He can’t eat as he instantly throws it back up and has runs , I’ve given him electrolytesIf people with diabetes don't eat and don't produce enough digestive glucose to satisfy brain requirements, the body will start absorbing body fat via the krebs/citric acid cycle to produce ketones that can more easily be converted to ATP to fuel the brain and body.
In fact the conversion of ketones to ATP gives more ATP (energy) than the conversion of glucose to ATP
I’ve rang and text and waiting for callIf it were me, I'd want him seen by a doctor tonight. Have you got an urgent care centre you can take him to or A&E? Or out of hours GP number? Failing that, call 111 but don't be fobbed off.
Has he been tested for Coeliac disease?Hi all , my son has got high keytones but he’s hypo , he’s been being treated for ibs as this last 3 months he’s been having tummy pains ,sick ,runs , he’s lost appetite due to pain and feeling sick , help any advice please
Thank you , keytones now 2.4. water yes , degludex has just been lowered , he has starvation keytones and gastropriosis ,with all the tests the last few weeks and what’s happening now its not good so it might not be ibs at all they said but gp was sent a letter for further investigation when he was admitted and nothing had been done , so all this time ,we’ve been waiting for answers and it’s now affecting his diabetes , he’s so poorlySorry to hear about your son @Kezz72
What levels of ketones did he have last time you checked?
Can he keep water down?
What is his BG level?
Do you have basal insulin he could have?
Glad you have called NHS 111.
Hope he gets prompt attention and recovers speedily.
No that was my first initial response due to the dairy products not settling , there saying it could be gastropriosis due to him having diabetes for such a long timeHas he been tested for Coeliac disease?
Unfortunately no matter what the problem is the first diagnoses is always it's your diabetes. So you have to point out to them that there is no such condition called it's your diabetes.No that was my first initial response due to the dairy products not settling , there saying it could be gastropriosis due to him having diabetes for such a long time
Thanks so much. I think it must be that. I wasn’t aware pumps put you at increased risk of DKA, useful to know.If she’s not eating, they could be so-called starvation ketones. IMO, it’s best to eat something and bolus some insulin to get them down. It doesn’t have to be a lot - a piece of toast, etc, or some crackers. If she finds food difficult, maybe some soup or jelly or ice cream.
Pump users are at increased risk of DKA so I’m always wary of ketones.
Thanks so much. I think it must be that. I wasn’t aware pumps put you at increased risk of DKA, useful to know.
Thanks so much. I think it must be that. I wasn’t aware pumps put you at increased risk of DKA, useful to know.If she’s not eating, they could be so-called starvation ketones. IMO, it’s best to eat something and bolus some insulin to get them down. It doesn’t have to be a lot - a piece of toast, etc, or some crackers. If she finds food difficult, maybe some soup or jelly or ice cream.
Pump users are at increased risk of DKA so I’m always wary of ketones.
No that’s very helpful, thank you. I will talk to the GP. You’re right, the worry about being sick and the ketones causes anxiety as well. Thanks very much indeed for your helpYes, it’s because we don’t have any long-acting insulin on board. Things can change quite quickly if you’re on a pump so I’m always very cautious. Getting some insulin and food in should help clear the ketones. Even sipping full sugar coke can help if she’s struggling to eat. I recommend little and often rather than large amounts.
There’s a medication you can get from a GP that treats nausea. I’ve been trying to remember the name but failing. One of my children had anxiety and nausea and it helped a lot - psychologically as well as physically. It might have begun with M but I’m not sure. Apologies, but hopefully your GP will know.
My understanding is that the reason that pump users are at higher risk of DKA is if the pump goes wrong, and we don’t do anything about it. This is because we have no long acting insulin working for us. Once the pump stops there is nothing present. Providing our pump is working effectively ketones are no more likely to develop.Thanks so much. I think it must be that. I wasn’t aware pumps put you at increased risk of DKA, useful to know
Hello, we don't log on every day so may be a bit late on this. When first diagnosed (2003) T1 in hospital with DKA was disgusted with my body's loss of control. Read a lot about diabetes and cell respiration, college level, research stuff. Decided to go on a zero-carb diet to try to beat the diabetes.was hoping @Pumper_Sue or @Robert459 you could expand on your answers a bit to help me. My 18YO daughter has T1. She has recently tended to get nauseous/vomit when stressed, then doesn't eat as she can't keep anything down, then gets fluctuating raised ketones over the next few days (not super high, 1- 1.4) which then (i presume) makes her feel sick even after the stress has passed, so she doesn't eat etc etc The whole cycle seems to take about 7 days, with her drinking masses of water to try to get rid of the ketones, till she feels up to eating properly (has happened 3 times in the last year). Her BG is well controlled throughout, even with the initial stress (4-8mmol/L) with occasional hypos treated with Glucogel.
I am baffled. Is the lack of food causing the raised ketones? I have read that as long as she is getting insulin via her pump that the ketone levels won't/can't go dangerously high- is that true? Any idea why they would be fluctuating? Any thoughts on how we can bring them down?
Thanks @Robert459 that's very interesting. Absolutely take your note of caution. Very useful to hear your experience and I am coming to that conclusion as well. I just want her to feel well, so will focus on that not get preoccupied with ketones while her BG is so well controlledHello, we don't log on every day so may be a bit late on this. When first diagnosed (2003) T1 in hospital with DKA was disgusted with my body's loss of control. Read a lot about diabetes and cell respiration, college level, research stuff. Decided to go on a zero-carb diet to try to beat the diabetes.
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Managed it for over a year, zero carbs, a sandwich would be two cheese slices with a chicken slice or smoked salmon inside, meals: meat, eggs, no veg or carbs. My bg level was 4-5 all the time so it works. It was hard. Ketones were high. A classic "Atkins" induction diet. We were in 'ketosis' all the time with no ill effects other than food boredom.
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Eventually succumbed to some pizza and gave up.
Asked DM consultants what the difference was between DKA and 'Atkins', they couldn't answer.
We assume it's the low BG levels of 'Atkins' no matter what the Ketone levels were.
So, in answer to your question...
I have read that as long as she is getting insulin via her pump that the ketone levels won't/can't go dangerously high- is that true? Any idea why they would be fluctuating? Any thoughts on how we can bring them down?
Maybe, as long as her BG level is good, forget about the ketones ?
NOTE: I am not a medical professional, it is just my personal experience
...so do NOT follow my experience, but everything above is the truth.
We wish you and your daughter well x