PAEDIATRIC ALTERED CONSCIOUS LEVEL GUIDELINE

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AIMS

SCOPE

CLINICAL QUESTIONS

EVIDENCE-BASED SEARCH

DELPHI PROCESS

RECOMMENDATIONS

COMMENTS

PARTICIPANTS

DRAFT GUIDELINE

 

 

These pages are now of historical interest only.

 

All the information is summarised in the Full Technical Document.

 

 

 

INTRODUCTION

 

 

A new paediatric guideline is under development and you are more than welcome to help in this process.

 

Children who present with a decreased conscious level do so for a variety of reasons. A recent study found that about 30 children out of every 100,000 children will present per year in a coma not caused by trauma, and the overall mortality in this group of children was 46% (Wong et al, 2001). With such a high mortality rate and a multitude of causes, a guideline to help health professionals investigate and treat children who present in this way will be very useful.

 

Health professionals will need to answer key clinical questions to inform their management decisions. The answers to these questions need to be based on the best available medical evidence and where there is no evidence available consensus opinions can be used to fill the gaps. The search strategies for finding the evidence to answer these questions can be viewed through this site, as can the formal consensus process known as the “Delphi panel”.

 

Recommendations based on the evidence and consensus opinion will form the final guideline which will be disseminated in 2005. A guideline development group has been formed to develop this guideline and this site aims to explain the developments as they happen. To help the guideline development group in this task please comment on the guideline process by emailing richard.bowker@nottingham.ac.uk and both your comments and responses to them will be posted on the comments board (anonymously unless specified).

 

The development of this guideline has been funded by The National Reye’s Syndrome Foundation of the United Kingdom, a registered charity (No. 288064) which was formed to provide funds for research into the cause, treatment, cure and prevention of Reye’s syndrome and Reye-like illnesses, to inform both the public and medical communities and to provide support for parents whose children have suffered from these diseases.