Equine Myopathies Flashcards

1
Q

What are the two main diagnostic techniques for investigating muscle disease?

A

Muscle enzymes
Muscle biopsy

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2
Q

What are the two main muscle enzymes how long do they take to peak after a muscle insult?

A

Creatine kinase: peaks at 4-6 hours
AST: peaks at 24 hours

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3
Q

What are the two types of CK and AST sampling?

A

Single
Dynamic

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4
Q

Why may you see myoglobinuria with myopathies and why is this a problem?

A

Myoglobin released from muscle cells as they break down
Nephrotoxic

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5
Q

When is myoglobinuria usually seen?

A

Rhabdomyolysis

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6
Q

What are the two types of muscle biopsy you can take?

A

Bergstrom needle or open method

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7
Q

For exertional rhabdomyolysis and for equine motor neurone disease, which muscles are used to biopsy?

A

Exertional rhabdomyolysis - semimembranosus
Equine motor neurone disease - sacrocaudalis dorsalis

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8
Q

What are the main clinical signs of sporadic exertional rhabdomyolysis?

A

Usually affects hindlimb muscles
Stiff gait
May refuse to move
Muscles may be hard, painful and swollen

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9
Q

What is the cause of sporadic exertional rhabdomyolysis?

A

Overtraining/overexertion above the level of fitness

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10
Q

How would you treat sporadic exertional rhabdomyolysis?

A

Rest
NSAIDs
IV fluids

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11
Q

Which breed often sees recurrent exertional rhabdomyolysis and what is it due to?

A

Thoroughbreds
Due to an abnormality in calcium regulation

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12
Q

How can you prevent recurrent exertional rhabdomyoslysis?

A

Diet - high fat low starch
Exercise/turn out daily
Dantrolene

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13
Q

What is the aetiology of polysaccharide storage myopathy?

A

Glycogen storage disorder characterised by increased skeletal muscle glycogen concentration and the accumulation of abnormal amylase resistant polysaccharide in type 2 muscle fibres

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14
Q

What is the main form of prevention/treatment of polysaccharide storage myopathy?

A

High fat-low starch diet

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15
Q

What are the clinical signs of an atypical myopathy?

A

Sudden onset muscle weakness and stiffness
Quickly progesses to recumbency and/or death
May show respiratory difficulty
Usually afebrile with normal appetite

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16
Q

Which toxin causes atypical myopathy?

A

Hypoglycin A toxin

17
Q

What is the treatment for atypical myopathy?

A

Intensive care and nursing
IV fluids
Analgesics

18
Q

How would you prevent atypical myopathy?

A

Avoid affected fields
Amount of toxin can vary
Fence off around trees
Pick up seeds/leaves
Ensure plenty of grass and supplementary feed