Exam 2 - GI Flashcards

(50 cards)

1
Q

when is the GI system formed during embryonic development

A

first 4 weeks

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2
Q

the GI tract arises from the ___ layer

A

endoderm

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3
Q

can an infant still breastfeed with a cleft lip

A

yes but depends on the severity

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4
Q

when is a cleft lip repair

A

1-2 months and again at 4-5 years

you want complete closure by 6-24 months

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5
Q

cleft lip puts children at higher risk for ___ ___ and ___ ___

A

ear infection; hearing loss

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6
Q

what is esophageal atresia

A

congenital malformation where the esophagus terminates before reaching the stomach

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7
Q

3 C’s for esophageal atresia

A

coughing
choking
cyanotic

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8
Q

HOB should be at least __ degrees for esophageal atresia

A

30

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9
Q

how often to suction with esophageal atresia

A

q5-10 minutes

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10
Q

what 2 meds need to be administered ASAP d/t aspiration risk

A

IVF
abx

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11
Q

what are the 4 motility disorders

A

GERD
constipation, encopresis
recurrent abdominal pain
IBS

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12
Q

s/sx of physiological GERD

A

painless emesis after meals
rarely occurs during sleep
weight gain
no aspiration
will outgrow by 1-2 y/o

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13
Q

s/sx of pathologic GERD

A

FTT
aspiration PNS and/or asthma
apnea
coughing, choking
frequent emesis with abdominal pain, crying
risk for aspiration, ear infection
meds and/or sx for treatment

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14
Q

GERD management

A

diet
positioning
meds
tx acute bleeding
surgery (fundoplication)

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15
Q

constipation/encopresis management

A

overcoming withholding
diet changes
change retention habits
emotional support
home care
evaluation
toileting schedule
keep a change of clothes on hand

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16
Q

IBD management

A

corticosteroids
immune suppressants (MTX)
abx
low fat, low fiber diet
high protein diet

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17
Q

appendicitis s/sx develop slowly over __ hour period

A

12

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18
Q

s/sx of appendicitis

A

pain
anorexia
N/V
fever

pain proceeding vomiting, appendicitis is likely

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19
Q

possible position of child with appendicitis

A

knee-chest

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20
Q

what are the 4 obstructive disorders

A

hypertrophic pyloric stenosis
intussusception
volvulus
Hirschsprung’s disease

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21
Q

when does hypertrophic pyloric stenosis occur

A

within the first few weeks after birth

22
Q

cause of hypertrophic pyloric stenosis

A

unknown but can be genetic predisposition

23
Q

what to assess with hypertrophic pyloric stenosis

A

frequency, consistency and amount

24
Q

concern with hypertrophic pyloric stenosis

A

dehydration
weight loss

25
where may there be a palpable mass with hypertrophic pyloric stenosis
R of the umbilicus
26
preop: hypertrophic pyloric stenosis
NPO IVF NGT elevate HOB
27
postop: hypertrophic stenosis
elevate HOB PO rehydrating solution (when bowel sounds return) formula started if PO hydration is tolerated x24 hours I&Os (weigh diapers, daily weight)
28
when does intussusception occur
5 months to 3 years
29
s/sx of intussusception
abdominal pain mass in RUQ red, currant jelly like stools vomiting fever lethargy
30
intussusception treatment
NPO until active bowel sounds radiographic air enema saline enema NGT sx is LAST resorT
31
what must always be documented with intussusception
see and document all characteristics of BM
32
Hirschsprung disease is commonly seen in individuals with ___ ___
Down Syndrome strong heredity
33
Hirschsprung disease is d/t ___ ___ in 1 part of the GI tract
inadequate immobility
34
s/sx of Hirschsprung disease
delayed meconium passage chronic constipation first month of life abdominal pain, distention FTT ribbon like stools
35
Hirschsprung disease can lead to a ___ ___
permanent colostomy
36
Hirschsprung pre op
NPO abx monitor abdominal circumference monitor electrolytes
37
Hirschsprung post op
bowel sounds s/sx infection BM anal dilators
38
most common malabsorption disorder
lactose intolerance
39
what are the 4 types of lactose intolerance
primary secondary congenital developmental
40
primary vs. secondary vs. congenital vs. developmental lactose intolerance
P: around 5 y/o S: secondary to illness or injury C: rare, hereditary D: seen in premature babies, gets better over time
41
where is tropical sprue Celiac disease seen mostly
Caribbean India SE Asia
42
what is short bowel syndrome
congenital malformation 50% less bowel than normal individual
43
lactose intolerance is more common in ___ and ___ ___
Asians Native Americans
44
how to dx lactose intolerance
stool test
45
where is gluten seen
protein seen in wheat, barely, rye, and oats
46
how to Dx Celiac
Bx jejunum IgA blood work
47
which form of hepatitis is most prevalent in children
hepatitis A
48
what is biliary atresia
inflammation, obstruction of the bile duct hard time with fats and bile salts
49
#1 indication for liver transplant in children
biliary atresia
50
treatment for cirrhosis of the liver in children
no treatment, supportive measures