Barts Research Centre for Women's Health, Queen Mary University of London, UK; Barts Health, NHS Trust, London, UK.
Barts Health, NHS Trust, London, UK; Wolfson Institute, Queen Mary University of London, UK.
Transfus Med Rev. 2020 Apr;34(2):101-107. doi: 10.1016/j.tmrv.2019.12.002. Epub 2020 Jan 28.
Fibrinogen levels drop early in postpartum hemorrhage (PPH), and low fibrinogen levels predict outcomes. There is increasing interest in replacing fibrinogen early in severe PPH and this systematic review's aim was to assess if early fibrinogen replacement therapy improves outcomes in severe PPH. We searched the following databases from inception to June 2019: CDSR and CENTRAL (The Cochrane Library), MEDLINE, Embase, CINAHL, PubMed, Transfusion Evidence Library, LILACS, Web of Science Conference Proceedings Citation Index-Science, ClinicalTrials.gov and the WHO International Clinical Trials Registry Portal. We included randomized (RCT) and well-designed controlled observational studies where fibrinogen replacement therapy was given early (within 90 minutes of bleeding) compared with standard protocol in pregnant women > 24 weeks' gestation who developed PPH, defined as estimated blood loss ≥500 mL up to 24 hours post-delivery. Two independent reviewers extracted and reviewed the data on the primary outcome of allogeneic blood transfusion at 24 hours after intervention and secondary outcomes including all-cause mortality, rate of thrombosis, and the need for surgical and non-surgical interventions. We identified 5 eligible studies: 2 completed (total of 299 women) RCTs comparing fibrinogen concentrate with placebo, and 3 ongoing RCTs. There was no completed study assessing cryoprecipitate transfusion. There was variation of: timings of intervention administration; severity of PPH; fibrinogen doses and use of tranexamic acid. There was insufficient evidence that early administration of fibrinogen in PPH reduces the need for allogeneic blood transfusion at 24 hours (risk ratio 0.83 (95% CI 0.54-1.26), P = 0.38) (2 trials, 299 participants) or improves other outcomes. Both studies were underpowered to answer our outcomes. There is a lack of evidence that early fibrinogen replacement therapy improves outcomes in PPH. Future studies are needed to address this, underpinned by data on the optimal fibrinogen dose, protocol-driven approaches versus targeted therapy, and cost-effectiveness of cryoprecipitate versus fibrinogen concentrate therapy in PPH.
纤维蛋白原水平在产后出血 (PPH) 早期下降,低纤维蛋白原水平预测结局。人们对严重 PPH 早期补充纤维蛋白原越来越感兴趣,本系统评价的目的是评估早期纤维蛋白原替代治疗是否改善严重 PPH 的结局。我们从建库至 2019 年 6 月检索了以下数据库:CDSR 和 CENTRAL(Cochrane 图书馆)、MEDLINE、Embase、CINAHL、PubMed、输血证据库、LILACS、Web of Science 会议论文引文索引-科学、ClinicalTrials.gov 和世界卫生组织国际临床试验注册平台。我们纳入了纤维蛋白原替代治疗在出血后 90 分钟内(早期)与标准方案相比,用于妊娠 24 周以上发生 PPH 的孕妇的随机对照试验 (RCT) 和设计良好的对照观察性研究,PPH 定义为产后 24 小时内估计失血量≥500mL。两名独立评审员提取并评估了干预后 24 小时异体输血的主要结局和次要结局(包括全因死亡率、血栓形成率以及手术和非手术干预的需求)数据。我们确定了 5 项符合条件的研究:2 项已完成(共 299 名妇女)的 RCT 比较纤维蛋白原浓缩物与安慰剂,以及 3 项正在进行的 RCT。没有已完成的研究评估冷沉淀输血。干预措施的实施时间、PPH 的严重程度、纤维蛋白原剂量和氨甲环酸的使用等方面存在差异。早期在 PPH 中给予纤维蛋白原可减少 24 小时异体输血需求的证据不足(风险比 0.83(95%CI 0.54-1.26),P=0.38)(2 项试验,299 名参与者)或改善其他结局。这两项研究都没有足够的能力回答我们的结局问题。目前尚无证据表明早期纤维蛋白原替代治疗可改善 PPH 的结局。需要进一步的研究来解决这个问题,研究应基于最佳纤维蛋白原剂量的数据、基于方案的方法与靶向治疗、以及冷沉淀与纤维蛋白原浓缩物治疗在 PPH 中的成本效益。