输血相关急性肺损伤危险因素的Meta分析

Meta-analysis of risk factors for transfusion-related acute lung injury

  • 摘要:
    目的 系统综述输血相关急性肺损伤(TRALI)的危险因素。
    方法 计算机检索PubMed、CINAHL、EMBASE、The Cochrane Library、CNKI、WanFang Data、VIP、CBM等数据库中TRALI危险因素的观察性研究, 检索时段为建库至2024年3月。对纳入研究进行质量评价, 2位研究者独立筛选文献并提取数据,采用RevMan 5.3软件进行Meta分析。
    结果 共纳入15项病例对照研究和2项队列研究,共计9 489例患者。Meta分析结果显示: ①受血者自身因素包括急性生理学及慢性健康状况评价(APACHE)评分(SMD=0.45, 95%CI: 0.09~0.80, P=0.01)、败血症(OR=3.01, 95%CI: 1.66~5.46, P=0.000 3)、肝脏疾病(OR=2.09, 95%CI: 1.25~3.50, P=0.005)、体外循环时间(WMD=83.71, 95%CI: 12.00~155.42, P=0.002)。②输血种类/量的因素包括血浆量(WMD=0.37, 95%CI: 0.23~0.51, P < 0.000 01)、输注女性捐献者的血浆量(WMD=0.32, 95%CI: 0.02~0.62, P=0.04)、新鲜冰冻血浆(FFP)(OR=2.62, 95%CI: 1.72~3.98, P < 0.000 01)、血小板量(WMD=0.31, 95%CI: 0.06~0.56, P= 0.01)、大量输血(24 h内>10 U)(OR=4.40, 95%CI: 2.05~9.41, P=0.000 1)。③捐赠因素包括棕榈酰溶血卵磷脂(Lyso-PC 16∶0)/硬脂酰溶血卵磷脂(LysoPC 18∶0)含量(WMD=18.78, 95%CI: 4.57~33.00, P=0.01)、人类白细胞抗原Ⅰ(HLA Ⅰ)抗体(OR=13.77, 95%CI: 1.13~167.28, P=0.04)、粒细胞抗体(OR=4.48, 95%CI: 1.54~13.04, P=0.006)与TRALI显著相关。
    结论 受血者的APACHE评分、败血症、肝脏疾病、体外循环时间,输注的血浆量、输注女性捐赠者的血浆量、输注FFP、输注血小板量、大量输血,捐赠中Lyso-PC 16∶0/LysoPC 18∶0含量、含HLA Ⅰ抗体、含粒细胞抗体等因素会影响TRALI的发生。

     

    Abstract:
    Objective To systematically review the risk factors of transfusion-related acute lung injury (TRALI).
    Methods Observational studies on the risk factors of TRALI were retrieved from databases including PubMed, CINAHL, EMBASE, The Cochrane Library, CNKI, WanFang Data, VIP, and CBM from the establishment of the databases to March 2024. Quality assessment of the included studies was conducted. Two researchers independently screened the literatures and extracted data, and Meta-analysis was performed using RevMan 5.3 software.
    Results A total of 15 case-control studies and 2 cohort studies were included, involving 9 489 patients. The results of the Meta-analysis showed that: ① Recipient-related factors included the Acute Physiology and Chronic Health Evaluation (APACHE) score (SMD=0.45, 95%CI, 0.09 to 0.80, P=0.01), sepsis (OR=3.01, 95%CI, 1.66 to 5.46, P=0.000 3), liver disease (OR=2.09, 95%CI, 1.25 to 3.50, P=0.005), and cardiopulmonary bypass time (WMD=83.71, 95%CI, 12.00 to 155.42, P=0.002). ② Transfusion-related factors (type/volume) included the volume of plasma (WMD=0.37, 95%CI, 0.23 to 0.51, P < 0.000 01), the volume of plasma from female donors (WMD=0.32, 95%CI, 0.02 to 0.62, P=0.04), fresh frozen plasma (FFP) (OR=2.62, 95%CI, 1.72 to 3.98, P < 0.000 01), the volume of platelets (WMD=0.31, 95%CI, 0.06 to 0.56, P=0.01), and massive transfusion (>10 U within 24 h) (OR=4.40, 95%CI, 2.05 to 9.41, P=0.000 1). ③ Donor-related factors included the content of palmitoyl lysophosphatidylcholine (Lyso-PC 16∶0)/stearoyl lysophosphatidylcholine (LysoPC 18∶0) (WMD=18.78, 95%CI, 4.57 to 33.00, P=0.01), human leukocyte antigen class Ⅰ (HLA Ⅰ) antibodies (OR=13.77, 95%CI, 1.13 to 167.28, P=0.04), and granulocyte antibodies (OR=4.48, 95%CI, 1.54 to 13.04, P=0.006), which were significantly associated with TRALI.
    Conclusion The APACHE score, sepsis, liver disease, cardiopulmonary bypass time of recipients, the volume of infused plasma, the volume of plasma from female donors, infused FFP, the volume of infused platelets, massive transfusion, the content of Lyso-PC 16∶0/LysoPC 18∶0 in donations, the presence of HLA Ⅰ antibodies, and the presence of granulocyte antibodies in donations are factors influencing the occurrence of TRALI.

     

/

返回文章
返回