I’m diabetic and I have stage 4 CKD. I am unfamiliar with the med Dapaglifozin. You say it is a med for diabetes? Your doc has you on “Losatan”? Do you mean Losartan? That is a med for treating blood pressure. I’m not understanding how swapping Dapaglifozin for Losartan makes sense?
Diabetes and high blood pressure are common leading causes of CKD. I see an endocrinologist for diabetes care and a nephrologist for kidney care. They are part of the same healthcare system. They have access to my records and can collaborate on my healthcare plan.
My nephrologist also prescribes blood pressure meds for me. One of which is Losartan. My blood pressure is well controlled and they have me monitoring it at home. You can get a cuff and recording system to use to share your records with your provider.
Is your nephrologist your main provider? Are you Afro-American? I read in a Mayo Clinic Press book that there is a gene that folks of African descent can have that predisposes them to kidney problems. The book is called “The Body’s Keepers” by Paul L. Kimmel MD I think. I don’t recommend reading the book because it was a terrible slog getting through it. But I never heard of that gene before and it’s potentially rotten effect on people of African descent. I think the gene was called APOL-1 or something like that. Various clinical trials and research have stemmed from it. Anyway it might be something you could ask your nephrologist about?
Hi,
"Do you mean Losartan? That is a med for treating blood pressure. I’m not understanding how swapping Dapaglifozin for Losartan makes sense?"
Yes Losartan is what I am currently on. I was initially put on Simvostatin when they first diagnosed CKD. However, when the High Cholestrol was diagnosed and the Cholestrol specialist advised I be put on Rosuvastatin, I was taken off Simvostatin and put on Losartin. (to ensure my blood pressure did not drop any further). I now remain on Atorvastatin & Ezetimibe for High Cholesterol and Losatin for my kidney function.
To be honest I can't keep up with the med changes and what they are meant to do. I wrote on here seeking advice and wondering if I had been too trusting of my medical team over the years.
I am Black British - and have been tested for the "the gene was called APOL-1 " I don't have it. My condition is a mystery to everyone. They don't know why my kidney function keeps dropping, and all the meds are just trial and error it seems.
I recall in my 20s during a holiday in India I had a urine test done. I was told then I had a lot of protein in my urine. At the time it didn't mean a lot to me. (that's only recently coming back to mind. that was 30+ years ago)