ER Admission for Chronic GP Pain

I have been going through some rough times recently. The weather is partially to blame in that the heat has made it difficult for my tpn to keep up with my hydration needs, often landing me in the ER with extreme stomach cramps, migraine headaches and unrelenting nausea. My heart rate soars to the mid and upper 140s as my vitals are taken. I get rushed back into an ER exam room where I can be hooked up to heart, respiratory and oxygenation monitors. Blood was taken, four whole vials for a standard panel of stats. Fluids were administered via IV through my chest portacath and anti-nausea medicine, Zofran, was also administered through the central line. And there I laid for what seemed like hours. The doctor finally comes in and asks the most condescending question a patient could hear in an ER room, “how are you feeling today?”

I usually go home the same day I get to the ER, 4-5 hours later, pumped up on fluids and on occasion, pain medication. However, the pain I have been experiencing lately has been very localized to a very specific spot. The pain runs along the leads of my gastric neurostimulator. It feels like a burning, tight, and crampy pain. I expressed this to my gastroenterologist and he suggested I do another GES to first check on the stimulator and see if it had any effect on my stomach. He was hoping the stimulation would sort of “kick-start” my stomach into working. The GES would show increased emptying times when compared to my previous GES done in 2009.

GES Experience

I arrived for my second GES study bright and early at 8:00am. I was not allowed anything by mouth for 12 hours prior to my appointment. This wasn’t a problem because I don’t eat anything by mouth, I am mostly NPO and receive my nutrition via TPN. I check in and get called back into the room where the large machine that is used to scan my stomach for food, is located. I’m instructed to eat eggs (egg white egg beaters that were microwaved) laced with radioactive tracer, bread with jam and drink a cup of water in 10 minutes. I look at him like he’s crazy. Who ever makes up these meals clearly makes them without their victims in mind, because there is no way a person with any motility disorder is going to be able to choke down that meal. I was able to get the eggs down, since I knew that was the most important part, and a piece of bread. My first solid meal in I don’t even know how long and it was painful, there were tears, but I hopped right up on that table and got him to start the four hour test before any of that food came back up.

The first scan is used to compare the rest of the scans. A scan is done at hour 1, 2 and 4. Between the scans you are free to do whatever you want. If you are scheduled to have this test done, bring something to entertain yourself because you are going to be there for awhile. I brought my iPad loaded with movies, and the hospital had Internet. Between scans I watched movies and chatted it up with people. Even with entertainment, I pretty much wanted to claw my eyes out from boredom. The results of the test were done using complicated equations combined with visual confirmation. The scanner detects the traces of radiation and maps them out in your stomach. The results are reported back in percentages of food left in the stomach at set intervals.

Normal results are:
T1: 90%
T2: 60%
T4: 10%-0%

My Results from 2009:
T1: 98%
T2: 86%
T4: 4%

Results from July 2011:
T1: 98%
T2: 96%
T4: 34%

My gastroenterologist was upset to see how fast my stomach had slowed down and how the gastric stimulator had zero affect on the stomach. The test in July was with the stimulator ON. It is not approved nor expected to pace the stomach, but it was the hope that it might start the stomach into working. This clearly is not the case. He has suggested vigorous stimulation and more powerful medications to help the stomach to empty. For now, TPN is still how I will be getting my nutrition. It is working, I’m gaining and maintaining weight, so I can’t exactly complain. The only downside to higher settings on the stimulator is that it wears out the battery at a much higher rate, requiring more surgeries. Guess we will address that when it comes time.

I hope everyone is enjoying their evening! Happy belly days!

  • 3 Responses

  • natalie says...

    Hey Kirby, sorry to hear you are still struggling so much! I think of you often…especially when I’m really low. It makes me feel less alone x Hope you start to feel better soon and the weather backs off lol x

  • Aunti says...

    What are we going to do with you!! I am sorry!!Hang in there!! Been thinking about you!! Love you lots, Auntie!!!

  • Kirby says...

    Things are getting better. Just taking it day by day. Taking the week to rest up for the weekend where I use all my energy. One crazy cycle. I hope you are doing OK! I need to catch up on your blog as it has been awhile! I hope you are doing better. Keep me updated!

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