Gastroenterology Flashcards

1
Q

What is “functional constipation”

A

children without an organic etiology for their constipation. Often the result of holding feces if having a BM is painful.

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2
Q

Rome III diagnostic criteria for functional constipation

A

Must have the following criteria 1x per week for at least two months:

Two of the following in a child with a dev age of 4 yrs:

  • Two or fewer defecations in the toilet per week.
  • At least one episode of fecal incontinence per week.
  • History of retentive posturing or excessive volitional stool retention.
  • History of painful or hard bowel movements.
  • Presence of a large fecal mass in the rectum.
  • History of large diameter stools that may obstruct the toilet.
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3
Q

At what transition periods is the developing child prone to constipation?

A

toilet training and the start of school

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4
Q

How do you diagnose fecal impaction?

A

identifiying a large and hard mass in the abdomen or a dilated rectum filled with stool. You do not need an x-ray!

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5
Q

What are the recommended methods of disimpaction?

A

oral (PEG) or rectal (enemas) medication. Digital disimpaction is not recommended

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6
Q

What is the maintenance dose of PEG?

A

0.4 g/kg/day to 1.0 g/kg/day

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7
Q

What is the disimpaction dose of PEG?

A

1 g/kg/day – 1.5 g/kg/day for 3 days

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8
Q

What can you use to treat constipation in infants < 18 months of age?

A

PEG (0.8 g/kg/day), lactulose, glycerin suppositories

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9
Q

How long do you treat for constipation?

A

Children with constipation should be treated for at least six months, and should have regular bowel movements without difficulty before considering a trial of weaning maintenance therapy.

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10
Q

Features of UC

A

Rectum involved, involves gut continuously, bowel wall may be normal, mucosa is hemorrhagic, strictures/fistulas are rare

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11
Q

Features of CD

A

Segmental involvement / skip lesions, TI is thick/inflammated, transmural inflammation, mucosa looks cobblestone, strictures/fistulas are common

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12
Q

What infection mimicks crohn’s disease?

A

yersinia

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13
Q

Investigations to do in IBD

A

CBC (microcytic anemia, thrombocytosis),
ESR, CRP,
albumin,
fecal calprotectin (stool test specific for gut inflammation),

P-ANCA (UC), ASCA (crohn’s)

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14
Q

Imaging for Crohn’s?

A

MRI-enterography, MR pelvis for peri-anal/fistulas, used to do UGI+small bowel follow-through

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15
Q

After how many weeks of life should a jaundiced baby have conjugated and unconjugated bili testing done?

A

2 weeks

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16
Q

Definition of acute liver failure?

A

INR >= 1.5 with encephalopathy
OR
INR >= 2.0 without encephalopathy

After you have attempted to correct INR with 1 dose of vit K IV

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17
Q

What is the only clotting factor made outside of the liver?

A

factor 8 (made in endothelium)

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18
Q

How does alpha-1-antitrypsin present in children?

A

liver cirrhosis

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19
Q

How do you prevent Hep B in at risk newborns?

A
  • vaccine within 12 hours

- immunoglobulin within 7 days

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20
Q

When can you return to school if you have Hep A?

A

7-10 days from first day of jaundice

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21
Q

Breast milk protein?

A

Higher in whey protein (70%) than casein (30%) than bovine sources (18, 82% respectively)

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22
Q

contraindications to breastfeeding?

A

HIV infection, chemotherapy / cytotoxic drugs, radiation therapy, active TB or if the infant has galactosemia

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23
Q

who should get 800 IU of vit d per day?

A
  • living north of latitude 55 degrees, October-April
  • living in community with high prevalence of vitamin D deficiency
  • children with dark skin
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24
Q

soy based phytoestrogens are contraindicated in what situation?

A

congenital hypothyroidism (phytoestrogens can inhibit thyroid peroxidase, potentially lowering free thyroxine concentrations, which could lead to abnormal thyroid function)

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25
Q

how do you manage mild dehydration?

A

replace with ORS 50 mL/kg over 4 hours, replace losses

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26
Q

how do you manage moderate dehydration?

A

rehydrate with ORS 100 mL/kg over 4 hours, replace losses

27
Q

how do you manage protein-losing enteropathy?

A

hydrolyzed formula

28
Q

how do you test for fat malabsorption

A

fecal elastase

29
Q

how do you test for carbohydrate malabsorption

A

stool reducing substances

30
Q

how do you test for protein malabsorption?

A

stool alpha-1-antitrypsin

31
Q

what is acrodermatitis enteropathica?

A

inability to absorb sufficient zinc (genetic)

32
Q

what is kwashiorkor?

A

hypoalbuminemia, edematous malnutrition due to inadequate protein intake. noted to have sparse yellow/red-tinged hair.

33
Q

what is marasmus?

A

severe protein-energy malnutrition, emaciated, < 70% of ideal weight, face like “old man”

34
Q

what should you supplement in a vegan breastfeeding mom?

A

B12

35
Q

What key nutrient is missing in goat’s milk?

A

folate

36
Q

does iron fortified formula increase risk of constipation?

A

nope!

37
Q

when should you recommend soy milk?

A

rarely! galactosemia, or for religious reasons

38
Q

what is a sign of vitamin c deficiency (scurvy)

A

bleeding gums

39
Q

sign of zinc deficiency

A

peri-oral / bum rash, diarrhea

40
Q

when do you remove a button battery?

A

within 48 hours, ASAP!

41
Q

what contains gluten

A

wheat, rye, barley

42
Q

pathologic findings of celiac

A

villous atrophy
crypt hyperplasia
intraepithelial lymphocytosis

43
Q

non-GI manifestations of celiac disease

A
  • dermatitis herpetiformis
  • osteoporosis
  • short stature
  • delayed puberty
  • iron-deficient anemia
  • hepatitis
  • arthritis
  • epilepsy with occipital calcifications
44
Q

conditions associated with celiac

A

type 1 DM, IgA deficiency, down syndrome, turner syndrome, williams syndrome, other autoimmune conditions, first degree relative with celiac (1:20)

45
Q

diagnosis celiac

A

anti-TTG, IgA (+/- deaminated gliadins), biopsy

46
Q

osmotic laxatives

A

lactulose, mineral oil

47
Q

stool softener

A

docusate

48
Q

prokinetic laxatives

A

dulcolax, senokot, prucalopride

49
Q

first line tx for pinworms

A

mebendazole

50
Q

Most likely cause of persistent unconjugated hyperbilirubinemia at 21 days of life…

A

Gilbert’s

51
Q

what to screen for in an infant with e.coli sepsis

A

galactosemia

52
Q

gilbert’s - inheritance

A

autosomal dominant

53
Q

gilbert’s - mutation in…

A

CGG repeats in glucoronyl transferase UDP1A1

54
Q

most common indication for liver transplant in children

A

biliary atresia

55
Q

which type of PFIC presents with elevated GGT?

A

type 3 (not type 1/2)

56
Q

most common metabolic etiology of hepatitis

A

A1AT deficiency (if unwell, think of galactosemia!)

57
Q

definition of fulminant hepatic failure

A

INR >2, or INR > 1.5 + encephalopathy

58
Q

elevated ALP in healthy child

A

familial hyperphosphatasemia (benign)

59
Q

ALP normal, other liver enzymes elevated

A

Think of Wilson’s disease

60
Q

ALP abnormally low

A

think of Zinc deficiency! (co-factors)

61
Q

coagulation factor not made in liver

A

factor VIII (8)

62
Q

treatment of Hep B

A
  • interferon-alpha

- other options: lamivudine (nucleoside analogue)

63
Q

side effect of interferon alpha (tx for hep b)

A

neutropenia, fever, myalgia, h/a

64
Q

most common type of gallstone

A

cholesterol