1/17
[Why] is furosemide susceptible to malabsorption from "gut edema"?

When a patient with heart failure is hospitalized with congestion I often hear "let's use IV furosemide; they're probably not absorbing the PO."

It's a comment unique to furosemide.

But is it accurate?
2/
In order to understand what happens in heart failure, we must first understand what happens under normal conditions.

🔑Furosemide absorption is in the small intestine and stomach
🔑Some data suggest greater absorption in the duodenum than stomach

t.ly/JjdK
3/
Regarding oral bioavailability:

🔑 It is highly variable (ranging from 11-100%) even in those without heart failure
🔑 This variability is both between patients and within the same patient

t.ly/a0CU
4/
Let's turn to heart failure (HF).

In 1985, Vasko et al. gave 11 patients with HF oral furosemide during decompensation and again when they were compensated.

When compensated,
➤ Absorption was faster
➤ Peak plasma concentrations were higher

BUT...

t.ly/6GWl
5/
...this study also found no significant difference in the area under the curve for plasma concentration when decompensated.

🔑Conclusion: there is no difference in the total amount of drug that reaches the blood for a given oral dose of furosemide, even when decompensated.
6/
A later study confirmed that there is little difference in total absorption of furosemide between compensated and decompensated states.

In fact, this study found no difference in speed of absorption (Tmax) or peak plasma either.

t.ly/J9Pt
7/
Assuming that decompensation leads to delayed absorption of furosemide and NOT decreased total absorption, what explains this?

I found little data for this being due to "gut edema".

Instead, many propose delayed gastric emptying as the culprit

t.ly/49ko
8/
Supporting this are experiments in mice demonstrating that:

➤ Injection of BNP &
➤ Left ventricular dysfunction induced by myocardial infarction

Both lead to delayed gastric emptying and decreased furosemide absorption.

t.ly/FtZG
t.ly/lSTM
9/
Patients with decompensation also have ↑ sympathetic and ↓ parasympathetic tone. This may lead to delayed gastric emptying.

If the small bowel is the preferred site of furosemide absorption, delayed delivery could be the cause of delayed absorption.

t.ly/Qcrx
10/
This explanation is supported by data in Roux-en-Y gastric bypass recipients. These patients have RAPID gastric emptying. This results in:

➤ Faster time to maximum plasma furosemide concentration
➤ Earlier natriuresis

t.ly/xCqW
11/
Other explanations have been offered for the observed differences. These include:

➤ Decreased renal blood flow and delivery to the nephron
➤ Altered blood flow
➤ Concomitant medications

And, of course, "gut edema".

t.ly/vGQb
12/
Given that there is little diuretic or natriuretic effect below a given plasma concentration (the “threshold”), it could be that reduced peak absorption results in less reliable natriuresis.

BUT...

t.ly/xnKq
13/
... furosemide pharmacodynamics seem unaffected by decompensation.

In fact, the study in tweet 4 found INCREASED urinary sodium excretion during decompensation.

t.ly/6GWl
14/
Before closing, let me offer a natural experiment supporting the idea that oral furosemide can be absorbed during decompensation.

In 2012 Ontario faced a shortage of IV furosemide. More oral furosemide was used, even in decompensated heart failure.

t.ly/kM8B
15/
Despite the shift from IV to PO furosemide, hospitals saw NO DIFFERENCE in:

➤ 30-day mortality
➤ ICU admission
➤ Length of stay <6 days
➤ 30-day readmission

The oral furosemide seemed to work just fine, even in decompensated heart failure.

t.ly/kM8B
16/
Clearly, many patients can achieve natriuresis with oral furosemide, even when decompensated.

But others have absorption issues, whether from delayed gastric emptying, "gut edema", or something else.

Here, as with much in medicine, the exceptions drive our practice.
17/17 CONCLUSIONS
⚡️Though furosemide absorption may be delayed during decompensated heart failure
⚡️Total absorption appears less affected
⚡️Delayed absorption may be related to delayed gastric emptying
I want to extend a HUGE thank you to...

🎗️Brooke Barlow (@theABofPharmaC)
🎗️Alex Pipilas (@apipilasMD)

...for their peer review of this tweetorial.

If you want to get smarter, give them a follow.

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More from @tony_breu

27 Nov 21
1/13
Why does adrenal insufficiency (particularly adrenal crisis) lead to hypotension?

I don't think of glucocorticoids as "pressors" and yet when they're lacking patients are at great risk for shock.

Let's have a look.
2/
Hypotension has long been associated with adrenal insufficiency.

For example, one report of 108 cases of Addison's Disease (i.e., primary adrenal insufficiency) found that:

⚡️88% of patients presented with hypotension

PDF: t.ly/aDzv
3/
In primary adrenal insufficiency (PAI), hypotension is partly due to volume depletion related to mineralocorticoid deficiency.

But even in PAI the hemodynamic profile isn't simply ↓cardiac output from ↓venous return (i.e., volume depletion).

PDF: t.ly/Ooej
Read 13 tweets
31 Oct 21
1/15
Why are statins administered at night?

In this tweetorial I'll discuss the mechanistic and historical reasons for the frequently used QHS dosing schedule. And why it's often unnecessary.

But before we get there, I'm curious: when do you prescribe/order/take statins?
2/
Early studies suggested that evening administration of statins led to a greater reduction in cholesterol when compared with morning dosing.

Two notes on the linked study:
➤It is small
➤The differences in LDL reduction weren't as clear

PDF: t.ly/6wfc Image
3/
As a result of this early data, the package insert for lovastatin, the first FDA-approved statin, suggested evening dosing.

And the landmark 4S trial did the same, administered simvastatin in the evening.

Insert: t.ly/GsOy
4S: t.ly/9mqS ImageImage
Read 15 tweets
14 Aug 21
As I noted in a recent tweetorial, Raymond Pearl reported a lower frequency of cancer in those with evidence of tuberculosis.

This finding led Pearl and others to treat patients with tuberculin.

Unfortunately, Pearl's original study methods suffered from bias.
More specifically, Pearl's study sample contained an overrepresentation of exposed controls (i.e., control subjects who had died from tuberculosis).

This led to an incorrect conclusion that tuberculosis is associated with decreased rates of cancer.
Pearl published a "retraction" in Science.

While arguing that "any serious student of the matter" would agree that TB and cancer are rarely found together in the same person, he admits that concluding a mechanistic connection "may have been erroneous".

pubmed.ncbi.nlm.nih.gov/17777405/
Read 5 tweets
14 Aug 21
1/16
Why do we use a vaccine (BCG) to treat an unrelated malignancy (bladder cancer)?

Can infections really prevent/treat cancer?

Let's find out.
2/
This story begins in 1813 when Arsène-Hippolyte Vautier reported that patients suffering from gas gangrene experienced a decrease in the size of their malignant tumors.

An explanation (or even the causative bacterium!) wasn't immediately apparent.

pubmed.ncbi.nlm.nih.gov/28202530/
Read 19 tweets
26 Jul 21
1/15
Why does clostridium difficile infection (CDI) cause marked leukocytosis?

Many of you have likely seen a new WBC >20k and wondered "could this patient have CDI?"

Are you right to wonder? If so, why?
2/
To start, is there a connection?

One of the earliest studies examined patients with WBC >30k. They reported the following rates of CDI:

🔹20% of all cases (excluding those with heme malignancy)
🔹34% of patients with an infectious etiology

pubmed.ncbi.nlm.nih.gov/12032893/
3/
In another study included 60 patients with unexplained leukocytosis (WBC >15k) and found:

⚡️58% had CDI⚡️

And: leukocytosis preceded recorded symptoms of colitis in half of the patients.

pubmed.ncbi.nlm.nih.gov/14599633/
Read 15 tweets
11 May 21
Great list Avi!

I'll add some relevant links for a few of these.
💻K/Mg repletion often unnecessary

Here is a tweetorial on potassium repletion/replacement.

💻Wilson disease evaluation in acute liver failure often not needed

@ebtapper and @ShaniHerzig wrote a great article in the @JHospMedicine Things We Do For No Reason Series on nondirected testing for inpatients with severe liver injury.

journalofhospitalmedicine.com/jhospmed/artic…
Read 6 tweets

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