Muscle Disease Flashcards
How do we diagnose muscle dz?
- CS
- enzymes
- EMG
- muscle biopsy
- exercise challenge test
Describe AST enzyme and it’s use:
- is it muscle specific?
- how long does it take to see/leave?
- NOT muscle specific
- increases slowly (12-24h)
- stays elevated longer (2+ weeks)
Describe CK enzyme:
- is it muscle specific?
- how long does it take to see/leave?
- YES, muscle specific
- very sensitive
- reflects muscle damage
- peak around 6-8h
- decreases within 3 days
What will the CK value look like with:
- Recumbency with colic
- Venipuncture
- Rhabdomyolysis
- 500-1,000
- 300-1,000
- Tens/hundreds of thousands!
Describe the method of obtaining muscle biopsy:
Include unaffected + affected muscle
6mm biopsy
Exercise challenge test:
- method
- normal values
- increases
- 15-30min of light exercise
- normally won’t see any CK elevations
- 5x increase or more = rhabdomyolysis
What is the signalment for Hyperkalemic Periodic Paralysis
Quarter horses
Impressive-line horses
CS for HyPP:
- variable!
- intermittent signs by 2-3yo and normal btwn episodes
HyPP episode triggers:
Stress Sudden cold Transportation Sudden diet changes Surgery/anesthetic recovery
What are the CS associated with HyPP?
Prolapse of 3rd eyelid
Sweating
Muscle fasiculations
Cramping
- episodes can last min-hrs*
- some young horses that are HOMOZYGOUS can get upper resp muscle paralysis and resp stridor*
T/F: HyPP is autosomal recessive inheritance
False!
Autosomal DOMINANT
What [in terms of electrolytes] is abnormal in HyPP?
Abnormal Na channels
Hyperkalemia
Why are the Na channels abnormal? What is wrong with them?
Resting potential is closer to firing
Na channels remain open
T/F: Hyperkalemia in HyPP is only seen during an attack
True!
During attacks, high efflux of K occurs
Risk factors for HyPP
- fasting
- general anesthesia
- concurrent illness
- exercise restriction
How do we diagnose HyPP?
Gene testing
CS
HyperK in an episode