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
Q

What is the pathogenesis of Hirchsprung’s disease?

A
  1. absent ganglion cells in meissner’s (submucosal) and auerbach’s (myenteric) plexuses
  2. failure of caudal migration
26
Q

how does Hirchsprung’s disease present?

A

neonatal failure to pass meconium and obstipation