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
why would you monitor blood glucose level
hypoglycemia R/Thypermetabolic state
Metabloic acidosis TX
1-2 mEq sodium bicarb
Hyperkalemia TX
10mEq/kg Ca+ chloride
10-50 mEq/kg Ca+ Gluconate
OR
1ml/kg of D50with 0.15 units/kg of Regular Insulin
(10 units usually)
Can us use Ca+ channel blockers with Dantrolene
HELL NO you will KILL them.
Increases K+ and can cause Asystole
Rhabdomyolysis Tx
get rid of the myoglobin form the kidneys with lasix and bicarb
MH kills by
Acidosis
Hyperkalemia
organ failure due to hyperthermia
DIC
Renal failure due to myoglobinuria
MH may be mimiced by
Fever with out muscle rigidity - thyrotoxicosis, sepsis, phenochromocytoma, iatrogenic overheating, anticholinergic syndrome
Fever with muscle symptoms - Neuroleptic maligant syndrome, Hypoxic encephalopathy, Ionic contrast agents in CSF, cocaine, amphetamines and ecstasy
Diagnostic test for MH
Caffeine Halothane test (CHCT)
Indications for CHCT
unexplained rabdo after surgery
MMR w rabdo
exercise induced rabdo
What Hx in a Pt increases your concern for MH
any muscular dystrophy increases the chance of MH
Central core myopathy
motor developement delay
lower limb muscle delay
mutation in the RYR-1
Duchenne muscualr dystrophy
X linked recessive affecting males
abnormal muscle fiber function
developmental motor delay
King Denborough Syndrome
dysmorphic facial features
Heat stroke
hyperthermia as a trigger
Neuroleptic Malignant syndrome
triggered by antipsychotic meds
surgical Tx for pt with a HX of MH
dont use triggering agents
TIVA
Regional
Ketamine
propofol / opoids
watch in PACU for 4 hrs post surgery