Hi
@Midchild54 - thanks for your tag
My kidney function deteriorated very rapidly due to the NSAIDs the OS had me on for over 18 months. In the medical world CKD is a well known identified side effect in relation to NSAIDs. It is often called the 'silent disease'. There is a lot of information regards the gastric side effect of this class of drugs, but GP's and Surgeons do not discuss the side effect regarding the kidneys.
Essentially, in my case, my kidney function was being tested, but sadly the path reports were not monitored by either the surgeon or the GP and my eGFR and Creatinine levels deteriorated very rapidly with in a couple of months. I was placed in the permanent care of a Renal Specialist for the rest of my life, who now monitors my kidney function closely. Yes, I now have CKD for life. There is NO kidney function recovery for me. The main aspects of this disease is to ensure my kidney function is monitored closely, along with my BP and weight.
At my worse stage, my eGFR was sitting just 1% above the severe stage. Had it dropped to the next level, I would have been placed immediately on dialysis and the kidney transplant list. This was identified just weeks/days before my original surgery date. My original surgeon refused to continue with the surgery until it was investigated. This resulted in my surgery being cancelled 3 times in the space of 2 weeks. It was a very stressful time of my life.
I stress this is my personal story and is not necessarily the case for you.
My advice is to ensure that your medical team are testing and monitoring your kidney function and reevaluating your NSAID meds accordingly. My medical team let me down!
Continuing ongoing discussions with my Renal Specialist over the past 3 years has resulted in a total ban on me taking NSAIDs in any form, not even 1 dose and close scrutiny of the class of antibiotics I may require for future infections. By the way, this was also taken into consideration as part of my surgical procedure. My Renal Specialist was part of my surgical team and at the first hint of any renal deterioration I would have been placed on short term dialysis - although I spent 5 days in ICU and 1 day in HDU, this was unrelated to my CKD, so I didn't have to go onto dialysis.
So what is my future prognosis regards my CKD - monitor, monitor, monitor.. and I do no take any NSAIDs, prescribed or over the counter. Watch my weight and self (and GP) monitoring of my BP and of course blood tests for my CKD.
Although, this disease is potentially life threatening for me, I do not focus on it.. I stress a little until I get the results of my blood tests, but other than that as it is a silent disease I have no obvious symptoms, maybe I get more tired than I did before. I can live a normal life and be conscious that I must have my tests and keep copies of the results myself and I have educated myself sufficiently to be able to discuss it at the medical detail level with my new team of medicos..
Please don't hesitate to tag me if you have further questions - happy to share my experience.
