We have a follow-up appointment with Dr. Barnhart next Friday. The results from the nissen seems to be optimal. I haven't noticed reflux symptoms. Andrew did gag and heave the first few days in the hospital, but since getting food again hasn't had any episodes.
Jul 24, 2010
Happy Again
We have a follow-up appointment with Dr. Barnhart next Friday. The results from the nissen seems to be optimal. I haven't noticed reflux symptoms. Andrew did gag and heave the first few days in the hospital, but since getting food again hasn't had any episodes.
Jul 15, 2010
Fundoplication Surgery
Well, after a lot of thought, research, discussion, and prayer, Ryan and I felt like it was time to go ahead with fundoplication surgery for Andrew. It's a surgery to stop reflux, where they wrap the upper part of the stomach around the esophagus, and then sew it back to the stomach.
We had known for a long time that this was a possibility because Andrew has such severe reflux, but were trying to avoid it. Now that he's had such problems with his stricture and his reflux has not improved as much as we had hoped, the surgeon recommended that we do the surgery to stop reflux from irritating the stricture.
We went in for the surgery Tuesday. Start time was expected to be 12:30 and it was going to be about a 3 hour surgery. Well, he didn't end up going in until 2:15 or so. Then they had a much harder time than they anticipated. The plan was to do the surgery with laparoscopy (5 little holes instead of an incision). Just after 8 pm the surgeon finally came out of the OR. We'd had updates throughout surgery, so we knew that Andrew was ok, but that things were not going as smooth as they had hoped.
They ended up making an incision after several hours of trying to do the surgery with the laparoscopy. They also ended up moving Andrew's G-tube sight. Which overall means they closed the old one and made a new one. Most of Andrew's small stomach was used for the surgery, so we'll have to stretch his stomach again. Overall he's doing fine. He's has decent pain control, and has been stable and healing fine. He is not interested in doing anything beyond being held and has slept 98% of the last 2 days, so far. The pain should decrease from here though. He has avoided coughing or clearing his throat at all, and did run a high fever Tues night, but an x-ray cleared him of any infection worry.
He got a PICC line placed today. Which is like a long IV that goes from the inside of the elbow, through the vein and ends just before entering the heart. He'll get IV nutrition, and all his medication through that until Sunday. Then he'll finally be able to start having G-tube feeds. He'll be starting all over, like he did in the NICU last year. They will start at a very slow rate, and use drip feedings to avoid having pressure build-up in his stomach. Then slowly increase the rate. When he gets to the full volume of feedings and tolerates it, then he can come home. The magic number is 36 cc's/hr, I think. That's just over 7 tsp/hr on a continuous feeding. We'll work on the rest at home.It's hard to see with all the tape, but you can probably tell what's what. The top bandage is the old G-tube site. The line below the tube is the incision site. The rest are the little holes used for laparoscopy. And, of course, the new tube. He'll have to have the long tube until the new site heals. This tube doesn't have a balloon on the inside because his stomach is so small again, that a balloon would possibly block to exit from the stomach to the intestine. Instead there is a plastic disc on the inside. I'm not sure how they get it in, or how they'll get it out, but that's how it was described to me.
Ryan and Ty have been staying at my parents at night and visiting the hospital in the day. I stayed with Andrew the last two nights. Tonight Ryan and I will switch, and I'll stay with Ty while Ryan is with Andrew at the hospital. Man how we love those hospital pull-out couch beds! At least we get to stay with him.