Cerebral Palsy Flashcards

1
Q

Risk Factors for CP

A
Prematurity
Low birth weight
Low maternal education
Poor prenatal care
Maternal or fetal infection or inflammation
Multiple pregnancy
Perinatal asphyxia
Brain malformation
Genetic disorders
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2
Q

Diagnosis of CP

A
12-18 months
History and physical
Neuroimaging studies, e.g., MRI, CT scan
Metabolic and genetic screening
Coagulation studies
Developmental surveillance, i.e., motor, speech and language, cognition, vision, hearing
Nutritional and growth status
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3
Q

Clinical Signs of CP

A
Qualitative movement differences
Muscle tone differences
Hypertonia
Hypotonia
Failure to attain, or asymmetrical development of, motor milestones
Decreased muscle strength for transitional movements
Deficits in postural control development
Deficits in voluntary motor control
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4
Q

Prenatal Causes of CP

A

Congenital problems causing defects in the developing brain
Maternal infections: rubella, cytomegalovirus, toxoplasmosis
Metabolic disorders
Rare genetic syndrome

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5
Q

Congenital problems causing defects in the developing brain

A

Microcephaly
Schizencephaly-cleft defect
Lissencephaly- smooth brain

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6
Q

Classification by Topography

A
Hemiplegia (33%) 
Diplegia (44%)
Triplegia
Quadriplegia (6%)
Monoplegia
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7
Q

Diplegia

A

primary motor impairment of lower limbs, limited involvement of upper limbs

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8
Q

GMFCS Level I:

A

Walks without restrictions; limitations in more advanced gross motor skills

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9
Q

GMFCS Level II:

A

Walks without assistive devices; limitations walking outdoors and in the community

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10
Q

GMFCS Level III:

A

Walks with assistive mobility devices; limitations walking outdoors and in the community

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11
Q

GMFCS Level IV:

A

Self-mobility with limitation; children are transported or use power mobility outdoors and in the community: most likely to have power wheelchair

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12
Q

GMFCS Level V:

A

Self-mobility is severely limited even with the use of assistive technology

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13
Q

GMFCS 0-2 Age Band

Level I

A
  • -Sits on floor with hands free­
  • -Moves in and out of floor sitting
  • ­‐Crawls on hands and knees
  • ­‐Pulls to stand and takes steps holding onto furniture
  • ­‐Walks between 18-­‐24 months without assistive mobility devices, AMD
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14
Q

GMFCS 0-2 Age Band

Level II

A
  • ­‐Maintains balance in floor sitting but may use hands for support
  • ­‐Creeps on stomach or crawls on hands and knees
  • ­‐May pull to stand and take steps holding onto furniture
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15
Q

GMFCS 0-2 Age Band

Level III

A

Maintains floor sitting with low back support

-­‐Rolls and creeps forward on stomach

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16
Q

GMFCS 0-2 Age Band

Level IV

A

Head control but trunk support required for floor sitting

-­‐Rolls to supine, may roll to prone

17
Q

GMFCS 0-2 Age Band

Level V

A

Limited voluntary control of movement

  • ­‐Unable to maintain head and trunk postures in prone and sitting
  • ­‐Requires assistance to roll
18
Q

GMFCS 2-4 age band

Level I

A
  • Sits on floor with hands free
  • Requires assistance to move in and out of floor sitting and standing
  • Walks without AMD as preferred mobility method
19
Q

GMFCS 2-4 age band

Level II

A

May have balance difficulty in hands free sitting on floor

  • Requires assistance to move in and out of sitting on floor
  • Pulls to stand on stable surface
  • Crawls using reciprocal pattern
  • Cruises holding onto furniture
  • Walks using AMD as preferred mobility method
20
Q

GMFCS 2-4 age band

Level III

A

Maintains floor sitting, often by “W-sitting”; may require assistance to assume

  • Creeps on stomach or crawls on hands and knees, often without reciprocal leg movements as primary means of mobility
  • May pull to stand on stable surface and cruise short distances
  • May walk short distances indoors using AMD and assistance for steering and turning
21
Q

GMFCS 2-4 age band

Level IV

A

Floor sits when placed but uses hands support to maintain alignment and balance

  • Frequently requires adaptive equipment for sitting and standing
  • Self-mobility for short distances in room through rolling, creeping on stomach, or crawling on hands and knees without reciprocal leg movement
22
Q

GMFCS 2-4 age band

Level V

A

Restricted voluntary control of movement and ability to maintain antigravity head and trunk postures

  • Limited motor function including sitting and standing that are not fully compensated for through use of adaptive equipment and assistive technology
  • No independent mobility and are transported; some achieve self-mobility using
23
Q

Manual Ability Classification System, MACS

A

observed ability to handle objects in daily activities, e.g., eating, dressing, playing, drawing, writing
5 levels, 4-18 years

24
Q

MACS Level I

A

handles objects easily and successfully

25
MACS Level II
handles most objects but with somewhat reduced quality and/or speed of achievement
26
MACS Level III
handles objects with difficulty; needs help to prepare and/or modify activities
27
MACS Level IV
handles a limited selection of easily managed objects in adapted situations
28
MACS Level V
does not handle objects and has severely limited ability to perform even simple actions
29
Primary Impairments
due to pathophysiology
30
Secondary Impairments
develop over time as a result of other impairments, activity limitations, participation restrictions, contextual factors, i.e., environmental, personal
31
Primary Impairments in | Children with Cerebral Palsy
Muscle tone and extensibility Muscle strength Postural control Selective motor control
32
Muscle Stiffness
abnormally high tone or muscle hypoextensibility requiring more force to produce length changes.
33
Differences between spastic muscle and normal muscle
``` decreased number of muscle fibers. shorter resting sarcomere length. increased collagen concentrations. poor organization and quality of extracellular material ```
34
Children with CP have:
decreased muscle strength Decreased EMG activity due to neuronal drive, co-activation of antagonist muscles, secondary myopathy, altered tissue properties. Biomechanical changes reducing torque, may also impact joint structures. More weakness in distal musculature, concentric contractions, faster movement speeds
35
Selective voluntary motor control:
the ability to isolate muscle activation that is a primary impairment
36
Poor SVMC is characterized by
reduced movement speed or mirror movements, i.e., reciprocal activation on the opposite side of the body. Co-activation of antagonist muscle groups may also be evident when moving a limb
37
Difficulties with SVMC result in
coupled flexion or extension patterns or abnormal movement synergies, sometimes described as posturing.
38
What is whole task practice recommended for:
discrete tasks, e.g., reaching and grasping for an object, and for continuous tasks that require longer movement duration and cyclical repetition of limb movements, e.g., walking or cycling
39
What is part task practice recommended for:
serial tasks that involve a combination of discrete tasks, i.e., wheelchair transfer training.