Again, I think you misunderstand the Libre. The Libre captures data in the same way as a "blind CGM" from Medtronic does. When you sleep, it still captures data and gives you the information about what happens overnight. It doesn't alarm, no, but it does provide you with continuous data.if you consider "libre" works in past way (past information), it only works 16 hours per day (when you sleep, it doesn´t work...), it lasts 14 days, but I think 90% dexcom users get 2 to 4 weeks (personally I always get 2 weeks, some 3, but I always replace it in 2 weeks)
As pointed out above, the cost of the two systems is very different. As soon as you introduce a transmitter into the sensor you need far more power - that's a huge benefit of NFC. NFC doesn't have the range for a permanent feed so you would need an alternative.I hope next "libre" will be released with alarms and automated read (it´s very easy... a wireless NFC device programmed to read every minute and transmit to receiver).
I'm not sure that blood is preserved, as that would require some form of pooling mechanism. I think what is more likely is that glucose is removed from the blood by the muscles/organs that need it such that when it reaches the peripheries, it is at a lower level.That is really interesting Pete R. I have a pet theory that glucose rich blood is preserved where it is needed and not in the peripheral tissue where we read BG from. No evidence other than anecdotal - eg a few days ago I read 1.8 mmol/L but I certainly was not in a coma or even feeling particularly bad, just a mild hypo sensation. Happens a lot that I get "impossible" fingerstick BG even when I am not low carbing.
Good theory - so the brain, organs and muscles are just "first in the queue" ahead of the peripheral tissue.I'm not sure that blood is preserved, as that would require some form of pooling mechanism. I think what is more likely is that glucose is removed from the blood by the muscles/organs that need it such that when it reaches the peripheries, it is at a lower level.
It's kind of in line with the difference between exogenous and native insulin - exogenous insulin acts initially on muscle tissue, which becomes the primary filter of Glucose from the blood, unlike a healthy individual for whom the liver undertakes 70% of this job following release of insulin into the hepatic portal vein.Good theory - so the brain, organs and muscles are just "first in the queue" ahead of the peripheral tissue.
That is really interesting Pete R. I have a pet theory that glucose rich blood is preserved where it is needed and not in the peripheral tissue where we read BG from. No evidence other than anecdotal - eg a few days ago I read 1.8 mmol/L but I certainly was not in a coma or even feeling particularly bad, just a mild hypo sensation. Happens a lot that I get "impossible" fingerstick BG even when I am not low carbing.
Hi Spiker and Diamattic,
this is great advice for me thank you both. I'll try the recommendations and see how things go. I've ordered some of the Opsite flexifix I saw recommended to help secure the sensor.
Diamattic, I find that the interstitial fluid measurements of the cgm systems always lag behind blood test when riding. I think unless blood glucose goes above optimal it goes straight from the stomach into the bloodstream and prioritised to the working muscles to an extent. For example, I was training 5 hours at a fair pace on Saturday and the cgm was alarming for the first 2 hours despite having optimal blood glucose levels. The team-mates I was with thought I had a reversing alarm on the bike when the dexcom was bleeping away! I don't know if this happens with other sports or what your experiences are.
thanks again,
Pete
Maybe, but that's a separate issue. I am talking about fingerstick tests below 2.0.I am not sure if i can agree with this or not. But i have had alarms telling me my BS are in the 1's and low 2's so i would rush to check my finger and find they are actually in the 5s and 6s.. I think the Dexcom is just plain wrong sometimes.
Forgive me as I don't know xDrip but I believe it's reading the same signal from the same sensor? So isn't this just a case of the Dexcom receiver and the xDrip receiver both being as wrong as each other? Or am I missing something.I'm also running a little experiment on the dex receiver, I haven't calibrated it for over 3 days now. Trend lines are in sync with xDrip and is currently only 0.2 mmol different, I can't pick any difference from when it was calibrated.
My understanding is that the transmitter sends raw data from the chemical reaction in the sensor (which I thought would vary as the sensor gets older).Forgive me as I don't know xDrip but I believe it's reading the same signal from the same sensor? So isn't this just a case of the Dexcom receiver and the xDrip receiver both being as wrong as each other? Or am I missing something.
My understanding is that the transmitter sends raw data from the chemical reaction in the sensor (which I thought would vary as the sensor gets older).
The receiver interprets the raw data into a BGL with the help of its calibration readings.
So yes, the xDrip and Dex get the same signal from the transmitter but they use their own formulas and calibration data to give you a BGL.
We use cookies and similar technologies for the following purposes:
Do you accept cookies and these technologies?
We use cookies and similar technologies for the following purposes:
Do you accept cookies and these technologies?