Orthopedics - The Spine (Jurkovic) Flashcards

1
Q

Deformities are defined by what the plane of the deformities. What defines a Scoliosis? What defines a Kyphosis or Lordosis?

A
  • Scoliosis is defined in the coronal plane by greater than 10 degrees
  • Kyphosis or Lordosis is defined by the sagittal plane. Kyphosis is usually 20-40 degree for the thoracic spine, and lordosis increases for the lumbar spine
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2
Q

Where is the curve location dictated by?

A

based upon apex of the curve

  • Cervical C1-C6
  • Cervical thoracic C7-T1
  • Thoracic T2-T11
  • Thoracolumbar T12-L1
  • Lumbar L2- L4
  • Lumbosacral L5-S1
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3
Q

What are the prominent features of adolescent idiopathic scoiosis (AIS)?
What is its prevalence?

A
  • lateral curvature occuring at or near the onset of puberty without etiology.
  • In 2-3% it is <10 degree curve
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4
Q

What two factors are known to predict curve progression?

A
  • Lesser maturity - as you are growing asymmetry can affect the growth of bones
  • Larger curve magnitude
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5
Q

How do you measure the Cobb angle?

A
  • Angle created by measuring the a line parallel with the top vertebrae of the top of the curve and another line parelell with the bottom vertebrae of the bottom of the curve.
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6
Q

Why is a double major curve harder to diagnose?

A
  • Because it is there is a compensatory curve for the primary curve thereby making the curve appear not as bad.
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7
Q

Curves under what degree tend not to progress?

What degree curve has the greatest likelihood of progressing?

A
  • Curves under 30 degrees do not tend to progress

- curves greater than 50 degrees

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8
Q

What types of curvatures put patients at an increased risk of cor pulmonale (increased RV due to hypertension in the lungs)
- What degrees does breathing issues result?
What will result in more pulmonary loss?

A
  • patients with a high-angle thoracic curve greater than 100 degrees;
  • do not occur until 100-120 degrees
  • Lesser curves with significant hypokyphosis (flatter thoracic spine)
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9
Q

What is curvature significance with pregnancy?

A
  • Does not worse during pregnancy and does not cause problems with preg.
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10
Q

What are the manifestations of the rib/vertebral structure in a scoliotic curve?

A

The ribs are pushed more lateral and anterior on the concave side, the spinous process is deviated to the concave side, the Lamina is thinner and verebral canal is narrower on the convex side. The vertebral body is distorted toward the convex side and the ribs are pushed posteriorly and thoracic cage narrowed on the convex side.

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11
Q

What can neurologic symptoms be indicative of in curvatures?

A

-progression of the the scolosis.

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12
Q

What is the Adams test?

A

-Bend forward and look for prominances

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13
Q

What are the big things to look for in a x-ray?

A

interpedicular widening, congenital abnoramalities, rib pencilling, skeletal maturity

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14
Q

What is the Risser Sign?

A

It is a # assigned to designate skeletal maturity, the lower the # the more mature and therefore the greater the risk of progression

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15
Q

What are the normal curve patterns?

A

Lumbar cuve - apex left

Thoracic curve - apex right

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16
Q

What is seen with an Atypical curve?

A
  • Lumbar curve - apex right
  • Thoracic curve apex left
  • Long C-shaped neuromusclular curve
  • Curve with short, sharp apex
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17
Q

What is the criteria for bracing?

A

A patient with allot of growth left and with a Risser 2 or less and:

  • Cobb angle > 25 degrees
  • Cobb angle > 20 degrees with documented 5 degrees progression
  • *Must have a flexible curve or they will not tolerate the brace
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18
Q

In infantile idopathic scoliosis (birth - 3 yrs) what is used to predict progressive scoliosis?

A
  • Measure the Mehta rib vertebral angle difference (measures sternal to rib angle) and a greater than 20 degree difference between the left and right sides indicates and 80% chance of progression (
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19
Q

For Juvenile Idiopathic Scoliosis (4-10 yrs) what RAD indicates possible progression?
- What else do you need to rule out the absence of an abnormality?

A
  • RAD > 10

- an MRI

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20
Q

What is diastemotomyelia?

- What is diplomyelia?

A
  • Boney or fibrous defect that splicts the spinal cord, as the spine elongates traction occurs on the cord
  • Spilt cord
21
Q

What are some main defects of neuromuscular scoliosis?

A
  • Boney defect
  • Interpedicular distance
  • Tethered cord: traction on end of cord, thickened filum terminale, lipoma ( fat pad - causes traction on the cord and effects the microcirculation on cord (resulting in leg pain and back pain)
22
Q

In neuromuscular scoliosis, what is a Myelomeningocele and what are its main attributes?

A
  • Myelonmeningocele
    • Neural tube defect: when flat it doesn’t close- high correlation with folate deficiency
    • Widened interpedicular distance
    • Missing posterior elements: no spinous processes, no lamina
    • Possible Arnold-currarie (brain stem herniating through the foramen magnum.
23
Q

In neuromuscular scoliosis, what is a Hydrosyrinx?

A

The expansion of the spinal cord occurs with CSF in the inner canal.
- Treating the hydrosyrinx can possibly improve the scoliosis

24
Q

What are the types of neuromuscular scoliosis and what are the subtypes?

A
    • Lower motor neuron:
      • ->Polio
      • -> Spinal musclular atrophy (SMA)
      • -> Dysautonomia
  • Myopathic
    • -> Muscular dystrophies
    • -> Arthrogryposis
25
Q

What are the 4 types of congenital scoliosis formation problems?

A
  • Wedge vertebrae (partial unilateral failure of formation)
  • Hemivertebra (complete unilateral failure of formation- 6 degrees a year with most at 50 degrees by 4 years
  • Congenital Bar (unilateral failure of segmentation. (5 degrees a year with most 50 degrees by 10 years)
  • Block vertebra: bilateral failure of segmentation.
26
Q

What is a VATER complex?

A

is an association of congenital anomalies consisting of vertebral defects, aortic problems, renal insufficiency, etc. Requires an MRI.

27
Q

What is Klippel-Feil and percentage of patients with congenital scoliosis has it?

A

Congenital fusion of any 2 of the 7 cervical vertebrae, approx. 25% have it

28
Q

What are the congenital scoliosis prognosis?

A
  • Unilateral unsegmented bar (4 degrees with most 50 degrees by 10 years)
  • Unilateral bar with contralateral hemivertebrae (6 degrees with most at 50 degrees by 4 years)
  • Two ipsilateral hemivertebrae ( often each 70 degrees by maturity)
  • Nonsegmented hemivertebrae ( rarely require treatment except at LS junction)
29
Q

What is the treatment for congenital scoliosis?

A
  • Hemiepiphyseodesis appears effective in correcting some below 7 years
  • dependent on fusion location
  • fuse early before the curve gets bad and an osteotomy is required
30
Q

What is the treatment for Congenital muscular Torticolis?

What is the prognosis?

A
  • Gentle stretching
  • Place crib toys, mirrors, etc. on opposite side
  • Greater than 80% resolve in 1 year - if not resolved by 1 year may require surgery
31
Q

What are some associated problems with Kippel-Feil syndrome?

A
  • Sprengel’s (33%)
  • GU anomalies (25-35%)
  • Hearing problems or deafness (15-36%)
32
Q

What is Sprengel Deformity?

A

Congenital deformity where one shoulder blade is higher than the other one

33
Q

What is Synkinesis?

What are some associated problems with Sprengel deformity?

A

20% - can occur in many normal preschool children
- sykinesis, pulmonary problems, congenital heart disease (14-29%), spinal cord (parrellels with vertebral congenital abnormalities),

34
Q

What are some long term concerns of Sprengel deformity?

A
  • worry of instability, disc herniations, instability, spontaneous paralysis, surgical indications are common sense.
35
Q

What are high risk patients?

A
  • patients that have
    • ->2 sets of block vertebrae with an open intervening disc
    • -> Craniocervical abnormalities with a congenital fusion below C2
    • -> Fusion of one or more levels associated with stenosis at any cervical level- the fusion and stenosis need not be at the same level.
36
Q

What bone orthopedic problems can occur in Down Syndrome’s?

A

Ligamentous Laxity

  • C1-C2 instability ( fusion can be difficult and hazardous, most people base upon symptoms, natural history is controversial, x-ray age 5 and 15
  • Occipital Cervical instability (easily overlooked)
37
Q

In skeletal dysplasias ( increase in the # of immature cells) what do you need to be especially aware of?

A
  • C1-C2 instability ( in all storage diseases, Spondyloepipyseal Dysiplasia- a defect in the ossification center -SED)
38
Q

What are some disorders associated with cervical kyphosis?

A
Diastrophic dysplasia
Larson syndrome (cervical kyphosis in children)
39
Q

What would require a workup with a back pain evaluation?

A
  • Persistance (3-4 weeks)
40
Q

What are the possible etiologies of a back pain diagnosis?

A
  • Trauma
  • Vertebral Stress Fracture
  • Bony abnormalities
  • Psychogenic pain
  • Benign
  • Malignant
  • Metastatic
  • Somatic dysfunction
  • Muscle spasm
  • Mechanical low back pain
  • Spinal Dysraphism (incomplete closure of the raphe)
  • Tumor
  • Juvenile Rheumtoid Arthritis
41
Q

What is the trend with benign mechanical back pain?
What are the contributing factors?
Are the symptoms continuous?

A
  • increasing - 50% of young adults reported pain
  • Deconditioning , backpacks
  • Symptoms are intermittent
  • *OMT is indicated
42
Q

What is a SPECT scan best used for?

A
  • Spondylolysis (common cause of back pain in kids)
43
Q

What is the best use for and MRI?

A

Intraspinal pathology, nerve involvement.

44
Q

What are two defects of the posterior elements?

A

Spondylolysthesis ( disc slippage )

Spondylothesis - pars inticularis break - tightness of hamstrings

45
Q

What is Scheuermann disease?

A

Inflammation of growth plates of vertebral bodies, increased throracic kyphosis (most common site)

46
Q

What are significant on the X-ray for Scheuermann Disease?

A
  • Lateral Cobb angle > 45 degrees
  • Wedging of 5 consecutive vertebrae
  • Schmorl’s nodes ( on lateral view can see when a lateral disk pushes up through the end plates)
47
Q

What are some symptoms of scheuermann
disease?
What is part of the differential diagnosis?

A
  • Thoracolumbar (kyphosis, pain)
  • Lumbar Scheuermann (pain and no deformity)
  • Discitis (IV disc inflammation –>narrowing disc space–>self-limiting- <5yrs old, S. aureus)***
48
Q

What is the corkscrew deformity?

A
  • anterior vertebral fusion - high risk of morbitity and mortality - want to wokr on them as close to skeletal maturity as possible.
48
Q

What is the corkscrew deformity?

A
  • anterior vertebral fusion - high risk of morbitity and mortality - want to wokr on them as close to skeletal maturity as possible.