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首页> 外文期刊>International Journal of Research in Medical Sciences >Prevalence of thalassemia and hemoglobinopathy in antenatal mothers with relation to complete hemogram and high performance liquid chromatography-a hospital based study of Eastern India
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Prevalence of thalassemia and hemoglobinopathy in antenatal mothers with relation to complete hemogram and high performance liquid chromatography-a hospital based study of Eastern India

机译:产前母亲地中海贫血和血红蛋白病的患病率与全血图和高效液相色谱法的关系-基于印度东部医院的一项研究

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Background: Iron deficiency anemia (IDA) and Beta thalassemia (BT) are two most common causes of microcytic hypochromic anemia in our country affecting the reproductive age group. It is important to discriminate between these two entities to prevent treatment with iron of individuals with thalassemia trait as well as prevent homozygous transmission of B thalassemia trait (BTT). Aim of the study was to investigate causes of microcytic anemia in antenatal mothers and to find out the role of Cell Counter and High Performance Liquid Chromatography (HPLC) so as to screen BTT and other hemoglobinopathies. Methods: This study was done over a period of six months (May 2017 to October 2017) in the Department of Pathology in R. G. Kar Medical College. We analyzed the blood samples of all antenatal mothers attending Department of Pathology for blood tests and a complete hemogram and hemoglobin A2 (Hb A2) quantitation was done. Results: Total cases evaluated were 2200 of which 442 patients were found to have microcytic hypochromic anemia (MCV<80%, MCH<27). Rest that is 1758 was normal. Of 442 cases of microcytic hypochromic anemia, 205 were found to have IDA, 115 BTT, 112 E trait, 1 case each of Hemoglobin E disease, E-Beta thalassemia and hereditary persistence of fetal hemoglobin (HPFH). Hemoglobinopathies like S trait and Hemoglobin J (Hb J) was found in 4 and 3 cases respectively. Conclusions: In India, Microcytic hypochromic anemia is common and may be due to IDA, BTT or other hemoglobinopathies Cell counter-based parameters and formulas, along with HPLC can be an effective method of thalassemia screening in a society.
机译:背景:缺铁性贫血(IDA)和β地中海贫血(BT)是我国影响生殖年龄组的小细胞性低铬性贫血的两个最常见原因。重要的是要区分这两个实体,以防止对患有地中海贫血特征的人进行铁治疗,并防止纯正地传播B地中海贫血特征(BTT)。该研究的目的是调查产前母亲小细胞性贫血的原因,并找出细胞计数器和高效液相色谱(HPLC)的作用,以筛查BTT和其他血红蛋白病。方法:本研究在R.G.Kar医学院的病理学系进行了六个月(2017年5月至2017年10月)。我们分析了所有参加病理学检查的产前母亲的血液样本,以进行血液检查,并完成了完整的血象图和血红蛋白A2(Hb A2)定量。结果:评估的总病例为2200例,其中442例患有小细胞性低铬性贫血(MCV <80%,MCH <27)。其余的是1758年是正常的。在442例小细胞性低色素性贫血中,发现205例具有IDA,115 BTT,112 E性状,1例血红蛋白E病,E-β地中海贫血和胎儿血红蛋白(HPFH)遗传性持久性。分别在4例和3例中发现了S性状和血红蛋白J(Hb J)等血红蛋白病。结论:在印度,小细胞性贫血性贫血很常见,可能是由于IDA,BTT或其他血红蛋白病所致。基于细胞计数器的参数和公式以及HPLC可以成为社会中地中海贫血筛查的有效方法。

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