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
hirschsprung disease
rare birth defect (1:5000) defined by absence of ganglion cells in the rectum and colon
26
what are ganglion cells responsible for
opening and closing of peristalsis
27
hirschsprung can cause?
megacolon
28
manifestation of hirschsprung
- no passing of meconium in the first 48hr - abdominal distention - feeding intolerance - bili emesis
29
treatment of hirschsprung
take out part of bowel that doesn't have ganglion cells and replace with the good bowel and connect to anus
30
complication of hirschsprung
- can cause enterocolitis - inflammation of the intestines - s/s of chrons
31
long term effect of hirschsprung
weight gain can be hard
32
nursing considerations for hirschsprung
- make sure the baby poops - watch for vomiting - newborn nutrition
33
gastroenteritis
inflammation of the stomach accompanied by vomiting and diarrhea
34
most severe complication of gastroenteritis
dehydration
35
appendicitis
inflammation of the vermiform appendix and is the most common cause of emergency surgery in children
36
when is appendicitis most common
- children ages 10-19 - younger = higher risk of perforation
37
manifestations of appendicitis
- PANT (only happen in this order) - Pain - Anorexia - Nausea - Temp
38
labs for appendicitis
- CBC (elevated WBC) - electrolytes
39
what is the preferred method to take images of appendicitis
- U/S is less radiation - Adults are CT
40
management of appendicitis
- IV fluids - NPO - incision care - antibiotics
41
hyperbilirubinemia
- elevated serum bilirubin level - very common in 84% of term newborns
42
patho of hyperbilirubinemia
shortened RBC life span
43
manifestations of jaundice
- lethargic - decreased PO intake
44
diagnostic for jaundice
total serum bilirubin
45
nursing management of jaundice
- educate breastfeeding - strict I/O - IV hydration - phototherapy - vital signs
46
nursing dx for jaundice
- FVD - Risk for impaired attachment - Risk for imbalanced body temp