Publications by authors named "Moira O'Meara"

Background: Children with acute liver failure (ALF) who meet the criteria are eligible for super-urgent transplantation, whereas children with end-stage chronic liver disease (ESCLD) are usually transplanted electively. Pediatric liver trans plantation (PLT) in ALF and ESCLD settings has been well described in the literature, but there are no studies comparing the outcomes in these two groups.

Aim: To determine if there is a difference in post-operative complications and survival outcomes between ALF and ESCLD in PLT.

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Article Synopsis
  • - The study investigates factors affecting post-transplant survival in pediatric liver transplant (PLT) patients over time, focusing on data from 2000 to 2019 at a single transplant unit.
  • - Key findings reveal that recipient age, weight, height, and transplant category significantly influence patient survival, with invasive ventilation noted as a critical factor for those transplanted after 2005.
  • - The research highlights that technical advancements and learning curves have positively impacted patient outcomes, suggesting a revision of the belief that smaller candidates have worse survival rates.
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Background: Immediate tracheal extubation of selected adult patients after orthotopic liver transplant (OLT) is common practice. We hypothesized that selected children may be safely extubated immediately after OLT and avoid potentially deleterious effects of artificial ventilation and sedation.

Methods: After June 2002, we chose immediate extubation unless a specific contraindication was identified.

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Background: Thromboelastography (TEG) is an established way of monitoring the coagulation status of children and adults requiring blood products during surgery. Serial measurements are performed using a nearside machine and blood product prescription may be titrated against changes in TEG. There may also be useful applications when the patient is remote from the TEG machine but these are limited because TEG is usually performed on fresh native whole blood within 6 min of venepuncture.

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Autoimmune polyglandular syndrome type 1 (APS-1) is an autosomal-recessive condition characterized by hypoparathyroidism, autoimmune Addison's disease, and chronic mucocutaneous candidiasis. Autoimmune hepatitis develops in 10-20% of affected patients and has a variable course ranging from asymptomatic chronic liver disease to lethal fulminant hepatic failure. Liver transplantation has been documented previously in only two patients.

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