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356A AASLD ABSTRACTS HEPATOLOGY, October, 2015<br />

greater than 10, 20 and 30, OR for development of SBP was<br />

4.62 (2.86-7.82), 7.9 (5.18-12.27) and 11.03 (4.92-28.1)<br />

respectively. MELD score cut-off level ≥ 17 had an area under<br />

the receiver operating characteristic curves (AUROC) 0.76 with<br />

sensitivity 63% and specificity 79%. PPI use was independently<br />

associated with development of SBP (OR 2.87, CI 1.78-4.69).<br />

There was an interaction between MELD score and PPI use, but<br />

MELD score was a stronger risk. Conclusion: MELD score and<br />

PPI therapy are associated with development of the first episode<br />

of SBP. Prospective <strong>studies</strong> are needed to validate these<br />

data and to determine the optimal MELD score above which<br />

patients would benefit from primary prophylaxis of SBP.<br />

18 and 24 months. Overall the included <strong>studies</strong> had a low risk<br />

of bias, except for two observational <strong>studies</strong> in which the risk<br />

was judged as moderate. Conclusions: Based on moderate<br />

quality evidence, the use of NSBBs was not associated with a<br />

significant increase in the risk of all-cause mortality in cirrhotic<br />

patients with ascites, including refractory ascites.<br />

Subgroup analyses of 12 <strong>studies</strong> included in meta-analysis<br />

Multivariate Logistic regression analyses of predictors the first<br />

episode of SBP<br />

Disclosures:<br />

Patrick S. Kamath - Advisory Committees or Review Panels: Sequana Medical<br />

The following authors have nothing to disclose: Sakkarin Chirapongsathorn,<br />

Rashid Khan, Ashwani K. Singal<br />

282<br />

Effect of Beta-Blockers on Survival in Patients with Cirrhosis<br />

and Ascites: A Systematic Review and Meta-analysis<br />

Sakkarin Chirapongsathorn 1,2 , Nelson Valentin 1 , Fares Alahdab<br />

3,4 , Chayakrit Krittanawong 5 , Patricia J. Erwin 6 , Mohammad<br />

H. Murad 3,7 , Patrick S. Kamath 1 ; 1 Gastroenterology and Hepatology,<br />

Mayo Clinic, Rochester, Rochester, MN; 2 Gastroenterology,<br />

Phramongkutklao Hospital and College of Medicine, Royal Thai<br />

Army, Bangkok, Thailand; 3 Robert D and Patricia E Kern Center<br />

for the Science of Health Care Delivery, Mayo Clinic, Rochester,<br />

Rochester, MN; 4 Knowledge and Evaluation Research Unit, Mayo<br />

Clinic, Rochester, Rochester, MN; 5 Cardiovascular Disease, Mayo<br />

Clinic, Rochester, Rochester, MN; 6 Mayo Clinic Libraries, Mayo<br />

Clinic, Rochester, Rochester, MN; 7 Preventive, Occupational and<br />

Aerospace Medicine, Mayo Clinic, Rochester, Rochester, MN<br />

Backgrounds: Recent <strong>studies</strong> have suggested that non-selective<br />

beta-blockers (NSBBs) are associated with negative impact<br />

on survival in patients with cirrhosis and refractory ascites.<br />

However, other <strong>studies</strong> showed contradictory findings and suggested<br />

that NSBBs are beneficial in these patients. We performed<br />

a systematic review and meta-analysis to evaluate the<br />

effect of NSBBs on all-cause mortality. Methods: We conducted<br />

a comprehensive search of MEDLINE, Embase, Web of Science<br />

and Scopus databases through January 2015 and manually<br />

reviewed the literature. Attempts were made to contact<br />

the corresponding authors of the relevant <strong>studies</strong> for additional<br />

information when needed. Trial-specific risk ratios (RRs) were<br />

calculated and pooled using random-effect model meta-analysis.<br />

Between-study heterogeneity was assessed using the I 2<br />

statistic. The quality assessment of included <strong>studies</strong> and publication<br />

bias were assessed. Result: We included 4 randomized<br />

control trials and 8 observational <strong>studies</strong> in which 1,206 deaths<br />

were reported in 2,486 patients with ascites. NSBBs users did<br />

not have an increase in all-cause mortality compared to NSBBs<br />

nonusers with overall ascites (RR, 0.94; 95% CI, 0.6-1.46; P<br />

= 0.77); non-refractory ascites (RR, 0.97; 95% CI, 0.45-2.09)<br />

or refractory ascites (RR, 0.86; 95% CI: 0.47-1.57; P = 0.63).<br />

Results were similar in RCTs and observational <strong>studies</strong>. Use of<br />

NSBBs was not associated with increased mortality at 6, 12,<br />

Disclosures:<br />

Patrick S. Kamath - Advisory Committees or Review Panels: Sequana Medical<br />

The following authors have nothing to disclose: Sakkarin Chirapongsathorn,<br />

Nelson Valentin, Fares Alahdab, Chayakrit Krittanawong, Patricia J. Erwin,<br />

Mohammad H. Murad<br />

283<br />

Increasing incidence and cost, but decreasing mortality<br />

in patients with hepatorenal syndrome: a study of the<br />

National Inpatient Sample 2005-2011<br />

Albert Do 1 , Ghideon Ezaz 2 ; 1 Internal Medicine, Yale-New Haven<br />

Hospital, New Haven, CT; 2 Internal Medicine, Beth Israel Deaconess<br />

Medical Center, Boston, MA<br />

Background: Hepatorenal syndrome (HRS) is significant in<br />

patients with cirrhosis, carrying a high morbidity and mortality<br />

risk. However, its burden on inpatient hospital care presently<br />

is unclear. We report the incidence, costs, and mortality<br />

trends of HRS in the American medical inpatient setting. Materials<br />

and Methods: The Nationwide Inpatient Sample contains<br />

discharge-level inpatient hospitalizations comprising 20% of<br />

non-government hospitals in the United States. We determined<br />

incidence rates, mortality rates, hospital length of stay, and<br />

hospital costs (adjusted to 2011 dollar terms to adjust for inflation)<br />

from 2005 to 2011 for patients with HRS (ICD-9 code<br />

572.4). Results: 153,057 cases of HRS were identified during<br />

2005-2011, comprising a cohort with mean age 57.6 years,<br />

primarily males (64.1%) of white race (55.9%), with public<br />

insurance payers (58.1%), and hospitalized at a teaching hospital<br />

(54.9%). Table 1 summarizes HRS-associated trends in<br />

incidence, mortality and cost, showing increased disease incidence.<br />

Overall hospital mortality was 34.4%, with decreasing<br />

mortality (43.8% in 2005 to 31.2% in 2011). $16.3 billion<br />

was spent in this time, with an annual expenditure increase<br />

from $1.4 billion to $3.5 billion. However, hospital length<br />

of stay did not change during this time period (range 10.1 to<br />

11.9 days). 5,268 patients (3.4% of all patients) received a<br />

liver transplant during their hospital stay. Conclusions: From<br />

2005 to 2011, the incidence and costs of HRS have increased.

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