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Prediction models for neonatal outcomes: are they useful? Are they feasible?
  1. Lisa Barker1,2,
  2. David Field1
  1. 1 Department of Health Sciences, University of Leicester, Leicester, UK
  2. 2 Neonatal Intensive Care Unit, Leicester Royal Infirmary, Leicester, UK
  1. Correspondence to Professor David Field, Department of Health Sciences, University of Leicester, 22-28 Princess Road West, Leicester LE1 6TP, UK; df63{at}

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Randolph and colleagues1 report their attempts to develop a prediction model for death and/or neurodevelopmental impairment (NDI) in a group of extremely low birthweight infants. They focused on the ability of low pH and or acidosis to enhance the precision with which prediction of this combined outcome could be achieved. Ultimately they were unsuccessful with other parameters being more important in the final model than measures of acidosis.

They conclude that NDI is not just the product of the early neonatal course, and as a result prediction based on condition at birth, or in the period immediately after birth, is perhaps not feasible. This may well be true but it is perhaps also worth reflecting on our rationale for seeking predictive models and whether there would be benefit from adopting a somewhat different approach.

In general these types of studies have had one or both of the following broad goals:

  • To provide a tool that permits risk adjustment between services that have different case mixes. The use of early data allows babies’ outcomes to be compared and adjusted based on their risk at the time they entered the service.

  • To provide clinicians and parents with a means of looking at the likely outcome of a child early in their course so that care can be orientated appropriately, perhaps from an intensive to a more palliative approach.

These goals are linked as the first (risk adjustment) looks at the risk for a population whereas the second (likely outcome) looks at …

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  • Contributors DF was invited to write this editorial. LB and DF were involved in designing the piece of work. The first draft was written by LB and DF drafted the work and revised it critically for important intellectual content. LB and DF agree and approve the version submitted.

  • Competing interests None.

  • Patient consent Obtained.

  • Provenance and peer review Commissioned; internally peer reviewed.

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