When was the last time you saw a pt with hepatic encephalopathy or lost a pt to cerebral edema from it?
Ever wondered why liver failure causes HE & Cerebral edema? What if conventional Rx fail?
If interested in journey to MARS, keep reading.
Bringing awareness to #neurologists.
Pt w/ MVA,G5 liver lac,hepatic art sacrificed,LFT 5k,NH3 250,GCS 4
Pt w/🍺cirrhosis,found down,severe rhabdo,CK📈,NH3 400s,renal shutdown,GCS 5
Pt w/ colon Ca on @KEYTRUDA w/jaundice DILI
Pt w/ liver transplant, p/w intractable pruritus
You got the gist-MARS aka Albumin dialysis
Pathyphysiology of cerebral edema in HE.
An article by @EWijdicks elegantly describes it. (PMID:27783916)
In Liver failure (LF), ⬆️NH3 cross BBB, converted to glutamine👉🏻osmotic gradient and CE.
Risk of cerebral edema (CE) ⬆️ with NH3 >200 micro moles/L.
Here is the toxin hypothesis of vicious cycle that occurs in LF, can lead to CE + herniation.
Basically states that liver injury does not only impair toxin clearance but also can cause impaired hepatic regeneration 👉🏻 further exacerbation of LF + toxin clearance. (PMID:22228886)
Rx for ICP:hypertonic,sedation,🤷🏻♂️from now on #verticalization@namorrismd
Last resort👉🏻may need Extracorporeal Liver Support-ECLS👉🏻3 goals:
✅remove toxin
✅synthesize protein
✅reverse inflamm by cytokines
MARS=Molecular Adsorbant Recirculating System👉🏻1 of many ways of ECLS.
ECLS are of 2 main types; (25438293,26311600)
Type 1:Artificial/acellular/non-biologic:Utilize artificial membrane 👉🏻adsorption+detoxification of🩸
Pros:
✅easy 2 use
✅reverses pathyphysiology of LF
✅cheap
Cons:
☑️no synthetic func
E.g.MARS (main focus here), SPAD, Prometheus
Type 2:Bio-artificial/Cellular/Biologic:Utilize live hepatocytes from human or 🐷 source soaked in a medium in cartridge through which🩸is passed for detoxification.
Pros:
✅+synthetic func
Cons:
☑️complex technology
☑️cell source supply issue
☑️Xenotransmission
☑️💰💵🤑
MARS has 2 different circuits merged together:
🟡albumin dialysate high-flux dialyzer(protein-bound ☠️+cytokine+drugs)
🟢renal dialysate low-flux filter(water sol☠️)
Basically,add albumin circuit b/w blood & CRRT
🛑for a sec.
Understand Dalton-unit of atomic mass of an atom in reference to C-12(g/mol)
For filter, 1000Da (1 kDa) =1.3nm pore size. 35 kDa filter allows everything <=35 kDa size to pass through.
Ammonia=17Da
Urea=60Da
Cr=113Da
Bile acid=500Da
Albumin=67 kDa
DNA=~156 billionDa
Molecules cleared by MARS:
Water soluble-NH3, Urea, Creatinine, (?? nitric oxide👉🏻improved hemodynamics)
Protein-bound-Bilirubin (indirect), Bile acid, Tryptophan, Fatty acids(low, medium chain), TNF & IL(CK), Cu, BZD & drugs.
8. MARS machine
✅pumps albumin dialysate circuit through HFD
9. Central venous access with VasCath / Trialysis
Now since we have all pieces together, let’s make a MARS circuit:
Hint:
Green-simplified renal dialysate circuit
Black/yellow-albumin dialysate circuit (black=used albumin, shades of yellow=dark to bright,more cleaner albumin.
Red-pt’s 🩸with toxins
Blue-pt’s 🩸free of toxins
✅🩸only passes through HFD,not LFD.
✅Used Albumin dialysate from HFD is diverted to LFD first to filter water sol☠️ before going to MARS PF, AC & IE filters for recycling.
✅pt’s Albumin never gets filtered, nor does it make contact w/ dialysate Albumin.
✅since we’re running 2 circuits(Alb dialysate+renal dialysate) w/ 2 machines (MARS+CRRT) in a single continuum, the flow rates must be the same in both machines. 150-200ml/min(usually 180)
✅circuit needs to be primed ~2 hrs before anticipated use.
✅don’t forget heparin/citrate
Duration of Rx=6-8hrs, max 10. Why?
👉🏻potential risk of Alb becoming culture medium w/ longer use
👉🏻AC & IE filters get saturated after 6-8hrs
✳️Usually 3-5 sessions are done, may be more.
✳️MARS is not a destination treatment, it’s bridge to spontaneous recovery or transplant
So what’s in it for 🧠👨⚕️?
We must know when to anticipate MARS in pt w/ HE and understand it’s effects on 🧠& recovery.
1.Effects on hemodynamics:
Confounded data but some suggest improved MAPs,others not. Almost everyone found improved SVR (may be nitric oxide clearance?)
2.Effects on CBF, 🧠O2 consumption:
✳️⬆️ Vmean in MCA w/ TCD (12950955)
✳️⬇️SjVO2(jug venous O2) from 86%->70%,marker of 🧠O2 consumption.
✳️Average ⬆️GCS by 4-6,independent of survival (11445681)
One study reported 5/8 pts improved from comatose to GCS>13 after just 1 Rx MARS
3.Effects on ICP & HE:
✳️⬇️⬇️ICP from 37 to 13 on average (12602522) & resolution of CE on CT.
✳️average ⬇️ HE grade by 2 (West Haven)
✳️55% likelihood of improvement in HE (meta-analysis 26311600)
4.Effects on drug clearance:
Conventional dialysate didn’t remove diazepam but when switched to Albimin,level dropped👉🏻potential protein-bound drugs clearance.(22077243)
Most data w/ MARS is CCB/acetaminophen/mushroom poison.
How about Phenytoin/Valproate/BZD/Phenobarb toxicity?
Briefly,
❇️SPAD:unlike MARS, albumin is not recycled, discarded.
❇️Prometheus:Uses 250kDa filter👉🏻separate pt’s own albumin w/ toxins from 🩸👉🏻albumin rich plasma like solution passed through IE+AC👉🏻clear albumin-plasma remixed into🩸at the end of filter👉🏻through LFD👉🏻back to pt.
Here’s one of our patient undergoing MARS for intractable pruritis..
So, if NH3 was the only culprit for HE, why not use just CRRT?
Yes, we can but NH3 clearance is UF rate dependent. Usual UF rate ~30ml/kg/hr is not enough to keep up w/ production of NH3. We need “high dose CRRT’- UF rate ~90ml/kg/hr.
Here’s the landmark study w/ data supporting.
If you want to learn further about how CRRT works, follow this link to a great tweetorial by my co-fellow @EricLawson90
Humanity has but three great enemies: fever, famine and war; of these, by far the greatest, by far the most terrible, is fever. -Sir William Osler
That’s why temperature is one of the “vital signs” (not pain🤨)
So if you have ever wondered how body controls🌡 & never got an answer beyond - somewhere in 🧠hypothalamus; here’s an explanation.
🤕 is admitted H&H 4 SAH + IVH. This is the temp📈-shows, patient started spiking 🌡@ 24hrs & peaked ~72hrs. Cultures ⏲ ABX started on admission.
38.3 C = magic number for most of us to trigger “pan-culture” + “broad spectrum ABX” to fight off infection.
Does every fever needs to be addressed with ABX?? - probably not.
This is a #MedTwitter about Central fever aka neurogenic fever. From basics to treatment approaches.
1/ Antiepileptic drugs: a constantly evolving frontier- like many other fields in #Neurology. It’s hard to know about every single medication in-depth. Here, I attempted to make AEDs simple, easy to understand and a handy layout of important facts to know about #AED#epilepsy.
2/ Let’s begin with understanding what is synapse and how it works, then only we can understand how the AEDs work. Look at the cartoon I created from references (acknowledged at the end) with help of an amazing app #Procreate. I’m a fan of @PeterMLawrence1 great art work !!
3/ Looks chaotic?Let’s break it down. You got this!
There are 2 main types of synapses.
A)Excitatory synapse-neurotransmitter is Glutamate- receptors are AMPA and NMDA
B)Inhibitory synapse-neurotransmitter is GABA-receptor is GABAa binding site on ligand gated Cl- channel