GASTRO GAP Flashcards

1
Q

INV FOR ZOLLINGER ELLISON

A

Diagnosis
fasting gastrin levels: the single best screen test
secretin stimulation test

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2
Q

Hepatic vs Cholestatic Picture

A

proportionate rise in ALT > proportionate rise in ALP = hepatitic
hePAtitic e alP kom thake

proportionate rise in ALT < proportionate rise in ALP = obstructive/cholestatic

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3
Q

GI Enzymes:
MALTASE
SUCRASE
LACTASE

A

MALTase = 2 glucose - NestoMALT - Double Glucose= Glucose + Glucose
sucRase = glucose + fRuctose
LACtase = glucose + gaLACtose

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4
Q

Alcoholic Liver Disease

A

gamma-GT is characteristically elevated
the ratio of AST:ALT is normally > 2, a ratio of > 3 is strongly suggestive of acute alcoholic hepatitis

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5
Q

Jejunal villous atrophy causes

A

Jejunal villous atrophy

Whilst coeliac disease is the classic cause of jejunal villous atrophy there are a number of other causes you need to be aware of

Causes
coeliac disease
tropical sprue
hypogammaglobulinaemia
gastrointestinal lymphoma
Whipple’s disease
cow’s milk intolerance

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6
Q

Hepa B Serology

A

‘S’ is sinister

HbsAg shows ongoing infection either Acute or chronic means sinister is there.

Anti-Hbs is anti sinister: means immunized against sinister through vaccine or developed immunity after sin.

‘C’ is caught: anti- Hbc means have caught the virus at some stage. not positive in vaccine. Igm is for 6 months then igG after 6 months implying chronic infection.

‘E’ for enfectivity. HbeAg means ongoing enfection.

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7
Q

Inv for Primary Biliary Cholangitis

A
  • anti-mitochondrial antibodies (AMA) M2 subtype are present in 98% of patients and are highly specific
  • smooth muscle antibodies in 30% of patients
  • raised serum IgM

imaging
required before diagnosis to exclude an extrahepatic biliary obstruction (typically a right upper quadrant ultrasound or magnetic resonance cholangiopancreatography (MRCP)

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8
Q

Pancreatic Cancer Presentation

A

The patient’s history (weight loss, jaundice, pruritis and steatorrhea), examination (palpable gallbladder - Courvoisier’s sign) and blood tests (obstructive jaundice) are most suggestive of pancreatic cancer. High resolution CT is the diagnostic investigation of choice.

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9
Q

Presentation of Biliary colic

A

The patient presents with colicky right upper quadrant pain after eating a fatty meal in the background of a raised body mass index. The likely diagnosis is biliary colic.

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10
Q

Inv for Gilbert

A

Investigation and management
investigation: rise in bilirubin following prolonged fasting or IV nicotinic acid
no treatment required

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11
Q

OGD finding of gastric cancer

A

Signet Ring

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12
Q

Villousb adenoma

A

Diarrhoea + hypokalaemia → villous adenoma

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13
Q

RX Ulcerative Colitis

A

Inducing remission:
1. Treating mild-to-moderate ulcerative colitis
proctitis:
- topical (rectal) aminosalicylate: rectal mesalazine
- oral aminosalicylate
- topical or oral corticosteroid

proctosigmoiditis and left-sided ulcerative colitis
- topical (rectal) aminosalicylate
- a high-dose oral aminosalicylate OR switch to a high-dose oral aminosalicylate and a topical corticosteroid
- if remission still not achieved stop topical treatments and offer an oral aminosalicylate and an oral corticosteroid
-
extensive disease
topical (rectal) aminosalicylate and a high-dose oral aminosalicylate:
if remission is not achieved within 4 weeks, stop topical treatments and offer a high-dose oral aminosalicylate and an oral corticosteroid

Severe colitis
should be treated in hospital
IV steroids are usually given first-line
IV ciclosporin may be used if steroids are contraindicated
if after 72 hours there has been no improvement, consider adding IV ciclosporin to IV corticosteroids or consider surgery

Maintaining remission

Following a mild-to-moderate ulcerative colitis flare
proctitis and proctosigmoiditis
topical (rectal) aminosalicylate alone (daily or intermittent) or
an oral aminosalicylate plus a topical (rectal) aminosalicylate (daily or intermittent) or
an oral aminosalicylate by itself: this may not be effective as the other two options
left-sided and extensive ulcerative colitis
low maintenance dose of an oral aminosalicylate

Following a severe relapse or >=2 exacerbations in the past year
oral azathioprine or oral mercaptopurine

Other points
methotrexate is not recommended for the management of UC (in contrast to Crohn’s disease)
there is some evidence that probiotics may prevent relapse in patients with mild to moderate disease

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14
Q

Maintainence of Remission of UC

A

Maintaining remission
1. Following a mild-to-moderate ulcerative colitis flare
a. proctitis and proctosigmoiditis
- topical (rectal) aminosalicylate alone (daily or intermittent) or
- an oral aminosalicylate plus a topical (rectal) aminosalicylate (daily or intermittent) or
- an oral aminosalicylate by itself: this may not be effective as the other two options

b. left-sided and extensive ulcerative colitis
low maintenance dose of an oral aminosalicylate
**
2. Following a severe relapse or >=2 exacerbations in the past year**
oral azathioprine or oral mercaptopurine

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15
Q

NICE Bariatric Referral Cut-offs

A

with risk factors (T2DM, BP etc): > 35 kg/m^2
no risk factors: > 40 kg/m^2

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16
Q

Achalasia XRay

A

oesophageal manometry
excessive LOS tone which doesn’t relax on swallowing
considered the most important diagnostic test

17
Q

Drugs causing hepatocellular disease

A

mnemonic for DRugs causing hepatocellular disease:
Peter- Paracetamol
Had- Halothane
Epilepsy- sodium valproated and phenytoin
And- amiodrone
Alcoholic- Alcohol
TB- anti-tbs
he Met- Methyldopa
dr. Mel Nora- MAOI, Nitrofurantoin
in the STATes- Statins

18
Q

The following drugs tend to cause cholestasis (+/- hepatitis)

A

combined oral contraceptive pill
antibiotics: flucloxacillin, co-amoxiclav, erythromycin*
anabolic steroids, testosterones
phenothiazines: chlorpromazine, prochlorperazine
sulphonylureas
fibrates
rare reported causes: nifedipine

MNEMONIC: PASS FOR
phenothiazines
antibiotics
anabolic steroids
sulphonylureas

FOR-
FIBRATES
OCPS
RARE- NIFEDIPINES.

19
Q

Drugs causing Liver cirrhosis

A

Methotrexate
Methyldopa
aMiodarone

20
Q

Pancreatitis causes

A

Popular mnemonic is GET SMASHED
Gallstones
Ethanol
Trauma
Steroids
Mumps (other viruses include Coxsackie B)
Autoimmune (e.g. polyarteritis nodosa), Ascaris infection
Scorpion venom
Hypertriglyceridaemia, Hyperchylomicronaemia, Hypercalcaemia, Hypothermia
ERCP
Drugs (azathioprine, mesalazine*, didanosine, bendroflumethiazide, furosemide, pentamidine, steroids, sodium valproate)

21
Q

Scorings of Liver Cirrhosis

A

Child Pugh
MELD score (Model for End-Stage Liver Disease)

22
Q

Child Pugh Score consists of

A

Bilirubin
Prothombin Time
Albumin
Encephalopathy
Ascites

23
Q

Rx of Achalasia Cardia

A
  1. pneumatic (balloon) dilation is increasingly the preferred first-line option
  2. surgical intervention with a Heller cardiomyotomy should be considered if recurrent or persistent symptoms
  3. Intra-sphincteric injection of botulinum toxin is sometimes used in patients who are a high surgical risk
  4. drug therapy (e.g. nitrates, calcium channel blockers) has a role but is limited by side-effects
24
Q

Rovsing sign
Psoas Sign

A

Rovsing’s sign (palpation in the LIF causes pain in the RIF) is now thought to be of limited value
psoas sign: pain on extending hip if retrocaecal appendix

25
Q

Some common factors indicating severe pancreatitis include:

A

However, some common factors indicating severe pancreatitis include:
age > 55 years
hypocalcaemia
hyperglycaemia
hypoxia
neutrophilia
elevated LDH and AST

26
Q

Causes of Pancreatitis

A

Gallstones
Ethanol
Trauma
Steroids
Mumps (other viruses include Coxsackie B)
Autoimmune (e.g. polyarteritis nodosa), Ascaris infection
Scorpion venom
Hypertriglyceridaemia, Hyperchylomicronaemia, Hypercalcaemia, Hypothermia
ERCP
Drugs (azathioprine, mesalazine*, didanosine, bendroflumethiazide, furosemide, pentamidine, steroids, sodium valproate)

27
Q

Alcoholic Ketoacidosis

A

It typically presents with a pattern of:
Metabolic acidosis
Elevated anion gap
Elevated serum ketone levels
Normal or low glucose concentration

28
Q

Haemochromatosis
Genetics

A

HFE gene on chromosome 6
Autsomal recessive

29
Q

Peutz-Jeghers syndrome

A
  • autosomal dominant
  • responsible gene encodes serine threonine kinase LKB1 or STK11
  • numerous hamartomatous polyps in the gastrointestinal tract
  • pigmented freckles on the lips, face, palms and soles.-
  • 50% of patients will have died from another gastrointestinal tract cancer by the age of 60 years.
30
Q

Dabigatran is reversed by

A

**Idarucizumab
**

Brand name of dabigatran is Pradaxa®, which is reversed by Praxbind (idarucizumab)

  • RivaroXaban, apiXaban, and edoXaban all ‘ban Xa’ = factor Xa inhibitors Antidote: andeXanet alpha

Da(BI)gatran (bi = 2) = factor 2a (thrombin) inhibitor
Antidote: (IDA)rucizumab = (I)nhibits (DA)bigatran*

31
Q

Angiodysplasia

A
  • IDA
  • GI Bleed (Positive FIT, but negative OGD/Colonoscopy- needs Capsule endoscopy)
  • Aortic Stenosis