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22个欧洲国家新生儿重症监护病房的血小板输注:一项前瞻性观察研究。

Platelet transfusion in neonatal intensive care units of 22 European countries: a prospective observational study.

作者信息

Houben Nina A M, Lopriore Enrico, Fijnvandraat Karin, Caram-Deelder Camila, Carrascosa Marta Aguar, Beuchée Alain, Brække Kristin, Cardona Francesco, Debeer Anne, Domingues Sara, Ghirardello Stefano, Grizelj Ruza, Hadžimuratović Emina, Heiring Christian, Krivec Jana Lozar, Malý Jan, Matasova Katarina, Moore Carmel Maria, Muehlbacher Tobias, Szabó Miklos, Szczapa Tomasz, Zaharie Gabriela, de Jager Justine, Reibel-Georgi Nora Johanna, New Helen V, Stanworth Simon J, Deschmann Emöke, Roehr Charles C, Dame Christof, le Cessie Saskia, van der Bom Johanna, Fustolo-Gunnink Suzanne

机构信息

Sanquin Research, Sanquin Blood Supply Foundation, Amsterdam, the Netherlands.

Leiden University Medical Centre, Leiden, the Netherlands.

出版信息

Lancet Reg Health Eur. 2024 Oct 10;47:101086. doi: 10.1016/j.lanepe.2024.101086. eCollection 2024 Dec.

Abstract

BACKGROUND

Platelet transfusions are given to preterm infants with severe thrombocytopenia aiming to prevent haemorrhage. The PlaNeT2/MATISSE trial revealed higher rates of mortality and/or major bleeding in preterm infants receiving prophylactic platelet transfusions at a platelet count threshold of 50 × 10/L compared to 25 × 10/L. The extent to which this evidence has been incorporated into clinical practice is unknown, thus we aimed to describe current neonatal platelet transfusion practices in Europe.

METHODS

We performed a prospective observational study in 64 neonatal intensive care units across 22 European countries between September 2022 and August 2023. Outcome measures included observed transfusion prevalence rates (per country and overall, pooled using a random effects Poisson model), expected rates based on patient-mix (per country, estimated using logistic regression), cumulative incidence of receiving a transfusion by day 28 (with death and discharge considered as competing events), transfusion indications, volumes and infusion rates, platelet count triggers and increment, and adverse effects.

FINDINGS

We included 1143 preterm infants, of whom 71 (6.2%, [71/1143]) collectively received 217 transfusions. Overall observed prevalence rate was 0.3 platelet transfusion days per 100 admission days. By day 28, 8.3% (95% CI: 5.5-11.1) of infants received a transfusion. Most transfusions were indicated for threshold (74.2%, [161/217]). Pre-transfusion platelet counts were above 25 × 10/L in 33.1% [53/160] of these transfusions. There was significant variability in volume and duration.

INTERPRETATION

The restrictive threshold of 25 × 10/L is being integrated into clinical practice. Research is needed to explore existing variation and generate evidence for various aspects including optimal volumes and infusion rates.

FUNDING

Sanquin, EBA, and ESPR.

摘要

背景

对患有严重血小板减少症的早产儿进行血小板输注旨在预防出血。PlaNeT2/MATISSE试验显示,与血小板计数阈值为25×10⁹/L相比,血小板计数阈值为50×10⁹/L时接受预防性血小板输注的早产儿死亡率和/或大出血发生率更高。该证据在多大程度上已被纳入临床实践尚不清楚,因此我们旨在描述欧洲目前的新生儿血小板输注实践。

方法

2022年9月至2023年8月期间,我们在22个欧洲国家的64个新生儿重症监护病房进行了一项前瞻性观察性研究。结果指标包括观察到的输血流行率(按国家和总体计算,使用随机效应泊松模型汇总)、基于患者组合的预期率(按国家计算,使用逻辑回归估计)、到第28天接受输血的累积发生率(将死亡和出院视为竞争事件)、输血指征、输血量和输注速率、血小板计数触发值和增加值以及不良反应。

研究结果

我们纳入了1143名早产儿,其中71名(6.2%,[71/1143])共接受了217次输血。总体观察到的流行率为每100个入院日0.3个血小板输血日。到第28天,8.3%(95%CI:5.5-11.1)的婴儿接受了输血。大多数输血是因阈值原因(74.2%,[161/217])。在这些输血中,33.1%[53/160]的输血前血小板计数高于25×10⁹/L。输血量和持续时间存在显著差异。

解读

25×10⁹/L的限制性阈值正在被纳入临床实践。需要开展研究以探索现有的差异,并为包括最佳输血量和输注速率在内的各个方面提供证据。

资金来源

荷兰血库、欧洲血液学协会和欧洲儿科研究学会。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83d1/11635195/5195f46de510/gr4.jpg

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