Taking PPIs with CKD : Hi. I have been stable... - Kidney Disease

Kidney Disease

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Taking PPIs with CKD

cmo999 profile image
31 Replies

Hi. I have been stable at CKD stage 3A for 10 years since initial diagnosis. I also have problems with a hiatus hernia/acid reflux which are helped by taking a PPI (Omeprazole). However, I have read that use of PPIs is damaging for kidneys so have been advised to stop taking them after 4 - 6 weeks and am worried about managing the symptoms without them. The doctors don't seem very clued up on this subject - does anyone have any experience of taking long term PPIs with CKD?

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cmo999 profile image
cmo999
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31 Replies
orangecity41 profile image
orangecity41NKF Ambassador

I am at CKD 3b and have been taking Omeprazole (lowest dose) for years. Being concerned about it I asked my gastroenterologist about connection to CKD. I was told best to keep taking them in my case. I too have hiatal hernia and GERD. I guess have to weigh all factors? Keep us posted on what your Doctor says.

cmo999 profile image
cmo999 in reply to orangecity41

Thank you, that's helpful. I will see how the symptoms are when I finish this round in mid-January. Can you just tell me by lowest dose, do you mean 10mg?

orangecity41 profile image
orangecity41NKF Ambassador in reply to cmo999

Yes, was 10 mg for years, many years ago, and it has been increased to 20 mg, since the 10mg was not working due to GERD. So far 20mg over the counter is working.

drmind profile image
drmind in reply to orangecity41

What low dose are you on? I had been on 10 mg of Omerprazole, but im on 20 mg now. I may try to get back on 10 mg. Have both GERD and hiatal hernia.

drmind profile image
drmind in reply to drmind

Oops. Just got my answer. I didn't read all the replies before i replied.

orangecity41 profile image
orangecity41NKF Ambassador in reply to drmind

The 20mg Omeprazole (OTC) seems to work for the GERD and Hiatal Hernia.

drmind profile image
drmind in reply to orangecity41

I have the same results....20 mg works for GERD and hiatal hernia. I have an appt.wirh my nephrologist in a week and an half and will check further with him

cmo999 profile image
cmo999 in reply to drmind

Thanks drmind. It would be very helpful to have a nephrologist’s opinion on use of Omeprazole. I was diagnosed with hiatus hernia and GERD 13 years ago and took either 20 or 40mg for a few months initially. Symptoms largely disappeared so I stopped but then found out I had CKD 3 years later. Not sure if the Omeprazole contributed to the damage or not but have not taken it again until this year when symptoms reappeared quite strongly and ongoing since February. Have started taking the PPI again (usually 20mg) but don’t want to keep taking it if it will cause further damage. Would be very interested to see if you can get any further guidance.

orangecity41 profile image
orangecity41NKF Ambassador in reply to drmind

Good idea. My PD also approves. One does not know what further damage to our bodies if we were not to take Omeprazole. Maybe there is a suitable substitute. In my case it does not appear to damage my kidneys according to eGFR.

drmind profile image
drmind in reply to orangecity41

Ill ask my nephrologist when i see him in a week and a half and report back to everyone. As i change.my diet, i may try to get back on 10 mg instead of 20mg.

cmo99 profile image
cmo99 in reply to drmind

Hi drmind. I hope you’re doing well. Just wondering if you managed to get any information from your nephrologist about taking PPIs?

drmind profile image
drmind in reply to cmo99

Had a hectic telehealth visit with my kidney doctor and never got to ask. His staff kept calling a wrong number for me while i waited on the right number. GFR continues to fall and im so worried. Back on old BP meds plus a new one and still can't get BP right. I see him in 2 weeks in a face to face appt and will ask. However, i go over my meds each visit and he never said anything negative about omeprazole.

Got my first vaccine shot this week and all went well. Hoping the same with the 2nd one. Stay safe and be well as possible

Love

FELICE2020 profile image
FELICE2020

I have this very same issue! Any suggestions out there?

MGNKF profile image
MGNKF

Hi cmo999, good advise from our fellow members. I was diagnosed with stage 3A recently. I have an appointment with a nephrologist in February, meantime I've changed my diet, no more meat, just fish/chicken veggies, etc. However, that change on diet made me lose weight 4 lbs in the last three weeks. It's great that you have been able to maintain stage 3A with no further damage to your kidneys, how is your diet and exercise routine?

drmind profile image
drmind in reply to MGNKF

Aside from info on Omeprazole, id also love to have info about your diet. Im struggling with mine once i found out that the frozen fish i was using in my new diet had too much phosphorous in it. Going out to buy fresh fish is difficult with covid19 around. Thanks

in reply to drmind

I have some information below that may help you get some general information. When you open the website look to the far left column and click on elements you'll see other items that you can check for in various foods. Just scroll down and get to the type of food you are looking for. I hope this helps. If you have trouble getting the link to open, try it a second time by copying the whole link and delete the www and then try it. That's what I had to do when I didn't go directly to the site. Sorry if this is confusing.

apjcn.nhri.org.tw/server/in...

drmind profile image
drmind in reply to

Thanks for this site. It opened without the Its helpful and i think that I downloaded this before. However, my recent problem dealt with phosphorous. I had been buying several slices of flounder frozen with my grocery pickup. then, someone on this forum mentioned that lots of frozen poultry and fish were frozen along with high doses of phosphorous. I checked my frozen flounder package and noticed that it was definitely frozen with a phosphate ingredient. So, all my recipes with frozen flounder and other frozen fish have to be changed and this is not easy. I'm still trying to find out if I can handle whatever phosphate is present in these items. Gosh, one has to be a food chemist to figure this all out. Buying fresh fish several times a week is not an option with covid around. I have a wonderful recipe with flounder fried with butter, lemon, and capers that I would hate to give up! Darn.... Waiting on a referral for a dietitian and i guess it will have to wait until my next nephrologist appointment in a week and a half.

in reply to drmind

Once the site opens and you click on Elements on the left side all of the various elements are listed on the right side and can be clicked on individually. I've used it mainly for the sodium and fat content since my gallbladder was removed.

drmind profile image
drmind in reply to

Sounds good. You've done so much good research thst you share so freely. Thank you

drmind profile image
drmind in reply to

Finally, I found the chart for Phosphorous by looking at the right. I was in too much of a rush to read your instructions carefully. I've got my charts now. Hope i can do better with checking out some of my old recipes. Thanks again.

Kacicircle9 profile image
Kacicircle9 in reply to drmind

My caregiver recently purchased "Renal-Friendly" food from momsmeals.com. The info on these says they are designed made by dietitians especially for those with kidney disease. The website also has "diabetes-friendly" meals" and offers other special needs meals. You might want check this site. The Renal-friendly meals are $7.99 but if you are a member of Davita you pay $6.99 for each meal and there are several meals to choose from. Best wishes for your health.

drmind profile image
drmind in reply to Kacicircle9

Thank you so much. Bless you and have a nice holiday

Buspasswalker profile image
Buspasswalker

Kidney.org gives advice on PPIs.

cmo999 profile image
cmo999 in reply to Buspasswalker

Thank you. You are right, there is information on PPIs on there but it only relates to damage done to previously healthy kidneys by taking PPIs. There is apparently no research on whether PPIs cause further damage to kidneys when you already have CKD which I find very surprising.

Raclette profile image
Raclette

Sorry no idea - but I take Peppermint Oil Capsules and manage my Hiatus Hernia as my reflux is very mild.

Mackembabe profile image
Mackembabe

I actually take 30mg of Lansoprazole have done for years and have CKD 3b, recently have had to up it to 60mg because of acid reflux which hasn't touched it so am now being treated for Helicobactor Pylia which I have already had 2 times already. That's the trouble we are given the tablets but don't tell you its bad for CKD so what can we do, I chew gum which helps because of all the swallowing you do keeps it down, hope you get sorted soon Love & Hugs Xx

Bond-007 profile image
Bond-007 in reply to Mackembabe

I believe H. Pylori can lead to peptic ulcers. Could it also cause GERD?

Mackembabe profile image
Mackembabe

That's very true that's why it has to be treated antibiotics 2 types before it takes a real hold and causes ulcers, so beware if it continues get to your Dr in case you have it. Love & Hugs Xx

RhenDutchess123 profile image
RhenDutchess123

Acid Reflux can also cause Esophagial Cancer....known as Barretts Disease

CatOnACloud profile image
CatOnACloud

Me too! Pantoprazole 40mg twice a day helps more than the omeprazole as my gerd is worsening as i age. It also helps my nausea but still i have symptoms, they said it was ok but not ran by nephrologist as I fired my last one. Not but one practice around me. If icould i wouldnt take ant PPIs but yeah i really need to…

medway-lady profile image
medway-lady

I have a CKD linked to Omeprazole but stress its very, very rare. I didn't even have any issues just used as a protector for another medication. It is now CKD over time. I crashed to 8GFR spent weeks in hospital and am now 26GFR. Just one of those things and entirely unpredictable its been life changing though. I'm not going to say you should worry over it just follow the advice of your medical team as it is so rare I'd still have taken it. Make sure you get regular blood tests which I did and that probably saved my life. But again sometimes these things are just so rare that it has to happen to someone and statistically it probably won't be you. I hope that helps.

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