
  • Broader in scope than a patients bill of rights.
    It would commit governments to work
    collaboratively towards a national plan that
    includes
  • A common basket of core health care services to
    be made available to all Canadians under uniform
    terms and conditions

30
CMA - Canadian Health Charter (contd)
  • National benchmarks for timeliness, accessibility
    and quality of health care
  • Investments in health system resources, including
    health human resources, information technology,
    and capital infrastructure
  • National goals and targets to improve the health
    of Canadians.

31
CMA - Rights and ResponsibilitiesPatients/Citize
ns
  • Rights
  • Access to timely, quality care
  • Recourse to alternatives if public system fails
    to meet guarantee
  • Choice of health care provider
  • Security and confidentiality of personal health
    information
  • Responsibilities
  • Responsible use of services
  • Financial contribution via taxes and patient
    cost-sharing

32
CMA - Rights and ResponsibilitiesProviders
  • Rights
  • Reasonable compensation with dispute resolution
  • Choice in the mode of practice and payment
  • Professional autonomy and clinical independence
  • Responsibilities
  • Advocate on behalf of patients
  • Prudent management of resources
  • Collaboration across disciplines

33
CMA - Rights and ResponsibilitiesProviders
(contd)
  • Rights
  • Access to resources needed to provide timely care
  • Consultation / participation in decision-making
    at all levels
  • Responsibilities
  • Providing high quality, evidence-based care
  • Uphold standards of professional practive
  • Prudent use of resources

34
CMA - Rights and ResponsibilitiesGovernments
  • Rights
  • Define scope of coverage
  • Set budget
  • Set goals and priorities
  • Access information necessary to measure system
    performance
  • Responsibilities
  • Provide adequate, stable funding
  • Set expectations or guarantee for timeliness and
    quality of care
  • Report publicly on the performance of the health
    care system
  • Respect for

35
The Kirby Report The Health Care Guarantee
  • A health care guarantee would ensure that for
    every type of major procedure or treatment, a
    maximum waiting time would be established and
    patients would be entitled to receive service
    within that time frame.

36
The Kirby Report The Health Care Guarantee
(contd)
  • For each type of major procedure or treatment, a
    maximum needs-based waiting time should be
    established and made public.
  • When this maximum waiting time is reached, the
    insurer (government) should pay for the patient
    to immediately receive the procedure or treatment
    in another jurisdiction including, if necessary,
    another country (e.g. the United States). This
    is called the Health Care Guarantee.

37
The NHS PlanA plan for investmentA plan for
reform
  • Reacting to a lack of national standards,
    old-fashioned demarcations between staff and
    barriers between services, a lack of clear
    incentives and levers to improve performance, and
    an over-centralisation and disempowered patients.

38
The NHS PlanPromises - Patient Empowerment
  • Letters about an individual patients care will
    be copied to the patient
  • Patients views on local health services will
    help deice how much cash they get
  • Patient advocates will be set up in every
    hospital
  • If operations are cancelled on the day they are
    due to take place the patient will be able to
    choose another date within 28 days or the
    hospital will pay for it to be carried out at
    another hospital of the patients choosing
  • Patients surveys and forums to help services
    become more patient oriented.

39
The NHS PlanPromises Deals with Private
Providers
  • By 2004 patients will be able to have a GP
    appointment within 48 hours and there will be up
    to 1,000 specialist GPs taking referrals from
    fellow GPs
  • Long waits in accident and emergency departments
    will be ended
  • By the end of 2005 the maximum waiting time for
    an outpatient appointment will be three months
    and for inpatients, six months.

40
The NHS PlanPromises Cancer, Heart Disease and
Mental Health treatment
  • A big expansion in cancer screening programmes
  • An end to the postcode lottery in the prescribing
    of cancer drugs
  • Shorter waits for heart operations
  • Hundreds of mental health teams to provide an
    immediate response to crises.

41
The NHS PlanPromises Seniors Health
  • Nursing care in nursing home will be free
  • By 2004 a 900 million package of new
    intermediate care services to allow older people
    to live more independent lives
  • National standards for caring for older people to
    ensure that ageism is not tolerated
  • Breast screening to cover all women aged 65 to 70
    years
  • Personal care plans for elderly people and their
    care-givers.

42
The NHS PlanPromises National Inequalities
Target
  • Increase and improve primary care in deprived
    areas
  • Introduce screening programmes for women and
    children
  • Step up smoking cessation services
  • Improve the diets for young children by making
    fruit freely available in schools for 4-6 year
    olds.

43
Good Health Through Good Governance A
Submission to the Commission on the Future of
Health Care in Canada from  The Good Health
Through Good Governance Working Group
44
Need for Good Governance
  • Lack of patient involvement in significant
    decisions in the health care system - leads to
    diminishing confidence and trust.
  • Lack of pan-Canadian governance structure - leads
    to duplication and limits opportunities for
    learning.
  • Lack of knowledge sharing and innovation and the
    perverse absence of incentives
  • Isolated information and feedback systems - leads
    to duplicated procedures, lack of portability of
    health records, and missed opportunities for
    quality improvement.

45
Key Elements for Good Health
  • System does not need total overhaul, but rather
    key adjustments and a formal recognition of the
    determinants of health.
  • Patients are the central reason for the health
    care system - they must be meaningfully engaged
    and treated as partners.
  • Health infostructure is a key enabler for
    integration of health care and public health,
    improved data systems and governance.
  • Good governance provides connectivity,
    leadership, innovation and accountability across
    the country.

46
Recommendations
  • Ensure that the governance of health is fair,
    transparent and actively involves citizens to
    ensure the ongoing confidence of all Canadians.
  • Establish a common set of principles for the
    governance of public health and health care at
    all levels that reflect a learning culture and
    the feedback inherent in a complex adaptive
    system.

47
Recommendations (contd)
  • Make patient empowerment a priority. The goal is
    to enable all Canadians to make better choices
    regarding their health situations and behaviour,
    use the health care system wisely, ask informed
    questions of practitioners, and compare their
    care to clinical guidelines.

48
Recommendations (contd)
  • Create an inclusive, transparent and ongoing
    process for debating what is medically
    necessary, whats covered and whats not, using
    principles of accountability for reasonableness.
    Give more emphasis to prevention and health
    promotion. Citizens would be involved in
    priority setting and review of outcomes.

49
Recommendations (contd)
  • Devise with the genuine participation of citizens
    a living charter of pan-Canadian standards
    regarding expectations of our public health and
    health care systems, as well as specific goals
    and targets for improving the health status of
    all Canadians. The possibility of a Heath
    Commissioner as an officer of Parliament and
    responsible for the Charter should be considered.
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