Tuesday, February 3, 2009
Update from Morning Rounds
During morning rounds we learned that Ryan has lost a substantial amount of weight because he has been fed primarily through a sugar water IV and has only been receiving a half ounce of breastmilk every 3 hours since yesterday. He is down 13 ounces from his birth weight of 7 pounds, so the doctor ordered that a protein mix (TPN) be added to his IV. They are hoping to be able to up the amount of breastmilk per feeding possibly tomorrow depending on how he is doing. He has a lot of mucus in his GI system and has spit up several times, but the nurse practitioner said that his GI motility should improve once they are able to increase his feeding quantity. Regarding his resipratory issues, he is doing a slight bit better maintaining his oxygen levels, but the doctors would like to see him doing much better before they consider trying to wean him down from the level of oxygen he is currently receiving in the hood. They are going to keep everything the same at least for the next 12 hours (including continuing to enforce very limited stimulation) and then re-evaluate him. Hopefully he will improve more dramatically during that time and they'll be comfortable trying to wean him off the oxygen. They also warned us that, assuming he improves and then tolerates slowly weaning him off the oxygen, he will likely have a lot of feeding difficulties. They said that the vast majority of babies who overcome pulmonary hypertension have problems with feeding. Unfortunately we are way too familiar with feeding difficulties from our experience with Ethan. Please pray that Ryan turns the corner within the next 12 hours and really shows improvement in keeping his oxygen saturation level up on his own and respiration rate down. Please also pray that the doctors are able to start weaning the oxygen in his hood down, that he tolerates it well, and that we are able to hold him as soon as possible. I am hopeful that he will "prove them wrong" about feedings and do much better than they are expecting him to do when it comes to eating/nursing. I asked if the nurse practitioner could guesstimate when we might be able to go home (assuming all goes well and his condition doesn't worsen), and she said her best estimate would be 1-2 weeks from today. We were a bit surprised (and definitely disappointed) that Ryan might need to be here that long.
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4 comments:
Please know that we will continue to pray for Ryan. We are thinking of you often.
Love~Staci (For the Middletons)
Julie-
I'm so sorry you have to go through this scary experience! Our thoughts and prayers are with you and your family and we're cheering Ryan on from afar. We pray that he will improve with his sats and O2 level and that he'll be strong enough to take larger feeds. He definitely can prove them wrong on feeding difficulties - I've seen it before!! Thank you for keeping us updated!! Thinking of you throughout the day!
Susie (Grunow) Baker
Keep your chin up, Julie! I know how hard it can be, but you'll all be home and together soon. And take heart, Ryan will learn to breastfeed if you stay with it. It took Evan two months to get it down, but once she did, she was a trooper. :) We're keeping you all in our prayers.
Dan and Julie,
Thanks for the update. We will continue to keep your family in our prayers.
Todd and Tracy Brandenburg
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