Neuro and MSK Management Flashcards

1
Q

what age group is MACS for?

A

4-18 yo

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

how is MACS performed?

A

ask someone who knows the child and how the child typically performs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

MACS I

A

handles objects easily and successfully

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

MACS II

A

handles most objects but with somewhat reduced quality and/or speed of achievement

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

MACS III

A

handles objects with difficulty
needs help to prepare and/or modify activities

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

MACS IV

A

handles a limited selection of easily managed objects in adapted situations

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

MACS V

A

does not handle objects and has severely limited ability to perform even simple actions

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

what is the purpose of the FMS?

A

describe functional mobility in children 4-18 yo with CP

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

how is mobility described in the FMS?

A

over 3 distinct distances: home (5m), school (50m), in wider community (500m)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

FMS 6

A

independent on all surfaces

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

FMS 5

A

independent on level surfaces
requires rail for stairs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

FMS 4

A

uses 1 or 2 sticks

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

FMS 3

A

uses crutches

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

FMS 2

A

uses walker or frame

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

FMS 1

A

uses WC

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

when is a C or N used for FMS?

A

C - crawling
N - does not apply (can’t complete full distance)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

what is the gold standard for classifying CP?

A

GMFM

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

what type of assessment is GMFM?

A

criterion referenced
observational assessment

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

what diagnoses is GMFM validated for?

A

CP
down syndrome

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

GMFM 88 vs 66

A

88: 5mo - 16 yo
66: 5-16 yo

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

what 5 dimensions does the GMFM include?

A

lying and rolling
sitting
crawling and kneeling
standing
walking, running, jumping

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

GMFM Score:
0
1
2
3

A

0: does not initiate task
1: initiates task
2: partially completes task
3: completes task

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

which GMFM should be used for down syndrome?

A

88

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

what other diagnoses could GMFM be used for?

A

TBI
spinal muscular atrophy
osteogenesis imperfecta
hereditary spastic paresis
acute lymphoblastic leukemia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
25
Q

you need at least ___ steps for GMFM

26
Q

you need a space for a ____ meter run for GMFM

27
Q

GMFM 88 vs 66

A

88: more items for level V, eval of ambulatory aids and/or orthoses or shoes of interest
66: barefoot

28
Q

which GMFM provides a more meaningful assessment of change?

29
Q

precautions for spina bifida

A

latex allergy
observe and assess hydrocephalus
VP shunt
tethered cord
sudden significant changes in foot posture and/or B&B function

30
Q

incidence of shunt malfunction

31
Q

1 year failure rate for VP shunts is ___% for pediatrics and ___ for adult

A

40-50% peds
29% adult
getting lower tho

32
Q

tethered cord signs

A

weakness, numbness in legs
tremors or spasms in leg muscles
changes in foot appearance (higher arches, curled toes)
loss or worsening of B&B function

33
Q

initial radiographs should be taken between what ages for children with down syndrome?

34
Q

assessment tools for down syndrome

A

GMFM
PDMS-2

35
Q

individuals with disability education improvement act Part B:
age group:
components:

A

3-21 yo
school aged services
components:
- IEP
- PTE
- NOREP

36
Q

how often is an IEP developed?

37
Q

what is a NOREP?

A

classifies type of classroom and programming

38
Q

individuals with disability education improvement act Part C:
age group:
components:

A

birth to 3 yo
early intervention services
IFSP
financial assistance to states for early intervention programs

39
Q

how often is IFSP reviewed?

A

at least every 6 mo

40
Q

purpose of section 504 of rehabilitation act of 1973

A

discrimination against individuals with disabilities illegal; protects students

41
Q

Americans with disabilities act of 1990

A

prohibits discrimination against individuals with disabilities in employment, transportation, public accommodation communities, and government activities

42
Q

_____ system is unreliable in young children (<4 yo)

A

thermoregulatory

43
Q

dense ordinary CT

A

heals tendons and ligaments

44
Q

a common complication of tendon regeneration is _____

A

development of fibrous adhesions b/w tendon and surrounding tissue

45
Q

what layer of embryonic development is bone, cartilage, and muscle derived from?

46
Q

Hueter-Volkman Principle

A

growth plates produce increase growth in response to tension and decreased growth in response to excessive compression

47
Q

how is bone age usually determined?

A

X-ray of L wrist, hand, and fingers

48
Q

what is a Risser sign used to assess?

49
Q

a ____ Risser sign indicates that a lot of growth is left and scoliosis will get worse

50
Q

when does the anterior fontanelle close?

A

7-18 months

51
Q

when does the posterior fontanelle close?

A

1-2 months

52
Q

T/F: therapeutic US is NOT safe over growth plates by diagnostic US is

53
Q

what occurs in dominant (classical) OI that leads to brittle bones?

A

too little or poor quality of type 1 collagen due to genetic mutation of 1 of the type 1 collagen genes

54
Q

what occurs in recessive OI that leads to brittle bones?

A

mutation in non-collagen genes

55
Q

how long does biochemical (collagen) and molecular (DNA) testing take to diagnose OI?

A

requires several weeks

56
Q

biochemical (collagen) and molecular (DNA) tests detect almost ___% of type 1 collagen mutations

57
Q

what meds will someone with OI usually be on?

A

bisphosphonate
vit D

58
Q

clinical characteristics of OI

A

hyperlaxity of ligaments
fragile skin
poor thermoregulation
blue sclerae
dentinogenesis imperfecta (teeth)

59
Q

how do you educate a parent on infant handling with OI?

A
  • carry w/ widespread hands over head/shoulders and bottom
  • diaper changes done by lifting butt not ankles
  • do not twist or pull body parts
60
Q

rules with MMT and OI

A

may NOT be possible
if tolerate - do a midshaft of bone

61
Q

what MMT should never be performed for OI pt?

A

no isolated trunk extension or flexion to assess core strength (d/t spine fx possible)