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. 2009 May;11(3):252–257. doi: 10.1111/j.1477-2574.2009.00047.x

Table 1.

Demographics, diagnoses, types of portosystemic shunt and outcomes in children with intrinsic liver disease

Patient Sex Diagnosis Age at shunt, years Type of shunt Follow-up, years Outcome
1 M Biliary atresia 2.8 DSRS 1.2 Patent shunt
2 M Biliary atresia 3.9 DSRS 0.2 Patent shunt
3 F Biliary atresia 5.5 DSRS 0.2 Patent shunt
4 M Biliary atresia 8.8 Mesocaval 14.1 Liver transplant
5 M Congenital hepatic fibrosis 16.7 DSRS 11.7 Liver transplant
6 M Congenital hepatic fibrosis 6.4 DSRS 1.1 Patent shunt
7 M Cryptogenic cirrhosis 18.0 DSRS 5.8 Patent shunt
8 F Cryptogenic cirrhosis 22.1 DSRS 3.6 Patent shunt
9 F Autoimmune hepatitis 18.6 DSRS 6.1 Death (non-adherence)
10 M Wilson's disease 10.7 DSRS 0.3 Patent shunt
11 F Cystic fibrosis 12.9 DSRS 4.7 Patent shunt
12 M Lymphoma 17.9 Proximal splenorenal 0.2 Death secondary to lymphoma

M, male; F, female; DSRS, distal splenorenal shunt