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822A AASLD ABSTRACTS HEPATOLOGY, October, 2015<br />

tion and patient and graft survival. Implications for the clinical<br />

setting are conscientiously monitoring of the GFR in the first<br />

months after liver transplantation and taking action as early<br />

as possible to prevent worsening of the creatinine clearance.<br />

Disclosures:<br />

Faouzi Saliba - Advisory Committees or Review Panels: Novartis, Roche, Genzyme,<br />

Vital therapies; Grant/Research Support: Astellas; Speaking and Teaching:<br />

Gambro, MSD, Gilead<br />

Rene Adam - Grant/Research Support: Merck Serono, Roche, Sanofi aventis,<br />

astellas, novartis, Merck Serono, Roche, Sanofi aventis, astellas, novartis, Merck<br />

Serono, Roche, Sanofi aventis, astellas, novartis, Merck Serono, Roche, Sanofi<br />

aventis, astellas, novartis<br />

Didier Samuel - Consulting: Astellas, MSD, BMS, Roche, Novartis, Gilead, LFB,<br />

Janssen-Cilag, Biotest, Abbvie<br />

The following authors have nothing to disclose: Noémie Minczeles, Valérie Delvart,<br />

Teresa Antonini, Rodolphe Sobesky, Philippe Ichai, Audrey Coilly, Bruno<br />

Roche, Marc Boudon, Eric Vibert, Denis X. Castaing, Daniel Cherqui, Gilles<br />

Pelletier, Jean-Charles Duclos-Vallee<br />

1238<br />

Value of Magnetic Resonance Cholangiography in<br />

Assessment of Non-Anastomotic Biliary Strictures after<br />

Liver Transplantation<br />

A. Claire den Dulk 1 , Martin N.J.M. Wasser 2 , Francois Willemssen<br />

3 , Melanie A. Monraats 2 , Marianne de Vries 3 , Rivka van den<br />

Boom 2 , Jan Ringers 4 , Hein W. Verspaget 1 , Herold J. Metselaar 5 ,<br />

Bart van Hoek 1 ; 1 Gastroenterology and Hepatology, Leiden University<br />

Medical Center, Leiden, Netherlands; 2 Radiology, Leiden<br />

University Medical Center, Leiden, Netherlands; 3 Radiology, Erasmus<br />

Medical Center, Rotterdam, Netherlands; 4 Transplant Surgery,<br />

Leiden University Medical Center, Leiden, Netherlands; 5 Gastroenterology<br />

and Hepatology, Erasmus Medical Center, Rotterdam,<br />

Netherlands<br />

Background Non-anastomotic biliary strictures (NAS) remain<br />

a frequent complication after orthotopic liver transplantation<br />

(OLT). The aim of this study was to evaluate whether Magnetic<br />

Resonance Cholangiography (MRCP) could be used to detect<br />

or exclude NAS and grade the severity of biliary strictures.<br />

Methods In total, 58 patients after OLT from two transplantation<br />

centres in whom endoscopic (ERCP) or percutaneous transhepatic<br />

cholangiography (PTC) and MRCP were performed<br />

within less than 6 months were included in the study. Of these<br />

patients, 41 had NAS and 17 were without NAS based on<br />

ERCP or PTC and follow-up. Four radiologists – two in each<br />

center – used an adapted validated classification –termed<br />

Leiden Biliary Stricture Classification (LBSC)– to evaluate the<br />

MRCP independently and assess NAS severity on a scale from<br />

0 to 3 points in three hepatobiliary regions.(Fig 1) A maximum<br />

of 15 points could be obtained. Interobserver agreement of the<br />

severity score and intra-observer agreement between ERCP/<br />

PTC and MRCP for each region was calculated with the kappa<br />

(κ) statistic. Results Optimal cut-off value of the LBSC to detect<br />

the presence of NAS with MRCP was calculated at ≥ 3 points<br />

for all readers. Applying this cut-off, sensitivity for each reader<br />

was >90%, with a corresponding specificity of 50-82%, positive<br />

predictive value (PPV) of 86-91%, and negative predictive<br />

value (NPV) of 80-100%. When the cut-off value was applied<br />

to the radiologists’ mean scores sensitivity was 98%, specificity<br />

65%, PPV 87% and NPV 92%. MRCP performance was better<br />

in evaluation of the intrahepatic bile ducts than of the extrahepatic<br />

bile ducts. The additional value of MRCP for grading<br />

severity (κ= 0.2 – 0.7) and localizing NAS (κ= 0.2 – 0.9) was<br />

limited. Conclusion MRCP is a reliable tool to detect or exclude<br />

non-anastomotic biliary strictures after OLT. MRCP cannot be<br />

used to reliably grade the severity of these strictures.<br />

Disclosures:<br />

Bart van Hoek - Advisory Committees or Review Panels: Janssen-Cilag, Bristol<br />

Meyers Squib, Gilead, Merck, Abbvie<br />

The following authors have nothing to disclose: A. Claire den Dulk, Martin N.J.M.<br />

Wasser, Francois Willemssen, Melanie A. Monraats, Marianne de Vries, Rivka<br />

van den Boom, Jan Ringers, Hein W. Verspaget, Herold J. Metselaar<br />

1239<br />

Are cirrhotic patients awaiting liver transplantation protected<br />

against vaccine preventable diseases?<br />

Mazzola Alessandra 1,2 , Margherita Tran Minh 1,3 , Raluca Pais 1 ,<br />

Pascal Lebray 1 , Denis Bernard 4 , Claire Goumard 5 , Yvon Calmus 1 ,<br />

Filomena Conti 1 ; 1 Unité Médicale de Transplantation Hépatique,<br />

APHP, Hôpital Pitié Salpétrière, Paris, France; 2 Sezione di Gastroenterologia,<br />

University of Palermo, Palermo, Italy; 3 Clinical<br />

and experimental Medecine, Università del Piemonte Orientale,<br />

Novara, Italy; 4 Service d’Anesthésie Réanimation, APHP, Hôpital<br />

Pitié Salpétrière, Paris, France; 5 Sevice de Chirurgie Hépatobiliaire<br />

et de Transplantation, APHP, Hôpital Pitié Salpétrière, Paris,<br />

France<br />

Background: Cirrhotic patients are spontaneously immunocompromised<br />

and are at increased risk of infection with higher<br />

morbidity and mortality. Vaccination may reduce the mortality<br />

related to infectious complications in those patients. Only<br />

few data regarding protection against vaccine preventable<br />

diseases and the results of vaccination are available in cirrhotic<br />

patients awaiting liver transplantation (LT). Aims: The aims of<br />

this prospective non-randomized study were to prospectively<br />

assess the prevalence of hepatitis A, B and varicella viruses<br />

(HAV,HBV,VZV) serological markers and to the evaluate the<br />

immunization status in a cohort of cirrhotic patient awaiting LT<br />

to determine the need of vaccination in this cohort. Patients and<br />

methods: All the cirrhotic patients registered on the LT waiting<br />

list in a single center were questioned about the prevalence of<br />

previous diseases and vaccinations by a questionnaire. The<br />

enzyme linked immunosorbent assay (ELISA) method was used<br />

to assess the presence of HBsAg, anti-HBc, anti-HBs, anti-HAV<br />

and anti-VZV antibodies. The positivity of serology was defined<br />

as: HBsAg ≥1 mUI/mL, anti-HBs ≥10 mUI/L, anti-HBc≥1 mUI/L,<br />

anti-HAV(IgG)≥1mUI/mL and anti-VZV(IgG)≥165 mUI/mL for<br />

HBV, HAV and VZV viruses, respectively. Results: 201 patients<br />

(male: 74%, mean age: 54±11years) have been evaluated.<br />

The indication for LT was HCV-related cirrhosis in 42.4%, HBV<br />

cirrhosis in 9%, alcoholic cirrhosis in 43.1%, NASH in 6.1%,<br />

hepatocellular carcinoma in 41.9%, and other indications in<br />

21.2%. Forty-five percent were class A, 33.2% B and 18.9%<br />

C according to Child-Pugh score; median MELD score was 12<br />

(6-33). Only 2.5% of patients had a vaccination book, 50%<br />

were anaware of having or having not a pasthistory of HBV,<br />

HAV or VZV infection. Twenty-nine percent, 6.7% and 4.0%,<br />

respectively, reported a vaccination against HBV, HAV and<br />

VZV. Seroprevalence was 11.1% for HBsAg, 32.2% for anti-

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