Misc. Stuff from PPTs - Exam 1 Flashcards
Factors that can prolong paralysis
Hypothermia
Aminoglycoside toxicity (MYCIN abx)
steroid myopathy
antihypertensives
antidysrhythmics
abx
steroids
volatile anesthetics
Dantrolene (do NOT give prophylactically)
Magnesium
Lithium
T/F Most abx can cause NM blockade without the use of NMBD
true
-scary
How do abx potentiate NMBD?
Inhibit PREjunctional release of ACh
Depress POSTjunctional nAChR sensitivity to ACh
T/F cephalosporins and penicillins can potentiate NMBD
false
Calcium antagonizes the interaction between NMBD and abx, should we use it to help with recovery?
No
-antagonism isn’t sustained and it can minimize positive effects of abx
What can be given prophylactically to prevent histamine release for NMBD?
H1 and H2 blockers
Amount of histamine release after administering a NMBD depends on _ and _ of injection
dose and speed
Atracurium and Mivacurium release _ amounts of histamine
modest
-can cause HoTN and tachycardia
Succinylcholine can release _ amounts of histamine
slight
-may see some tachycardia initially but repeat dosing can cause bradycardia
Pancuronium is _ and causes slight _ release causing tachycardia.
vagolytic
catecholamine
-not histamine mediated
If an allergic reaction happens, blocking _ helps prevent cardiovascular collapse
H2 (famotidine, etc)
-GIVE BOTH H1 AND H2 BLOCKERS THO
If an allergic reaction happens, blocking _ helps with bronchoconstriction
H1 (benadryl)
-GIVE BOTH H1 AND H2 BLOCKERS THO
Which medications metabolize via Hoffman Elimination?
Benzylisoquinoline Relaxants
-Cisatracurium(Nimbex)
-Atracurium
T/F Drugs metabolized via Hoffman Elimination cause toxicity and metabolism varies pt to pt
false
T/F Drugs that metabolize via Hoffman Elimination form toxic byproducts
True
-not of much concern tho
The toxic byproducts formed by Hoffman Elimination are _ and _
LAUDANOSINE
Acrylates
Hydrolysis via Hoffman Elimination requires which 2 factors:
-temperature change
-pH change
Drugs that metabolize via Hoffman Elimination could be useful for patients with:
renal or liver disease
Hoffman Elimination contributes to -% of the metabolism for Atracurium
10-40%
-remainder is metabolized by nonspecific ester hydrolysis
Hoffman Elimination contributes to _% of the metabolism for Cisatracurium
77%
-remainder is metabolized by nonspecific ester hydrolysis
NMBD that cause histamine release:
Succinycholine
Mivacurium
Atracurium
NMBD that cause cardiac muscarinic effects (vagal block)
Succinylcholine (stim or block)
Pancuronium (moderate block)
NMBD metabolized via hepatic and renal systems:
Roc
Vec
NMBD eliminated via hepatic and renal systems:
Roc- R (10-30%) H (70-90%)
Vec - R (40-50%) H (50-60%)
NMBDs that only are metabolized via the liver
Vec + Pancuronium
NMBD metabolized via plasma cholinesterase
Succinylcholine
Mivacurium
Steroidal NMBD with toxic metabolites
Vec (metabolite has 80% of potency of parent drug)
Pancuonium (has 66% potency of parent drug)
-both make 3-OH, accumulates, bad for renal and liver pts
Pancuronium should be avoided in which patients
renal disease
-eliminated primarily via kidneys (~85%)
T/F Sugammadex can reverse Cisatracurium, Mivacurium, and Atracurium
false, these are benzylisoquinoline relaxants and sugamadex only works on steroidals