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| ID | Type | Description | Link |
|---|---|---|---|
| 2021-A01869-32 | Other Identifier | IDRCB |
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Autoimmune hepatitis (AIH) is a chronic liver disease, which is characterized by the increase of immunoglobulin G (IgG) level, the presence of auto-antibodies and a typical histology, in the absence of other liver disease.
Due to the heterogeneity of AIH manifestations, different scoring systems have been validated in order to make a reliable diagnosis. The two most recent scoring systems are: the revised International Autoimmune Hepatitis Group (IAIHG) criteria and the IAIHG simplified criteria. The second one is recommended by the European Association for the Study of the Liver (EASL) clinical practice guidelines (CPGs).
The EASL clinical practice guidelines suggests that the treatment of ASAIH (Acute Severe AIH) is high doses of corticosteroids (superior to 1mg/kg/day) as early as possible and a lack of improvement within seven days should lead to listing for emergency liver transplantation (LT). However, the "lack of improvement" is not objectively defined and the grading of recommendation is III (Opinions of respected authorities).
The hypothesis of the study is that the previously developed decisional score on a retrospective series will prospectively allow the differentiation between patients with ASAIH (Acute Severe AIH) who respond to corticosteroid therapy and should be maintained on treatment and patients who do not respond and should be rapidly evaluated for LT. The score will be computed at day 3 since corticosteroid introduction.
All the interventions (blood samples, imagery examinations, visits, liver biopsy, corticosteroid therapy, liver transplantation) will be performed following the standard of care for ASAIH. The investigators of the participating centers will not change their standard management for the study protocol. The management will follow the recommendation of EASL CPGs.
The prognostic score will allow to distinguish between patient's responders and non-responders to corticosteroid therapy in ASAIH. This knowledge will avoid the prolonged duration of the corticosteroid therapy in patients for whom this therapy is futile or harmful and rapidly select the patients for LT. Of course considering that the created score is decisional whether a patient is a candidate for LT, a prospective validation is mandatory to use it as a clinical tool for the day-to-day practice. This is the first prospective study on ASAIH.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Corticosteroid therapy | Experimental | Prednisone or Prednisolone or Methylprednisolone : Patient with ASAIH will be treated in oral or intravenous (IV) with high doses ( ≥ 1mg/kg/day) of corticosteroids (Prednisone or Prednisolone or Methylprednisolone) until relapse (confirmed by blood tests and clinical status) requiring an emergency Liver Transplantation (LT) or death. |
|
| Patient without corticosteroid therapy | No Intervention | Patient not treated will undergo to emergency Liver Transplantation (LT) or death. |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Corticosteroid therapy | Other | Administration of high doses of corticosteroids as early as possible. Patient non-responder to treatment should lead to listing for emergency liver transplantation (LT). |
| Measure | Description | Time Frame |
|---|---|---|
| Prospectively validate the previously elaborated SURFASA-score, evaluating its ability to predict non-response outcome to corticosteroid therapy in a new population of patients with acute severe autoimmune hepatitis. | Patient response within 90 days to corticosteroid therapy defined as: responders (alive without LT) or non-responders (dead or transplanted) within 90 days since corticosteroid therapy introduction. | Day 90 |
| Measure | Description | Time Frame |
|---|---|---|
| The association between infection occurrence and death during hospitalization | Documented infections during hospitalization | participation period (treatment+follow-up): 12 months |
| the management of infected ASAIH patients in usual practice |
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Inclusion Criteria:
Exclusion Criteria:
Previous medical history of chronic liver disease including autoimmune liver disease (AIH, Primary Biliary Cholangitis (PBC), Primary Sclerosing Cholangitis (PSC) , alcoholic hepatitis etc.)
Other causes of acute severe hepatitis:
Use of corticosteroids 1 month before inclusion
Pregnant or lactating woman
Curator or guardianship or patient placed under judicial protection
Participation in other interventional research during the study
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Eleonora DE MARTIN, MD, PhD | Contact | 33 (0)1.45.59.64.33 | eleonora.demartin@aphp.fr | |
| Jean-Charles DUCLOS-VALLEE, MD, PhD | Contact | 33 (0)1.45.59.64.28 | jean-charles.duclos-vallee@aphp.fr |
| Name | Affiliation | Role |
|---|---|---|
| Eleonora DE MARTIN, MD, PhD | Assistance Publique - Hôpitaux de Paris | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| CHU Angers, Service Hepato-gastro-enterologie | Angers | 49933 | France |
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This is a multicenter, prognostic, non-randomized, comparative, longitudinal, prospective, external validation cohort, which aims to evaluate a decisional score previously developed in a retrospective cohort.
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Antibiotic therapy : doses
| participation period (treatment+follow-up): 12 months |
| The risk factors for early AIH flair after corticosteroid therapy response. | The frequency of AIH flair | D90 |
| The risk factors for AIH recurrence after liver transplantation | AIH recurrence | participation period (treatment+follow-up): 12 months |
| The evolution of patients after LT | Retransplantation, alive, death | participation period (treatment+follow-up): 12 months |
| The evolution of patients not treated with corticosteroids but meeting the inclusion and non-inclusion criteria | Retransplantation, alive, death | participation period (treatment+follow-up): 12 months |
| The prognostic factors for survival in patients treated with corticosteroids who underwent or not LT | quality of the graft, immunosuppression, rejection episode, | participation period (treatment+follow-up): 12 months |
| The association of histological features (liver biopsy) with response to corticosteroids and survival at 90 days since admission | Presence of centrilobular necrosis and inflammatory infiltration | 90 days |
| CHU Jean Minjoz Besançon, Service d'hepatologie et de soins intensifs digestifs | Besançon | 25030 | France |
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| APHP, Hopital Avicenne, Service Hepatologie et Oncologie Hépatique | Bobigny | 93000 | France |
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| CHU Brest, Hopital de la Cavale Blanche Service Gastro-enterologie | Brest | 29609 | France |
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| CHU de Caen, Hopital de la Cote de Nacre, Service Hepato-Gastro-Enterologie et Nutrition | Caen | 14033 | France |
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| CHU Trousseau Chambray, Service Gastro-enterologie et hepatologie | Chambray-lès-Tours | 37170 | France |
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| CHU Dijon, Service Hepato-gastroenterologie et cancerologie digestive | Dijon | 21079 | France |
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| CHRU de Lille, Hopital Claude Huriez, Service des maladies de l'appareil digestif et de la nutrition | Lille | 59037 | France |
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| CHU Limoges, Hopital Dupuytren, Service Hepato-gastroenterologie et nutrition | Limoges | 87042 | France |
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| CHU Hopital Edouard Herriot, Service Hepato-gastro-enterologie | Lyon | 69003 | France |
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| CHU Lyon, Hopital Croix Rousse, Service Hepato-gastro-enterologie | Lyon | 69317 | France |
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| Hopital Saint Joseph, Service Hepato-gastro-enterologie | Marseille | 13285 | France |
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| CHU Montpellier, Hopital Saint Eloi, Service Hepato-gastro-enterologie | Montpellier | 34295 | France |
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| CHU Nice, Hopital de l'Archet 2, Service Hepatologie | Nice | 06200 | France |
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| CHU Orleans, Hopital de la Source, Service Gastro-enterologie et hepatologie | Orléans | 45100 | France |
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| AP-HP, Hopital St Antoine, Service Hepato-gastro-enterologie | Paris | 75012 | France |
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| APHP, Hopital Pitie-Salpetriere, Service d'hepatologie et de gastroenterologie | Paris | 75013 | France |
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| AP-HP, Hopital Cochin Service Hepatologie | Paris | 75014 | France |
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| CHU Bordeaux, GH Sud Haut-Leveque, Service Hepato-gastro-enterologie | Pessac | 33604 | France |
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| CHU La Miletrie, Service Hepato-gastro-enterologie | Poitiers | 86000 | France |
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| CHU Reims, Hopital Robert Debré, Service Hepato-Gastroenterologie et de Cancerologie digestive | Reims | 51092 | France |
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| CHU de Rennes, Hopital de Pontchaillou, Service Maladie du foie | Rennes | 35000 | France |
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| CHU Rouen, Service d'hepatogastro-enterologie | Rouen | 76031 | France |
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| CHU Strasbourg, Hopital de Hautepierre, Service Hepato-gastro-enterologie | Strasbourg | 67200 | France |
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| CHU Toulouse, Hopital Rangueil, Service Hepatologie | Toulouse | 31059 | France |
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| AP-HP, Paul Brousse Hospital, Centre Hepato-Biliaire | Villejuif | 94800 | France |
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| ID | Term |
|---|---|
| D017114 | Liver Failure, Acute |
| D019693 | Hepatitis, Autoimmune |
| ID | Term |
|---|---|
| D017093 | Liver Failure |
| D048550 | Hepatic Insufficiency |
| D008107 | Liver Diseases |
| D004066 | Digestive System Diseases |
| D006521 | Hepatitis, Chronic |
| D006505 | Hepatitis |
| D001327 | Autoimmune Diseases |
| D007154 | Immune System Diseases |
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