Jump to content
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

Emergency Room


lotusgem

Recommended Posts

lotusgem Rookie

This question goes out to those of you who have accidentally ingested gluten and have then made a trip to the emergency room because of extreme pain. I've read this scenario numerous times on the message board, yet, it only just occurred to me to wonder what, if any, treatment is administered at the hospital. Can they actually do anything for someone in this situation?

:huh: Paula


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



MySuicidalTurtle Enthusiast

I sometomes wish doctors could give you something to take at home. Ow, it can hurt.

flagbabyds Collaborator

if it hurts so much you can go to the ER and they can give you anti-nausea pills and such, sometimes the pain can be from dehydration because you are getting rid of so much stuff, so they will give you IVs and that can make you feel better.

KaitiUSA Enthusiast

Before I went gluten free I was in there 4 or 5 times for IV's and they would give me a few of them then release me. I felt so much better after getting pumped with IV's...of course at this point I was undiagnosed and had no clue what was wrong.

After I went gluten free I haven't had to go back there. There have been times when I have been glutened and almost felt like I needed to go but I always was able to hold out. IV's really do help though I can say that...if I get glutened now and a reaction gets really bad I will go to this place we found that will give you IV therapy.

cdford Contributor

The times it has happened to me they gave me IV phenergan and demerol until the gastro symptoms and pain were under control. It usually only takes a couple of hits and then they send me home with darvocet and phenergan tablets to get through the next few days. Once last year it took four days in the hospital to get it under control to where I could hold down mashed potatoes and juice. I hope to never repeat that experience again.

cdford Contributor

Oh yes, and remember to be sure they clearly mark your chart to verify gluten free meds with the pharmacy. I also carry a letter with me stating that.

*****

If you have children, be sure you have with you an authorization and phone numbers for someone to take care of your children or they will be placed with Social Services (DFACS or whatever they call it in your state) until you get out of the hospital.

*****

I found that one out the hard way when it took my husband more than 15 minutes to get to us. The ambulance drivers are often required by law to call them in for minor children even if there is someone the kids know there with you. I was too sick to contact anyone and luckily we were at a pharmacy where they knew us well and they contacted my husband for us.

anewsprue Newbie

Just before I was diagnosed I was in the ER with extreme pain, before they could do any testing they had to give me some pain killer IV, wish I knew what it was becasuse it really helped. It would be nice to have pill form on hand at home.


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



plantime Contributor

It seems to me that painkillers, antinausea, antidiarrheal, and fluids is all they can do to help. They have stronger meds at the ER than we can get OTC, so it does help to alleviate the symptoms. I'm not sure that having the meds in pill form would help us, though, since the problem is in the intestines.

lotusgem Rookie

Thank you, everybody! I just had no idea. Good advice, Donna, on looking after the kids. That would be so scary for them, both to have to see mom go away in an ambulance and then for them to be taken out of the family setting! Well, I hope that none of you has need of the emergency room again.

Take care. :)

Paula

cdford Contributor

Yeah, I don't which scared me more--the nasty neurological symptoms I was having or the thought of my kids under the jurisdiction of the state for any period of time!

Generic Apprentice

They also give steroids, it actually really helps aleviate the reaction.

Noneformethanks Newbie

I got glutened big time in December after a visit to Rubio's Baja Grill (basically, I found out later, that the only gluten-free items on the menu are the black beans and lettuce). I was in such pain the next day that I could hardly walk and couldn't stop crying.

Walk-in clinic sent me to the ER, where I told them I thought it was a reaction to gluten. They were convinced otherwise; thought it was diverticulitis (sp?). Started an IV, mprphine, and I got a CAT scan, which of course, showed nothing. Six hours and 3 doses of morphine later, I wasn't any better.

Finally, the nurse decided to try another opiate, fentenal, and viala' the relief was nearly instant. Although, I hurt like I'd been sucker punched for another week.

I learned for the ER dr. that the majority of people in there for abdominal pain are sent home without a diagnosis. I'm thinking that perhaps a simple little blood test for celiac disease would seem like common sense, afterall they are already doing a CBT.

I hope never to relive that experience, but if I do, I'm asking for the fentenal first!

Barbara

lotusgem Rookie

Well, thank you for MORE interesting replies! Barbara, you answered another question that had been running through my mind, which is, do doctors take you at your word when you inform them that you are having a gluten reaction. I suppose that the response is different with each doctor, but since the medical profession in the U.S. seems to be largely ignorant of Celiac Disease, it wouldn't be surprising for them to ignore and go off in another direction, entirely. I'm glad that you finally got relief.

Paula

cdford Contributor

Once you have it on your hospital's medical records that you are celiac disease, they tend to ask if it is a typical reaction and, if so, treat it as such. Otherwise, you can count on them questioning everything and writing you off. My symptoms take such a specific pattern when I get into something that there is no question anymore. They just hit me with IV phenergan and some demerol without question. It has happened once each of the last two years and the last time it took three hospital trips to get it under control. They kept sending me home and it would flare back up again once the drugs got out of my system.

  • 3 weeks later...
pmrowley Newbie

Just a note; if you DO end up in the ER in the United States, make damn sure they don't hook you up to a Dextrose drip. They do not monitor for gluten-based dextrose sources here.

-Pat

celiac3270 Collaborator

What do you mean? :huh: Dextrose is always gluten-free because it's sugar. Do you mean dexTRIN which can be made from corn or wheat?

Archived

This topic is now archived and is closed to further replies.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,164
    • Most Online (within 30 mins)
      7,748

    JennyK
    Newest Member
    JennyK
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • trents
      Welcome to the forum, @Mmoc! Please include the reference ranges for the IGA and the TTG tests in your next post if you have access to them. We cannot comment much otherwise as different labs use different reference ranges for these tests and also different units of measurement. There are no universal standards as of yet so the raw test numbers are not always helpful. Having said that, if your IGA (what we usually call "total IGA") is low, the TTG-IGA score will be skewed and cannot be trusted. Other kinds of tests for celiac disease would need to be run, particularly those in the IGG family of tests. Perhaps this will be helpful:  
    • Mmoc
      Hi there any advice welcomed. I have had 4 years of symptoms ranging from immune related anaphylactic symptom sudden onset food allergy to peppers/paprika/chilli/capsicum family derivatives. all these allergies fizzled out and following a food challenge test in hospital I reintroduced them a few months ago. Since then my digestive system is a mess. i have since noticed that 4 years ago when testing for iga allergies my iga level was .62 and my ttg was less than .1 (due to symptoms I was probably eating very plainly at that time). should I insist on being retested for celiac? I’ve since read two indicators for celiac include: sensitive to spicy foods when in flare up tooth enamel weakness and symmetrical discolouration patches on teeth which I have had since childhood on my two front teeth     thanks
    • trents
      This article does not address migraines at all.  Yes, red wine and sulfites are often mentioned in connection with migraine triggers. With me, any kind of alcoholic beverage in very modest amounts will reliably produce a migraine. Nitrous oxide generators, which are vaso dialators, also will give me migraines reliably. So, I think most of my migraines are tied to fluctuations vascular tension and blood flow to the brain. That's why the sumatriptan works so well. It is a vaso constrictor. 
    • knitty kitty
      Excessive dietary tyrosine can cause problems.  Everything in moderation.   Sulfites can also trigger migraines. Sulfites are found in fermented, pickled and aged foods, like cheese.  Sulfites cause a high histamine release.  High histamine levels are found in migraine.  Following a low histamine diet like the low histamine Autoimmune Protocol diet, a Paleo diet, helps immensely.    Sulfites and other migraine trigger foods can cause changes in the gut microbiome.  These bad bacteria can increase the incidence of migraines, increasing histamine and inflammation leading to increased gut permeability (leaky gut), SIBO, and higher systemic inflammation.   A Ketogenic diet can reduce the incidence of migraine.  A Paleo diet like the AIP diet, that restricts carbohydrates (like from starchy vegetables) becomes a ketogenic diet.  This diet also changes the microbiome, eliminating the bad bacteria and SIBO that cause an increase in histamine, inflammation and migraine.  Fewer bad bacteria reduces inflammation, lowers migraine frequency, and improves leaky gut. Since I started following the low histamine ketogenic AIP paleo diet, I rarely get migraine.  Yes, I do eat carbs occasionally now, rice or potato, but still no migraines.  Feed your body right, feed your intestinal bacteria right, you'll feel better.  Good intestinal bacteria actually make your mental health better, too.  I had to decide to change my diet drastically in order to feel better all the time, not just to satisfy my taste buds.  I chose to eat so I would feel better all the time.  I do like dark chocolate (a migraine trigger), but now I can indulge occasionally without a migraine after.   Microbiota alterations are related to migraine food triggers and inflammatory markers in chronic migraine patients with medication overuse headache https://pmc.ncbi.nlm.nih.gov/articles/PMC11546420/  
    • trents
      Then we would need to cut out all meat and fish as they are richer sources of tyrosine than nuts and cheese. Something else about certain tyrosine rich foods must be the actual culprit. 
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.