Showing posts with label GI. Show all posts
Showing posts with label GI. Show all posts
Monday, July 23, 2012
Each week the Preemie Resource Blog will look at one issue that effects preemies and their parents.This week we will discuss reflux, one of the most common issues among premature babies. Read Stacy's story about her son's struggle with reflux.
REFLUX
Reflux is one of the most common but
least diagnosed issues with preemies. I’ve found that many doctors do not want
to start a medication regimen for preemies in the NICU. What that means is that
many babies go home and continue to suffer out loud or in silence.
If you have ever had reflux or
heartburn, you can imagine what a little baby is feeling every time they eat. I
remember crying 8-10 times a day- every time my son ate. It was heartbreaking
to have to feed him when he was in so much pain. Then the spitting up got
worse. I was told; “babies spit up.” This was not a baby just “spitting up”.
WHAT IS GER?
“GER is Gastroesophageal Reflux. Gastro means
stomach, and esophageal refers to the esophagus, the tube inside the throat
that connects the mouth to the stomach. A muscle at the top of the stomach
(also called the Lower Esophageal Sphincter or LES) naturally opens and closes
to allow swallowing, burping, and vomiting. Refluxing occurs when the stomach
acid and partially digested food flow back up through the LES into the
esophagus. All children and adults will naturally reflux throughout the day,
especially after eating. However, if the muscle opens too frequently and
refluxing occurs too often, complications can develop.
Premature infants have an increased risk of
developing GER. There are several medical conditions that can cause reflux, but
in preterm infants, the most common causes are immature muscles and abnormal
breathing from chronic lung disease. If the lower esophageal sphincter is weak
or underdeveloped, it can remain open when it should be closed, letting the
stomach contents flow back up the esophagus. When an infant or child breathes
abnormally because of chronic lung disease, the muscles used for breathing work
harder. As these muscles work hard to breathe, they can pull on the muscles
near the top of the stomach, stretching the sphincter and causing it to remain
open.
When the stomach contents flow inappropriately up
into the esophagus they bring acid from the stomach. As the acid irritates the
tissue inside the esophagus, it becomes inflamed and reddened. This condition
is called esophagitis. Esophagitis is painful, similar to the pain of
heartburn. This is why an infant will refuse to eat or stop eating - she is
protecting herself from the pain of the acid touching the damaged tissue. If
the reflux is severe, the stomach contents may go high enough into the
esophagus to be aspirated or spilled into the lungs causing choking, color
changes, frequent respiratory infections, apnea (breathing slows or stops)
and/or bradycardia (slowed heart rate).”
SYMPTOMS:
As I said, “babies spit up” but reflux is much more
than that. Here are some common signs and symptoms:
•
spitting up frequently (more than
2 times a day);
•
fussy often throughout the day
(specifically before, during or after eating)
•
refusing to eat,
•
fighting eating;
•
taking only small amounts of
formula or food, regardless of the amount of time since the last feeding;
•
back arching during feedings;
•
bradycardia;
•
choking or apnea during or after
eating;
•
skin color turns pale or grayish
during or after eating;
•
poor weight gain; and/or frequent
respiratory infections.
Many parents say, "She acts like it hurts to
eat" or "It just seems like she is in pain."
My son would spit up every time he ate, even if he was held upright for
an hour after he ate. He refused to eat and would only eat a small amount every
2 hours. He would arch his back and cry and scream. It broke my heart because
he was a happy baby when he wasn’t eating or refluxing. Although his weight
gain was slow, he was always gaining so the doctors weren’t concerned. But
mother’s intuition told me that it was more than just spitting up. Eventually, my son spit up so badly that he stopped
breathing and my husband and I had to bulb syringe him until color came back to
his face. It was after that point that we finally got our diagnosis.
For more on reflux--how is it diagnosed, treated, and other how helpful information--click here
Labels:
bradycardia,
feeding,
GI,
reflux
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Sunday, February 5, 2012
Meet Addison… my ex-26 week preemie… twin sister to Blake.
Addison is primarily G-tube fed.
Addison is primarily G-tube fed.
What is a G-tube? A G-tube is a gastric feeding tube that is surgically placed directly into one’s stomach for the purpose of providing nutrition. Medical advancements have come a long way since the first G-tube, now days many individuals sport what we call a “button”.
No more long tube set left to dangle, to be tugged on or tucked away in effort to disguise. The bottom portion (including the balloon) stays inside the stomach while the top part lies against the skin. The balloon is filled with water and is deflated to insert or remove the button. There is a“snap” on the top that opens and allows the extension set (feeding tube) to be connected for feeding.
Why is Addison Tube fed? As a preemie Addison faced several obstacles, one major obstacle was reflux. Her case was so severe that the NICU refrained from even attempting oral feeding via bottle. To complicate things even more she was diagnosed with a cleft palate (opening in the roof of her mouth that did not close in utero), which hinders her ability to gain good suction to suck on a bottle. Those two things alone paired with a very very late start to oral feeding since created a huge obstacle including major oral aversions as well as never developing the suck swallow breathe reflex.
At 3 months 2 weeks (actual)/2 weeks (adjusted) of age doctors performed surgery to place a Nissin Fundo (to control reflux and prevent aspiration) and the G-tube, (these two almost always go hand in hand). After she recovered she was discharged to home and begun feeding therapy. We meet with OT thru Early Intervention once a week, and practice eating by spoon & drinking from a Sippy cup 3 times a day. Some days she does pretty awesome and will eat up to half a jar of Stage 1 purees, other days she is less then interested and we are lucky if she will take one bite.
Feeding a tube fed child is a fine art, a balance of tube feedings and oral feedings. It’s a fine line between making sure Addison isn’t getting over full from tube feedings (and hence making her not hungry, and refusing to eat by mouth) and making sure she is getting adequate nutrition. It’s also a lot of trial an error to find out what works to get the best results.
In our case, instead of just filling a spoon and putting it in her mouth, we have to do what I like to call “warm ups”… Exercises where we stimulated her mouth and help Addison get organized to eat. This begins with brushing her gums with a Nuk brush, 3 times on each side of her mouth & tongue, while giving her a moment to swallow in between…we repeat this about 3-5 times each. Then we encourage her chewing reflex by placing a Chewy Tube (shaped like a T) near her molar area and allowing her to bite down & chew. After 5 seconds we take it out and give her a chance to swallow and repeat. Then comes the spoon and Sippy.
Like I said…it’s quite the process. We are also learning that she really isn’t all that crazy about baby purees and she really likes “self feeding”. She is a lot less resistant if she is the one putting things in her mouth, so we try to give her lots of opportunities to do this as well.
Her oral surgeon promises that things will get MUCH better once she has her cleft palate repair this summer, and her GI doctor is convinced we’ll be saying “Bye Bye Tube” by age 2. Until then we continue to work with her every day, and pray.
It can be very overwhelming. In public people stare and wonder why you aren’t feeding your child, and what is worse is they even stare when we’ve tube fed her in public. I understand children being nervous and curious but grow adults stare and gawk which is frustrating. We also meet a lot of misunderstanding or even denial, from grandparents, family & friends. None of which have ever fed Addison. It’s not their fault and all we can do is teach them.
I think one of the biggest fears as a tubie mom is that someone will naively feed Addison something that is not safe without our permission. And again that’s why knowledge is so important. Holidays such as Thanksgiving can be especially tough with all the food around. But there are also many positives to the feeding tube, when she is sick, I never have to worry about keeping her hydrated and I can administer meds without any fuss or fighting. If it wasn't for her feeding tube things could be very different. In the beginning I had a love/hate relationship with her feeding tube, but now I know it was the best choice and I couldn't love the tube more (but I will still be glad to see it go).
She continues to develop, thrive, and astonish us all by defing all the odds. She is your typical little lady, in fact for the first time since their birth she's actually outgrown her "little" brother. Now if I could just get her to lay still and stop trying to run away when it’s time to “eat”. J
Labels:
g-tube,
GI,
Nissin Fundo,
reflux,
tubie
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