Common GI Tract disorders Flashcards

1
Q

What is Diarrhoea?

A
  • Defined as passage of >200g faeces per day
  • Increases in faecal mass of 500 – 1000g /day require attention
  • Needs to be more severe to result in dehydration
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2
Q

What are the results of Diarrhoea physiologically?

A
  • Lower GI losses results in loss of bicarbonate - metabolic acidosis
  • Dehydration - increased Urea
  • Electrolyte disturbances – especially decreased K+ and Mg2+, decreased HCO3
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3
Q

What are the different types of Diarrhoea?

A
  • Osmotic: Due to solution of high osmotic potential, generally salt or sugar. Water is drawn from the body to equilibrate the chyme. Can also be due to malabsorption
  • Secretory: Increased secretion or reduced absorption of water and ions e.g. enterotoxins (such as cholera) open membrane channels leading to export of water, Na, K and HCO3 into the intestine
  • Inflammatory: Damage to intestinal mucosa e.g Ulcerative Colitis/Crohn’s disease or infective e.g Shigella (Dysentary)
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4
Q

What results from Vomiting physiologically?

A

One of the most common causes is gastroenteritis leading to upper GI losses

  • Loss of acid – increased bicarbonate
  • Decreased chloride - metabolic alkalosis
  • Dehydration can result in low K (2°Hyperaldosteronism)
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5
Q

What can causes Upper GI bleeds?

A
  • Peptic ulcer
  • Oesophageal varices
  • Gastric erosions
  • Gastric cancer (rarely )
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6
Q

What is the results of Upper GI bleeds physiologically?

A
  • Red blood cells released and reabsorbed
  • Increased potassium (from intracellular release)
  • Increased urea from protein metabolism
  • Raised urea:creatinine ratio
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7
Q

What is Irritable Bowel Syndrome?

A
  • Bowel disorder with no detectable organic cause
  • Signs and symptoms include cramping, abdominal pain, bloating, gas and diarrhoea or constipation
  • Does not cause changes to the bowel tissue, does not increase risk of colorectal cancer
  • Diagnosis of exclusion
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8
Q

What is Inflammatory Bowel Disease?

A
  • Similar symptoms to IBS
  • Caused by chronic inflammation of the digestive tract
  • Crohn’s Disease and Ulcerative colitis
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9
Q

What are features of Crohns Disease?

A
  • Age of onset between 15-35 years of age
  • Symptoms: Abdominal pain, Diarrhoea, Weight Loss and Fatigue, Bloody stool, malnutrition
  • Can affect any part of GI tract from mouth to anus
  • Most commonly starts in terminal ileum
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10
Q

What are features of Ulcerative Colitis?

A
  • Age of onset between 15-35 years of age
  • Symptoms: Stool Urgency, Fatigue, Increased Bowel Movements, Mucous In Stools, Nocturnal Bowel Movements, Abdominal pain
  • Restricted to colon and rectum
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11
Q

What are some biochemical tests for Inflammatory Bowel Disease?

A
  • Faecal calprotectin identifies patients who require colonoscopy
  • CRP/ESR can give an indication of the level of inflammation
  • Nutritional assessment
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12
Q

What is Coeliac Disease?

A

Gluten sensitive enteropathy

  • Wheat protein contains gliadin. Gliadin metabolised by tissue transglutaminase
  • In Coeliac disease, an autoimmune reaction happens. Upon exposure to Gliadin, there is an immunological response to Tissue transglutaminase.
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13
Q

How is Coeliac Disease screened?

A
  • Screened by ELISA (TTG)
  • Histology to confirm
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14
Q

How is Bowel Cancer screened biochemically?

A
  • National screening programme for men and women aged 60 to 74
  • Offered test ever 2 years
  • Uses Faecal Immunochemical Test (FIT)
  • Detects small amounts of faecal occult blood
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15
Q

What is intestinal failure?

A
  • Defined as intestinal failure when the ability of intestine to absorb fluids and nutrients threaten’s the health of patient
  • Intestines have considerable reserve capacity
  • Maybe short term while awaiting surgery on the small intestine
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16
Q

What are the types of Pancreatitis?

A

Acute

  • Abdo pain, nausea & vomiting
  • At worst can lead to multi-organ failure!
  • Amylase, Lipase & CRP
  • U&E, LFT, Calcium, Blood gases

Chronic

  • Follows acute
  • Most commonly due to alcohol (in UK)
  • Faecal elastase

Hereditary

17
Q

What is Pancreatic Insufficiency, lab tests and the treatment?

A
  • Usually due to long term damage to organ
  • Lab Tests
    • Faecal enzymes (e.g elastase)
  • Treatment
    • Supplementation (Creon- protease, amylase, lipase)
    • Insulin (for DM)
18
Q

What are complications of Pancreatic Insufficiency?

A
  • Malabsorption
  • Malnutrition
  • Vitamin deficiencies
  • Weight loss
  • Fatty stools (steatorrhoea)
  • Diabetes
19
Q

What are the types of patterns demostrated in Liver Function Tests?

A

Hepatocellular pattern:

  • Disproportionate elevation in the serum aminotransferases compared with the alkaline phosphatase
  • Serum bilirubin may be elevated
  • Tests of synthetic function may be abnormal

Cholestatic pattern:

  • Disproportionate elevation in the alkaline phosphatase compared with the serum aminotransferases
  • Serum bilirubin may be elevated
  • Tests of synthetic function may be abnormal

Isolated hyperbilirubinemia

  • Elevated bilirubin level with normal serum aminotransferases and alkaline phosphatase
20
Q

What are causes of Cholestasis?

A

Obstruction of bile flow

  • Pregnancy
  • Gallstones
  • Pancreatic carcinoma

Non-obstructive causes

  • Drug induced- e.g ampicillin/erythromycin
  • Inherited
  • Primary Biliary Cirrhosis, Primary SclerosingCholangitis – inflammatory conditions
  • Total Parenteral Nutrition
21
Q

What is Acute Hepatitis?

A
  • Damage to hepatocyte characterised biochemically by short term increased in transaminases and then rising bilirubin as excretory capacity if reached
  • Usually caused by viral infection (Hep A, B, C, D and E, EBV, CMV) or toxins (e.g. alcohol, drugs)
  • Great variation in severity and time course
22
Q

What is Chronic Hepatitis?

A
  • >6 months of Hepatitis
  • Autoimmune, Hep B and C and alcohol very commonx
23
Q

What are features of Autoimmune Hepatitis?

A

Autoimmune hepatitis:

  • Onset ~45yrs
  • Association with other autoimmune diseases
  • More common in women
  • Antinuclear and anti smooth muscle antibodies often very high
  • Raised IgG
24
Q

What are Gallstones formed from?

A
  • 80% Mainly comprised of cholesterol
  • 20% ‘pigment stones’ of calcium bilirubinate/polymers containing calcium & copper
25
Q

What is Cholecystitis?

A

Cholecystitis is inflammation of the gall bladder

26
Q

What is Cholagitis and how does it present?

A
  • Inflammation of common bile duct (usually infection e.g bacterial but can occur due to roundworm/fluke)
  • Typical presentation: ‘Charcot’s triad’; 1:fever/chills/rigor, 2:upper right quadrant pain & 3:jaundice’
  • Biliary obstruction which can be complete or intermittent
  • Mixed hepatocellular & cholestatic picture
27
Q

What are biochemical features Primary Sclerosing Cholangitis?

A
  • 60+% cases are pANCA Ab +ve

Strongly associated with IBD (85%UC, 15% Crohn’s)

28
Q

What is Steatosis?

A
  • In certain metabolic conditions and alcoholism, fat is laid down in the liver. This leads to an inflammatory response
  • Collagen deposition occurs and this leads to cirrhosis in 10-30% of patients within 10 years (NASH)
29
Q

What are some features of Liver and Pancreatic Cancers?

A

Symptoms: Weight loss, Painless jaundice

  • Liver (& bone) carcinoma often secondary due to metastases
  • Endocrine tumours of pancreas such as insulinoma, glucagonoma, VIPoma
  • Hepatocellular carcinoma
30
Q

What is Cirrhosis?

A
  • Late stage of scarring of liver
  • End stage liver failure