lecture 6: common neuro conditions Flashcards

1
Q

Which of the following is not a PRECAUTION for PT session w/ child with spina bifida?

-latex
-hip dislocation
-fracture risk
-fragile skin
-decreased endurance
-thermoregulation
-UTI

A

UTI
(not a precaution, just something to be aware of…incontinence IS a precaution and related to UTI)

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

list all the 9 precautions for Spina Bifida during PT

A
  1. decreased endurance
  2. fracture risk
  3. hip dislocation
  4. fragile skin
  5. latex allergies
  6. incontinence
  7. thermoregulation
  8. fall risk
  9. spasticity increase
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

list all the COMPLICATIONS of Spina Bifida interfering with PT

A

-UTI
-spasticity
-Arnold Chiari malformation
- fracture
- pressure sore
- tethered cord
-VP shunt failure
-symptomatic hydromelia
-symptomatic hydrocephalus

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

A child with spastic diplegic CP functions at GMFCS level 3 has

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

What is the FMS?

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

MACS is what

A

GMFCS scale for the UE

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

an important feature of the activity-focused model is the integration of ______ with ________

A

impairment-focused interventions WITH functional practice

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

What are the 3 classification systems, not assessment tools, for cerebral palsy?

A

GMFCS -mobility level
FMS - mobility
MACS - UE function

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

GMFCS level 1

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

GMFCS level II

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

GMFCS level III

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

GMFCS level IV

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

What is the MACS and what is it for?

A

Manual Ability Classification System:
ability 4-18 years with CP to handle objects in daily activities, categorized into 5 levels
1: good, 5: bad

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

What is the FMS and how does it work?

A

describes functional mobility in children with CP, 4-18 years (scored over 3 distances)

how do they walk for 5 meters? (house)
how do they walk for 50 meters? (classroom)
how do they walk for 100 meters? (community)

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

Ratings 1-6 for FMS and rating C and N
Describe these:

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

GMFM is what?

A

standardized, criterion referenced, observational ASSESSMENT (measure changes over time) for children with CP

*GMFM-66, GMFM-88

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

What is a dorsal rhizotomy

A

cut dorsal nerve rootlets
to decrease spasticity for children with CP

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

GMFM is validated for children with

A

CP and also been validated for children with Downs Syndrome

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

GMFM-88 original is for children ___ years of age

A

5 months - 16 years

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

GMFM-66 newer is validated for ages _____

A

5 years to 16 years

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

GMFM includes what 5 dimensions?

A
  1. lying and rolling
  2. sitting
  3. crawling and kneeling
  4. standing
  5. walking, run, jumping
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

GMFM scored how?

A

NT: not tested
0 = does not initiate
1 = initiates task
2 = partial complete task
3 = COMPLETES TASK

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

GMFM items are appropriate for children with motor skills at or below those of _____

A

at or below those of a 5 year old child without any motor disability

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

GMFM-88 is evidenced for use in children with ______

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

GMFM equipment and space needed

A

mat, bench, stairs (5 steps)
space for 4.5 meter run

*any differences should be documented for consistency to measure change over time

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
26
Q

The GMFM-88 vs -66

A

-88:
more descriptive for complex or very young children

-88: use if evaluating kid with ambulatory aids and/or orthoses/shoes

-66: barefoot, teaks less time, more meaningful assessment of change bc items ordered by level of difficulty

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
27
Q

Administering GMFM-88 takes about -__ to ___ minutes for someone familiar with the measure

A

45-60 minutes

28
Q

GMFM-66 takes about ___ min

A

20-30 minutes

29
Q

precautions for children with spastic diplegic CP

A

lever arm dysfunction, midfoot breakdown

30
Q

What are precautions for children with CP at age 8?

A

be aware of growth spurt

*extra affected due to tight gastroc/spastic diplegic CP
*MSK is progressive, so weakness with age and tightness as they grow

31
Q

Spina Bifida case study: myelominengocele presentation

A

▪ Diminished or absent trunk or lower extremity
strength and sensation
▪ Impaired bowel and bladder
▪ Possible poor motor control
▪ Changes in posture and alignment
▪ Decreased mobility and activity tolerance
▪ Deficits depend on level of injury
▪ Monitor for Scoliosis***

32
Q

Shunt malfunction signs:

A

▪ Headaches
▪ Vomiting
▪ Lethargy
▪ Irritability
▪ Vision issues or changes
▪ Decreased school performance
▪ Cognitive challenges/mild dementia.
▪ Periods of confusion
▪ Seizures
▪ Difficulty walking/gait disturbances
▪ Urinary urgency or incontinence
▪ Fever (sign of shunt failure or infection)
▪ Redness or swelling along shunt tract

33
Q

VP shunt as mainstay of treatment for ____ in both adult and pediatric patients

A

hydrocephalus

34
Q

signs of tethered cord syndrome

A

Weakness, numbness or problems with muscle function
in the legs.
▪ Tremors or spasms in the leg muscles.
▪ Changes in the way the feet look, like higher arches or
curled toes.
▪ Loss or change of bladder or bowel control that gets
worse

35
Q

What is the 1 year failure rate for VP shunts?

A

40-50% of pediatric patients until few decades ago….shunt malfunctions are found to be approx 15%

36
Q

PT interventions for SB includes…

A

-risk for obesity, osteoporosis, UTIs,
functional mobility training, what life will look like…
-exercises

37
Q

symptoms of hydrocephalus in infants

A
  1. enlarged head
  2. bulging/tense soft spot on top of head
  3. downward looking eyes
  4. high pitched cry
  5. problems sucking/feeding
  6. recurrent vomiting
  7. seizures
38
Q

symptoms of hydrocephalus in children/adults

A
  1. headaches
  2. blurred/double vision
  3. loss of bladder control
  4. nausea/vomiting
  5. problems with balance
  6. vision problems
  7. decline in school or job performance
  8. poor coordination
  9. sleepiness or hard time waking up
  10. irritability
39
Q

symptoms of hydrocephalus in older adults

A

difficulty walking or slow shuffling
memory problems, dementia
problems with balance, coordination
tremor or shaking

40
Q

Initial radiographs for children with down syndrome should be taken when?

A

between 3-5 years of age

*atlanto-axial instability
*possible cervical instability

41
Q

children with DS have higher incidence of ________

A

cardiac (heart defects)
hearing
endocrine
developmental
dental defects/health issues
*cervical instability
*AA instability in about 15%

42
Q

IDEA PART B is what?

A

federal legislation for school-aged services for students 3-21 years with disabilities

43
Q

What is the IEP?

A

legally binding document developed annually for students

44
Q

IDEA PART C

A

federal legislation establishes early intervention services for infants and toddlers (birth to 3 years) with disabilities

45
Q

What is IFSP?

A

Individualized family service plan for those receiving early intervention. Educated at least 1x/year and reviewed at least every 6 months

46
Q

Section 504 of the rehabiliation Act of 1973:

A

Federal legislation that makes discrimination against individuals
with disabilities illegal

▪ Section 504 provides that students who do not require specially
designed instruction may receive accommodations and services
including physical therapy if they are considered to have a
disability that impacts a major life function

47
Q

Americans with Disabilities Act of 1990 (ADA)

A

▪ Federal civil rights legislation that prohibits discrimination against
individuals with disabilities in employment, transpiration, public
accommodations communications, and governmental activities

▪ Treating across life-span and education families

48
Q

Are children tiny adults?

A

NO! growth plates!
-physiologically: young children under 4 yrs have an unreliable thermoreg system

-risk of hypothermia is higher in children as they are less efficient in generating heat, lose heat more readily

49
Q

CANNOT DO THERAPEUTIC ULTRASOUND OVER GROWTH PLATES, OK?

A

epiphyseal plates!!!

*you CAN do diagnostic ultrasound, they do this for hip dysplasia dx

50
Q

What influences body structures (connective tissues, bone, mm)?

A

force
shape
genes
nutrition
drugs
hormones
actiivites/lack of

51
Q

bone, cartilage and mm are derived from what embryonic layer?

52
Q

growth plates
produce increase growth in response to
tension and decreased growth in response to
excessive compression
What principle is this?

A

Hueter-Volkman Principle

53
Q

What is Bone age?

A

helps docs estimate skeletal maturity
take single x ray of left hand, wrist, fingers

54
Q

scoliosis: x ray of iliac crest to see how much bone growth is left
What is this called?

A

RISSER SIGN
1: 25 (lot of ossificiation of iliac epiphysis left, bad sign if u have scoliosis)
2: 50
3. 75
4: 100
5: fused to ilium

55
Q

posterior fontanelle closes ___, anterior fontanelle closes _____

A

posterior: 1-2 mo
anterior: 7-18 mo

56
Q

fontanelle closure has implications for what child population?

A

children with plagiocephaly and torticollis!
REFER WAY BEFORE 18 MONTHS

57
Q

What is the principle where bones develop in response to mechanical forces placed on them?

A

Wolff’s Law

58
Q

Difference between epiphyseal plates and lines

A

plates: occur at various locations at epiphyses of long bones, GROW

lines: plates have fused, growth not possible

59
Q

What is osteogenesis imperfecta?

A

genetic disorder where bones break easily

20-50,000 people in USA

60
Q

dominant/classical OI is a condition where

A

person lacks TYPE 1 COLLAGEN or has poor quality of type 1 due to mutation in one of those genes

61
Q

In recessive OI, mutations in -___ interefere with -____

A

other genes mutation interfere with collagen production

62
Q

What tests help diagnose OI?

A

-clinical features
-biochemical biopsy (collagen) test
-molecular (DNA) tests
(tests require several weeks)

*detect almost 90% of all type 1 collagen mutations

63
Q

What is the medical management of “brittle bone disease” or OI?

A

▪ Bisphosphonate
▪ Infusions & Vitamin D

64
Q

clinical characteristics of OI

A

▪ Hyperlaxity of Ligaments
▪ Fragile Skin
▪ Poor Thermoregulation
▪ Blue Sclerae
▪ Dentinogenesis imperfecta – issues
with teeth

65
Q

PT precautions with INFANT HANDLING if they have osteogenesis imperfecta

A

Carry with widespread hands over head/shoulders and
bottom
▪ Diaper changes done by lifting buttocks, not ankles

*open laces/braces WIDE, do not twist, pull on body parts
*MMT ONLY at midshaft of bone, ONLY if osteoporosis is not advanced, prob not tolerated

*no trunk extension/flexion for core strength (spine fx)

*caution with managing joint contractures