Malabsorption Flashcards

(59 cards)

1
Q

What is the definition of malabsorption?

A

“Defective mucosal uptake and transport of adequately digested protein, fat, carbohydrates or nutrients”

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2
Q

What is intraluminal digestion?

A

Pancreatic enzyme secretion and emulsification by bile salts

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3
Q

What is terminal digestion?

A

Enzymatic hydrolysis in brush border of small intestine

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4
Q

What is transepithelial transport?

A

Nutrients, fluid and electrolytes transported across epithelium

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5
Q

What can disturbance in electrolyte absorption lead to?

A

Osmotic diarrhoea

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6
Q

What are proteins, starches and triglycerides digested to?

A

Proteins → peptides
Starches → α-dextrins and disaccharides
Triglycerides → fatty acids and monoglycerides

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7
Q

What are a-dextrins and disaccharides hydrolysed by?

A

α-dextrins and disaccharides are hydrolysed by brush border enzymes and absorbed into cells

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8
Q

What do amphipathic bile salts form?

A

tiny spheres called micelles

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9
Q

What do long chain fatty acids require for absorption?

A

bile salts

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10
Q

What happens when Fatty acids and monoglycerides reach the epithelial cells of the villi?

A

Fatty acids and monoglycerides reach the epithelial cells of the villi and diffuse into the cells, leaving micelles behind in chyme

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11
Q

Where are bile salts reabsorbed?

A

the terminal ileum (enterohepatic circulation)

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12
Q

How do you identify steatorrhoea?

A

Stools may float in the pan – difficult to flush

Oily appearance and be foul smelling.

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13
Q

Which vitamins are fat soluble?

A

Vitamins A, D, E and K are fat-soluble

If fat absorption is impaired, deficiencies in these vitamins may occur

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14
Q

How does vitamin D deficiency affect calcium absorption?

A

Calcium absorption is greatly reduced in vitamin D deficiency and sometimes in generalized malabsorption

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15
Q

What is osteoporosis?

A

reduced bone density, inc risk of fragility fractures

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16
Q

What are some causes of osteoporosis?

A

Anorexia, smoking, alcoholism, malabsorption, steroid therapy, vitamin D/ calcium deficiency

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17
Q

How is osteoporosis diagnosed?

A

WHO osteoporosis criteria, DEXA bone scan T-SCORE -2.5 or worse

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18
Q

What is Osteomalacia and what causes it?

A

Definition:
Normal amount of bone but its mineral content is low.

Causes:
Vitamin D deficiency - inadequate sunlight, malabsorption (coeliac, intestinal resection, cholestasis), renal disease.

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19
Q

What can vitamin A deficiency cause?

A

blindness (begins with inability to produce tears)

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20
Q

What can vitamin B1 (thiamine) deficiency cause?

A

Beriberi; Wernickes

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21
Q

What can vitamin B2 deficiency cause?

A

angular stomatis; cheilitis

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22
Q

What can vitamin B6 deficiency cause?

A

polyneuropathy

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23
Q

What can vitamin B12 deficiency cause?

A

anaemia, SCDC

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24
Q

What can vitamin C deficiency cause?

25
What can vitamin D deficiency cause?
osteomalacia
26
What can vitamin E deficiency cause?
bleeding disorders
27
What can vitamin K deficiency cause?
bleeding disorders
28
What can lead to B12 deficiency?
Gastric mucosal atrophy (pernicious anaemia) and terminal ileal disease
29
What does B12 require for absorption?
intrinsic factor
30
What is folate necessary for?
efficient thymidilate synthesis and production of DNA.
31
3 things to consider in deficiencies
Is the patient - not getting enough in not absorbing enough losing too much
32
3 mechanisms of iron deficiency
iron intake (dietary) ↓ iron absorption (principally in the duodenum) ↑ iron loss (sloughed mucosal cells, bleeding)
33
What is coeliac disease?
Inflammatory condition of the small intestinal mucosa induced by an autoimmune reaction to the ingestion of gluten
34
What can be seen in coeliac disease from a histology point of view?
Villous atrophy/ intraepithelial lymphocytosis
35
How common is coeliac disease?
1 in 100 in the UK
36
What is the clinical presentation of coeliac disease in infants?
impaired growth, diarrhoea, vomiting, abdominal distension
37
What is the clinical presentation of coeliac disease in older children?
anaemia, short stature, pubertal delay, rickets, recurrent abdominal pain or behavioural disturbance
38
What is the clinical presentation of coeliac disease in adults?
chronic/recurrent iron deficiency anaemia, diarrhoea, abdominal pain, bloating, isolated nutritional deficiencies, reduced fertility, osteoporosis, osteomalacia abnormal liver function tests
39
How is Coeliac disease diagnosed?
Clinical history Serological tests – endomysial (EMA) and tissue transglutaminase (tTG) antibodies Duodenal biopsy via upper GI endoscopy
40
How is coeliac disease treated/managed?
gluten-free diet
41
What can lead to B12 deficiency?
Gastric mucosal atrophy (pernicious anaemia) and terminal ileal disease
42
What does B12 require for absorption?
intrinsic factor
43
What is folate necessary for?
efficient thymidilate synthesis and production of DNA.
44
3 things to consider in deficiencies
Is the patient - not getting enough in not absorbing enough losing too much
45
3 mechanisms of iron deficiency
iron intake (dietary) ↓ iron absorption (principally in the duodenum) ↑ iron loss (sloughed mucosal cells, bleeding)
46
What is coeliac disease?
Inflammatory condition of the small intestinal mucosa induced by an autoimmune reaction to the ingestion of gluten
47
What can be seen in coeliac disease from a histology point of view?
Villous atrophy/ intraepithelial lymphocytosis
48
How common is coeliac disease?
1 in 100 in the UK
49
What is the clinical presentation of coeliac disease in infants?
impaired growth, diarrhoea, vomiting, abdominal distension
50
What is the clinical presentation of coeliac disease in older children?
anaemia, short stature, pubertal delay, rickets, recurrent abdominal pain or behavioural disturbance
51
What is the clinical presentation of coeliac disease in adults?
chronic/recurrent iron deficiency anaemia, diarrhoea, abdominal pain, bloating, isolated nutritional deficiencies, reduced fertility, osteoporosis, osteomalacia abnormal liver function tests
52
How is Coeliac disease diagnosed?
Clinical history Serological tests – endomysial (EMA) and tissue transglutaminase (tTG) antibodies Duodenal biopsy via upper GI endoscopy
53
How is coeliac disease treated/managed?
gluten-free diet replace nutritional deficiencies monitor bone density
54
What are investigations for chronic pancreatitis?
Faecal elastase-1 Produced by pancreas and passed in stool largely unaltered Plain abdominal X-ray Ultrasound/ CT MRCP vs ERCP
55
What are some clinical features of pancreatic disease?
epigastric pain, often radiating to the back, food or alcohol may exacerbate the pain, weight loss.
56
How is chronic pancreatitis managed?
``` Remove precipitant (eg. alcohol) Pain control Treat diabetes (often need insulin) Pancreatic enzyme supplements – Creon Lipase, protease, amylase Vitamin supplementation ``` Nerve plexus blocks Endoscopic stenting of strictures, surgery
57
What is cholestasis?
Cholestasis is the impairment of bile formation / bile flow
58
What is Primary sclerosing cholangitis (PSC)?
Inflammatory/ fibrotic process affecting intra/extrahepatic bile ducts Leads to bile duct strictures Aetiology unknown, but ~80% associated with IBD Presents as pruritis, fatigue, jaundice Ultimately leads to cirrhosis and liver failure - only proven treatment is liver transplantation
59
What drug can cause malabsorption?
orlistat - inhibits gastric and pancreatic lipase