Pediatric GI Flashcards

1
Q

Age of Infantile Hypertrophic Pyloric Stenosis?

A

3-5 weeks

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2
Q

Vomiting in Infantile Hypertrophic Pyloric Stenosis?

A

Projectile vomiting after eating, hungry after

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3
Q

Appearing of baby with Infantile Hypertrophic Pyloric Stenosis?

A

“Thin” or “emaciated”

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4
Q

What’s palpable in Infantile Hypertrophic Pyloric Stenosis? When?

A

“Olive” on lateral edge of rectuc abdominus in RUQ after vomiting

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5
Q

DX for Infantile Hypertrophic Pyloric Stenosis?

A

Ultrasound. Endoscopy if U/S inconclusive.

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6
Q

What labs to check in Infantile Hypertrophic Pyloric Stenosis?

A

Lytes to assess hydration

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7
Q

What first thing to treat in Infantile Hypertrophic Pyloric Stenosis?

A

Correct hydration status

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8
Q

Treatment of choice in Infantile Hypertrophic Pyloric Stenosis?

A

Surgical pylormyotomy

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9
Q

Etiology of Intussusception?

A

75% idiopathic

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10
Q

What is most common obstruction in 6-36mo old?

A

Intussusception

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11
Q

Intussusception most common in what age?

A

3-5 months

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12
Q

Intussusception due to?

A

Intestinal invagination most commonly at ileocecal junction

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13
Q

Where does Intussusception happen most?

A

Ileocecal junction

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14
Q

Describe pain in Intussusception

A

Severe, sudden, crampy pain. Legs drawn up, inconsolable. 15-20 minutes long then OK until next episode.

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15
Q

Describe stool in Intussusception

A

Blood or currant jelly in stool

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16
Q

Describe mass in abdomen in Intussusception

A

Sausage shape abdominal mass

17
Q

Dx of Intussusception?

A
  • X-ray

- U/S

18
Q

What will U/S show in Intussusception?

A

Bulls Eye or Coiled Spring

19
Q

Tx of Intussusception if stable and no perforation?

A

Edema with barium or pressurized air. 80-95% success.

20
Q

Tx for Intussusception if perforation or necrosis?

A

Surgery

21
Q

Etiology of Phenylketonuria?

A

Deficiency of Phenylalanine Hydroxyurase (PAH) to convert Phenylalanine to Tyrosine

22
Q

What disability does Phenylketonuria cause?

A

Intellectual disability

23
Q

Blood and urine smell in Phenylketonuria?

A

“Mousy” smell

24
Q

Dx of Phenylketonuria?

A

Newborn screening from heel stick

25
Q

Tx of Phenylketonuria?

A

Restrict Phenylalanine from diet ASAP, definitely <1 week

26
Q

How often to monitor Phenylketonuria?

A

Weekly in first year, twice a month 1-12 years, monthly in 12+ years

27
Q

Most common age in Appendicitis?

A

5-12 y/o

28
Q

Fever and pain where in Appendicitis?

A

Low grade fever, complain of hip pain

29
Q

WBC in Appendicitis shows what?

A

Elevated WBCs with increased polys

30
Q

U/S in Appendicitis if what?

A

Young and thin

31
Q

What test to use if U/S inconclusive in Appendicitis?

A

CT

32
Q

Tx of non-perforated Appendicitis?

A
  • NPO, IV fluids, control pain/puke/fever

- Surgery w/n 6h

33
Q

Pre-op abx in Appendicitis if non-perforated?

A

Cefoxitin

34
Q

Tx of perforated Appendicitis?

A
  • NPO, IV fluids, control pain/puke/fever

- Surgery ASAP

35
Q

Abx in perforated Appendicitis?

A

Triple Amp/Gent/Flagyl

36
Q

Tx of constipation in infants?

A

Flycerine suppositories, lubricated thermometer

37
Q

Tx of constipation in older kids?

A

Glycerine suppositories, Miralax