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. Author manuscript; available in PMC: 2017 May 12.
Published in final edited form as: Pediatr Transplant. 2011 Nov 17;16(1):41–49. doi: 10.1111/j.1399-3046.2011.01598.x

Table 1.

Pediatric liver transplant recipients by weight status at transplant

Pediatric liver transplant recipients by weight status at transplant, children 6 months–2 yr at transplant
Underweight (weight-for-length <5th percentile) Normal weight (weight-for-length 5th–95th percentile) Overweight (weight-for-length >95th percentile) Total p-value (χ2 or Kruskal–Wallis)





Weight status at transplant n (%) n (%) n (%) n
Number 533 (17) 2119 (69) 441 (14) 3093
Female 287 (17) 1193 (70) 221 (13) 1701 0.05
Male 246 (18) 926 (67) 220 (16) 1392
Age at transplant in months (median, IQR) 10 (7–13) 11 (8–16) 12 (8–18) 11 (8–16) 0.0001
Primary diagnosis
 Biliary atresia 369 (20) 1312 (70) 204 (11) 1885 <0.0005
 Metabolic disease* 31 (13) 166 (68) 47 (19) 244
 Acute liver failure 10 (6) 122 (71) 39 (23) 171
 Tumor 15 (14) 79 (72) 15 (14) 109
 Other cholestatic conditions 72 (14) 318 (63) 111 (22) 501
 Other 36 (20) 122 (67) 25 (14) 183
Race/ethnicity
 White 282 (17) 1128 (68) 238 (14) 1648 0.027
 Black 112 (20) 380 (68) 63 (11) 555
 Hispanic 85 (14) 432 (70) 103 (17) 620
 Asian 32 (20) 102 (64 26 (16) 160
 Other§ 22 (20) 77 (70) 11 (10) 110
Ethnicity
 Hispanic 95 (15) 446 (69) 105 (16) 646 0.069
 Non-Hispanic 438 (18) 1673 (68) 336 (14) 2447
Months of follow-up (median, range)
Includes 2380 patients
68 (24–119) 67 (23–125) 67 (23–112) 67 (24–121) 0.8331

Pediatric liver transplant recipients by weight status at transplant, children 2–20 yr at transplant

Underweight (BMI <5th percentile) Normal weight (BMI 5th–85th percentile) Overweight (BMI 85th–95th percentile) Obese (BMI >95th percentile) Total p-value (χ2 or Kruskal–Wallis)






Weight status at transplant n (%) n (%) n (%) n (%) n

Number 321 (7) 2962 (64 751 (16) 624 (13) 4658
Female 121 (5) 1469 (61) 478 (20) 333 (14) 2401 <0.0005
Male 200 (9) 1493 (66) 273 (12) 291 (13) 2257
Age at transplant, yr (median, IQR) 12.3 (4.6–16.3) 11.6 (6.7–16) 10 (5.2–15.7) 5.7 (3.3–13.3) 10.7 (5.3–15.8) 0.0001
Primary diagnosis
 Biliary atresia 42 (5) 505 (63) 128 (16) 132 (16) 807 <0.0005
 Metabolic disease* 54 (6) 571 (67) 126 (15) 105 (12) 856
 Acute liver failure 51 (6) 529 (59) 175 (20) 138 (16) 893
 Tumor 27 (9) 200 (67) 30 (10) 42 (14) 299
 Other cholestatic conditions 74 (10) 492 (67) 85 (12) 80 (11) 731
 Other 73 (7) 665 (62) 207 (19) 127 (12) 1072
Race/ethnicity
 White 190 (7) 1855 (66) 418 (15) 336 (12) 2799 <0.0005
 Black 50 (6) 461 (58) 138 (17) 145 (18) 794
 Hispanic 55 (7) 479 (59) 153 (19) 123 (15) 810
 Asian 20 (13) 107 (68) 19 (12) 11 (7) 157
 Other§ 6 (6) 60 (61) 23 (24) 9 (9) 98
Ethnicity
 Non-Hispanic 264 (7) 2472 (65) 594 (16) 499 (13) 3829 0.016
 Hispanic 57 (7) 490 (59) 157 (19) 125 (15) 829
Months of follow-up (median, range)
Includes 3621 patients
63 (27–119) 69 (25–121) 66 (24–119) 71 (24–137) 69 (25–122) 0.5914
*

Metabolic disease includes: alpha-1-antitrypsin deficiency, Crigler–Najjar syndrome, cystic fibrosis, glycogen storage disease, inborn errors in bile acid metabolism, neonatal hemochromatosis, primary hyperoxaluria, tyrosinemia, urea cycle defects, and Wilson’s disease.

Other cholestatic conditions includes: Alagille syndrome, Byler disease, progressive intrahepatic cholestatic syndromes, total parenteral nutrition cholestasis, sclerosing cholangitis, and idiopathic cholestasis.

Other diagnosis includes: congenital hepatic fibrosis, Budd–Chiari syndrome, autoimmune hepatitis cirrhosis, drug toxicity, hepatitis C cirrhosis, and unknown cirrhosis.

§

Other race includes: Native American/Alaskan, Pacific Islander/Hawaiian, multiracial, and unknown.