Chp 27 - Nursing Care of the Child Born With a Physical or Developmental Challenge Flashcards

(51 cards)

1
Q

Also known as “tongue tied”. The abnormal restriction of tongue by abnormally tight frenulum

A

ANKYLOGLOSSIA

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2
Q

This is a simple surgical procedure to release the frenulum. It’s often performed quickly and with minimal discomfort

A

Frenotomy

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3
Q

A more complex surgical procedure that may be needed if the frenulum is very thick.

A

Frenuloplasty

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4
Q

It is a failure of the maxillary & median nasal processes to fuse that range from small notch in the upper lip to total separation of lip & facial structure up into floor of the nose, with even upper teeth and gingiva absent

A

Cleft Lip

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5
Q

Cleft Lip comes in high incidence in ______ population, and lower incidence in African-American population

A

Asian

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6
Q

It is a palate opening that usually on the midline & involves anterior hard palate, posterior soft palate, or both

A

Cleft Palate

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7
Q

a triad of micrognathia (small mandible), cleft palate, and glossoptosis (a tongue malpositioned downward).

A

Pierre Robin Syndrome

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8
Q

orifice/passage in body that is closed or absent

A

ATRESIA

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9
Q

abnormal/surgically made passage between hollow or tubular organ & body surface, between 2 hollow, or tubular organs

A

FISTULA

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10
Q

obstruction of esophagus

A

ESOPHAGEAL ATRESIA

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11
Q

Abdominal contents protruding through wall of abdomen at the junction of UC and abdomen. Intestines are usually herniated but sometimes it included stomach and liver.

A

Omphalocele

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12
Q

what is the difference between Gastroschisis and Omphalocele

A

Gastroschisis: the intestines are outside the abdomen through a hole in the abdomen

Omphalocele: the intestine, liver, and other organs reamin outside of the abdomen in a sac

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13
Q

Anal stricture is
narrowing the end of tube
that takes stool out of the body. The other term is “anal stenosis

A

IMPERFORATE ANUS

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14
Q

Newborns with imperforate anus are usually identified upon the first physical examination

A

-Absence of stool
-Passing of stools in other openings
-Swollen belly
-Absence of anal opening

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15
Q

protrusion of an abdominal organ (usually the stomach or intestine) through a defect in the diaphragm into the chest cavity. This usually occurs on the left side, causing cardiac displacement to the right side of the chest and collapse of the left lung

A

Diaphragmatic Hernia

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16
Q

How does a diaphragmatic hernia occur

A

the chest and abdominal cavity are one; at approximately week 8 of growth, the diaphragm forms to divide them. If the diaphragm does not form
completely, the intestines can herniate through the diaphragm opening into the chest cavity

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17
Q

how to manage cleft lip and palate

A

-fetal surgery
-surgical repair
-nasal mold apparatus shape better nostril
-revision of original repair

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18
Q

how to manage TRACHEOSOPHAGEAL ATRESIA AND FISTULA

A

-emergency surgery
-antibiotics
-gastrostomy
-close monitoring until suture dissolves

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19
Q

management of omphalocele

A

-surgery within 24hrs
-silastic pouch/”silo”
-TPN

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20
Q

management for imperforate anus

A

-NPO until surgery is done
-temporary colostomy
-OGT/NGT insertion
-in for fluid and electrolytes

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21
Q

management for diaphragmatic hernia

A

-laparoscopy
-semi fowlers
-NPO
-NGT/gastrostomy insertion

22
Q

protrusion of a portion of the intestine through the umbilical ring, muscle, and fascia surrounding the umbilical cord

A

Umbilical Hernia

23
Q

an excess of CSF in the ventricles or the subarachnoid space

A

Hydrocephalus

24
Q

How to assess hydrocephalus

A

For assessing this kind of condition, ultrasound, CT scan, and transillumination test in order to identify abnormalities in the body.

25
tube that is surgically implanted to drain excess CSF from the brain to another part of the body, usually the abdomen
Shunt placement
26
surgical procedure that creates an opening in the floor of the third ventricle to allow CSF to drain.
Endoscopic third ventriculostomy
27
This happens when the fusion of posterior laminae of vertebrae fails
SPINA BIFIDA
28
when the meninges herniate through unformed vertebrae
MENINGOCELE
29
Meningocele is a protruding mass appears and usually have same size of an _______ at the center of back
orange
30
the spinal cord & meninges protruding the vertebrae same with meningocele
MYELOMENINGOCELE
31
what can be used to differentiate meningocele to myelomeningocele
-CT scan -Ultrasound -MRI
32
The higher the myelomeningocele, the ______ the chance hydrocephalus accompany it
higher
33
cranial meningocele or myelomeningocele occurs most often in the occipital area of the skull but may occur as a nasal or nasopharyngeal disorder
Encephalocele
34
the absence of cerebral hemispheres. The mother may experience difficult in labor, most of this condition present as breech
ANENCEPHALY
35
slow growth of brain that falls more than 3x below normal on growth charts
Microcephaly
36
underdevelopment or imperfect hip can affect the head, acetabulum, or both. The femur head don’t lie deep enough within acetabulum & slips out in movement
DEVELOPMENTAL HIP DYSPLASIA
37
mildest form; femoral head remains in acetabulum
Acetabular dysplasia
38
most common form; femoral head partially displaced
Subluxation
39
femoral head not in contact with acetabulum; displaced posteriorly and superiorly
Dislocation
40
management for hip dysplasia
-surgical intervention -positioning of legs slightly flexed and abducted -pavlik harness; spica cast from the waist to below knees
41
This condition can result from ingestion of maternal drug, viral invasion, and amniotic band formation. Prostheses of lower extremity are fitted as early as 6 months while upper extremity are fitted this early so infant can handle and explore objects readily
ABSENT OR MALFORMED EXTREMITIES
42
presence of one or additional fingers or toes. These are usually amputated off early.
POLYDACTYLY
43
when two fingers or toes are fuse
SYNDACTYLY
44
indention of lower portion of sternum. There can be decreased lung volume, heart is displaced to the left.
PECTUS EXCAVATUM
45
when the sternum is displaced anteriorly, increasing AP diameter of the chest
PECTUS CARINATUM
46
2 types of chest deviations
-PECTUS EXCAVATUM -PECTUS CARINATUM
47
occurs as a congenital anomaly when the sternocleidomastoid muscle is injured and bleeds during birth
Torticollis (Wry Neck)
48
The sutures of the skull is closing prematurely and may occur in utero or early infancy
CRANIOSYNOSTOSIS
49
CRANIOSYNOSTOSIS needs to be detected early because sealed skull will compromise _______ ________
Brain Growth
50
failure of bone growth inherited as a dominant trait. It causes a disorder in cartilage production in utero
Achondroplasia
51
deformities are ankle–foot disorders, popularly called clubfoot
Talipes