I've been a DE for about 1.5 years, work in a rural area, don't have endocrinologists anywhere near us, and therefore my experience with patients and insulin pumps is very, very slim. I have recently gotten a referral that is wanting to get information on and start an insulin pump. I have the literature, I have not met with this patient yet, but I will next week, they are type 2, been on meal time and basal insulin for years, their diabetes is UNCONTROLLED for years (A1C is double digits), and they stated to me they have never had any diabetes education.
My plan is to first educate them on how to get their diabetes under control or at least better control and then see why they want an insulin pump and why they think an insulin pump will help them gain control? Now I'm certainly not against pumps and I think they are a great idea, but if someone has been really out of control for years with large doses of insulin, do they think that they can simply add a pump and everything will be perfect, that would be my concern.
I suppose my question here is, when giving or getting information to help someone get started on a pump, what do you do as educator? Any certain process? Any specific information? I have information from the pump company the patient suggested and I have the request form from the company for the patient to fill out, send into the company so they can work with the patient, provider, and insurance. What else would be good to do?
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I've been a DE for about 1.5 years, work in a rural area, don't have endocrinologists anywhere near us, and therefore my experience with patients and insulin pumps is very, very slim. I have recently gotten a referral that is wanting to get information on and start an insulin pump. I have the literature, I have not met with this patient yet, but I will next week, they are type 2, been on meal time and basal insulin for years, their diabetes is UNCONTROLLED for years (A1C is double digits), and they stated to me they have never had any diabetes education.
My plan is to first educate them on how to get their diabetes under control or at least better control and then see why they want an insulin pump and why they think an insulin pump will help them gain control? Now I'm certainly not against pumps and I think they are a great idea, but if someone has been really out of control for years with large doses of insulin, do they think that they can simply add a pump and everything will be perfect, that would be my concern.
I suppose my question here is, when giving or getting information to help someone get started on a pump, what do you do as educator? Any certain process? Any specific information? I have information from the pump company the patient suggested and I have the request form from the company for the patient to fill out, send into the company so they can work with the patient, provider, and insurance. What else would be good to do?