Neural Tube Defects Flashcards

1
Q

Is used to describe many distinctly malformations of the neural tube

A

Neural Tube Defect

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2
Q

It is the developing brain & spine od the fetus at 3-4 weeks of gestation

A

Neural Tube

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2
Q

Why is the neural tube susceptible to malformations?

A

Because NT forms in utero firet as a flat plate and then molds to form the brain & spinal cord.

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3
Q

It is the process in which the neural plate bends up and later fuses to form the holloe tube that will eventually differentiate into the brain & the spinal cord of the CNS.

A

Neurulation

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4
Q

Risk Factors of NTDs

A
  • Folic acid deficiency
  • Family hx of NTDs
  • Maternal age under 20 or over 40
  • Maternal educaction
  • Low socioeconomic status
  • Maternal diabetes
  • Maternal obesity
  • Certain drugs such as valproic acid - used to treat seizure disorders
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5
Q

Two most common NTDs

A
  1. Anencephaly - brain defect
  2. Spina Bifida - spinal cord efect
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6
Q

When does neural folds fuses?

A

Around Day 21-28 (3-4 weeks of gestation)

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7
Q

Order or sequence of fusion of neural folds

A
  1. Begins midline
  2. Cranial
  3. Going downward to caudal
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8
Q

Two possible outcomes of neural fusion

A
  1. Complete fusion of neural tube
  2. Unfused neural tube segment (incomplete)
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9
Q

Is the most severe type of NTD in which both the brain and spinal cord remain open

A

Cranioachischisis

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10
Q

Is a condition in which major portions of the brain, skull, and scalp are absent or failed to develop

A

Anencephaly

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11
Q

How is Anencephaly diagnosed?

A
  • Amniocentesis
  • Prenatal UTZ
  • Elevated MAFP (Maternal Alfa-fetoprotein)
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12
Q

Outcomes of anencephaly

A

An infant with this condition may die in utero or may survive for several days after birth but cannot survive further because they have little or no cerebral function

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13
Q

Treatment or cure for anencephaly

A

No known treatment or cure and no surgical management available

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14
Q

What happens if the condition is discovered prenatally?

A

Parents are offered the option of pregnancy termination

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15
Q

Degrees of Spinal Cord Abnormalities

A
  1. Spina Bifida Occulta
  2. Meningocele
  3. Meningomyelocele
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16
Q

It is the mildest form of all NTDs
- a malformation caused by the non-closure or incomplete closure of the posterior portion of the vertebrae

A

Spina bifida occulta

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17
Q

Assessment findings for spina bifida occulta

A
  • May be first noticed as dimpling on the skin at the point of incomplete fusion
  • Abnormal tufts of hair or discolored skin may also be present
18
Q

How do nurses help in clarifying the degree of spina bifida occulta to parents?

A

Explain that this degree simply means a surface of bone is missing and the spinal cord is intact

20
Q

Why do children with spina bifida occulta need no surgical correction?

A

No tissue protruding from the vertebrae

21
Q

Surgery in children with spina bifida occulta is done in order to?

A

Prevent vertebral detorioration because of the unbalanced spina column

22
Q

Three layers of meninges

A
  1. Pia mater
  2. Arachnoid
  3. Dura mater
23
Q

Meninges herniate through an incompletely closed or unformed vertebrae, they will protude as a circular mass called…?

A

Meningocele

24
Q

Meningocele is accompanied by no sensory or motor deficit unless?

A

Membrane sac ruptures

25
Q

Why is immediate surgery necessary for meningocele?

A

To replace the meninges & to close the gap in the skin to prevent infection

26
Q

When is surgery done for meningocele?

A

24-48 hours after birth to prevent infection & trauma to the exposed tissue

27
Q

Most severe form of spina bifida
- Meninges protrude through the vertebrae & the spinal cord usually ends at the point of protrusion

A

Meningomyolocele

28
Q

What happens to the nerves function?

A

Motor & sensory function will be decreased or absent beyond the point of protrusion

29
Q

Why is talipes (club feet) a complication of meningomyelocele

A

Due to lack of innervation to the feet/ankles

29
Q

Complications associated with meningomyelocele

A
  • Loss of bowel & bladder control
  • Permanent weakness or paralysis of legs
  • Talipes (club feet)
  • Hydrocephalus
30
Q

Why is hydrocephalus a complication of meningomyelocele?

A

Due to obstruction of CSF circulation from the spinal deformity
- Higher the meningomyelocele occurs on the cord, the more likely it is that hydrocephalus will be present.

31
Q

Therapeutic management for mingomyelocele

A
  • Immediate surgery
  • Simultaneous VP shunting during a primary meningmyelocele repair
32
Q

VP shunting may not be necessary if meningomyelocele repair is done in?

33
Q

After surgery, the child will continue to have partial or complete paralysis of the lower extremities & loss of bowel & bladder function. why is that?

A

Lesions on the back can be reparied but the absence of a lower cord cannot be replaced

34
Q

How are NTDs diagnosed?

A
  • Prenatal UTZ
  • Fetoscopy
  • Screening amniotic fluid for alpha-fetoprotein
  • analysis of maternal alpha-fetoprotein
35
Q

How can a lesion be closed if the condition is discovered in utero?

A

Thru fetoscopic surgery

36
Q

Why is an infant with NTD can be born via C-section?

A

To avoid pressure & injury to the spinal cord.

37
Q

Surgical closure of open lesion in an infant with myelomeningocele is usually recommended in the?

A

First 24 hours to reduce the incidence of infection & trauma to the exposed tissues

38
Q

Plan of care after deliver of the baby with myelomeningocele is focused on?

A

Potential for infection

39
Q

What is the baby’s position prior to surgery for a myelomeningocele?

A

Prone position

40
Q

Why is the baby placed in prone position prior to surgery for a myelomeningocele?

A

To minimize pressure on the sac & reduces potential trauma to the area.

41
Q

Why is maintaing skin integrity necessary in caring for an infant with myelomeningocele?

A

Because skin problems can develop due to limited movement, muscle weakness, poor sensation, bowel & bladder incontinence