GI Motility and Functional Disorders Flashcards

1
Q

What is ileus?

A

disruption of normal propulsive ability of the gastrointestinal tract due to a failure of peristalsis in the absence of mechanical obstruction

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2
Q

What are the consequences of ileus? (5)

A
  1. constipation
  2. distension
  3. discomfort
  4. nausea
  5. absent bowel sounds
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3
Q

What are the causes of ileus? (5)

A
  1. post surgery/trauma
  2. severe illness
  3. electrolyte and acid-base abnormalities
  4. drugs - anti-muscarinics, opioids
  5. hypothyroidism
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4
Q

What is the ROME III criteria for IBS?

A

abdominal pain that improves with defaecation, onset is associated with change in stool frequency and change in stool form/appearance

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5
Q

What is the cause of IBS?

A

multifactorial

bio-psycho-social model

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6
Q

What are the subtypes of IBS? (4)

A
  1. IBS-Constipation
  2. IBS-Diarrhoea
  3. IBS-Mixed
  4. IBS-Unsubtyped
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7
Q

What IBS subtypes are associated with aberrant autonomic nervous system function? (2)

A
  1. excess sympathetic tone in IBS-D

2. Insufficient parasympathetic tone IBS-C

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8
Q

What are the triggers for IBS? (3)

A
  1. Gut flora
  2. Food triggers
  3. psychosocial triggers
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9
Q

How is IBS managed? (5)

A
  1. identify dietary triggers
  2. manipulate dietary fibre and exercise
  3. manipulate gut flora
  4. pharmacologically modulate gut motility
  5. investigate, explain, reassure
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10
Q

What is chronic idiopathic intestinal pseudo-obstruction?

A

intestinal dilation

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11
Q

What is the cause of intestinal pseudo-obstruction?

A
  1. insufficient actin in the inner circular smooth muscle layer
  2. auto-immune inflammatory mixed connective tissue disorder
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12
Q

What is the diameter of the lumen in slow transit constipation?

A

normal diameter

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13
Q

What cells are decreased in slow transit constipation?

A
  1. interstitial cells of cajal (pacemakers)

2. enteric neurofilaments

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14
Q

What are the characteristics of systemic sclerosis?

A
  1. chronic inflammation
  2. widespread small vessel damage
  3. progressive perivascular and interstitial fibrosis
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15
Q

In whom is systemic sclerosis most severe?

A

African-American women

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16
Q

What auto antibodies are seen in systemic sclerosis? (3)

A
  1. anti-nuclear antibodies (all)
  2. anti DNA topoisomerase (10-20%)
  3. anti centromere antibody (20-30%)
17
Q

What are the classifications of systemic sclerosis?

A
  1. diffuse cutaneous SScl

2. limited cutaneous SScl (60%)

18
Q

What autoantibody is associated with diffuse cutaneous SScl?

A

anti-DNA topoisomerase 1

19
Q

What autoantibody is associated with limited cutaneous SScl?

A

anti-centromere antibody

20
Q

What is limited cutaneous SScl associated with? (5)

A
  1. Calcinosis
  2. raynaud’s
  3. esophageal dysmotility
  4. sclerodactyly
  5. telangiectasia
21
Q

What is the causative agent of Chaga’s disease?

A

trypanosoma cruzi

22
Q

What is the presentation of acute Chaga’s disease?

A
  1. papule
  2. fever
  3. adenopathy
  4. myocardial damage
23
Q

What is Hirchsprung’s disease?

A

congenital aganglionic megacolon

24
Q

What is Hirchsprung’s disease associated with? (2)

A
  1. trisomy 21

2. loss of function mutation of RET gene

25
What is the pathogenesis of Hirchsprung's disease?
1. absent ganglion cells in meissner's (submucosal) and auerbach's (myenteric) plexuses 2. failure of caudal migration
26
how does Hirchsprung's disease present?
neonatal failure to pass meconium and obstipation