The conventional diuretic treatment of ascites in patients with cirrhosis is high doses of spironolactone w/furosemide (classic 100/40 ratio). This was also mentioned recently on @thecurbsiders. Where does this come from and is it true? A quick🧵. #MedTwitter#nephtwitter
In 1981 Fogel et al compared 3 diuretic strategies in 90 patients w/cirrhosis
🔥Furosemide alone appeared to perform worst for weight loss though not statistically sig. Required sig up-titration and massive KCl
In 1983 Perez-Ayuso et al: lasix v spiro. in 40 pts w/cirrhosis and nml kidney function
If🚫response (UNa excretion <50mmol/d) alt. tx given
🔥Lasix grp: 50% response
🔥90% of non-responders responded to spiro.
🔥spiro. grp: 95% responded: 1 non-responder🚫response to lasix
Conclusions from the above:
🔥Furosemide alone is a poor choice - perhaps ineffective and comes with more electrolyte disturbances like hypokalemia which can precipitate encephalopathy
🔥spiro alone seems effective but takes longer to work
🔥combo therapy works faster
In modern times a 2003 study from Santos et al randomized 100 pts w/cirrhosis to spiro + lasix or spiro alone.
🔥No difference in mobilization of ascites
🔥No diff. in response time
🔥No diff in AEs
🔥⬆️need to reduce diuretic dose in combo group to avoid excessive diuresis
In 2010 Angeli et al randomized 100 pts to combo spiro + lasix or spiro alone with addition of lasix in case of non-response. Both in escalating doses.
🔥Overall response rate was the same b/w groups
🔥Combo therapy worked faster
🔥Increased AEs w/sequential therapy (mainly⬆️K)
So: mostly older studies suggesting poor response to lasix and superiority of spiro. Even if true then why? Conclusions will cite activation of the RAAS but that's not true in HF (or most causes of volume overload) where the RAAS is also revved⬆️and loops are preferred diuretic
Another theory is impaired tubular secretion
💡Loop diuretics have to be secreted into the tubule via OATs to reach their site of action, whereas spironolactone doesn't
Although this study suggests a significant increase in tubular secretion (at least of creatinine) in patients with compensated cirrhosis as shown by a significant decrease in creatinine based GFR with cimetidine administration, which inhibits tubular secretion. (PMID: 11749665)
Conclusion
🔥idea that spiro is a better diuretic in cirrhosis seems to be perpetuated from small studies
🔥questionable pharmacologic basis
🔥maybe true for outpatients but inpatients I still prefer loops
I also don't treat a lot of these anymore so curious what experts think
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Right off the bat let's acknowledge that the following trials show no mortality benefit in critically ill patients with vasopressin. But that's not the point - we only care about the kidneys right now because I'm a Nephrologist.
Before we get to hearts we need to borrow from the sepsis literature.
First a small study from 2002
💥24 pts w/septic shock
💥vasopressin v norepinephrine x4 hrs, titrated to BP
💥Vasopressin group = better UOP and CrCl
First, it's important to recognize how crucial adequate decongestion is.
👇study: pubmed.ncbi.nlm.nih.gov/29544928/ which assessed pts in the PROTECT trial showed lack of decongestion was a predictor of mortality and HF re-hospitalization
Great case of hypokalemia presented by chief fellow @Laurenaring yesterday.
60 y/o woman with a h/o nasopharyngeal cancer, nephrology consulted for hypokalemia.
Sk 2.5, bicarb 30, normal kidney function. No diuretic use, denies vomiting or diarrhea. #nephtwitter#medtwitter
She was on pembrolizumab, which is a/w tubulointerstitial disease and subsequent hypokalemia d/t an RTA, however this was just started 5 days ago and her urine was bland.
Next step? As Nephrologists we want to know urine composition. In this case I would want a Uk, UCr and UCl
Spot values are sufficient and hers were Uk 43, UCr 18 and UCl 50
If you live in the US then you have to deal with unit conversions: discussed here pbfluids.com/tag/potassium/
Her Uk/Ucr ratio was 27 (>2.5 is c/w renal K wasting)
Why are thiazides effective in augmenting natriuresis when added to loops?
We all know that exposure to loops➡️increase in NCC channels in the distal tubule
BUT there's more
Did you know that there's a mechanism for thiazide sensitive NaCl reabsorption in the collecting duct?
Electroneutral NaCl absorption can also occur in the collecting duct through the parallel action of pendrin and NDCBE (Na-dependent Cl/HCO3 exchanger) which is upregulated by Ang II and mineralocorticoids (when Ang II present)
2 cycles of pendrin = 2HCO3- to the lumen for 2Cl-. 1 Cl- is recycled to NDCBE resulting in net reabsorption of 1 NaCl and 2 HCO3- (Cl- through CLCK2 and Na and HCO3- through AE4 in the basolateral membrane)
The whole mechanism appears to be thiazide sensitive
This study showed a ⬇️need for antihypertensives if dietary K+ was ⬆️
💥RCT 47 pts w/ htn
💥⬆️ K+ vs usual K+ diet
💥45% ⬆️ in dietary K+ in ⬆️ K+ group
🔥Hypertensive therapy ⬇️by at least 50% in 81% of intervention group v 29% in control group at 1 yr