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Liver and lung transplantation in cystic fibrosis: an adult cystic fibrosis centre's experience.
Sivam, S; Al-Hindawi, Y; Di Michiel, J; Moriarty, C; Spratt, P; Jansz, P; Malouf, M; Plit, M; Pleass, H; Havryk, A; Bowen, D; Haber, P; Glanville, A R; Bye, P T P.
Affiliation
  • Sivam S; Department of Respiratory and Sleep Medicine, Royal Prince Alfred Hospital, Camperdown, New South Wales, Australia.
  • Al-Hindawi Y; Sydney Medical School, University of Sydney, Sydney, New South Wales, Australia.
  • Di Michiel J; Department of Respiratory and Sleep Medicine, Royal Prince Alfred Hospital, Camperdown, New South Wales, Australia.
  • Moriarty C; Sydney Medical School, University of Sydney, Sydney, New South Wales, Australia.
  • Spratt P; Department of Respiratory and Sleep Medicine, Royal Prince Alfred Hospital, Camperdown, New South Wales, Australia.
  • Jansz P; Sydney Medical School, University of Sydney, Sydney, New South Wales, Australia.
  • Malouf M; Department of Respiratory and Sleep Medicine, Royal Prince Alfred Hospital, Camperdown, New South Wales, Australia.
  • Plit M; Sydney Medical School, University of Sydney, Sydney, New South Wales, Australia.
  • Pleass H; Lung Transplantation Unit, St Vincent's Hospital, Sydney, New South Wales, Australia.
  • Havryk A; Lung Transplantation Unit, St Vincent's Hospital, Sydney, New South Wales, Australia.
  • Bowen D; Lung Transplantation Unit, St Vincent's Hospital, Sydney, New South Wales, Australia.
  • Haber P; Lung Transplantation Unit, St Vincent's Hospital, Sydney, New South Wales, Australia.
  • Glanville AR; Sydney Medical School, University of Sydney, Sydney, New South Wales, Australia.
  • Bye PT; Liver Transplant Unit, Royal Prince Alfred Hospital, Camperdown, New South Wales, Australia.
Intern Med J ; 46(7): 852-4, 2016 Jul.
Article in En | MEDLINE | ID: mdl-27405894
ABSTRACT
Liver disease develops in one-third of patients with cystic fibrosis (CF). It is rare for liver disease to have its onset after 20 years of age. Lung disease, however, is usually more severe in adulthood. A retrospective analysis was performed on nine patients. Three patients required lung transplantation approximately a decade after liver transplant, and another underwent combined liver and lung transplants. Four additional patients with liver transplants are awaiting assessment for lung transplants. One patient is awaiting combined liver and lung transplants. With increased survival in CF, several patients may require more than single organ transplantation.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Liver Transplantation / Lung Transplantation / Cystic Fibrosis / Liver Diseases Type of study: Observational_studies / Risk_factors_studies Limits: Adolescent / Adult / Child / Female / Humans / Male Country/Region as subject: Oceania Language: En Journal: Intern Med J Journal subject: MEDICINA INTERNA Year: 2016 Document type: Article Affiliation country: Australia

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Liver Transplantation / Lung Transplantation / Cystic Fibrosis / Liver Diseases Type of study: Observational_studies / Risk_factors_studies Limits: Adolescent / Adult / Child / Female / Humans / Male Country/Region as subject: Oceania Language: En Journal: Intern Med J Journal subject: MEDICINA INTERNA Year: 2016 Document type: Article Affiliation country: Australia