gastroenterology Flashcards

1
Q

Mx of Dyspepsia

A

review meds
lifestyle
trail of PPI for 4 weeks OR test & treat approach for H.pylori

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2
Q

testing for H.pylori, what if they took PPI and came back and symptoms still not resolved?

A

carbon-13 urease breath test
there is no need to check for H.pylor eradication if symptoms have resolved

still not resolved?…..do UREA BREATH TEST

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3
Q

Ix & Mx of PUD

Ix & Mx of Celiacs

A

PUD
Ix–> upper OGD + boipsy, CLO if hpylori
Mx–> lifestyle, trial PPI for 4 weeks

celiacs
put them on a gluten diet for 6 weeks first…..
Ix–> IgA (serum and total count) , Anti TTG, Anti EDM, endoscopic intestinal biopsy
Mx–> gluten free diet, pneumococcal vaccine

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4
Q

Chrons Mx
UC Mx
IBS Mx

A

IBS
LOW FODMAP, limit high fibre, limit fresh fruit to 3x a day
bloating–> oats and linseeds 1 TBS a day
constipation–> isaphagula husk
pain–> mebeverine, buscupan
Diahrrea–> loperamide

Chrons
right sided–> bumetinide
azathioprine or mercaptopurine
if CI–> methotrexate

UC
mesalezine
severe–> IV hydrocortisone

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5
Q

Ix & Mx GORD (when would u do upper OGD)
Ix & Mx Achalasia
Ix & Mx barrets oesophagus

A

GORD
Ix–> upper OGD if (over 55, cancer symp, relapsing), if - then consider 24 hr esops. PH monitoring
Mx–> PPI for 4-8 weeks, offer H2 antagonist of not work, fundoplication

Achalasia
Ix–> oesophageal MANOMETRY, barium swallow (birds beak) CXR
Mx–> nifedipine while waiting Sx, Pneumatic balloon dilation, hellers cardiomyotomy, in can’t Sx–> botulinum toxin

barret’s oesophagus
Ix–> upper OGD (salmon pink)
Mx–>HIGH DOSE PPI

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6
Q
Ix & Mx Cirrhosis
scoring?
How to check for liver fibrosis?
Ix & Mx Alcoholic liver disease
Ix & Mx & complix PBC
Ix & Mx & complix PSC
A

Ix

bedside: BM, urine dip
bloods: basic, bilirubin, clotting, lipid profile, PT high, albumin low, plate low

Autoimmune: ANA, AMA, SMA
AFP: HCC
Alpha 1 antitrypsin 
Ceaeruplasmin--> LOW in wilson
Ferritin, TIBG, total iron--> haemachromoatosis

Imaging:
USS–> increased echogenecity
FIBROSCAN ( transient elastography) measure stiffness of liver

ENHANCED LIVER FIBROSIS TEST
check 3 molecules involved in liver metabolism ( TIMP, PIIMP etc)

SCORING–> child Pugh and MELD (guide referral for l. transplant)

Mx
if Ascites–> ascitic tap, fluid restrict, spironolactone, prophylactic oral ciprofloxacin if protein is 15 g/L or less
if have SBP give–> intravenous cefotaxime
if encephalopathy–> give laxatives, antibiotics rifaximin

Alcoholic liver disease
Ix–> GgT highhh, AST:ALT ^^2
Mx–> prednisone–> acute episodes of alcoholic hepatitis

PBC
Ix–> IgM, Antimitchondreal antibodies,
Mx–> urseodeoxyxholic acid , for itching, cholestramine
complx: heptocellular carcinoma

PSC (UC)
Ix–> ERCP/ MRCP
Mx–> itching: cholestramine, liver transplant is curative
complix: cholangiocarcinoma

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7
Q

Ix & Mx Wilsons 1st line and GOLD
Ix & Mx Haemochromatosis
Ix & Mx Alpha 1 Antitrypsin Deficiency

A

WILSONS
Ix–> low serum caeruloplasmin, reduced total serum copper (bc its deposited in the tissue), Liver biopsy is GOLD standard
Mx–> Penicillamine

Haemochromatosis
Ix–> transferrin high, high ferritin , low TIBC, Liver biopsy w/ Perl’s stain can be used to establish the iron concentration in the parenchymal cells used to be the gold standard
Mx–> Venesection is the first-line treatment,
desferrioxamine may be used second-line

Alpha 1 Antitrypsin Deficiency
Ix–> A1AT concentrations
spirometry: obstructive picture
Mx–> no smoking
supportive: bronchodilators, physiotherapy
intravenous alpha1-antitrypsin protein concentrates
surgery: lung volume reduction surgery, lung transplantation

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8
Q

black liver vibes?
stressed teenager w/ jaundice?
does not survive through adulthood due to absolute deficiency?

A

dubin johnson
gillbert
Criggler najjaar

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9
Q

triad of sudden onset abdominal pain, ascites, and tender hepatomegaly?
triad of sudden onset of severe chest pain, vomiting, Subcuta emphysema
triad high serum ketone levels , low G
dysphagia, regurg, halitosis
dysphagia (2ndry to oesophageal webs), glossitis, iron-deficiency anaemia

A
Budd-Chiari syndrome
mackler's triad--> Boerhaave's syndrome
Alcoholic ketoacidosis
Pharangeal pouch
Plummer-Vinson syndrome
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10
Q

PPI
4 SE
interactions

A

hyponatraemia, hypomagnasaemia
Osteoporosis → increased risk of fractures
microscopic colitis
increased risk of C. difficile infections
Diharrea

Interaction
Clopidogrel–>. reduces it

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11
Q

Mx of Variceal haemorrhage

Prophylaxis of variceal haemorrhage

A
ABC
correct clotting: FFP, vitamin K
vasoactive agents: terlipressin 
prophylactic IV antibiotics  Quinolones 
both terlipressin and antibiotics should be given before endoscopy in patients with suspected variceal haemorrhage

endoscopy: endoscopic variceal band ligation
Sengstaken-Blakemore tube if uncontrolled haemorrhage
TIPSS if above measures fail

Prophylaxis:
Propranolol: reduced rebleeding and mortality
endoscopic variceal band ligation (EVL)

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12
Q

Pernicious anaemia Mx

A

3 IM per week for 2 weeks –> followed by—> by 3 monthly treatment of vitamin B12 injections

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