ZDogg does it again! The man is unstoppable!
Consult team with their new Renal Merit Badges
Custom dialysate solutions
I get nervous when I need to dialyze someone who is severely hyponatremic. Dialysis has the power to change the sodium concentration very fast. Patients with chronic, compensated hyponatremia need their sodium corrected slowly. Experts recommend increasing the sodium by less than 12 mEq/L/day and to actually undertarget only 6 mEq/L/day to give you some margin for error.
Over the week-end we were consulted on a patient with a sodium of 106 and acute renal failure. By the time we were forced to dialyze the patient the sodium was up to 112. To do this safely we selected CVVHD and then diluted our dialysate down to 120 mEq/L.
Here is a Keynote (100 mb), PDF (155 kb) and a narrated version of that presentation (118 mb) where I walk through the algebra on how to mix a dialysate of any final sodium concentration.
The movie available for download is very high quality. Below is a YouTube conversion of that video to save you the 118 mb download.
This is some serious Sodium Jujitsu and I awarded my team the first Nephrology Merit Badge: Sodium Ninja (pages | pdf). Designed for Avery 5163 2×4 labels.
Nephrology Merit Badge, updated for the 21st century as a sticker for your iPad |
PBFluids breaks into the medical literature.
The first time PBFluids was referenced in the medical literature was in Matt Sparks’ article on nephrology internet resources.
Extremely high levels of serum creatinine have been reported in the literature.3 The highest level of serum creatinine reported was 37 mg/dL.3
So what is the highest previous creatinine reported in the literature? Well according to the author, Said Abuhasna, it’s 37 from this post at PBFluids. Nice to see blogs being included in the canon of medical literature. Though it would be even nicer if they spelled my name right.
The death of MobileMe and a whole mess of broken links at PBFluids–Updated
One of the best stories about Steve Jobs was his tirade is response to the MobileMe disaster.
He gathered the MobileMe team together and asked,
“Can anyone tell me what MobileMe is supposed to do?”
Having received a satisfactory answer, he continues,
“So why the f*** doesn’t it do that?”
He then picked another executive to run the project on-the-spot. Ultimately, this resulted in the service being shuttered and replaced with iCloud.
I never had any problems with MobileMe; it always worked fine for me. However, I foolishly relied on it to host files for PBFluids. This includes all of the presentations and handouts that are the highest trafficked pages of the site. Well, MobileMe stopped accepting new subscriptions a year ago and as of June 30th the hosted files are no longer accessible. I have downloaded all of the material and will start re-uploading the files to DropBox. The problem is rewiring all of the past links to the new file locations. This will take some time.
As I looked through the collection of files that used to be hosted at MobileMe I found a lot of journal articles and other copyrighted works. I have no idea how popular these links were but I remember when I uploaded them, PBFluids was a lonely backwater, where I was the sole source of traffic. I put the files the files online for my own use in teaching and on rounds. I don’t plan on replacing these files.
July 3, first lecture of the year
For the past few years I have had the honor of giving the July 1st morning lecture for the internal medicine residents at St John Hospital and Medical Center. Unfortunately, July 1st was a Sunday and Monday mornings are dedicated to a formal sign out rounds in our division. So July 3rd was my first lecture.
I gave my Fluids, Diuretics and Sodium for the Terrified Intern lecture. You can down load it here:
Twitter, kidney transplants and misinformation–Updated
Last week Indiana University (@IU_Health) live-tweeted a kidney transplant. They claimed it was the first unrelated-living-donor transplant Live tweeted.
It was dramatic and there was a lot of buzz among the kidney folk on Twitter about this. You can read some of the coverage here. It was exciting but it tasted too much like a publicity stunt for my taste. The counter argument, of course, is that raising the profile of living unrelated donors increases the likelihood that people will come forth and donate and I should just swallow my distaste and be supportive of the outreach effort.
As part of the Twitter publicity campaign, IU_health tweeted various facts about transplant. This one seemed wrong to me:
This is a very cool website
Endobible arranges a database of endocrine diseases in widely searchable manner. They lead physicians through the diagnosis, work-up and treatment of most endocrine diseases. They skip diabetes, but outside of that is looks awesome. Nice reminder that endocrine is more than diabetes.
I perused the Conn’s Syndrome section (primary hyperaldosteronism). The history and physical were great. The work-up was less impressive. They don’t advise saline loading and they still recommend stopping ACEi and beta-blockers before performing a Aldo Renin Ratio. Good luck keeping a resistant hypertension patient from stroking while you wash all those drugs out for 4 weeks.
Overall a clever design and great resource.
Lupus nephritis, MMF and maintenance therapy
I love it when I have a clinical question and I’m able to find a well executed study that’s exactly fits my question. It’s like fitting the last piece of a puzzle.
A year ago I was referred a patient with heavy proteinuria. Initial assessment showed 7 grams of proteinuria, a cholesterol over 300, edema and an albumin of 0.7. Classic nephrotic syndrome.
Before he returned for his first follow-up appointment disaster struck. He developed chest pain and shortness of breath from a pulmonary embolism. This was a patient my age, two kids, professional. Looking at him was like looking in the mirror, but for the grace of G-d that could be me sitting in that exam chair.
black arrow points to tubuloreticular inclusions seen in SLE and HIV. |
After a month of anti-coagulation I was able to convince pulmonology and hematology to reverse the Coumadin for a few hours to get a kidney biopsy. It was membranous nephropathy with endothelial tubuloreticular inclusions. Along with consistent ANA and DS DNA we made a diagnosis of SLE WHO V and began mycophenolate mofetil. We titrated the MMF up to 3g a day and after 6 months he was in remission.
After a few months of sub nephrotic proteinuria, a normal albumin and a year of anti-coagulation he stopped his Coumadin. He has weaned his prednisone to 10 mg every other day and stopped the alendronate and rosuvastatin. Now he wants to get off the mycophenolate. Given how frightening the PE was, my preference would be to treat him forever. I casually surveyed my peers and got answers as varied as:
- I never lower the MMF, every time I do the patient relapses
- I taper it off after 6 months of remission
When I consulted the literature to look into this I found this paper:
Bet he has Gitelman’s syndrome
This post on BuzzFeed makes me so glad I never suffered the indignity of on-line dating. My favorite is this guy:
What are the odds he has Bartter’s or Gitelman’s. Every patient I have encountered with Bartter’s or Gitelman’s has admitted to drinking pickle juice, so it’s sensitive but I don’t know how common this is among norms so its specificity has yet to be determined.