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
Profile of a child with pyloric stenosis
- < 2 months old | - first born male
26
Classic metabolic picture of child with pyloric stenosis
- hypochloremic - hypokalemic - metabolic alkalosis
27
What is needed for a definitive diagnosis of hirshsprung
Rectal biopsy
28
Findings suggestive of hirshsprungs
1) palpable stool throughout abdomen 2) empty rectal vault 3) of never having unassisted stooling
29
Failure to pass meconium in first 24-48 hours of life
Hirshsprungs