成人重症监护病房血小板减少症患者的血小板输注:PLOT-ICU初始队列研究的一项子研究。

IF 1.9 4区 医学 Q2 ANESTHESIOLOGY Acta Anaesthesiologica Scandinavica Pub Date : 2024-09-01 Epub Date: 2024-06-05 DOI:10.1111/aas.14467
Carl Thomas Anthon, Frédéric Pène, Anders Perner, Elie Azoulay, Kathryn Puxty, Andry Van De Louw, Sanjay Chawla, Pedro Castro, Pedro Povoa, Luis Coelho, Victoria Metaxa, Matthias Kochanek, Tobias Liebregts, Thomas Kander, Mirka Sivula, Jo Bønding Andreasen, Lene Bjerregaard Nielsen, Christine Lodberg Hvas, Etienne Dufranc, Emmanuel Canet, Christopher John Wright, Julien Schmidt, Fabrice Uhel, Louai Missri, Mette Krag, Elisabet Cos Badia, Cándido Díaz-Lagares, Sophie Menat, Guillaume Voiriot, Niels Erikstrup Clausen, Kristian Lorentzen, Reidar Kvåle, Andreas Barratt-Due, Thomas Hildebrandt, Aleksander Rygh Holten, Kristian Strand, Morten Heiberg Bestle, Pål Klepstad, Damien Vimpere, Carolina Paulino, Catherina Lueck, Christian Svendsen Juhl, Carolina Costa, Per Martin Bådstøløkken, Lia Susana Aires Lêdo, Morten Hylander Møller, Lene Russell
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引用次数: 0

摘要

背景:重症监护病房(ICU)经常使用血小板输注,但目前的做法,包括使用的产品类型、数量、剂量和效果尚不清楚:研究设计:"重症监护室血小板减少症和血小板输注(PLOT-ICU)"初始队列研究的子研究,包括急性入院的重症监护室成人血小板减少症患者(血小板计数为 9/L)。主要结果是按产品类型分列的在重症监护室接受血小板输注的患者人数。次要结果包括血小板输注详情、血小板增量、出血、其他输血和死亡率:在来自欧洲和美国 10 个国家 43 家医院的 504 名血小板减少症患者中,20.8% 的患者接受了 565 次血小板输注;61.0% 的患者接受了集合产品,21.9% 的患者接受了无细胞产品,17.1% 的患者同时接受了两种产品。每次输血量的中位数为 253 毫升(180-308 毫升),集合产品占输血量的 59.1%,但各国的情况有所不同。大多数中心(73.8%)使用固定剂量(中位数范围为 2.0 至 3.5 × 1011 个血小板/次输血),而一些中心(主要在法国)则使用基于体重的剂量(范围为每 10 千克体重 0.5 至 0.7 × 1011 个血小板)。单次预防性血小板输注的血小板计数增量中位数为 2(-1 至 8)×109/L。接受和未接受血小板输注的血小板减少症患者的预后各不相同:结论:在急性入院的成人血小板减少症重症监护病房患者中,20.8%的患者在重症监护病房接受了血小板输注,其中大部分患者接受的是集合产品,但不同国家的产品类型、输注量和剂量存在很大差异。预防性血小板输注对血小板计数的增加作用有限。
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Platelet transfusions in adult ICU patients with thrombocytopenia: A sub-study of the PLOT-ICU inception cohort study.

Background: Platelet transfusions are frequently used in the intensive care unit (ICU), but current practices including used product types, volumes, doses and effects are unknown.

Study design and methods: Sub-study of the inception cohort study 'Thrombocytopenia and Platelet Transfusions in the ICU (PLOT-ICU)', including acutely admitted, adult ICU patients with thrombocytopenia (platelet count <150 × 109/L). The primary outcome was the number of patients receiving platelet transfusion in ICU by product type. Secondary outcomes included platelet transfusion details, platelet increments, bleeding, other transfusions and mortality.

Results: Amongst 504 patients with thrombocytopenia from 43 hospitals in 10 countries in Europe and the United States, 20.8% received 565 platelet transfusions; 61.0% received pooled products, 21.9% received apheresis products and 17.1% received both with a median of 2 (interquartile range 1-4) days from admission to first transfusion. The median volume per transfusion was 253 mL (180-308 mL) and pooled products accounted for 59.1% of transfusions, however, this varied across countries. Most centres (73.8%) used fixed dosing (medians ranging from 2.0 to 3.5 × 1011 platelets/transfusion) whilst some (mainly in France) used weight-based dosing (ranging from 0.5 to 0.7 × 1011 platelets per 10 kg body weight). The median platelet count increment for a single prophylactic platelet transfusion was 2 (-1 to 8) × 109/L. Outcomes of patients with thrombocytopenia who did and did not receive platelet transfusions varied.

Conclusions: Among acutely admitted, adult ICU patients with thrombocytopenia, 20.8% received platelet transfusions in ICU of whom most received pooled products, but considerable variation was observed in product type, volumes and doses across countries. Prophylactic platelet transfusions were associated with limited increases in platelet counts.

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来源期刊
CiteScore
4.30
自引率
9.50%
发文量
157
审稿时长
3-8 weeks
期刊介绍: Acta Anaesthesiologica Scandinavica publishes papers on original work in the fields of anaesthesiology, intensive care, pain, emergency medicine, and subjects related to their basic sciences, on condition that they are contributed exclusively to this Journal. Case reports and short communications may be considered for publication if of particular interest; also letters to the Editor, especially if related to already published material. The editorial board is free to discuss the publication of reviews on current topics, the choice of which, however, is the prerogative of the board. Every effort will be made by the Editors and selected experts to expedite a critical review of manuscripts in order to ensure rapid publication of papers of a high scientific standard.
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