26.neuro_exam Flashcards

1
Q

6 parts of a neuro exam

A
  1. sensorium and behavior2. posture and gait3. postural reactions4. spinal reflexes, muscle mass, muscle tone5. cranial nerves6. cutaneous sensation
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2
Q

obtunded vs stupor vs coma

A

—obtunded—decreased arousal in response to touch/voicedepression—stupor—arousable to vigorous stimuli but response is incomplete or inadequate–coma—sustained unresponsiveness to stimuli

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3
Q

alteration in sensorium is typically due to what disturbances

A
  1. disturbance in the ascending reticular activating system2. disturbance in cerebrum3. disturbance in the limbic system (cerebrum/brainstem–diencephalon)suggests intracranial disease
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4
Q

define lower motor unit

A
  1. ventral horn cell2. axons of peripheral nervous system3. NMJ4. innervated muscle
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5
Q

decerebrate vs decerebellate rigidity

A

both indicate disruption of descending inhibitory influence on the nerves going to extensor musclesdecerebrate—opisthotonous, mentation changes/menace, rigid neck x 4 limbs—-indicate midbrain or rostral cerebellar lesiondecerebellate—opisthotonous, do not always affect mentation, rigid neck x 4 limbs but hind limbs FLEXED—-indicate SEVERE cerebellar lesion

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6
Q

area of nervous system leading to gait abnormalities

A

midbrainstem and caudal (caudal brainstem, spinal cord, peripheral nerve)ataxia (vestibular, cerebellar, proprioception)weakness (can be UMN or LMN)lameness (LMN or ortho)

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7
Q

T/Fchronic structural changes in prosencephalon do NOT result in obvious gait abN

A

TRUEchronic structural changes in prosencephalon do NOT result in obvious gait abN

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8
Q

variation in LMN paresis/gait

A

mild-moderate LMN dz: ambulatory with short, choppy, stilted gaitSevere LMN dz: non ambulatory or tetraplegicnot usually ataxic bc GP pathways are unaffected

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9
Q

modified franked scoring

A

0 plegia with no deep pain1 plegia with no superficial pain2 plegia with nociception intact3 nonambulatory paresis4 ambulatory paresis , ataxic5 spinal hyperesthesia only

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10
Q

variation in UMN paresis/gait

A

long strided, spastic gaitgeneral proprioceptive ataxia

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11
Q

why is it difficult to separate general proprioceptive ataxia vs UMN dz

A

adjacent pathway anatomicallytherefore it is difficult to separate the effect on gait caused by dysfunction of descending UMN path vs dysfunction of ascending proprioceptive pathwaysdogs w only proprioceptive ataxia are assumed to have UMN dz

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12
Q

T/Fanimals with LMN dz/neuromuscular dz actually have NORMAL postural rxn

A

TRUEanimals with LMN dz/neuromuscular dz actually have NORMAL postural runbecause a LACK of disruption of general ascending proprioceptive pathways. Therefore, rely on spinal reflexes to dx

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13
Q

what do normal postural run depend on

A

intact conscious AND UNCONSCIOUS proprioception and intact UMN and LMNSENSORY –>DORSAL HORN (IPSILATERAL SPINAL CORD TO MIDBRAIN Unconscious Proprioception, CONTRALAT PROESNCEPHLAON Conscious Proprioception)

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14
Q

T/Fa dog with NM dz (ie. myasthenia gravis) may still have proprioceptive deficits

A

TRUEeven though the lesion is NOT in the proprioceptive pathway the dog is too weak to return paw to normal anatomic position

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15
Q

most reliable spinal reflexes

A

patellar withdrawal

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16
Q

patellar reflex

A

L4-L6femoral nstifle extension(maybe abN in older dogs without signs of neuro dz)

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17
Q

the finding of an absent or hyporeflexia spinal reflex indicates a problem where?

A
  1. afferent limb2. efferent limb3. spinal cord segment involved in reflex arc
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18
Q

the finding of a hyper reflexive spinal reflex indicates a problem where?

A

lesion cranial to the spinal cord segment containing the reflex arc

19
Q

biceps and triceps spinal reflex

A

biceps reflex–musculocutaneous n (C6-8)–slight flexion of elbow, and movement over muscletriceps reflex–radial n (C7-T2)–slight extension of elbow, contraction of triceps

20
Q

pelvic vs thoracic withdrawal spinal reflex

A

pelvic withdraw–sciatic n (L6-S1)thoracic withdraw–brachial plexus n (C6-T2)(S-S)-M-A-R-M-UComplete flexion of all joints!!

21
Q

stance of dogs with sciatic nerve injury

A

PLANTIGRADE due to tibial nerve dysfunction (which is a branch of sciatic, courses medially to innervate gastrocnemius muscle)PAW MISPLACED ONTO DORSUM due to peroneal nerve dysfunction (which is a branch of sciatic, courses laterally to cranial tibialis muscle)LMN dz BUT pelvic limb is not usually short strided but rather exaggerated and “flings” foot forwardlimb will be able to support weight if femoral nerve is intact bc stifle can be extended to bear weight; hip is flexed

22
Q

where do the median and ulnar nerves innervate

A

PALMAR

23
Q

where does the ulnar nerve innervate

A

LATERAL aspect of DIGIT 5

24
Q

where does radial nerve innervate

A

dorsum of footcranial and lateral antebrachium

25
Q

where do ulnar and musculocutaneous nerves innervate

A

caudal and medial antebrachium (ulnar n) and brachium (musculocutaneous n )

26
Q

where do perineal and tibial branches of the sciatic nerve innervate

A

dorsal (peroneal n ) and plantar (tibial n)

27
Q

where does the saphenous branch of femoral nerve innervate

A

medial aspect of pelvic limb (digit 1)in some patients, innervation by the saphenous nerve is not present distally.

28
Q

perineal spinal reflex

A

sacral and caudal branches of pudendal nerveS1-S3

29
Q

Cutaneous trunci reflex

A

sensory input via dermatomes lateral thoracic nerve C8-T1—>cutaneous trunci musclereflex is preserved for 1-2 vertebral bodies caudal to the level of the spinal cord lesion

30
Q

cranial nerves

A

ooottafvgvah pg 332olfactoryopticoculomotortrochleartrigeminalabducensfacialvestibularglossopharyngealvagus accessoryhypoglossal

31
Q

menace reflex

A

most reliable for visiontests 2 optic, 7 fascial innervation orbicularis oculi mlearned response 10-12 wk of age

32
Q

why does an indirect PLR occur

A

PLR tests 2 optic, 3 oculomotor nindirect/consensual response occurs bc crossing over fibers at optic chasm and pretectal nuclei to stimulate parasympathetic oculomotor nerve and iris muscle–> constriction of pupil

33
Q

horners syndrome

A

loss of sympathetic innervation to the eye1. ptosis2, third eyelid elevation3. miosis4. enophthalmos

34
Q

course of autonomic nervous system four sympathetic fibers

A

preganglionic neuron–CNS (throughout TL spinal cord, join vagus/vagosympathetic trunk,ascend in sheath to cranial cervical ganglion)post ganglionic neuron–PNS (synapse at CC ganglion–near bullae, go to cranium via ophthalmic branch of trigeminal n to innervate muscle)effector muscle (muscle innervated dilator muscle of the pupil in the iris)

35
Q

ventrolateral strabismusmedial strabismuseyeball extorsion with CN dysfunction

A

ventrolateral strabismus–oculomotor n dysfunction (3)medial strabismus–abducens n dysfunction (6)eyeball extorsion–trochlear n dysfunction (4)trochlear dysfunction in cats also displays itself as lateral rotation of the dorsal aspect of the pupil

36
Q

palpebral reflex

A

5 trigeminal sensory (branches ophthalmic medially maxillary lateral)7 facial motor (branch–palpebral)

37
Q

trigeminal sensory function is tested with

A

nasal sensation 1. ipsilateral branch of ophthalmic and maxillary2. nociceptive path to contralateral thalamus / cortex

38
Q

what nerves control the GAG reflex

A

glossopharyngealvagushypoglossal

39
Q

how many spinal cord segments C, T, L, S

A

cervical 8thoracic 13lumbar 7sacral 3at least 2 caudal coccygealC1-5 C6-T2 (cervicothoracic intumescence) T3-L3 L4-S3 (lumbosacral intumescence)

40
Q

typical gait for C6-T2 lesions

A

2 engine gaitthoracic limbs–short choppy (LMN)pelvic limbs–long strides (UMN) with GP ataxia

41
Q

when is schiff-sherrington syndrome seen

A

peracute T3-L3 lesionsmarked increased extensor tone in thoracic limbsdue to disruption in ascending inhibitory axons arising from interneurons

42
Q

describe spinal shock

A

may occur as T3-L3 lesions in which pelvic limbs display LMN signsdue to transient disconnection btwn the facilitatory descending UMN that modulate function of LMN of the LS intumescence and the spinal neurons

43
Q

NM or LMN diseases

A

localized to NMJ, nerves (neuropathy) or muscles (myopathy); can be focal, multifocal, or diffusemay need ancillary testingCK, AST, electrolytesTick borne disease panelsTensilon testingAch Ab titerNerve/Muscle bxEMG