Adherence to a restrictive red blood cell transfusion strategy in critically ill patients: An observational study.

IF 1.9 4区 医学 Q2 ANESTHESIOLOGY Acta Anaesthesiologica Scandinavica Pub Date : 2024-07-01 Epub Date: 2024-03-07 DOI:10.1111/aas.14402
Martin F Bjurström, Ylva C Linder, Jens Kjeldsen-Kragh, Jesper Bengtsson, Thomas Kander
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Abstract

Background: Randomized controlled trials relatively consistently show that restrictive red blood cell (RBC) transfusion strategies are safe and associated with similar outcomes compared to liberal transfusion strategies in critically ill patients. Based on these data, the general threshold for RBC transfusion was changed to 70 g/L at a 9-bed tertiary level intensive care unit in September 2020. Implementation measures included lectures, webinars and feedback during clinical practice. The aim of this study was to investigate how implementation of a restrictive transfusion strategy influenced RBC usage, haemoglobin trigger levels and adherence to prescribed trigger levels.

Methods: In this registry-based, observational study, critically ill adult patients without massive bleeding were included and divided into a pre-cohort, with admissions prior to the change of transfusion strategy, and a post-cohort, with admissions following the change of transfusion strategy. These cohorts were compared regarding key RBC transfusion-related variables.

Results: In total 5626 admissions were included in the analyses (pre-cohort n = 4373, post-cohort n = 1253). The median volume (interquartile range, IQR) of RBC transfusions per 100 admission days, in the pre-cohort was 6120 (4110-8110) mL versus 3010 (2890-4970) mL in the post-cohort (p < .001). This corresponds to an estimated median saving of 1128 € per 100 admission days after a restrictive RBC transfusion strategy was implemented. In total, 26% of the admissions in the pre-cohort and 19% in the post-cohort (p < .001) received RBC transfusion(s) during days 0-10. Both median (IQR) prescribed trigger levels (determined by intensivist) and actual haemoglobin trigger levels (i.e., levels prior to actual administration of transfusion) were higher in the pre- versus post-cohort (90 [80-100] vs. 80 [72-90] g/L, p < .001 and 89 [82-96] g/L vs. 83 [79-94], p < .001, respectively). Percentage of days without compliance with the prescribed transfusion trigger was higher in the pre-cohort than in the post-cohort (23% vs. 14%, p < .001). Sensitivity analyses, excluding patients with traumatic brain injury, ischemic heart disease and COVID-19 demonstrated similar results.

Conclusions: Implementation of a restrictive transfusion trigger in a critical care setting resulted in lasting decreased RBC transfusion use and costs, decreased prescribed and actual haemoglobin trigger levels and improved adherence to prescribed haemoglobin trigger levels.

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重症患者坚持限制性红细胞输注策略:一项观察性研究。
背景:随机对照试验相对一致地表明,在重症患者中,限制性红细胞(RBC)输注策略是安全的,与自由输注策略相比,结果相似。基于这些数据,一家拥有 9 张床位的三级重症监护病房于 2020 年 9 月将红细胞输注的一般阈值改为 70 g/L。实施措施包括讲座、网络研讨会和临床实践中的反馈。本研究旨在探讨限制性输血策略的实施如何影响 RBC 的使用、血红蛋白触发水平以及对规定触发水平的遵守情况:在这项以登记为基础的观察性研究中,纳入了无大出血的成年重症患者,并将其分为前队列和后队列,前者在输血策略改变前入院,后者在输血策略改变后入院。对这两个队列中与输注红细胞相关的主要变量进行了比较:共有 5626 例入院患者纳入分析(前队列 n = 4373 例,后队列 n = 1253 例)。组群前每 100 个入院日输注 RBC 的中位数(四分位数间距,IQR)为 6120(4110-8110)毫升,组群后为 3010(2890-4970)毫升(P 结论:组群前每 100 个入院日输注 RBC 的中位数为 6120(4110-8110)毫升,组群后为 3010(2890-4970)毫升:在重症监护环境中实施限制性输血触发后,输注红细胞的次数和费用持续减少,处方血红蛋白触发水平和实际血红蛋白触发水平均有所下降,处方血红蛋白触发水平的依从性也有所提高。
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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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