Rehab Exam FINAL Review Flashcards

1
Q

Gait Pattern Deficits of Parkinson’s Disease

A
  • Slow speed
  • Festinating
  • Decreased arm swing
  • Decreased trunk movement
  • Flexed Posture, Kyphosis
  • Narrow BOS
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2
Q

Motor Control

A
  • Area of study dealing with the understanding of the neural, physical and behavioral aspects of movements
  • Everything related to movement
  • How brain talks to rest of body (amt of force, speed at which person moves)
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3
Q

Motor Skill

A
  • Purposeful and functionally based movement

- Learned through interaction and exploration of environment

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4
Q

Motor Plan

A
  • Idea or plan of action for purposeful movement
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5
Q

Motor Program

A
  • Set of commands that results in production of coordinated movement
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6
Q

Motor Memory

A
  • Perform the movements of the sub-routines of the motor program without thought
  • Components: Initial movement conditions, sensory, specific movement patterns, outcome of movement
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7
Q

Neuroplasticity

A
  • Ability of the nervous system to respond to intrinsic or extrinsic stimuli by reorganizing its structure, function and connections
  • Can occur during development, response to environment, learning new task, response to disease, relationship to therapy
  • Adaptive: Good, postitive; re-routing occurs
  • Mal-Adaptive: Does not generate new routes; allows compensation changes
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8
Q

Motor Learning

A
  • CNS integrates sensory and motor input to produce motor action - leads to relatively permanent changes
  • Skill must be important to pt; demonstrate task exactly as it should be done; relate skill to previous skill with which pt is familiar; clear, concise verbal instructions and cues
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9
Q

Feedback

A
  • Info received about movement and corrective movement response occurs in response to info
  • Feedforward: Signals sent in advance of movement to ready sensimotor system
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10
Q

Motor Control Theories

A
  • Dynamical Systems Control Theory: Organized around specific task demands
  • Hierarchal Control Theory: Top-Down
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11
Q

Tests and Measures Terms

A
  • Validity: Test measures parameters it says it measures
  • Reliability: Consistency of results obtained by tester (intra-rater - single examiner over repeated trials, inter-rater - several examiners)
  • Sensitivity: Abnormality is present (True positive)
  • Specificity: Abnormality is absent (True negative)
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12
Q

Types of Aphasia

A
  • Receptive (Wernicke’s - fluent): Can talk, but does not understand
  • Expressive (Broca’s - nonfluent): Difficulty talking, but can understand
  • Global: Receptive + Expressive Aphasia
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13
Q

Types of CVA

A
  • Ischemic (Clot blocks blood flow - most common 80%)

- Hemorrhagic (Blood vessel ruptures)

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14
Q

TIA vs. CVA

A
  • TIA: Temporary interruption of blood flow lasts few minutes to no more than 24 hours
  • CVA lasts longer than 24 hours; permanent deficits
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15
Q

Gait Deficits of CVA

A
  • Difficulty walking
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16
Q

Choreoathetosis

A
  • Rapid, worm-like movements
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17
Q

Hemiballism

A
  • Jerking movements on one side
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18
Q

Delirium

A
  • Clouding of consciousness (acute state of confusion, dulling of cognitive processing, impaired alertness)
  • Inattention
  • Incoherent
  • Fluctuations in LOC
  • Sometimes hallucinations and/or agitation
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19
Q

Attention

A
  • Capacity of brain to process info from the environment or from long-term memory
  • Ability to select and attend while suppressing extraneous stimuli
  • Selective: screen and process relevant info while screen out irrevelant info
  • Sustain: length of time pt maintains attention
  • Alternating: Switching between 2 different tasks
  • Divided: Perform two tasks simultaneously
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20
Q

Memory

A
  • Store experiences and perceptions for recall
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21
Q

Confabulation

A
  • Pt fills in missing info (missing because lack of memory, lack of knowledge)
  • Not attempt to be deceptive, pt actually believes what they’re saying
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22
Q

Perseveration

A
  • Pt “gets stuck”

- Continued repetition of words, thoughts, actions

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23
Q

Pusher Syndrome

A
  • Ipsilateral pushing with stronger extremities towards hemiplegic/weaker side - WS to weaker side
  • Active pushing with strong towards weaker side –> fall toward weaker side
  • Instability, Asymmetry, difficulty in transfers, standing
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24
Q

Working with pt in Pusher Syndrome

A
  • Visual cues
  • Sit stand with mirror, tape to show midline, reach across midline
  • Tapping to promote muscular activation
  • Doorway or corner to facilitate symmetry
  • If cane, shorten it to facilitate WS to stronger side
  • Walk around table (wall) - push into wall
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25
Q

Pathophysiology for TBI

A
  • External forces act on brain
  • Acceleration, deceleration, rotational forces relative to bony skull
  • Compression, strain, shearing, displacement of brain tissue
  • Penetrating object (ex bullet) –> laceration and contusion of brain tissue
  • Glial cells get damaged and die - send toxins from cell death that kill off neurons
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26
Q

Rancho Los Amigos Levels

A
  • I,II, III: Decreased or Low-Level Response - ROM, Positioning, Improving arousal through sensory stimulation, spasticity management, Guided Techniques for ADL: sitting, grooming
  • IV: Confused-Agitated - Work near pt level of function and improve endurance rather than progress; Pt and family education; positive reinforcement
  • V, VI: Confused-Inappropriate/Confused-Appropriate - Confused, but with structure, can follow commands; Pt education on safety, BWSTT, CIMT, Facilitation techniques; break down complex tasks into simple commands
  • VII, VIII: Appropriate: Late Confused/Appropriate, early stage Automatic-appropriate - Simulate or integrate real-word/community skills, ADLs, Include in decision-making
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27
Q

SCI - Manually assist to cough

A
  • Work distal to xiphoid

- Push diaphragm in and up while pt coughs

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28
Q

Autonomic Dysreflexia - Signs

A
  • Occurs in SCI T6 and above
  • Noxious stimulus below level of tension
  • Sudden onset of symptoms: Pounding, excruciating headache; Profuse sweating; Vasodilation above level of lesion; Vasoconstriction below level of lesion; HTN; Bradycardia; Increased spasticity; Constricted pupils; Nasal congestion; Goosebumps; Blurred vision
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29
Q

Autonomic Dysreflexia - How to treat/prevent

A
  • Check clothing, catheter; when was last time voided bladder
  • Noxious stimulus: Urinary retention, catheter kink, tight clothing
  • Immediate intervention: Activate code (some facilities); if pt flat, bring to sitting (lowers BP); Identify stimulus and relieve it (bladder); If do not immediately find stimulus, relieve bladder
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30
Q

Pressure sores - How often to change position

A
  • Bed: Change position every two hours
  • W/C: Change position every 10-15 minutes
  • Bony prominences: Sacrum, heels, ischium, greater trochanter, scapula, elbow, ASIS, knees
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31
Q

Brown-Sequard Syndrome

A
  • Hemisection of SC (usually stabbing)
  • Ipsilateral loss: proprioception and vibration
  • Contralateral loss: pain and temperature
  • Loss is several dermatome levels below lesion level - spinothalamic tract ascends 2-4 segments on same side prior to crossing
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32
Q

Central Cord Syndrome

A
  • UE involvement > LE involvement
  • Can walk, but not move arms
  • Cause: cervical hyperextension injury
  • Compressive forces –> hemorrhage and edema in central SC
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33
Q

Posterior Cord Syndrome

A
  • Very rare
  • Loss or proprioception, epicritic sensation
  • Wide base steppage gait
  • Intact pain, light touch, motor
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34
Q

Anterior Cord Syndrome

A
  • Loss of pain and temperature (spinothalamic tract damaged)
  • Loss of motor (corticospinal tract samaged)
  • Proprioception and vibration preserved
  • Cause: Cervical flexion innjury –> damage to anterior SC
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35
Q

Sacral Sparing

A
  • Incomplete lesion
  • Sacral tracts are spared from injury
  • Intact perianal sensation; external sphincter contract
    Often first sign of incomplete cervical SCI
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36
Q

Cauda Equina Injury

A
  • Usually incomplete - b/c large number of nerve roots and large surface area
  • Peripheral injury, not central, LMN
  • Has potential to regenerate like peripheral nerve
  • Full neurological recovery is uncommon (long axons make location of injury far from site of innervation, scarring on axon may block regeneration, muscle may not be functional once regeneration occurs)
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37
Q

ASIA Levels

A

A: “Worst” - complete, No sensory or motor function preserved
B: Incomplete - Sensory but not motor is preserved below neurological level; includes S4-S5 segments
C: Incomplete - Sensory preserved; motor function preserved below neuro level; more than half of key muscles below neuro level have muscle grade less than 3
D: Incomplete - Sensory preserved; motor function preserved below neuro level; at least half of key muscles below neuro level have muscle grade of 3 or more
E: “Best” Normal - motor and sensory function is normal

38
Q

Reflexogenic erections

A
  • Response to external physcial stimulation of genitals and perineum
  • Intact reflex arc is required; UMN lesion (above conus medullaris)
39
Q

Psychogenic erections

A
  • Cognitive activity (i.e., erotic fantasy)
  • Imagination: brain to SC to end organ communication
  • Reflex lost; psychogenic response preserved; LMN lesion (conus medullaris and cauda equina)
40
Q

Types of Prosthetic Feet (Non-articulated)

A
  • Foot and lower shank are one section, no joint

- SACH, SAFE, Carbon Copy II, Seattle foot, Flex foot and Springlite foot

41
Q

Types of Prosthetic Feet (Articulated)

A
  • Metal bolt or cable joins the foot and lower shank
  • Single-axis (DF, PF, Toe Break)
  • Multiple-axis (Slight movement in all planes)
  • Rotators (Absorbs shock in tranverse plane, allows socket to rotate with skin, used by single-foot axis)
42
Q

Residual Limb Care

A
  • Edema control
  • Proper hygiene
  • Skin care (avoid abrasion/cut, skin inspection)
  • PT handling of residual limb
  • Scar tissue: Friction Massage
  • Avoid “home remedy” of “touching up skin”
43
Q

Parts of Transtibial prosthesis

A
  • Foot-ankle assembly
  • Shank
  • Socket
  • Suspension
44
Q

Parts of Transfemoral prosthesis

A
  • Foot-ankle assembly
  • Shank (exo or endo skeleton)
  • Knee Unit
  • Socket
  • Suspension
45
Q

Reliefs

A
  • Concavities
  • Pressure relief of sensitive areas
  • Fibular head, tibial crest, tibial condyles, anterior-distal tibia
46
Q

Build-ups

A
  • Convexities
  • Contact of pressure-tolerant areas
  • Belly of gastroc, patellar tendon, proximal-medial tibia, pes anserinus, tibial and fibular shafts
47
Q

Cotton Socks

A
  • Absorb perspiration
  • Least allergenic
  • 2, 3, 5 ply
48
Q

Wool Socks

A
  • Good cushioning
  • Hot
  • Expensive
  • Require special laundering
  • 3, 5, 6 ply
49
Q

Synthetic Socks

A
  • Orlon/Lycra
  • Resilient
  • Easily washed (don’t shrink)
  • Does not absorb as much perspiration - wicking materials
  • 2, 3 ply
50
Q

How long do you wear a shrinker?

A
  • Worn 24-7, except for bathing

- Edema control: wear until edema is managed, don’t wear with prosthesis

51
Q

Post-Conceptual Age

A
  • AA prior to achieving term age

- GA + CA

52
Q

Term Adjusted Age

A
  • CA - # weeks missed in utero
53
Q

Chronological Age

A
  • Age based on birthday
54
Q

Gestational Age

A
  • Length of time in utero
55
Q

Types of Spina Bifida

A
  • Spina Bifida Occulta (Asymptomatic): Dimpling of skin, tuft of hair
  • Meningocele (No neuro deficits): Meninges of SC protrude through opening in vertebrae; form fluid filled sac
  • Myelomeningocele (Neuro deficits present): Meninges and part of SC protrude through opening in vertebrae
56
Q

Cerebal Palsy (Occurrence)

A
  • Ante- Natal (vascular events, maternal infections): In utero
  • Perinatal: Labor and delivery (obstructed labor, neonatal strokes
  • Post-Natal: trauma, infection, shaken baby syndrome
  • Not diagnosed until 12 months for definitive dx (quality of movement, MRI, Ultrasound)
57
Q

Types of CP

A
  • Spastic CP (70%): Most common; Diplegic, Hemiplegic, Quadraplegic/Tetraplegic
  • Dyskinetic and movement disorders (20%): Uncontrolled, involuntary movements - includes athetosis, ataxia, rigidity, tremors, dystonia, ballismus, choreoathetosis
  • Ataxia CP (10%): Deficits in balance and coordination
  • Hypotonic CP: Can be permanent; most likely transient as atheotosis or spasticity develops
58
Q

Primitive reflexes exist in which neurological issues?

A
  • TBI

- Cerebral palsy

59
Q

Selective Dorsal Rhizotomy

A
  • Non-reversible surgery
  • Cut across selected nerve rootlets L2-S2 or L2-S1
  • Reduce spasticity and tone, enhance quality of life
60
Q

Piaget’s Theory: Sensorimotor Stage

A
  • 0-18 mo
  • Learn primarily through exploring senses, movements
  • Discoveries made through trial and error (experimentation)
  • Manipulate environment with strategies that create new understandings = accomodations
  • Severe MR will not progress past stage, will continue discovery stage
61
Q

Piaget’s Theory: Preoperative Stage

A
  • 2-7 yo
  • Development of language
  • Beginning of abstract thought
  • Use of symbols for objects: Group, classify objects
  • Moderate IQ 35-55, may not develop beyond this stage
62
Q

PIaget’s Theory: Concrete Stage

A
  • 7-12 yo
  • Ability to order, classify, relate experience to an organized whole
  • Increase problem solving
  • Recognize another person’s point of view
  • Mild IQ - Cannot progress beyond this stage
63
Q

Piaget’s Theory: Formal Operations Stage

A
  • 12 yo and older
  • Ability to reason and hypothesize
  • Child with MR seldom reaches this stage
64
Q

Tactile Defensiveness

A
  • Aversion to touch
  • Aversion to certain stimuli
  • Avoidance reaction of hands, feet, face
  • Seen in children with hyperactivity or distraactibility
  • Affects exploration of environment and learning
  • Compensatory - labile, threatened, unable to cope, withdrawn, irritable, distractable
65
Q

Tactile Defensiveness Treatment

A
  • Focus on tactile and proprioceptive systems
  • Heavy touch, pressure, WB
  • Avoid light touch and tickling
66
Q

Stridor

A
  • Crowing sound during inspiration

- Airway obstruction or laryngospasm

67
Q

Expiratory grunting

A
  • Physiological attempt to prevent premature airway collapse
68
Q

Gurgling

A
  • Copious amounts of secretion in larger airways
69
Q

Wheezes

A
  • Musical sounds produced by airflow through narrowed airways during inspiration or expiration
70
Q

Crackles

A
  • Non-musical sounds during inspiration or expiration; previous deflated airway opens
71
Q

Rubs

A
  • Coarse, leathery sounds indicating tissues rubbing on one another
72
Q

Crunches

A
  • Crackling sounds when air leaks into the area; usually heard over mediastinum
73
Q

Predisposing Principles of Acute RF

A
  • High incidence of respiratory infections
  • Small airway size and poor mechanical advantage of respiratory muscles
  • Poor ability to cough
  • Small airway size and ound
  • Spending time in supine –> harder to ventilate
74
Q

How to assess MMT of children under age 3?

A
  • Observe movement and function
75
Q

Individualized Education Plan (IEP)

A
  • Comprehensive individualized plan developed by multi-disciplinary team
  • Determined within 30 calendar days of determining eligibility
  • Child’s present level of academic achievement and functional performance
  • Measurable annual goals
  • Child’s progress towards goals
  • Special Education and related services
  • Explanation of extent to which child WILL NOT participate with non-disabled children in regular classroom
  • Accommodations necessary to measure academic achievement and functional performance
  • Projected date of services
  • Updated annually
76
Q

Special Education

A
  • Refers to children who need special provisions to facilitate education
  • Provisions are only for children who have special education needs
  • Not for children with disabilities without special education needs
77
Q

Respiratory Distress Syndrome

A
  • Pulmonary immaturity, inadequate pulmonary surfactant
78
Q

Patent Ductus Arteriosus

A
  • Bypass circulation to lungs pre-birth
  • Normal: a hole in R ventricle and L pulmonary artery allows blood to celebrate; closes 10-15 hrs after delivery
  • If does not close, prevents oxygenation of blood
  • Results in hypotension, poor perfusion, CHF
79
Q

Hyperbilirubinemia

A
  • Accumulation of bilirubin (liver enzyme) in the blood; can accumulate in the brain and cause neuronal damage
  • Cause: immature hepatic function
80
Q

Gastroesophageal Reflux

A
  • Esophageal lining can be damaged –> inflammation, dysmotility, pain
  • Can lead to poor oral feeding patterns, oral aversion, and excessive crying due to pain
81
Q

Necrotizing Enterocolitis

A
  • Acute inflammation of the immature intestine causes acute intestinal necrosis
  • Cause: Injury to intestinal mucosal lining
82
Q

Germinal Matrix - Intraventricular Hemorrhage

A
  • Most common brain lesion in premature infants

- Hemorrhage deep in brain extends to area between lateral ventricles

83
Q

Periventricular Leukomalacia

A
  • Death of neurons in areas of white matter adjacent to the lateral ventricles
84
Q

Retinopathy of Prematurity

A
  • Alteration in the normal development of blood vessels in the eye
  • Vasoproliferative disease of immature retina
85
Q

Chorioamnionitis

A
  • Most common cause of preterm labor
  • Cervicovaginal bacteria invades the amniotic cavity causing inflammatory response in the membranes of the developing fetus
  • More susceptible to brain damage and intestinal abnormalities
86
Q

Osteopenia

A
  • Decreased bone density
87
Q

Bronchopulmonary Dysplasia

A
  • Most common chronic lung disease associated with prematurity
  • O2 toxicity, barotrauma, volutrauma from mechanical ventilation
88
Q

Meconium Aspiration Syndrome

A
  • During delivery, fetus may pas BM into amniotic fluid. As infant gasps first breath, may aspirate meconium-tainted fluid
  • Meconium particles obstruct airway, interfere with gas exchange
89
Q

Down’s Syndrome - Characteristics

A
  • Short stature
  • Hypotonia
  • Ligamentous laxity due to collagen deficit
  • Small hands and feet
  • Pes Planus
  • Patellar instability
  • Scoliosis
  • Atlanto-axial instability
  • Brachycephaly (flattened back of head)
  • Larger fontanels
  • Flat contour of face
  • Slightly slanted eyes
  • Umbiical hernia
  • Delayed integration of primitive reflexes
  • Single crease in palm of one or both hands
  • Wide space between 1st and 2nd toes
90
Q

Down’s Syndrome - Goals

A
  • Align compression and WB forces to stimulate longitudinal bone growth
  • Align WB support to promote joint stability and formation
  • Facilitate normal co-contraction, force production and increased muscle tone