Showing posts with label IV Infiltrate. Show all posts
Showing posts with label IV Infiltrate. Show all posts

12.27.2011

Primary Children's Medical Center 8-27-11

Sorry, I had to skip a day this time around. I took off Thursday evening and left Daddy here with Miss K and a good supply of frozen milk. I went to my parents house to have cake with Roo for his birthday then I took him home for the night and all day Friday. I don't take my laptop with me when I do this because I don't even want the temptation to be there when I'm trying to spend all the time I can with my little boy. It was a great day and night with him. He was getting very cranky being at my parents, he's decided it's time to be home, I don't blame him at all it really is time to be home. He's starting to freak out a bit when I try to leave him anywhere. Thursday evening he worried I was leaving without him, he kept a close eye on me and when I started gathering things to leave he cried and ran around trying to grab all his stuff as fast as he could to get to the door before I did. It broke my heart, I was so glad I was taking him with me so I didn't have to break his heart and leave him! He was so happy to be home with me! When we got there I asked him if he wanted to get in his bed and he said "Mommy's bed?", I didn't think he'd remember napping with me in our bed last Sunday, lol! Luckily I got him to sleep in his own bed and he slept all night just fine :o). Friday was kind of crazy with him, he was so cranky and easy to make mad! But I enjoyed my time with him and I know he enjoyed it as well. I miss him so much and can't wait to be home as a family again!

Daddy had a pretty good night and day with Miss K. I guess she had to get another new IV Thursday night :o(. She also had a few more episodes of SVT. Friday morning the Cardiology team dropped by and announced they were putting her back on the Amiodarone IV drip for another 24 hours :o(, they weren't happy with how many times she'd been in SVT for the day. Daddy was very vague on any details with me so I really don't know what the real plan is or what's going on as of right now, I'll find out sometime this morning when they come by again.

Miss K has another infiltrated IV :o(, it's her left arm this time, which means we've run out of limbs to put IV's in, she's down to just her right arm :o(. I'm hoping and praying with all my might that she doesn't need the IV's anymore now so we don't have to do a central line, every time she's infiltrated an IV they've thought about a central line but dismissed the thought because she shouldn't be on IV's much longer, if she was going to get a central line it should have been done 2 weeks ago, I'm wishing they had done that in the first place to save her poor little body :o(. Amiodarone infiltrates look horrible, and they can't feel good at all :o(.

Cardiology is very happy with Miss K's latest progress, she's only gone into SVT 3 times in about 24 hours, YAY! But those 3 times were pretty long and she had to have help to come out of it, they don't really like that. But they said they think they've gone as far as they can with the medications and that since she can be brought out of SVT with natural methods that can be done at home they are willing to consider a closer go home date! So, they want her to be kept on the Amiodarone IV drip for 24 more hours just in case it helps steady her even more then they'll take her off of it tomorrow morning! They also said that if she blows another IV or infiltrates or whatever then we should just take the Amiodarone off and forget about the 24 hours, YAY again! Sadly, within an hour of them saying this Miss K's last IV went bad, luckily it's not infiltrated and it had nothing to do with her vein, the IV line itself had a leak in it near the entry so we had to remove it, but she has to have an IV in her just in case it's needed so they will be calling the IV team in again to place a new one, but we're just happy she can have a new one and that it was the IV itself that was having trouble.

The Cardiologist that talked to me today was new to me, I haven't seen him before. He is a great Doctor as far as I can tell. He told me that they would prefer she have some type of heart monitor for her to go home with since she's still going into SVT and they're sure she will most likely still be going into it very occasionally at home. So he suggested we buy a sports Heart Rate Monitor to put on her. Daddy had previously asked about these when talking to nurses and other Doctors but he never mentioned it to Cardiology because the others told him it wouldn't work because she's an infant. Today's Cardiologist told me they've put these monitors on trial in the clinic and that they work just great so he wants us to get one for her so we can monitor when she's in SVT and make sure she comes out of it. Daddy is so excited, it's what he wanted to do from the beginning so he's now currently researching the best of the best out there and we'll be getting one, no matter the cost. This is something we think saving money on an affordable one won't be acceptable so he's been instructed by me to ignore price and look only at reviews and quality, we'll pay what we have to to keep our baby girl safe.

The pediatric team came by and they are impressed as well, though less impressed than Cardiology, they aren't as easy going about the SVT as others are. In fact one of the Doctors came and sat through an SVT episode in the night and was on edge the whole time getting ready to call for Adenosine. I got her out of it by blowing in her face, he was impressed that worked, and then he relaxed (See Physical Maneuvers). So they aren't happy with Cardiology telling me just to take her off the Amiodarone drip if she looses her IV, lol! But they are happy with everything else, they're glad to see her on her way to recovery.

I have strict instructions to get her in to the pediatrician as soon as we're home and then in about a month her pediatrician needs to send her in for an MRI to see if she was/is having seizures. None of us think she really is but we need to make sure, better safe than sorry. They're keeping her on the Keppra for at least another 2 weeks just in case then they'll talk about whether she really needs it or not.

Her infiltrated IV locations on her two feet don't look great at all. I'm not happy, her cute little feet look so horrible and painful! But they can't really do anything about it but watch and monitor them. Her little arm that joined the party looks bad too, she has a "Popeye" bulge in it and it's all red :o(. I guess they've had a ton of Amiodarone infiltrates this week but they can't really do anything to help them heal, just watch them. So here's to hoping they heal well and quickly on their own! I haven't been able to get a good picture of them yet but I will post as soon as I do.

Forgot to mention we had a little birthday party for Roo here at the hospital last night. It was nice to have my parents, little sister and 1 brother and Daddy's mom and Grandma Dot come celebrate with us :o). Roo had a blast, he got to open more presents, he got a TON of Mater stuff, lol! Don't know what we'll do with it all! He got an awesome cake made by a friend of a friend and we all loved it :o), these girls are such sweethearts for doing this for me :o). We celebrated outside on the court and had a blast for an hour or so.

8-27-11 A New Report:
Whew! What a long day! We hopped for boring as usual but got a little bit of excitement thrown in :o(.

We took Miss K off the Amiodarone drip totally today because of the non-working IV, they called the cardiology team and they told us to keep it off, they're confident she'll be fine :o). We got a new IV put in, now it's just there in case they need one for whatever reason, but she's not hooked up to any drips :o).

Around 3:00pm Miss K had her first SVT episode in 12 hours. I had a new nurse who was sort of panicky, she didn't really know exactly how to handle SVT so seeing Miss K in it made her nervous. After 25 minutes she begged me to do something so I blew in Miss K's face...about 10 times...and it didn't work so the nurse pulled out a bag of ice, she started to panic then because Miss K's heart rhythm was coming up as VTACH on the screen instead of regular SVT. She took Miss K from me and applied the ice, it worked for a split second and then she went back into SVT, we went through this about 5 times before she finally came out of it. But, 5 minutes later she went right back into it, as soon as the ice was applied she went into what looked like VTACH again, the nurse then panicked more and after frantically (and not very effectively because she was so freaked out) trying the ice about 10 times in a row (without giving poor Miss K much of a break between) she pushed the Code Blue button. I had no idea she had done this until a whole team of Doctors and nurses came running and whipped open our doors and crowded into the room turning on lights, pushing furniture out of the way, throwing tables and chairs and bringing in equipment! The next thing I knew they had applied the patches for the crash cart to Miss K's little body ready to shock her if her heart stopped! She had an oxygen mask on and was suddenly hooked up to all kinds of things. I was pushed into a corner watching about 8-10 people crowded around my baby girl making it impossible for me to see her or anything that was going on. I didn't panic much though, I knew she was fine but I couldn't understand what the nurse thought was so important to need all that. They started getting out the Adenosine and about that time a calm Doctor applied the ice one more time and Miss K came right out of SVT and fell asleep. She was totally fine. The nurse got a little bit reprimanded by the charge nurse. I felt bad for her, she was a little embarrassed for what she had caused.

The good news is when the nurse and Doctors reported the whole episode to the cardiology team and asked them if we should turn the Amiodarone drip back on the cardiologists all said she was doing as well as expected without it and to keep it off :o). So hopefully tomorrow morning the decision is still the same and we can hopefully be moved back upstairs to regular care and not ever be back in here again! I am worried about what that last episode was though, her rhythm really didn't look good at all to me, it had me a little worried. I really don't want her doing that at home at all!

Tonight I'm going to start having the nurses teach me how to check her profusion efficiently and how to feel her pulse in her ankle to make sure she's pumping blood throughout her body, if I can do this correctly then IF she does go into SVT at home then I will be able to know if she's handling it well enough to ride it out or if we need to bring her back in. It'll make me feel a lot better.

So we'll just keep praying that she's really doing as well as they say she is and that we can all be home together as a family again very soon!

Primary Children's Medical Center 8-25-11

Good news, good news, good news today! YAY!

Miss K hasn't had an SVT episode since yesterday morning. The nurse and I were thinking that maybe she was still having SVT occasionally was because of her infiltrated IV, the Amiodarone wasn't getting into her system fast enough. Now that's been fixed and she's been great since! So the Cardiology team came by and said they are very impressed, we lowered her Amiodarone IV drip a little in the middle of the night, they asked that we lower it even more today so we are officially onto the weaning side of things!

The PICU pediatrician team came by, they haven't seen anything significant in her recent belly x-rays. She was supposed to have 3 more stool samples and all 3 needed to come back negative for blood but she hasn't had a poop in almost 24 hours, kind of hard to do that on an empty tummy when it's been empty for over 48 hours right? Today they decided to let me feed her, YAY! So now we could use all the prayers we can get that she's 100% OK in the tummy area, they are still weary about it and want to see absolutely no blood in her stool ever again, they think it should be fine since her heart rate has been normal for so long and should stay normal from here on out.

So this means no more Amiodarone drip within the next 24 hours sometime, no more IV fluid drip as soon as I start feeding her, and no more Zantac drip as soon as her stomach acids get used to food again. I guess that just leaves weaning her off the Keppra drip and getting her onto oral with that, as soon as this happens there will be no more IV's, YAY YAY YAY! I believe tomorrow they will be transferring us upstairs to the regular care unit :o). We're hoping to be home by Sunday, the Doctors laughed at me when I said this but I'm trying to think positively, if not Sunday then hopefully no later than Tuesday morning...Here's to hoping and praying!

It's Roo's 2nd birthday today, I'm so sad I can't be with him right now :o(. But I'm escaping tonight to head down to my parents for icecream and cake with him :o). He and I will spend a peaceful night at home together tonight and a great day together tomorrow then head back down here tomorrow evening for icecream and cake again :o). Daddy will spend Saturday and Sunday at home with Roo and then we'll see what we need to do for next week, we're still hoping to be home all together but if not we'll make some plans for Roo again.

Primary Children's Medical Center 8-24-11

Last night was a very rough night. The PICU team came in to tell me they were seeing the same thing in the 3rd x-ray as they saw in the second so they were going to assume it wasn't just poop and could be more serious. Then they dropped the horrible bomb on me...I was ordered not to feed her all night. They put her on IV for fluids and I spent the night getting up every few hours to pump and freeze my milk. Luckily Daddy was here, I couldn't hold her without her freaking out she was so hungry and she could smell me. Daddy took care of her all night long while I tried to sleep a little between pumping. She only had 1 episode of SVT, but she never ate or burped or was even bugged except that one time so we don't know if she didn't have SVT because her medications are finally working full swing or if it's because she was sleeping soundly and left alone most of the time.

The Cardiology team came in early this morning, a first early visit in a few days! They are impressed with Miss K's progress and they like what they're seeing, in the past 24 hours she's only had 8 or 9 SVT episodes :o). So they are starting on the oral version of Amiodarone, YAY! We are on to the weaning process! I can finally see a light at the end of the tunnel, though it may still be a little farther away than I want it to be. They also doubt there's anything wrong with her belly but they're letting the PICU pediatric team treat her as they wish, better safe than sorry.

The PICU pediatric team stopped by soon after the Cardiologists. They had taken 3 belly x-rays throughout the night and they said all of them looked the same except the last one, which looked more normal but not satisfying enough for them so they've ordered a strict no feeding diet all day today and maybe all night tonight :o(. I'm heartbroken, it's so hard to listen to her cry and hold her while she eats my shirt and cries :o(, it's such an easy fix to make her stop crying and be happy, not to mention it's one of the only things I can do to comfort her through all of this, and they've taken it away. So here's to a very long day of consoling an inconsolable baby and trying to pump somewhere in between to keep my milk supply going good and strong through all this.

8-24-11 A New Report:
Just got some bad news from a PICU pediatric team member...Miss K had 2 stool samples come back fine and the last belly x-ray came back perfect but her latest stool sample has blood in it again :o(. And they did blood tests and they came back positive for a high white blood cell count :o(. So now they know she's trying to fight some infection somewhere but they're not completely sure where, they're assuming it's her bowls. They have ordered that she not be fed the rest of today and all night then we'll go from there. They won't put her on antibiotics, they want to see it resolve itself if possible :o(. They've put her on Zantac to help with stomach acids from her empty tummy. It's so sad, she's beyond hunger now just rooting around trying to find food but she does it like she knows there isn't any, she's just being hopeful :o(. Luckily she's not really being too fussy much of the time, but I feel so bad for her :o(. We're just praying this bowl issue sorts itself out within the next 24 hours so she can eat again and get out of here!

She's only had 1 SVT episode so far today, it did last 1 hour though and my blowing in her face didn't stop it so we did the ice treatment, it worked like a charm and she came out of the SVT very quickly.

She had an infiltrated IV in her foot :o(, yesterday it looked angry and red but we thought it was a reaction to the tape, now the nurse and I both feel really bad :o(. Her poor little foot is all swollen and puffy and red and purple, it looks really awful :o(. The wound team said just to watch it though and it should clear up, but I'm worried because her other foot has the same issue only it didn't get that bad before we caught it and it's still looking the same :o(.

Miss K is quite the cutie though :o). She's changing like crazy. She already has quite the personality, so sweet and mellow :o). She is smiling now, I know it's quite early for this, we're all very surprised to see it but it's not just her making gas look good, lol! She has those smiles as well but it's so easy to tell the difference :o). She loves to smile at her Daddy mostly but I get a few good ones here and there :o). Luckily she LOVES her binky, this has been a huge lifesaver through everything. I never thought I'd say it was a good thing for a baby to like the binky until now.

I keep myself sane by writing all of this down for you guys to read and working on Heritage Makers projects, mostly Roo's year 2 book trying to get it done very soon, it helps me to work on his book because it makes me feel like I'm still trying to be a good mommy to him even though I can't be with him right now.

I want to thank all of you for all your thoughts and prayers again. I also want to thank everyone who's offered/given help in whatever way you've done, it's all greatly appreciated, I have no idea how I'll ever repay any of you. I've got some awesome friends and family in all of you :o).