Week 5: CH 25 GI Flashcards

1
Q

stomach of a newborn

A

20mL

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2
Q

stomach of a 30 day old

A

90mL

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3
Q

stomach of a 1 year old

A

360mL

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4
Q

why is gas not uncommon

A

stomach enzymes are deficient until 4-6 months

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5
Q

cleft lip

A

failure of the maxillary processes to fuse by 6 weeks gestation and failure of the tongue to move down at the correct time prevents the palatine from fusing

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6
Q

cleft palate vs cleft lip

A

cleft palate is harder to detect

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7
Q

approach to therapy for a cleft defect

A

plastic surgeon, dentist, audiologist, speech, ENT, lactation, and social work

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8
Q

post op care of cleft defect

A
  • vitals
  • monitor I/O
  • observe for s/s of infection
  • place upright and burp frequently
  • use special feeder or dropper to start clear liquids
  • nothing in the mouth
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9
Q

GER

A

return of gastric contents into the esophagus

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10
Q

3 mechanisms that allow reflux to occur

A
  • lower esophageal relaxations
  • incompetent lower esophageal sphincter
  • anatomic disruption of esophagogastric junction
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11
Q

manifestations of GER

A
  • regurgitation
  • spitting up
  • vomiting
  • hungry/irritable
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12
Q

treatment of GER

A
  • depends on severity
  • medications or specific formula can be used if severe
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13
Q

pyloric stenosis

A

hypertrophied pyloric muscle causes symptoms of projectile vomiting and visible peristalsis

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14
Q

nursing considerations of pyloric stenosis

A
  • avoid oral feeding
  • IV therapy
  • NG tube
  • Strict I/O
  • minimize weight loss
  • promote rest/comfort
  • prevent infection
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15
Q

omphalocele

A

congenital malformation that results when the intra-abdominal contents herniate through the umbilical cord

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16
Q

when does omphalocele occur

A

in week 11 of gestation when abdominal contents fail to return to the abdomen

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17
Q

where are the abdominal contents stored in omphalocele

A

in a sac that if ruptured the organs are eviscerated

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18
Q

what causes omphalocele

A
  • multiple causes
  • 50-70% of infants with omphalocele will have an associated anomaly
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19
Q

gastroschisis

A

congenital defect in which the bowel protrudes through the abdominal wall

20
Q

difference in omphalocele vs gastroschisis

A

omphalocele has a sac and has higher % of anomaly

21
Q

intussusception

A

portion of the intestine goes inside another part of the intestine

22
Q

most common site of intussusception

A

ileocecal valve

23
Q

manifestations of intussusception

A
  • abdominal pain
  • JELLY STOOLS
  • vomiting
24
Q

treatment of intussusception

A
  • air reduction enema
  • surgical reduction if needed
25
Q

hirschsprung disease

A

rare birth defect (1:5000) defined by absence of ganglion cells in the rectum and colon

26
Q

what are ganglion cells responsible for

A

opening and closing of peristalsis

27
Q

hirschsprung can cause?

28
Q

manifestation of hirschsprung

A
  • no passing of meconium in the first 48hr
  • abdominal distention
  • feeding intolerance
  • bili emesis
29
Q

treatment of hirschsprung

A

take out part of bowel that doesn’t have ganglion cells and replace with the good bowel and connect to anus

30
Q

complication of hirschsprung

A
  • can cause enterocolitis
  • inflammation of the intestines
  • s/s of chrons
31
Q

long term effect of hirschsprung

A

weight gain can be hard

32
Q

nursing considerations for hirschsprung

A
  • make sure the baby poops
  • watch for vomiting
  • newborn nutrition
33
Q

gastroenteritis

A

inflammation of the stomach accompanied by vomiting and diarrhea

34
Q

most severe complication of gastroenteritis

A

dehydration

35
Q

appendicitis

A

inflammation of the vermiform appendix and is the most common cause of emergency surgery in children

36
Q

when is appendicitis most common

A
  • children ages 10-19
  • younger = higher risk of perforation
37
Q

manifestations of appendicitis

A
  • PANT (only happen in this order)
  • Pain
  • Anorexia
  • Nausea
  • Temp
38
Q

labs for appendicitis

A
  • CBC (elevated WBC)
  • electrolytes
39
Q

what is the preferred method to take images of appendicitis

A
  • U/S is less radiation
  • Adults are CT
40
Q

management of appendicitis

A
  • IV fluids
  • NPO
  • incision care
  • antibiotics
41
Q

hyperbilirubinemia

A
  • elevated serum bilirubin level
  • very common in 84% of term newborns
42
Q

patho of hyperbilirubinemia

A

shortened RBC life span

43
Q

manifestations of jaundice

A
  • lethargic
  • decreased PO intake
44
Q

diagnostic for jaundice

A

total serum bilirubin

45
Q

nursing management of jaundice

A
  • educate breastfeeding
  • strict I/O
  • IV hydration
  • phototherapy
  • vital signs
46
Q

nursing dx for jaundice

A
  • FVD
  • Risk for impaired attachment
  • Risk for imbalanced body temp