peads Flashcards

1
Q

how brachial plexus injury happens

A

trauma to shoulder or spine during vag delivery

traction on shoulder
traction/ rotation of head during delivery of shoulder

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2
Q

complicating factors fr brachial plexus injury

A
maternal diabetes
high birth weight
prolonged labour
sedated hypotonic infant
heavily sedated mum

difficult c section

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3
Q

brachial plexus segments

A

c5-t1

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4
Q

most common impairment from brachial plexus injury

A

erbs palsy

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5
Q

erbs palsy segments / impact

A

c5-6
Grasp is INTACT
sensory loss

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6
Q

position of erbs palsy

A
waiters tibe
shoulder - ext, IR, add
elbow - ext
forearm - pro
wrist/fingers - flexed
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7
Q

T/F erbs palsy is lower plexus injury

A

F - UPPER PLEXUS

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8
Q

whats klumpkes palsy

A

lower plexus injury

c7-t1

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9
Q

whats erb klumpke injury

A

whole arm

c5-t1

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10
Q

what do you see in ppl with brachial plexus injury

A

paralysis / weakness
mm imbalance
learned non use

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11
Q

what kind of mm imbalance would you see in brachial plexus injury

A
abnormal substitution movements
weird arm postures
contractures
subxlactions / dislocation 
deformity
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12
Q

PT management in brachial plexus injury

A
functional training
ROM
Splinting 
education 
sensory awareness
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13
Q

T/F brachial plexus injury can be surgical

A

t

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14
Q

T/F impairment in AROM and PROM of UE supination and shoulder IR are common for kids with brachial plexus injury

A

F - External rotation

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15
Q

is balance rehab relevant to brachial plexus injuries

A

yes

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16
Q

development dysplasia of the hip

DDH

A

hip disorders that are unstable, sublax or dislocate

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17
Q

T/F normal development of femoral head and acetabulum are co dependent

A

T

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18
Q

risk factors for DDH

A
breech position
position
incorrect LE swaddling
positive family history
first born 
foot abnormalities
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19
Q

most important risk factors in screening for DDH

A

breech position

positive family history

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20
Q

is DDH very apparent in infancy / early childhood

A

no its silent but early detection is critical

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21
Q

can mild forms of DDH resolve without treatment

A

yes

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22
Q

when is there a poor prognosis for DDh

A

unstable and morphologically abnormal by 2-3 yrs old

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23
Q

how to screen for DDH

A
ultrasound 
leg length discrepancy 
asymmetric gluteal folds
limited hip abd
gentle Barlow / Ortolani test
safe swaddling 
abnormal gait
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24
Q

Ortolani

A

dislocated femoral head is reduced with ABD

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25
Q

the most important clinical test for detecting newborn dysplasia

A

ortolani

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26
Q

barlow

A

you dislocate it with ADD

tests laxity / instability

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27
Q

is ortolani or Barlow test better

A

orto

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28
Q

management of DDH

A

observe
abduction brace
surgical

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29
Q

long term implications of DDH

A
degenerative arthritis
leg length discrepancy 
limited hip abd
pain
early hip replacement 
avascular necrosis
30
Q

osteogenesis imperfecta

A

congenital disorder of collagen synthesis - all connective tissue

31
Q

T/f osteogenesis imperfecta presents widely differently

A

T - as osteoporosis , excessive fractures, spinal deformities , mm weakness, lig laxity

32
Q

medical management of osteogenesis imperfecta

A
bisphosphonates
orthopaedic solutions (splint, case, rod)
33
Q

T/F vitamin C / D are effecting in preventing fractures

34
Q

bisphosphonates

A

reduced fracture rate
improve bone density
improve functional status

35
Q

physiotherapy management in osteogenesis imperfecta

A

function and participation

36
Q

idiopathic toe walking (ITW)

A

atypical in kids after 3

37
Q

what is ITW associated with

A

positive family history
language/ learning delays

out of phase firing of gastroc, soleus , tib ant

38
Q

ITW symptoms

A

toe walking
pain in legs
frequen tripping
ankle injuries

39
Q

ITW mangement

A

cast, PT, botox, surgery

40
Q

whats PT do with ITW

A

stretch, strengthen, manual therapy, balance , gait training

41
Q

does ITW impact activities

A

not really

42
Q

Legg calve perthes disease

A

AVN of femoral head

43
Q

when does legg calve perthes happen

A

3-13

but most common is boys 5-7

44
Q

stages of legg calve perthes

A

condensation
fragementation
reossificaiton
remodelling

45
Q

clinical presentation of legg calve perthes

A
limp 
pain 
trendelenburg
decrease ROM
mm spasm
46
Q

how is range impacted in Legg calve perthes

A

ABD, IR, hip flexion limited

47
Q

managing legg calve perthes

A

relieve pain
contain the femoral head while bone remodels
restore ROM, strength, balance, gait

partial WB crutches
casting
surgerical

48
Q

T/f you could be in a cast for over 1 year with legg perthes

A

true up to 2 years

49
Q

what causes slipped capital femoral epiphysis SCFE

A

excessive force on growth plate
fat
trauma
puberty

50
Q

clinical prevention SCFE

A

pain in groin / knee
leg ER
limited hip F, ABD, IR
can’t WB

51
Q

Management of SCFE

A

surgery
bed rest
casting
pT

52
Q

Osgood Schlatter

A

apophysitis of tibial tubercle
boys 10-15
girls 8-13

53
Q

osgood schlatter presentation

A

anterior pain at tibial tubercle
bump on tibial tubercle
worse with activity

54
Q

how to assess osgoods

A

palpation

radiograph

55
Q

OSD management

A

ice rest, stretch ham and quads

Strengthen

56
Q

can they return to sport with OSD

A

yes, you might have mild discomfort during growth but crack on

57
Q

whats OCD

A

osteochondritis dissecans

58
Q

whens OCD

59
Q

what causes OCD

A

trauma
uneven / excessive pressure
disruption of blood to bone
genetics

60
Q

clinical presentation of OCD

A
pain with activity
pain with rotational 
swelling
instability
locking
61
Q

acromegaly

A

pituitary gland produces too much growth hormone

increase in bone size

62
Q

too much growth hormone

63
Q

signs and symptoms acromegaly

A

enlarged hands and feet

changes in face shape (protrude low jaw and brow, enlarged nose, thickening lips, gap in teeth)

64
Q

complications of acromegaly

A
hypertension
OA
diabetes
sleep apnea
carpal tunnel 
vison loss
65
Q

T/F dwarfism is mostly genetic

66
Q

most common type of dwarfism

A

achondroplasia

67
Q

t/F dwarfism mostly happens in families where both families are average height

68
Q

difference disproportionate and proportionate dwarfism

A

some parts are small vs all parts are small

69
Q

proportionate dwarfism when do you have it

A

present at birth

early childhood

70
Q

management dwarfism

A

early diagnosing / treatment helps
shunt to relieve brain pressure
correct surgeries
physio ROM, strength