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GI tube, Ports???

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A GI tube /button are for extra nutrition ,or for kids who are orally unable

to eat .The kids /babies/adults get nutrition thru the tube into their

stomach.The port /infusaport is for IV medication thru a permanently placed

tube in a vein for those with bad veins or who have a hard time with

IV's.Please understand this is a very simple explaination you could look in

the archives for GI-feeding tube,NG Feeding tube. Port,or Infusaport,or

Portacath.These are slightly different items that do similar things.I hope

this helps a little.BeckyB.

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A GI tube /button are for extra nutrition ,or for kids who are orally unable

to eat .The kids /babies/adults get nutrition thru the tube into their

stomach.The port /infusaport is for IV medication thru a permanently placed

tube in a vein for those with bad veins or who have a hard time with

IV's.Please understand this is a very simple explaination you could look in

the archives for GI-feeding tube,NG Feeding tube. Port,or Infusaport,or

Portacath.These are slightly different items that do similar things.I hope

this helps a little.BeckyB.

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Can someone tell me what these are, what are the differences. Does a child only

need one if it is undernourished, possibly from being picked up at a later stage

in life?? I am a bit foggy on this. My hope is that not all child with CF need

to get one of these tubes. Would appreciate some clarification here

Thank you

mum to baby Liam

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My daughter got her G-tube almost 2 years ago. We don't

regret it one bit. It has help Jess keep weight on that noramlly she

would lose when she would have a flair up. She can eat during the day

but when she is having more congestion she won't eat she she gets

hooked up to her tube feedings. So if these kids are having trouble

with their weight the feeding tubes are great( NG -through the

nose...G-tube - right into the stomach and a J-tube - goes into the

intestines)

As for the port, Jess is getting ready to get her first. After 12

PICCs since 1998 her veins are getting harder and harder to get the

lines in. she is getting tired of getting stuck and stuck over again.

Dana

> Can someone tell me what these are, what are the differences. Does

a child only need one if it is undernourished, possibly from being

picked up at a later stage in life?? I am a bit foggy on this. My

hope is that not all child with CF need to get one of these tubes.

Would appreciate some clarification here

> Thank you

> mum to baby Liam

>

>

>

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My daughter got her G-tube almost 2 years ago. We don't

regret it one bit. It has help Jess keep weight on that noramlly she

would lose when she would have a flair up. She can eat during the day

but when she is having more congestion she won't eat she she gets

hooked up to her tube feedings. So if these kids are having trouble

with their weight the feeding tubes are great( NG -through the

nose...G-tube - right into the stomach and a J-tube - goes into the

intestines)

As for the port, Jess is getting ready to get her first. After 12

PICCs since 1998 her veins are getting harder and harder to get the

lines in. she is getting tired of getting stuck and stuck over again.

Dana

> Can someone tell me what these are, what are the differences. Does

a child only need one if it is undernourished, possibly from being

picked up at a later stage in life?? I am a bit foggy on this. My

hope is that not all child with CF need to get one of these tubes.

Would appreciate some clarification here

> Thank you

> mum to baby Liam

>

>

>

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