Peds Final Practical Flashcards
What do thoracic level spina bifida patients present with?
“frog leg deformity”- legs abducted, ER, and flexed w/ feet in plantarflexion
What do high lumbar level spina bifida patients present with?
some active hip flexion and adduction, but no other strong movements
What do low lumbar level spina bifida patients present with?
strong hip flexors and adductors (no hip ext)
strong dorsiflexors (no plantarflexion)
In-toeing
Ambulatory with use of orthotics and glut med lurch/lumbar lordosis
What do sacral level spina bifida patients present with?
strong knee flexors and hip abduction
weak plantarflexors
mostly independent with gait
What would you include in the examination of a patient with spina bifida?
History (development, surgical, etc.)
MMT, ROM, sensory assessment, gait
Functional status
What interventions would you provide to a patient with spina bifida?
Encourage upright positioning to integrate equilibrium and righting reactions and to active abdominals
ROM and stretching to prevent contracture
Balance activities
Strengthen hip flexors to counteract weak PFs (active facilitated, resisted step ups, etc.)
Pressure relief
What are some special considerations for spina bifida?
Latex allergies
Skin breakdown
Hydromyelia (hypertonus, weakness in UEs, scoliosis)
Tethered cord (hypertonus, weakness, gait, etc.)
What would you include in the examination of a patient with TBI?
History: onset and MOI, medical precautions, vital signs, Cogntition Sensory exam (skin integrity) Functional mobility ROM (check for heterotopic ossification)
What is the Pediatric Rancho Scale?
I- oriented to self and surroundings II- responsive to environment III- localized response IV- generalized response V- no response
What is the modified ashworth scale?
0: no increase in tone
1: slight increase in tone
1+: slight increase through less than half of ROM
2: marked increase, full ROM available
3: considerable increase, PROM difficult
4: affected part is rigid
What is low cognitive level TBI and what interventions would you do?
Pediatric V-III –> Stimulation
Prevent complications from immobilization (Skin breakdown, contracture development, respiratory issues)
Vestibular, Visual, Olfactory, Tactile, Auditory
What is mid cognitive level TBI and what interventions would you do?
Pediatric II –> Structure
Agitation: work in a dimly lit room with no distractions. perform simple activities that are familiar to the child (ROM, sitting, standing, walking)
Confusion: simplify environment or instructions, promote functional tasks, constantly orient the child to surroundings, don’t rely on memory
What is higher cognitive level TBI and what interventions would you do?
Pediatric I –> School/community reintigration
Evaluate for orthotics, AD, recommendations for environmental home or school modifications
Wean child from structure and cueing
Focus on treating residual motor deficits
What are some special considerations for patients with TBI?
autonomic dysreflexia, heterotopic ossification
What is the ASIA impairment scale?
A: complete
B: incomplete
C: incomplete, muscle grade 3 below level
D: incomplete, muscle grade 3 and above below level
What would you include in the examination of a patient with SCI?
MOI, loss of consciousness?, treatment received, developmental history, medications
Vital signs (risk for orthostatic hypotension)
Integumentary screen
ROM, strength, tone
Funcional measure (QIF, SCIM)
What are the muscles added for the spinal cord levels?
C5: addition of biceps
C6: addition of pectorals
C7: addition of triceps
T4-T6: upper abdominals
T9-T12: lower abdominals
L2-L4: gracilis, iliopsoas, and quadratus lumborum
L4-L5: hamstrings, quadriceps, anterior tibialis
What interventions would you provide to patient with a spinal cord injury
Skin health (positioning and pressure relief Contracture prevention (ROM, stretching) ADL and ambulation training depending on level
What are some special considerations for a patient with SCI?
autonomic dysreflexia
hip subluxation
scoliosis
bone density
What are some signs and symptoms of Duchenne muscular dystrophy?
Between ages 2-5 Pseudohypertrophy of calves Wide base of support during gait Lumbar lordosis Gower's sign Reluctance to or incoordination with gait
What should you include in the examination of a patient with DMD?
Developmental history, child and parental concerns
Pulmonary history
Functional abilities (time testing important)
MMT, ROM
What interventions would you provide to a patient with DMD?
Goal = prolong ambulation and independence, improve pulmonary function
Stretching, strengthening
Diaphragmatic and breathing exercises
W/C safety: pressure relief, etc.
What are the 3 main phases of DMD?
Early/ambulatory stage
Transitional stage
Later/wheelchair stage
What are the symptoms of Type I (Werdnig-Hoffman) SMA?
Present in the first 3 months of life
Floppy baby with head lag
Never learn to sit
What are the symptoms of Type II SMA?
Present around 1 year Weakness and wasting of extremities and trunk Fasciculations with tone Fine tremor when using UE Never learn to walk without an AD
What are the symptoms of Type III (Kugelberg-Welander) and IV SMA?
Diagnosed later in life
DTRs decreased
Progressive spinal deformities and contractures uncommon
Typically walk independently
What would you include in the examination of a patient with SMA?
History: medical, developmental, medications, etc.
ROM, MMTs
Functional testing to track progression
Respiratory abilities
What interventions would you provide to a patient with SMA?
Goal=maintenance of function and flexibility
Type I: percussion and postural drainage, switch toys, quality of life
Type II: prone and quadruped skills, distmal muscle strengthening, ROM and stretching to prevent contractures
Type III: maintain function and flexibility, WB activities
What are the main musculoskeletal concerns in patients with Downs Syndrome?
Hypotonia, slow reaction time, joint hyperflexibility, ligamentous laxity, foot deformities, scoliosis, atlanto-axial instability, congenital heart defects