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HEPATOLOGY, VOLUME 62, NUMBER 1 (SUPPL) AASLD ABSTRACTS 929A<br />

were significant. On multi-variate analysis, recent alcohol (OR<br />

4.0, p=0.003) and illegal turns (OR 1.4, p=0.005) remained<br />

significant predictors of real-life crashes. Conclusion: In this<br />

largest-studied cirrhosis cohort, MHE subjects were likely to<br />

have worse simulator and real-life crash rates that remains<br />

stable over 1 year. Only MHE patients who performed poorly<br />

on navigation and had quit alcohol within 3 years were likely<br />

to be unsafe drivers.<br />

Summarized of results<br />

Table shows summarized of results from driving simulation, real<br />

life traffic history and 6-month follow up in 163 patients.<br />

Disclosures:<br />

Richard K. Sterling - Advisory Committees or Review Panels: Merck, Vertex, Salix,<br />

Bayer, BMS, Abbott, Gilead, Baxter, Jansen; Grant/Research Support: Merck,<br />

Roche/Genentech, Pfizer, Gilead, Boehringer Ingelheim, Bayer, BMS, Abbott<br />

Puneet Puri - Advisory Committees or Review Panels: Health Diagnostic Laboratory<br />

Inc.; Consulting: NPS Pharmaceuticals Inc.<br />

Arun J. Sanyal - Advisory Committees or Review Panels: Bristol Myers, Gilead,<br />

Genfit, Abbott, Ikaria, Exhalenz; Consulting: Salix, Immuron, Exhalenz, Nimbus,<br />

Genentech, Echosens, Takeda, Merck, Enanta, Zafgen, JD Pharma, Islet<br />

Sciences; Grant/Research Support: Salix, Genentech, Intercept, Ikaria, Takeda,<br />

GalMed, Novartis, Gilead, Tobira; Independent Contractor: UpToDate, Elsevier<br />

Douglas M. Heuman - Consulting: Bayer, Grifols, Genzyme; Grant/Research<br />

Support: Exilixis, Novartis, Bayer, Bristol Myers Squibb, Scynexis, Ocera, Mannkind,<br />

Salix, Globeimmune, Roche, SciClone, Wyeth, Otsuka, Ikaria, UCB, Celgene,<br />

Centocor, Millenium, Osiris, AbbVie, Gilead; Speaking and Teaching:<br />

Otsuka, Astellas<br />

Jasmohan S. Bajaj - Advisory Committees or Review Panels: Salix, Merz, otsuka,<br />

ocera, grifols, american college of gastroenterology; Grant/Research Support:<br />

salix, otsuka, grifols<br />

The following authors have nothing to disclose: Mette M. Lauridsen, Vishwadeep<br />

Ahluwalia, Ariel Unser, Melanie White, R. Todd Stravitz, Scott C. Matherly,<br />

Velimir A. Luketic, Mohammad S. Siddiqui, Michael Fuchs<br />

1473<br />

Randomized Controlled Trial on Efficacy of Nutritional<br />

Therapy on Cognitive Functions and Health Related<br />

Quality of Life in Patients of Liver Cirrhosis with Minimal<br />

Hepatic Encephalopathy<br />

Sudhir Maharshi, Barjesh C. Sharma, Sanjeev Sachdeva, Siddharth<br />

Srivastava; Gastroenterology, G B Pant Institute of Post<br />

graduate Medical Education and Research, New delhi, India<br />

Background & Aims: Minimal hepatic encephalopathy impairs<br />

health related quality of life (HRQOL), predicts development of<br />

overt hepatic encephalopathy and associated with poor prognosis.<br />

There is no study on nutritional management in patients<br />

with minimal hepatic encephalopathy. We assessed the effects<br />

of nutritional therapy on cognitive functions and HRQOL in<br />

patients of cirrhosis with minimal hepatic encephalopathy.<br />

Methods: A randomized controlled trial conducted in a tertiary<br />

care setting on patients of cirrhosis with minimal hepatic<br />

encephalopathy who were randomized to nutritional therapy<br />

(group A: 30-35 kcal/kg/day and 1 . 0-1 . 5 gram of vegetable<br />

protein/kg/day) and no nutritional therapy (group B: diet as<br />

patients were taking before) for 6 months. Minimal hepatic<br />

encephalopathy was diagnosed based on psychometry hepatic<br />

encephalopathy score (PHES). HRQOL was assessed by sickness<br />

impact profile (SIP) questionnaire. Primary endpoints were<br />

improvement or worsening in minimal hepatic encephalopathy<br />

and improvement in HRQOL. Results: 120 patients were<br />

randomized to group-A (n = 60, age 42 . 1±10 . 3 yr, 48 men)<br />

and group-B (n = 60, age 42 . 4±9 . 6 yr, 47 men). There was<br />

no significant difference in baseline characteristics between<br />

the two groups. Baseline PHES (-8 . 12±1 . 32 vs -8 . 53±1 . 38;<br />

p=0 . 08) and SIP score (14 . 25±5.8 vs 15 . 44±5 . 03; p=0 . 85)<br />

were comparable in both the groups. Reversal of minimal<br />

hepatic encephalopathy was higher in group A (71 . 1% vs<br />

22 . 8%; p=0 . 001). Improvement in PHES (ΔPHES 3 . 86±3 . 58<br />

vs 0 . 52±4 . 09; p=0 . 001) and HRQOL (Δ SIP 3 . 24±3 . 63 vs<br />

0 . 54±3 . 58; p=0 . 001) were also higher in group A compared<br />

to group B. Overt hepatic encephalopathy developed in 10%<br />

of patients in group A vs 21 . 7% in group B (P=0 . 04). Conclusions:<br />

Nutritional therapy is effective in treatment of minimal<br />

hepatic encephalopathy and associated with improvement in<br />

HRQOL.<br />

Disclosures:<br />

The following authors have nothing to disclose: Sudhir Maharshi, Barjesh C.<br />

Sharma, Sanjeev Sachdeva, Siddharth Srivastava<br />

1474<br />

Usefulness of Balloon-Occluded Retrograde Obliteration<br />

(B-RTO) as a Therapeutic Procedure to Improve Liver<br />

Function in Cirrhotic Patients with Porto-Systemic Shunts<br />

Manabu Nakazawa, Yukinori Imai, Satsuki Ando, Kayoko Sugawara,<br />

Mie Inao, Nobuaki Nakayama, Satoshi Mochida; Gastroenterology<br />

& Hepatology, Saitama medical university hospital,<br />

Saitama, Japan<br />

Aim: Porto-systemic shunts cause refractory hepatic encephalopathy<br />

in patients with liver cirrhosis. The shunts also contribute<br />

to derange liver function through reduction of blood flow in<br />

the portal vein. The usefulness of B-RTO as a therapeutic procedure<br />

for improvement of liver function as well as attenuation of<br />

refractory hepatic encephalopathy was evaluated in cirrhotic<br />

patients. Methods: The subjects were 34 cirrhotic patients with<br />

porto-systemic shunts showing refractory hepatic encephalopathy.<br />

The extent of liver dysfunction classified according to the<br />

Child-Pugh classification were grade A, B and C in 3, 18 and<br />

13 patients, respectively. A balloon catheter was inserted into<br />

the shunts followed by injection of 5% ethanolamine oleate<br />

through the catheter under balloon inflation. The balloon was<br />

kept inflation for between 6 and 48 hours depending on<br />

sizes of the shunts. Results: Drainage vessels of the targeted<br />

shunts were the splenorenal, mesocaval, paraumbilical, azygos<br />

and splenorenal plus azygos veins in 20, 4, 6, 2 and<br />

2 patients, respectively. B-RTO was successfully done in 29<br />

patients (85%), and hepatic encephalopathy did not recur in<br />

24 (83%) patients. In patients receiving successful B-RTO procedures,<br />

HH15, LHL15 and LU15 values assessed by Tc-99m<br />

GSA scintigraphy were not different between at baseline and<br />

1 months after the procedures, while doppler ultrasound examinations<br />

revealed that blood flows in the portal vein (cm 3 /sec;<br />

mean±SD) increased significantly (from 2.2±0.9 to 8.4±2.4,<br />

p

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