NEURAL TUBE DEFECTS Flashcards

(41 cards)

1
Q
  • A CNS defect resulting from failure of neural tube to close during the embryo’s early development (the first 3 to 5 weeks)
  • constitute the largest group of congenital anomalies with multifactorial inheritance
A

neural tube defects

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2
Q

deficits for those with NTDs

A

sensorimotor disturbance
dislocated hips
talipes equinovarus (clubfoot)
hydrocephalus

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3
Q

Globally, more than ___ pregnancies are estimated to be
affected by NTDs, and ___% of the NTD live births result in
under-5 deaths.

A

260,000
75%

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4
Q
  • In the Philippines, about 0.9 % (around 1 in 5) are folate-deficient
    based on ___, while 38.7% (around 2 in 5) are folate deficient based on ___ (Ostrea, 2022)
A

red cell folate count
serum folate

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5
Q

In 1992, US Public Health Service: All woman childbearing age, capable of becoming pregnant –
should take 0.4 mg (400 mcg) ___ per day for purpose of reducing risk of NTD’S.

A

folic acid

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6
Q

etiology and risk factors of NTDs

A
  • Folic acid deficiency
    *Chemicals: Alcohol
    *Medications: Anti-epileptic and isotretinoin for acne
  • Exposure to radiation
    *Maternal obesity; GDM
  • Previous NTD pregnancy
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7
Q

a malformation where the brain is
totally exposed or herniated through a
skull defect

A

exencephaly

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8
Q

a protrusion of the brain
and meninges into a fluid filled sac through a skull defect

A

encephalocele

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9
Q
  • a skull defect through
    which various tissues
    protrude
  • Failure of the bones of the
    skull to close
A

cranioschisis

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10
Q
  • a disorder in which the
    brain growth is so slow
    that it falls more than
    three standard deviation
    below normal growth
    charts
A

microcephaly

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11
Q
  • brain is degenerated to a
    spongiform mass with no bony
    covering in a fetus
  • absence of the cranial vault with
    cerebral hemispheres either
    completely missing or greatly
    reduced in size.
A

anencephaly

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12
Q

2 most common types of NTDs

A

anencephaly
spina bifida

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13
Q

*there is an incomplete closure
of the vertebrae & neural tube
*fissures in the spinal column
that leaves the meninges and
spinal cord exposed

A

spina bifida / rachischis

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14
Q

types of spina bifida

A

spina bifida occulta
spina bifida cystica

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15
Q
  • failure of the posterior vertebral
    arches to fuse
  • at the 5th lumbar or 1st sacral
    vertebrae
  • there is no herniation of the
    spinal cord or meninges
A

spina bifida occulta

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16
Q

spina bifida occulta

spinal cord -
meninges -
neurological deficits -

A

spinal cord - intact and not visible
meninges - not exposed on skin surface
neurological deficits - not usually present

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17
Q

sign of spina bifida occulta

A

Small dimple, birthmark, or patch of
hair over the lower back

18
Q
  • Protrusion of the spinal
    cord and meninges
  • a defect in the closure of
    the posterior vertebral
    arch
A

spina bifida cystica

19
Q

2 anomalies of spina bifida cystica

A

meningocele
myelomeningocele

20
Q
  • Protrusion involves meninges and a saclike cyst that contains CSF in the midline of the back (lumbosacral area)
  • No spinal cord or nerves in the sac
  • No or mild neuro deficits
21
Q
  • Sac-like Protrusion of the meninges, CSF, nerve roots, and a portion of the
    spinal cord occurs
  • Neurological deficits are evident
  • Most serious type of Spina Bifida
A

Myelomeningocele

22
Q

sign of meningocele

A

: Fluid-filled sac on back, covered
by skin

23
Q

sign of myelomeningocele

A

The sac (defect) is covered by a
thin membrane prone to leakage or
rupture

24
Q

prognosis of meningocele

A

Generally good if no
nerves involved

25
prognosis of myelomeningocele
Variable; often lifelong physical and cognitive disabilities
26
assessment during intrauterine life
* Sonography * Fetoscopy *Amniocentesis
27
assessments done after birth
* Ultrasound * Transillumination (if with lesion) * Radiologic studies * CT scans & MRIs * Flat plate films of the spinal column * Neurological examination of the extremities
28
a medical technique where light is shined through a body part to assess its internal structure and identify abnormalities
transillumination
29
true or false - the higher the defect, the greater neurologic dysfunction
true
30
clinical menifestations
* visible spinal defect * flaccid paralysis of the legs * altered bladder & bowel function * orthopedic problems (hip and joint deformities) * weakness * sensory loss * Hydrocephalus
31
neurosurgical repair of meningocele and myelomeningocele is usually done within ___ hour after birth
24-48 hours
32
what is done to repair meningocele
sac removes and spinal defect is closed
33
Cover the sac on the newborn’s back with a ___
sterile saline dressing
34
Place the infant in a prone position with hips ___ & legs ___
hips slightly flexed & legs abducted
35
true or false - Feed the infant with the head turned to one side
true
36
signs of increased ICP may indicate
hydrocephalus development
37
post op - Placed in the ___ position with head ___
prone or side-lying head elevated
38
If a Ventriculoperitoneal (VP) shunt was placed: *monitor for:
* hydrocephalus * increased intracranial pressure * infection
39
diet for long term home care
low fat, low CHO, high CHON, high fiber
40
___ (act on smooth muscle of the bladder) to increase bladder capacity and improve continence
anitspasmodics
41
Bowel program for long term home care
high-fiber diet, increased fluids, suppositories