Platelet transfusion stated practices among neonatal and paediatric veno-arterial extracorporeal membrane oxygenation providers: A survey.

IF 1.8 4区 医学 Q3 HEMATOLOGY
Vox Sanguinis Pub Date : 2025-03-17 DOI:10.1111/vox.70018
Trupti Ingle, Brian Simms, Jesse Bain, Melania M Bembea, Jill M Cholette, Madhuradhar Chegondi, Eva Cheung, Robert Niebler, Caroline Ozment, Matthew Paden, Ofer Schiller, Marianne E Nellis, Oliver Karam
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Abstract

Background and objectives: Extracorporeal membrane oxygenation (ECMO) provides cardiopulmonary support to over 4000 neonates and children annually worldwide. Although potentially lifesaving, ECMO carries bleeding and thromboembolic risks, often managed with platelet transfusions to maintain specific thresholds. Platelet transfusions themselves carry many risks. This survey aimed to describe stated prophylactic platelet transfusion practices among paediatric veno-arterial (VA)-ECMO providers and identify factors influencing transfusion decisions.

Materials and methods: This is a cross-sectional electronic survey of paediatric ECMO providers from 10 centres evaluating platelet transfusion thresholds based on six patient scenarios (non-bleeding, minimally bleeding and resolved bleeding in neonates and children). Descriptive statistics were used for analysis.

Results: The survey response rate was 56% (114 of 204). Paediatric intensivists comprised 66% of respondents. The median pre-transfusion platelet count varied across VA-ECMO scenarios, with a threshold of 50 × 109/L (interquartile range [IQR] 45-75) for non-bleeding children and 70 × 109/L (IQR 50-85) for non-bleeding neonates. The threshold for minimally bleeding children, minimally bleeding neonates and resolved bleeding in children was 75 × 109/L (IQR 50-100). The threshold for resolved bleeding in neonates was 80 × 109/L (IQR 50-100). There was significant heterogeneity between and within sites (p < 0.001). Uncertainty about the level of evidence was high (59%), with clinical judgement being the most influential factor in transfusion decisions (85%).

Conclusion: Prophylactic platelet transfusion practices in paediatric ECMO vary widely, highlighting uncertainty and the need for clinical trials to improve patient outcomes.

血小板输注说明了新生儿和儿科静脉-动脉体外膜氧合提供者的做法:一项调查。
背景和目的:体外膜氧合(ECMO)每年为全球4000多名新生儿和儿童提供心肺支持。尽管ECMO有可能挽救生命,但它有出血和血栓栓塞的风险,通常通过血小板输注来维持特定的阈值。输血小板本身就有很多风险。本调查旨在描述儿科静脉-动脉(VA)-ECMO提供者的预防性血小板输注做法,并确定影响输注决策的因素。材料和方法:这是一项来自10个中心的儿科ECMO提供者的横断面电子调查,基于6种患者情况(新生儿和儿童无出血、轻度出血和缓解出血)评估血小板输血阈值。采用描述性统计进行分析。结果:调查回复率为56%(114 / 204)。儿科重症医师占应答者的66%。输血前血小板计数中位数在VA-ECMO方案中有所不同,无出血儿童的阈值为50 × 109/L(四分位数范围[IQR] 45-75),无出血新生儿的阈值为70 × 109/L (IQR 50-85)。轻度出血儿童、轻度出血新生儿和缓解性出血儿童的阈值为75 × 109/L (IQR 50-100)。新生儿出血消退阈值为80 × 109/L (IQR 50-100)。结论:儿科ECMO预防性血小板输注实践差异很大,这突出了不确定性,需要临床试验来改善患者的预后。
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来源期刊
Vox Sanguinis
Vox Sanguinis 医学-血液学
CiteScore
4.40
自引率
11.10%
发文量
156
审稿时长
6-12 weeks
期刊介绍: Vox Sanguinis reports on important, novel developments in transfusion medicine. Original papers, reviews and international fora are published on all aspects of blood transfusion and tissue transplantation, comprising five main sections: 1) Transfusion - Transmitted Disease and its Prevention: Identification and epidemiology of infectious agents transmissible by blood; Bacterial contamination of blood components; Donor recruitment and selection methods; Pathogen inactivation. 2) Blood Component Collection and Production: Blood collection methods and devices (including apheresis); Plasma fractionation techniques and plasma derivatives; Preparation of labile blood components; Inventory management; Hematopoietic progenitor cell collection and storage; Collection and storage of tissues; Quality management and good manufacturing practice; Automation and information technology. 3) Transfusion Medicine and New Therapies: Transfusion thresholds and audits; Haemovigilance; Clinical trials regarding appropriate haemotherapy; Non-infectious adverse affects of transfusion; Therapeutic apheresis; Support of transplant patients; Gene therapy and immunotherapy. 4) Immunohaematology and Immunogenetics: Autoimmunity in haematology; Alloimmunity of blood; Pre-transfusion testing; Immunodiagnostics; Immunobiology; Complement in immunohaematology; Blood typing reagents; Genetic markers of blood cells and serum proteins: polymorphisms and function; Genetic markers and disease; Parentage testing and forensic immunohaematology. 5) Cellular Therapy: Cell-based therapies; Stem cell sources; Stem cell processing and storage; Stem cell products; Stem cell plasticity; Regenerative medicine with cells; Cellular immunotherapy; Molecular therapy; Gene therapy.
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