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SURVEY: Seeking intensivists views of ethical challenges of rapid genomic sequencing

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Should genomic testing go ahead without parental consent? When results could drastically impact a child’s quality of life, should parents be allowed to decline testing?

Share your views in this 10-minute survey. 

We are seeking the views of English-speaking paediatric or neonatal intensivists (either practising or in training) on the use of rapid genomic sequencing for critically ill infants. Our short survey will ask about two different ethical scenarios surrounding gaining consent for genomic testing and how a genomic test might influence treatment decisions. 

This will be the first study to collect global intensivist perspectives on this topic.

If you are able to participle, please click on the following link:

Please feel free to forward this ad to relevant colleagues!

Any questions, please email: biomedicalethics@mcri.edu.au

Christopher Gyngell
Senior Lecturer, Department of Paediatrics, The University of Melbourne
Team Leader, Biomedical Ethics Research Group, Murdoch Children’s Research Institute


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