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An Evaluation of the Infant with Motor Delays: When and How Much?

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An Evaluation of the Infant with Motor Delays: When and How Much? Sarah Winter, MD Neurodevelopmental Pediatrician Division of General Pediatrics – PowerPoint PPT presentation

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Title: An Evaluation of the Infant with Motor Delays: When and How Much?


1
An Evaluation of the Infant with Motor Delays
When and How Much?
  • Sarah Winter, MD
  • Neurodevelopmental Pediatrician
  • Division of General Pediatrics
  • University of Utah
  • Terry Holden, PT CHSCN
  • February 23, 2010

2
Objectives
  • Discuss hallmarks of motor delays in infants such
    as tone patterns, primitive reflexes, milestone
    delays, and deviances
  • Using cases to prompt discussion, compare
    differences in the approach to evaluation
  • Review brain MRI abnormalities with patterns of
    motor impairment
  • Review the purpose of the Neuromotor Team

3
Developmental Disorders in Children
Disorders of brain function
4
Neuromotor TeamChildren with Special Health Care
Needs
  • Specialty team within the Child Developmental
    Clinic
  • Types of patients seen
  • Typically birth to 36 months
  • Older children with motor impairment with case
    management needs
  • Team members
  • Sarah Winter, MD, Terry Holden, PT, Scott Jerome,
    PT, and Alison Seppi, RN
  • Oversight Jim Taliaferro, LCSW

5
My developmental path to understanding gross
motor delay
6
  • But how do you apply this disparate knowledge and
    be helpful to this child and family?

7
Developmental Progress
  • Move from chaotic pieces of knowledge
  • A systematic approach of identification,
    evaluation, and intervention

To
8
A Systematic Approach
9
References for Screening
  • 2001 AAP Policy Statement Developmental
    Surveillance and Screening of Infants and Young
    Children
  • EPSDT Early Periodic Screening, Diagnosis, and
    Treatment
  • 2006 AAP Policy Statement Identifying Infants
    and Young Children with Developmental Disorders
    in the Medical Home An algorithm for
    Developmental Surveillance and Screening

10
References to Screening and Surveillance
  • Society for Development and Behavioral Pediatrics
    website www.dbpeds.org
  • Grand Rounds by Paul Young and Charlie Ralston
  • Podcast produced by Dr. Paul Carbone
    www.utah.edu/podcast

11
Features of a Good Developmental History
  • Parents describe gross motor skill delays well
  • People both parents and medical care providers,
    dont tend to pay attention to fine motor skills
    e.g. when are kids supposed to have a hand
    preference?
  • Ask about language, it is a clue to cognitive
    development

12
The Pediatric Neurodevelopmental Exam
  • Gross Motor findings
  • Fine Motor findings
  • Language findings
  • Expressive
  • Receptive
  • Social/Behavioral findings

13
Focused exam findings
  • Tone patterns
  • Low tone mild or severe?
  • High tone is it symmetric?, is it typical
    (LEgtUE)?
  • weird tone ataxia, tremor, fluctuating
    (dystonia)

14
Gross Motor Exam Findings
15
Focused exam
  • Reflexes
  • High or absent
  • Primitive reflexes see figure
  • Postural or protective responses
  • Lateral, anterior, posterior supports
  • parachute

16
Examples of primitive reflexes
  • The Moro is normal in a newborn and should be
    gone by 4 months
  • The ATNR is normal in a newborn and should be
    gone at 6 months

17
Postural (or protective) responses
Parachute response (appears at 10 months)
Lateral support (appears at 6 months)
  • Anterior (comes 1st) , lateral (2nd), and
    posterior (3rd) support responses
  • Parachute response

18
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19
Increased tone
20
gross motor examination
  • This child presents with delays in gross motor
    milestones. His tone is likely low
  • Differentiate between tone and strength

21
Focused Exam
  • Deviant (atypical but not always delayed) motor
    patterns
  • Bottom scooters
  • Circling hands and feet while balanced on the
    bottom (hypotonia) Some confuse this for a sign
    of autism
  • Commando crawling (hemiplegia)

22
Gross motor testing standardized measures of
gross motor function
  • Frequently used tools
  • Peabody Developmental Motor Scales
  • Bayley Scales of Infant Development
  • Gross Motor Function Scale
  • TIMP
  • Alberta Infant Motor Scales
  • Purpose
  • Further diagnostic information
  • Qualifying children for therapeutic services
  • Developmental measure or mark in time

23
Motor Assessment Tools
24
Narrowing the Differential Diagnosis
  • Patient A in top graph 18 months with negative
    past medical history.
  • Patient B 12 month old with history of failure
    to thrive

25
Medical Diagnostic Considerations
26
Case 1
  • 10 month old not sitting or rolling
  • Pregnancy/Labor/birth HX Uncomplicated
    pregnancy, NSVD, BW 8 3 oz. Apgars normal
  • FHx noncontributory

27
1
  • Physical exam cute blonde, fair skinned, growth
    parameters weight gtgt95, hgt 75, OFC, 75 rest
    of exam normal
  • Neuro exam low trunk tone, high extremity tone
    upper extremities more involved than lower
    extremities. Hyperreflexia throughout
  • Neurodevelopmental exam GM no sitting balance,
    prominent extensor thrust , FM fisted hands,
    language smiling, babbling

28
What is an appropriate work-up?
  • Imaging?
  • CT vs. MRI
  • Metabolic Studies?
  • Genetic Studies?

29
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30
Case 2
  • 24 month old with language delay, not using left
    arm as well as right arm
  • Pregnancy.labor /delivery uncomplicated
  • Family History negative
  • Physical exam
  • Neuro exam reflexes, tone, strength intact
  • Neurodevelopmental exam walking, asymmetric use
    of hands LltR, language delay

31
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32
How helpful is imaging?
  • Practice Parameter Diagnostic assessment of the
    child with cerebral palsy Ashwal and Russman et
    al, Neurology (2004)
  • Yield of abnormal brain CT in children with CP
    77
  • Yield of abnormal brain MRI in kids with CP 89
    and it is helpful in determining timing of injury
  • Depended on type (n264)
  • (dyskinetic CP 100, quadriplegia 98, hemi 96,
    diplegia 94 ataxic 75)

33
How helpful are metabolic and genetic studies?
  • In children with dx of CP
  • 0 4 of children have a metabolic or genetic
    cause (Ashwal, Russman)
  • In almost all cases there were atypical features
  • Hx suggestive of regression
  • Neuroimaging suggesting genetic or metabolic
    injury
  • Family history of childhood neurologic disorder
  • If clinical history or findings on neuroimaging
    do not determine a specific structural
    abnormality or if there are atypical or
    additional features on the history or clinical
    exam, metabolic and genetic testing should be
    considered.

34
What if the child doesnt have CP but a broader
presentation of global developmental delay?
  • Moeschler J, Shevell M and the Committee on
    Genetics Pediatrics, 2006
  • Describes what pediatricians can anticipate as an
    optimal clinical genetics evaluation
  • Karyotype, FISH for subtelomere abnormalities,
    Frag X, molecular genetic testing, imaging,
    metabolic testing
  • Report on the usefulness of high resolution
    chromosome studies (9 36) in patients
    evaluated for DD/MR
  • Routine metabolic screening of all patients with
    DD/MR is not required

35
Gross motor delay and its relationship to other
brain functions
  • Cognition function and CP, depends of the type
  • For children with spastic quadriplegic CP
    (Strauss, DMCN, 2005)
  • 95 with MR
  • If had dyskinetic CP only 40 with profound MR
    and 20 no MR

36
Gross motor delay and its relationship to other
brain functions
  • Cognitive Function and Developmental Coordination
    Disorder or mild motor delays
  • No good epidemiologic data

37
Using CP as a paradigmChildren Who Outgrew CP
Nelson, Ellenberg Pediatrics, 1982
  • 229 infants age 12 months with diagnosis of CP
  • Examined again at 7 y. o.
  • 118 free of motor handicap
  • 13 of white children and 25 of black children
    with MR
  • Nonfebrile sz, abnormalities of speech, behavior,
    and extraocular movements were more frequent than
    controls

38
When do you not need a brain MRI when evaluating
a child with motor delays?
  • Mild delay
  • Looking for an inutero infection that would leave
    calcifications (CT is better)
  • Ultrasound in the NICU showed cystic
    encephalomalacia and development is consistent
    with this pattern of CP (generally SQ CP but can
    have mixed tone)

39
Treatment/Intervention
  • Cure vs. maximize functional abilities
  • Only one cure in my clinical years

40
National Center for Medical Rehabilitation
Research
(1995)
  • Model to assist in the direction of research
  • Paradigm for chronic disorders
  • Good fit for persons with motor disorders such as
    CP, muscular dystropy, spinal cord injury or
    birth defect (SB)

41
Neuromotor Team Evaluations
  • Medical Evaluation and Diagnosis
  • Therapy PT performs PDMS for evaluation
  • Educational Concerns frequent referrals to EI
  • Technology assistive devices
  • Social Supports referrals to programs as needed

42
Questions??
  • Sarah Winter, MD
  • Phone 801-581-7877
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