Frequency in the change of insulin catheter.

Via's profile photo   05/05/2011 7:26 p.m.

Hello everyone.
I carry insulin bomb and when they put it to me, they told me that I could adjust the changes of 2 times a week, that is, a period would be 3 days and the next 4.
On my last visit with the endo, he recommended, I made the change of catheter at 3 days, without exceeding me, because it could be a cause of my bad glycemic controls.

My question: What is the frequency in the change of your cateters, between the insulin bomb?Have you noticed worse results if you spend the recommended 3 days?

Thank you.
Greetings.

Via's profile photo
Via
05/05/2011 7:26 p.m.
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Via, everything depends on how you see the controls ... have you noticed that on the third day you have higher values?Where do you put the catheter? ... I tell you, my daughter lasts quietly and without any sequel to the skin 4 or 5 days.My husband if he has the cannula in the buttock up to 4 days without problems, but if he puts it on the gut at 2.5 days he is already working badly ... I know children who have to change it at 2 days ...That everyone has to do with their rhythm.They advise the change every 3 days, but as everything, this is variable depending on the user.
Another thing, are you very thin? What canula do you use 6 or 9 mm?
Greetings.
We are going to move this thread to the pump section, so that it is better located.

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Velia
05/06/2011 4:08 a.m.

De los buenos tiempos, siempre quiero más...
Mamá de Ángela, ¡16 añitos, fiera!. Debut: octubre de 2003.
Bomba insulina Medtronic Paradigm Veo desde junio 2005
Última hemo 6.1

  

I usually last 4 days, especially in the buttock, but if I see that the third day the controls go up I change it.It is true that when I changed my bomb in October, Medtronic's girl stressed a lot that we did not pass from 3 days, which was not convenient to abuse.

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DiabetesForo
05/06/2011 5:09 a.m.
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Thanks Prado and Velia for your answers.

It has cost me a bit to locate the message again, because I was looking for it in the diabetes forum, and there are many issues about bombs, until I have gone to the general and rescued it.

Well, I answer in parts:
* Yes, I am thin and I use the 9mm cannulas.When at first they put it to me, I proposed because of 6mm.They looked at me with a certain "sneer", and they told me that those were for the children.¿,,?I have not proposed it again, but the truth is that I feel pain in insertion, which then disappears.But when I spend it badly it is with the insertion of the sensor.There are times that I stay paralyzed for a few moments for pain.It may be that I get some tendon or muscle, but the first 12 hours, I feel, most of the time very sore.
* Since January, I am putting - both the catheter and the sensor - on the thighs.The endo suggested, to see if I had better results, and less discomfort than in the gut, because I have little adipose tissue, they bothered me a lot.
Now, the sensor change, I leave it normally to go to sleep, because so, those first hours, I am at rest, and it seems that I lift me barely.
* Yesterday, the catheter, I put it in the buttock, at the top near the thigh.It cost me a little more work to turn, the pain TB was strong, but then, it has let it upset.
* The best thing is that today has been, I think, the day with better results, since I am with a bomb and of course since years, because I have been almost all day with unusual values ​​for me _ the highest 220, afterof breakfast, when usual is around 300 or exceeding them_
Then, at the time after finishing the food, I have had a 66 hicc.
* For my tremendous instability and decompensation, I cannot appreciate whether or not the glycemia are worse from the 3rd day of the catheter, because they are always bad.
* I think that Friday's stability, it may be due to modifications in the basal and ratios that we made in the last consultation and today, the sensor and capillary values ​​were very close, very close (nothing of 120, 140 and up to 200 of a difference betweenthey)

Tomorrow I have to change sensor, and I wanted to tell you, Velia, some recommendations that you gave me in your answer.But I will do it in the other section, because this will be endless.
Thanks Prado and Velia for being there.
Ciao

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Via
05/06/2011 8:20 p.m.
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What mania that the 6mm catheters are for children: Evil: ... Well, I've been using them for 6 years and I have stopped being a girl :)) :)), instead of saying those bullshit why I don't knowThey set a little more in the physical constitution of each patient?

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DiabetesForo
05/07/2011 6:39 a.m.
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I endure the catheter 3-4 days, and well, I do not notice any variability .... What I have not tried is to put on the catheter in the culete ... I do not know, it gives me fear ... I imaginethat there when sitting (I work sitting) you have to throw a lot. Or I know, I start imagining, that the pompis when sitting, a pelin is tense, and maybe with it the catheter folds ... :))that jaleos do ... for now I have only dared in the gut ...:-/

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kekiya
05/08/2011 5:52 p.m.
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Hello, my 8 -year -old daughter has the bomb and I do believe that if the glycemia values ​​can be exceeded, especially in summer, because with high temperatures the insulin may lose qualities.

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carpa
05/10/2011 8:24 a.m.
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