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43 Cards in this Set

  • Front
  • Back
PHASE II BLOCK
-post junctional membrane repolarizes but does not respond normally to ACh
-usually doses > 3-5 mg/kg IV
-resembles non depolarizing block
ATYPICAL PLASMA CHOLINESTERASE
-gene, unable to hydrolyze the ester bonds in drugs like Sux, mivacurium
-usually don't know until given Sux and block time prolonged
-test with dibucaine
2 CHEMICAL CLASSIFICATIONS OF NON DEPOLARIZERS
STEROID DERIVATIVES-Pan, Roc, Vec, Pipercuronium *vagolytic usually (increase HR)
BENZYLLISOQUINOLINES-d-tubo, atracurium, mivacurium* tend to release histamine
DIBUCAINE TEST
-local anesthetic that will inhibit normal plasma cholinesterase by 80% (normal is 80)
-40-60 heterozygous atypical prolonged block (20-40)
-20-40 Block >60 min homozygous atypical
LONG ACTING NON DEPOLARIZERS
Pancuronium longest, Doxacurium,pipe, d-tubo, metocurine and gallamine
SIDE EFFECTS OF SUX
-can also stimulate muscarinic receptors causing bradycardia
-Fasiculations can cause myalgia
-prevent fasiculations by giving subparalyzing dose 3-5% of ED95 non depolarizing drug
-hyperkalemia from sustained opening of channels and K out
-don't use in burns, upper motor neuron lesions, musc. dystrophy
MORE SIDE EFFECTS OF SUX
myoglobinuria from fasiculations, Increase IOP, increase ICP, increase IGP, Trismus in children -jaw doesn't relax, may be a sign of suseptibility to MH,
-trigger for MH
INTERMEDIATE NON DEPOLARIZER
Vec, atracurium, cisatracurium, Roc
SHORT ACTING NON DEPOLARIZER
mivacurium
PAVULON (PANCURONIUM)
LONG ACTING
-DOSE intub. .08-.12 mg/kg
main. .01 mg/kg
ONSET 3-5 min
DURATION 60-90 min
EXCRETION primarily renal (only one)
***can stimulate and block vagus -> increase HR, CAD caution
NUROMAX (Doxacurium)
LONG ACTING
DOSE intub. .05 mg/kg
main. .005 mg/kg
ONSET 4-6 min
ARDUAN (Pipercuronium)
LONG ACTING
DOSE intub. .06-.1 mg/kg
**hypotension, bradycardia
EDROPHONIUM
ANTICHOLINESTERASE
onset like atropine
trade names TENSILON, ENLON, REVERSOL
DOSE 0.5-1 mg/kg
give with atropine 0.014 mg per mg of edrophonium
PROSTIGMIN, VAGOSTIGMIN (Neostigmine)
ANTICHOLINESTERASE
DOSE .037-0.07 MG/KG
give with glycopyrrolate 0.2 mg per mg of neostigmine
PHYSOSTIGMINE
ANTICHOLINESTERASE
-tertiary amine crosses BBB
-used to tx anticholinergic toxicity
NOT USED FOR REVERSAL
***too much anticholinesterase will cause weakness and blockade due to excessive ACh in NMJ
-this drug will prolong/potentiate the block of Sux
TRACURIUM (Atracurium)
INTERMEDIATE
-DOSE intub. .5 mg/kg over 30-60 sec
main .1mg/kg
infusion 5-10 mcg/kg/min
EXCRETION hoffman elimination, spontaneous non enzymatic degredation (at normal temp and pH), 2nd non specific tissue esterases.
-can cause seizures
-good for renal pts
-Laudanosine product of metab. CNS stimulant
-if push too fast histamine release
CHOLINERGIC SYNDROME (CRISIS)
-excessive use of cholinesterase inhibitors or organic insecticides
-excessive ACh peripherally or centrally
-s/s miosis, salivation, brochoconstriction, bradycardia, abd. cramping
-weakness
CNS dysphoria, confusion, seizures, coma
(inhibits parasympathetic, CNS excitatory)
NIMBEX (cisatracurium)
INTERMEDIATE ACTING
-stereoisomer of atracurium
-slower onset less histamine
DOSE intub. .1-.15 mg/kg
infusion 1-2 mcg/kg/min
EXCRETION Hoffman elimination
Laudanosine but less than atracurium
ANTICHOLINERGIC SYNDROME
-develops in response to increased doses of atropine and scopolamine
s/s CNS restless, shiver, mania, hallucinations, delerium, drowsiness, agitation disorientation
-peripheral - blurred vision, dry mouth, Increase HR, dry flushed skin, hypoTN, rash on face, neck and upper chest
TREATMENT FOR CHOLINERGIC SYNDROME
Atropine 35-70 mcg/kg
Pralidoxime 15 mg/kg IV Q 20min (reactivates acetylcholinesterase)
****then treat s/s
ZEMURON (Rocuronium)
INTERMEDIATE ACTING
-low s/e profile, alternate for Sux for RSI
DOSE intub. .6 mg/kg
RSI double the intub dose- will make onset more rapid and longer duration
EXCRETION little metab. largely excreted unchanged in the urine
MIVACRON (Mivacurium)
SHORT ACTING
DOSE intub. .15-.2 mg/kg
infusion 4-10 mcg/kg/min
EXCRETION hydrolysis via plasma cholinesterase * so if atypical plasma cholinesterase increases block time
-histamine release- push slowly
-spontaneous recovery need for reversal controversial
REVERSAL AGENTS
ANTICHOLINESTERASES
-inhibit the enzyme that breaks down ACh (acetylcholinesterase)
-Therefore INDIRECTLY increase the amoung of ACh available to compete with the non depolarizing agent which will therefore reestablish neuromuscular transmission
PHASE I BLOCK
-depolarizing NMB
-"fasiculations"
DTc d-tubocurarine
not used for NMB but pre tx for sux to prevent fasiculations
DOSE 3 mg IV 3-5 min before sux
***causes histamine release
TREATMENT FOR ANTICHOLINERGIC SYNDROME
Physostigmine 15-60mcg/kg
crosses the BBB
ANTICHOLINESTERASES SIDE EFFECTS
-increase in ACh affects more than nicotinic receptors of skeletal muscle
CV Brady,
RESP bronchospasm
GI N/V
so give with anticholinergic agents
NORCURON (Vecuronium)
INTERMEDIATE ACTING
DOSE intub. .08-.12 mg/kg
main. .01 mg/kg
infusion 1-2 mcg/kg/min
ONSET 3-5 min
DURATION 20-60 min under an hour
EXCRETION prim biliary, 2nd renal (25%)
ULNAR NERVE
adductor pollicis, adduction of thumb,
ASSESS FOR READY TO EXTUBATE
comes back last
MANDIBULAR NERVE
masseter muscle, electrode in front of and below zygomatic arch and forehead
POST TIBIAL NERVE
plantar flexion of big toe
FACIAL NERVE
ASSESS FOR READY TO INTUBATE
-first to go down first to come back
-orbicularis oculi
-has similar sensitivity to NMB as diaphragm and laryngeal
-recover sooner than adductor pollicis, orbicularis, diaphragm, rectus abdominus, and laryngeal
POST TETANIC FACILITATION
-response to TOF following tetanus is increased yet still fades as before
-typical of non dep block usually means you can start reversal
DOUBLE BURST
-3 short high frequency bursts 50 Hz separated by 0.2 msec followed by another 3 or 2 750 msec later
-considered gold standard easier to assess
-depolar 2 twitches diminished no fade
-non depolar 2 twitches with fade
TETANY
-sustained 5 sec 50-100 Hz
-sustained without fade indicates adequate recovery from block
TOF
-4 stimuli at 2 Hz delivered Q 0.5 sec
SINGLE TWITCH
-frequency 1 Hz
-used as control twitch
RECEPTOR BLOCKADE
-100%- flaccid no response
-95%- no twitches but diaphragm may move
-90%- 1 twitch adequate for abd. surg.
-70%- 75%- 4 twitches TOF, VC and TV can be normal
-50%- can pass inspriatory pressure test (NIF)
-30%- head lift and hand grasp sustained
MIOSIS
CONSTRICT
MYDRIASIS
DILATE
CHOLINERGIC CRISIS
-too much anticholinesterases
AKA muscarinic crisis
s/s abd pain, n/v, blurred vision, bronchial hypersecretion
TX PRALIDOXIME 15 MG/KG Q 20 min (reactivates acetylcholinesterase
ATROPINE 35-70 MCG/KG
ANTICHOLINERGIC SYNDROME
-opposite of cholinergic syndrome ( TOO MUCH ANTIMUSCARINICS, atropine, glycopyrolate, pralidoxime)
s/s Increase of SNS efffects
Increase HR, blurred vision, rash neck, face, and chest
TX PHYSOSTIGMINE 15-60 MCG/KG
CROSSES BBB
PYRIDOSTIGMINE
ANTICHOLINESTERASE
DOSE 0.15- 0.35 mg/kg
give with glycopyrrolate 0.05 mg per pyridostigmine