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Localization of the nero system
Intracranial
Forebrain, brainstem, cerebellum
Spinal cord
C1-5, C6-T2, T3-L3, L4-S1
PNS
Somatic nerve, muscle, NMJ, autonomic nerve,
Enteric nerve
Mentation/behavior
Brainstem dx:
LOA, dull, coma
Use ascending reticular activating system (ARAS)
level of awareness
Foerbrain dx:
Confusion, disorientation, loss of learned behaviour, compulsive behaviours
Gait
slowly, strait, turns, fatigue, free, joint flexion or extension
Plegia: absent gait generation
Paresis: weakness, min gait generation
LMN: maintains tone, short strided
UMN: gait generation, slower protraction and longer stride, ataxia
Ataxia: without order, long stride and has unpredictable foot placement
Cerebellar: hypermetric, head tilt/listing/falling, Slow nystagmus (<60 per min), sm circles, rolling
Cerebrum: Lg circles, contralateral sign, precept issues, side step
forebrain dosnt’t influence gait
Posture
Postural Reactions: test 2x, support, do all limbs
Paw position, hopping, bracing
Muscle tone: symmetry
focal loss in 8d from nerve dx
Cranial tibial from L7-S1 disk/stenosis
Decerebrate: head up, legs strait down
Decerebellate: downward dog posture
Schiff Sherrington: extended front limbs
T3-L3
Reflex testing
Done standing or lateral
Pelvic Limb: patellar, cranial tibial, calcaneal or gastrocnemius, and withdrawal
Thoracic Limb: biceps, extensor carpi, triceps and withdrawal
Cutaneous trunci
key for localization
Perineal
Withdrawal in reflex testing
LMN stimuli to withdrawal limb
continued emotional rxn post stimuli = deep pain
Squeeze toes and watch
Which joints flex? Is it complete? does the animal kick?
Crossed extensor in lateral = UMN
LMN signs
Weakness, decreased tone, decreased reflexes
withdrawal
Short stride, proprioceptive deficit
Slow to rise/slow to sit, dribble urine or drop stool
L7S
UMN Signs
Descending Tract Failure
Weakness, Increased reflex, long stride, Increased tone
Ascending Tract Failure
Proprioceptive ataxia, Postural deficit
Peripheral neuropathy/myopathy
LMN signs
Short stride, weakness, good proprioception
Frequently normal cranial nerves??
Systemic signs
WBC, temperature, malaise
Cranial Nerves
CN II: menace, tracking, obstacle course, PLR
CN III: PLR, head movement, Strabismus
CN IV: head movement, Strabismus
CN V: facial sensation/tone
CN VI: head movement, Strabismus
CN VII: facial sensation/tone
CN VIII: head movement, Strabismus
CN IX: gag reflex, resp sounds, tounge
CN X: gag reflex, resp sounds, tounge
CN XI: gag reflex, resp sounds, tounge
CN XII: gag reflex, resp sounds, tounge
Mence response
CN II
dev @ 12-16w
Forebrain dx
Contralateral to the lesion
opp if its cerebellar (rare)
Abnormal PLR and menace = Rostral to the diencephalon
Normal PLR but abnormal menace: Caudal to the diencephalon
Horner’s Syndrome
MOA: Long pathway within the CNS and periphery
Brain, cervical, thoracic, and middle ear disease
Consider both CNS and systemic diseases
can be partial or complete
CS: Miosis, Ptosis, Nictitans protrusion, Enophthalmos, Sweating (horse)
DDX: parasympathetic dx
2 cat an 5 dog branches
weird pupils (D in cats)
Retention/Storage of urine
Pontine storage to hypogastric nerve (T10-11) detrusor and trigone
Pudendal nerve to external urethral and anal sphincter
Voluntary control regulated by the forebrain
Cerebellar inhibition of urination
Dysfunction in different parts of the brain
Forebrain
Seizures, near normal gait, compulsive behaviours, inappropriate urination
Lg circles to lesion, contralateral sensory deficits
Brainstem
Altered gait, altered LOA, proprioception
Cerebellum
Intention tremor, postural reaction issues,
hypermetric gait, wide stance, normal strength
Vestibular
• Central: gait and proprioceptive issues
• Peripheral: normal tone, proprioception, nystagmus opp lesion, head tilt, rolling to lesion
Disfunction in different parts of the spine
C1-5: Long stride and ataxia, proprioceptive deficits, weakness, increased tone and reflexes to all four limbs
C6-T2: Short stride, decreased reflexes, withdrawal changes and tone in front, long stride with ataxia, increased tone and reflexes in hind, proprioceptive deficits, in all four
T3-L3: Normal front, long stride with ataxia in hind, proprioceptive deficits, altered tone, and reflexes, cutaneous trunci changes, bladder control.
L4-S1: Normal front, short stride in hind, flopping of the distal limb, altered withdrawal, decreased reflexes and tone, slow to rise/sit, tail drop, incountenance
Seizure-like Episodes
Cataplexy, narcolepsy, REM sleep disorder
Vestibular episodes
Panic attack
Episodes of neuromuscular disease or encephalitis
Myoclonus
Syncope
Cervical muscle spasm
Head bobbing & breed associated muscle disorders
Seizure terms
Seizure: a sudden attack or convulsion
Status epilepticus: a persistent seizure >5 min, lowers lifespan
Cluster seizures: >1 in 24hrs, lowers lifespan
Non-convulsant seizure: sensorium only, lowers lifespan, common w/ clusters, ECG req
Refractory seizure: multi tx fail
Super-refractory: ER tx fail
Seizure causes
NT changes: High excitatory NT or Low inhibitory NT
Young (<1y): infectious, anomalous, metabolic, trauma, toxin
1-5y: idiopathic
>5y: neoplasia, infarct, inflam, metabolic, infection
Refractory seizure cases
MOA:
multi tx fail
Aussie, colie, Italian Spinoni
Tx:
Be aggressive >2 anticonvulsants
Rescue and emerg plan
Set expectations
6m monitoring & CBC
General treatment of seizure cases
Goal: <1seziure every 3m
Establish:
emerg, monitoring, tracking plan
maintenance, post episode tx
Consider:
Who, what, where, when, why?
Postictal phase behaviour (recovery)
takes 5 ½ lifes to reach steady state w/ meds
Phenobarbital
Use: anticonvulsant
MOA: Ca/Na channel, Gaba
Monitor:
Liver, Bone Marrow, Skin, Endocrine toxic
BW 2w after changes then 6m
high metab of T4 and P450
Loading: 16-30 mg over 24hrs in 1-6 doses
Keppra
Use: anticonvulsant
DEA not req
MOA: Ca channel, NT release
Loading: 60-100mg/kg IV
Potassium Bromide
Use: anticonvulsant
not in cats: pneumonia
MOA:
Membrane stabilization/hyperpolarization
24hrs ½ life
Monitor: Pancreatitis, Esophagitis
3m after changes then yearly
high Cl
Loading: 400-600mg/kg over 5d
1/2 dose q12 to avoid nausea
Zonisamide
Use: anticonvulsant
MOA: Na channel
Monitor: idiosyncratic/acidosis
Emergency and rescue plan
Home
Repeat maintenance meds 1-3x
New med w/ short half life for 1-3d
Diazepam/midazolam: IN 80% or rectal 60%
ER/Clinic
Hospitalization after >3 till 24hrs clear
Supportive care
Load meds or new meds
Diagnostics, MRI, EEG
Benzo
AKA: Diazepam/Midazolam
Use: active seizures
MOA: Gaba
Action of 15-30min
Tolerance 1-2w
Ketamine
Use: Refractory Status Epilepticus
no rxn w/ benzos
MOA: NMDA
Steps:
see EEG w/ active seizure
give w/ Propofol to stop movement
super-refractory epilepsy treatment
Meds:
Ketamine-Dexdomitor
Propofol to stop movement
Other:
Induce hypothermia (36.7-37.7)
Indications:
no rxn to benzos
continues seizure
Stages of Feline seizures
Prodromal: behavior/personality change
Aura: sensory type change/anticipation
Ictus: seizure phase
Post-ictal: persistent deficits min-days
High ALP/ALT, ataxia, aggression, disoriented, vison loss
Feline seizure causes
Neoplasia: meningioma #1
cats see changes in behaviour
dogs have seizures
FIP: ventriculitis & diffuse inctercranial/spinal signs, high protien fluid
Ischemic encephalopathy: Parasite migration through the brain, variable forebrain signs, sneezing
Stroke: renal, endocrinopathies, hypertension, systemic disease
Idiopathic: bimodal, normal neuro exam, 9-12y cats
Seizures maintenance in cats
Leviteracitam, Zonisamide, Phenobarbital, Topomax
NO KBr: pneumonia
Treating disk disease
NSAIDS: better QOL score & recovery
Sx: best tx, timeline does not impact has recovery or success
Acupuncture: faster recovery
Physical therapy: better recovery
Glucocorticoids: contradicted
Methylprednisolone: no benefit, reduces bld flow & PMN’s
Cage rest: no benefit
Evaluating disk disease prognosis
Moderate reoccurrence for rx and low for sx
Higher grade worse rx prognosis, sx indicated
Thoracolumbar
Paraplegia/deep pain negative: poor rx, moderate sx
Paraplegia/deep pain positive: moderate rx, good sx
Non-ambulatory paraparesis: moderate rx, good sx
Ambulatory paraparesis: moderate rx, good sx
Paraspinal hyperasthesia: good rx, good sx
Cervical
Grade I-III: moderate rx, good sx
Grade IV-V: low sx, moderate sx
Testing for disk disease
Deep pain negative: eval w/ MRI
Evalute breed, focality, progressiveness
??????Myomalasia: diaphragm innervation issues, risk w/ acute
C6-7 keep u from heaven, C5-4 keeps you from the door (diaphragm)
DDX: Fibrocartilagenous emboli, Acute non-compressive nucleus pulposus extrusion, cancer, metabolic dx, malformations
Hydrocephalus
MOA: Active distention of ventricular system obstruction flow
breed mesencephalic stenosis, acquired
CS: High ICP, white matter pressure, cortical atrophy, dome head, altered behavior, seizures, stupid, ataxia, circling, blindness
ID:
Congenital: MRI, CT, US
Acquired: MRI, CSF
Tx: Long term pred & Omeprazole, ventriculoperitoneal shunt sx, ventriculostomy sx
Atlanto-occipital or axial junction malformations
MOA:
AO: overlap, concussive, medulla compression
AA luxation: cranial/cervical spine concussion
CS: paresis, plegia, vestibular signs
ID: CT, MRI, C2 rads (AA)
Tx: sx stabalization, braces (1” rolled gauze “dough nuts” in emerg)
Avoid ventroflexion
Caudal occipital junction malformations
MOA: overcrowding of fossa, poor fluid dynamics, herniation, cerebellum/medulla compression
CS: hyperesthesia, phantom scratching, ataxia, vestibular signs, paresis, vocalization, face rubbing, seizures
ID: CT, MRI
Tx: Long term, NSAID, Steroid, gabapentin/lyrica, omeprazole, sx w/ short term success but reoccurs
Vertebral malformation
MOA: segment failure or trama
transition, butterfly, block, wedge, hypoplasia (pugs/frenchies), hemivertebra
Scoliosis, lordosis, kyphosis: brachiocephalic breeds
young T3-L3 myelopathy or old w/ multi disk injuries
CS: paraspinal discomfort, paresis, plegia, incontinence, ataxia
UMN signs
ID: MRI, rads
Tx: NSAID, gabapentin, sx stabilization
gliosis/atrophy of spinal cord = guarded the prognosis,
Arachnoid diverticula
MOA: ?
Dilation of the arachnid space in caudal cervical/thoracolumbar spine
Brachycephalic, Rotty
Tx: decompressive/stabilizing sx
Localizing spinal cord/myelopathies based on CS
C1-2
UMN: all limbs and bladder
C6-T2:
UMN: hind limb and bladder
LMN: front limb
T3-L3
UMN: hind limb and bladder
L4-S1:
LMN: hind limb and bladder
Steroid responsive meningitis arteritis
MOA: 6m-2y Beagle, Berner, Boxer
CS: low head, stiff
ID: Febrile 103-105, neutrophilia, high IGA, CSF
Tx: Steroids, cyclosporine
Discospondylitis
MOA: Infection of the disk/endplate
lg dogs
CS: Pain, empyema/disk extrusion
ID: difficult, rad, MRI, CRP, culture, urine analysis
Tx: C&S antibiotics (6-12m), analgesic, euth w/ brucella
Infection/empyema of the spine
MOA: Grass awn from resp into L4 @ diaphragm
CS: Cough, pain
Tx: Sx, long term antibiotics
Tetanus
MOA: 1-3w post wound or sx
Travels retrograde to block interneuron
CS: rhesus sardonus, extensor rigidity, light/sound hypersensitivity, saw horse stance, lock jaw
Tx: antibiotics, clean, antitoxin, high mortality
Degenerative Myelopathy
MOA: Progressive degeneration SOD 1 mutation
GSD, Boxer, Corgi (still RARE
CS: Non painful, Ataxia
ID: genetic screening (purple top MSU/OFA)
neg, carrier, affected
Tx: fucked, PT, 6-18m till euth
Trigeminal neuritis
CS: Drop jaw/bilateral
Tx: assist feed, 6w to fix
Polyradiculoneuritis
AKA: Coonhound paralysis
MOA: Rapid porgression
CS: LMN signs w/ intact sensation, Rapid atrophy 8d, normal cranial nerves
Tx: 4-6w recovery, can relapse, spontaneous
Laryngeal paralysis
MOA: Vibration of larynx causes
think horses
CS: Roaring, heat/exercise intolerance
Tx: Tie-back
Nerve sheath tumor
MOA: Trigeminal, brachial plexus, pelvic plexus
CS: focal rapid atrophy, progressive
ID: palpate, US
DDX: mononeuropathy
Endocrinopathies
CS: Classic Cushing’s signs, stiff stilted gait
Tx: Do not recover motor function
Immune myopathies
MOA: location dependent, Immune attack on musle/NMJ
Masticatory muscle embryo distinct
CS: swelling, pain, progresses atrophy, fibrosis
ocular myositis: eye bulge
Junctionopathy: aspiration
ID: AB titer, biopsy, eosinophils, high CK/CPK/AST
Poly myositis is tricky
Tx: Immune suppress (steroids)
Myasthenia Gravis
MOA: acquired or congenital, thymoma
CS: Exercise intolerance, fatiguable palpebral, megaesophagus, regurge, sits
Tx: Tensilon, pyridostigmine, mass remvoal sx
Dealing with Head trauma
ID:
Breathing patterns, Postures, Diaphragm, forebrain CS
Brainstem evaluation: LOA, UMN function, reflexes
Score of 1-6 for each, total >8 = 50% survival @ 48hrs
Cushing’s reflex: high ICP, low CBF, high CO2
life threatening
Tx: replace fluids, NSAIDS, fentanyl, benzodiazepines, ketamine, dexmetatomidine, propofol, anticonvulsant medications
Short acting reversible drugs
High ICP
MOA: Cushing’s reflex
high ICP, low CBF, slow HR, high CO2
life threatening brainstem issue
CS: Slow HR (<60), high BP (>150), brain stem CS
Tx: incline to 30o, lower metab (barbiturate/sedation), anticonvulsants (Keppra/phenobarbital), electrolytes (Mannitol/hypertonic saline)
Hyperosmolars
Mannitol: sugar, osmotic diuretic, decrease CSF production, draws extracellular fluid into vessels, rheologic/improve cerebral blood flow
Hypertonic saline: Salt, osmotic diuretic, draws extracellular fluid into vessels, improved cerebral blood flow, less diuretic effect
Can dehydrate a patient if used alone
Contradictions: not for intracranial hemorrhage
Meningoencephalitis
MOA: inflam of brain/meninges
Sm dogs: pug, korkie, Maltese
CS: rapid progression (3-7d), status epileptics, blindness
DDX: peripheral vestibular disease
Caudal Fossa
MOA: immune CNS dx
bacti, fungi, viral, parasites
forebrain/brain stem issue
CS: balance loss, side stepping, peripheral vestibular dx
ID: MRI, CSF, Myringotomy
Peripheral vestibular dx
Nystagmus greater than 60bpm
Head tilt
Falling/rolling
Normal proprioception, mentation
Cranial nerve 7 dysfunction
Myringotomy
Otoscope/endoscope w/ tom cat catheter
Puncture TM
Culture material beyond TM
Otitis
ID: Culture canal or myringotomy
Tx:
Antibiotic/fungal, topical if tympanum is intact
Media/interna will require long tx
Sx
Meningitis
ID: MRI, CSF
Tx: Immune suppress (steroids, cyclosporine), chemotherapeutics
long tx