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Phenotype Submission - Portal Hypertension

Cohort Definition Name: “Portal Hypertension”
Contributor name: Joel N. Swerdel
Contributor OrcId: 0000-0001-9491-2737
Logic Description: First occurrence of Portal Hypertension.
Recommended study application: outcome, indication
Assertion statement: This cohort definition was executed on at least one real person-level observational health data source and resulted in a cohort with at least 1 person.
Submitted cohort definition:
portHtn.txt (1.9 KB)

Target Clinical Description

Portal hypertension is a medical condition characterized by the elevation of blood pressure within the portal venous system, which carries blood from the digestive organs to the liver. This condition most commonly results from liver disease, particularly cirrhosis, and can lead to serious complications due to increased pressure within the portal vein. These complications include variceal bleeding, ascites (fluid buildup in the abdomen), and hepatic encephalopathy. Managing portal hypertension is crucial to prevent life-threatening events and improve the quality of life for affected individuals.

Presentation for Portal Hypertension:

  1. Variceal bleeding, often manifested as bloody vomit or black, tarry stools
  2. Ascites, leading to abdominal swelling and discomfort
  3. Splenomegaly (enlarged spleen)
  4. Hepatic encephalopathy, causing confusion, personality changes, and impaired cognition
  5. Easy bruising and bleeding due to reduced production of clotting factors
  6. Jaundice (yellowing of the skin and eyes) in advanced cases
  7. Fatigue and weakness

Assessment for Portal Hypertension:

  1. Doppler ultrasound of the liver and portal vein
  2. Upper endoscopy to detect and monitor esophageal varices
  3. Imaging studies (CT or MRI) to evaluate liver and spleen size
  4. Liver function tests, including assessment of liver enzymes and bilirubin
  5. Measurement of portal vein pressure through hepatic venous pressure gradient (HVPG) measurement

Differential Diagnoses for Portal Hypertension:

  1. Heart failure
  2. Budd-Chiari syndrome (blockage of the hepatic veins)
  3. Portal vein thrombosis
  4. Alcoholic liver disease
  5. Non-alcoholic fatty liver disease (NAFLD)

Treatment Plan for Portal Hypertension:

  1. Medications to reduce portal pressure (e.g., beta-blockers)
  2. Endoscopic variceal band ligation or sclerotherapy to prevent variceal bleeding
  3. Paracentesis or diuretics to manage ascites
  4. Shunt procedures (e.g., transjugular intrahepatic portosystemic shunt, or TIPS) to reduce portal pressure
  5. Liver transplantation for severe cases or when other treatments are ineffective

Prognosis for Portal Hypertension: The prognosis for individuals with portal hypertension largely depends on the underlying cause, the extent of liver damage, and the effectiveness of treatment. Complications such as variceal bleeding and hepatic encephalopathy can be life-threatening but are manageable with appropriate medical care. In cases of advanced liver disease, liver transplantation may be necessary, offering the possibility of a cure and improved long-term outcomes.

Imported to the OHDSI Phenotype Library. It may be expected to be found with id = 774 in the next release. Thank you ‘Joel Swerdel’,‘Eva-maria Didden’;

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