GI 229&237 Nutrition and Chronic Diarrhoea Flashcards

1
Q

What is short bowel syndrome?

A

A state of malabsorption and malnutrition that occurs following massive anatomical or functional loss of the SI

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2
Q

What is necrotizing enterocolitis?

A

Ischaemia and necrosis of the SI in neonates causing 22-50% of SBS - a surgical emergency in neonates

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3
Q

What is intusseption of the bowel?

A

Part of the intestine folds into another part - presents in childhood

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4
Q

What is the function of the ileocaecal valve?

A

To slow transit time and to prevent bacterial reflux from the large intestine to the small

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5
Q

What happens in ileal adaptation?

A

Usually when there has been a jejunum resection

epithelial hyperplasia within 24hours, with villi changes resulting in increased macronutrient absorption

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6
Q

What must be given after jejenal resection?

A

Enteral feeding as it stimulates ileal adaptation

containing: arginine, TG’s, glutamine and AA’s

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7
Q

What diet is recommended after jejenal resection?

A

Diet higher in fat and protein

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8
Q

What are the main complications that must be managed with an ileal resection?

A

Massive fluid and electrolyte loss due to malabsorption of bile salts and Vitamin B12

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9
Q

What are some complications of Short Bowel Syndrome?

A

Hypergastrinaemia, malabsorption of bile acids, therefore fat soluble vitamins, clotting disorders, osteoporosis and nephrolithiasis

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10
Q

What is hypergastrinaemia and why does it occur in SBS?

A

(mostly in jejenal resection) the negative feedback mechanism for inhibiting gastrin secretion has been removed
can lead to oesophagitis or PUD but is often only transient

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11
Q

Why can gallstones occur in SBS?

A

A decreased bile acid:cholesterol ratio and stasis allowing gallstone formation

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12
Q

Why can nephrolithiasis occur in SBS?

A

Bile salts in the colon stimulates increased oxalate absorption giving rise to renal oxalate stones

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13
Q

What are the indications for enteral feeding?

A

Functioning gut but cannot meet the nutritional requirements with normal food
3 months of >10% unintentional weight loss and a hypermetabolic state e.g. sepsis or trauma

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14
Q

What are the indications for parenteral feeding?

A

Non-functioning gut, gut rest needed, >7 days inadequate nutrition
e.g. in severe pancreatitis, post chemo, IBD, intestinal atresia and other motility disorders
Use short term only (2/52)

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15
Q

Explain refeeding syndrome

A

When a state of starvation is quickly reversed the catabolic processes and state of gylcogenolysis and gluconeogenesis switch to anabolic. There is sudden increase in insulin in response to feeding leading to increased protein and glycogen synthesis
This leads to rapid uptake of vitamins into cells with Na and water retention
Can be fatal due to mineral and electrolyte deficiencys

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16
Q

What minerals is there rapid uptake of in refeeding and therefore what problems?

A
hypoPhosphate = tissue hypoxia
hypomagnesium
hypokalaemia = cardiac dysrhythmias
decreased thiamine = confusion
Na+/water = oedema 
there is also thrombocytopaenia
17
Q

What are the risk factors for refeeding syndrome?

A

One of:
BMI 15% weight loss in 3-6 months
Low minerals to begin with

Two of:
BMI 10% in 3-6months
intake decreaed in >5/7
Alcohol/drug abuse

18
Q

How do you prevent refeeding?

A

Decrease rate of feeding initially
Vitamin B for the 1st 10 days
Supplement electrolytes assessing daily and comparing to baseline
If refeeding occurs then slow feeding rate

19
Q

What do you get with a Vitamin A deficiency?

A

compromised mucosa, night blindness and benign intracranial HTN

20
Q

What do you get with a Vitamin D deficiency?

A

Ricketts/Osteomalacia

21
Q

What do you get with a Vitamin E deficiency?

A

Increased susceptibility to oxidant stress th. CVS disease
Haemolysis
Neurological symptoms

22
Q

What do you get with a Vitamin K deficiency?

A

Coagulopathy - prolonged PT

23
Q

What happens in lactose intolerance?

A

There is a lack of digestion of lactose by brush border enzymes resulting in its accumulation in the lumen - has an osmotic effect leading to diarrhoea and it also ferments in the intestine leading to gas, bloating and acidic stools

24
Q

How would you investigate a suspected lactose intolerance?

A

Lactose breath test - give lactose to ingest then if there is an intolerance there will be increase hydrogen

25
Q

What are some causes of lactase deficiency?

A

Primary - can develop later, often after 5 years of age is an AR disorder
Congenital extremely rare and infant fails to thrive
Secondary to mucosal injury - often transient

26
Q

What is the breakdown of Lactose?

A

By lactase into glucose and galactose

27
Q

What does the SGLT transporter do?

A

Transports glucose and galactose coupled with Na+

28
Q

Where is CCK released from?

A

I cells in duodenum and jejenum

29
Q

Where does CCK act on and what are its actions?

A

Pancreas: increase enzyme secretion
Gallbladder: Contraction and sphincter of oddi relaxation

30
Q

What are the actions of Gastrin?

A

Parietal cells: H+ release

31
Q

Where is glucagon released from?

A

alpha cells of pancreas (islets of langerhans)

32
Q

What is the action of glucagon?

A

Opposes insulin: increase production of glucose and breakdown of glycogen

33
Q

What is ghrelin and where is it released from?

A

Hormone released from stomach that stimulates appetite

34
Q

Describe somatostatin

A

Released from stomach and D cells in pancreas - inhibits secretion and action of most hormones!

35
Q

What is the action of guanylin?

A

Stimulates fluid absorption from the SI/LI

36
Q

Where is VIP released rom?

A

ENS neurones

37
Q

What is the action of VIP?

A
SI/Pancreas = increased secretions
SI = relaxes smooth muscle