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Archives of Disease in Childhood logoLink to Archives of Disease in Childhood
. 1994 Oct;71(4):349–352. doi: 10.1136/adc.71.4.349

Liver transplantation for hepatic cirrhosis in cystic fibrosis.

G Noble-Jamieson 1, J Valente 1, N D Barnes 1, P J Friend 1, N V Jamieson 1, A Rasmussen 1, R Y Calne 1
PMCID: PMC1030018  PMID: 7979532

Abstract

Five children with cystic fibrosis complicated by hepatic cirrhosis received liver grafts. They all had portal hypertension with varices and three had variceal bleeding; respiratory function was only moderately impaired, but four were colonised with pseudomonas and one with aspergillus. Liver transplantation was well tolerated and there was no increase in respiratory or other early postoperative complications. Four of the children were fully well from 14 to 35 months after transplantation; the most recently transplanted had problems from a biliary stricture. In spite of the need for immunosuppression there was no increase in infection and respiratory function improved or remained stable. Once the children were stabilised after transplantation their nutrition and general health were greatly improved.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

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