Wednesday, July 15, 2009

Watching & Waiting

Day Eighteen: Tuesday, July 14

Well, I took the day off today. That is one fringe benefit of having your baby in the hospital, you can do that. I needed an emotional and physical break and I don't think Will has been up to much visiting either.

I kept in contact with Will's nurse in the morning and I spoke with his nurse practitioner in the afternoon. The nurse informed me that they had decided to keep taking x-rays of Will's tummy every six hours. They wanted to make sure that the distention and dilation was just air or stool and not something worse. She said they wanted to be sure that it was not air being let in from a ruptured bowel. She told me that the Anderson tube was still looking quite clear. Also at rounds (the huddle that the doctors have each morning to discuss the game plan for each baby) they decided to help him out with the pain by increasing his morphine dosage. I was glad to hear that.

Later this afternoon, Will's nurse practitioner called. She said that the x-rays were continuing to look good. They are fairly sure that it is not a ruptured bowel. They determined that he just has some air or stool that he hasn't been able to pass on his own. To give him a little help they are going to give him a suppository and hope that he will be feeling better after his bowels start moving things along. They have continued checking his blood count and it sounds like those began to normalize after the antibiotics they gave him yesterday, so that's good. The blood & urine cultures and a spinal that they did yesterday are all looking clear so far and we should have the final results sometime tomorrow night. These were all to check for any infection.

I am so relieved that we haven't run into any worse case scenarios yet. So far it sounds like he was hurting and just needed a little help. So we are still just waiting for his little system to get up and running.

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About Gastroschisis

I have posted some links for your information and research, but here's the run down on gastroschisis.

What is it?
Gastroschisis is a birth anomaly in which the baby's abdominal wall does not close all the way during early development. These abdominal defects can result in several problems, the least of which is gastroschisis. This is when some of the intestines escape through the small opening in the abdomen and are now outside the baby's body. During pregnancy these organs are exposed to the amniotic fluid for some time which makes the once maliable and functional bowel stiff and swolen.

How is it treated?
Since gastroschisis is not as serious as other similar defects, it is not dangerous to still deliver the baby vaginally. Upon delivery the baby will go to the NICU and be examined by the pediatric surgeons. At this point of evaluation, there are several courses of action. What needs to happen eventually is that the bowel needs to be surgically put back into the abdomen of the baby.

Option 1: If the bowel has little damage, is quite maliable and healthy, and the baby's belly seems to have the room to accept all of the intestine at once, the surgeons will perform a "primary closure". The surgery is fairly simple. They will make an incision to enlarge the opening enough to push the bowel back inside and sew it up once it is finished.

Option 2:
If the bowel is stiff and swolen and or the baby's belly does not have the room to accept it all at once, they will perform a "staged closure". This is more complicated and takes some time. This invloves placing a "silo" over the bowel (this is basically a bag that holds the bowel suspended above the opening). This silo will be somewhat inserted into the baby's belly so as to allow the abdominal fluids to enter and thus healing the bowel by bringing the swelling down and making it malleable again. As the bowel heals and with a little assistance from the doctors the bowel will slowly but surely re-enter the baby's abdomen.

Recovery
A staged closure can take up to a week or two. So you may ask why does he have to be in the hospital for 5 to 6 weeks. Since the baby's system is not used to the pressure introduced by this bowel that is now inside the abdomen, and the bowel has been exposed to the amniotic fluid for so long, it simply takes time for the baby's digestive system to normalize. Aside from the digestive system, other things may be affected such as breathing due to the increased pressure inside the body. The baby's recovery can be broken down into three distinct stages. Pre-Surgery, Post-Surgery/Pre-Feedings, and Post-Feedings.

The first is simply the waiting period before the baby's bowel can be put back inside.

The next period is after surgery, the baby's system is still very fragile and can only be fed interveinously. During this time the amount of nutrients is slowly increased until the baby is ready for the final stage, when his body can accept real food.

Once on breast milk feedings from a bottle, the baby is closely monitored. The process is slow as the baby must phase into these feedings from the IV. Once the baby is up to full feedings and is gaining weight, we can all go home!

Long term effects
Once the baby has fully recovered and is ready to go home, he should be fit as a fiddle and have little or no related complications thereafter. The main thing that he may experience is a case of acid reflux, but this can be treated with medication and it usually will go away as he grows and gets older.