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Factors XI and XII in extracorporeal membrane oxygenation: longitudinal profile in children.
Drop, Joppe; Letunica, Natasha; Van Den Helm, Suelyn; Heleen van Ommen, C; Wildschut, Enno; de Hoog, Matthijs; van Rosmalen, Joost; Barton, Rebecca; Yaw, Hui Ping; Newall, Fiona; Horton, Stephen B; Chiletti, Roberto; Johansen, Amy; Best, Derek; McKittrick, Joanne; Butt, Warwick; d'Udekem, Yves; MacLaren, Graeme; Linden, Matthew D; Ignjatovic, Vera; Attard, Chantal; Monagle, Paul.
Affiliation
  • Drop J; Department of Paediatrics, Division of Paediatric Hematology, Erasmus Medical Centre-Sophia Children's Hospital, Rotterdam, South Holland, The Netherlands.
  • Letunica N; Department of Paediatrics, Division of Paediatric Intensive Care and Paediatric Surgery, Erasmus Medical Centre - Sophia Children's Hospital, Rotterdam, South Holland, The Netherlands.
  • Van Den Helm S; Haematology Research, Murdoch Children's Research Institute, Melbourne, Victoria, Australia.
  • Heleen van Ommen C; Haematology Research, Murdoch Children's Research Institute, Melbourne, Victoria, Australia.
  • Wildschut E; Haematology Research, Murdoch Children's Research Institute, Melbourne, Victoria, Australia.
  • de Hoog M; Department of Paediatrics, The University of Melbourne, Melbourne, Victoria, Australia.
  • van Rosmalen J; Department of Paediatrics, Division of Paediatric Hematology, Erasmus Medical Centre-Sophia Children's Hospital, Rotterdam, South Holland, The Netherlands.
  • Barton R; Department of Paediatrics, Division of Paediatric Intensive Care and Paediatric Surgery, Erasmus Medical Centre - Sophia Children's Hospital, Rotterdam, South Holland, The Netherlands.
  • Yaw HP; Department of Paediatrics, Division of Paediatric Intensive Care and Paediatric Surgery, Erasmus Medical Centre - Sophia Children's Hospital, Rotterdam, South Holland, The Netherlands.
  • Newall F; Department of Biostatistics, Erasmus University Medical Center, Rotterdam, South Holland, The Netherlands.
  • Horton SB; Department of Epidemiology, Erasmus University Medical Center, University Medical Center Rotterdam, Rotterdam, South Holland, The Netherlands.
  • Chiletti R; Haematology Research, Murdoch Children's Research Institute, Melbourne, Victoria, Australia.
  • Johansen A; Department of Paediatrics, The University of Melbourne, Melbourne, Victoria, Australia.
  • Best D; Department of Clinical Haematology, The Royal Children's Hospital, Melbourne, Victoria, Australia.
  • McKittrick J; Haematology Research, Murdoch Children's Research Institute, Melbourne, Victoria, Australia.
  • Butt W; Haematology Research, Murdoch Children's Research Institute, Melbourne, Victoria, Australia.
  • d'Udekem Y; Department of Paediatrics, The University of Melbourne, Melbourne, Victoria, Australia.
  • MacLaren G; Department of Clinical Haematology, The Royal Children's Hospital, Melbourne, Victoria, Australia.
  • Linden MD; Department of Paediatrics, The University of Melbourne, Melbourne, Victoria, Australia.
  • Ignjatovic V; Department of Cardiac Surgery, The Royal Children's Hospital, Melbourne, Victoria, Australia.
  • Attard C; Department of Intensive Care, The Royal Children's Hospital, Melbourne, Victoria, Australia.
  • Monagle P; Paediatric Intensive Care Research Group, Murdoch Children's Research Institute, Melbourne, Victoria, Australia.
Res Pract Thromb Haemost ; 7(8): 102252, 2023 Nov.
Article in En | MEDLINE | ID: mdl-38193071
ABSTRACT

Background:

Extracorporeal membrane oxygenation (ECMO) is used in children with cardiopulmonary failure. While the majority of ECMO centers use unfractionated heparin, other anticoagulants, including factor XI and factor XII inhibitors are emerging, which may prove suitable for ECMO patients. However, before these anticoagulants can be applied in these patients, baseline data of FXI and FXII changes need to be acquired.

Objectives:

This study aimed to describe the longitudinal profile of FXI and FXII antigenic levels and function before, during, and after ECMO in children.

Methods:

This is a prospective observational study in neonatal and pediatric patients with ECMO (<18 years). All patients with venoarterial ECMO and with sufficient plasma volume collected before ECMO, on day 1 and day 3, and 24 hours postdecannulation were included. Antigenic levels and functional activity of FXI and FXII were determined in these samples. Longitudinal profiles of these values were created using a linear mixed model.

Results:

Sixteen patients were included in this study. Mean FXI and FXII antigenic levels (U/mL) changed from 7.9 and 53.2 before ECMO to 6.0 and 34.5 on day 3 and they recovered to 8.8 and 39.4, respectively, after stopping ECMO. Function (%) of FXI and FXII decreased from 59.1 and 59.0 to 49.0 and 50.7 on day 3 and recovered to 66.0 and 54.4, respectively.

Conclusion:

This study provides the first insights into changes of the contact pathway in children undergoing ECMO. FXI and FXII antigen and function change during ECMO. Results from this study can be used as starting point for future contact pathway anticoagulant studies in pediatric patients with ECMO.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Observational_studies / Prognostic_studies Language: En Journal: Res Pract Thromb Haemost Year: 2023 Document type: Article Affiliation country: Netherlands Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Observational_studies / Prognostic_studies Language: En Journal: Res Pract Thromb Haemost Year: 2023 Document type: Article Affiliation country: Netherlands Country of publication: United States