Malignant Hyperthermia Flashcards
MH Characteristics
sustained hypermetabolism
Inherited
abnormal handeling of intracellular Ca+
Triggered by Pharmacologic agents possibly heat/exercise
Who gets MH
1 : 15,000 children
1 : 20,000 - 50,000 Adults
1 : 2,000-3,000 have trait
Clinical manifestations of MH
hypercarbia
tachycardia
muscle rigidity (masterator muscle)
cyanosis
hyperthermia > 38.8 C
cola colored uring (myoglobin)
Labs with MH
elevated ETCO2
decreased Ph
ABG will show what
Mixed metabolic and resp acidosis
hyperkalemia
What receptor regulates the SR Ca+ exchange
RYR-1 ( ryanodine) receptor
what happens if the Ca+ is not returned to the SR
sustained contraction
Agents that will trigger a MH event
SUCs
volital agents
waht agents will NOT trigger a MH event
NDNMB
N2O
Propofol, ketamine, etomidate, opoids and benzos
Local anesthetics
Treatement for MH
Dantrolene 2.5 mg/kg rapid IV
100% O2
Removal of triggering agent
Core temp and Ice pack with COLD NS levages
GET HELP
Dantrolene contains what other medication with it
Mannatol so your pt will diurese
How much dantrolene do you give
repeat 2.5 mg/kg dose until Sx stop or max at 10 mg/kg
Why do you not give LR to these Pts
they are already building up lactic acid you dont need to add to this acidosis
Labs that need to be ordered
serial blood gases
coags
UA myoglobin
lactic acid
creatine kinase
Maintance dantrolene dose
1mg/kg Q6hrs for 36 hrs