My sister (a SAHM) had her 4th child at 11:40 pm on Good Friday. Tate is beautiful, but Saturday afternoon he was having trouble nursing. When the ped came through for his routine exam, they discovered that Tate has a membrane closing off his left nostril (the membrane is up in the pharynx (sp)). In the early afternoon he was admitted to the NICU so his O2 sat could be monitored. They discovered that anytime his head fell forward, it dropped. It also dropped if he was laying looking to his right.
They told my sister that he couldn't be discharged until she and her husband (a pharmacist at the hospital where he was born) learned infant CPR. My mom told my sister to insist that she won't take him home unless Tate has a pulse-ox monitor.
At first they were saying that they would surgically remove the membrane, but now they are saying that any surgery would be too rough on the little guy (he was full term, 7lbs 6oz and 20-1/2").
Any insight from either ENT or peds would be greatly appreciated. Of course when I told DH about it last night, he said that they should insist on taking the baby to the Children's Hospital where he is doing medical school. It is a great hospital, but it is nearly 4 hours away.
They told my sister that he couldn't be discharged until she and her husband (a pharmacist at the hospital where he was born) learned infant CPR. My mom told my sister to insist that she won't take him home unless Tate has a pulse-ox monitor.
At first they were saying that they would surgically remove the membrane, but now they are saying that any surgery would be too rough on the little guy (he was full term, 7lbs 6oz and 20-1/2").
Any insight from either ENT or peds would be greatly appreciated. Of course when I told DH about it last night, he said that they should insist on taking the baby to the Children's Hospital where he is doing medical school. It is a great hospital, but it is nearly 4 hours away.
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