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Clinical Practice Guideline, May 2004
 10-30% of upper gastrointestinal
haemorrhage
 is a major cause of death in patients with
cirrhosis.
 The aetiology of cirrhosis in Malaysia is
mainly due to hepatitis B or alcohol
 In alcoholic liver disease, continued
abstinence from alcohol may result in a
decreasing in size or even disappearance of
varices.
• Severe consequence of portal hypertension secondary
to cirrhosis
• Core symptoms co-exist with other emotional,
behavioral & learning disorders
Definition
Co-
morbidities
• varies from 24-81% in oesophageal varices in patients
with cirrhosis
• 60% of decompensated cirrhosis and 30% of
compensated cirrhosis patients
Prevalence
Classification
Japanese US VATrial Paquet
Absent Absent Absent Absent
Grade 1: small, straight varices not
disappearing with insufflation
Small < 5 mm I
Grade 2: medium varices occupying
less than one third of the lumen
Medium 5-9 mm II
Grade 3: large varices occupying
more than one third of the lumen
Large >9 mm III
Giant IV
Increase
resistance to
portal flow
Increase portal
pressure
Varices
Variceal
growth
Decrease
arteriolar
resistance
Increase portal
blood inflow
Cirrhosis
 Severity of the liver dysfunction
 Size of the varices (large greater than
small)
 Presence of endoscopic red wale signs.
 Hepatic venous pressure gradient (HVPG)
- ---- variceal bleeding will not occur if the
HVPG is below 12mmHg.
Management
Active
bleeding
episode
Prevention
of
rebleeding
Prophylactic
measure to
prevent the first
haemorrhage
 Non-selective ß-adrenergic antagonists such as
propranolol and nadolol.
- Propranolol 20mg bd titrated to achieve a 25%
decrement in resting pulse rate or a pulse rate
of 55-60 bpm)
 Screening endoscopy 1-2 yearly from the onset
of diagnosis of liver cirrhosis
 General Management:
IV access and fluid resuscitation
Prepare for blood transfusion if haemodynamic
unstable
Correction of coagulopathy and thrombocytopenia
Intubation if severe uncontrollable bleeding,
encephalopathic, inability to maintain O2 saturation
adequately and to prevent aspiration
Specific therapy:
 Pharmacological therapy with vasoactive drugs to arrest
the bleeding (vasopressin/it's analogue, somatostatin/it's
analogue)
a) IV Terlipressin 2 mg stat bolus and 1 mg QID for 2-5
days or;
b) IV Somatostatin 250 mcg bolus followed with 250
mcq/h infusion for 2-5 days or;
c) IV bolus Octreotide 50 mcg stat followed with IV
infusion 50 mcg/h for 2-5 days
Generic
name
Time to
maximum
effect
Duration of
action
Half -life
Somatostatin
Terlipressin 6 hour
Octretide
Terlipressin was not inferior to octreotide in its
effi cacy for controlling variceal bleed.
 Endoscopic Sclerotherapy or Endoscopic
banding or Adrenaline injection
 If bleeding uncontrolled a Minnesota tube or
Sangstaken-Blakemore tube is used.
a) Non-selective ß-adrenergic antagonists such as
propranolol and nadolol
b) Endoscopic sclerotherapy every 10-14 days until
the varices are obliterated (5-6 sessions)or
endoscopic variceal banding
c) Combination of pharmacological and endoscopic
management may be considered
d) Transjugular Intrahepatic Portosystemic Shunts
(TIPSS)
e) Surgical therapy (selective shunts or
devascularisation procedures)
 Antibiotic prophylaxis in patients with cirrhosis
 Antibiotic treatment should be continued for 7
days
 Norfloxacin 400mg bd
 OR Ciprofloxacin 500mg bd or IV 200mg bd
 OR Third generation cephalosporins (e.g.
Ceftriaxone 1g daily)
 Terlipressin vs. Octreotide in Bleeding EsophagealVarices as an AdjuvantTherapy With Endoscopic Band
Ligation:A Randomized Double-Blind Placebo-ControlledTrial

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Management of acute variceal bleeding

  • 2.  10-30% of upper gastrointestinal haemorrhage  is a major cause of death in patients with cirrhosis.  The aetiology of cirrhosis in Malaysia is mainly due to hepatitis B or alcohol  In alcoholic liver disease, continued abstinence from alcohol may result in a decreasing in size or even disappearance of varices.
  • 3. • Severe consequence of portal hypertension secondary to cirrhosis • Core symptoms co-exist with other emotional, behavioral & learning disorders Definition Co- morbidities • varies from 24-81% in oesophageal varices in patients with cirrhosis • 60% of decompensated cirrhosis and 30% of compensated cirrhosis patients Prevalence Classification
  • 4. Japanese US VATrial Paquet Absent Absent Absent Absent Grade 1: small, straight varices not disappearing with insufflation Small < 5 mm I Grade 2: medium varices occupying less than one third of the lumen Medium 5-9 mm II Grade 3: large varices occupying more than one third of the lumen Large >9 mm III Giant IV
  • 5. Increase resistance to portal flow Increase portal pressure Varices Variceal growth Decrease arteriolar resistance Increase portal blood inflow Cirrhosis
  • 6.  Severity of the liver dysfunction  Size of the varices (large greater than small)  Presence of endoscopic red wale signs.  Hepatic venous pressure gradient (HVPG) - ---- variceal bleeding will not occur if the HVPG is below 12mmHg.
  • 8.  Non-selective ß-adrenergic antagonists such as propranolol and nadolol. - Propranolol 20mg bd titrated to achieve a 25% decrement in resting pulse rate or a pulse rate of 55-60 bpm)  Screening endoscopy 1-2 yearly from the onset of diagnosis of liver cirrhosis
  • 9.
  • 10.  General Management: IV access and fluid resuscitation Prepare for blood transfusion if haemodynamic unstable Correction of coagulopathy and thrombocytopenia Intubation if severe uncontrollable bleeding, encephalopathic, inability to maintain O2 saturation adequately and to prevent aspiration
  • 11. Specific therapy:  Pharmacological therapy with vasoactive drugs to arrest the bleeding (vasopressin/it's analogue, somatostatin/it's analogue) a) IV Terlipressin 2 mg stat bolus and 1 mg QID for 2-5 days or; b) IV Somatostatin 250 mcg bolus followed with 250 mcq/h infusion for 2-5 days or; c) IV bolus Octreotide 50 mcg stat followed with IV infusion 50 mcg/h for 2-5 days
  • 12. Generic name Time to maximum effect Duration of action Half -life Somatostatin Terlipressin 6 hour Octretide Terlipressin was not inferior to octreotide in its effi cacy for controlling variceal bleed.
  • 13.  Endoscopic Sclerotherapy or Endoscopic banding or Adrenaline injection  If bleeding uncontrolled a Minnesota tube or Sangstaken-Blakemore tube is used.
  • 14. a) Non-selective ß-adrenergic antagonists such as propranolol and nadolol b) Endoscopic sclerotherapy every 10-14 days until the varices are obliterated (5-6 sessions)or endoscopic variceal banding c) Combination of pharmacological and endoscopic management may be considered d) Transjugular Intrahepatic Portosystemic Shunts (TIPSS) e) Surgical therapy (selective shunts or devascularisation procedures)
  • 15.  Antibiotic prophylaxis in patients with cirrhosis  Antibiotic treatment should be continued for 7 days  Norfloxacin 400mg bd  OR Ciprofloxacin 500mg bd or IV 200mg bd  OR Third generation cephalosporins (e.g. Ceftriaxone 1g daily)
  • 16.  Terlipressin vs. Octreotide in Bleeding EsophagealVarices as an AdjuvantTherapy With Endoscopic Band Ligation:A Randomized Double-Blind Placebo-ControlledTrial

Editor's Notes

  1. Decompensated liver cirrhosisCompensated liver cirrhosis
  2. Add in prepare for blood transfusion if haemodynamic unstable.
  3. Why antibiotic prophylaxis?