TY - JOUR
T1 - Factors XI and XII in extracorporeal membrane oxygenation
T2 - longitudinal profile in children
AU - Drop, Joppe
AU - Letunica, Natasha
AU - Van Den Helm, Suelyn
AU - Heleen van Ommen, C.
AU - Wildschut, Enno
AU - de Hoog, Matthijs
AU - van Rosmalen, Joost
AU - Barton, Rebecca
AU - Yaw, Hui Ping
AU - Newall, Fiona
AU - Horton, Stephen B.
AU - Chiletti, Roberto
AU - Johansen, Amy
AU - Best, Derek
AU - McKittrick, Joanne
AU - Butt, Warwick
AU - d'Udekem, Yves
AU - MacLaren, Graeme
AU - Linden, Matthew D.
AU - Ignjatovic, Vera
AU - Attard, Chantal
AU - Monagle, Paul
N1 - Funding Information:
The authors thank the participants and their families for participating in this study and the Royal Children's Hospital PICU Extracorporeal Life Support Nurses for collecting samples, This research project was funded by the National Health and Medical Research Council (1129317). J.D. N.L. S.H. C.A. J.R. and P.M. conceived and designed the study. J.D. N.L. S.H. C.O. E.W. M.H. J.R. R.B. H.Y. F.N. S.H. R.C. A.J. D.B. J.M. W.B. Y.U. G.M. M.L. V.I. C.A. and P.M performed analysis and interpretation of data and critical writing and revision of the intellectual content and gave final approval of the version to be published. The authors have no competing interests to disclose.
Funding Information:
This research project was funded by the National Health and Medical Research Council (1129317).
Publisher Copyright:
© 2023 The Authors
PY - 2023/11
Y1 - 2023/11
N2 - 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.
AB - 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.
KW - extracorporeal membrane oxygenation
KW - factor XI
KW - factor XII
KW - infant
KW - newborn
UR - http://www.scopus.com/inward/record.url?scp=85179053672&partnerID=8YFLogxK
U2 - 10.1016/j.rpth.2023.102252
DO - 10.1016/j.rpth.2023.102252
M3 - Article
C2 - 38193071
AN - SCOPUS:85179053672
SN - 2475-0379
VL - 7
JO - Research and Practice in Thrombosis and Haemostasis
JF - Research and Practice in Thrombosis and Haemostasis
IS - 8
M1 - 102252
ER -