Let's take a step back and introduce an analogy: imagine a home with a thermostat and a radiator.
When the temperature drops below a set-point, the THERMOSTAT turns the RADIATOR on, increasing the temperature. When the desired temperature is reached it turns off.
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This is an example of a controlled system: a CONTROLLER (the thermostat) directs a PLANT (the radiator) to regulate a process variable (the temperature).
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This closed loop system carefully regulates the temperature in our homes.
We'll call this HOMEostasis...! 😂
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It also turns out this simple Control Theory Model is also a pretty good analogy of how our respiratory system functions:
A CONTROLLER (the pons/medulla) activates a PLANT (the respiratory muscles) in response to a PROCESS VARIABLE (PaCO2).
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Just like our home thermostat regulates temperature, our pons/medulla activates our respiratory muscles using a closed loop controlled system.
Normally, this adjusts VE to maintain homeostasis, tightly controlling our PaCO2, PaO2 & pH.
Full disclosure: As you can see, I've simplified the model & omitted the math (this is a #tweetorial not a textbook!).
If I've piqued your interest in the topic I recommend reading this paper (don't worry you won't have to do any Laplace transforms!) jstage.jst.go.jp/article/jpfsm/… 12/
Now that we understand how the system works, we're ready to understand how it's perturbed in CHF.
Using our analogy:
1️⃣weaker radiator
2️⃣radiator is farther from the thermostat
These result in delayed response to temperature shifts & thus big swings in room temperature. 13/
Why is the radiator smaller?
Because of low cardiac output, less blood is delivered to the lungs. This increases physiologic DEAD SPACE & alters the relationship between VE and PaCO2.
Due to low cardiac output, it takes longer for blood to circulate from lungs to chemoreceptors. This means that there is a DELAY (circulation time) between plant output and sensor.
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How much longer is circulation time in CHF?
In 1933, researchers injected volunteers in the leg with a tracer compound and measured how many seconds until the volunteers could taste it.
🚨 Clinical aside: This fact can save a life!
Increased circulating time really matters when you intubate people with CHF:
-Expect your sedation & paralytics to take longer to work!
-There will be a longer delay in SpO2 recovery once the tube is in!
Be patient!
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Adding a delay between plant output & controller input can destabilize a controlled system.
For the mathematically inclined, adding a time delay (τ) has an *exponential* effect on the Lapacian. This is why a small delay (just 13 seconds) can profoundly destabilize things! 18/
Altered plant gain & prolonged circulating time can make feedback loops overcorrect; VE is constantly overshooting (hyperventilation) or undershooting (apnea).
Each correction leads to another cycle of larger corrections, until large oscillations develop: Cheyne-Stokes! 19/
Let's summarize:
- the respiratory "plant" is triggered by the medulla/pons "controller"
- people with CHF have more dead space (a smaller plant) & delay in sensing CO2; this causes Periodic instability in PaCO2 and respirations!
- think of the thermostat overcorrecting!
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But why did an inotrope "fix" the Cheyne-Stokes respirations?
- the inotrope increased the SV & CI
- this reduced physiologic dead space, making the lungs work better (improved plant gain!)
- this also reduced circulating time (eliminating the instability from the delay!)
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If you like my thermostat analogy, imagine that adding an inotrope is like putting a fan in that big room!
The fan improves the efficiency of the radiator & reduces the delay in sensing. This "fixes" the problem of big swings in temperature, restoring HOMEostasis!
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Let's go over the incorrect answers.
- Opioids exacerbate Cheyne-Stokes (CSR)
- Oxygen can help CSR but wouldn't have doubled the SV or CO!
- This was CSR not Kussmaul. If it was Kussmaul due to DKA, insulin would have helped.
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To summarize everything, we learned:
- how control theory helps us understand control of respiration (thermostat analogy)
- why people with CHF develop Cheyne-Stokes: more dead space & prolonged circulatory time (big room, small radiator)
- how inotropes correct CSR (add a fan)
It occurs to me that a slightly better analogy would be a thermostat turning on central AC:
Rising temp (analogous to PaCO2) leads to AC plant activation (analogous to ventilation), which normalizes the temp!
🥶But frankly it’s way too cold out to think about AC!
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Fact check: Marik was fired (he claims he resigned) from EVMS in late 2021. With no institution willing to hire him, he was *unable* to renew his university limited license. His license to practice medicine expired in 2022.
A man comes to the ICU after uncomplicated cardiac surgery. He is hypertensive and a nicardipine infusion is started. 10 minutes later he becomes hypoxemic. A chest radiograph is obtained.
What happened?
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Here's some followup: an intervention was performed & hypoxemia resolved. These two CXR are taken 15 minutes apart.
What was done?
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Pre: Post:
This case illustrates two of the my favorite (and IMO 2 of the most clinically important) pulmonary concepts in the ICU: 1. diagnosis of lobar collapse on chest radiograph 2. loss of hypoxic pulmonary vasoconstriction due to calcium channel blockers (CCB)
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Here's a physiology case that *everyone* who touches a ventilator needs to understand:
A 60 yo woman is intubated for hypoxemia from multifocal pneumonia.
She has a SpO2 of 89% on PEEP +12 and 100% FiO2.
PEEP is increased to +16 & her SpO2 drops to 80%!
What happened?
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Before we get into the answer, let's make it interesting with some multiple choice.
Which mechanism(s) could cause worsening hypoxemia with increasing PEEP?
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Wow! 6000 votes! Im amazed by how many people share my love for 🫁 physiology!
I’ll post the answer tomorrow. If you can’t wait there’s a complete explanation on #MedMastodon.
Important ICU teaching case:
A woman with AL amyloidosis presents with hemorrhagic shock from a GI bleed. HR 130, BP 80s/40s, Hb 4.5. She’s been receiving CyBorD-Dara chemotherapy up until 1 month ago.
What crucial fact do you need to remember when ordering blood transfusions?
The answer is that daratumumab (an anti-CD38 monoclonal) interferes with antibody screening & crossmatch!
In order to understand *why* this occurs we need to step back and review how blood is tested for compatibility.
Buckle up for a🧵! Let’s get our Coombs on, indirectly. 2/
To safely transfuse blood, we test for:
-major antigens (ABO, Rh)
-minor antigens (everything else)
Testing patient ABO & Rh is called “typing”
Testing for antibodies against minor antigens is called “screening”
Mixing donor blood w/ recipient serum is “cross matching”
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During my undergrad @BrownUniversity I remember when researchers did this in *humans*: A man with quadriplegia controlled a computer or robotic limb using a brain-machine interface. It was on the cover of @Nature. That was in 2006.
More hilarious is in a “groundbreaking paper” ostensibly written by Elon & published in the Journal of Internet Medical Research, they claim it’s “plausible a person may someday control a digital mouse” w/ this technology.
Ignoring the fact that it was accomplished >15 yrs ago!
Here’s an ECG with a pathognomonic finding that everyone ought to know, especially at this time of year.
Explanation: this is an example of Osborn Waves seen in a person whose core temp was 28°C.
Osborn waves are positive deflections that occur at the J point. They are seen in hypothermia (T usually <32C) and typically more pronounced at lower temperatures.
I said pathognomonic because by definition an Osborn Wave is associated with hypothermia.