vomiting + malabsorption in children Flashcards
pyloric stenosis features
projectile non-bilious vomiting
weight loss
dehydration +/- shock
pyloric stenosis characteristic electrolyte disturbance
metabolic alkalosis
hypochloraemia
hypokalaemia
effortless vomiting
regurgitation
involuntary passage of gastric contents through the mouth
self limiting and resolves spontaneously in vast majority of cases
when may effortless vomiting not resolve spontaneously with age
cerebral palsy
progressive neurological problems
oesophageal atresia +/- TOF operated
generalised GI motility problem
what is effortless vomiting almost always due to
gastro-oesophageal reflux
pathophysiology of reflux in infants
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
presenting symptoms GOR
vomiting haematemesis feeding problems failure to thrive apnoea cough wheeze chest infection sandifer's syndrome
sandifer’s syndrome
association of GOR disease with torticollis and dystonic body movements
diagnosing GOR
hx and exam often sufficient
oesophageal pH study/impedance monitoring
endoscopy
radiological investigations: video fluroscopy, barium swallow
GOR treatment
feeding advice, nutritional support
medical treatment
surgery
GOR feeding advice
- thickeners for liquids
- appropriateness of foods: texture, amount
- behavioural stimulation: oral stimulation, removal of adverse stimuli
- feeding position
- check feed volumes
GOR nutritional support
calorie supplements
exclusion diet - cows milk protein free trial for 4 weeks
NG tube
gastrostomy
GOR medical treatment
feed thickener - gaviscon, thick + easy
acid suppressing drugs; H2 receptor blockers, proton pump inhibtors
GOR indications for surgery
failure of medical treatment
persistent: failure to thrive, aspiration, oesophagitis
vomiting without complications may not be an indication
GOR surgery
nissen fundoplication
fundus is wrapped round LOS
bilious vomiting
should always ring alarm bells
due to intestinal obstruction until proven otherwise
causes of bilious vomiting
intestinal atresia - newborns only
intussusception
ileus
crohn’s disease w strictures
bilious vomiting investigations
abdo x-ray
consider contrast meal
surgical opinion re exploratory laparotomy
chronic diarrhoea
4+ stools per day for more than 4 weeks
causes of diarrhoea: motility disturbance
toddler diarrhoea
irritable bowel syndrome
causes of diarrhoea: active secretion
(secretory)
acute infective diarrhoea
inflammatory bowel disease
causes of diarrhoea: malabsorption of nutrients
(osmotic)
food allergy
coeliac disease
CF
osmotic diarrhoea
movement of water into bowel lumen to equilibrate osmotic gradient
usually a feature of malabsorption: enzymatic defect, transport defect
osmotic diarrhoea: enzymatic defect
e.g. secondary lactase deficiency due to loss of brush-border enzymes after diarrhoeal illness
osmotic diarrhoea: transport defect
e.g. glucose-galactose transported defect
secretory diarrhoea
classically assoc with toxin productions from vibrio cholerae and enterotoxienic e.coli
intestinal fluid secretion predominantly driven by active Cl- secretion via CFTR
clinical approach to chronic diarrhoea
thorough history
consider growth + weight gain of child
faeces analysis: appearance, stool culture, determination of secretory vs osmotic
history taking chronic diarrhoea
age onset abrupt/gradual onset Fam Hx travel history/local outbreaks nocturnal defecation suggests organic pathology
fat malabsorption causes
pancreatic disease: diarrhoea due to lack of lipase and recurrent steatorrhoea, classically CF
hepatobiliary disease: chronic liver disease, cholestasis
coeliac disease
autoimmune condition
gluten sensitive enteropathy
wheat, rye, barley
presenting features coeliac disease
abdo bloating dirrhoea failure to thrive short stature constipation tiredness hepatiformis
coeliac disease screening tests
serological screens
- anti-tissue transglutaminase
- anti-endomysial
- serum IgA
duodenal biopsy
genetic testing: HLA DQ2, DQ8
treatment of coeliac disease
gluten-free diet for life
gluten must not be removed prior to diagnosis as serological and histological features will resolve
histology coeliac duodenum
lymphocytic infiltration surface epithelium
partial/total villous atrophy
crypt hyperplasia
when to do endoscopy + biopsy for coeliac
- symptomatic
- anti TTG +ive
- anti-endomysial +ive
- HLA DQ2, Q8 +ve
all present diagnosis without endoscopy
any missing then endoscopy