- Shuffle
Toggle OnToggle Off
- Alphabetize
Toggle OnToggle Off
- Front First
Toggle OnToggle Off
- Both Sides
Toggle OnToggle Off
Front
How to study your flashcards.
Right/Left arrow keys: Navigate between flashcards.right arrow keyleft arrow key
Up/Down arrow keys: Flip the card between the front and back.down keyup key
H key: Show hint (3rd side).h key
![]()
PLAY BUTTON
![]()
PLAY BUTTON
![]()
85 Cards in this Set
- Front
- Back
|
What are the 4 major categories of musculoskeletal disorders?
|
(1) Abnormal electral conductions resulting in fasiculations or abnormal tone
(2) Muscle atrophy (3) Rhabdomyolysis (4) Muscle dysfunction w/normal CK |
|
Usually myopathies are characterized into which three divisions?
|
Exertional, non-exertional, or miscellaneous
|
|
What are some signs to look for on physical exam for a myopathy?
|
Lameness or pain
Alterations in muscle texture/tone Symmetry Atrophy Muscle response to percussion |
|
How long does it take CK to peak? Elevated CK indicates damage within what time period?
|
CK peaks in 4-6 hours.
Indicates damage within 3 days. |
|
How long does it take AST to peak? Elevated AST indicates damage within what time period?
|
AST peaks in 24-48 hours.
Indicates damage within 14 d. |
|
How may significant muscle damage manifest in the urine? What is the "CK cutoff" for this?
|
Myoglobinuria occurs when CK >20000.
|
|
How high must the CK be before brown urine is seen?
|
CK>40000
|
|
Which tube type and blood fraction is best for measuring vitamin E? Selenium?
|
Serum or plasma in a plain or heparin tube for vitamin E.
Whole blood in EDTA for Se. |
|
When performing a muscle biopsy, should the sample be formalin fixed or frozen?
|
Frozen provides better results!
|
|
Where is a good place to take a muscle biopsy in the horse?
|
Semimembranousus halfway between tuber ischii and achilles tendon
|
|
How should normal muscle behave in electromyography?
|
Minimal spontaneous activity
|
|
Abnormal EMG can confirm:
a) myopathy b) neuropathy c) denervation d) HYPP |
a) myopathy
b) neuropathy c) denervation d) HYPP |
|
What are some clinical signs of exertional rhabdomyolysis?
|
Sweating
Stiff & reluctant to move fasiculations Firm muscles Brown-red urine (other non-specific signs) |
|
What are the two types of exertional rhabdomyolysis?
|
Chronic and Sporadic
|
|
Which muscle fibers are affected in equine ER?
|
Type II fibers
|
|
Which drug is great for preventing further muscle damage? What is a possible side effect?
|
Dantrolene (can induce hyperkalemia)
|
|
Predict the relative electrolyte levels in a horse with exertional rhabdomyolysis.
|
K and P UP
Ca, Na, and Cl DOWN |
|
What are the 2 forms of chronic equine exertional rhabdomyolysis? How can they be differentiated?
|
Recurrent ER
Polysaccharide Storage Myopathy (differentiate by biopsy) |
|
PSSM is more common in which horse breeds?
|
Drafts, QH related breeds, warmbloods
|
|
Recurrent ER is more common in which horse breeds?
|
Thorobreds, Arabs, Standardbreds
|
|
What is the typical signalment for RER?
|
Nervous 2yo thoroughbred filly
|
|
What is the pathogenesis for RER?
|
Abnormal intracellular Ca regulation
|
|
How can RER be prevented?
|
Reduce stress
Good warm-up b4 exercise Good quality grass hay Electrolyte supplement Address lameness |
|
How is RER transmitted?
a) ticks b) flies c) autosomal recessive d) autosomal dominant |
d) autosomal dominant
|
|
What is a common presentation of a draft horse with PSSM?
|
Asymptomatic w/normal CK
|
|
What is a common presentation of a QH with PSSM?
|
Classic ER signs; persistent increase in muscle enzymes
Occasional epaxial wasting |
|
What mutation causes PSSM in draft horses? In quarterhorses?
|
Glycogen Synthase 1 mutant in BOTH (just different signs)
|
|
How can PSSM be diagnosed?
|
Genetic testing for GYS1 gene (type I)
Biopsy (type I or type II) |
|
What are the two types of PSSM and how do they differ?
|
Type I (has mutant GYS1 gene)
Type II (no mutated gene but positive biopsy) |
|
What is seen on a positive PSSM biopsy?
|
High muscle glycogen (purple)
Amylase-resistant PAS-positive inclusions Subsarcolemmal vacuolations |
|
How can PSSM be managed?
|
Regular exercise + low starch, high fiber, and fat supplemented diet.
|
|
What are the categories of non-exertional myopathies of large animals?
|
Inflammatory
Trauma Toxic Nutritional Metabolic Idiopathic |
|
Clostridial myositis is often associated with:
|
IM banamine or ivermectin
Also vaccines, furosemide, xylazine, and vitamin B acupuncture |
|
What are signs of clostridial myositis?
|
Rapid onset of pain (48hrs)
Fever gas pockets in affected region Tachycardia/tachypnea lame discolored membranes sometimes cool region develops |
|
How can clostridial myositis be diagnosed?
|
Clinical signs mostly
Ultrasonography (fluid pockets, gas, edema) Mild to moderate CK/AST increase Toxemia and inflammation Anaerobic culture Cytology |
|
What organisms cause clostridial myositis? What is the prognosis for each?
|
C. perfringens (better prognosis but higher degree of IMHA)
C. septicum (worse prognosis) |
|
How can the urine fractional excretion be determined?
|
Measure serum and urine creatinine along with electrolyte concentration in serum and urine. Normalize ratio using creatinine.
|
|
Which drugs are currently used to treat clostridial myositis in horses?
|
Metronidazole
Oxytetracycline Choramphenicol |
|
How can clostridial IMHA be determined?
|
See autoagglutination in the blood after venipuncture
|
|
What are some non-pharmaceutical management techniques for clostridial myositis?
|
Debride and flush
IV fluids hydrotherapy topical wound therapy fly control |
|
What go-home antibiotics should be given to a horse with clostridial myositis?
|
Metronidazole or doxycycline
|
|
What is the prognosis for clostridial myositis?
|
68% mortality!
|
|
What is the common signalment for a ruminant with clostridial myositis?
|
Dead feedlot cow.
If they're alive, then fever, tachypnea, anorexia, depression with swelling and pain at affected site |
|
How can clostridial myositis be prevented in ruminants? In horses?
|
Ruminants (vaccinate)
Horses (no vaccine; avoid inappropriate IM injections) |
|
What are two causes of viral myositis in horses?
|
EHV1 and Equine Influenze A2
|
|
How is sarcocystis myositis treated in ruminants? Horses?
|
Ruminants (amprolium or ionophore abx)
Horses (anti-inflammatories, TMS + pyramethamine or ponazuril, steroids??) |
|
What are the three forms of myopathies associated with respiratory pathogens? Which is most common?
|
Immune-mediated polymyositis (most common)
Acute S. equi-associated rhabdomyolysis Infarctive hemorrhagic purpura |
|
Which respiratory pathogens can cause myopathies? What is the most common one?
|
S. equi most common
Also S. zooepidemicus, R. equi, C. pseudoTB) |
|
Which of the following are associated with respiratory-associated myopathies?
a) atrophy b) significantly elevated CK c) mildly elevated CK/AST d) asymptomatic presentation |
a) atrophy
b) significantly elevated CK |
|
What horse breed is typically impacted by immune-mediated polymyositis?
|
young quarterhorse
|
|
What is a typical finding upon physical exam of an animal with immune mediated polymyositis?
|
severe and rapidly progressive muscle atrophy of the gluteal and epaxial muscles
|
|
What will be seen on a biopsy of a horse with immune-mediated polymyositis?
|
Lymphocytic inflammation
Anguloid atrophy Fiber necrosis and regeneration |
|
How is immune-mediated polymyositis treated?
|
Immunosuppress (dexamethasone and prednisolone)
|
|
What proportion of immune-mediated polymyositis cases have a respiratory infection?
|
only ~30%
|
|
What laboratory anomalies are seen with S. equi rhabdomyolysis?
|
(CBC) mature neutrophilia, hyperfibrinogenemia
(Chem) marked elevations in CK; LOW serum protein M |
|
If you see a horse with lymphadenopathy and/or gutteral pouch empyema with stiffness and muscle pain, what should you be thinking? What is the prognosis?
|
Strangles and S. equi rhabdomyolysis; very poor prognosis
|
|
If a horse develops stiffness and colic within 3 weeks of vaccination against S. equi, what should you be thinking? What is the prognosis?
|
Infarctive purpura; very poor prognosis
|
|
What lab abnormalities will be seen with infarctive purpura?
|
Left shift neutrophilia & toxic change
Hypoalbuminemia Marked high CK and AST HIGH serum M protein |
|
What are two main differences in labwork that differentiate infarctive purpura from S. equi rhabdomyolysis?
|
HIGH Serum M, Left shift neutrophilia in Purpura;
LOW serum M, mature neutrophilia in rhabdomyolysis |
|
Traumatic myopathies are frequently related to what event?
|
Anesthesia
|
|
What are common sites for traumatic myopathies?
|
Gluteals
Triceps Adductor muscles (draft horses) |
|
How can traumatic myopathies be treated?
|
Dantrolene (maybe pre-med)
Anti-inflammatories and analgesics IV fluids keep patient standing! |
|
What are some differentials for heat stress myopathy in the down camelid?
|
Meningeal worm
Trauma Systemic illness |
|
What conditions are associated with Atypical Myopathy?
|
Spring
Sudden, inclement weather Animals at pasture >12h/day |
|
What are the major syndromes in nutritional myopathies? Which nutrients are they linked to?
|
Skeletal muscle necrosis
Myocardial and diaphragmatic involvement Masseter muscle inflammation; (both due to VitE and/or Se deficiencies) |
|
Which nutritional myopathy has a slower onset?
|
Skeletal muscle necrosis
|
|
Which nutritional myopathy involves sudden death?
|
Myocardial and diaphragmatic involvement
|
|
Describe the pathophysiology of nutritional myopathies?
|
Oxidative damage; (Vit E is a free-radical scavenger; Se is necessary in glutathione peroxidase)
|
|
If you see a seizing foal with high CK, muscle weakness, and persistent leukopenia, what might you think about?
|
Glycogen Branching Enzyme Deficiency
|
|
What are the two manners in which muscle can atrophy?
|
Myogenic
Neurogenic |
|
T or F:
Myogenic atrophy affects both type 1 and 2 fibers while neurogenic only affects type 1. |
False!
Neurogenic affects both Myogenic only affects type 2 |
|
Neurogenic atrophy due to prolonged vitamin E deficiency is called...
|
Equine Lower Motor Neuron Dz
|
|
What are some causes of muscle fasciculations?
|
Physiological response
Viral encephalitis Hypocalcemia Ear ticks HYPP Myotonia |
|
Which tick can cause fasciculations? What is the pathogenesis?
|
Otobius (ear tick); toxin alters Ach release from presynaptic terminals
|
|
Delayed muscle relaxation is known as...
|
...myotonia
|
|
Describe the pathogenesis of myotonia.
|
Abnormal membrane excitability due to reduced permeability to Cl.
|
|
Percussion dimpling is a sign of...
|
...myotonia
|
|
What is a pathognomic test for myotonia?
|
EMG ("dive bomber pattern")
|
|
Biopsy of an animal with myotonia will show...
|
...fiber size variation; hypertrophy of type 1 fibers
|
|
Which channel is impacted in HYPP?
a) Ca channel b) K channel c) Na channel d) Cl channel |
c) Na channel
|
|
What are signs of HYPP?
|
Episodic weakness
Protrusion of 3rd eyelid Facal myotonia Sweating and fasciculations Dog-sitting |
|
Which of the following are congruent with HYPP?
a) High CK/AST b) Normal biopsy c) Abnormal EMG d) Hyperkalemia |
b) Normal biopsy
c) Abnormal EMG Note - CK/AST is NORMAL; hyperkalemia is VARIABLE |
|
How can HYPP be treated acutely? How can it be managed?
|
Acute (IM adrenaline; feed grain or corn syrup; maybe Ca gluconate, dextrose, and/or NaHCO3)
Manage with low K in ration |
|
Hypocalcemia in horses is assocated with...
|
...lactation and transport
|
|
Hypocalcemia must be differentiated from what infectious disease?
|
Infectious tetanus!
|