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Two-dimensional Shear Wave Elastography for Assessment of Cirrhosis and Portal Hypertension

Not yet recruiting
Conditions
Cirrhosis, Liver
Portal Hypertension
Interventions
Diagnostic Test: Hepatic venous pressure gradient
Diagnostic Test: Two-Dimensional Shear Wave Elastography
Registration Number
NCT06358092
Lead Sponsor
Third Affiliated Hospital, Sun Yat-Sen University
Brief Summary

Exploring and establishing new non-invasive risk stratification techniques for portal hypertension based on E imaging technology for measuring liver and spleen stiffness is an urgent need in this field of research.

Detailed Description

Portal hypertension is an important risk factor affecting the clinical prognosis of patients with liver cirrhosis. According to clinical practice guidelines, risk stratification based on portal vein pressure levels is crucial for predicting the prognosis of patients with cirrhotic portal hypertension, and it is one of the most important aspects in the diagnosis and treatment chain of end-stage liver diseases such as cirrhosis. The most reliable method for assessing portal vein pressure in patients with cirrhosis is the measurement of hepatic venous pressure gradient (HVPG). This is achieved by inserting a catheter into the hepatic vein via jugular vein puncture, measuring the free and wedged pressures, and calculating the difference to obtain HVPG. HVPG provides important information regarding treatment response, complication risks, and long-term prognosis for patients with cirrhotic portal hypertension: HVPG ≥ 10mmHg indicates an increased risk of varices, decompensation events, and hepatocellular carcinoma in compensated cirrhosis patients, HVPG ≥ 12mmHg is a high-risk factor for variceal bleeding, HVPG ≥ 16mmHg suggests an increased risk of death in patients with cirrhotic portal hypertension, and HVPG ≥ 20mmHg indicates higher failure rates of hemostatic treatment and increased mortality risk in patients with acute variceal bleeding. However, there are some issues with measuring HVPG, including invasiveness, technical requirements, and high costs, which limit its clinical application. The development of non-invasive assessment techniques for portal hypertension in cirrhosis has always been a hotspot and difficulty in this field.

In recent years, with the rapid development of ultrasound elastography technology, it has also been widely used in the field of liver diseases. Transient elastography, point shear wave elastography, and two-dimensional shear wave elastography (referred to as E imaging) all have important value in the non-invasive assessment of portal hypertension in cirrhosis. Ultrasound elastography, due to its advantages of non-invasiveness, rapidity, ease of operation, repeatability, safety, and ease of follow-up monitoring, is of great significance in risk stratification, precise management, and efficacy evaluation of portal hypertension in cirrhosis. Although liver stiffness has been applied in the diagnosis, treatment, and prognosis assessment of cirrhotic portal hypertension, transient elastography is still the main ultrasound elastography technique used clinically, and there are relatively few original studies related to spleen stiffness. Therefore, there is currently a lack of high-level clinical evidence based on E imaging technology for evaluating portal hypertension in cirrhosis in China, as well as a lack of original research on spleen stiffness assessment in cirrhotic portal hypertension.

In summary, exploring and establishing new non-invasive risk stratification techniques for portal hypertension based on E imaging technology for measuring liver and spleen stiffness is an urgent need in this field of research.

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
112
Inclusion Criteria
  1. Age: 18-75 years old;
  2. Clinical diagnosis of liver cirrhosis (confirmed by pathological biopsy, imaging findings, or occurrence of relevant complications);
  3. Scheduled for hepatic venous pressure gradient (HVPG) examination;
  4. Planned to undergo measurement of liver and spleen stiffness using E imaging technology;
  5. Voluntary signing of informed consent form.
Exclusion Criteria
  1. Contraindications to hepatic venous pressure gradient examination;
  2. Liver intervention surgery scheduled between E imaging examination and HVPG examination;
  3. Interval between E imaging examination and HVPG examination exceeds 14 days;
  4. Presence of liver cancer;
  5. Concurrent active, severe, life-threatening diseases;
  6. History of the following surgeries: ① Transjugular intrahepatic portosystemic shunt (TIPS) procedure; ② Hepatectomy; ③ Splenectomy; ④ Liver transplantation.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Training cohortHepatic venous pressure gradientTo explore the cut-off value of LSM and SSM by 2D-SWE for assessment of CSPH in cirrhosis.
Validation cohortHepatic venous pressure gradientTo validate the cut-off value of LSM and SSM by 2D-SWE for assessment of CSPH in cirrhosis.
Training cohortTwo-Dimensional Shear Wave ElastographyTo explore the cut-off value of LSM and SSM by 2D-SWE for assessment of CSPH in cirrhosis.
Validation cohortTwo-Dimensional Shear Wave ElastographyTo validate the cut-off value of LSM and SSM by 2D-SWE for assessment of CSPH in cirrhosis.
Primary Outcome Measures
NameTimeMethod
the diagnostic performance of liver and spleen stiffness by E imaging technology for clinically significant portal hypertension1 year

Using HVPG as the gold standard, the diagnostic performance of measuring liver and spleen stiffness based on E imaging technology for clinically significant portal hypertension.

Secondary Outcome Measures
NameTimeMethod
the diagnostic performance of microvessel imaging of hepatic microcirculation by E imaging technology for clinically significant portal hypertension1 year

Using HVPG as the gold standard, the diagnostic performance of microvessel imaging of hepatic microcirculation based on E imaging technology for clinically significant portal hypertension.

the difference among left, middle and right hepatic venous pressure gradient1 year

the difference among left, middle and right hepatic venous pressure gradient

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