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594A AASLD ABSTRACTS HEPATOLOGY, October, 2015<br />

Disclosures:<br />

Simona Bota - Speaking and Teaching: Janssen Pharmaceutica, Bristol-Myers<br />

Squibb<br />

Mattias Mandorfer - Consulting: Janssen; Speaking and Teaching: AbbVie, Gilead,<br />

Janssen, Boehringer Ingelheim, Bristol-Myers Squibb, Roche<br />

Michael Trauner - Advisory Committees or Review Panels: MSD, Janssen, Gilead,<br />

Abbvie; Consulting: Phenex; Grant/Research Support: Intercept, Falk Pharma,<br />

Albireo; Patent Held/Filed: Med Uni Graz (norUDCA); Speaking and Teaching:<br />

Falk Foundation, Roche, Gilead<br />

Markus Peck-Radosavljevic - Advisory Committees or Review Panels: Bayer, Gilead,<br />

Janssen, BMS, AbbVie; Consulting: Bayer, Boehringer-Ingelheim, Jennerex,<br />

Eli Lilly, AbbVie; Grant/Research Support: Bayer, Roche, Gilead, MSD, AbbVie;<br />

Speaking and Teaching: Bayer, Roche, Gilead, MSD, Eli Lilly, AbbVie, Bayer<br />

Thomas Reiberger - Consulting: Xtuit; Grant/Research Support: Roche, Gilead,<br />

MSD, Phenex; Speaking and Teaching: Roche, Gilead, MSD<br />

The following authors have nothing to disclose: Philipp Schwabl, Theresa Bucsics,<br />

Remy Schwarzer, Arnulf Ferlitsch<br />

772<br />

Does Haemodynamic or Clinical Rebound Exist in<br />

patients with Cirrhosis after Abrupt Interruption of<br />

Beta-blockers?<br />

Audrey Payance 2 , Julien Bissonette 2 , Olivier Roux 2 , Laure Elkrief 2 ,<br />

claire francoz 2 , Ouardia Nekachtali 1 , Dominique C. Valla 1 , Didier<br />

Lebrec 1 , Francois Durand 2 , Pierre-Emmanuel Rautou 1 ; 1 Paris VII<br />

University and INSERM, BEAUJON HOSPITAL, Clichy, France;<br />

2 HEPATOLOGY, BEAUJON HOSPITAL, Clichy, France<br />

Background and Aims: Beta-blockers (BBs) may be interrupted<br />

in patients with portal hypertension. The concept of rebound<br />

after abrupt interruption of BBs is based on animal <strong>studies</strong><br />

showing a transient β-adrenergic hypersensitivity state following<br />

propranolol withdrawal and on few case reports of<br />

variceal bleeding following abrupt interruption of this drug.<br />

However, no human study addressed this issue yet. Our aim<br />

was thus to determine if a rebound after abrupt interruption of<br />

BBs exists in patients with cirrhosis both on a hemodynamic<br />

and a clinical point of view. Patients and Methods: This prospective<br />

observational study included all patients with cirrhosis<br />

undergoing right heart and hepatic vein catheterization in our<br />

hemodynamic laboratory. Four groups of patients were a priori<br />

defined: “no BBs” defined as patients not receiving BBs;<br />

“≥ 1day” defined as patients having received BBs within 1<br />

day before catheterization; “2-3 days”, defined as patients<br />

having interrupted BBs 2 or 3 days before catheterization;<br />

and “≥4days” defined as patients having interrupted BBs 4<br />

days or more before catheterization. Results are presented as<br />

median (interquartile range). Results: A total of 150 patients<br />

were included (men, 76%; median age, 57 yrs; alcoholic cirrhosis,<br />

75%; large varices, 73%). Indications for right heart<br />

and hepatic vein catheterization included evaluation prior to<br />

liver transplantation (n=90) or liver surgery (n=8) and assessment<br />

of cirrhosis severity (n=52). There were 81, 44, 11, 14<br />

patients in the “no BBs”, “≥1day”, “2-3 days” and “≥4days”<br />

groups, respectively. MELD and Child-Pugh scores were not<br />

different among the groups. Hepatic venous pressure gradient<br />

was not different between patients in groups “≥ 1day” (18.5<br />

mm Hg, 15-23), “2-3 days” (17 mm Hg, 13-23) and “≥4days”<br />

(19.5 mm Hg, 17-26). Cardiac index remained low up to 3<br />

days after BBs interruption. Patients in the “≥4days” group<br />

had higher cardiac index than those in the “≥1day” group<br />

[4.6 (3.5-5.1) vs 3.4 (2.6-4.0); p=0.001)] or in the “2-3 days”<br />

group [4.6 (3.5-5.1) vs 3.1 (2.7-3.7); p=0.007], but only borderline<br />

significantly higher than patients not receiving BBs [4.6<br />

(3.5-5.1) vs 3.7 (3.0-4.5); p=0.052]. Among the 25 patients<br />

in the groups “2-3 days” and “≥4days”, median duration of<br />

BBs interruption was 4 (3-6) days. No gastrointestinal bleeding<br />

occurred during that period. Conclusions: Abrupt interruption<br />

of BBs may slightly increase cardiac index without rebound<br />

in hepatic venous pressure gradient and with no apparent<br />

increase in the risk of variceal bleeding. Thus, interruption<br />

of BBs in cirrhotic patients with portal hypertension does not<br />

require particular dosing or surveillance.<br />

Disclosures:<br />

Francois Durand - Advisory Committees or Review Panels: Astellas, Novartis,<br />

BMS; Speaking and Teaching: Gilead<br />

Pierre-Emmanuel Rautou - Speaking and Teaching: Gilead<br />

The following authors have nothing to disclose: Audrey Payance, Julien Bissonette,<br />

Olivier Roux, Laure Elkrief, claire francoz, Ouardia Nekachtali, Dominique<br />

C. Valla, Didier Lebrec<br />

773<br />

High risk of misclassifying liver stiffness using 2D shearwave<br />

and transient elastography during a moderate or<br />

high calorie meal<br />

Maria Kjærgaard 1 , Maja Thiele 1 , Bjørn S. Madsen 1 , Christian<br />

Jansen 2 , Jonel Trebicka 2 , Aleksander Krag 1 ; 1 Odense University<br />

Hospital, Odense, Denmark; 2 University of Bonn, Bonn, Germany<br />

Introduction: Transient Elastography (TE) (FibroScan) and<br />

real time 2D shear wave elastography (2D-SWE) (Aixplorer)<br />

are widely used in the grading and staging of liver fibrosis.<br />

In patients with chronic viral hepatitis a meal of 600 kcal<br />

increases liver stiffness (LS) measured by TE. Thus, food intake<br />

may hamper interpretation of results and clinical decision-making.<br />

This study aimed to investigate the impact of a meal on<br />

LS measured by both TE and 2D-SWE in patients with alcoholic<br />

fibrosis, the role of the meal size and the time it takes<br />

to return to baseline. Methods: Patients with a liver biopsy<br />

or known cirrhosis participated in a two-day protocol with a<br />

250ml/625 kcal liquid meal (49% carbohydrates, 36% fat,<br />

15% protein) and 500ml/1250 kcal meal on day 1 and 2<br />

respectively. TE and 2D-SWE were measured at 0, 20, 40, 60,<br />

120 and 180 minutes. DLS are the highest increase in LS from<br />

baseline. Results: 51 patients participated: 71% male, median<br />

age 61years, 88% with alcoholic etiology, 8% HCV and 4%<br />

NASH. 14 patients showed none or minimal fibrosis (METAVIR<br />

F0-1), 9 patients moderate or severe fibrosis (F2-3) and 28<br />

patients cirrhosis (F4). On day 1 and 2, post-meal LS increased<br />

significantly in all fibrosis groups (see table). The highest DLS<br />

was measured after a median of 60 minutes (range 20-180)<br />

and the largest DLS were observed in patients with cirrhosis<br />

(43% increase). In these patients, LS increased similarly on day<br />

1 and 2, despite twice the volume and calories (P= 0.93). In<br />

patients with F0-F3 fibrosis there was a trend towards a higher<br />

DTE on day 2; F0-1 (P= 0.08) and F2-3 (P=0.07). In patients<br />

with baseline TE

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