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474A AASLD ABSTRACTS HEPATOLOGY, October, 2015<br />

are needed. Our process demonstrated the possibility that a<br />

reduction in readmission rates could be achieved with a multifaceted<br />

process that incorporates nurse directed education with<br />

performance feedback and telephonic symptom assessment,<br />

coupled with rapid provider communications. A larger study<br />

will be required to confirm these findings.<br />

Disclosures:<br />

Simona Rossi - Consulting: BMS; Speaking and Teaching: gilead<br />

Eyob L. Feyssa - Advisory Committees or Review Panels: Gilead; Grant/Research<br />

Support: J&J, BMS, Abbot, Salix, Conatus, Cumberland, Merck; Speaking and<br />

Teaching: Gilead, BMS, Abbvie<br />

The following authors have nothing to disclose: Manisha Verma, Catherine Reynolds,<br />

Dee Morrison, June Smith, Cindy Mcglone, Victor J. Navarro<br />

531<br />

Thirty-day Readmission Following Liver Transplant in<br />

Medicare Beneficiaries – Incidence, Etiology, Outcomes,<br />

and Cost<br />

Lorna M. Dove 1 , Mary Jo Braid-Forbes 2 , Kevin F. Forbes 2 , Daniel<br />

J. Lerner 3 ; 1 Internal Medicine, Columbia University College of<br />

Physicians and Surgeons, New York, NY; 2 Braide-Forbes Health<br />

Research, Silver Spring, MD; 3 Health Sciences West, Scarsdale,<br />

NY<br />

BACKGROUND: Readmission of Medicare beneficiaries (MBs)<br />

within 30 days of hospitalization (30dRA) is considered a<br />

quality indicator, and it increases the total amount of annual<br />

Medicare spending. In 2015 the Centers for Medicare and<br />

Medicaid Services (CMS) can reduce reimbursements by up to<br />

3% for hospitals with high 30dRA rates for specific conditions.<br />

More than one-third of liver transplant (LT) recipients in the US<br />

are MBs, but little is known about 30dRA following LT in this<br />

group. PURPOSE: The purpose of this study is to define the<br />

incidence, etiology, outcomes, and cost of 30dRA following<br />

LT in adult MBs. METHODS: A total of 1,359 adult Medicare<br />

fee-for-service beneficiaries who underwent LT and survived<br />

to discharge in 2011 were identified and used to define the<br />

incidence of 30dRA following LT, and the principal diagnoses,<br />

outcomes, patient characteristics, and inpatient costs associated<br />

with those 30dRA. RESULTS: The incidence of 30dRA<br />

following LT in MBs was 37%. This is substantially higher than<br />

published 30dRA rates for MBs following acute myocardial<br />

infarction (AMI), heart failure (HF), pneumonia, and coronary<br />

artery bypass grafting (CABG). The most common principal<br />

diagnoses for 30dRAs were complications of a device implant<br />

or graft (21.5%) or medical or surgical care (12.9%), fluid and<br />

electrolyte disorders (5.4%), septicemia (4.4%), and acute/<br />

unspecified renal failure (4.0%). The most common procedures<br />

at readmission were transfusion of blood products (11.7%),<br />

non-cardiac vascular catheterization (8.4%), and non-operating<br />

room GI procedures (8.2%). Factors associated with<br />

increased risk of readmission after risk adjustment were being<br />

Medicaid eligible (dual eligible) (OR 1.64, 95% CI [1.26-<br />

2.13]), and having renal failure at the time of transplantation<br />

(OR 1.44 95%CI [1.06-1.94]). The association of dual-eligibility<br />

with 30dRA is important because more than one-third<br />

of the MBs who underwent LT were dual-eligible, significantly<br />

more than in the general Medicare population. The mean cost<br />

of a 30dRA was $21,054. One year after hospitalization<br />

for LT, patients who had a 30dRA had significantly reduced<br />

survival (11.7% vs. 3.7%; P=0.01), and their total inpatient<br />

care costs were 34% higher, compared to patients without a<br />

30dRA ($252,985 vs. $189,352). CONCLUSIONS: In MBs,<br />

the 30dRA rate following LT was 37%, higher than reported<br />

for AMI, HF, pneumonia, or CABG. Complications were the<br />

most common cause for 30dRA. Patients with a 30dRA had<br />

decreased survival and increased inpatient costs at one year.<br />

Future research should focus on strategies to reduce complications<br />

from LT, and reduce 30dRA in patients at increased risk.<br />

Disclosures:<br />

The following authors have nothing to disclose: Lorna M. Dove, Mary Jo Braid-<br />

Forbes, Kevin F. Forbes, Daniel J. Lerner<br />

532<br />

Epidemiology and survival in patients with cirrhosis in a<br />

large commercial insurer database<br />

Steven J. Scaglione 1,3 , Leanne N. Metcalfe 2 , Stephanie Kliethermes<br />

3 , Rebecca Tsang 1 , Vik Goyal 4 , Allyce Caines 4 , Shaham<br />

Mumtaz 4 , Amy Luke 3 , Scott Cotler 1 ; 1 Hepatology, Loyola University<br />

Medical Center, Maywood, IL; 2 Enterprise Clinical Analytics,<br />

Health Care Services Corporation, Chicago, IL; 3 Preventive Medicine,<br />

Loyola University Medical Center, Maywood, IL; 4 Internal<br />

Medicine, Loyola University Medical Center, Maywood, IL<br />

Background: There are limited data regarding the epidemiology<br />

of cirrhosis in the general population (Scaglione, Volk,<br />

2014). We analyzed a large commercial insurance provider<br />

database to investigate the prevalence of cirrhosis, differences<br />

in survival in compensated versus decompensated cirrhosis,<br />

and differences in survival between NASH and HCV-related<br />

cirrhosis with and without diabetes. Methods: Retrospective<br />

matched case-control analysis estimating the prevalence in<br />

clinical-demographic, risk factors and survival associated with<br />

cirrhosis from Sept 2008-Aug 2013 by Health Care Services<br />

Corporation (HCSC), a commercial insurer providing healthcare<br />

coverage in 5 states. Cirrhosis was defined as ICD-9 code<br />

571.2, 571.5, or 571.6. The index date was the date of the<br />

first cirrhosis ICD-9-code occurring in the database after the<br />

first 6 months of continuous enrollment. Decompensated cirrhosis<br />

was defined as ICD-9 571.2, 571.5, or 571.6 AND a<br />

2nd diagnostic code for decompensation (any ICD-9: 070.44,<br />

070.71, 348.3x, 456.0, 456.1, 456.2x, 572.2, 572.3,<br />

572.4, 782.4, 789.59). Compensated cirrhosis is defined<br />

as those with ICD-9 571.2, 571.5, 571.6 and lacking ICD-9<br />

for decompensation as above. HCV Cirrhosis was defined by<br />

diagnostic codes for chronic HCV (ICD-9: 070.54 or 070.70)<br />

on at least two occasions a month or more apart. NAFLD<br />

was defined as by ICD-9 571.8 at any time in the absence<br />

of codes for other causes of liver disease. Results: During the<br />

study period, there were 18,202 persons with cirrhosis among<br />

3,478,093 enrollees, yielding a prevalence of 0.52%. Cirrhotics<br />

were older (55.6 vs 43.7,p

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