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. Author manuscript; available in PMC: 2021 May 1.
Published in final edited form as: Hepatology. 2020 Jan 24;71(5):1802–1812. doi: 10.1002/hep.30926

TABLE 2.

Recipient Characteristics at Time of LT

Recipient Characteristic Resident (n = 43,026) Presumed Unauthorized Immigrants (n = 166) P
Age (years) 58 (51–63) 49 (39–58) <0.001
Male 28,336 (66) 100 (60) 0.13
Medicaid as Payer of LT 6,035 (14) 85 (51) <0.001
Private Insurance as Payer of LT 22,543 (52) 53 (32) <0.001
Race/Ethnicity
 Caucasian 30,678 (71) 29 (18) <0.001
 Black 3,889 (9) 10 (6)
 Hispanic 6,026 (14) 98 (59)
 Asian 1,789 (4) 26 (16)
 Other 644 (2) 3 (2)
Highest Education Level
 High School or Below 19,694 (46) 102 (61) <0.001
 College or Above 21,576 (50) 54 (32)
 Unknown 1,756 (4) 10 (6)
Body Mass Index 28.5 (25.0–32.7) 26.7 (23.7–30.2) 0.001
Diabetes* 12,138 (28) 33 (20) 0.05
Renal Replacement Therapy 6,621 (15) 51 (31) <0.001
Portal Vein Thrombosis at LT 5,798 (14) 22 (13) 0.93
MELD Score at LT 21 (14–31) 29 (20–37) <0.001
Simultaneous Liver Kidney Recipient 3,710 (9) 22 (13) 0.03
Living Donor 1,723 (4) 5 (3) 0.51
Days on Waitlist 108 (20–307) 56 (7–270) <0.001
indication for LT Resident (n = 43,026) Presumed Unauthorized immigrants (n = 166) P
Alcohol 10,568 (25) 38 (23) 0.62
Hepatitis C 9,764 (23) 22 (13) 0.004
Hepatitis B 977 (2.3) 16 (10) <0.001
Nonalcoholic Fatty Liver Disease or Cryptogenic 8,083 (19) 26 (16) 0.30
Autoimmune§ 4,167 (9.7) 18 (11) 0.61
Other 3,103 (7.2) 20 (12) 0.02
Hepatocellular Carcinoma 14,703 (34) 42 (25) 0.2

Note: Data are presented as n (%) or median (IQR).

*

For diabetes status, 75 (0.2%) missing values among residents, 0 (0%) missing values among presumed unauthorized immigrants.

For portal vein thrombosis at LT, 237 (0.6%) missing values among residents, 0 (0%) missing values among presumed unauthorized immigrants.

The indication for transplant was categorized as hepatitis C, hepatitis B, alcohol-associated liver disease, nonalcoholic fatty liver disease, cryptogenic, autoimmune (includes autoimmune hepatitis, primary biliary cholangitis, primary sclerosing cholangitis), and other (e.g., acute liver failure, drug-induced liver injury, Wilson’s, amyloidosis, glycogen storage diseases) based on primary listing diagnosis. The diagnosis of HCC was based on any primary or secondary diagnosis of HCC at listing or LT.

§

Includes autoimmune hepatitis, primary sclerosing cholangitis, and primary biliary cholangitis.