The plan is still to ween her from her ivs and remove the PIC line within a day or two. The caffeine can be given orally. They are restricting fluids a little more and have moved up to CPAP level 6 (from 5). The CPAP will just be giving her some more pressure now to help. There's are of course side effects to increased pressure and increased oxygen. Hopefully, Taylor will respond quickly and she can get back on room air and less pressure.
They don't want to remove the CPAP anymore during holdings. And they are recommending that we consider going down to one kangaroo care sitting a day (but perhaps a little longer). We had already decided to give her a break this morning. Last night's session with me didn't go to well. The mustache piece that holds the CPAP on her face was coming loose, and the CPAP wasn't functioning very well. Her oxygen sat levels were all over the place and there were a lot of alarms during it. It was still nice to be able to hold her though.
Today is Tristan's birthday. Michelle and the kids are on the way to the hospital right now to pick me up. Beth is coming to spend the day with Taylor so that Michelle and myself can be with Tristan. We really appreciate it. Hopefully tonight we will get one of the family rooms here in the NICU and we can be together as a family. I haven't heard yet if we got a room (there are 2) or not. I begged pretty hard this morning for one though.
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