1/THREAD
Ever wonder why fluoroquinolones increase the risk of tendon rupture?

It seems so random that a whole class of antibiotics could cause tendon injuries, but the risk is real.

#medtwitter #tweetorial
2/
Fluoroquinolones inhibit bacterial function by blocking topoisomerase activity.

They first emerged as an antibiotic class in the 1960s, as byproducts of antimalarial quinine development.

Nalidixic acid = the first quinolone discovered.

pubmed.ncbi.nlm.nih.gov/14056431/
3/
The first report of fluoroquinolone-associated tendinopathy occurred in 1983.

2 renal transplant patients received norfloxacin and subsequently developed achilles tenosynovisitis.

Their symptoms spontaneously resolved w/ cessation of the norfloxacin.

pubmed.ncbi.nlm.nih.gov/6223241/
4/
Subsequent studies confirmed this association, with an overall odds ratio (OR) of 4.3 for achilles tendinopathy (tendonitis or rupture) resulting from fluoroquinolone use.

Patients on corticosteroids (OR 9.1) or dialysis (OR 20) are at highest risk.

pubmed.ncbi.nlm.nih.gov/23026288/
5/
In 2008, on the strength of this evidence, the FDA issued a black box warning for fluoroquinolone-associated tendinopathy.

pubmed.ncbi.nlm.nih.gov/18632714/
6/
Before we explore mechanisms, let's review tendon structure.

Tendons are composed of collagen fibers surrounded by extracellular matrix (ECM). Tendon-specific fibroblasts called tenocytes produce the collagen and ECM, supporting a tendon' strength.

physio-pedia.com/Tendon_Anatomy
7/
So what are the mechanisms by which fluoroquinolones can injure tendons, or even make them spontaneously rupture?

Theorized answers fall under 3 main categories:

🔑Tenocyte toxicity
🔑Inflammatory responses
🔑⬇️ production and ⬆️ destruction of collagen
8/
Let's start w/ impacts on tenocytes.

A 1996 study found that incubation of human tenocytes w/ ciprofloxacin led to increased cell death.

Addition of a steroid increased fluoroquinolone cytotoxicity.

pubmed.ncbi.nlm.nih.gov/20650258/
9/
Animal models have found edema and increased mononuclear infiltration into the tendons of rats treated with high doses of various fluoroquinolones.

This isn't surprising if tenocyte cytotoxicity is occurring.

pubmed.ncbi.nlm.nih.gov/9371338/
10/
Under normal circumstances, as we've seen, tenocytes secrete collagen into the ECM, contributing to tendon structure/stability.

Fluoroquinolones impair tenocyte function and survival, which leads to decreased collagen production.

pubmed.ncbi.nlm.nih.gov/10843129/
11/
Next let's examine collagen degradation.

It turns out that fluoroquinolones can upregulate matrix metalloproteinase-2 (MMP-2) activity.

This leads to increased collagen degradation and further weakening of the tendon.

pubmed.ncbi.nlm.nih.gov/20602464/
12/
Tendons constantly undergo a cycle of stress-strain and repair.

In patients w/ other risk factors (eg ESRD, steroid use), fluoroquinolones hamper tendon repair mechanisms, altering this stress-strain relationship and increasing the risk of rupture.

pubmed.ncbi.nlm.nih.gov/18261674/
13/
A convenient way to conceptualize this overall process is that fluoroquinolone tendinopathy is essentially an accelerated form of overuse injury.
14/
Fluoroquinolones also are associated with an increased of risk of aortic aneurysm and dissection.

This 2019 metanalysis found an overall relative risk elevation for aortopathy of 2.1.

pubmed.ncbi.nlm.nih.gov/30947680/
15/
The mechanisms for fluoroquinolone-associated aortopathy appears to be similar to tendinopathy.

This mouse study found increased aortic MMP activity and more elastic fiber degradation after ciprofloxacin exposure.

pubmed.ncbi.nlm.nih.gov/30046809/
16/SUMMARY
🦶Fluoroquinolones increase the risk of tendinopathy
🦶Mechanisms include tenocyte toxicity, inflammatory responses, ⬇️ collagen production, and ⬆️ collagen degradation
🦶Aortopathy can occur by a similar mechanism

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More from @AvrahamCooperMD

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A short 🧵 on my 3️⃣-prong approach to rounding with resident teams in the MICU…

I emphasize 3️⃣ themes to the residents and fellows:

1️⃣ Clinical care
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#MedTwitter #MedEd
1️⃣ Clinical care

I ask teams to focus on efficiency, ⬆️ time for teaching/ discussion

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🧠I ❤️ to teach but avoid overwhelming residents by teaching high yield points on 2-3 patients max. I supplement w/ PM chalk talks after lunch and notes are done

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How does the immune system achieve "self-tolerance", knowing not to attack and destroy the body's own tissues, like it does invading microbes?

This story involves scientific skepticism, T cell self-destruct signals, the thymus, and much more.

#tweetorial #medtwitter
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The focus will be on the adaptive immune system more than innate.
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Why is the liver able to regenerate itself?

Somehow the liver has the incredible capacity to both heal itself after toxic injury and regrow after resection. No other solid organ in the body can regenerate like this.

#medtwitter #tweetorial
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It's assumed that the ancient Greeks knew of the liver's unique regenerative capacity, based on the myth of Prometheus (his liver regrew daily after an eagle ate it).

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pubmed.ncbi.nlm.nih.gov/20472318/
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Have you ever wondered why Pseudomonas aeruginosa smells like grapes 🍇?

The answer relates to the ability of Pseudomonas to cause chronic airway infections and also coincidentally explains certain spoiled wine flavors.

#medtwitter #tweetorial
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Pseudomonas was first isolated in 1882 by the French pharmacist Carle Gessard, after he cultured it from the blue-green pus on bandages of injured soldiers.

academic.oup.com/cid/article/6/…
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It was widely observed that Pseudomonas aeruginosa produces a grape-like smell when growing in cultures or on wounds.

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ncbi.nlm.nih.gov/pmc/articles/P…
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1/THREAD
Why would adenosine, a purine nucleoside, be able to treat supraventricular tachycardias (SVT)?

And why are its effects so short lived (e.g. <2 seconds)?

The answers will change the way you think about this drug.

#tweetorial #medtwitter
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Adenosine is an endogenous purine nucleoside that gets incorporated into RNA, ATP, and cAMP.

It has pleomorphic effects as a signaling molecule via A1, A2A, A2B, and A3 receptors.

pubmed.ncbi.nlm.nih.gov/25687993/
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Adenosine was first found to be able to terminate supraventricular tachycardias (SVT) in 1927 in animal experiments.

💡It's mechanism of action was unknown.

pubmed.ncbi.nlm.nih.gov/16994064/
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