I talked to the doctor today and she's ordered another echo of both babies. DD has a pretty large PDA and DSs is smaller, but both have decreased in size since they restricted fluids. The doctor said she doesn't think they're small enough and we're running out of time to treat it with medicine. So, she wants the cardiologist to take a look again. She is concerned because dd is still 6 below her birth weight and is two weeks today. DS is at his birth weight. She said they will have to stop breast milk when giving the meds so they'll go back on nutrients.
Does anyone have experience with this issue?
Re: Treating PDA with meds
I'm a lurker, but thought I'd share my experience. Both my girls were born with moderate to large PDAs. We went through two rounds of meds before they finally decided to do surgery at 30ish weeks. Deep down we knew they would have to
Both my twins (27 weekers) had PDAs. Each of them were given three rounds of indocin. For my DD, the medicine closed the PDA. However, it didn't work for my son so he had a PDA ligation at 2 weeks old (29.5 weeks).
I know the idea of your
Beta#1 (12dp3dt)= 353, Beta#2 (15dp3dt)= 1466, Beta#3 (22dp3dt)= 14,139, First u/s: TWINS!!
After 10 weeks of bedrest, our two little ladies joined us at 28w6d
My DD had a very large PDA that closed after 3 rounds of indomethacin at 3 week
www.virginiakkent.blogspot.com
Peanut Butter and Jelly!
<a href="http://s568.photobucket.com/albums/ss122/AliceNP/?action=view