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We propose adopting a systematic and integrated approach to the design and provision of information to clinical oncologists and breast cancer patients in a routine clinical environment. The basis of the proposal is to pool the required multidisciplinary expertise to design two specific information support, software tools that link to the prognostic information available about the individual patient, and present this in a user-centered, flexible way, so as to maximise the utility to the oncologist and to the patient. This requires skills in intelligent systems, bioinformatics and interface design. The eventual systems follow the main requirements of the Medical Devices Directives, in being design assured by use of best practice in statistical, neural and expert system inference, together with risk assessment, to verify the inferences made against clinical knowledge and also to assure the integration of the software system as a whole, and finally an evidence-based evaluation of effectiveness to the two types of users. This approach complies with a solid framework for the development and evaluation of complex interventions to improve medical care (http://www.mrc.ac.uk/complex_packages.html).

Such an approach, unlike traditional decision-making techniques including multi-criterion, will provide breast cancer clinicians and patients with a high-assurance, decision support that is adaptive to their decision practices yet allowing for evolutions of decision models, decision resources (data) and other users concerns. This novel approach will provide important insight into the development of an integrated decision support infrastructure for high-assurance decision activities.

Required Research

The evidence-based approach to the delivery of medical care has gained wide recognition within the healthcare community, advocating that decision-making should use current knowledge and clinical evidence from systematic research (Sackett et al 1996). In breast cancer care, there are currently few staging methods in widespread use by clinicians, namely the Nottingham and Manchester staging systems. Patients are provided with key information mainly during one pre-set appointment with the clinician and perhaps the breast care nurse. This can lead to patients being given information that they are not able to rationalise, or is pitched at an inappropriate level of detail, perhaps also missing out on the opportunity to ask for further clarification as doubts and queries set in after the event. In both the case of the patient, and of the clinician, there is a need not just for accurate and relevant information, but also to make this accessible at the time when the user requests it, in a form that the user will relate to, and with the opportunity to follow-up levels of detail under control of the user.
Enabling such decision-making processes will require addressing a number of issues including:

  • How to integrate support models for clinicians and for patients within a common reasoning framework.

  • How to identify and fetch evidence that is relevant to a specific clinician?s and/or patient?s decision point, and to validate the advice given by recourse to explicit reasoning models.

  • How evidence and decision traceability is best presented to each group of users.

To address these questions, we will study and model the information needs of clinicians and patients, developing techniques tailored to the level of complexity of the users, but providing also the capability to trace the advise given in progressively greater levels of detail. While the goals we have set ourselves are ambitious, we believe that they are realisable in the proposed timescale of 3 years, as follows:

Given the multi-disciplinary nature of the specification, design, implementation and evaluation aspects of this health informatics system, the project will actively involve clinicians, statisticians, computer scientists and public health researchers, who will participate in the modelling, specification development and evaluation of the proposed work. In short, it will require active participation by the complete patient care team, in dialogue with psychologist, sociologist, statisticians and computing specialists who will implement the informatics system. The expertise to do this is currently in the consortium.

  • The starting point for the provision of patient specific information are prognostic groups allocations by statistical survival models, together with rule-based reasoning captured from expert clinicians and other members of the care team. This will progress to include an interactive user interface supported by a reasoning model, which sophistication at first will be kept as simple as possible to facilitate verification and validation of informatics system as a whole, and building user acceptance and trust in the system. It will then be augmented with a visualisation tool with self-organising data maps and data segmentation facility.

  • The survival and segmentation models may be used to define metrics for data access. Principled statistical and pattern recognition methodologies to model censored data and for visualisation and segmentation are already in the domain of expertise of the core team of researchers, as are the aspects of rule-based reasoning and multimedia engineering.

 

Project Title

Towards a Disciplined Approach to Integrating Decision-Support Systems for Breast Cancer Care Activities

Sponsors


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