Clinical PotpourriDevelopment and validation of the new ICNARC model for prediction of acute hospital mortality in adult critical care
Introduction
Risk prediction models for critical care take information from early in a patient's critical illness to make a prediction about the patient's likely outcome. They are predominantly aimed at the health care provider level – allowing fair comparisons between different providers, adjusted for case mix. In the UK, the risk prediction model used to underpin the national comparative benchmarking programme for adult critical care is the Intensive Care National Audit & Research Centre (ICNARC) model [1].
As critical care populations change and new diagnostic, therapeutic and prognostic techniques become available, risk prediction models need to be updated and improved [2]. Many of the existing risk prediction models for critical care, including the ICNARC model, are constructed around a numeric severity score. While this approach has the advantage that the score can be used as a simple description of severity of illness – either for a population or an individual patient – such an approach restricts the statistical techniques that can be used for risk prediction. It is well-recognised that dividing continuous predictors, such as physiology, into categories is not the best approach to modelling [3].
The aim of our study was to develop and validate a new predictive model to improve the accuracy of comparisons between UK critical care providers. To achieve this, we decided to leave behind the paradigm of the severity score, allowing us to employ up-to-date statistical techniques for handling missing data and for continuous nonlinear modelling of physiological parameters.
Section snippets
Selection of data
The Case Mix Programme is the national clinical audit for adult critical care in England, Wales and Northern Ireland. Participation is 100% among adult general critical care units delivering Level 3 (intensive) or combined Level 2/3 (intensive/high dependency) care and many specialist critical care units (e.g. neurocritical care units and cardiothoracic critical care units) and standalone Level 2 units also participate. For all participating units, data on consecutive admissions are recorded
Results
There were a total of 155,239 eligible admissions to 232 adult critical care units from 1 January 2012 to 31 December 2012 included in the development dataset and 90,017 admissions to 216 critical care units from 1 January 2013 to 30 September 2013 in the validation dataset. The characteristics of the included critical care units are reported in the Supplementary appendix (Table S1) and the characteristics of included patients are summarised in Table 2. Pupil reactivity was found to have poor
Discussion
In this paper we present an improved and updated risk prediction model for UK critical care services. On external validation, the model performed well both overall and across different specialised critical care units, including cardiothoracic critical care units, neurocritical care units and standalone high dependency units. The new ICNARC model improves on previous risk prediction models through better handling of missing data, introduction of new predictors, continuous nonlinear modelling of
Conclusions
The main aim of the project was to improve risk prediction that underpins quality improvement programmes for critically ill patients in the UK. The new risk prediction model developed in this study showed good performance across all types of units and when evaluated in specific patient subgroups. This will enable more accurate comparison across critical care units including, for the first time different types of critical care units. We believe it should be the model of choice for benchmarking
Conflicts of interest
None.
- APACHE
Acute Physiology and Chronic Health Evaluation
- ICNARC
Intensive Care National Audit & Research Centre
- MPM
Mortality Probability Models
- SAPS
Simplified Acute Physiology Score
Abbreviations
Acknowledgements
This work forms part of a project supported by the National Institute for Health Research NIHR Health Services and Delivery Research (HS&DR) Programme (project number 09/2000/65) which has been published in full [6]. This manuscript has been prepared in accordance with the NIHR dual publication policy (http://www.journalslibrary.nihr.ac.uk/information-for-authors/dual-publication). The funder had no involvement in study design; in collection, analysis and interpretation of data; in the writing
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