Malignant Hyperthermia Flashcards

1
Q

MH Characteristics

A

sustained hypermetabolism

Inherited

abnormal handeling of intracellular Ca+

Triggered by Pharmacologic agents possibly heat/exercise

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2
Q

Who gets MH

A

1 : 15,000 children

1 : 20,000 - 50,000 Adults

1 : 2,000-3,000 have trait

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3
Q

Clinical manifestations of MH

A

hypercarbia

tachycardia

muscle rigidity (masterator muscle)

cyanosis

hyperthermia > 38.8 C

cola colored uring (myoglobin)

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4
Q

Labs with MH

A

elevated ETCO2

decreased Ph

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5
Q

ABG will show what

A

Mixed metabolic and resp acidosis

hyperkalemia

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6
Q

What receptor regulates the SR Ca+ exchange

A

RYR-1 ( ryanodine) receptor

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7
Q

what happens if the Ca+ is not returned to the SR

A

sustained contraction

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8
Q

Agents that will trigger a MH event

A

SUCs

volital agents

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9
Q

waht agents will NOT trigger a MH event

A

NDNMB

N2O

Propofol, ketamine, etomidate, opoids and benzos

Local anesthetics

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10
Q

Treatement for MH

A

Dantrolene 2.5 mg/kg rapid IV

100% O2

Removal of triggering agent

Core temp and Ice pack with COLD NS levages

GET HELP

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11
Q

Dantrolene contains what other medication with it

A

Mannatol so your pt will diurese

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12
Q

How much dantrolene do you give

A

repeat 2.5 mg/kg dose until Sx stop or max at 10 mg/kg

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13
Q

Why do you not give LR to these Pts

A

they are already building up lactic acid you dont need to add to this acidosis

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14
Q

Labs that need to be ordered

A

serial blood gases

coags

UA myoglobin

lactic acid

creatine kinase

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15
Q

Maintance dantrolene dose

A

1mg/kg Q6hrs for 36 hrs

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16
Q

why would you monitor blood glucose level

A

hypoglycemia R/Thypermetabolic state

17
Q

Metabloic acidosis TX

A

1-2 mEq sodium bicarb

18
Q

Hyperkalemia TX

A

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)

19
Q

Can us use Ca+ channel blockers with Dantrolene

A

HELL NO you will KILL them.

Increases K+ and can cause Asystole

20
Q

Rhabdomyolysis Tx

A

get rid of the myoglobin form the kidneys with lasix and bicarb

21
Q

MH kills by

A

Acidosis

Hyperkalemia

organ failure due to hyperthermia

DIC

Renal failure due to myoglobinuria

22
Q

MH may be mimiced by

A

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

23
Q

Diagnostic test for MH

A

Caffeine Halothane test (CHCT)

24
Q

Indications for CHCT

A

unexplained rabdo after surgery

MMR w rabdo

exercise induced rabdo

25
Q

What Hx in a Pt increases your concern for MH

A

any muscular dystrophy increases the chance of MH

26
Q

Central core myopathy

A

motor developement delay

lower limb muscle delay

mutation in the RYR-1

27
Q

Duchenne muscualr dystrophy

A

X linked recessive affecting males

abnormal muscle fiber function

developmental motor delay

28
Q

King Denborough Syndrome

A

dysmorphic facial features

29
Q

Heat stroke

A

hyperthermia as a trigger

30
Q

Neuroleptic Malignant syndrome

A

triggered by antipsychotic meds

31
Q

surgical Tx for pt with a HX of MH

A

dont use triggering agents

TIVA

Regional

Ketamine

propofol / opoids

watch in PACU for 4 hrs post surgery

32
Q
A