GI Flashcards

(47 cards)

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

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

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
mgmt. after cleft lip surgery
feed them - po | logan bow arm restraints - to keep hands away form incision
26
complications of cleft
hearing problems w/recurrent otitis media infections dental problems (missing teeth) recurrent respiratory infections (usually unrepaired cleft)
27
with cleft palate surgery what would you encourage
drinking for a cup | do not insert straws or pacifier
28
what is esophageal atresia
esophagus ends in pouch
29
what do we worry about with esophageal atresia
aspirations respiratory issues risk for pneumonia
30
when feeding a baby with esophageal atresia what can happen (three c's)
choking coughing cyanosis - bag baby/oxygen - critical!
31
what happens when you stick an NG tube through nose with a baby with esophageal atresia
It stops
32
goals for child with esophageal atresia
``` npo maintain patent airway intubation hob elevated iv fluids suction ```
33
can esophageal atresia be repaired
yes, thoracotomy | end-to-end anastomosis of esophagus
34
what will happen to esophagus after esophageal atresia surgery
flappy airway, not as sturdy
35
what happens if child cries/coughs
esophagus can collapse/close
36
after surgery goals/mgmt. for esophageal atresia
chest tubes do not place tension on sutures make sure esophagus is patent before feeding
37
discharge teaching for esophageal atresia
go home with apnea monitor cpr training preventing reflux
38
what is biliary atresia
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
when will we see s/s of biliary atresia
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
what happens in biliary atresia
``` 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
ultimate treatment for biliary atresia
liver transplant
42
cause of biliary atresia
unknown
43
dx of biliary atresia
labs | liver biopsy - determines
44
**what is kasai procedure***
segment of intestine is anastomosed for bial drainage
45
treatment for biliary atresia**
kasai procedure - supportive | liver transplant
46
what age do children with biliary atresia have the best success rate
dx and surgically treated before 2 months of age
47
mgmt. for biliary atresia
failure to thrive itching - prevent secondary infections - oatmeal baths support for parents