Module 1 Flashcards
(276 cards)
What causes Myasthenia Gravis?
Autoimmune B cell activation d/t infectious agent attacks acetylcholine receptors
What is Myasthenic Syndrome?
What causes it?
Decreased release of acetylcholine.
Usually paraneoplastic
Strength actually increases with exercise.
What is Neostigmine?
Acetylcholinesterase Inhibitor.
Increases amount of circulating acetylcholine.
What is HyperPP?
What channel does it effect?
Hyperkalemic Periodic Paralysis.
Na channel defect.
Basically can’t regulate changes in K level greater than 5.
What is HypoPP?
What channel is effected?
Hypokalemic Periodic Paralysis
Can’t tolerate K less than 3.0
CALCIUM or SODIUM CHANNEL DEFECT
What should be considered when administering anesthesia to a patient with any skeletal muscle channelopathy?
No succ. Susceptible to MH.
Optimize electrolytes
What is Anderson - Tawil Syndrome?
K channel defect with LOTS of cardiac conduction issues.
Develop periodic paralysis with that may or may not be associated with K level (hypo/hyper/normo).
Ten percent suffer a cardiac arrest!
What is Myotonic Dystrophy?
What considerations should be made for their anesthesia? (3)
Skeletal muscles are unable to repolarize after contraction.
- Extreme reaction to succ.
- PNS unreliable.
- Can get resp depression from narcs
What is Congenital Myopathy?
What anesthesia considerations should be made? (2)
Hypotonia and weakness at birth.
- Lots of respiratory mm dysfunction.
- SUSCEPTIBLE TO MH.
What is Duchenne Muscular Dystrophy?
How does it manifest?
What anesthesia considerations should be made? (3)
X linked recessive.
absence of Dystrophan.
Progressive paralysis, starts around age 12.
- Need cardiac eval every 2 years.
- No succ (rhabdo and hyperkalemia). Avoid halogenated inhalants
- Dysfunctional GI tract means increased risk of aspiration.
What is Becker Muscular Dystrophy?
Less severe than DMD. Later onset. Reduced cardiac risk, eval every 5 years.
What causes Guillain - Barre?
What are the manifestations?
Anesthesia considerations?
Autoimmune response to an infection causes the body to attack your nerves, moving from distal to proximal.
Resp dysfunction. Autonomic dysfunction can cause hypotension/tachycardia.
Noxious stimuli like intubation can cause large autonomic response.
Malignant Hyperthermia Common Triggers (4)
Succinylcholine
Halogenated Inhalants
Extreme physiologic stress
Heat exhaustion
MH Cause
Mutation of the ryanodine recepter
permits uncontrolled releast of Ca from sarcoplasmic reticulum
First Sign of MH
Increased ETCO2 that does not respond to increased ventilation
Acute Malignant Hyperthermia S/S
Muscle rigidity
Masseter Spasm
Respiratory AND metabolic acidosis
Hyperthermia may develop early or late
Dantrolene
Inhibits pathologic release of Ca
Initial dose 2.5mg/kg
May require up to 10-20 mg/kg
Which drugs are safe for MH susceptible patients?
What precautions should be taken in MH susceptibility?
OK: prop, benzos, opioids, NDMA, Nitrous
Remove or close all vaporizers
Flush machine with 100% O2
Charcoal filters
Have dantrolene readily available
What is Porphyria?
Manifestations?
Enzyme deficiencies in the Heme synthesis pathway cause a buildup of heme precursors that are toxic to the nervous system
Acute: Fever, tachycardia, N/V, ab pain, weakness, seizures, confusion, hallucinations
SEVERE Muscle weakness with resp failure
Hyponatremia (2/2 SIADH)
What drugs should be avoided with Porphyria?
When should porphyria be suspected?
barbituates and etomidate.
Delayed emergence or prolonged mm weakness after anesthesia
How is Acute Porphyria detected?
Urinary porphobilinogen detected within 5 minutes
What is Plasma Cholinesterase?
Enzyme synthesized in the liver to break down acetylcholine
ALSO Breaks down succinylcholine, mivacurium, procaine, chloroprocaine, tetracaine and cocaine.
What usually causes Cholinesterase Disorders?
What are some anesthetic concerns?
Usually caused by hepatic disease (cholinesterase is synthesized in the liver)
It hydrolyzes certain drugs, making them much more potent and long lasting
Since cholinesterase disorders are often undiagnosed until surgery, what is a prudent practice to prevent prolonged apnea?
Be certain that recovery from the initial dose of succ has occured before administering more muscle relaxant (succ or nondepolarizing)