Hi!
My post is for anyone who has had nitrous oxide during a dental procedure either adults or children with cf. My son had a small cavity that needed taken care of, and the dentist thought "giggle gas" would be best rather than giving him a shot.
The dentist is the head of the dental department at Children's Hospital Pgh., and treats lots of kids with special needs.
About 2 minutes in, my son stopped responding. His eyes were closed, and the dentist was shaking him and asking him if he was ok, (he was shaking his head yes that he was ok prior when the dentist asked), but now nothing. I jumped up, grabbed my sons hand, and nothing. He was lifeless. Kept calling his name and be wasnt responding. After what seemed like forever, but was probably a minute, he opened his eyes and seemed fine. He has no memory of this happening.
i said to the dentist after he was ok, that that scared the crap out of me, he looked right at me and said yeah, me too.
today we saw his peditrician and i told him about it. He said, after checking the internet that nitrous oxide is safe and used with all ages, but it has contraditions for people with respirtory disease, pulmonary disease, and cystic fibrosis. i wa stunned. The dentist is fully aware of all my sons diagnoses.
my question is if any of you or your children have had any similar experiences or told it could not be used on you based on your cystic fibrosis?
We will never use this again, thats for sure. I just worry what the heck was going on with him while this was happening. Doctor asked if they checked his pulse or breathing while this was happening, and no one did.
the only otherthing was that my son was super tired the rest of the day.
sorry for such a long post. Thank you in advance, jshet
My post is for anyone who has had nitrous oxide during a dental procedure either adults or children with cf. My son had a small cavity that needed taken care of, and the dentist thought "giggle gas" would be best rather than giving him a shot.
The dentist is the head of the dental department at Children's Hospital Pgh., and treats lots of kids with special needs.
About 2 minutes in, my son stopped responding. His eyes were closed, and the dentist was shaking him and asking him if he was ok, (he was shaking his head yes that he was ok prior when the dentist asked), but now nothing. I jumped up, grabbed my sons hand, and nothing. He was lifeless. Kept calling his name and be wasnt responding. After what seemed like forever, but was probably a minute, he opened his eyes and seemed fine. He has no memory of this happening.
i said to the dentist after he was ok, that that scared the crap out of me, he looked right at me and said yeah, me too.
today we saw his peditrician and i told him about it. He said, after checking the internet that nitrous oxide is safe and used with all ages, but it has contraditions for people with respirtory disease, pulmonary disease, and cystic fibrosis. i wa stunned. The dentist is fully aware of all my sons diagnoses.
my question is if any of you or your children have had any similar experiences or told it could not be used on you based on your cystic fibrosis?
We will never use this again, thats for sure. I just worry what the heck was going on with him while this was happening. Doctor asked if they checked his pulse or breathing while this was happening, and no one did.
the only otherthing was that my son was super tired the rest of the day.
sorry for such a long post. Thank you in advance, jshet