paeds GI Flashcards

1
Q

signs to look out for in GORD

A
Chronic cough
Hoarse cry
Distress, crying or unsettled after feeding
Reluctance to feed
Pneumonia
Poor weight gain
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2
Q

mx for GORD?

A

Small, frequent meals
Burping regularly to help milk settle
Not over-feeding
Keep the baby upright after feeding (i.e. not lying flat)

  • Gaviscon mixed with feeds
  • Thickened milk or formula
  • Ranitidine
  • Omeprazole where ranitidine is inadequate
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3
Q

what is Sandifer’s syndrome?

A

GORD with abnormal movements- the baby is neurologically fine tho

torticollis: forceful contraction of the neck muscles causing twisting of the neck

Dystonia: abnormal muscle contractions causing twisting movements, arching of the back or unusual postures

resolves as reflux gets better

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4
Q

Pyloric stenosis

A

hypertrophy of pyloric

failure to thrive
Projectile vomitting!!!!
firm round mass in upper abdomen- feels like a large olive

hypochloric (low CL) and metabolic alkalosis

dx: abdominal USS

Tx: laparoscopic pyloromyotomy (known as “Ramstedt’s operation“

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5
Q

main concerns with gastroenenteritis in a child?

A

isolate- easily spread.

Dehydration

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6
Q

Cystic fibrosis?

A

Steatorrhoea means greasy stools with excessive fat content.

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7
Q

most common cause of viral gastroenteritis?

A

Rotavirus

Norovirus

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8
Q

E.coli and gastroenteritis?

A

produces Shiga toxin:
bloody diarrhoea and vomitting
-> HUS

don’t use abs!!- increase risk of HUS

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9
Q

travellers diarrhoea causes?

A

Campylobactor

Raw or improperly cooked poultry
Untreated water
Unpasteurised milk

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10
Q

abx for campylobacter diarrhoea?

A

azithromycin or ciprofloxacin.

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11
Q

Shigella diarrhoea?

A

1-2 day incubation

bloody diarrhoea and cramps

  • can cause HUS
  • > Azithromycin/ ciprofloxacin (like campylobacter)
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12
Q

Bacillus ceros diarrhoea?

A

guy eats rice and

vomiting within 5 hours,

diarrhoea after 8 hours,

then resolution within 24 hours.

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13
Q

gastroenteritis ccx?

A

Lactose intolerance
Irritable bowel syndrome
Reactive arthritis
Guillain–Barré syndrome

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14
Q

Coeliac antibodies?

A

anti-tissue transglutaminase (anti-TTG) -raised

anti-endomysial (anti-EMA)

-> these 2 are IgA, need to test for TOTAL IgA

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15
Q

coeliac presentation?

A
Failure to thrive 
Diarrhoea
Fatigue
Weight loss
Mouth ulcers

Anaemia secondary to iron, B12 or folate deficiency

!!!!Dermatitis herpetiformis is an itchy blistering skin rash that typically appears on the abdomen

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16
Q

what disease associated with Coeliac?

A

test all patients with a new diagnosis of type 1 diabetes for coeliac disease, even if they don’t have symptom, because the conditions are often linked.

17
Q

how does Crohns present?

A

N – No blood or mucus (these are less common in Crohns.)

E – Entire GI tract

S – “Skip lesions” on endoscopy

T – Terminal ileum most affected and Transmural (full thickness) inflammation

S – Smoking is a risk factor (don’t set the nest on fire)

18
Q

UC presentation?

A

C – Continuous inflammation

L – Limited to colon and rectum

O – Only superficial mucosa affected

S – Smoking is protective

E – Excrete blood and mucus

U – Use aminosalicylates!!

P – Primary sclerosing cholangitis

19
Q

how to test for IBD?

A

Faecal calprotectin

endoscopy- gold standard!

20
Q

how to treat IBD?

A

steroids!!- Prednisalone/ IV hydrocortisone

21
Q

How does Biliary atresia present?

A

presents shortly after birth

-significat conjugated jaundice (dark pee, pale poo)

lasting more than 14 days in term babies and 21 days in premature babies.

22
Q

how to manage biliary atresia?

A

Surgery!!

Kasai portoenterostomy

23
Q

what can cause surgical obstruction?

A
Meconium ileus
Hirschsprung’s disease
Oesophageal atresia
Duodenal atresia
Intussusception
Imperforate anus
Malrotation of the intestines with a volvulus
Strangulated hernia
24
Q

presentation of abdominal obstruction?

A

bilious vomitting

abdo pain and distention

failure to pass stool or wind

high pitched tinkling

25
Q

ix and management of abdominal obstruction?

A

abdo xray!- dilated loops of bowel

absnece of air in rectum

Surgery!! nil by mouth, IV fluids

26
Q

what is Hirshsprungs disease?

A

nerve cells in myenteric plexus in nervous system absent

Absence of parasympathetic ganglion cells

loss of movement of poo and obstruction of bowel-> listened and full

27
Q

genes and hirshsprungs?

A

FH!!

associated with: downs, neurofibromatosis, waadernburg syndrome

multiple endocrine neoplasia type II

28
Q

presentation of hurshprungs

A

acute intestinal obstruction shortly after birth

gradually developing symptoms

delay passing meconium

abdo pain and distention

vomitting

poor wight gain and FTT

29
Q

what is Hirschsprung-assosiated enterocolitis?

A

2-4 weeks of birth with fever, abdominal distention, diarrhoea (often with blood) and features of sepsis.

life threatening-> toxic megacolon and perforation of the bowel.

urgent antibiotics,
fluid resuscitation and decompression of the obstructed bowel.

30
Q

mx of hirshprungs?

A

abdo xray

rectal biopsy confirms diagnosis- there will be no ganglionic cells

need fluid rhesus, and mx of obstruction

definitive mx- surgical removal!!- but can be left with incontinence

31
Q

Intussesception?

A

associated with concurrent viral illness
HSP
Cystic fibrosis

presentation:
Recurrent Jelly stool!!!!!
RUQ mass- Sausage shaped!!!
-usually kid would of had URTI before and sx of bowel obstruction

32
Q

ix of choice for intussusception?

A

USS!!

33
Q

mx of intussusception?

A

therapeutic enemas

surgery