Introduction: The pancreatic disorders (PDs) acute pancreatitis (AP), chronic pancreatitis (CP) and pancreatic ductal adenocarcinoma (PDAC) are the leading causes of gastrointestinal hospital admissions and cancer death. PDs have a higher incidence and prevalence in blacks but there is a paucity of data on the impact of PD on other racial groups. Our aim is to further determine racial differences in health care utilization and outcomes of PD in the United States. Methods: Using the Nationwide Inpatient Sample, adult patients (≥18 years) with a primary discharge diagnosis of AP, CP or PDAC from 2011 were identified and studied. Results: A total of 340,231 discharges were identified with a primary diagnosis of AP (83%), CP (5%), or PDAC (12%). Racial distribution demonstrated that 65.5% were white (WH), 16.9% black (AA), 12.2% Hispanic (H), 1.7% Asian/Pacific Islander (AP), 0.7% Native American (NA) and 2.9% other race. Demographics were significantly different between populations. The majority of AA and NA populations were in the lowest income quartile. The majority of AP populations were in the top 2 income quartiles. On univariate analysis, NAs had the lowest mortality rate (0.5%; p<0.001), length of stay (LOS; 2.8 days; p<0.001) and total hospital charge ($15,646; p<0.001). APs had the highest total hospital charge ($32,836; p<0.001). On multivariate analysis (Table 1), compared to WHs, LOS was shorter for AAs, Hs, and NAs. Compared to WHs, hospital charges were less in AAs but higher in H and AP populations.Table 1: Multivariate Analysis of Race and Pancreatic Disease Health Care Utilization and OutcomesConclusion: Of the races evaluated, the immigrant minorities, Hispanic, and Asian/Pacific Islanders have different income demographics and length of stay yet have higher total hospital charges compared to Blacks, Native Americans, and Whites in pancreatic disorders. Our study demonstrates that significant pancreatic disorder health care utilization and outcome differences exist within minority groups that require additional investigation.
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