Gastroenterology Flashcards

1
Q

Antibiotics used for prophylaxis in variceal UGIB

A

Broad spectrum, to cover SBP, ofer quinolones in people with cirrhosis

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2
Q

Management of variceal upper GI bleed

A

1) A-E and escalation status!
A, B
C: Examination, IV access X 2, bloods (G&S, coag, VBG, FBC, U&E, LFT)
Fluids / blood transfusion if needed

patient needs to be stable before endoscopy

2) Review medications
Stop NSAIDs, anticoagulant, antiplatelets, antihypertensives, clopidogrel, reverse if can

3) Correct coagulopathy - ?FFP, vit K, platelets

4) Antibiotics - prophylaxis in cirrhosis against SBP (b4 endoscopy)

5) Terlipressin - splanchnic vasoconstriction, reduce portal pressures, reduce bleeding (b4 endoscopy)

6) Endoscopy - are they fit? can they lie for 15 mins? Glasgow blatchford score.
- Band, glue

7) NBM, fluid balance, stool chart

not work
Sengstaken blakemore tube
Interventional radiology - CT + embolisation
Surgery
TIPS (transjugular intrahepatic porto-systemic shunt) connects hepatic vein to portal vein

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3
Q

Prophylaxis of UGIB in varices

A

1) Propranolol
2) Endoscopic variceal ligation
For medium- large varices,
every 2 weeks until eradicated, give prophylactic PPI as well to endoscopic variceal ligation induced ulcers
3) Tranjugular intrahepatic portosystemic shunt (TIPS)

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4
Q

Assessment of severity of UGIB

A

1) Pre-endoscopy = Glasgow blatchford = need for endoscopy
2) Post-endoscopy = rockall = mortality post endoscopy

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5
Q

Antibiotic prophylaxis in variceal upper GI bleeds

A

broad spectrum antibiotics, often quinolone

give for 5-7 days

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5
Q

Terlipressin in variceal upper GI bleeds

A

1) Give 2mg QDS for 3-5 days or until definitive endoscopic haemostasis achieved

reduces portal pressure and helps control haemorrhage

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6
Q

75mg aspirin in UGIB - what to do

A

can continue!

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7
Q

Heparin reversal in UGIB
dose timing

A

Give protamine
8 hrs before = half the dose

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8
Q

Warfarin reversal in UGIB

A

Give PCC and IV vitamin K if actively bleeding

If stable, give vitamin K IV

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9
Q

endoscopy - what’s done in variceal management

A
  • band ligation
  • gastric = intravariceal injection of N-butyl-2-cyanoacrylate glue.
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10
Q

non variceal endoscopy management

A
  • Clips + adrenaline
  • Thermal coagulation + adrenaline
    -fibrin/ thrombin injection + adrenaline
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11
Q

Alternative to UGIB if endoscopy doesn’t work

A

1) Sengstaken blakemore tube
2) Interventional radiology - CT + embolisation
3) Surgery - tie off artery

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12
Q

Who needs re-scoping after UGIB?

A

Bleeding due to
1) Varices
2) PUD - in 6-8 weeks, to ensure resolution and no underlying carcinoma

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13
Q

How long NBM for post endoscopy?

A

over night - may need further endoscopy, especially if concern about haemostasis

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14
Q

When to offer platelet transfusion in upper GI bleed patients?

A

Actively bleeding AND platelets < 50 x 10^9

if not actively bleeding AND stable - don’t offer

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15
Q

Who give fresh frozen plasma to?

A

Actively bleeding and INR / activated partial thromboplastin > 1.5 times normal

If fibrinogen level remains less than 1.5 g/litre despite fresh frozen plasma use, offer cryoprecipitate as well

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16
Q

Coagulopathy correction in UGIB

A

1) Platelets if platelet < 50 AND actively bleeding

2) INR > 1.5 or activated partial thrombplastin time ratio > 1.5 = give fresh frozen plasma
If INR > 1.5 and on warfarin, give PCC and vit K!

3) Fibrinogen < 1.5 = fresh frozen plasma -> if still low despite FFP, give cryoprecipitate

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17
Q

Refeeding syndrome - electrolyte disturbances

A

phosphate
potassium
magnesium
thiamine
calcium
sodium

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18
Q

Symptoms of re-feeding syndrome

A

1) No ATP = muscle cannot contract = myocardium cannot (heart failure) diaphragm cannot (respiratory failure)
2) Low calcium and K+: Cardiac: Arrhythmia
3) Neurological: Weakness, paresthesia, tetany, seizure
4) low thiamine: Wernicke encephalopathy
5) Peripheral oedema
5) Low phosphate - low ATP in muscles = can cause rhabdomyolysis

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19
Q

High risk patient for re-feeding, going to re-feed, what want to do?

A

1) Check baseline electrolytes (phosphate, K+, Mg2+, calcium, sodium, thiamine)
2) Give thiamine first 200mg
3) feed < 50% normal intake 10kcal/kg/day, slowly increase
4) monitor bloods & electrolytes, replace as appropriate, balance fluids

20
Q

Ascitic fluid - what is sent off in an ascitic TAP?

A

1) Cytology
2) MC&S
3) Gram stain
4) Protein, albumin, glucose, LDH, amylase, WCC

21
Q

Management of ascites

A

1) Low sodium diet
2) Aldosterone antagonist (increase sodium excretion) +/- loop diuretics
3) Review meds - stop NSAIDs, ACEI, not give aminoglycosides, alpha blockers
4) Can fluid restrict
aim to reduce sodium and water if sodium < 125

exudate: underlying cause manage if possible

tense ascites: therapeutic paracentesis
TIPS - refractory ascites in cirrhosis

ascites + cirrhosis + ascitic protein < 15 g/L give prophylactic abx, ciprofloxacin, until resolution of ascites, reduce risk of SBP

  • ascites + cirrhosis -> consider transplant
22
Q

What is ascites?

A

Excess ascitic fluid in the peritoneal cavity

23
Q

Causes of ascites

A

Transudate, SAAG > 11g/L
Liver: Cirrhosis (portal hypertension), liver failure (low albumin), mets
Heart: Right sided heart failure, constrictive pericarditis
Other: Budd chiari syndrome (hepatic vein thrombus), portal vein thrombus, veno-occlusive disease

SAAG < 11g/L
Transudate: Low albumin
Exudate
Infection - TB, SBP
Inflammation - serositis in connective tissue disorders, pancreatitis
Cancer - peritoneal mets - GI, ovarian

24
Q

Presentation of ascites

A

Need 500ml of fluid for symptoms

  • Abdominal distension, discomfort
  • Loss of appetite, nausea, vomiting
  • Weight gain (gain fluid)
  • ## SOB (diaphragmatic splinting)
25
Q

Ascitic fluid analysis

A

MC&S, cytology, gram stain,
albumin, protein, glucose, amylase, LDH, WCC

26
Q

Ascitic fluid analysis - protein

A

0.3-4g d/L is normal
> 4 = SBP

27
Q

Ascitic fluid analysis - WCC

A

WCC > 250u/L = abnormal
Mostly neuts - SBP
Mostly lymphocytes = TB

28
Q

Ascitic fluid - glucose

A

Similar to serum = normal
Less = infection, ca (used up!)

29
Q

Ascitic fluid - amylase

A

Same as serum = normal
More = pancreatitis

30
Q

Red cell count in ascitic fluid

A

0 = normal
> 100 = cancer, TB
> 1000 haemorrhage, haemorrhagic pancreatitis, trauma

31
Q

SAAG

A

More albumin in serum than in ascitic fluid!

Serum albumin - ascitic fluid albumin

> 11g/L = cirrhosis/ liver failure, heart, thrombus (BCS, portal vein)

< 11g/L = cancer, infection (SBP, TB), inflammation (pancreatitis, serositis), low albumin

32
Q

Cirrhosis -how cause ascites

A

1) portal hypertension
Increase capillary hydrostatic pressure
NO released, splanchni vasodilation, reduce renal perfusion, RASS activated, retain more sodium and water - worsen ascites
2) Failure of hepatic function
Low albumin = reduce oncotic pressure

Transudate, but SAAG can be < 11g/L or > 11g/L

33
Q

Medications to avoid in ascites secondary to cirrhosis

A

NSAIDs
ACEI - renal hypoperfusion, activate RAAS more, more sodium and water retention
Alpha blockers - as above
Nephrotoxic medications - aminoglycosides!

34
Q

When give prophylaxis in ascites patients? what give?

A

1) Had 1 episode SBP
2) Ascites + cirrhosis + protein < 15 -> give until ascites resolved

ciprofloxacin

35
Q

What is SBP?

Why happens?

A

Infection of ascitic fluid, no other source identified that cannot be treated surgically

Overgrowth bacteria in gut -> enter portal vein -> portal hypertension force out into ascitic fluid
Patient likely compromised immune system (liver is toast and cannot make normal immune system proteins)

Normally 50% due to E.Coli

36
Q

Presentation of SBP

A

1) Diffuse abdominal pain
2) Fever - normally due to a dampened immune system and slightly lower temperature, so take temp spike seriously!
3) Worsening ascites / symptoms of cirrhosis/ liver failure (encephalopathy, jaundice)

may have had diarrhoea before - bacterial overgrowth sign!

37
Q

Why give pabrinex IV not oral?

A

Alcohol inhibits absorption of vitamin B1 up to 50%

38
Q

What is wernicke’s encephalopathy?

A

Acute reversible encephalopathy secondary to low thiamine (B1)

39
Q

Causes of wernicke’s encephlopathy?

A

Reduced intake, reduced absorption, increased losses
- Eating disorders
- Chronic alcoholics
- Hyperemesis of pregnancy
- IBD/ bariatric/ upper GI surgery

40
Q

Symptoms of wernicke’s encephlopathy

A

Triad, don’t often have all 3
- Ataxia: Broad-based gate
- Altered mental status: confusion, disorientation, inattention
- Ophthalmoplegia: VI palsy, conjugate gaze palsy III/IV/VI, sluggish pupils, anisocoria (unequal pupil sizes)

41
Q

Management of ? wernickes

A

Give pabrinex IV thiamine 500mg TDS for 3-5 days
If improve = wernickes -= give 250mg OD for another 3-5 days or until improved fully

No improve after 500mg IV TDS - then high dose oral thiamine 100mg

Can give IM, but need good muscle mass to absorb, alcoholics less likely to have this!

42
Q

What can wernicke’s cause?

A

Korsakoffs

43
Q

Korsakoffs – what is it?

A

Irreversible encephalopathy secondary to prolonged thiamine deficiency

44
Q

Korsakoff’s symptoms

A
  • retrograde and antegrade amnesia
  • confabulation
  • apathy
  • no insight
45
Q

Medication review in ascites

A

ACEI, ARB, NSAIDs, alpha blockers, nephrotoxic drugs

46
Q

Ascites in cirrhosis refractory to management options

A

TIPS!

47
Q

FFP VS PCC

A