MH Flashcards

1
Q

MH mutation genes

A

RYR 1 chr 19
CACNA1S chr 1
STAC3 chr 12

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2
Q

Hypermetabolism: ATP needed for what 3 things

A

Ca release, reuptake into SR, and troponin decoupling

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3
Q

MH: succ vs VA causes cell level

A

Succ sustained depolarization at nAChR. VA at ryanodine receptor, ca release from SR

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4
Q

Earliest s/s MH

A

Hypercarbia, tachypnea, tachycardia

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5
Q

Confirmatory lab in kids w masseter spasm after sux

A

> 20,000 CPK

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6
Q

MMR: what is normal, check what, MH occurs how often

A

Mild inc masseter tone after sux w limb flaccidity. Check K and ABG. MH occurs in 20% of cases of MMR

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7
Q

3 symptoms that occur w rhabdo

A

Muscle pain, myoglobinuria, arrhythmias from high K

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8
Q

CPK correlates

A

In >20k well w rhabdo, less well w fever and acidosis

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9
Q

Rapid v slow rhabdo

A

K dangerously high/quick in rapid, in slow its safer, K is redistributed before blood levels increase

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10
Q

Sympathetic response leads to 3 things in heart/vessels

A

Inc catecholamines lead to inc HR, cutaneous vasoconstriction, inc SVR
Inc CO

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11
Q

What to do in isolated MMR

A

D/c volatiles, give propofol, turn up flows, get another IV/give vol/ABG. Observe 24h if other symptoms. Maybe muscle bx

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12
Q

Gold standard MH test

A

Halothane caffeine contracture test. Muscle in halothane, sustained contracture. 80% specificity

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13
Q

How dantrolene works, 1/2 time

A

Reduces muscle tone and metab. Dec release of Ca from SR. Blocks external entry of Ca into sarcoplasm. Inhib ca thru ryanodine receptors. 10-15 e 1/2

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14
Q

Dantrolene: doesnt potentiate effects of what

A

Non depolarizing muscle relaxants or interfere w reversal. Can cause weakness if pre existing NM disease

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15
Q

DONT use dantrolene with what

A

CCB, life threatening hyperkalemia and myo depression

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16
Q

How many vials need to be in facility if sux is used, what else needs to be there

A

36 minimum. Sterile water, 60 ml/vial

17
Q

Dantrolene dosage

A

2.5 mg/kg bolus, then maintenance dose 2 mg.kg q 5 min. Total 10 mg/kg. Then 1 mg/kg q6 for 72 hours

18
Q

Where we want temp. Saline bolus dose.

A

38 c. 15 ml/kg q 10 min

19
Q

Hyperkalemia treatment

A

1 ml/kg d50 glucose and 0.15 u/kg regular insulin and/or CaCl 5-10 mg/kg IV

20
Q

Monitoring how long after, recrudescence how often. Avoid what, measure what

A

36h in icu. 25%. No LR (K). Coag profile for DIC and CKs q6h

21
Q

Lab supplies needed

A

6 abg kits, Ck myoglobin, sma 19, pt/ptt, fibrinogen, fsps, CBC, LA level. Urine myoglobin level x2, urine dipstick hgb

22
Q

Muscle diseases assoc w MH 3

Not assoc w which one

A

Central core disease, king denborough syndrome, and Evans myopathy. Not: MD but can still develop rhabdo so still avoid triggering agents

23
Q

Neuroleptic malignant syndrome presentation. Who is susceptible

A

Fever, muscle rigidity, ANS instab, delirium, elev CPK. Pts on haldol, prolixin, thorazine

24
Q

Sudden cardiac arrest after sux in young males can be what

A

R/t hyperkalemia in undx myopathy. 50% mortality rate, may also have rigidity and hyperthermia

25
Q

Meds/tx for sudden unexpected cardiac arrest

A

Ca cl, hco3, insulin, glucose, hyperventilation. May need dialysis and CPB

26
Q

Report MH to who

A

North American mh registry. In CHOP in Pittsburgh. Barbara Brandon