Dias Joao D, Levy Jerrold H, Tanaka Kenichi A, Zacharowski Kai, Hartmann Jan
Haemonetics SA, Signy, Switzerland.
Departments of Anesthesiology, Critical Care and Surgery, Duke University School of Medicine, Durham, NC, USA.
Anaesthesia. 2025 Jan;80(1):95-103. doi: 10.1111/anae.16463. Epub 2024 Nov 14.
Patients undergoing major surgery frequently experience major uncontrolled bleeding. The aim of this systematic review and meta-analysis was to evaluate the clinical efficacy of using viscoelastic haemostatic assays to manage peri-operative bleeding in elective surgery.
We searched PubMed/MEDLINE and Embase databases for randomised controlled trials according to pre-determined criteria. The primary outcomes were blood product requirements; duration of stay in the operating theatre or ICU; and surgical reintervention rate.
We included 20 randomised controlled trials. The overall risk of bias was low to moderate. Twelve studies used thromboelastography-based transfusion algorithms, while eight used thromboelastometry. Viscoelastic haemostatic assay-guided therapy was associated with a statistically significant reduction in transfusion of red blood cells (standardised mean difference (95%CI) 0.16 (-0.29 to 0.02)), platelets (standardised mean difference (95%CI) -0.33 (-0.56 to -0.10)) and fresh frozen plasma (standardised mean difference (95%CI) -0.64 (-1.01 to -0.28)). There was no evidence of an effect of viscoelastic haemostatic assay-guided therapy on surgical reintervention (relative risk (95%CI) 1.09 (0.70-1.69)). Viscoelastic haemostatic assay-guided therapy was associated with lower blood loss and shorter ICU duration of stay. There was no evidence of any effect on total duration of stay and all-cause mortality.
Viscoelastic haemostatic assay-guided therapy may reduce peri-operative blood product transfusion requirements and blood loss during major elective surgery, with no discernible effect on patient-centred outcomes. The overall quality of evidence was modest.
接受大手术的患者经常会出现严重的失控性出血。本系统评价和荟萃分析的目的是评估使用粘弹性止血检测来管理择期手术围手术期出血的临床疗效。
我们根据预先确定的标准在PubMed/MEDLINE和Embase数据库中检索随机对照试验。主要结局包括血液制品需求量、在手术室或重症监护病房的停留时间以及手术再次干预率。
我们纳入了20项随机对照试验。总体偏倚风险为低到中度。12项研究使用基于血栓弹力图的输血算法,而8项研究使用血栓弹力测定法。粘弹性止血检测指导的治疗与红细胞输注量(标准化均数差(95%CI)0.16(-0.29至0.02))、血小板输注量(标准化均数差(95%CI)-0.33(-0.56至-0.10))和新鲜冰冻血浆输注量(标准化均数差(95%CI)-0.64(-1.01至-0.28))的统计学显著减少相关。没有证据表明粘弹性止血检测指导的治疗对手术再次干预有影响(相对危险度(95%CI)1.09(0.70 - 1.69))。粘弹性止血检测指导的治疗与失血量减少和重症监护病房停留时间缩短相关。没有证据表明对总住院时间和全因死亡率有任何影响。
粘弹性止血检测指导的治疗可能会减少大择期手术期间的围手术期血液制品输注需求和失血量,对以患者为中心的结局没有明显影响。证据的总体质量一般。