Portal Hypertension
Dr Harsh J Shah
MS, FMAS, DNB, MCh (GI)
GI & HPB Surgeon
Kaizen Hospital, Ahmedabad
Portal Hypertension
• Anatomy & Physiology
• Diagnosis
• Etiology
• Management of Bleed
Hepatic
vein
Sinusoids
Portal
vein
Liver
Splenic
vein
Coronary
vein
SMV IMV
Characteristics
• Starts & ends in capillaries
• Major source of blood supply to liver
• No Valves in portal circulation
– Blood can flow in either directions
• Portosystemic collaterals
Portal Hypertension
• Normal Portal venous pressure – 5-8 mm Hg
• Portal Hypertension >10mmHg
• Variceal bleeding > 12mm Hg
• HVPG (Hepatic venous portal gradient)
Physics
Ohm’s law
P (Pressure) = R (Resistance) x Q ( Flow)
• Resistance
– Cirrhosis
– NCPF
– EHPVO
• Flow
– Cirrhosis
– AV fistula
Porto-systemic collaterals
Sites of portal hypertension
Extrahepatic Presinusoidal Sinusoidal Postsinusoidal
EHPVO NCPF Cirrhosis Budd-chiari
syndrome
Manifestations of Portal HT
• Asymptomatic – Detected
Incidentally
• Ascites
• Splenomegaly
• Hypersplenism
• Jaundice
• Encephalopathy
Investigations
Haematology
• CBC, Platelets count
Chemistry
• Liver Functions
• Synthetic function – Protein, Albumin
• Renal functions- Urea, Creatinine
• Coagulation profile – PT, APTT
USG Abdomen in PHT
• Liver architecture & Size
• Portal vein, Splenic vein diameter
• Spleen enlargement
• Ascites
• PV thrombosis & cavernoma
• Hepatic veins & IVC
 Doppler for blood flow direction
Flexible UGI Endoscopy
• Oesophageal Varices
• Gastric varices
• Grade of Varices ( I-IV)
• Gastropathy
• Risk factor bleed - Red spots
Endoscopic view of Esophageal
Varices
Normal Low Grade High Grade
Colonoscopy
Rectal varices
Liver Biopsy in PHT
- For Diagnosis of Cirrhosis if unclear on clinical grounds
- For prognosis
- As a guide to antiviral treatment
- Contra-indication – Massive Ascites, prolonged PT
Causes of portal hypertension
• Cirrhosis of liver
• Extrahepatic portal venous obstruction
• Non-cirrhotic portal fibrosis
Cirrhosis of liver
• End stage liver disease
Causes of liver cirrhosis
• Alcohol
• Viral hepatitis (Hep B & C)
• Biliary obstruction
• Hemochromatosis
• Wilson’s disease
• Autoimmune
• Drugs and toxins
• Metabolic diseases
• Idiopathic
Clinical Stages
1. No varices
2. Varices but no bleeding
3. Ascites
4. Variceal bleed
5. Renal failure, infected ascites or encephalopathy
Child Pugh Scoring
1 2 3
Ascites None Mild Severe
Encephalopathy None Low grade High grade
S. Bilirubin < 1 mg % 1-2 mg % >2mg%
S. Albumin >3.5 gm% 2.8 –3.5 <2.8
Pro. Time <3 Sec 4-6 Sec >6 sec
Childs A -5,6, B - 7-9, C>9 Score
EHPVO & NCPF
Portal Cavernoma
Portal Hypertension
Cirrhotic
• Coagulopathy
• Altered LFT, Albumin
• Ascites
• Bleed
• Encephalopathy
• Renal failure
• Liver tumour(HCC)
• Limited survival without
Transplant
Non cirrhotic (EHPVO,
NCPF)
• Normal coagulation
• Normal LFT, Albumin
• Bleed
• Shunt surgery
Management of Variceal Bleed
Endoscopic
(Sclerotherapy, Band, Glue)
+
Medical
(Somatostatin, Octreotide, Terlipressin)
Endoscopic Banding
Endoscopic Sclerotherapy (EST)
• Agents – Polidocanol,
Absolute Alcohol
• Methods – Intra /
Paravariceal
• Mechanism – fibrosis of
connective tissue
Endoscopic Glue Injection
• Cyanoacrylate glue (Histoacryl)
• Mainly used for gastric variceal bleed
• Mech. of action – obliteration of varix
• Hazardous to eyes & endoscopes
Surgical shunts in cirrhosis results in
high morbidity..
Esophageal & Gastric Devascularization
Transjuglar intrahepatic
Portosystemic stent shunt (TIPSS)
• Percutaneous transjugular technique
• Tract between hepatic vein & Portal vein created &
expandable stent - 8 Fr placed.
• Indication-Temporary control of bleed in poor risk
cirrhotic patient waiting for liver transplant
• Problems –Expertise, cost, complications, thrombosis
TIPSS (Transjugular Intrahepatic
Portosystemic stent shunt)
MELD (Model for End stage liver disease)
(9.57 x loge creatinine mg/dl + 3.78 x loge bilirubin mg/dl +
11.20 x loge INR + 6.43)
• Range : 6-40
• Candidate for liver transplant: >14
Liver transplant
• Definitive treatment for end stage liver disease
• MELD score >14
• Two types of donors
– Diseased donors (Brain dead)
– Living related donors
• Blood group matching is required
• 5 year survival – 75-80 %
Splenectomy & Spleno-Renal Shunt
• One time treatment
• For EHPVO & NCPF
• Emergency or elective
• Effective in bleed control
• Relieves hypersplenism
• Low post-operative morbidity
Completed PSRS
Pancreas
Renal vein
Splenic vein
Take Home Message
• Variceal bleed is the most common symptom of PHTN
• Cirrhosis - most common cause of PHTN
• Endoscopic management is successful in >90% cases
• Surgical devascularization or TIPSS in cirrhotics
• Stage 3,4,5 cirrhosis – Liver transplant
• EHPVO & NCPF – Easily treated with shunt surgery

Portal Hypertension

  • 1.
    Portal Hypertension Dr HarshJ Shah MS, FMAS, DNB, MCh (GI) GI & HPB Surgeon Kaizen Hospital, Ahmedabad
  • 2.
    Portal Hypertension • Anatomy& Physiology • Diagnosis • Etiology • Management of Bleed
  • 3.
  • 4.
    Characteristics • Starts &ends in capillaries • Major source of blood supply to liver • No Valves in portal circulation – Blood can flow in either directions • Portosystemic collaterals
  • 5.
    Portal Hypertension • NormalPortal venous pressure – 5-8 mm Hg • Portal Hypertension >10mmHg • Variceal bleeding > 12mm Hg • HVPG (Hepatic venous portal gradient)
  • 6.
    Physics Ohm’s law P (Pressure)= R (Resistance) x Q ( Flow) • Resistance – Cirrhosis – NCPF – EHPVO • Flow – Cirrhosis – AV fistula
  • 7.
  • 8.
    Sites of portalhypertension Extrahepatic Presinusoidal Sinusoidal Postsinusoidal EHPVO NCPF Cirrhosis Budd-chiari syndrome
  • 9.
    Manifestations of PortalHT • Asymptomatic – Detected Incidentally • Ascites • Splenomegaly • Hypersplenism • Jaundice • Encephalopathy
  • 10.
    Investigations Haematology • CBC, Plateletscount Chemistry • Liver Functions • Synthetic function – Protein, Albumin • Renal functions- Urea, Creatinine • Coagulation profile – PT, APTT
  • 11.
    USG Abdomen inPHT • Liver architecture & Size • Portal vein, Splenic vein diameter • Spleen enlargement • Ascites • PV thrombosis & cavernoma • Hepatic veins & IVC  Doppler for blood flow direction
  • 12.
    Flexible UGI Endoscopy •Oesophageal Varices • Gastric varices • Grade of Varices ( I-IV) • Gastropathy • Risk factor bleed - Red spots
  • 13.
    Endoscopic view ofEsophageal Varices Normal Low Grade High Grade
  • 14.
  • 15.
    Liver Biopsy inPHT - For Diagnosis of Cirrhosis if unclear on clinical grounds - For prognosis - As a guide to antiviral treatment - Contra-indication – Massive Ascites, prolonged PT
  • 16.
    Causes of portalhypertension • Cirrhosis of liver • Extrahepatic portal venous obstruction • Non-cirrhotic portal fibrosis
  • 17.
    Cirrhosis of liver •End stage liver disease
  • 18.
    Causes of livercirrhosis • Alcohol • Viral hepatitis (Hep B & C) • Biliary obstruction • Hemochromatosis • Wilson’s disease • Autoimmune • Drugs and toxins • Metabolic diseases • Idiopathic
  • 19.
    Clinical Stages 1. Novarices 2. Varices but no bleeding 3. Ascites 4. Variceal bleed 5. Renal failure, infected ascites or encephalopathy
  • 20.
    Child Pugh Scoring 12 3 Ascites None Mild Severe Encephalopathy None Low grade High grade S. Bilirubin < 1 mg % 1-2 mg % >2mg% S. Albumin >3.5 gm% 2.8 –3.5 <2.8 Pro. Time <3 Sec 4-6 Sec >6 sec Childs A -5,6, B - 7-9, C>9 Score
  • 21.
  • 22.
  • 23.
    Portal Hypertension Cirrhotic • Coagulopathy •Altered LFT, Albumin • Ascites • Bleed • Encephalopathy • Renal failure • Liver tumour(HCC) • Limited survival without Transplant Non cirrhotic (EHPVO, NCPF) • Normal coagulation • Normal LFT, Albumin • Bleed • Shunt surgery
  • 24.
    Management of VaricealBleed Endoscopic (Sclerotherapy, Band, Glue) + Medical (Somatostatin, Octreotide, Terlipressin)
  • 25.
  • 26.
    Endoscopic Sclerotherapy (EST) •Agents – Polidocanol, Absolute Alcohol • Methods – Intra / Paravariceal • Mechanism – fibrosis of connective tissue
  • 27.
    Endoscopic Glue Injection •Cyanoacrylate glue (Histoacryl) • Mainly used for gastric variceal bleed • Mech. of action – obliteration of varix • Hazardous to eyes & endoscopes
  • 28.
    Surgical shunts incirrhosis results in high morbidity..
  • 29.
    Esophageal & GastricDevascularization
  • 30.
    Transjuglar intrahepatic Portosystemic stentshunt (TIPSS) • Percutaneous transjugular technique • Tract between hepatic vein & Portal vein created & expandable stent - 8 Fr placed. • Indication-Temporary control of bleed in poor risk cirrhotic patient waiting for liver transplant • Problems –Expertise, cost, complications, thrombosis
  • 31.
  • 32.
    MELD (Model forEnd stage liver disease) (9.57 x loge creatinine mg/dl + 3.78 x loge bilirubin mg/dl + 11.20 x loge INR + 6.43) • Range : 6-40 • Candidate for liver transplant: >14
  • 33.
    Liver transplant • Definitivetreatment for end stage liver disease • MELD score >14 • Two types of donors – Diseased donors (Brain dead) – Living related donors • Blood group matching is required • 5 year survival – 75-80 %
  • 34.
    Splenectomy & Spleno-RenalShunt • One time treatment • For EHPVO & NCPF • Emergency or elective • Effective in bleed control • Relieves hypersplenism • Low post-operative morbidity
  • 35.
  • 36.
    Take Home Message •Variceal bleed is the most common symptom of PHTN • Cirrhosis - most common cause of PHTN • Endoscopic management is successful in >90% cases • Surgical devascularization or TIPSS in cirrhotics • Stage 3,4,5 cirrhosis – Liver transplant • EHPVO & NCPF – Easily treated with shunt surgery