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80 Cards in this Set

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  • Back
What elements are involved in the motor exam?
Strength, muscle bulk, reflexes, muscle tone, coordination, resting posture, gait
What is the scale by which strength is measured and what do each of the numbers stand for?
Strength is measured on a 0-5 scale.
5 = normal
4 = slight weakness
3 = just strong enough to move against gravity but not additional resistance
2 = can move, but not against gravity
1 = can see/palpate movement of muscle, but no actual motion of body
0 = no motion at all
Some people add plus and/or minus signs in.
What is an important aspect when assessing strength during a neuro exam?
Trying to assess effort. Collapsing weakness or breakaway weakness is different than not trying weakness. Is it physiological? Or is this person trying to get workman's comp.
What nerve roots are involved with Shoulder abduction?
C5-6
What nerve roots are involved with shoulder external rotation?
C5
What nerve roots are involved with elbow flexion?
C5-C6
What nerve roots are involved with elbow extension?
C7
What nerve roots are involved with wrist flexion?
C7-C8
What nerve roots are involved with wrist extension?
C7
What nerve roots are involved with intrinsic hand muscles?
C8-T1
What nerve roots are involved with hip flexion?
L2-3
What nerve roots are involved with hip extension?
L4-5
What nerve roots are involved with knee flexion?
L5-S1
What nerve roots are involved with knee extension?
L3-4
What nerve roots are involved with ankle plantar flexion?
S1-2
Whatever nerve roots are involved with ankle dorsiflexion?
L4-5
What nerve roots are involved with ankle inversion and eversion?
L5-S1
What is the best way to test limb strength?
Test them in a physiological way... maybe with pronator drift, toe walk/ heel walk, hop or climb a step, arise from chair, circle rotation test, closing of hand, rapid alternating movements (RAM)
What are the 4 types of weakness to the muscles?
1) Upper motor neuron- damage to central descending motor pathways (think CORTICOSPINAL tract)
2) Lower motor neuron- damage to the anterior horn cell or its axon (in nerve roots and peripheral nerve)
3) Muscle disease- usually see weakness in the proximal (big) muscles
4) Disease of the neuromuscular junction- presents with muscle fatigue typically starting with muscles that work all the time such as the eye muscles.
What are the two types of atrophy and what causes them?
1) Disuse: this can be due to many causes such as bedrest or casting and can be reversed with exercise.
2) Neutrogenic atropy: It is severe and indicates lower motor neuron involvement (anterior horn cell or its axon).
What is breakaway weakness a sign of?
malingering aka functional weakness
What are signs of functional weakness or malingering?
Pronator drift test is different, Hoover's sign, hold weak arm over face, able to use legs sitting down but unable to stand on them, breakaway weakness
What are the two types of reflexes and what are they helpful in?
Reflexes are helpful in assessing the cause of muscle weakness.
1) Deep tendon (myotatic) reflexes
2) Superficial reflexes
What do the myotactic reflexes represent and what inhibits them?
Monosynaptic spinal reflex which are lower motor neurons with the muscle stretch afferent pathway. These pathways are under inhibitory control by descending motor pathways the cerebral cortex via pyramidal pathways aka upper motor neurons (UMN)
How are deep tendon reflexes graded?
It is graded on a 0-4+ scale.

1+ sluggish
2+ normal
3+ brisk
4+ sustained clonus
You must try reinforcement before you can consider the reflex to be "0"
What's the most important observation you can make about deep tendon reflexes?
Checking that they are symmetrical and correlate with other motor and sensory signs. Remember that there is a wide range of normal!!
What does pathological spread of reflexes look like?
Only the muscle whose tendon is struck normally contracts... will see "crossed adduction". Remember the video he showed.
What is clonus?
It is something that can occur when the myotatic reflexes are tested. The muscle contracts with manual stretching of the tendon. It is most common at the ankle but can also test at the wrist or patella. Clonus can be sustained or unsustained. Want to notice how many "beats". Sustained clonus is always abnormal.
What nerve level are the biceps and brachioradialis reflexes at?
C6
What nerve level is the triceps reflex at?
C7
What is the nerve level of the finger flexor muscle reflexes?
C8
What nerve level is the knee reflex?
L4 (with a little L3)
What nerve level is the ankle jerk reflex at?
S1
What kind of reflex is the response to scratching the skin? What do the different responses to it mean?
It is a superficial reflex.
A plantar response is the normal response to lateral plantar stimulation (so downgoing toe). When trying to elicit the response you scrape along the lateral side of the foot and across the ball of the the foot to the base of the great toe. If you don't get a response, try it again faster and deeper. Stay lateral and take care to avoid plantar grasp reflex. No response suggests damage to descending motor tracts or sensory deficit.
What is the abdominal reflex?
It is a superficial reflex where the muscle in the quadrant of the abdomen you scratch contracts.
What is the Cremaster reflex?
It is rapid, brief elevation of the testicle on the side of the scratch of the medial thigh. It tests nerve levels L1-L2.
What is the most important consideration with superficial reflexes?
symmetry! Absence of symmetry or of a reflex suggests upper motor neuron damage.
What is the Babinski sign?
It is dorsiflexion of the toe in response to scratching the bottom of the foot which normally elicits the plantar response. It indicates upper motor neuron damage( somewhere along the corticospinal track pyramidal/UMN) though it is normal in babies.
Besides the Babinski sign, what are some other pathological reflexes?
Tromner's: volar surface of the fingers are tapped.
Hoffmann's: You flick the fingers and look for flexion of the thumb.
What if a patient is too ticklish and a proper babinski test can not be performed?
There are alternative tests you can do!
Oppenheim maneuver: painful rub along the anterior tibia with thumb and forefinger can elicit an upgoing plantar reflex.
Chaddock maneuver: Firm pressure along the lateral foot can elicit an upgoing plantar reflex
Gonda's maneuver: extensor plantar response by flicking the little toe or 4th toe
Schafer maneuver: pinching the Achilles tendon can elicit it also.
What are the regressive/primitive reflexes?
Grasp, snout, routing, palmomental, glabellar, nuchocephalic
What does an increased jaw jerk signify?
It is suggestive of UMN pathology above the brainstem.
What does decreased muscle tone indicate? What might you see (symptoms)?
Decrease in muscle tone typically is due to lower motor neuron dmage or damage to sensory fibers. Decreased muscle tone=flaccidity. Usually decreased muscle tone is associated with decreased myotatic reflexes
What are the 3 patterns of increased muscle tone?
1) Rigidity: constance increased tone throughout like a lead pipe = a basal ganglia disease. Usually the limb doesn't return to original position like spasticity does.
2) Spasticity: clasped knife rigidity=corticospinal tract disease. With rapid passive displacement, resistance of muscle tone increases then suddenly relaxes (clasp-knife phenomena)
3) Paratonia: Gegenhalten, an inhability to relax= this is seen with frontal lobe dysfunction.
What is the exception to what UMN lesions cause?!
Usually they cause spasticity, but acutely they can cause flaccidity!! Be careful in evaluating a patient to not just assume it's LMN damage if there is flaccidity acutely!
What is the prototype neuromuscular junction disease?
Myasthenia Gravis
Muscular dystrophies: what is seen in regards to weakness and reflexes?
Usually proximal weakness and anyway from normal to diminished reflexes.
Do acquired myopathies usually affect proximal or distal muscles?
Usually proximal.
What causes UMN syndrome?
Damage to the motor tracts either via the spinal cord, brainstem, internal capsule or cerebral cortex
What causes LMN syndrome?
Damage to motor neurons either in anterior horn of the spinal cord, nerve root, plexus, or peripheral nerves.
What are the changes that occur with UMN damage with reflexes, tone, and muscle bulk?
Reflexes- increased; tone- increased (spasticity) Remember acutely may be flaccidity though; Bulk: disuse atrophy
What are the changes that occur with LMN damage with reflexes, tone, and muscle bulk?
Reflexes: decreased; Muscle tone: decreased (flaccidity); muscle bulk: severe
How is coordination tested?
usually coordination is tested with rapid alternating movements or finger to nose testing. Any skilled movements can be used such as sliding your heel along your shin (as another example). Coordination testing tests strength, tone, and sensation
How does cerebellar damage affect coordination?
It decreases coordination without affecting other motor functions.
What is Dysdiadochokinesis?
Then say it five times fast haha.
Dysdiadochokinesis is the clinical term for an inability to perform rapidly alternating movements.
What causes dysdiadochokinesia?
Dysdiadochokinesia is often caused by multiple sclerosis in adults and cerebellar tumors in children. There may be a false impression of dysdiadochokinesia secondary to weakness in patients with Parkinson's disease (or other movement disorders) and UMN lesions. This is because they can have abnormal rapid alternating movements secondary to weakness, akinesia, or rigidity creating the false impression.
What can you gain about the motor exam just from observation?
Posture, frequency/speed of movement, abnormal movements at rest. You can often make a diagnosis just carefully watching the patient walk into the clinic exam room!
What are some abnormal movements at rest?
Tremor- resting, postural (attention), intention; chorea; athetosis; dystonia; Hemiballism; Tourette's; Myoclonus; asterixis; fasciculations
What is chorea?
Chorea consists of repetitive, brief, jerky, large-scale, dancelike, uncontrolled movements that start in one part of the body and move abruptly, unpredictably, and often continuously to another
What is athetosis?
athetosis is a continuous stream of slow, sinuous, writhing movements, generally of the hands and feet.
What is one of the conditions associated with chorea?
Huntington's Disease
What types of dystonia are there?
Torticollis, writer's camp, task specific dystonias
What's dystonia? How many people get it? What characterizes it?
Women develop it more than men. Less than 1% of people are affected. It is benign when it's in a single region (hand or foot for example). Occurs with a specific action. Worsens with stress fatigue, or anxiety. Quality of life impact depends on the body part affected.
What are the common places dystonia can occur and what are the effects?
Eyelids: rapid blinking or squinting (blepharospasm) can be so severe as to make a person functionally blind;
Neck: Cervical dystonia may cause the head to twist and turn painfully to one side or to pull forward or backwards
Jaw and tongue: Oromandibular dystonia may cause slurred speech or difficulty eating or swallowing
Hand and forearm: writer's cramp or musician's cramp causes pain during a single repetitive motion such as writing or playing an instrument
A lot of cases of dystonia have no obvious cause... but what are some of the underlying problems that can cause it?
TBI, stroke, brain tumor, O2 deprivation, infections such as tuberculosis or encephalitis, reactions to certain drugs, heavy metal or carbon monoxide poisoning
What is a therapy for dystonias and how does it work?
Botox! It blocks the release of acetylcholine at the NMJ by blocking cleavage of SNAP25 and hence binding of synaptosome to cell membrane and release
What are the different types of tremor?
1) Resting: usually with Parkinson's
2) Postural: usually "essential" or "familial". May be due to thyrotoxicosis, anxiety, caffeine, excessive sympathetic/ adrenal activity
3) Action (intention)- may be essential or cerebellar
What is an essential tremor?
It is an idiopathic tremor that is one of the most common neuro diseases with a prevalence of approximately 4% in persons aged 40 and older and considerably higher among persons in their 60s, 70s, 80s, and 90s. Many cases are inherited.
What is myoclonus?
Myoclonus is sudden activation of muscles which can be normal, can be due to damage to several levels of the nervous system, or can be due to encephalopathy.
What is asterixis?
Asterixis is a sudden, erratic loss of muscle tone. It can be due to encephalopathy/ delerium, toxic chemicals, metabolic causes, or drugs.
What causes fasciculations?
They can be normal or can happen with damage to lower motor neurons.
What are the different gait disorders?
Antalgic gait of joint pain (hip) – less time spent weight bearing on affected joint
Trendelenburg gait (unilateral weakness of hip abductors – gluts) – leaning to lesioned
side with every contralateral leg swing
Waddling gait of proximal myopathy (osteomalacia, polymyosites, etc.)
Fatiguing gait of MG
High stepping gait of foot drop or proprioceptive loss
Dragging leg of UML (stroke) – scissor gait in CP
Ataxic ‘drunken’ gait of cerebellar lesions - broad based, leaning to lesioned side
Shuffling gait of PD
Apraxic gait (small, ‘magnetic’ steps)
Normal pressure hydrocephalus - triad of gait apraxia, urinary incontinence, and
dementia (often reverible with shunt). “Magnetic gait”
Frontal lesions ("frontal apraxia")
Bizarre, non-falling, inconsistent gait of hysteria. “astasia-abasia”
Astasia refers to the inability to maintain station (stand upright) unassisted.
Abasia refers to lack of motor coordination in walking. The term literally means that the
base of gait (the lateral distance between the two feet) is inconstant or unmeasurable.
When seen in conversion disorder, the gait is bizarre and is not suggestive of a specific
organic lesion: often the patient sways wildly and nearly falls, recovering at the last moment
What does a reeling gait suggest?
cerebellar problems
What does apraxic gait suggest?
Frontal lobe disease
What does limping suggest?
orthopedic problem
What is a spastic gait?
stiff-legged, circumducting... dragging one spastic limb around the body.
What is the parkinsonian gait?
rigid, narrow base
What are the various gaits of weakness?
Steppage: lift knee high with foot-drop
Waddling: due to gluteal weakness
Lock knees with quadriceps weakness
What is needed for station? What tests station?
Station requires sensory, extrapyramidal, motor, cerebellar, and frontal lobe systems.
It is tested with the Romberg test (increased instability with eye closure due to sensory/ proprioceptive loss).
What disease causes issues with station?
Parkinsons causes delayed postural corrections and retropulsion.