氨甲环酸对严重脊柱畸形矫形术止血疗效及安全性的荟萃分析
DOI:
作者:
作者单位:

1.山西医科大学第二医院;2.山西医科大学第二医院骨科;3.骨与软组织损伤修复山西省重点实验室;4.山西医科大学;5.骨与软组织损伤修复重点实验室

作者简介:

通讯作者:

中图分类号:

基金项目:

科技部国家国际合作项目;国家自然科学基金项目(面上项目);国家自然科学基金项目(青年基金)


The efficacy and safety of tranexamic acid in corrective surgery for severe spinal deformity: a meta-analysis
Author:
Affiliation:

1.The Second Hospital of Shanxi Medical University;2.Key Laboratory of Bone and Soft Tissue Injury Repair of Shanxi Province;3.Shanxi Medical University

Fund Project:

International S&T Cooperation Program of China(2015DFA33050); National Natural Science Foundation (81772415;81601949)

  • 摘要
  • |
  • 图/表
  • |
  • 访问统计
  • |
  • 参考文献
  • |
  • 相似文献
  • |
  • 引证文献
  • |
  • 资源附件
  • |
  • 文章评论
    摘要:

    [目的] 通过对已有随机对照试验进行数据提取及荟萃分析,为严重脊柱畸形患者的术中止血药物选择提供循证医学证据。[方法] 检索PubMed、Web of Science、EMBASE、CNKI及万方5个中英文数据库中所有使用氨甲环酸止血的脊柱矫形手术文献,时间限定在建库至2019年8月。采用Review Manager 5.3软件数据进行统计学分析。[结果] 共检索相关研究306篇,参照纳入与排除标准,最终纳入9项随机对照实验468例患者,其中氨甲环酸组292例,年龄分布为11-65岁;安慰剂组纳入患者289例,年龄分布11-68岁。严重脊柱畸形患者中,氨甲环酸组术中失血量较安慰剂组少311ml(-311.47 [-385.72, -237.21]);围手术期总失血量亦较安慰剂组少,该差异有统计学意义(-159.41ml [-188.12, -130.70])。氨甲环酸显著降低了患者的输血需求(-186.44ml [-294.59, -78.30]),氨甲环酸组患者输血量较对照组减少-186ml。但氨甲环酸并不能减少手术时间,两组患者在手术时间上并无差异(-1.46 [-15.92, 13.00])。氨甲环酸也并未增加相应的血栓相关并发症发生率(1.16 [0.44, 3.08]),氨甲环酸组与安慰剂组的血栓事件发生率为5.1% VS 4.2%(P=0.76)。[结论] 对于严重脊柱畸形矫形手术,氨甲环酸能够有效的降低围手术期总失血量及输血量,同时并不增加血栓形成的风险。未来仍需大样本多中心的实验提供更高的证据等级支持。

    Abstract:

    [Objective] To determine the optimal hemostatic drug in corrective surgery for severe spinal deformity, data were extracted from randomized controlled trials to performed a meta-analysis. [Methods] A search of tranexamic acid (TXA) infusion in spinal corrective surgery was conducted in PubMed, EMBASE, Web of Science,CNKI and Wanfang database.The results were limited to August 2019 and all the statistics were analyzed by Review Manager 5.3 software.[Results] A total of 306 relevant literatures were searched. According to the inclusion and exclusion criteria, 9 randomized controlled trials including 468 patients were eventually enrolled in this meta-analysis, which 292 patients were included in the TXA group with an age ranging from 11 to 65 years, while 289 patients were included in the placebo group ranging from 11 to 68 years old. Compared to the placebo group, the volume of blood loss in the TXA group decreased in 311ml (-311.47 [-385.72, -237.21]) for patients with severe spinal deformity. As for total blood loss, there was a significant decrease in TXA group (-159.41ml [-188.12, -130.70]).TXA significantly reduced the transfusion need (-186.44 ml [-294.59, -78.30]), which in TXA group the requirement of transfusion was lower in 186ml. However, there was no difference in the operation time between the TXA groups and placebo group (-1.46 [-15.92, 13.00]). The administration of TXA did not increase the rate of thrombosis-related complications (1.16 [0.44, 3.08]). The incidence of thrombotic events in the TXA group and placebo group were 5.1% and 4.2%, respectively (P=0.76). [Conclusion] In corrective surgery for severe spinal deformity, tranexamic acid can effectively reduce the the volume of perioperative blood loss and transfusion without increasing the risk of thrombotic events. There is a need for the larger sample size and multicenter trails in the future to provide higher levels of evidence.

    参考文献
    相似文献
    引证文献
引用本文
分享
文章指标
  • 点击次数:
  • 下载次数:
  • HTML阅读次数:
  • 引用次数:
历史
  • 收稿日期:2019-11-05
  • 最后修改日期:2019-11-05
  • 录用日期:2019-12-06
  • 在线发布日期:
  • 出版日期: