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Title: EMROAFRO Research Project: Estimating Patient Harm in Developing


1
EMRO-AFRO Research ProjectEstimating Patient
Harm in Developing Transitional Countries
  • Dr Ross Wilson,
  • Dr Ahmed Abdellatif, Dr Philippe Michel, Dr Sisse
    Olsen, Prof Charles Vincent
  • International Forum for Quality Safety in
    Health Care Paris 2008

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"I am called eccentric for saying in public that
hospitals, if they wish to be sure of
improvement, must find out what their results
are. Must analyze their results to find their
strong and weak points. Must compare their
results with those of other hospitals...
Such opinions will not be eccentric a few years
hence."
E. A. Codman MD (1869 - 1940)
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Background
  • Patient Safety becomes an international issue in
    the 1990s through measurement publication
  • Multiple publications on regional and then
    national levels, showing unacceptable levels of
    preventable patient harm (adverse events) not
    just one country
  • Beginning of many nationally led efforts to
    improve patient safety

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  • Operation 39.3
  • Admin system 10.6
  • Diagnosis 9.3
  • Therapy 8.4
  • Drug 6.7
  • Procedure 4.3
  • Fracture 2.2
  • Falls 1.7
  • 16.6 of hospitalisations associated
    with AE
  • 50 of AEs were preventable
  • 18.6 caused permanent disability/death

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CMAJ 2004170(11)1678-86
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Knowledge is the enemy of unsafe care
Harvard Practice Medical Study 1984
Canadian Adverse Event Study 2004
Danish Adverse Event Study 2001
Adverse events in British Hospitals 1999-2001
Utah Colorado Study 1992
French Adverse Event Study 2004
The Commonwealth Fund Survey 2005
Australian Quality in Healthcare Study 1992
Adverse Events in New Zealand Study 2002
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  • A worldwide agenda
  • In May 2002 the World Health Assembly passed
    resolution WHA55.18, which urged countries to pay
    the greatest possible attention to patient safety
    and requested the Director-General of WHO to
    carry out a series of actions to promote patient
    safety, including
  • development of global norms and standards
  • promotion of evidenced-based policies
  • promotion of mechanisms to recognize excellence
    in patient safety internationally
  • encouragement of research
  • provision of assistance to countries in several
    key areas.
  • The resolution has ensured that the drive for
    safer health care is now becoming a worldwide
    endeavour, bringing significant benefits to
    patients in countries rich and poor, developed
    and developing, in all corners of the globe.

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Dublin 2003
  • Expert Advisory Group formed to develop strategic
    and operational direction

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  • The Launch of the World Alliance for Patient
    Safety,Washington DC, USA 27 October 2004
  • The World Alliance for Patient Safety was
    launched in Washington, DC, on 27 October 2004.
    This was the first time that heads of agencies,
    health policy-makers, patients' groups and the
    World Health Organization came together to
    advance the patient safety goal of "First do no
    harm" and reduce the adverse health and social
    consequences of unsafe health care.
  • The Director-General of WHO, Dr LEE Jong-wook,
    launched the Alliance followed by keynote
    speeches by the Chief Medical Officer of the UK ,
    Sir Liam Donaldson, and the Director of Agency
    for Healthcare Research and Quality, Dr Carolyn
    Clancy.

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Leadership
  • Essential element

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Key Action Areas
  • Research epidemiology of patient harm and
    solutions
  • Global Challenge
  • Effective role of consumers
  • Taxonomy
  • Reporting Systems

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Key Action Areas
  • Research epidemiology of patient harm and
    solutions
  • Global Challenge
  • Effective role of consumers
  • Taxonomy
  • Reporting Systems

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  • LONDON DECLARATION
  • Patients for Patient Safety
  • WHO World Alliance for Patient Safety
  • We, Patients for Patient Safety, pledge to help
    create a world in which health care errors harm
    fewer people. We, gathered in London from 27-30
    November 2005 to join together in partnership in
    an effort to reduce the massive burden of
    avoidable harm in health care. Risk and
    uncertainty are constant companions. So we come
    together in dialogue, participating in care with
    providers. We unite our strength as advocates
    for care with less harm in the developing as well
    as the developed world.
  • We are committed to spreading the word from
    person to person, town to town, country to
    country. There is a right to safe health care
    and we will not let the current culture of error
    and denial continue. We call for honesty,
    openness and transparency. We will make the
    reduction of health-care errors a basic human
    right that protects human life around the world.
  • We, Patients for Patient Safety, will be the
    voice of all patients, but especially of those
    who are now unheard. Together, as partners, we
    will collaborate in
  • Devising and promoting programmes for patient
    safety and patient empowerment.
  • Developing and driving a constructive dialogue
    with all partners concerned with patient safety.
  • Establishing systems for reporting and dealing
    with health-care harm on a worldwide basis.
  • Defining best practices that deal with
    health-care harm of all kinds and promote those
    practices throughout the world.
  • In honor of those who have died, those who have
    been left disabled and our loved ones today, we
    will strive for excellence, so that all people
    receiving health care are as safe as possible, as
    soon as possible. This is our pledge of
    partnership.
  • January 17, 2006

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Key Action Areas
  • Research epidemiology of patient harm and
    solutions
  • Global Challenge
  • Effective role of consumers
  • Taxonomy
  • Reporting Systems

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More than words?
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Key Action Areas
  • Research epidemiology of patient harm and
    solutions
  • Global Challenge
  • Effective role of consumers
  • Taxonomy
  • Reporting Systems

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Key Action Areas
  • Research epidemiology of patient harm and
    solutions
  • Global Challenge
  • Effective role of consumers
  • Taxonomy
  • Reporting Systems

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Knowledge Is the Enemy of Unsafe Care 1st
Meeting on the Global Research Program for
Patient Safety WHO World Alliance for Patient
Safety in Collaboration with AHRQ Washington
November 1, 2005
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Sources of Data on Patient Harm
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Broad based published studies
  • Strong (larger) hospital focus
  • Obstetric and mental health care often excluded
  • necessarily under-estimate the size of the
    problem
  • divide into negligence studies with AE rates
    3-4 and improvement studies with AE rates
    around 10
  • have reasonable reliability on AE causation, but
    less on preventability
  • The harder you look the more you find

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Adverse events and near miss reporting in the NHS
R Shaw, F Drever, H Hughes, S Osborn and S
Williams 1 National Patient Safety Agency,
London, UK2 Hammersmith Hospitals NHS Trust,
London, UK
  • Results A total of 28,998 incidents were
    reported including
  • 11,766 (41) slips, trips and falls,
  • 2514 (9) medication management incidents,
  • 2429 (8) resource issues, and 2164 (7)
    treatment issues.
  • 138 catastrophic and 260 major adverse outcomes
    were reported.
  • Slips, trips and falls (n 11,766) were the
    most common type of incident

Qual Saf Health Care. 2005 Aug14(4)279-83
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Reporting systems?
  • Voluntary anonymous reporting
  • Does not give prevalence or incidence data and
    hence does not allow prioritisation of
    improvement activities
  • Requires new infrastructure
  • Is heavily dependent on organisational culture
    (which groups are willing to report)
  • Biased toward errors of commission with very
    short latent interval
  • But provides unique contextual information
    unobtainable by other sources!

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Observational Study
  • An alternative strategy for studying adverse
    events in medical care. Andrew LB, Lancet 1997
    349309-313
  • observational study in 3 clinical units in
    tertiary referral hospital
  • 17.7 of patients had at least one serious AE
    leading to longer hospital stays
  • AE risk increased by 6 for each day in hospital
  • 38 of AEs caused by an individual, 10 by
    administrative decisions.

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Observation
  • Useful for a defined clinical process
  • Injection, blood transfusion, IV cannulation,
    delivery, medication administration
  • Useful where there are already agreed standards
    for the process
  • Obtaining the data is low cost and low technology
    and training needs
  • Analysis can be challenging

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Research Stream Focus
  • Using measurement to understand the size and
    nature of patient harm in developing/transitional
    countries
  • Development of measurement tools for data-poor
    environments
  • Expert Group Ross Wilson, Philippe Michel,
    Sisse Olsen, Charles Vincent, Ross Baker
    supported by Alliance team (Itziar Laritzgoitia,
    Helen Hughes and Martin Fletcher)

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Project Objectives
  • To estimate the size and nature of patient harm
    from health care, in developing and transitional
    countries
  • To develop methodologies for measuring patient
    harm in data-poor environments
  • To provide input into the future development of a
    global patient safety study agenda
  • Through measurement, to build local awareness of
    patient safety problems and build will to act to
    reduce patient harm

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Process
  • Countries volunteered workshop Cairo Dec 2005
    then agreed to the task
  • Generating patient safety interest/activity
    through measurement
  • Methodological selection with Philippe Michel,
    Charles Vincent, Sisse Olsen and Ross Baker
  • Peak stakeholder group directly connected to
    Ministry
  • Ethical approval required in most countries
  • Project management and training May 2006
  • Reviewing commenced 2006-7 after funding made
    available from World Alliance
  • 2008 - Draft reports now being reviewed prior to
    publication

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EMRO December 2005
35
Cairo December 2005
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  • Commencement of Patient Safety measurement
    project in 9 African countries (EMRO and AFRO)
    December 2005
  • Egypt, Tunisia, Morocco, Sudan, Yemen, Kuwait,
    Jordan, Kenya, South Africa
  • National teams with representatives from
    Ministry, senior clinicians, health information
    managers etc
  • Goal was to build a research collaboration

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Sources of Data on Patient Harm
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Project Scope
  • 8 countries Egypt, Jordan, Kenya, Morocco,
    South Africa, Sudan, Tunisia, Yemen
  • 26 hospitals (13,500 beds),
  • gt15,000 patient records in the database,

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Outcomes so far..
  • Health care is causing permanent disability and
    death in developing and transitional countries
  • Much of this harm is preventable (75)
  • Medical record review is a (surprisingly) viable
    methodology
  • Research expertise is variable, but enthusiasm is
    high
  • There is agreement to publish results
  • There is hunger to use the results to drive
    improvement efforts in all participating
    countries

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30 years old female admitted twice for drainage
of liquor. In last admission, the patient
complained of labour like pain. breech
presentation and pt underwent C/S . Uterus
ruptured and repaired
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35 old woman complained of amenorrhea for 7/12.
Patient diagnosed as diabetes with pregnancy. She
was given insulin to control her blood glucose
level. Patient refused to stay in hospital and
discharged .
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85 years old male admitted through A/E with
history of inability difficult in micturition,
diagnosed as BPH operated on 12/02/2005, and died
the following day
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18 years old girl admitted through A/E with
complaint of headache, fever, convulsion. Patient
received medication and referred to psychiatric
department and later died
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Lessons Learned So Far
  • Building a team is essential for completion of
    project as well doing something with the results
  • Patient safety can galvanise attention and
    interest such that it leads to huge local effort
  • Connecting the project through EMRO to Health
    Ministries in each country is crucial
  • Medical record quality is improved by
    promulgation of standards (Egypt Kenya)

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Alexandria 2008
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Future Issues
  • How to use the data to drive change locally and
    internationally
  • Publication/presentation
  • Data ownership
  • How much data is enough (and how local) in order
    to inform/energise local efforts
  • How to improve medical records (and
    disease/procedure coding)
  • Leaving the countries with a measurement tool
    that is locally manageable
  • The further development of measurement tools for
    data-poor environments rural and non-hospital

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Pilot testing agreed to in 2007
  • To test the feasibility of for measuring patient
    harm in data-poor environments using
  • Combining medical record review with structured
    interview with clinical staff
  • Using nominal group methods to obtain information
    from a clinical focus group
  • Using observation of a clinical interaction
    against agreed standards

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Looking forward by looking back
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