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Poor Access to Liver Transplantation and Survival of Children With Acute Liver Failure, Acute-on-chronic Liver Failure or Chronic Liver Disease.
Estrada-Arce, Emma Valeria; Aguila-Cano, Renata; Lona-Reyes, Juan Carlos; Flores-Fong, Laura Esther; Rivera-Chávez, Elva.
Afiliação
  • Estrada-Arce EV; From the Pediatric Gastroenterology Service, Hospital Civil de Guadalajara "Dr. Juan I. Menchaca" Salvador Quevedo y Zubieta, Guadalajara, Jalisco, México.
  • Aguila-Cano R; Universidad de Guadalajara, University Center for Health Sciences.
  • Lona-Reyes JC; From the Pediatric Gastroenterology Service, Hospital Civil de Guadalajara "Dr. Juan I. Menchaca" Salvador Quevedo y Zubieta, Guadalajara, Jalisco, México.
  • Flores-Fong LE; Universidad de Guadalajara, University Center for Health Sciences.
  • Rivera-Chávez E; Pediatric Infectology Service, Hospital Civil de Guadalajara "Dr. Juan I. Menchaca".
JPGN Rep ; 4(3): e318, 2023 Aug.
Article em En | MEDLINE | ID: mdl-37600617
We describe the survival of children with acute liver failure (ALF), chronic liver disease (CLD), or acute-on-chronic liver failure (ACLF) with poor access to liver transplantation (LT). A retrospective cohort study of 42 patients <18 years of age was conducted in the Hospital Civil de Guadalajara "Dr. Juan I. Menchaca". The median age was 76 months; 57.1% were female, 40.5% presented with ALF, 35.7% with CLD, and 23.8% with ACLF. Also, 38.1% (16/42) presented liver disease of unknown etiology. Death occurred in 45.2%; 14.3% were transferred to another hospital, and none received LT. Mortality in ALF, CLD, and ACLF was 76%, 0%, and 60%, respectively. In the survival analysis, within the first 20 months after diagnosis, the mortality rate was greater than 50% with ALF. The importance of having referral programs that perform liver transplantation is highlighted by the poor prognosis of the patients, despite conservative treatment.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Observational_studies Idioma: En Revista: JPGN Rep Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Observational_studies Idioma: En Revista: JPGN Rep Ano de publicação: 2023 Tipo de documento: Article