SaltyAndSweet
New member
Here's what the letter says:
"This appeal was reviewed by an independent external consultant, Board Certified in Internal Medicine with a Sub Speciality Certificate in Endocrinology Diabetes & Metabolism....
... Although the patient has met the criteria of being on on intensified insulin therapy program, and has a hemoglobin A1C of greater than 7%, there is no documentation to support low endogenous levels in the member. Her C-peptide level is within nomal limits, which is not <i>un</i>expected, since cystic fibrosis is associated with impared glucose tolerance rather than primarily decreased insulin production."
Now, I am quite confused. I thought that CFRD was caused because of decreased insulin production because the pancreas is damaged and not able to produce enough insulin to keep blood glucose at safe levels?
"The continuous glucose monitor was denied again because it "is still considered experimental and investigational, with the theraputic benefit yet to be proven in large-scale long-term studies. ... continuous glucose monitoring system is considered experimental / investigational/ unproven and is not in accordance with generally accepted standards of medical practice athe the present time, it would not be considered medically necessary."
Any one have any comments or suggestions about how to refute this claim??
"This appeal was reviewed by an independent external consultant, Board Certified in Internal Medicine with a Sub Speciality Certificate in Endocrinology Diabetes & Metabolism....
... Although the patient has met the criteria of being on on intensified insulin therapy program, and has a hemoglobin A1C of greater than 7%, there is no documentation to support low endogenous levels in the member. Her C-peptide level is within nomal limits, which is not <i>un</i>expected, since cystic fibrosis is associated with impared glucose tolerance rather than primarily decreased insulin production."
Now, I am quite confused. I thought that CFRD was caused because of decreased insulin production because the pancreas is damaged and not able to produce enough insulin to keep blood glucose at safe levels?
"The continuous glucose monitor was denied again because it "is still considered experimental and investigational, with the theraputic benefit yet to be proven in large-scale long-term studies. ... continuous glucose monitoring system is considered experimental / investigational/ unproven and is not in accordance with generally accepted standards of medical practice athe the present time, it would not be considered medically necessary."
Any one have any comments or suggestions about how to refute this claim??