Portal hypertension
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Patients scheduled for treatment of complications associated with portal hypertension (splenomegaly, portal hypertension, esophagogastric varices, refractory ascites) or patients suspected of having cirrhotic cardiomyopathy or portopulmonary hypertension due to respiratory distress, etc. 2) Age 20 years or older 3) Patients who have received sufficient explanation about the study after receiving sufficient explanation about their medical conditions and treatment methods, and who have obtained written consent of their own free will with sufficient understanding.
Exclusion criteria
Exclusion criteria: (1) Patients whom the principal investigator or sub-investigator judges to be inappropriate as subjects. (2) Patients for whom outpatient follow-up at our hospital is difficult.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Frequency of cirrhotic cardiomyopathy and portopulmonary hypertension in patients with portal Hypertension and at 3 months and 1 year | — |
Secondary
| Measure | Time frame |
|---|---|
| a. Examine the relationship between liver reserve values (blood chemistry, Child-Pugh score, MELD score, and liver elasticity) and cardiac and portopulmonary hypertension factors. b. Examine the relationship between portal hemodynamic severity (hepatic venous pressure gradient, Doppler flow factors in portal vein and portosystemic shunt) and cardiac function factors and pulmonary hypertension factors. c. To examine changes in cardiac function and pulmonary hypertension factors after treatment of complications associated with portal hypertension. d. Examine the relationship of prognosis to cardiac function and pulmonary hypertension factors. e. Examine differences in endothelin, cytokines, and BMP9 by angiographic site and changes after treatment. | — |
Countries
Japan
Contacts
Chiba University Hospital Department of Gastroenterology