So when I was about 29 weeks pregnant they noticed during an ultrasound that LO had a dilated right kidney but her left was fine. Throughout the remainder of my pregnancy I had to keep getting U/S every few weeks and then it started to slowly match with the left. It looked well enough that I was still able to deliver at the hospital of my choice and that the baby wouldnt need immediate attention.
At one month they wanted to check her kidneys again and reported that they were almost perfectly matched and nothing further needed to be done but to have one more U/S at 6 months just to be safe.
Well Monday we took LO in and got her U/S.......today we got a call finally from her doctor and the news was not what we were hoping for. Her right kidney is "stable" but dilated outside of normal range again.
I know she has two kidneys and that this can be very common in newborn babies and they usually self correct within a year. I am just wondering if anyone else out there has experienced the same type of situation? did it correct? any advise would be appreciated. TIA
Re: Dilated Kidney
Yes---We are going through the same exact problem.... both of my DDs kidneys have the issue,dealing with the reflux too. We are also on an antibiotic.We are on Septra, taken everynight. I agree with the PP. Call you DR and see why they dont think you LO needs to be on it. They found my daughters dialation while she was in the womb also. And as soon as she was born then took her for a abdominal scan... since then we've gone to a specialist and had scans/tests done. We will have another test done at 8 months. My Dr. Said this issue rates on a scale...1-5. 5 being the worst, and damage has already occured. My LOs is a 3. My Dr also said LOs with a 1 and sometimes 2 usually clear up. some by 1, but most by 3. I Hope when we go for the 8 month scan we get good news and can get off these antibiotics!!! GL to you ladies and your LOs!!!!
PS--I LOVE that Ive found women on here whos LOs are having the same issue. People who hear alot LOs issue, are like 'wtf', like Im speaking a crazy language!
this!
And Yes, I was told its alot more common in boys then girls.
Oh and BTW. I wrote that soo late/half asleep...but I sound wayy too happy about finding other women/LOs with the kidney issues. I just meant I knw I have ppl on here who can understand and relate. And maybe one day I can go to you with questions! Im not happy that other babies have it!

I wish allll our LOs didnt have this stinky kidney issue.
To clear up the antibiotic issue...
My DS had the same issues, but very mild just like the OP. Our pedi put him on a low dose of Septra as a preventative measure. We had a second u/s and a VCUG and then visited with a pediatric urologist who said that the swelling was still there, but the VCUG showed that the urine was flowing in the correct direction with no serious backflow or blockage. He said the Septra/antibiotic was not necessary to take because it was such a mild case. At this point we do nothing but sit and wait and get u/s done every 3mo for the next year to monitor everything.
So... just to clarify, just because your LO has mild hydronephrosis, it does not automatically buy you a ticket to the pharmacy for Septra.
Thats what I started thinking.....so I called my mother who oddly enough works for an adult nephrologist and she said to calm down and because it was normal at one month old and they used "stable" to describe it now(even tho its dilated) that most likely it is working fine and just larger. She said to call double check but said that the dr we go to is really part of the best childrens division around and they would have explained more if it was serious(such as reflex or urethers being enlarged) or called us in for an in person check back. The fact that they dont even want her to get another one for 6 months is good she said and would signify a mild case. But I know you all understand......im her mother and any problem with an important organ is not going to settle well!
And about PP I know you are not excited that other babies are going through it but yes it is nice to know your not alone and now have people to turn to. Plus knowing that your child isnt the only one with this issues does bring a little peace of mind in knowing that it just happens sometimes but can be fixed.
2 of my 3 boys had dialated kidney pelvis'. My oldest's went away about 1 month after birth. The second one's didn't go away, so they ran some tests and found that he has posterior urethral valves and had to get them removed at 8 months, his was checked at age 1, 2 and 3 and his kidneys are fine. Not sure if this is the same as what you are going through.