None listed
Conditions
Brief summary
This study will investigate the proportion of adults patients who undergo liver transplantation who receive an ultra massive transfusion. Ultra-Massive Transfusion is a relatively new term that has generally been accepted to describe the transfusion of >20 units of packed red blood cells in 24 hours. There is a paucity of literature on ultra massive transfusion, which has almost exclusively been studied in the context of trauma surgery, where it is associated poorer postoperative outcomes and increased mortality. This retrospective single centre study will use electronic medical records from the Austin Health database from 1st Jan 2019 to to 1st January 2023. We will evaluate the outcomes and complications in patients undergoing liver transplant surgery who receive ultra-massive transfusion. These results may be used to aid prognostication of post-operative liver transplant patients, as well as identify, and therefore modify, factors that may predispose patients to poorer post-operative outcomes, ultimately aiming to reduce overall morbidity and mortality in this patient cohort.
Interventions
This study will use patient data from a single-centre to investigate the association of ultra-massive transfusion and in-hospital complications in adult patients undergoing liver transplantation from 1 January 2019 to 1 January 2023. Ultra-Massive Transfusion is a relatively new term that has generally been accepted to describe the transfusion of >20 units of packed red blood cells (RBC) in 24 hours. Using routinely collected in-hospital data from the patients electronic medical records, this study will identify the proportion of adult patients who undergo liver transplantation who receive an ultra-massive transfusion. Ultra-massive fluid transfusion will defined a priori as a total transfusion > 20 liters of crystalloids, colloids, blood, and coagulation factors adminsitered intraoperatively and within 24-hours post surgery. Pre-operative risk factors for necessitating ultra-massive transfusion will be investigated. Secondary aims will investigate the relationship between the amount of pack red blood cells transfused and postoperative complications until hospital discharge. Mortality will be collected until 3 years post transplant. Finally, we will evaluate the effects of the co-transfused fresh frozen plasma to packed red blood cells ratio on postoperative complications. and mortality up until 3 years post-transplant.
Sponsors
Eligibility
Inclusion criteria
Inclusion Criteria: 1. Adult patient 2. Undergoing liver transplantation surgery 3. Patient receives ultra-massive transfusion
Exclusion criteria
1. Paediatric patients