Acoustic Radiation Force Impulse Imaging (ARFI) : a New Technique to Assess Liver Elasticity

Not Applicable

Completed

• Conditions: Liver Cirrhosis; Viral Hepatitis; Liver Fibrosis; Liver Tumour; Cardiac Failure; Biliary Cholestasis.
• Interventions: Device: ARFI measurement

• Registration Number: NCT01082419
• Lead Sponsor: University Hospital, Bordeaux

Brief Summary

Liver stiffness measurement (LSM) by non invasive methods is increasingly used to estimate liver fibrosis in patients with chronic liver diseases. However, there is growing evidence that fibrosis is not the only determinant of liver stiffness. Indeed inflammation, cholestasis, congestion could also interfere with stiffness measurements. Acoustic radiation force impulse imaging (ARFI) is a new technology to perform real time LSM. Using a standard ultrasonographic probe, it offers elastography with a flexible metering box at variable depth, allowing the examination of specific area.

Detailed Description

There are many causes of chronic liver diseases such as hepatitis C infection, hepatitis B infection, alcohol, NAFLD (non-alcoholic fatty liver disease), drugs and auto-immune liver disease.

Although the causes differ the pathological response to injury tends to be similar leading to fibrosis and cirrhosis.

Liver biopsy is the current gold standard for the assessment of liver fibrosis but is poorly suited for active monitoring because of its expense and morbidity. Thus, development of alternatives that are safe, inexpensive, and reliable is a priority.

Liver stiffness measurement (LSM) by non invasive method is increasingly used to estimate liver fibrosis in patient with chronic liver disease. Acoustic radiation force impulse imaging (ARFI) is a new technology to perform real time LSM. Using a standard ultrasonographic probe, it offers elastography with a flexible metering box at variable depth, allowing the examination of specific area.

The purpose of this work was to evaluate by ARFI, the efficiency of this new technique, the reproducibility inter and intra observer, and the liver elasticity obtained by this method in different patient groups.

The primary endpoint of this work is to evaluate by ARFI, the efficiency of the technique, the reproducibility inter and intra observer, and the elasticity of liver in 6 different patient groups and healthy volunteers.

The different population groups are:

* healthy volunteers Group A

* patients with supposed disease free liver (normal hepatic and pancreatic biochemistry). Group B

* patients with non cirrhotic hepatopathy. Group C

* patients with cirrhosis. Group D

* patients with liver tumour and surgery indication. Group E

* patients with reversible liver diseases:

* patients with acute left cardiac insufficiency. Group F

* patients with biliary cholestasis. Group G

ARFI measurements will be performed in a single liver ultrasound exam visit except for patients with reversible liver diseases who will have a second visit with ARFI measurement after clinical healing. The ARFI values are expressed as a speed in m/s.

Study Timeline

• Study First Submitted: 2010-03-05
• Study First Submitted QC: 2010-03-05
• Study First Posted: 2010-03-08
• Study Start: 2010-04
• Primary Completion: 2013-04
• Study Completion: 2013-04
• Status Verified: 2014-11
• Last Update Submitted: 2014-11-06
• Last Update Posted: 2014-11-07

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 109

Inclusion Criteria

• Man or Woman
• Age> 18 years old
• Able to understand the study and to give informed consent
• Informed consent signed by patient and investigator before any study required examination
• With a valid health insurance
• Groups specific inclusion criteria are:
• Group A : healthy volunteers without known liver disease
• Group B : voluntary patients without known liver disease
• Group C and D Patient with a diagnosed chronic liver disease
• Group E : patients with liver tumors (benign or malignant) with surgical indication
• Group F : patients with acute right heart insufficiency diagnosed by a cardiologist
• Group G :patients with biliary cholestasis and imaging evidence of biliary dilatation

Exclusion Criteria

• Patient under 18 years old
• Not able to understand the study or to give their consent.
• Pregnant woman
• Severe respiratory insufficiency
• Unable to perform a "light" apnea .
• hemodynamic instability (cardiogenic shock, septic or anaphylactic) possibility of disruption of the elasticity and inability to carry patient.
• Chronic heart insufficiency.
• deprived of their liberty by court

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Group B	ARFI measurement	patients with supposed disease free liver (normal hepatic and pancreatic biochemistry)
Group E	ARFI measurement	patients with liver tumour and surgery indication
Group F	ARFI measurement	patients with reversible liver diseases and with acute left cardiac insufficiency
Group G	ARFI measurement	patients with reversible liver diseases and with biliary cholestasis
Group A	ARFI measurement	healthy volunteers
Group D	ARFI measurement	patients with cirrhosis
Group C	ARFI measurement	patients with non cirrhotic hepatopathy

Primary Outcome Measures

Name	Time	Method
The elasticity parameter will be for each patient the median of ten ARFI values (m/s) in the right liver.	One or two 30 min visit according to the patient group

Secondary Outcome Measures

Name	Time	Method
Median (m/s) of ARFI values between before and after effective treatment for liver reversible disease	From patient admission until patient healing in groups F&G.
Inter and intra observer reproducibility	Three 30 min visits in healthy volunteer group.

Trial Locations

Locations (1)

University Hospital Bordeaux; 🇫🇷 Bordeaux, France