MH Flashcards
(35 cards)
incidence of malignant hyperthermia
1:8000 or 1:30,000
incidence of malignant hyperthermia is higher in
children
MH is linked to mutations in
RYR-1 gene mutation.
RYR1 on chromosome 19
CACNA1S - chromosome 1
and STAC3 of chromosome 12
all volatile agents (except N2O) can trigger MH via
direct action on RYR-1
Depolarizing NMB trigger MH via
over activation of VGCC that lead to opening of RYR-1 ( on the SR) –> indirect
early signs of MH
Hypercarbia tachypnea tachycardia MMR Hyperthermia*
MMR is a common SE of
succinylcholine
Of the people with MMR
20% will have an MH episode
rate of temperature rise in MH
1-2 degrees Celsius ever 5 minutes
milder MH triggers =
exercise in hot conditions
neuroleptic drugs
alcohol
infections
mild increase in masseter tone + limb flaccidity following succinylcholine =
normal reaction after succinylcholine
if MH is suspected immediately draw:
potassium and ABG
MH mortality without dantrolene =
70%
MH mortality with dantrolene =
5%
Dantrolene MOA
reduces muscle tone and metabolism -> stabilizes and restores balance between release and uptake of Ca++
- prevents on going release of calcium from muscle (@SR)
- Blocks external entry of Ca++ into cell
- Hypothesized to inhibit calcium conductance through RYR1
half life of dantrolene =
10 to 15 hours
calcium channel blockers + dantrolene =
life threatening hyperkalemia and myocardial depression.
avoid calcium channel blockers with history of MH
phlebitis often follows
administration of dantrolene
traditional minimum and ryanodex minimum
traditional minimum: 36 vials (20 mg/vial)
or 3 vials of (250 mg/vial) of ryanodex must be available
h2o mixed with traditional dantrolene =
60 mL sterile H2O PER VIAL.
36 vials = average loading dose
dantrolene dosing
- 5 mg/kg bolus.
maintenance: 2 mg/KG IV q 5 minutes to a total of 10 mg/kg
then 1 mg/kg q 6 hours for 72 hours
goal temperature in cooling for MH
38 degrees C
ABG drawn
q 15 min with active MH
Iced IV NS bolus =
15 mL/kg q 10 min