Chronic Diarrhea Flashcards

1
Q

Recipe for homemade ORS

A

half a teaspoon of salt
• six level teaspoons of sugar
• 1 litre of water

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2
Q

Formula for Estimated
Ideal Weight for Age

1-6 yo

A

Age 1-6
Wt in kg = age in yrs x 8 +2

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3
Q

Wt in kg= age in yrs x 7–5
` 2

Sample: 7 yo
• Wt= (7 x 7) – 5 = 22kg
2

A
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4
Q

Definition of Chronic Diarrhea

A

Diarrheal episode that lasts for >14 days

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5
Q

As stool leaves the colon, fecal osmolality
is equal to the serum osmolality

A

(290
mosm/kg)

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6
Q

how to estimate stool osmolality?

A

The stool osmolality may be estimated by
using the formula: (stool Na + stool K) × 2

(multiplied by 2 to account for the anions)

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7
Q

Osmotic vs. Secretory

A

• OSMOTIC

  • • 290 mosm/kg
  • -2(actual stool Na +
  • stool K) >100
  • • An “Osmotic” gap
  • • Stool with low
  • electrolytes
  • • Cause of diarrhea:
  • indigestible solutes (lactose, sucrose or fructose)

SECRETORY

  • 290 Osm/kg - 2(actual
  • stool Na + stool K) <100
  • • A stool rich in electrolytes
  • • Cause of diarrhea:
  • actively secreted
  • electrolytes by crypt
  • cells
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8
Q

Sudan red stain: neutral fat - a sign of

A

maldigestion (pancreatic insufficiency,
including cystic fibrosis)

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9
Q
A
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10
Q

visualized fat after acid hydrolysis of the
stool (split fat) :

A

malabsorption (celiac
disease)

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11
Q

What indicates the presence of reducing CHOH ( CHOH malabsorption)

A

A pH <5 or the presence of moderate
reducing substances indicates the
presence of reducing carbohydrates

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12
Q

Hemoccult testing: evaluate for occult
blood
• A positive test indicates

A

indicates intestinal mucosal
damage, which may be caused by
gastrointestinal infection, protein
intolerance or inflammatory bowel disease.

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13
Q

Fat globules in the stool may be
**normal or abnormal **in the first few months of life.

A

Normal

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14
Q

• In an older child, the presence of fat
globules suggests

A

steatorrhea

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15
Q

Other Laboratory Evaluation

hydrogen breath test for

A

carbohydrate
malabsorption,

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16
Q

72-hour fecal fat test for

A

fat
malabsorption

17
Q

sweat chloride test for

A

cystic fibrosis

18
Q

upper gastrointestinal series with smallbowel
follow-through for _____________

A

anatomic
abnormalities and Crohn’s disease

19
Q

Causes of Chronic Diarrhea

Neonatal Age of Onset

A

0-30 days

  • Microvillus inclusion disease
  • Short bowel syndrome
  • Food allergy
  • Hirschsprung’s disease
  • Neonatal Lymphagectasia
  • Primary bile salt malabsorption
20
Q

autosomal recessive disorder

\at birth: profuse watery secretory
diarrhea, dehydration and failure to
thrive

A

Microvillus inclusion
disease

21
Q

What is the characteristic of Microvillus inclusion disease in light microscopy?

A

Light microscopy of small bowel
mucosa:

diffuse thinning of the
mucosa, with hypoplastic villus
atrophy and no inflammatory
infiltrate

22
Q

What is the prognosis of Microvillus inclusion
disease?

A

fatal without long-term parenteral
nutrition support- Refer to
GASTROENTEROLOGIST

23
Q

What is the treatment of Microvillus inclusion
disease

A

Tx: somatostatin analog octreotide
may reduce the volume of stool

24
Q

Definitive Tx: Microvillus inclusion
disease

A

Intestinal
transplantation

25
Q

results from congenital malformations
or resection of the small bowel

A

Short Bowel Syndrome

26
Q

If greater than 50% of the small bowel is loss, what happens?

A

decreased transit time à geralized
malabsorption disorder + specific
nutrient deficiency

27
Q

Short Bowel Syndrome
TREATMENT:

A
  • Hospitalization for FLUID AND ELECTROLYTES management
  • May require Parenteral nutrition until bowel’s absorptive function normalizes
  • Referral to a Gastroenterologist for NUTRITIONAL SUPPORT
28
Q

A diagnosis in neonates and young infants age:
- Necrotizing enterocolitis in term newborns
- Allergic colitis of neonate/young infant: bloody
stool without other symptoms
- Eosinophilic enteropathy: Profuse Vomiting,
Chronic diarrhea, FTT, Pallor, Edema

A

COW’S MILK ALLERGY

(Food Proten Allergy)

29
Q

What is the TX for COW’S MILK ALLERGY

(Food Proten Allergy)

A
  • Eliminate milk in maternal diet if the baby is
  • breast-fed OR
  • v Use protein hydrolysate formula OR
  • v In refractory cases, amino acid–based formulas are often beneficial
30
Q
  • Migratory failure of neural crest cells
  • Ø 90% fail to pass meconium in first 24-48 hrs
  • Ø Abdominal distension, bilious emesis, obstructive enterocolitis
  • Ø Rectal Biopsy: Absence of Ganglion cells
A
31
Q

What is the TX Hirschsprung Disease

A

Referral to SURGERY

32
Q

What is the TX Hirschsprung Disease in NEONATEs?

A

In neonates: primary pull-through–
bringing normal colon down to anorectal
junction

33
Q

What is the treatment of Hirschsprung Disease in older infants

A

In older infants: 2 steps:
1. may need diverting colostomy first to
decompress the distended colon
2. Anorectal Pull-through

34
Q
A