Home > Cases > Avert-IT Project for the prediction of adverse events

Avert-IT Project for the prediction of adverse events

Acronym of the case:

Avert-IT

Web address of the case:

Country of the case:

United Kingdom , Pan european

City/region:

Highlands of Scotland

medical | intensive_care | hypotension


Posting Date: 21 July 2008
Last Edited Date: 09 October 2009

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Author:

Steve Reeves (Avert-IT project)United Kingdom
Type of initiative
  • Project or service
Case Abstract

Intensive Care patients can experience Adverse Events associated with sudden episodes of low blood pressure. These Adverse Events may impact all of the main organs resulting in longer lengths of stay, increased care costs and reducing quality of outcomes. Existing technologies enable to clinicians to know when these events have occurred and treat the effects. Medical techniques for avoiding Adverse Events currently exist, but clinicians don’t have a reliable way to predict the occurrence, so there’s no opportunity for intervention. A model for predicting Adverse Events offers potential for improving outcomes across a wide range of conditions and or illnesses.

Description of the case
Domain
Sector
January 2008 to January 2011
Date operational
January 2008
Target Users
Add Patients | Health authorities | Health professionals
Target Users Description

Intensive care decision support

Scope
International
Status
Research
Language(s)
English
Policy Context and Legal Framework

Research indicates average lengths of stay can be reduced by up to 30%, and outcomes improved for a similar proportion of patients, if these Adverse Events can be avoided through prediction and intervention. Potential savings across the EU exceed 5 billion euros, annually.

Project Size and Implementation
Type of initiative
Participation
Overall Implementation approach
Partnerships between administration and/or private sector and/or non-profit sector
Technology choice
Standards-based technology
Funding source
Public funding EU
Project size
Implementation: €1,000,000-5,000,000
Implementation and Management Approach

Research study involving six university hospitals and the private sector

Impact, innovation and results
Economic effects
Larger than €10,000,000
Impact

Objectives

The primary objective of our research is providing clinicians with advanced notice of upcoming hypotensive episodes.

In order to achieve this result we're needing to solve a number of issues:

   * Agree a common definition of hypotensive episode - all six of our centres currently work to different definitions
   * Build a software interface which collects data from patient monitoring devices - all centres have different equipment
   * Find a way of transmitting patient data from the research centres to our data warehouse
   * Build software which collects observation, treatment and outcome data at the bedside
   * Build a Bayesian Artificial Neural Network and train it to recognise patterns which precede hypotensive episodes
   * Build software to enable researchers to analyse actual data, identifying circumstances in which the BANN achieves an accurate prediction and those in which if provides false positives
   * Build software which alerts clinicians to potential upcoming episodes.
   * Multi stage clinical trial.

In parallel the project includes the need for multi stage ethics approval, support from IT staff in each of the centres, identification and protection of foreground IPR, and multiple routes to market.

We're also required to promote Framework 7 research and collaborate with other FP7 projects as appropriate.


Results


The starting point for our research has been a database of patient care data amassed as part of the Brain IT project, previously funded under Frameworks 4 and 5.  This data is minute by minute readings from monitors, and comprises more than 200 patients with traumatic brain injuries.  In some cases the data is incomplete and possibly inaccurate.

In the first stage we analysed the legacy data testing the various definitions of hypotension used by the research centres. Comparison of the definitions and events indicated by them enabled us to agree between all six centres a common definition, on which we could train the BANN.

In the second stage the BANN was used to examine patterns of parameters preceding episodes.  Subsequent monitoring of those patterns suggested approximately 35% of future episodes could be identified as outputs from the pattern recognition.  In addition some false positive predictions indicated ways the monitored parameters and definitions could be refined to improve accuracy.

In the third stage, working with IT staff at the centres data capture and transmission software has been built and installed. Software for collecting data at the bedside has been built in conjunction with clinical staff and installed. Software enabling researchers to monitor and enhance the accuracy of the prediction engine has been installed and is now in production use.

in the fourth stage we'll be monitoring and enhancing the BANN prediction capabilities, preparing data which will support our application for ethics approval for stage five - live monitoring and alerting of upcoming episodes.

Throughout the project we've been researching questions related to the protection of IPR in the worlds major markets.  As of yet we've made no application for patent - because we haven't finished the research.  We're still refining our understanding of monitored parameters and which patterns offer which levels of accurate prediction.

We've also collaborated with multiple public bodies, promoting FP7 and offering guidance to potential applicants.

The Avert-IT project has been selected by the Use and Diffuse project as an example of best practice and features in the projects publications.

Lessons learnt

The project is just starting, so no lessons learned as yet but we'll post something interesting here as soon as we can be sure that isn't predjudicing our ability to get a patent on the IPR

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