Evaluation of Flow Cytometry and Kleihauer Techniques for Quantification of Fetomaternal Hemorrhage: A Prospective Cohort Study in Southwestern Iran

Z. Keshavarz, L. Moezzi, R. Ranjbaran, A. Behzad-Behbahani, M. Abdullahi, M. Mahmoodi, S. Sharifzadeh
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Abstract

Background: Quantification of fetal red blood cells (RBCs) in maternal blood is of great importance to calculate appropriate dose of post-deliver anti D immunoglobulin in a rhesus D (RhD)-negative woman. Objective: The aim of this study is to evaluate a direct immunofluorescence flow cytometry technique in artificial and clinical samples and compared it to the Kleihauer-Betke test (KBT). Methods: This study was a prospective cohort design. Blood samples from 26 pregnant women who gave birth to RhD positive babies were tested using direct immunofluorescence flow cytometry and KBT techniques to determine the amount of FMH in the maternal circulation. The zone of D-positive cells was identified employing artificial samples including 0.3%, 0.6%, 1%, 1.5%, 2%, 5%, 10%, and 50% of D-positive fetal cells in D-negative maternal cells. Results: Analysis of 26 clinical samples for FMH showed consistent quantification with the flow cytometry and Kleihauer techniques. Although a good correlation was found between the KBT and flow cytometry results, in artificial samples containing more than 2% of fetal RhD positive cells, the flow cytometry results were closer to theoretical percentages. In a patient with FMH >4 mL, the FMH and consequently the required vial of Ig were overestimated using KBT. Conclusion: Most of the FMH calculated could have been neutralized by doses less than 625 IU, whereas the routine dose in Iran is more than double that amount (1500 IU). This achievement demonstrates that adjusting between the RhD immune globulin (RhDIg) dose and FMH size is inevitable.
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评价流式细胞术和Kleihauer技术量化胎儿出血:伊朗西南部的一项前瞻性队列研究
背景:母体血液中胎儿红细胞(rbc)的定量测定对于计算RhD阴性妇女产后抗D免疫球蛋白的合适剂量具有重要意义。目的:评价直接免疫荧光流式细胞术在人工和临床标本中的应用,并将其与Kleihauer-Betke试验(KBT)进行比较。方法:采用前瞻性队列设计。使用直接免疫荧光流式细胞术和KBT技术检测了26名生下RhD阳性婴儿的孕妇的血液样本,以确定母体循环中FMH的数量。采用人工样本鉴定d阳性细胞区,包括d阴性母细胞中d阳性胎儿细胞的0.3%、0.6%、1%、1.5%、2%、5%、10%和50%。结果:对26例临床标本进行FMH定量分析,结果与流式细胞术和Kleihauer技术一致。虽然在KBT和流式细胞术结果之间发现了良好的相关性,但在含有超过2%的胎儿RhD阳性细胞的人工样本中,流式细胞术结果更接近理论百分比。在FMH患者中,使用KBT高估了FMH和所需的Ig瓶。结论:计算出的大多数FMH可以通过低于625 IU的剂量被中和,而伊朗的常规剂量是该剂量的两倍多(1500 IU)。这一成果表明,在RhD免疫球蛋白(RhDIg)剂量和FMH大小之间进行调整是不可避免的。
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审稿时长
18 weeks
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