Malignant Hyperthermia Flashcards
(35 cards)
2 things that trigger MH
Volatile anesthetic agents
Sux
What happens in MH
Uncontrolled increase in oxidative metabolism in skeletal muscle
What kind of genetic disorder is MH?
Autosomal dominant disorder
When does MH occur?
Upon or shortly after exposure to certain general anesthetic agents
9 typical signs of MH:
- Hyper catabolic state
- High temp
- Tachycardia
- Tachypnea
- Hypercarbia
- Hypoxia
- Muscle rigidity
- Mixed acidosis
- Rhabdomyolysis
4 1st signs of MH:
Hypoxia
Hypercarbia
Sinus tachycardia
Massager spasm
Most common pattern of MH:
Respiratory acidosis and muscular abnormalities
EtCO2 suspect of MH:
> 55
Arterial pCO2 suspect of MH:
> 60
Arterial pH suspect of MH:
<7.25
Percent of respiratory acidosis, metabolic acidosis, and muscular abnormalities
99%
26%
80%
Suspect of MH by monitor with pulse ox, capnography, temp
- 3%
- 2%
- 9%
Percent of MH with use of only sux
.7
Percent of MH with use of sux and volatile
53.9
Percent of MH with use of only volatile
45.1
Percent of MH with no sux or volatile
.4
5 steps to treatment of MH
- Declare MH
- Discontinue triggering agents
- Abandon machine
- 100% O2 at high flow
- Give dantrolene
- Postsynaptic muscle relaxant that lessens excitation-contraction coupling in muscle cells
- inhibits Ca++ ions release form SR stores by antagonizing ryanodine receptors
Dantrolene
Primary drug used to treat and prevent MH
Dantrolene
Amount of minimum stock of dantrolene in hospitals
36 vials
Dantrium/revonto amount should be in each institution
36 vials
Ryanodex amount should be in each institution
3 vials
Percent of release rate for MH
19%
Systemic activation of blood coagulation, which results in generation and deposition of fibrin, leading to microvascular thrombi in various organs and contributing to multi organ dysfunction syndrome
Disseminated intravascular coagulopathy (DIC)