9:15pm: No real updates to note (other than he was moved into a "big boy" crib. We are anxiously waiting for the next gas test around midnight tonight... In the meantime, here are a couple of pictures that Kristen took today:







2:30pm: They have moved the tube going through his mouth into his stomach to his nose and will hopefully reduce some of the excess secretions that he has been having. I asked the nurse last night about this as I was concerned about the amount of fluids that he was losing and wondering if this had any impact on his electrolytes and indirectly on his CO2. Not sure if it is the answer, but I am glad that they are giving Reid a chance to prove himself and try to make small tweaks to see if they can isolate some of his issues of a higher CO2.

When Kristen text messaged me earlier, his O2 was at 38% and zonked out. I love how he has a bib on in this picture to help absorb the saliva that seems to steadily pour out of his mouth.

11:45am: Kristen just took off to the NICU and is meeting my sister, Shannon. I am going to take a break from the hospital today so that I can get some much needed work done. I am starting to hate Sunday's because I always put work off until after dinner and then I start to get grumpy (and nobody likes a grumpy Chad). So today, I am going to attempt to get ahead of the game and get some work done early. There are a couple of errands that I want to run today too --- but we will see if that happens. :)

Not much news this morning on the Reidster. Kristen called about 9am and he was on 35% oxygen and they probably weren't going to take another gas until 4pm.

4:30am: Reid's gas tests didn't go as well tonight as we hoped they would. Around 1am, his gas had a CO2 of 72 and at 4am, it had come down a little bit to 67. Ideally, he needs to be below 65 to be acceptable, but are hesitant in taking any action. The next steps would be either to go up on the pressures again, or go to CPAP. However, being that he is fighting an infection and is taking antibiotics, they want to give him the benefit of the doubt to see if he can rebound on his own. He was able to have normal CO2 readings following the first two days of extubation, so I am hoping that he can turn the corner. They are also curious to see what happens when they give him his lasix to see if that can help take away some of the fluids on his lungs to help bring down the CO2 as well.

On a different front, Reid was weighed again tonight - 4.13kg or 9lbs 2oz. This is a gain of about 3 oz since he was last measured.

11:00pm: We just got back from a great dinner with both of my sisters and their husbands and it is time for bed! Kristen just got off the phone with the nurse and his oxygen is at 35%. His next gas test is at or around midnight and we are anxious to see what it is. We are crossing our fingers and hoping that we can end such a wonderful day on a good note.


3:30pm: Do you know what is better than holding your son, looking at him only to have him stare back at you and start cooing? Nothing. This has made my day.

Unfortunately, Reid's blood work came back with a gram positive infection. The two antibiotics that they started last night will do the job and he will probably be on them for the next 10 days. Luckily, the can be administered through his central line and doesn't need another IV. With his steroids, his immune system takes a hit and isn't as strong as it could be.

His blood gasses this morning were high and they subsequently went up to 16 liter flow. His last gas was acceptable and they will do another gas tonight.

Dr. Cornish said his xray looked really good and better than before he came off the vent. We are just praying that we can turn this corner and steadily make some progress. His respiratory condition remains steady and is currently at 40%.

10:30am: after the Tylenol kicked in, Reid became a little more active and a little more like himself. His temperature came back down to 98.6. They took another set of labs, but still no results. Oxygen ranged anywhere from 40 to 60% and was at 45% when Kristen talked to the nurse.

A little bit of unfortunate news, Reid' arterial line came out this morning. This was a source of being able to monitor his blood pressure and also a mechanism to getting blood for his gas tests and lab work. Now that it is gone, we will go back to getting his blood from a prick on his heal. Not sure if they will try to get another art line in his other arm.

12:30am: Reid has been fighting a mild temperature for most of the afternoon and evening. They sent cultures to the labs to see if he had an infection, but nothing has come back as of yet (this could be a good sign). His temperature has ranged from about 99.6 to about 101. When I called to check just a few minutes ago, it was right about 100. His heart rate is elevated which usually comes along with a temperature. The good news though is that he is not showing any other signs of sickness. Morphine withdraw can produce these symptoms, and he is about at the time when you would start seeing these withdraws. To be on the safe side, they have started two antibiotics and will follow up with another set of cultures in the morning. They will be able to compare the two sets to see if anything has changed in the time between. They are also prescribing Tylenol to help with the temperature.

Oxygen requirements are still hovering in the 40 to 45% range as they have for most of the day. This is also a promising sign that he is not sick... seems like when he has been sick before, his respiratory stability was usually the first to go.

Dr. Piazza called me this evening but I had missed his phone call. He did, however, leave a message and said that today was his last day of service for the month and that a new Dr. will be taking over on Monday. Just when we were getting used to his styles, we will need to adapt to another style for the month of February. This is life at Egleston and we are becoming fairly used to the rotations now. At first, we didn't like it, but we are now seeing the benefits of being at a teaching hospital with the chance to interact with so many stellar doctors and nurses.

Bedtime for us. Keep your prayers coming and let's hope that this temperature is not a sign of sickness. Good night.

2:45pm: Unfortunately, Reid's hernias came back today. We knew it was a matter of time before they did, but was hoping that we could make a ton of progress before we even had the idea of surgery back in our heads. The nurse was not able to reduce them, so she had asked Dr. Clifton (the doctor that was supposed to do the hernia surgery in the first place) to come look at them. He was able to reduce them. This news makes me very nervous, but we won't talk about the surgery until they become very difficult to reduce (and who knows when that will be???).

Other news, the treatment of dexamethasone is over with. This drug did wonders for Reid and hopefully he will not have any side effects from its use later in life. I guess time will tell, but for the moment, we made a HUGE leap in the past few days and very grateful that we are where we are now.

11:00am: Sorry that we haven't blogged earlier - Kristen wrote the blog for me to post and for some reason, the computer decided to reboot and we lost her entry. So, now that she is out having coffee with Rachel and heading to the hospital, I am going to have to see if I can summarize what she had written...

Reid had a pretty uneventful night last night and his oxygen stayed in the 40-45% range all evening. His CO2 was around 60 this morning, but we have started to see that Reid has maybe stabilized a little bit. His work of breathing seems to have increased since the first day of his extubation, but today hasn't shown any increase over what he was doing yesterday.

Kristen and I went to the hospital after she picked me up from the airport last night and we were there from about 8 to 9:30pm. It was so good to see him! I forgot what it was like to be able to hear him make noises, whether it be crying or cooing. He was wide awake for the first half of our visit and was looking around and we entertained him with his bedside stuffed animals.

The pressures that are be exerted by the HFNC are pretty high and causes him to blow continuous spit bubbles. He has a pad of gauze that sits by his face as it is a constant stream of droll. Kristen and I like using the suction device and keep his face clean, but it is a losing battle to take on. Not until his pressures lessen, will we start to see this drool and bubbles subside.

Anyway, not much has changed over the past 2 days... but we are working on our third day of extubation and so far, things seem to be going as planned. His morphine is completely out of the picture now and they reduced the methadone dose even further.

Time for me to get back to work. Hope everyone has a good weekend.

2:47pm: [Kristen's Blog Entry] Reid is having an OK day. He's had several desats and his current O2 is at 50%. He had two diaper changes in a row thanks to the glycerin he had early this morning, his central line dressing was changed and a culture was done to see if he still has MRSA. He didn't like any of that attention and thus the desats. The nurse also noticed that he was working harder to breathe during all of the hands-on activity but once she gave him his daily dose of methadone his work of breathing returned to normal and he stopped desat'ing. His methadone was decreased from 1 mg to .08 mg and the goal for today is to keep him as quiet as possible so that he does not have to go back on the ventilator. When I called he was resting peacefully and sucking on his pacifier. We will go visit our little guy tonight after I pick up Chad from the airport and in the meantime I am heading to the spa to get an hour long massage. I can't wait!!

9:45am: Reid had a pretty stable night last night - his O2 fluctuated between 40% and 60%, but he was back down to 40% when Kristen called this morning at 8am. Their plan is to keep him somewhat sedated over the next couple of days, as the first 72 hours are the most critical of being off the vent. His blood gasses continue to be good.

2:15am: it's been a long day and just now getting around to put a blog together. Dr. Piazza had called me earlier today to let me know how well the extubation went , so it was good to hear from him that things looked promising. Kristen was able to hold Reid even though he was pretty drugged up and out of it.

Reid sat on 35% O2 for quite some time until they gave him his "sleeping" medicine which totally knocked him out. His breathing became a little shallow and required 50% O2. However, they noticed that after the drugs wore off a little that his breathing improved. This led them to believe that they gave him too much medicine at one time. Going forward, they are going to staggar the two drugs so that he doesn't get completly zonked out. As of 2am, he was back down to 40%, on his belly and sleeping soundly.

A big, successful day for Reid and we are hopeful that he can continue to have a quiet night and an even better tomorrow. So far, a big breath of fresh air.

Good night.

3:30pm: Reid was extubated about 3:00 today! He is on 13 litre high flow (weaned from 15 at extubation) and seems to be doing well. They started off at 40% O2 and was on 37% when I talked to the nurse at 3:30. In fact, when I was getting off the phone, his alarms were going off as he was high-sat'ing at 99 and were about to go down on the O2 again. Listening to his lungs, they sound pretty good.

His blood gas test was good - CO2 of 54 - which is acceptable, but even on the vent last night and this morning, he had low-60s and upper-50s, so actually, he might be doing a little better on his own right now. They will continue to get gas tests to ensure that he is able to handle the change and make sure they are staying on top of the changes he just had.

He is "fidgety", but doesn't seem to be agitated.

So far, so good. The next hours and days are going to be the true test to see if he can handle it. They will look for changes in his blood gasses and also monitor his work of breathing (retractions that show that he is having a harder time breathing on his own). We have been ready for this day and upset that I have to wait until tomorrow night to see him. I will have Kristen send me pictures later and will post them this evening.

12:00pm: Doctors have made their rounds and they have decided to extubate Reid after lunch. Not sure what time frame that means... but they have ordered it and that is all that matters!!!

On a side note, I was incorrect this morning when I had mentioned that he was off the morphine drip. They have cut the dose, but I guess because it takes awhile to get out of your system, last night was the time frame as to when he probably would have experienced that drop in dosage. Not sure if they will get him off the morphine all the way today... or if that is something that will be done in the next few days.

Reid is getting "range of motion" exercises now, as the physical therapist had requested. He tolerated these just fine today and maintained his sats.

Reid is also experiencing tremors like he did last time he came off the norcuron. Doctors are keeping a watchful eye on this, but are hoping that it will soon subside when the drugs start making their way out of his system. Most commonly, his hand/arm will shake and if you place your hand on top of his, he usually calms down quickly.

8:00am: Reid had a "test" last night as he came off the morphine and is now 100% on the methadone. Supposedly this can be a big event... and he passed with flying colors. His O2 this morning was at 34%. Hopefully this is paving the way to a great day. They weighed him again last night - 8lbs 15oz. He has lost quite a bit of water weight over the past few days and looks really good.

6:30pm: Just wanted to post some pictures that Kristen took today. She was able to hold Reid for about two hours and he stayed awake the entire time. He has a new best friend in the stuffed dog the Hospital gave him:








2:30pm: Sorry that I haven't posted earlier as I have been either on a flight or slammed with work. I did, however, get a chance to talk to Dr. Piazza this afternoon, so I wanted to let you in on the details:

• PEEP was reduced to 6 (from 7). Vent settings are now as low as they are going to get. BMP to remain at 14.



• Methadone drip was started last night to start the weaning process for the Morphine. Today, the morphine drip was cut in half. Tomorrow, he will be fully weaned off the morphine and be 100% on the methadone. We will probably see some side effects from this: 1) Return of the "shakes"; 2) diarrhea; 3) fussiness.



• The dexamethasone will be fully weaned in about 3 to 4 days. They have already significantly reduced the dose, and will continue to do so until he is 100% off. To compensate, last night, they started an increased dose of the hydrocortisone and this will eventually take the place of the dexamethasone. He is expected to be on the hydrocortisone for the next two and a half months. We were originally told that the prednisone steroid would take the place, but endocrinology decided for hydrocortisone instead.



• No eye test this week. Instead, he will have one next week (Thursday), and one probably every two weeks until he is 2 months old (gestational corrected) --- about the end of February or beginning or March. If everything checks out OK, he won't have another test until he is 1 year old.



• I haven't talked about this much, but he has been producing quite a large amount of saliva and was actually needing fluid replacement as this saliva was being pulled out of his stomach and collected (for about 3 days now). This extra production has now stopped and they have subsequently stopped the replacement fluids. This is most likely a result of the dexamethasone.



• And lastly, and most importantly, they are going to attempt an extubation tomorrow if everything remains steady as it has over the past 4 days. He seems to be stable enough and his vent settings are low enough, so this is the next logical step. When asked, Dr. Piazza said that he is going to attempt to put him straight onto the high-flow nasal cannulas (HFNC) (instead of going back to CPAP) at a rate of 10 liters per minute. CPAP, apparently is very traumatic on older babies, and will only be used as a possible back up to the HFNC. This is very exciting news, but also makes me very nervous. Unfortunately, I am out of town and Kristen has to work tomorrow, so we will be on pins and needles until we hear of the outcome of the extubation. Kristen and I have been ready for this day to come for quite some time!!!

7:00pm: We are starting to get a little frustrated as no one seems to know the game plan for Reid. When I called tonight to talk to the doctor, he had already left for the evening, so I guess I will try again tomorrow. I want to know what was said with the endocrinologist today, if the meeting even took place. We are on day 7 of the dexamethasone, and not sure when he plans on removing it completely. His vent settings are near extubation numbers - we have a few BPM to go and I imagine another wean of the PEEP, but there really isn't much room to go.

We are at the NICU now and about to go eat some yummy cafeteria dinner. I probably won't post again until tomorrow morning as there isn't a whole lot to write about - his O2 is still between 30 and 36 at the moment. I am leaving tomorrow for DC and will be back on Thursday night. I am crossing my fingers that when I get back that he has been extubated!!

12:00pm: Extubation is still not on the agenda for today. We haven't talked to the doctor yet, but the nurse said it was not discussed in rounds. His agitation is continuing to grow, and I am anxious for something to happen. As a result of this, they have increased his anxiety medicine and his morphine to help curb this. On the vent, they have further reduced his PEEP to 7 and his last blood gas after the change was "beautiful". BPM still at 14. Oxygen is ranging anywhere from 30 to 40%.

7:45am: Reid's O2 varied between 32-36% overnight and they further weaned his pressure support from 6 to 5. He got a bath last night that he "tolerated". Not much else to report on this end...

10:30pm: Where did this weekend go? Again, another weekend of feeling like I accomplished NOTHING. Well, I did get one thing done on my list - moving the old refrigerator down to the basement from the garage which involved talking off the door to the basement and the doors of the fridge (thanks Justin). Ugh. But hey, at least Reid has a dedicated freezer for his ever-growing supply of breast milk. He must have a 2 to 3 month supply saved up for him... and he better get back to full feeds soon or I am going to have to go buy another freezer.

Kristen and I drove to the NICU around 3:30 today and faced torrential downpours and flooding interstates. It seems like the streets flooded really quick, and it made for an exciting trip into downtown Atlanta. We made it safe... and that is all that matters.

Kristen was able to hold Reid again today. He has had kind of a "fussy" day, but his oxygen requirements have stayed fairly stable. When we got to the NICU, he was around 50% as he broke into sweats from being under a heater and being fully clothed. He had on his new "one tough cookie" outfit that he was supposed to wear home from hernia surgery (that never happened). Anyway, he got too hot and it took him awhile to cool off and regain his composure.

He has had quite a bit of mucus coming up his ET tube that has a tinge of old blood. They think this blood might be from the extubation/intubation that he had the other day, and it is getting lighter every day... but it worries me a little bit. It seems like quite a bit of mucus, but it doesn't seem to be bothering him too much.

Tonight has been a restless night as well. The nurse ended up giving him 3 boluses of morphine (don't think that he has had any in awhile), but his O2 is still at 39%. At least he seems to be able to control his breathing...

I got some work done tonight, and was able to watch the majority of the second half of the Saints/Vikings game and now that that game is over, it is time for bed. A little ticked that Favre couldn't pull his team for a win; better luck next year (that is if he doesn't decide to retire, again). Anyway... good night. Hope everyone had a good weekend.

12:00pm: Reid was on 40% oxygen when I called this morning but was sat'ing 96-97 and was about to be turned down. So, over the past 2 or 3 days, his oxygen requirements have remained steady. He was awake this morning and looking all around... we will make it into the NICU later this afternoon. Kristen and I are trying to get some work done (lesson planning and project planning) this morning so that we don't have to mess with it later today.

11:50pm: Reid is still at 38% O2 and has had a pretty uneventful evening. We left the NICU around 7pm and he has been asleep pretty much ever since. There isn't much weaning left to do and the nurse said the logical next step would be extubation. She was going to weigh him and bathe him, so hopefully we continue to have another good night.

The nurses have noticed a large amount of secretions coming out of his stomach - clear liquid that has a consistency of saliva (which is what they assume it is). They are curious as to why this isn't being digested so they ordered an ultrasound on his stomach and bowels to see if there was something that they were missing. His milk is obviously being digested normally, but it is being fed to him past his stomach. The ultrasound was looked at by the tech this morning/afternoon but has not been formally read by the doctor. We are assuming no news is good news. Probably not worth mentioning... but there really isn't a whole lot going on in room 2258 these days.

It felt awesome to hold him today... Kristen held him for about an hour and I held him for maybe a little longer than that. He needed some male bonding time as I hadn't held him since about the 15th of December. At one point, we both took a little snooze together. :) Anyway, hope you guys enjoy the pictures (the main reason I wanted to blog tonight).

3:45pm: things are holding pretty steady today. He is currently on 38% O2 and they have reduced his pressure support to 6 and his BPM to 14. Inspiration time down to .55. PEEP is still at 8. He looks like a whole new baby though as he has lost about a pound of water weight. It was about 10.5 pounds a few days back and when they weighed him last night, he was at 9.4 lbs. I am going to keep this blog short as they just finished a blood gas (7.38 pH, 39 CO2 is 39) and he is about to be put into Kristen's arms. Pictures will come at some point tonight.


9:00am: Reid decided to throw up again last night --- the same kind that he did about 3 weeks ago when he had come off of nurcuron and also when he was getting stress levels of hydrocortisone. These steroids tear up his intestines and causes ulcers to form that eventually bleed. Luckily, he only had one episode of that last night, but they did take his feedings away.

I just got off the phone with the nurse and his O2 was at 42 and was wide awake. She said he was looking at his balloons and at the nurse when she was talking to him. He was also holding her hand and just very content, so hopefully when we go in today, he can be as wide awake as he is now.

They are about to start resuming his feedings at a cautious 1cc per hour just to make sure that he can tolerate it. They looked in his stomach and the only thing that was found was a normal clear liquid - so it looks like he got rid of all of the old blood by himself.

I can't remember if I posted this yesterday or not, but his IV in his scalp had fallen out. His nurse at the time couldn't get a new one started (and she is one of the best IV-givers in the unit), so they decided to let him rest and wait and try again later. The nurse this morning found a good vein on his foot and tried that one two times, but she said the vein forked like a road and could get it threaded... so, they are letting him rest again. If there is someone that is working today that is really good at giving IVs, they will try again, and if not, they will keep administering the medicine through his central line. This isn't ideal (as I believe the IV was used for the morphine) as it goes straight to his heart, but they will make use of it for the time being. What they don't want to do is stress him out.

Long story short... Reid is doing pretty good and is requiring a little more O2 than he was yesterday, but I think he is quite a bit more alert now. Looking back a week or so ago when they tried this (taking him off the nurcuron), he was at 100% O2 (compared to 42% today). This kid has some fight in him!


12:15am: It is getting late but I wanted to get the video up on the website that Alison made today. It is so wonderful to see his eyes open again!! Kristen and I have felt very disconnected with Reid over the past week as there has been zero interaction, but with the visit today, it makes everything that we have been going through worth it.



Reid has a meeting with endocrinology on Monday. Dr. Piazza has started the weaning of the dexamethasone today, but is very cautious as to how to move forward with the finalizing doses. Reid has been on hydrocortisone for quite a while now, and he is a little concerned with weaning both steroids at the same time. The dexamethasone can have some impacts on the pituitary gland and he wants to make sure that he is weaning the drug at the correct times. The endocrinology team will help devise a plan.

When I asked Dr. Piazza tonight, he was very pleased with Reid's progress. I had also asked when a possibility of extubating him was... and was thinking that it might be a week or so away, but he had hoped it would be sooner than that. If his oxygen requirements can maintain where they are at, I am curious to see if they could skip the CPAP and move straight to the high flow cannulas. Wouldn't that be the best thing in the world?!?!

Currently, his rate (BPM) on the vent is 16 and his PEEP is 8. We are starting to get close to extubation numbers and it is overwhelming to even begin to think about it.I can't even begin to tell you how excited we are... and are dreaming again about the day that he gets to come home. We deal with this constant fear of the unknown... and it wears on us... but we have a new focus on what we have in front of us and cannot wait for the day that we get to load him up in the car and bring him home.

OK, bed time for me. Thank you to all that have kept Reid in their prayers --- It means the world to us!

4:00pm: Reid is finally off the nurcuron as of about 11am today. It will take a little bit of time to get out of his system, but he is slowly starting to wake up. His oxygen has been fluctuating between 21% and 40% today, but we knew this was going to be this way once he starts breathing on his own again. The PEEP pressures have been lowered to 8 (needs to get to about 6 before extubation) and things seem to be looking good. The dexamethasone dose has been cut in half.

He had some visitors today: Grandma & Grandpa Elley and Mrs. Alison. The nurse even dressed him for the occasion --- heaven forbid he isn't dressed for company. :)

I still haven't been able to see him since Monday. I think I am finally over my cold, but I wanted to give it one more day before I go in there. There is no use risking getting him sick for my own benefit, so I just have to hear the stories from everyone else

6:45am: God has been good to us again and has allowed Reid to be on room air (21%) for the past two and a half hours. The nurse said he is like a new baby today as he has tolerated her touching him. While his heart rate still goes up (a sign of agitation), his oxygen requirements remain the same. His blood gasses are back to normal again and they have further weaned the pressure (PIP) down to 21 (24 yesterday). It is pitch black outside, still very tired from working 14 hours yesterday, and Kristen is dancing around and singing. Life is good -- for the moment anyway.

5:00pm: Reid is still holding fairly steady. He has marginally increased on is O2 to 30%. At one point, he went up a little higher, but it was because he was swimming in his own pee. He does not tolerate a wet diaper and as soon as they changed his diaper and his bedding (leaked out of his diaper), he came right back down. His urine output was 130cc for one diaper and 160cc for another diaper. That is a TON of urine.

He just had a blood gas test and his CO2 was at 39, which is awesome, but for some reason his base was at -8. They like to be -3 to +3, and will tolerate up to -5, so he is a little off. The doctor is scratching his head and wanted to think about it because it was strange. His pH was a little low too, at 7.29 (normal is 7.35 to 7.45).

Lastly, I am going to leave you with a picture of his vent and his "loops". The loops, defined by their height and length, paint a picture of the size of breath that he is actually taking. In weeks past, the loops were about a quarter of the size, even with all of the pressures the vent was expelling. From this picture, I would think that his lungs have a lot less inflammation and are probably a lot more "pliable". "Good loops" as a respiratory therapist might say.

1:00pm: We have some really exciting news to share (and hopefully the trend can continue)!!! Reid had his eye test and there apparently wasn't any change from the past few exams. Looks like he has crossed the age/maturity threshold for ROP and the doctors determined that he will need no further exams. One of the eye nurses mentioned that she would like to do one more exam, but the doctor is fairly confident that this chapter is behind us. So, we will see if he has another one or not (I am guessing not). Long story short: no laser surgery needed!!

The other great news... which is even better news than the eyes.... Reid's O2 is down to 26%. And I would have to look back at my notes, but I don't think that he has been that low since the first couple of days of his life. The next step now is to start weaning on the vent pressures, which they have already started. His Pinsp (PIP) is down to 24. His PEEP is still at 10 and the doctor had told us a week or two ago, that it would need to get down into the 6 or 7 range before he could be switched over to CPAP. Of course, the next hurdle is to wake him up and get him off the nurcuron and morphine (this is probably a huge battle in itself). But, we are taking this one step at a time, and we are going to embrace this HUGE leap that our little rock star did over the past few days. We are so proud of him (but we wont tell him that we are in the event that he has some other things up his sleeve...err... diaper... that he wants to pull out).

9:30am: Reid had a good night last night and his O2 is down to 43%. Doctors have not done their rounds yet, so we are not sure what is in store for him today. I would assume that they may start weaning on the pressures of the vent. He eyes are currently dilated for his eye exam, so that should probably take place in the next hour or two. Curious to see how he is going to react to the exam as this boy does not like being bothered with. Just hoping that with all of the progress we have made in the past 2 days that this eye exam doesn't set him back again. Every day brings something new for him...

10:15pm: Reid seems to have maybe had a "traumatic" experience with the ET replacement this afternoon and required substantially more oxygen. Before the procedure, he was down to 53% and afterwards, he got all the way up to 82% (around 6:30 tonight). Since then, he has been steadily coming down and is currently at 65% and sat'ing 96. Talking to the nurse, there is an adjustment with a new tube: irritation (old one being taken out and new one inserted), a larger tube consuming more of his windpipe, etc. But she said this one should be much more comfortable in the long run for him and the room is much quieter without him squeaking every time the vent takes a breath. I would also assume there would be some sort of vibration with every breath, which is gone now too. So, we will see where tonight goes. Hopefully we can be back down into the low 50s again (and if we are super lucky, down into the 40s??).

4:15pm: Dr. Piazza just gave me a call to give me an update as to where Reid stands. I am loving the fact that he is much more available to Kristen and I after the nurse had put a kind word in for us. He is much more likely to stop by and see us when we are in the NICU, or to give me a call. Overall, he is pleased with the progress, but would have hoped to see maybe an additional 10% drop in O2 requirements. If Reid is to continue to progress, he would like to start weaning the dexamethasone starting sometime tomorrow… however, he will need to be in the 40-50% O2 range for him to start.

I was mistaken about the ECHO… he actually had an EKG done today. There were no issues, so that was good news. He said one of the common side effects of the drug is to increase the blood pressure, and when it is high, the heart doesn’t need to beat as fast. A heart rate of 80 for a baby Reid’s size is not uncommon, it was just the fact that Reid’s heart rate is usually in the 130-140 range; hence the slight alarm. No arrhythmia was found in the EKG.

The ET replacement went “smoothly” and had zero issues. Dr. Piazza was very hesitant of doing this, but knew that ultimately, when Reid comes down into the 30-40% O2 range and they start to wake him up (stop nurcuron), they wanted better control over the vent and be sure that no air was escaping around the smaller tube. The larger tube fills his windpipe and makes it much more easy for the vent to do its job correctly. He was glad that he did it, but was a little nervous about the whole procedure, but commented that Reid did well.

He did mention that his O2 was still at 67% but peaked into his room and said that his sat’s were high and could be turned down a little bit. So, let’s keep up the prayers and hope that Reid can get into the 40s tomorrow so that he can start the dexamethasone weaning process!


3:00pm: Reid's catheter was removed and his new ET tube was put in by Dr. Piazza. I think this stressed him out a little bit and his O2 is back up to 67. I don't think that getting a tube down your throat, regardless of how sedated you are, would feel good. We are hoping that he can settle down and get off the higher O2 soon. Nurse and Doctor were both pleased with the progress he has made today. ECHO hadn't taken place yet when Kristen called at 2:45.

11:00am: Just talked to the nurse and Reid seems to be continuing to have a good day. Currently, his O2 is down to 57 with a BPM of 27 (he was at 35 yesterday). His latest gas tests had a CO2 of 41. All very good news!

On the agenda for today:

* ECHO scheduled for today to take a look at his heart. Today, his nurse said that his rate hasn't dipped below 100... and they aren't sure if his heart's rhythm is disrupted or if it is just a general speeding up or slowing down. Hopefully the ECHO can show one way or another.

* His ET tube (breathing tube) is going to be replaced. The current one is too small and causes him to squeak when he breathes. Not really an issue now, but they don't want to get into a sticky situation where if his breathing condition worsens and they needed a larger tube. His current one was inserted on December 23 (day of his surgery) and he has already outgrown it.

* His catheter is going to be removed. They feel that his urine output is just fine and the catheter is only another source of infection.

Today has been a good day and I am praying that it will continue to last!

7:30am: It appears that the dexamethasone is doing its job. Between 10:45pm last night and 6:30am this morning, his O2 dropped from 97% to 65%. But with every bit of good news, we also have bad news to accompany it. It appears that the medicine is causing his heart to have arrhythmia. His heart rate will go way up, come back down to normal and then later go way down, only to go up again. His blood pressure is doing the same, but the good news is that he is able to maintain his oxygenation when this all happens. The doctors will be discussing this in rounds this morning and we will follow up to see what the course of action is... maybe supplementing it with another drug, discontinuing the dexamethasone, or nothing at all. They will have to determine if the risks of using the dexamethasone outweigh the risks of not using it at all. Not really sure if I am supposed to be concerned about this right now, but I am going to focus on the good news right now that his O2 is at 65.

I had a horrible night last night. I have been under the weather for the past couple of days, and last night, I tossed and turned, got hot and cold, sneezed, coughed and woke up around 5am with a pounding headache (probably one of the worst I have ever had). I cancelled my 8am call with my offshore India team, and going to go back to bed. I know what is on my plate for work today, so my bed rest will be short lived. Kristen is getting ready to go to work this morning; she had off on Monday for MLK day, so her one day of work this week must be really nice. If only she could support the Elley household on her teacher salary... I think I could manage being Mr. Mom for awhile. This work thing sucks and I am ready for retirement... or maybe at least a nice vacation from our daily lives. The past 7 months has been a wild ride.

10:15pm: down to 97% O2 and sat'ing 96. Nurse seemed a little concerned that we hadn't seen more progress, but we are counting on tonight and tomorrow to start seeing the downward trend. All babies respond differently...

12:45pm: Still at 100%. Doctor's rounded and didn't make any changes other than they increased his pressures on the vent.

I forgot to mentioned yesterday that they are now giving him arginine which is an amino acid that plays an important role in cell division. Some of the benefits include: Precursor for the synthesis of nitric oxide (NO); Reduces healing time of injuries; Quickens repair time of damaged tissue.

9:15am: Reid's O2 is back at 100% and has been there for most of the night. His hypertension doesn't appear to be the issue, his vital signs all look good (blood pressure, heart rate, etc)... which makes them believe that it is all related to his poor lungs. The doctors haven't rounded yet today, so we will see what they suggest... but the nurse feels that they will just wait to see the effects when the dexamethasone kicks in (~36 to 48 hrs).

3:30pm: After a discussion with the pulmonologists, the doctors have suggested that we move forward with the use of daxamethasone. They were originally going to wait until the antibiotics were finished, but took another culture and noticed a drastic drop of white blood cells (which are a sign of infection) from the last culture. This leads them to believe that the infection is either gone, or on its way out and the issues that Reid is facing is probably not due to this infection/bacteria.

With that being said, Dr. Patel had asked Kristen and I today if we were comfortable with the use of this drug (they need consent before they do). The plan would be for the dexamethasone to be administered twice daily for 3 to 7 days, followed by a three week treatment of prednisone.

I gave Dr. Metcalf at Cobb Hospital a call this afternoon and he was in favor of using the drug as Reid is getting too big to be dealing with the issues that he is. Dr. Metcalf's only concern was that a 3 day treatment of dexamethasone would probably not yield many results as it usually takes 48-72 hours to start seeing anything.

Reid will get his first dose today and then two a day until they feel that he has made enough progress (3 days initially, then evaluate. If needed, two additional days and then re-evaluate. If needed, two additional days for a max of 7 days). At that point, they will start the prednisone for the three weeks.

We are scared of the unknown, but studies have shown that low doses (less than 9 days) of this medicine are "safe". We feel the risks of not starting this drug outweigh the risks of taking it and we will deal with the consequences later in life if they ever present themselves.

12:30pm: Still at 80% O2, but found out that his hematocrit level was 29... time for a blood transfusion. This may partially explain some of the reason as to why it is taking some time for him to rebound from yesterday...

8:10am: Reid is down to 80% O2 as of 8:00am. When Kristen called at 4am, he was at 90%, so hopefully we can continue this downward trend today.

10:45pm: Still at 100% O2. Nurse said she was about to turn him down to 95% as he was sat'ing in the 95/96 range and then he fell down to about 91/92. We are crossing our fingers that we can make some progress tonight! Kristen is making our cat say his kitty prayers with us tonight.

6:45pm: Success is short-lived in the Elley household these days... the results of taking off the nurcuron finally caught up to Reid and he was back on 100% oxygen. About 30 minutes after my last post, his O2 started creeping up and eventually got up to 100% and they started the nurcuron drip once again. When Reid gets back down to the 40s/50s, they will attempt to remove the nurcuron again. If this doesn't work, looks like the dexamethasone might be our next path, but they are wanting to see the results of the antibiotic first (6 more days).

3:30pm: They took Reid off the paralytic at 9:30 this morning and have had to go up on the oxygen to 63, but I think for the most part, it has been a fairly quiet day. He wiggles around when we touch him, so it is nice to see some movement out of him. Still on the morphine drip and pretty drugged up, so we have yet to see him open his eyes.

They also weighed him this morning and he is 10 lbs 5oz - some of which is water weight and is still puffy. Nonetheless, he has put on quite a bit of weight in the past month since we have been here at Egleston. We are probably going to miss the joys of having a small baby, but the larger he is, the closer we are to bringing him home.

5:30pm: Pretty uneventful visit at the hospital today. He has been fluctuating between 45% and 50% all day and is currently at 48%. Met with the weekend doctor today and if all holds up over the next 12 hours, they are going to pull him off the paralytic tomorrow to see how he can handle being semi-awake. If he can handle that well, they will start weaning the pressures on the vent. Feedings were increased minimally to 7.5cc per hour.

7:00am: last night was the first stable night that we have seen in quite some time. Reid's O2 stayed at 45% the entire night, even when the nurse moved and adjusted him. Keep in mind he is still heavily drugged, but this is definitely progress!

11:00pm: is tonight our night? So far, this is the news we have been waiting to hear. Every night, we call right before bed and cross our fingers that things are going well. Lisa, our nurse tonight, said that she had been waiting for us to call as she had good news for us. Right now, his O2 is at 45% and sat'ing at 97. She is ready to bump him down to 40%, but she was cautious and wanted to take things slow. He has had quite a lot of urine tonight, which can also help with the stress that body fluids can put on the lungs. So, a breath of fresh air tonight, but don't want to get over excited as we know what can happen. But, good news is good news and we will take everything we can get right now.

6:30pm: down to 65% O2 and sat'ing 95. They have made a change on his feedings in another attempt to keep him dry: 6cc milk fortified to 24 calorie and starting the hyperal again. They want to ensure that he is getting the most calories possible for him to continue to grow, while trying to restrict the amour of fluids that he is getting. During rounds today, he had had a group of about 6 that was composed of doctors, pharmacists, nutritionists, etc. And they feel like they have formulated the best nutrition possible for him.

On a lighter note, his chin and neck weigh about a pound and his hands look like those of a fat kid. I will post pictures later tonight when I am home. :). Hopefully we can get some of these fluids off of him soon so that he starts looking like our baby again.

2:30pm: Reid is on 75% oxygen and they ended up giving him a catheter to help relieve some of the excess fluids. With him being very sedated and paralyzed, his urine output is less than stellar. We are about to head into the hospital soon...

9:45am: Reid had an up and down night: O2 fluctuated from the 50s to the 80s and was currently on 80% when Kristen called. He had recently been turned onto his back and caused his levels to go slightly up. On a different front, it looks like Reid packed on some serious weight over the past few days. The nurses have attributed it to the fact that the nurcuron causes fluid retention and with him on nearly full feeds and being paralyzed (little caloric burn). They have dropped his feeds down to 11cc per hour to help compensate against the fact that he is retaining the fluids.

2:30pm: Dr. Piazza, in his attempt to be more involved with Kristen and myself, gave me a call to touch base with where Reid stands:

1. Eyes: Good news is that he is at the same Stage and Zone as last week (and possibly slightly better if you look at the past several eye exams). The bad news is that we are not out of the woods yet, and will have another exam next week. He did mention that we are getting close to the cusp of being out of the danger zone though (in relation to his age and when it is no longer a concern).

2. Cultures: He came back positive (again) for Enterobacter even though he finished up his last dose of the current antibiotic the other day. After talking to Infectious Diseases, they had determined that the current antibiotic wasn't doing the job that it used to. This suggests that the bacteria may have slightly morphed and they are now giving another 10-day course of a new drug - gentamicin. Good that they found something, bad in the sense that he has to have his IVs (in addition to his central line) for another 10 days --- and we know how this kid goes through his IVs...

3. Pulmonary Hypertension: After reviewing his ECHOs over the past few weeks, Dr. Piazza is quite pleased as to the direction Reid has gone down. He suggests that the PPHN is no longer a factor in his poor oxygenation. He was previously thinking the other day that it may still play a role in his sickness and that is why he had gone up on the sildenafil once again. However, he is now second guessing himself and thinking that the sildenafil actually might have an adverse effect on the oxygenation. I don't think I understand the entire reason why, but it has something to do with the fact that the lungs have too much blood in them, and with Chronic Lung Disease, he is not capable of oxygenating all that blood at once. He is "scratching his head" and wondering if he should cut back on the dose of sildenafil.

12:15pm: So, the nurse lied to us and got her numbers mixed up when she told Kristen his O2 numbers this morning. He was in the 60s and 70s over the night (not 40s and 50s). How frustrating is that?!? He is currently at 65.

Eye test was this morning and we are good for one more week. Another test next Thursday.

9:15am: I don't have a lot of time to post, so I will keep this one short and sweet. His O2 fluctuated throughout the night ranging anywhere from the upper-50s and into the 40s. The nurse was up in the front of the NICU when Kristen called this morning, so she wasn't aware of the current number, but thought it was in the lower 50s. So, over night, he was able to gain at least 10 percentage points!

10:30pm: Down to 62% O2!!! This little stinker is giving his father a heart attack.

Reid is officially a drug addict and has developed a strong resistance to the morphine and nurcuron. Not only is he on a drip of these two drugs, but he also gets the chloralhydrate at night so that he sleeps for at least 6 hours. Tonight, shortly after touch times when he was given the chloralhydrate, he was smacking/sucking on his ET tube and waiving his hand in the air. Between these three drugs, he should be **gone**. The nurse decided to give him an extra bolus of morphine and nurcuron and no more than 10 minutes later, he is doing the exact same thing. After talking with the nurse practitioner, they gave him yet another dose of both drugs.... and he is finally out for the count. Hope he doesn't expect mom and dad to hook him up with the drugs when he comes home. :) I don't like the fact that he is on so many medications, but if it is what it takes to get this guy home to us, so be it.

5:30pm: Down to 82% O2. Doctors think this is Chronic Lung Disease at it's finest... an up and down roller coaster.

2:45pm: I don't have a lot of news as I am catching it all second hand from a very brief conversation with Kristen (she is teaching today and I have been in back to back meetings), but Reid's O2 is back down to 88 and his BPM to 24. Recent blood gas test back well. Lowered his feedings to 12cc per hour to help keep him "dry".

I did some reading this morning about Gastroesophageal Reflux in Premature Infants as this is something that the doctor is keeping a watchful eye on. He is concerned that his feedings are causing aspirations into his lungs when he refluxes... and if you read the article, it shows that this can lead to respiratory infections. This is something that I want to further discuss with Dr. Piazza next time I see him as we are starting to see a trend (not sure if it is related) that when Reid starts feeling better, he resumes his feedings, and then the vicious cycle starts all over again. Hmmm...

5:30am: They have changed Reid's position to be on his stomach and his sats have come up marginally to the 93 to 95 range. They have also repositioned his ET tube and moved it slightly down 1.5cm to see if that would help but is only sat'ing 95.

Feeds are going to continue as the hyperal/iv fluids tend to make babies retain more fluids which could impact his lungs. The bowel sounds are still present so they are fairly confident that he is still moving his food along well.

If Reid doesn't make any changes in the next couple of hours, they are going to switch over from the vent to the high frequency (oscillator) -- which was something that they had talked about yesterday in our meeting. This machine, while not pretty, can actually remove some of the stress that the vent puts on the lungs by mechanically inflating and deflating the lungs.

I am heading to the airport now and wish I wasn't going, but if need be, I can always change my flight and come back early. It is only a 1.5 hr flight and can be back fairly quick.

4:30am: Still at 100% oxygen since last night's touch time and has been hovering in the 89 to 92% saturation range. They have done chest and stomach xrays and don't see anything different than what they saw in yesterday's xrays.

They were able to suction about 8cc of milky fluid out of his stomach which appeared to be a mixture of medicine and partially digested milk. Since he is being fed into his intestine and not his stomach, this shows that his bowel had refluxed some of the milk. They aren't sure if they are going to stop feeds yet.