Department of Paediatrics, Division of Paediatric Hematology, Erasmus Medical Center Rotterdam - Sophia Children's Hospital, Rotterdam, the Netherlands; Department of Paediatrics, Division of Pediatric Intensive care and Pediatric surgery, Erasmus Medical Center Rotterdam - Sophia Children's Hospital, Rotterdam, the Netherlands.
Department of Paediatrics, Division of Pediatric Intensive care and Pediatric surgery, Erasmus Medical Center Rotterdam - Sophia Children's Hospital, Rotterdam, the Netherlands.
J Thromb Haemost. 2023 Dec;21(12):3383-3392. doi: 10.1016/j.jtha.2023.08.007. Epub 2023 Aug 12.
Extracorporeal membrane oxygenation (ECMO) provides cardiopulmonary support for children with severe cardiac and/or pulmonary failure. The incidence of bleeding complications during ECMO support is high. Acquired von Willebrand disease (AVWD) might contribute to the development of bleeding complications.
To study the incidence and longitudinal profile of AVWD during the first 14 days of ECMO support in children and to investigate the association between AVWD and bleeding complications.
This prospective observational study included pediatric patients (0-17 years) receiving ECMO. Blood was sampled prior to and after ECMO start, daily and 12 to 24 hours after stopping ECMO. von Willebrand factor (VWF) parameters and multimer patterns were determined. Clinical data were collected for each patient. AVWD was defined as loss of high-molecular weight multimers (ie, decreased compared with baseline) or a VWF:collagen binding/VWF: antigen (Ag) ratio or VWF:activity/VWF:Ag ratio below 0.7.
All of 50 (100%) patients developed AVWD during ECMO. The VWF:collagen binding /VWF:Ag ratio, VWF:activity/VWF:Ag ratio, and high-molecular weight multimers decreased during the initial days and recovered to baseline level within 24 hours after stopping ECMO. The incidence and longitudinal profile of AVWD were similar in patients with and without major bleeding complications.
Children receiving ECMO support commonly develop AVWD. AVWD develops rapidly after ECMO initiation and recovers quickly after ECMO cessation. Importantly, AVWD appears to be independent of major bleeding.
体外膜肺氧合(ECMO)为严重心肺衰竭的儿童提供心肺支持。在 ECMO 支持期间,出血并发症的发生率很高。获得性血管性血友病(AVWD)可能导致出血并发症的发生。
研究儿童在 ECMO 支持的前 14 天内发生 AVWD 的发生率和纵向特征,并探讨 AVWD 与出血并发症之间的关系。
这项前瞻性观察性研究纳入了接受 ECMO 的儿科患者(0-17 岁)。在 ECMO 开始前和开始后、每天以及停止 ECMO 后 12-24 小时采集血液样本。测定血管性血友病因子(VWF)参数和多聚体模式。为每位患者收集临床数据。AVWD 的定义为高分子量多聚体丢失(即与基线相比减少)或 VWF:胶原结合/VWF:抗原(Ag)比值或 VWF:活性/VWF:Ag 比值低于 0.7。
所有 50 例(100%)患者在 ECMO 期间均发生 AVWD。VWF:胶原结合/VWF:Ag 比值、VWF:活性/VWF:Ag 比值和高分子量多聚体在初始几天内下降,并在停止 ECMO 后 24 小时内恢复至基线水平。有和无重大出血并发症的患者的 AVWD 发生率和纵向特征相似。
接受 ECMO 支持的儿童通常会发生 AVWD。AVWD 在 ECMO 启动后迅速发展,并在 ECMO 停止后迅速恢复。重要的是,AVWD 似乎与重大出血无关。