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1960’s
Study of MSD’s including dysarthria began
Speech
Motor speech disorder is a _________ disorder
Brain injury
In order to diagnose an MSD, you must have a _______________
Disorder in clear speech (Disordered utterance)
Meaning of dysarthria
Speech
Unique, complex, dynamic motor activity
Cognitive linguistic process (memory, attention, EF, reasoning)
Motor speech planning and programming (apraxia)
Neuromuscular execution (dysarthria)
Motor Speech Process
MSD
“Speech disorders resulting from the neurological impairments affecting the motor planning, programming, neuromuscular control, or execution of speech”
Dysarthria
“Collective name for group of neurological speech disorders resulting from abnormalities in strength, speed, range, steadiness, tone or accuracy of movements required for speech control …. Aspects of speech production.”
Apraxia of Speech
“Neurological speech disorder reflecting impaired capacity to plan or program sensorimotor commands necessary for … normal speech. Can occur in absence of physiologic disturbances associated with dysarthria and in absence of disturbances in any component of language.”
NIH stroke scale
How neurologists are trained to score dysarthria
Palilalia (mimics MSD)
Compulsive repetition of words or phrases usually in context of accelerating rate and decreasing loudness
Echolalia (mimics MSD)
Repetition of sounds, words, or phrases
Aprosodia (mimics MSD)
Without rhythm, stress, etc.
Most likely psychogenic
Refer to psychiatrist (not treated like accent modification)
Exercises - reading samples, speak in other accents, sing passages, emphasize stress on certain words in passage
Foreign accent syndrome
Dysarthria 53%
Aphasia 25.8%
Apraxia 3.9%
Prevalence of speech/lang disorders
Age of onset (congenital, acquired)
Course (congenital, chronic, progressive, degenerative)
Site of lesion
Neurological diagnosis
Pathophysiology (spasticity, weakness)
Categorizing MSD’s
Flaccid (LMN) - Execution — Weakness
Spastic (Bilateral UMN) - Execution — Spasticity
Ataxic (Cerebellum) - Control — Incoordination
Hypokinetic (Basal ganglia) - Control — Rigidity
Hyperkinetic (Basal ganglia) - Control — Involuntary movement
UUMN (UUMN) - Control/execution — UUMN weakness, incoordination, spasticity
Mixed (>1) - Control and/or execution — >1
Apraxia - Left hemisphere - motor planning/programming — planning/programming errors
Mayo Clinic Classification & Table 1.1
Establish diagnostic possibilities
Establish diagnosis
Establish implication for localization and diagnosis
Specify severity
Purpose of MSD examination
Abnormal speech?
Neurological?
MSD?
Dysarthria?
What kind?
Apraxia?
Other neurogenic lang disorder?
Organic?
Psychogenic?
Whether it is neurological or not, ask whether it is long standing? Recently acquired? Dev stuttering, lang disorder, lang disability?
Establishing diagnostic possibilities - questions to ask
Always determine the type (ex. Flaccid dysarthria not just dysarthria) = huge diagnostic value
Important to remember when diagnosing
No lab test can diagnose it - it is diagnosed based on med hx, symptoms, phys exam
Parkinson’s - usually hypokinetic dysarthria
Why is Parkinson’s a working diagnosis?
Neuromuscular junction Disorder
Type of Flaccid dysarthria
When they speak for prolonged periods of time, speech for the first few min is normal then begins to decline after minutes. When breaks are given, speech improves again
Myasthenia Gravis
Speech stress testing - have them read a passage out loud multiple times and see how long/how many times it takes for intelligibility to decrease. Give a break and have them read again. If speech improves after break, it is Myasthenia Gravis
How to assess for Myasthenia Gravis (we do not diagnose, but refer)
measure progress
Match patient complaints to reality
Prognosis and management
Determining severity of MSD helps
90%; patient history
_____% of neurological diagnosis depends on __________
Looks at client’s
Strength
Speed
Range
Steadiness
Tone
Accuracy
Salient features
reduced muscle weakness
Laryngeal (VF weakness = breathy voice)
Velopharyngeal (hypernasality)
Articulators (tongue weakness)
LMN = CN & SN
Salient features: strength
Flaccid
Weakness is a sign of what type of dysarthria
Fast: uncommon (hypokinetic dysarthria)
Slow: common (spastic dysarthria - reduced speed)
AMR & SMR
Salient features: Speed
AMR (Alternating Motion Rate): pa pa pa
SMR (Sequential Motion Rate): pa ta ka
people with apraxia will struggle with SMR
AMR vs. SMR
Increased range of motion: uncommon (some hyperkinetic dysarthria)
Decreased range of motion: common (majority of dysarthria’s)
Salient Features: range
Involuntary movements or hyperkinesis
Resting tremor
Action tremor
Postural tremor (sticking tongue out, lifting arms)
Terminal tremor (towards end of an action)
Abnormal movements
Dystonia
Dyskinesia
Chorea
Athetosis
Salient Features: Steadiness
Increased (Spastic/Hypokinetic Dysarthria)
Reduced (flaccid dysarthria)
Salient Features: Tone
Regulation of tone, strength, speed, range, steadiness, timing
Outcome of well coordinated features above
Salient Features: Accuracy (coordination)
Do not need to diagnose MSD
Gait (wide shuffling walk)
Atrophy (weakness)
Fasciculations (twitching) [LMN lesion]
Laughing & crying excessively [UMN lesion]
Confirmatory Signs
Ask patient to cough
If they do not have good strong cough but have glottal coup, problem is at the respiratory level (do not have great breath support but VF are still working)
Assessing the larynx during non-speech tasks
Gag reflex
Stroke back of tongue, faucial pillars, pharyngeal wall
Jaw Jerk
Tongue blade under chin, tap with reflex hammer
Sucking Reflex
Stroke upper lip with tongue blade (lip pucker = unusual response)
Snout Reflex
Lightly tap the philtrum (pucker, protrusion, elevation of lower lip)
Palmomental reflex
Vigorously stroke blunt object on palm of hand
Automatic: numbers, names of months, happy birthday song
Volitional: speech you have to come up with
AOS patients may do well producing common words (automatic speech) but not uncommon words, multisyllabic words, repetition, etc.
Automatic vs. Volitional Speech
Flutter: rapid, relatively low-amp voice
Tremor: slower, more rhythmic (more severe)
Vocal Flutter vs. Vocal Tremor
Standardized test for Dysarthria (not the types)
Frenchman Dysarthria Assessment (FDA)
Standardized test for Apraxia of Speech
Apraxia Battery for Adults 2nd edition (ABA-2)
Intelligibility
the degree to which a listener understands the auditory signal produced by a speaker
Comprehensibility
the degree to which a listener understands speech on the basis of the auditory signal plus all other information that may contribute to understanding what is said
Efficiency
rate at which intelligible or comprehensible information is conveyed
Important supplement to measure intelligibility and comprehensibility because it contributes to both the perception of speech normalcy and the normalcy of communication by whatever means is social context
Comprehensibility
________ is superior to intelligibility
1: abnormal
7: normal
Functional Communication Measures (FCM)
Communicative effectiveness survey
Dysarthria Impact Profile
living with dysarthria
QOL analysis (filled out by patient or fam members)
look at notes
CN chart
Cortical speech planning & Programing
Direct activation pathway
Final common Pathway
Speech
Sensory system
Control circuits
sensory system
Indirect activation pathway
Final common pathway
Speech
Sensory system
Indirect activation pathway
Final common pathway
Speech
Sensory system
MSD Model
LMN
The final common pathway is a
PNS = CN & SN
LMN includes
final common pathway (nucleus, axon, neuromuscular junction)
When flaccid dysarthria occurs, the break down is in the ________________
weakness
Main issue associated with flaccid dysarthria
where the line ends & muscle begins (Myasthenia Gravis is a problem in the neuromuscular junction)
Neuromuscular junction - Final common pathway
CNS = brain and spinal cord
UMN include the
UMN: tracts
LMN: nerves
UMN are referred to as _______
LMN are referred to as ________
Speed, range, accuracy
Because there is weakness, ____, _____, & ______ can be the issue
Weakness
Hypotonia & reduced reflexes
Atrophy (bulk of muscle is lost)
Fasciculation (twitching)
Fibrillation
Progressive weakness with use
Characteristics of Flaccid Dysarthria
Congenital
Demyelinating
Infectious/Inflammatory
Degenerative (ALS)
Metabolic
Neoplastic (cancer)
Traumatic (spinal cord injury)
Vascular disease (stroke)
Etiologies of flaccid dysarthria
R side facial weakness
Chin fasciculations
R facial lesion (VII) =
affected resonance & voice
Glossopharyngeal lesion (IX) =
VF movement, breathiness, vocal flutter
(L vagus nerve affects VF more if there was a heart procedure)
Vagus nerve lesion (X) =
Tongue movement (fasciculations)
Hypoglossal Nerve (XII) lesion =
Jaw & Tongue = weak side
Everything else in oral cavity = strong side
Which structures deviate to the weak side and which ones deviate to strong side
we cannot be 100% certain where lesion is (could be UMN or LMN - LMN deviates to same side, UMN deviates to opposite side)
If there is atrophy or fasciculation, 100% LMN
If there is only tongue deviation (no atrophy or fasciculation), __________________
CN V
Ophthalmic (sensation)
Maxillary (sensation)
Mandibular (MOTOR) - mandible movement
Trigeminal Neve 3 Branches
Unilateral - Decent speech (other side compensates)
Bilateral - Imprecise Articulation & Prosody (slow rate)
Unilateral vs bilateral damage to Trigeminal nerve
Jaw deviate to weak side (unilateral)
Jaw hangs open (bilateral)
Difficulty chewing, drooling, opening/closing jaw
Decreased face, cheek, tongue, palate sensation
Trigeminal Nerve lesion - mandibular branch - flaccid dysarthria
Non speech Trigeminal nerve issues
Open/close jaw, move sideways (mandibular branch)
Touch face in areas and see if they can feel it (ophthalmic & maxillary branches)
Cranial nerve V (Trigeminal) examination
Sensory: Taste
Motor: Speech
R or L upper & lower weakness (ipsilateral) (LMN)
R or L lower weakness (contralateral) (UMN)
Facial Nerve lesions (VII)
Unilateral = articulation
Bilateral = articulation & prosody (slow rate)
Twitching of facial muscles (only jaw movement is CN V; every other facial movement is CN VII)
Unilateral & Bilateral Facial nerve (VII) lesions
Taste (sensory)
Tongue/velum movement (motor)
Gag reflex (vagus also plays role)
Glossopharyngeal Nerve (IX)
CN IX
CN X
CN XI
Pharyngeal plexus consists of what cranial nerves
Pharyngeal branch
Superior laryngeal branch (SLN) - pharynx/larynx
Recurrent laryngeal branch (RLN)
Vagus nerve (CN X) branches
pharyngeal consrtriction
Palatial elevation/retraction (speech/swallowing)
Hypernasality (resonance)
Pharyngeal branch of vagus nerve
Internal laryngeal branch (sensation)
Epiglottis, mucous membrane of larynx, base of tongue, aryepiglottic folds)
External laryngeal branch (Motor)
Inferior pharyngeal constrictors
Cricopharyngeus muscle
Thyropharyngeus muscle
Cricothyroid muscle (lengthen VF for pitch adjustment)
Superior laryngeal nerve branch of vagus nerve
SLN - Cricothyroid only
RLN - all other intrinsic laryngeal muscles
Which intrinsic laryngeal muscles are innervated by SLN and RLN of vagus
innervates all intrinsic laryngeal muscles
Sensory fibers: vocal folds and below
After it loops around subclavian artery, it becomes the RLN (not just vagus nerve)
Recurrent laryngeal branch of vagus nerve
Vagus (above pharyngeal branch)
Uni/Bi respiratory-phonatory
Uni/Bi resonance
Uni/Bi articulation
Uni/Bi prosody
Vagus (below pharyngeal branch, superior branch, recurrent branch)
Uni/Bi respiratory-phonatory
Uni/Bi Prosody
Cranial nerve lesions chart
Intermingles with CN X
Part of pharyngeal plexus
Clinically impossible to evaluate
Accessory nerve (CN XI)
If tongue is weak - imprecise articulation
Useful task: connected speech and AMR
Innervates all intrinsic and extrinsic muscles except palatoglossus (innervated by CN X)
Hypoglossal nerve (CN XII)
Breathing
short phrases (shortness of breath)
Reduced loudness (not enough breath support)
Spinal nerve lesions are always associated with _______
Sounds like two voices
Diplophonia
F - Flaccid
L - LMN
I/P - Ipsilateral
Tips for dysarthria FLIP