Status
Conditions
About
The principle is to propose dedicated monthly screening days bringing together the health personnel involved (hepatologist, addictologist, nurse in charge of the program, addictology nurse and social worker) and to propose appropriate management for each situation assessed.
Full description
Information on screening, the days are announced by :
Conduct of a SCANVIR day in the non-conventional structure " Hors les murs " :
Each patient presenting during the screening day will have an individualized welcome.
Addictological and hepatological data will be collected throughout the process by the various workers on the individual Scanvir form (attached).
Method for routine management of patients according to results :
HCV HBV HIV TROD are negative and FibroScan® > 7.1 KPa:
The patient meets directly with the hepatologist to screen for risk factors for chronic liver disease (alcohol, medications ...).
The HCV HBV HIV TROD are negative and the FibroScan ® < 7.1 KPa :
The nurse at the facility reviews with the patient the modes of transmission of the viruses and discusses with him/her risk reduction and harm reduction and what to do in case of recent exposure.
Positive HCV TROD:
The hepatologist offers to do an immediate and on-site HCV RNA by delocalized PCR (GeneXpert). If the HCV RNA is positive, HCV treatment is started immediately (excluding comorbidity). An appointment is proposed 3 months after treatment to control the cure by delocalized PCR on site (RVS12)
HIV or HBV TROD positivity:
The hepatologist proposes to do immediately and on site a complete blood test (HIV serology, HBV serologies (HBsAg, HBcAb, HBsAb) by the nurse present, assesses other risk factors and schedules an appointment for the results and management.
For all situations, a prevention action to reduce the risks of transmission of HCV and HBV will be carried out at the same time.
An anti-viral B vaccination may be offered.
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
Exclusion criteria
Loading...
Central trial contact
Marilyne DEBETTE-GRATIEN, MD; Véronique LOUSTAUD-RATTI, Prof
Data sourced from clinicaltrials.gov
Clinical trials
Research sites
Resources
Legal