Pediatric GI (Newman) Flashcards

1
Q

problems with free unconjugated bilirubin

A
  • can cross the blood brain barrier

- is toxic to CNS

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2
Q

total serum bilirubin with visible jaundice early in life

A

> 5 mg/dL

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3
Q

Is conjugated hyperbilirubinemia pathologic?

A

always

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4
Q

describe breast feeding jaundice

A

function of dehydration and decreased excretion of bilirubin in the stool (more supply related) *nonpathologic

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5
Q

describe breast milk jaundice

A

presence of bilirubin deconjugating enzymes in milk *nonpathologic

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6
Q

What type of hyperbilirubinemia does blood group incompatibility cause?

A

unconjugated

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7
Q

When to test for blood group incompatibility

A

if mom is type O or mom is Rh(D) negative

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8
Q

How to test from blood group incompatibility

A

infants cord blood should be evaluated for:

1) direct Ab (Coomb’s test)
2) blood type
3) Rh determination

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9
Q

What type of bilirubin is seen with biliary atresia

A

conjugated

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10
Q

Signs and Sx of biliary atresia

A

1) cholestatic jaundice
2) hepatomegaly
3) acholic stools

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11
Q

First phase acute bilirubin toxicity (timing and Sx)

A
  • first 1-2 days
  • poor suck
  • high pitch cry
  • stupor
  • hypotonia
  • seizures
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12
Q

Second phase acute bilirubin toxicity (timing and Sx)

A
  • middle of first week of life
  • hypertonia of extensor muscles
  • opisthotonus
  • retrocollis
  • fever
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13
Q

Third phase acute bilirubin toxicity (timing and Sx)

A
  • after first week of life

- hypertonia

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14
Q

how does jaundice advance in newborns?

A

cephalo-caudally

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15
Q

Assessing jaundice in newborns

A
  • turn on lights and blanch skin with digital pressure
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16
Q

Some risk factors for hyperbilirubinemia

A
  • jaundice in 1st 24 hours
  • previous sibling requiring phototherapy
  • exclusive breastfeeding, not going well
17
Q

treatment of mild jaundice

A
  • increase frequency of feedings

- continue breast feeding

18
Q

What does phototherapy do?

A

isomerizes bilirubin, making it water soluble

19
Q

describe GER

A
  • passage of gastric contents into the esophagus

- the happy spitter

20
Q

describe GERD

A
  • when symptoms or complications are present as a result of GER
  • hard to feed, cry a lot, arch and scream, hard to gain weight
21
Q

Diagnosis of GER/GERD

A
  • esophageal pH monitoring with impedance testing (direction of bolus movement)
  • tells frequency of GER
  • association of low esophageal pH with Sx
22
Q

Treatment of GERD

A
  • kids sleep on back
  • smaller amounts of food more frequently
  • upright position during feeding and for 30-45 minutes after feeding
  • medications (H2 antagonists)
  • surgery
23
Q

Where does intussusception occur most frequently?

A

most are ileocecal: ileum invaginates into the colon at the ileocecal valve/junction

24
Q

Frequent physical exam finding with intussuception

A

palpable tubular mass in their abdomen (RUQ)

25
Q

Profile of a child with pyloric stenosis

A
  • < 2 months old

- first born male

26
Q

Classic metabolic picture of child with pyloric stenosis

A
  • hypochloremic
  • hypokalemic
  • metabolic alkalosis
27
Q

What is needed for a definitive diagnosis of hirshsprung

A

Rectal biopsy

28
Q

Findings suggestive of hirshsprungs

A

1) palpable stool throughout abdomen
2) empty rectal vault
3) of never having unassisted stooling

29
Q

Failure to pass meconium in first 24-48 hours of life

A

Hirshsprungs