
Brandt's surgery was this morning at 8:30. He was on a fast all night/morning, but thankfully didn't realize it until right around the time anesthesia came to take him back to the OR. I wasn't able to go back with him this time, but they gave him some medication to keep him calm until they could give him the gas. Worked like a charm! His eyes were a little glazed over, but he didn't fuss at all!

Tanner and I grabbed breakfast, then headed back up to the hospital to wait in the parents' lounge. Usually, I'm a professional couch potato when the opportunity arises, but I have to admit that those four hours weren't fun. Eventually, we were paged back to talk to Dr. Chen, who was very pleased with how everything had gone. They were able to do everything the way he had wanted to, he'd taken care of the stent that was starting to become an issue, and Brandt was already being extubated! The latter, especially, was a big deal for us. The last time he woke up with a tube in his nose, he panicked, and the ensuing struggle wasn't pretty.
He's also been incredibly thirsty, which is expected. We gave him his sippy cup after the bunch of us came back from dinner, and that was a big hit. Until the morphine-nausea made him throw it all up. Moving him around to change his bedding isn't a big hit, either, because ouch.

I guess I haven't really gone into the details of this surgery! The Fontan is basically completing what we started with the Glenn. Basically, we're taking the heart, which is normally a two-cycle-pump, and turning it into a one-cycle-pump. We'd already rerouted half the blue blood, leaving the other half to mix. Now we've finished rerouting all of the blue blood, and completed the cycle. Because the amount of mixing blood is minimal, now, his sats are automatically higher. However, there's a 90% chance we'll still go home on oxygen.
The main reason Brandt needed his Fontan this early was because of those pesky AVMs. They're little blood vessels that pull the blood away from the lungs before it can get oxygen, and that drops his sats pretty dramatically, at times. Those will start disappearing, now that he's getting enzymes from the liver to his lungs, but it takes time. While he's got the capacity to have higher sats, he's still got those little leeches keeping him low, so we'll have to wean over time. It'll probably be a few more months of oxygen, but at least the end is in sight.
So there's tonight's update...I'm off to go get a little sleep while I can. I have a feeling that tonight's not going to be the most restful one I've had lately, between the hospital couch and the cranky toddler.
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Yay water! And our first glimpse of his eyes this evening. |
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This doesn't seem to get easier to look at. |
Oh, my! Pictures do tell a thousand words! Thanks for sharing all of this with us. Glad it went well!
ReplyDeleteGreat post! Thank you.
ReplyDeleteThanks for the info and the photos. Nice to be on the other side of that big milestone, and so glad it went well. - The Benedicts
ReplyDeleteSending prayers and love to this brave little boys and his loving and strong (beyond words) parents.
ReplyDeleteSo glad the surgery went well! Nice for Wade to have his Auntie to take care of him. Wishing you all the best.
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