GI Flashcards

1
Q

Hirschberg disease in children is a

A

birth defect

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2
Q

what happens in Hirschberg disease

A

part of lg intestine is unable to move waste properly causing blockage of lg intestine in newborn. ganglion cells either don’t reach area or don’t function.

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3
Q

s/s of Hirschberg

A

infection may develop (enterocoloitits)
vomiting/failure to thrive
swelling of lg intestine/abdomen

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4
Q

does Hirschberg require a surgical procedure

A

yes, laproscopicaly assisted trans-anal pull through

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5
Q

what procedure is necessary until surgery can be done

A

recto-irrigations, removes gas and waste, to prevent infection

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6
Q

in a laproscopicaly assisted trans-anal pull through what happens

A

loosen and remove diseased intestine; circular incision in rectum, inside of anus; pulled out through anus for removal

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7
Q

s/s of pyloric stenosis

A
vomiting
constipation
green diarrhea
weight loss
stomach pain after eating
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8
Q

symptoms of pyloric stenosis begin when baby is

A

3 weeks old

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9
Q

how is pyloric stenosis treated

A

surgery, loosen muscle so fluid can be easily out of the stomach

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10
Q

what causes pyloric stenosis

A

muscle is too big; doesn’t relax, stays tight

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11
Q

how is failure to thrive classified

A

growth failure; weight below the 5th percentile on growth chart

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12
Q

3 categories of failure to thrive

A

idiopathic - unknown cause
organic - r/t physical problem - look to disorders
non-organic - r/t not being fed - possible neglect

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13
Q

NFTT s/s

A

behavior - apathy, interested more in toys, no fear of strangers (issues)

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14
Q

goals for FTT

A

reverse malnutrition - provide calories needed
observe parent/child interactions
primary nursing - same assignment when possible

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15
Q

what is primary nursing

A

same assignment to learn cues/behaviors of child

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16
Q

if child is getting attention for feeding will they feed

A

no - if that is the only way I get attention - extending time

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17
Q

what tools do we use for cleft palate/lip

A

haberman feeder

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18
Q

mgmt. of cleft lip/palate

A

elevate child for feedings - 45 degrees (reduce risk for infections & aspiration)
encourage mom to breast feed
use teach back so parents know how to use tools

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19
Q

which surgery would come first if child had both a cleft lip and palate

A

cleft lip

20
Q

when would you do the cleft lip procedure/surgery

A

10
10 weeks
10 pounds
hemoglobin = 10

21
Q

what is the name of cleft lip surgery

A

cheiloplasty

22
Q

cleft palate surgery is usually performed at what age

A

between 6-12 months

23
Q

goal for cleft palate surgery

A

normal speech development

24
Q

is cleft lip same day surgery

A

yes - discharged, same day, if child is doing okay after surgery

25
Q

mgmt. after cleft lip surgery

A

feed them - po

logan bow arm restraints - to keep hands away form incision

26
Q

complications of cleft

A

hearing problems w/recurrent otitis media infections
dental problems (missing teeth)
recurrent respiratory infections (usually unrepaired cleft)

27
Q

with cleft palate surgery what would you encourage

A

drinking for a cup

do not insert straws or pacifier

28
Q

what is esophageal atresia

A

esophagus ends in pouch

29
Q

what do we worry about with esophageal atresia

A

aspirations
respiratory issues
risk for pneumonia

30
Q

when feeding a baby with esophageal atresia what can happen (three c’s)

A

choking
coughing
cyanosis - bag baby/oxygen - critical!

31
Q

what happens when you stick an NG tube through nose with a baby with esophageal atresia

A

It stops

32
Q

goals for child with esophageal atresia

A
npo 
maintain patent airway
intubation
hob elevated
iv fluids
suction
33
Q

can esophageal atresia be repaired

A

yes, thoracotomy

end-to-end anastomosis of esophagus

34
Q

what will happen to esophagus after esophageal atresia surgery

A

flappy airway, not as sturdy

35
Q

what happens if child cries/coughs

A

esophagus can collapse/close

36
Q

after surgery goals/mgmt. for esophageal atresia

A

chest tubes
do not place tension on sutures
make sure esophagus is patent before feeding

37
Q

discharge teaching for esophageal atresia

A

go home with apnea monitor
cpr training
preventing reflux

38
Q

what is biliary atresia

A

bile ducts may not form completely, or they close; bile cannot come out of liver and go into duodenum
can be intra or extrahepatic - bile ducts didn’t form properly

39
Q

when will we see s/s of biliary atresia

A

2 weeks - prolonged jaundice (progression)
swollen abdomen
acholic stools
hepatomegaly(enlarged liver)
pruritis - intense itching from toxins and irritants building up in the body

40
Q

what happens in biliary atresia

A
cholestasis - bile stays in liver
causes damage to liver
get cirrhosis/liver damage
life threatening disease
difficulty absorbing fat soluble vitamins A,D,E,K
41
Q

ultimate treatment for biliary atresia

A

liver transplant

42
Q

cause of biliary atresia

A

unknown

43
Q

dx of biliary atresia

A

labs

liver biopsy - determines

44
Q

what is kasai procedure*

A

segment of intestine is anastomosed for bial drainage

45
Q

treatment for biliary atresia**

A

kasai procedure - supportive

liver transplant

46
Q

what age do children with biliary atresia have the best success rate

A

dx and surgically treated before 2 months of age

47
Q

mgmt. for biliary atresia

A

failure to thrive
itching - prevent secondary infections - oatmeal baths
support for parents