Case 4 - Change In Bowel Habit Flashcards

1
Q

Differential diagnosis of colitis

A

Infectious - bacterial i.e. E. coli, diverticulitis
Inflammatory - IBD, Ischaemic
Cancer?

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2
Q

What is pancolitis?

A

Inflammation of the whole colon

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3
Q

What is the most common cause of pancolitis?

A

Ulcerative colitis

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4
Q

Pancolitis is usually caused by UC, what are other causes?

A

C. difficile, rheumatoid arthritis

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5
Q

Ulcerative colitis VS Crohn’s disease

Which one has ‘skip’ lesions?

A

Crohn’s disease

UC has continuous segments

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6
Q

Ulcerative colitis VS Crohn’s disease

Which one has ‘mucosal inflammation’

A

UC

Crohn’s has transmural inflammation

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7
Q

Ulcerative colitis VS Crohn’s disease

Which one has ‘granulomas?’

A

Crohn’s - UC does not have granulomas

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8
Q

Ulcerative colitis VS Crohn’s disease

Which one has ‘fistulae’?

A

Crohn’s has fistulae

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9
Q

Ulcerative colitis VS Crohn’s disease

Which one is in colon only?

A

UC - Crohn’s disease is anywhere in GIT

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10
Q

Fistulae is a common complication of what IBD?

A

Crohn’s

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11
Q

How to treat a fistulae associated with Crohn’s

A

Treat any infection
Remove distal obstruction
Reduce flow
(Rehydrate)

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12
Q

Management of Fistula mnemonic - SNAP

A

S = Sepsis - identify whether there is sepsis and it’s source, manage appropriately
N = Nutrition - optimise oral and/or enteral intake
Initiate parenteral nutrition if appropriate
A = Anatomical Mapping
P = Plan for potential surgical intervention

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13
Q

Extraintestinal manifestations - aphthous ulcers - which IBD?

A

Crohn’s

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14
Q

Pyoderma gangrenosum is a potential complication of both IBD types (more common in UC) - what is it?

A

Lesions in skin filled with pus, ulcer has indistinct edges and a unique purplish colour
Painful and slow to heal

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15
Q

Erythema nodosum is a skin condition that most often affects people with …

A

Crohn’s disease

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16
Q

What is this showing?

A

Erythema nodosum - an inflammatory condition characterised by inflammation of the fat cells under the skin, resulting in tender red nodules or lumps that are usually seen on both shins. Typically seen in Crohn’s (15% develop this), also idiopathic causes and some infections, medications, autoimmune disorders and potentially pregnancy

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17
Q

What is episcleritis?

A

Persistent irritated red eye - discomfort, not severe pain
No visual change
Vessels mobile over sclera
Usually localised

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18
Q

What is the most common eye manifestation of IBD?

A

Episcleritis - persistent red irritated eye, no vision loss, usually localised

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19
Q

What is neutropenic sepsis?

A

Potentially life-threatening complication of neutropenia (low neutrophil count)
Complication of anti cancer or immunosuppressive drug treatment
Temp of greater than 38 and any symptoms/signs of sepsis, in a person with a neutrophil count of 0.5 x 10^9/L or lower

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20
Q

Neutropenic sepsis is a complication of what treatments?

A

Immunosuppressive drugs and anti cancer treatment

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21
Q

Define septic shock

A

Sepsis with hypotension not responsive to 20ml/kg or requiring vasopressors

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22
Q

Define sepsis

A

Life-threatening organ dysfunction (medical emergency) caused by a dysregulated host response to infection

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23
Q

Severe sepsis - define

A

Sepsis with Organ dysfunction or high lactate

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24
Q

Sepsis 6

A

Take - blood cultures, lactate and Hb, urine output

Give - oxygen, antibiotics, fluid challenge

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25
Types of shock:
Cardio genie, hypovolaemic, obstructive, distributive (septic, anaphylactic, neurogenic)
26
3 types of distributive shock
Septic, anaphylactic, neurogenic shock
27
Neutropenic sepsis - what bacteria is it? And how do we treat?
Gram + or negative bacteria Broad spectrum antibiotics Anti-fungals +/-
28
Primary sclerosing cholangitis is associated with …
Ulcerative colitis
29
‘Beads on a string’ appearance is seen in a cholangiogram in what condition?
Primary sclerosing cholangitis
30
What is a cholangiogram?
X-ray of bile ducts
31
Abnormal LFTS - Hepatitic vs cholestatic
``` Hepatitic = very high ALT/AST, slightly high ASP/bilirubin/GGT Cholestatic = very high ALP/bilirubin/GGT, slightly high ALT/AST ```
32
``` … = very high ALT/AST, slightly high ASP/bilirubin/GGT … = very high ALP/bilirubin/GGT, slightly high ALT/AST ```
``` Hepatitic = very high ALT/AST, slightly high ASP/bilirubin/GGT Cholestatic = very high ALP/bilirubin/GGT, slightly high ALT/AST ```
33
ALT>AST is associated with what?
Chronic liver disease
34
AST>ALT is associated with … and …
Cirrhosis and acute alcoholic hepatitis
35
Common causes of acute hepatocellular injury (3)
Poisoning i.e. paracetamol overdose Infection (Hep A/B) Liver Ischaemia
36
Common causes of chronic hepatocellular injury (3)
Alcoholic fatty liver disease Non-alcoholic fatty liver disease Chronic infection (Hep B/C) Primary biliary cirrhosis
37
What is prothrombin time? (PT)
Prothrombin time is a measure of the blood’s coagulation tendency, specifically assessing the extrinsic pathway. In the absence of other secondary causes such as anticoagulant drug use and vitamin K deficiency, an increased PT can indicate liver disease and dysfunction. The liver is responsible for the synthesis of clotting factors, therefore hepatic pathology can impair this process resulting in increased prothrombin time
38
Albumin levels can fall due to:
Liver disease resulting in a decreased production of albumin (e.g. cirrhosis) Inflammation triggering an acute phase response which temporarily decreases the liver’s production of albumin Excessive lots of albumin due to protein-losing enteropathies or nephrotic syndrome
39
Bilirubin is a breakdown product of what?
Haemoglobin
40
Jaundice usually occurs when bilirubin levels are …
>60umol/L
41
Darker urine indicates the patient has … hyperbilirubinaemia
Conjugated - as this can pass into the urine as urobilinogen
42
The stool colour can help to differentiate the causes of jaundice - if bile and pancreatic lipases are not able to reach the bowel due to blockage, fat is not absorbed, meaning the stool is …
Pale, bulky and more difficult to flush
43
Normal stools + normal urine = … hepatic cause of jaundice
Pre hepatic cause
44
Normal stools + dark urine = … hepatic cause of jaundice
Hepatic cause
45
Pale stools + dark urine = … hepatic cause of jaundice
Post-hepatic cause (obstructive)
46
Causes of unconjugated hyperbilirubinaemia include:
Haemolytic (e.g. haemolytic anaemia) Impaired hepatic uptake (E.g. drugs, congestive cardiac failure) Impaired conjugation (e.g. Gilbert’s syndrome)
47
Causes of conjugated hyperbilirubinaemia include:
Hepatocellular injury | Cholestasis
48
The liver’s main functions are … (4)
Conjugation and elimination of bilirubin Synthesis of albumin Synthesis of clotting factors Gluconeogenesis
49
If the patient is jaundiced but ALT and ALP levels are normal - it is suggestive of a … cause of jaundice
Pre-hepatic
50
Causes of an isolated rise in bilirubin include:
Gilbert’s syndrome: the most common cause | Haemolysis - check a blood film, full blood count, reticulocyte count, haptoglobin and LDH levels to confirm
51
A greater than 10-fold increase in ALT and a less than 3-fold increase in ALP suggests a predominantly … injury
Hepatocellular injury
52
A less than 10-fold increase in ALT and a more than 3-fold increase in ALP suggests …
Cholestasis
53
Is it possible to have a mixed picture of hepatocellular injury and Cholestasis?
Yes
54
If there is a rise in ALP, it is important to review the level of GGT also - why?
A raised GGT can be suggestive of biliary epithelial damage and bile flow obstruction. It can also be raised in response to alcohol and drugs such as phenytoin. A markedly raised ALP with a raised GGT is highly suggestive of Cholestasis.
55
A markedly raised ALP with a raised GGT is highly suggestive of …
Cholestasis
56
Causes of an isolated rise in ALP include:
Bony metastases or primary bone tumours Vitamin D deficiency Recent bone fractures Renal osteodystrophy
57
… is found in high concentrations within hepatocytes and enters the blood following hepatocellular injury.
ALT
58
… is particularly concentrated in the liver, bile duct and bone tissues. It is often raised in liver pathology due to increased synthesis in response to Cholestasis.
ALP - so it is a useful indirect marker of Cholestasis
59
If the ALT is raised decide if this is a more than a … fold rise of less than a … fold rise
10 fold (more or less)
60
If the ALP is raised decide if this is a more than a … fold rise of less than a … fold rise
3 fold rise (more or less)
61
ALT, AST, ALP and GGT are used to distinguish between … damage and ….
hepatocellular damage and Cholestasis
62
Bilirubin, albumin and PT are used to assess what?
Livers synthetic function
63
What blood tests are used to assess liver function?
``` ALT AST ALP GGT Bilirubin Albumin Prothrombin time (PT) ```
64
In pre-hepatic jaundice, there is excessive red blood cell breakdown which leads to what?
Overwhelms the livers ability to conjugate bilirubin - causing an unconjugated hyperbilirubinaemia
65
Hepatocellular jaundice - dysfunction of hepatic cells - bilirubin is …
Mixed - both conjugated and unconjugated
66
Post-hepatic jaundice refers to obstruction of biliary drainage - so the result is ..
Conjugated hyperbilirubinaemia
67
Differential diagnosis of abnormal LFTS (hepatitic)
Alcoholic fatty liver disease Non alcoholic fatty liver disease Viral hepatitis Paracetamol overdose
68
Differential diagnosis of abnormal LFTS (cholestatic)
``` Gallstones Drugs Primary sclerosing cholangitis Primary biliary cirrhosis Cancer ```
69
What is primary biliary cirrhosis (cholangitis)?
A chronic disease of the small intrahepatic bile ducts that is characterised by progressive bile duct damage (and eventual loss) occurring in the context of chronic portal tract inflammation. Fibrosis develops as a consequence of the original insult and the secondary effects of toxic bile acids retained in the liver, resulting ultimately in cirrhosis. The almost universal presence of autoantibodies in PBC patients (classically anti-mitochondrial antibodies) has led to the widely held view that the disease has an autoimmune component to its aetiology.
70
Key diagnostic factors in primary biliary cirrhosis (cholangitis) - age and sex
Typically female sex, age 45-60years
71
Which condition is largely associated with IBD? | - Primary sclerosing cholangitis? Or Primary biliary cirrhosis?
Primary sclerosing cholangitis - usually have a history of IBD, male sex more common, age in 40s/50s
72
Primary biliary cholangitis vs primary sclerosing cholangitis - key diagnostic factors
Primary biliary cholangitis predominantly affects middle-aged women and is not associated with IBD, whereas primary sclerosing cholangitis typically in men and with people with a history of IBD
73
Will people with primary biliary cholangitis have a normal cholangiogram?
Usually it is normal but hard to distinguish from intrahepatic PSC
74
What autoantibody is present in 95% of those with primary biliary cholangitis?
Antimitochondrial autoantibody is present in 95% of cases
75
The classic histopathological finding of … is presence of periductal concentric “onion skin” fibrosis
Primary sclerosing cholangitis
76
Someone that is thin, but not cachectic is less likely to have what?
Crohn’s with ileitis and malabsorption
77
Neutrophil count of 0.1 is suggestive of …
Agranulocytosis- can be due to side effects of immunosuppressive drugs or anti cancer therapy
78
‘Onion skin’ fibrosis =
Cirrhosis due to PSC
79
Tender brushes on skin - usually shins indicates …
Erythema nodosum
80
‘Skip lesions’ on colonoscopy and transmural inflammation with granulomas =
Crohn’s disease
81
Positive antimitochondrial antibody =
Primary biliary cirrhosis
82
‘Beads on a string’ appearance on ERCP =
Primary sclerosing cholangitis
83
Abdominal distension in acute colitis - important to do an abdominal X-ray to look for what?
Toxic mega colon - dilated transverse colon - it is life-threatening
84
Ursodeoxycholic acid is used to help … drainage in patients with PSC and PBS
Bile drainage