Automated quantitation of fetomaternal hemorrhage by flow cytometry for HbF-containing fetal red blood cells using probability state modeling

被引:15
作者
Wong, L. [1 ]
Hunsberger, B. C. [2 ]
Bagwell, C. Bruce [2 ]
Davis, B. H. [1 ]
机构
[1] Trillium Diagnost LLC, Brewer, ME USA
[2] Ver Software House, Topsham, ME USA
关键词
KB assay; automated analysis; fetomaternal hemorrhage; GemStone; probability state modeling; fetal red blood cells; F cells; hemoglobin F; laboratory improvement; measurement error; quality practice improvement; MATERNAL BLOOD; QUIKQUANT;
D O I
10.1111/ijlh.12060
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BackgroundFlow cytometric methods (FCMs) are the contemporary standard for fetal red blood cell (RBC) quantitation and fetomaternal hemorrhage (FMH) detection. FCM provides greater sensitivity and repeatability relative to manual microscopic Kleihauer-Betke methods. FCM assays are not totally objective, employing subjective manual gating of fetal RBCs with measureable interobserver imprecision. We investigated Probability State Modeling to automate analysis of fetal RBCs using an assay for hemoglobin F (HbF)-containing RBCs. MethodsTwo hundred human bloods were processed using the FMH QuikQuant assay (Trillium Diagnostics, Brewer, ME, USA). A Probability State Model (PSM) was designed to enumerate fetal RBCs by selecting the three RBCs subpopulation based on differences in intensity levels of several parameters. The GemStone program uses a PSM that requires no operator intervention. Routine manual analysis by experienced users was performed, along with replicate analyses for both methods. ResultsThe PSM by GemStone correlates strongly with the expert manual analysis, r(2)=0.9986. The mean absolute difference of the FMH results between GemStone and manual expert' analysis was 0.04% with no intermethod bias detected. Manual gating demonstrated coefficient of variations (CVs) of 10.6% for intra-analyst replicates and 22.6% for interanalyst imprecision. The interanalyst agreement in GemStone is a perfect correlation, r(2)=1.00, and no imprecision with a 0.00% CV. ConclusionAutomated PSM analysis of fetal RBCs strongly correlates with expert traditional manual analysis. PSM enumerates fetal RBCs accurately with significantly greater objectivity and lower imprecision than the traditional manual gating method. Thus, PSM provides a means to markedly improve interlaboratory variance with FMH assays based upon subjective gating strategies.
引用
收藏
页码:548 / 554
页数:7
相关论文
共 20 条
  • [1] [Anonymous], LAB HEMATOLOGY PRACT
  • [2] [Anonymous], ADV BIOINFORMATICS
  • [3] [Anonymous], 2010, FLOW CYTOMETRY DRUG
  • [4] Bagwell CB, 2011, METHODS MOL BIOL, V699, P31, DOI 10.1007/978-1-61737-950-5_2
  • [5] Mixture modeling approach to flow cytometry data
    Boedigheimer, Michael J.
    Ferbas, John
    [J]. CYTOMETRY PART A, 2008, 73A (05) : 421 - 429
  • [6] Measurement of feto-maternal haemorrhage: A comparative study of three Kleihauer techniques and two flow cytometry methods
    Bromilow, IM
    Duguid, JKM
    [J]. CLINICAL AND LABORATORY HAEMATOLOGY, 1997, 19 (02): : 137 - 142
  • [7] Comparison of haemoglobin F detection by the acid elution test, flow cytometry and high-performance liquid chromatography in maternal blood samples analysed for fetomaternal haemorrhage
    Chambers, E.
    Davies, L.
    Evans, S.
    Birchall, J.
    Kumpel, B.
    [J]. TRANSFUSION MEDICINE, 2012, 22 (03) : 199 - 204
  • [8] A chromatic explosion: the development and future of multiparameter flow cytometry
    Chattopadhyay, Pratip K.
    Hogerkorp, Carl-Magnus
    Roederer, Mario
    [J]. IMMUNOLOGY, 2008, 125 (04) : 441 - 449
  • [9] Multicenter clinical experience with flow cytometric method for fetomaternal hemorrhage detection
    Chen, JC
    Davis, BH
    Wood, B
    Warzynski, MJ
    [J]. CYTOMETRY, 2002, 50 (06): : 285 - 290
  • [10] Detection of fetal red cells in fetomaternal hemorrhage using a fetal hemoglobin monoclonal antibody by flow cytometry
    Davis, BH
    Olsen, S
    Bigelow, NC
    Chen, JC
    [J]. TRANSFUSION, 1998, 38 (08) : 749 - 756