CUH

Nasophayngeal airways

Cleft (East of England Cleft Network)

 

Some operations narrow the airway a great deal. Indeed, this may be required to give your child a better speech result.

 

In some cases the airway may need to be held open by a temporary device called a nasopharyngeal airway (NPA).

 

nasopharyngeal tube

 

The tube goes from the nose to the back of the throat and keeps the tongue from blocking the airway and so allows your child to breathe easily. The tube usually stays in for 48 hours and will need to be kept open by suctioning regularly by the nursing staff on the ward.

 

It will be taken out by the anaesthetist – this is not a painful process.

 

Often children don't feel like feeding until the NPA is out. In the meantime they are fed with fluids through an intravenous line.

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

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On this site:

> Neonatal Cleft lip and palate

 



On other websites:

> CLAPA - The Cleft Lip and Palate Association (Cambridge branch)

 

Offers information about cleft lip and palate as well as support for families.

 

> NDCS - The National Deaf Children's Society

Offers help and support to deaf children and their families.

 

> NHS Direct - Includes a series of pages about cleft lip and palate