Observational Study
Copyright ©The Author(s) 2015.
World J Gastroenterol. Aug 28, 2015; 21(32): 9638-9647
Published online Aug 28, 2015. doi: 10.3748/wjg.v21.i32.9638
Figure 1
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Figure 1 Geographical distribution of children with biliary atresia (n = 188).
Figure 2
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Figure 2 Caseload of children with biliary atresia from 2006 to 2012 (n = 188).
Figure 3
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Figure 3 Flowchart providing outcomes of children with biliary atresia. BA: Biliary atresia; KP: Kasai procedure; LDLT: Living donor liver transplantation; LT: Liver transplantation; SLT: Split liver transplantation; WLT: Whole liver transplantation.
Figure 4
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Figure 4 Patient and graft survival after liver transplantation for biliary atresia (n = 122). A: Comparison between patients using different donor types (P = 0.286); B: Comparison between patients with or without a prior Kasai procedure (KP) (P = 0.701); C: Comparison between patients in stages I and II (P = 0.358); D: Comparison between the two stages within the living donor liver transplantation (LDLT) group (P = 0.107). NA: Not available.