vomiting + malabsorption in children Flashcards

1
Q

pyloric stenosis features

A

projectile non-bilious vomiting
weight loss
dehydration +/- shock

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2
Q

pyloric stenosis characteristic electrolyte disturbance

A

metabolic alkalosis
hypochloraemia
hypokalaemia

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3
Q

effortless vomiting

A

regurgitation
involuntary passage of gastric contents through the mouth

self limiting and resolves spontaneously in vast majority of cases

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4
Q

when may effortless vomiting not resolve spontaneously with age

A

cerebral palsy
progressive neurological problems
oesophageal atresia +/- TOF operated
generalised GI motility problem

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5
Q

what is effortless vomiting almost always due to

A

gastro-oesophageal reflux

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6
Q

pathophysiology of reflux in infants

A

LOS lax, mainly lying down and feeds are mainly liquid –> all predisposes them to GOR

tends to improve w age when solids are introduced from 6mo and when begin to sit/stand/walk

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7
Q

presenting symptoms GOR

A
vomiting 
haematemesis 
feeding problems 
failure to thrive
apnoea 
cough 
wheeze
chest infection 
sandifer's syndrome
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8
Q

sandifer’s syndrome

A

association of GOR disease with torticollis and dystonic body movements

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9
Q

diagnosing GOR

A

hx and exam often sufficient
oesophageal pH study/impedance monitoring
endoscopy
radiological investigations: video fluroscopy, barium swallow

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10
Q

GOR treatment

A

feeding advice, nutritional support

medical treatment
surgery

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11
Q

GOR feeding advice

A
  • thickeners for liquids
  • appropriateness of foods: texture, amount
  • behavioural stimulation: oral stimulation, removal of adverse stimuli
  • feeding position
  • check feed volumes
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12
Q

GOR nutritional support

A

calorie supplements
exclusion diet - cows milk protein free trial for 4 weeks
NG tube
gastrostomy

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13
Q

GOR medical treatment

A

feed thickener - gaviscon, thick + easy

acid suppressing drugs; H2 receptor blockers, proton pump inhibtors

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14
Q

GOR indications for surgery

A

failure of medical treatment

persistent: failure to thrive, aspiration, oesophagitis

vomiting without complications may not be an indication

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15
Q

GOR surgery

A

nissen fundoplication

fundus is wrapped round LOS

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16
Q

bilious vomiting

A

should always ring alarm bells

due to intestinal obstruction until proven otherwise

17
Q

causes of bilious vomiting

A

intestinal atresia - newborns only
intussusception
ileus
crohn’s disease w strictures

18
Q

bilious vomiting investigations

A

abdo x-ray
consider contrast meal
surgical opinion re exploratory laparotomy

19
Q

chronic diarrhoea

A

4+ stools per day for more than 4 weeks

20
Q

causes of diarrhoea: motility disturbance

A

toddler diarrhoea

irritable bowel syndrome

21
Q

causes of diarrhoea: active secretion

A

(secretory)
acute infective diarrhoea
inflammatory bowel disease

22
Q

causes of diarrhoea: malabsorption of nutrients

A

(osmotic)
food allergy
coeliac disease
CF

23
Q

osmotic diarrhoea

A

movement of water into bowel lumen to equilibrate osmotic gradient

usually a feature of malabsorption: enzymatic defect, transport defect

24
Q

osmotic diarrhoea: enzymatic defect

A

e.g. secondary lactase deficiency due to loss of brush-border enzymes after diarrhoeal illness

25
Q

osmotic diarrhoea: transport defect

A

e.g. glucose-galactose transported defect

26
Q

secretory diarrhoea

A

classically assoc with toxin productions from vibrio cholerae and enterotoxienic e.coli

intestinal fluid secretion predominantly driven by active Cl- secretion via CFTR

27
Q

clinical approach to chronic diarrhoea

A

thorough history
consider growth + weight gain of child
faeces analysis: appearance, stool culture, determination of secretory vs osmotic

28
Q

history taking chronic diarrhoea

A
age onset 
abrupt/gradual onset
Fam Hx
travel history/local outbreaks 
nocturnal defecation suggests organic pathology
29
Q

fat malabsorption causes

A

pancreatic disease: diarrhoea due to lack of lipase and recurrent steatorrhoea, classically CF

hepatobiliary disease: chronic liver disease, cholestasis

30
Q

coeliac disease

A

autoimmune condition

gluten sensitive enteropathy

wheat, rye, barley

31
Q

presenting features coeliac disease

A
abdo bloating
dirrhoea 
failure to thrive
short stature
constipation 
tiredness
hepatiformis
32
Q

coeliac disease screening tests

A

serological screens

  • anti-tissue transglutaminase
  • anti-endomysial
  • serum IgA

duodenal biopsy

genetic testing: HLA DQ2, DQ8

33
Q

treatment of coeliac disease

A

gluten-free diet for life

gluten must not be removed prior to diagnosis as serological and histological features will resolve

34
Q

histology coeliac duodenum

A

lymphocytic infiltration surface epithelium
partial/total villous atrophy
crypt hyperplasia

35
Q

when to do endoscopy + biopsy for coeliac

A
  • symptomatic
  • anti TTG +ive
  • anti-endomysial +ive
  • HLA DQ2, Q8 +ve

all present diagnosis without endoscopy
any missing then endoscopy