Malabsorption Flashcards
Malabsorption
occurs when an individual is unable to absorb macro/micronutrients from their diet
4 causes of malabsorption:
- alterations to secretions
- alterations in structure/absorptive capacity
- alteration in motility
- reduction in blood flow
Diagnostic features of malabsorption:
- change in bowel movements or contents
- abdominal distension
- flatulence
- loss of weigth/growth failure
- hypoproteinaemia (low serum albumin)
- iron deficiency anaemia or low serum ferritin
Presenting features of fat malabsorption:
- steatorrhoea (pale, malodorous, greasy. unformed
stools) - often difficult to flush
- may leave greasy residue in the toilet
Presenting features of carbohydrate malabsorption:
- typically water
- frothy diarrhoea
- presence of fermented sugars
Dietary treatment for malabsorption:
- replace large fluid and electrolyte losses
- treat the primary disorder if appropriate
- provide symptom relief
- restore optimal nutritional status with
supplementation for micronutrients - increasing the amount taken orally may not lead to
increased absorption - vitamin B12 is absorbed in terminal ileum, if this is
removed no B12 will be absorbed therefore need
injections
gastric resection- gastric function disturbances
Alteration in gastric motility
- markedly accelerated gastric emptying can induce
dumping syndrome with malabsorption of fluids and
nutrients leading to diarrhoea - dumping syndrom: following gastric resection:
- early dumping: sweating, dizziness, faintness, rapid
weak pulse, hypotension; causes rapid and early
delivery of hyperosmolar load into the jejunum - late dumping: symptoms of weakness, cold, faintness, sweating 2 hours after a meal; cause: overproudctoion of insulin in response to rapid absoprtion of glucose
Early dumping syndrom symptoms often reced after how long
how can symptoms be helped
- 2-3 months
- small meals, limiting consumption of rapidly
absorbed carbs and not having drinks with meals
Alterations to secretions: Enzyme deficiencies (small intestine):
- disaxxharidase deficiency: primarly alactasia or secondary lactase deficiency
Alterations to secretions: Intraluminal deficiencies (small intestine):
- high pH in duodenum: achlorhydria
- low pH in duodenum: Zollinger-Ellinson syndrome
varying degrees of lactase deficiency can lead to lactose remaining in the small intestine leading to
osmotic diarrhoea
colonic bacteria further ferment the lactose resulting in symptoms such as abdo distension, flatulence and explosive watery diarrhoea
Three main types of lactase deficiency:
- congenital alactasia
- primary lactase deficiency
- secondary lactase deficiency
Congenital alactasia
- rare autosomal recessive disorder
- complete absence of lactase requiring total and
permanent lactose exclusion
Primary lactase deficiency
- gradual reduction in lactase production causes
symptoms of lactose maldigestion in older children
and adults - undigested lactose and products of its bacterial
fermentation can cause GI symptoms