torticollis Flashcards

1
Q

definition of CMT

A

a postural deformity evident shortly after birth, typically presenting as side bending of the neck to one side and head/chin rotation to opposite side

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2
Q

cause of CMT

A

shortening of SCM muscle and may be accompanied by other MSK or neuro conditions

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3
Q

right sided torticollis

A

right SB
left rotation
tight R SCM

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4
Q

incidence

A

as many as 16% of newborns (1 in 6) experience torticollis

more prevalent in males, with ratio of 3:2

CMT frequently accompanied with cranial deformation

15% of babies with CMT also have hip dysplasia

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5
Q

3 types of CMT

A

postural
muscular
SCM MASS

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6
Q

postural CMT

A

the infant exhibits a postural preference WITHOUT muscle tightness or restriction to PROM

mildest form

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7
Q

muscular CMT

A

characterized by tightness of the SCM muscle and limitation of PROM

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8
Q

SCM mass

A

presents with thickening of the SCM muscle and restricted PROM

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9
Q

etiology of CMT - prenatal factors

A

longer body length

intrauterine crowding

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10
Q

etiology of CMT - perinatal factors

A

birth trauma

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11
Q

etiology CMT - post natal factors

A

positional preference
containers
GI reflux

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12
Q

prognosis - referral before 1 month

A

98% of infants achieve near normal range within 1.5 months

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13
Q

prognosis w referral between 1-6mos

A

prolongs intervention to about 6 months

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14
Q

prognosis referral after 6 months

A

requires 9+ months of interventions with fewwer infants achieving near normal range

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15
Q

possible complications if untreated

A

trouble bringing hands to midline

delayed visual development and visual tracking

problems w motor planning

decreased protective responses on affected side

asymmetrical motor skills and transitional movements

cranial deformation

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16
Q

ket takeaways

A

named by side of tight muscle

frequently accompanied with cranial deformation

early diagnosis is key

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17
Q

family interview - history

A

Age at initial visit (chronological and corrected age)
* Age of onset of symptoms
* Pregnancy history including maternal sense of whether the baby was “stuck” in one
position during the final 6 weeks of pregnancy
* Delivery history including birth presentation (cephalic or breech); use of assistance
during delivery such as forceps or vacuum suction
* Head posture/preference and changes in the head/face
* Family history of torticollis or any other congenital or developmental conditions
* Other known or suspected medical conditions
* Developmental milestones appropriate for age

18
Q

family interview - routines

A

feeding
sleeping
tummy time
time in equipemnt/devices
daycare/sitter

19
Q

posture and positioning - supine

A

Document the side of
torticollis, asymmetrical
hip, trunk, and extremity
positions, facial and skull
asymmetries, restricted
AROM

20
Q

prone posture

A

Document asymmetry of
the spine, the head on
the trunk, asymmetrical
use of the extremities,
and the infant’s tolerance

21
Q

supported upright positions posture

A

Document asymmetrical
preferential postures and
compensations in the
shoulders, trunk, and hip

22
Q

sidelying posture

A

Document asymmetries,
trunk flexion or
extension, head lifting,
leg position

23
Q

bilateral AROM - cervical rot and lateral flexion

A

Assess in supine and supported upright if age
appropriate
* Asymmetrical and compensatory movements
can indicate muscle tightness, restrictions or
weakness
* Treatment to improve AROM consistent with
goals of early intervention

24
Q

bilateral PROM - cervical rot and lateral flexion

A

Severity of CMT determined by difference between left and right PROM measures of
cervical rotation
* Normal value passive cervical rotation for child < 12 months: 110 ± 6 degrees
* Normal value passive lateral flexion for child < 12 months: 70 ± 2.4 degrees

25
bilateral AROM/PROM - UE anD LE
Document infant’s natural movements * Passively move arms and legs through all available range at each joint * Passively move ribs and spine * Rule out: * Developmental dysplasia of hip (DDH): observe for symmetry and stability of hip, leg length symmetry, gluteal skin folds, hip scour test, Barlow and Ortolani Maneuvers * Brachial plexus injuries or clavicle fractures * Neurological impairments * Hypermobility * CNS lesions * Scoliosis
26
pain or discomfort
Document any behaviors reflective of discomfort, or pain reactions in the infant and child during the examination process * Pain is not typically associated with the initial presentation of CMT * The FLACC is recommended to document baseline status * The PT should work with the parents and caregivers to differentiate actual pain responses from discomfort or behavioral reactions to stretching, anxiety, or the stress of an unusual environment.
27
skin integrity
Document skin integrity * Symmetry of neck and hip skin folds * Presence and location of SCM mass * Size, shape and elasticity of SCM muscle and secondary muscles
28
craniofacial asymmetries and head/skull shape
Up to 90% of infants with CMT will also have craniofacial asymmetry * Document cranial deformities, including plagiocephaly, brachycephaly, and dolichocephaly * Craniofacial asymmetries on the side of the torticollis may include: * smaller and elevated eye with changes in the orbit * recession of the ipsilateral ear * a reduced jaw height with malocclusion * possible gum line asymmetry
29
cranial deformation
plagiocephaly brachycephaly dolichocephaly
30
plagiocephaly
most common type of infant flat head syndrome. Generally, the back of the baby’s head is flat on one side.
31
brachycephaly
second most common type of flat head syndrome. The back of the head is flattened instead of curved.
32
dolichocephaly
less common type of flat head synfrome head is flattened on both sides
33
craniosynostosis vs plagiocephaly
Premature closure of one or more cranial sutures * Prevalence ranges from 0.4% to 0.07% * Requires referral to neurosurgery
34
gross motor function
Test of Infant Motor Performance (TIMP): 0-4 months * Alberta Infant Motor Scale (AIMS): 0-18 months * Peabody Developmental Motor Scales (PDMS-2): 0-5 years
35
muscle function scale
0 = head below horizontal line 1 = head on the horizontal line 2 = slightly above line 3 = high above line but below 45dg 4 = head high above and more than 45 dg 5 = head very high almost vertical
36
treatment - first choice
Neck PROM – Gentle stretching. Should not be painful to baby and stopped if infant resists or parent perceives changes in breathing or circulation. Each cheek on caregiver’s chest or floor. Neck & Trunk AROM – Exciting things to the non-preferred side. Tummy time, short spurts, total > 1hr/day. Symmetrical Movement Development – Both sides, both ways. Sidelying, rolling, reaching. Want bend and twist, not arching. Environmental Adaptations – Carry baby vs keeping them in holders, use towel rolls inside of swing or holder Parent/Caregiver Education – Alternate sides for holding, feeding and changing diaper
37
discharge criteria
PROM within 5 dg of non affected side symmestrical active movement patterns age appropriate motor development no visible head tilt parents understand what to monitor in growth
38
re eval should include
positional preference symmetry of movement developmental milestones
39
consult primary care
When asymmetries of the head, neck, and trunk are not starting to resolve after 4-6 weeks of comprehensive intervention. 2. After 6 months of treatment with a plateau in resolution
40
cranial reshaping helmet
head shaping not improving with positioning 4-10 months old length depends on severity
41
key takeaways
Key Takeaways 1) Examination includes infant history, routines, body structures/posture, strength and mobility 2)Use decision tree to classify severity level 3) Follow first choice interventions 4)Use discharge criteria for developing goals and plan of care