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Modelling Medical Knowledge and Processes

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Title: Modelling Medical Knowledge and Processes


1
Modelling Medical Knowledge and Processes
  • Tony Rose
  • Software Development Manager
  • Advanced Computation Lab

2
Contents
  • CR-UK and the Advanced Computation Lab
  • Cognitive science the clinical context
  • Clinical guidelines modelling languages
  • The Credo Trial
  • Usability issues

3
Cancer Research UK
  • History
  • Europe's largest independent cancer research
    organisation
  • 2002 merger of ICRF and CRC
  • Vision
  • to conquer cancer through world-class research,
    aiming to control the disease within two
    generations
  • Funding
  • research spend for 2002/2003 191 million
  • Structure
  • In-house research labs
  • External research grants

4
Advanced Computation Lab
  • One of CR-UKs in-house labs, based in London
  • Mission
  • research in the computer and cognitive sciences,
    including AI and cognitive psychology, as a basis
    for developing innovative information
    technologies to support patient care
  • Structure
  • Scientists developers

5
Research Aims
  • To carry out fundamental research in theories of
    computation and intelligent systems
  • To develop novel technologies based on
    theoretical results
  • To demonstrate the practical value of these
    technologies in biomedical applications for
    clinical research and patient care

6
Research at the ACL
7
The Clinical Context
  • Perhaps 16,000 lives could be saved if all
    current knowledge of cancer were properly
    applied
  • ICRF Vision for Cancer, 1995
  • Up to 97,000 unnecessary deaths p.a. in the US
    are due to medical error. Total national costs
    between 17B and 29B
  • Institute of Medicine, To Err is Human 1999

8
The Knowledge Crisis
  • Modern medicine is becoming a humanly impossible
    task
  • New knowledge is being generated too quickly for
    individuals to absorb and for organisations to
    assimilate into mainstream clinical practice

9
The Role of Clinical Guidelines
  • CGs based on best available evidence from
    systematic research
  • Following clinical guidelines helps to save lives
  • improve care quality and standardize care
  • Various sources
  • National Institute for Clinical Excellence
  • National Guideline Clearinghouse
  • many more

10
CGs and CIGs
  • Most CGs are deployed in textual form
  • Narrative, flowcharts, diagrams
  •   BUT
  • busy clinicians have little time to read
  • memories are unreliable, working pressures acute
  • conventional guidelines address general
    principles of care, not the needs of individual
    patients
  • Our aim is to provide evidence-based decision
    support in executable form

11
CIG Modelling Languages
  • Various paradigms, e.g.
  • procedural
  • rule-based
  • e.g. Arden syntax
  • task-based
  • GLIF, Eon, Asbru, PROforma

12
PROforma
  • Formal language for modelling clinical knowledge
    and processes
  • supports the definition of clinical guidelines
    and protocols in terms of
  • a set of primitive tasks which are composed into
    networks representing clinical processes
  • logical constructs that allow the details of
    tasks and their inter-relationships to be defined

13
Task hierarchy
  • Uses Argumentation for decision making
  • weigh up arguments for or against a particular
    proposition

14
PROforma
  • Plans container structures that hold any number
    of task instances
  • Enquiries requests for information or data from
    an external agent (e.g. the end-user)
  • Actions typically clinical procedures (such as
    the administration of an injection) to be carried
    out
  • Decisions choices of some kind, such as a choice
    of investigation, diagnosis or treatment

15
Tallis
  • Software environment for developing and executing
    clinical decision support and workflow
    applications
  • Clinical processes are modelled using the Tallis
    Composer
  • Processes can be enacted to provide workflow and
    DS via a web browser

16
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17
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18
Knowledge Sharing
  • Tallis supports knowledge sharing through a
    repository server, e.g. OpenClinical.net
  • leverage work done by others
  • reduce development costs
  • Leads to knowledge publishing lifecycle
  • iterative development and review process

19
Formalised in PROforma
Protocols, guidelines, care pathways

Tested in silico (in the lab)
Trials

Feedback into research and policy
Routine use
20
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21
The Credo Trial
  • as a basis for developing innovative
    information technologies to support patient care
    -gt the Credo Trial
  • multi-centre trial of integrated software package
    designed to support breast cancer care throughout
    the patient journey
  • Collaborators
  • Guys Hospital Breast Unit, London
  • Addenbrookes Hospital Breast Unit, Cambridge
  • Carol Franc Buck Breast Care Centre, UCSF

22
Trial Questions
  • What is the baseline quality and safety of
    decision-making in the management of breast
    cancer?
  • Can PROforma yield improved consistency, quality
    and safety of clinical decision making through
    the patient journey? How and where?
  • Can such services be acceptable to and valued by
    clinicians? Freeing them from administrative and
    operational burdens?
  • Can this result in improved experience for the
    patient?

23
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24
Credo Core Service Model
25
Phase 1
  • Total of 222 clinical, patient and communication
    services identified
  • about 65 require professional decisions
  • Software demonstrator constructed
  • A number of prototypes implemented in PROforma
    and web technologies
  • Pilot trials initiated

26
Phase 2
  • Continue pilot trials
  • Initiate clinical trials of specific services
  • Develop infrastructure
  • Clinical database
  • Patient records
  • Communications messaging
  • Plan multi-centre trial of integrated care
    manager

27
Phase 3
  • Phase 3
  • RCT of integrated patient journey system
  • Quantitative assessment of clinical outcomes
  • compliance with pathway
  • effectiveness and timeliness of communication
  • patient satisfaction

28
Credo Phase 1 Results
  • Aim trial of support for initial assessment
    (Triple Assessment) of women with breast symptoms
  • Methodsoftware assists clinician in calculation
    of familial risk, selection of appropriate
    investigations and subsequent management of
    patient
  • Study design Crossover experiment with balanced
    blocked design, each clinician managing a set of
    10 simulated cases, 5 with and 5 without DS

29
Credo Phase 1 Results
  • Aim to evaluate potential effect of PROforma DS
    on clinical decision making in Triple Assessment
  • Decision model
  • Pathway included 4 decisions familial risk, type
    of imaging, type of biopsy, and management
  • Materials and methods
  • 15 hypothetical paper cases developed by an
    expert panel of 5 judges (2 breast surgeons, 1
    breast pathologist, 1 radiologist and 1
    geneticist). Optimal management for each case was
    agreed by consensus
  • 24 doctors asked to manage 5 cases with and 5
    without DS. Balanced block design used to
    allocate cases

30
Triple Assessment
Hurt C, Patkar V, Steele R, Rose T, Fox J (in
preparation) Steele R, Fox J Proceedings of
European conference on AI in Medicine, 2003
31
Triple Assessment Study Results
24 participants (17 consultants, 5 specialist
registrars, 1 nurse practitioner) Average number
of years in speciality 9.3 (range 1 - 23)
Would patient care improve with TA decision
support? In favour 16 Undecided 1 Against
7 Would they personally wish to work with TA
decision support? In favour 12 Undecided
3 Against 9
32
Credo Phase 1 Results
  • Outcome measures deviation from the guidelines
    (as agreed in advance by a panel of experts

33
Usability Issues
  • High level (conceptual)
  • How best to model medical knowledge?
  • What kind of conceptual structures do clinicians
    use?
  • What kind of decision making framework?
  • How should those concepts be represented by the
    system (UI)?
  • Low(er) level
  • Does the UI employ HCI best practice?
  • Does it support the users task appropriately?

34
The Tallis Usability Trial
  • Aim to compare Tallis Composer 1.3 with Tallis
    Composer 1.5
  • Hypothesis Tallis 1.5 is more usable for new
    users
  • Study design between-groups trial with each
    participant performing 6 tasks with 1.3 or 1.5
  • Outcome measures
  • For each task
  • Classify as successful / unsuccessful / partial
    completion
  • Assign score based on each level of completion
  • Overall average score across all
    tasks/participants

35
Paper Prototyping
  • Tallis 1.3 is a working prototype, BUT -
  • Tallis 1.5 is a design proposal it exists on
    paper only
  • How do we test a design on paper?
  • Use paper prototyping
  • paper versions of screens widgets
  • one person acts as computer
  • both UIs are mocked up
  • think-aloud protocol

36
Collaboration
  • MEDAL (Prof. Sriram)
  • Extensive online repository of medical algorithms
  • www.medal.org
  • Integrate Tallis Medal
  • Ontologies, EMRs, lab IS, etc.
  • Create an online, open access repository of
    executable medical knowledge

37
Questions?
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