Screening of antenatal patients for anaemia and haemoglobinopathies

Tejal Ahuja, Nidhi Bhatnagar, Mamta Shah, Sangita Shah
{"title":"Screening of antenatal patients for anaemia and haemoglobinopathies","authors":"Tejal Ahuja, Nidhi Bhatnagar, Mamta Shah, Sangita Shah","doi":"10.15406/htij.2023.11.00306","DOIUrl":null,"url":null,"abstract":"Introduction: Anaemia is an extremely common condition in pregnancy worldwide, conferring a number of health risks to mother and child. Iron deficiency is most widespread micronutritional deficiency in the world and disproportionately affects female because of increased iron requirements during menstruation, pregnancy and lactation. Haemoglobinopathies are a group of inherited disorders because of abnormalities in haemoglobin synthesis or structure. Thalassemia and Sickle cell anaemias are the most prevalent haemoglobinopathies and a national health burden in India so identifying these disorders during antenatal period is necessary to take appropriate measures. Methods: A prospective study of screening for haemoglobin variants in Antenatal Patients due to low haemoglobin and evaluation of other causes was performed for 1 year with 570 samples. In Low Hb patients’ CBC, Reticulocyte staining and sickling test was performed. Haemoglobin analysis was done by HPLC BIO RAD VARIANT II. In Iron Deficiency Anaemia (IDA) Serum ferritin & Serum Iron level were done and in Megaloblastic Anaemia(MA) Vitamin B12 level were done. Result: Prevalence of anaemia in antenatal patients was 90.25%; in this IDA presented with 84.21%, MA with 4.73% and Dimorphic anaemia 1.27%. Prevalence of haemoglobinopathies in this study was 9.75%; in this Beta Thalassemia Minor present with 5.08%, Sickle Cell Trait 4.03%, Hb D Punjab 0.52% and Hb Q india 0.17%. Conclusion: Antenatal screening for genetic disorders, such as Beta thalassemia, Sickle Cell Anaemia, aims to reduce the burden of these diseases by offering information to individual with a high likelihood of giving birth to affected babies and giving parents more choices regarding their reproductive decisions. For this, premarital and antenatal screening should be mandatory to prevent the birth of affected offspring.","PeriodicalId":103294,"journal":{"name":"Hematology & Transfusion International Journal","volume":"1 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-07-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Hematology & Transfusion International Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.15406/htij.2023.11.00306","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Introduction: Anaemia is an extremely common condition in pregnancy worldwide, conferring a number of health risks to mother and child. Iron deficiency is most widespread micronutritional deficiency in the world and disproportionately affects female because of increased iron requirements during menstruation, pregnancy and lactation. Haemoglobinopathies are a group of inherited disorders because of abnormalities in haemoglobin synthesis or structure. Thalassemia and Sickle cell anaemias are the most prevalent haemoglobinopathies and a national health burden in India so identifying these disorders during antenatal period is necessary to take appropriate measures. Methods: A prospective study of screening for haemoglobin variants in Antenatal Patients due to low haemoglobin and evaluation of other causes was performed for 1 year with 570 samples. In Low Hb patients’ CBC, Reticulocyte staining and sickling test was performed. Haemoglobin analysis was done by HPLC BIO RAD VARIANT II. In Iron Deficiency Anaemia (IDA) Serum ferritin & Serum Iron level were done and in Megaloblastic Anaemia(MA) Vitamin B12 level were done. Result: Prevalence of anaemia in antenatal patients was 90.25%; in this IDA presented with 84.21%, MA with 4.73% and Dimorphic anaemia 1.27%. Prevalence of haemoglobinopathies in this study was 9.75%; in this Beta Thalassemia Minor present with 5.08%, Sickle Cell Trait 4.03%, Hb D Punjab 0.52% and Hb Q india 0.17%. Conclusion: Antenatal screening for genetic disorders, such as Beta thalassemia, Sickle Cell Anaemia, aims to reduce the burden of these diseases by offering information to individual with a high likelihood of giving birth to affected babies and giving parents more choices regarding their reproductive decisions. For this, premarital and antenatal screening should be mandatory to prevent the birth of affected offspring.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
筛查产前患者的贫血和血红蛋白病
导读:贫血是全世界妊娠期极为常见的疾病,给母亲和儿童带来许多健康风险。缺铁是世界上最普遍的微量营养素缺乏症,由于月经、怀孕和哺乳期对铁的需求增加,对女性的影响尤为严重。血红蛋白病是由于血红蛋白合成或结构异常而引起的一组遗传性疾病。地中海贫血和镰状细胞性贫血是印度最普遍的血红蛋白病,也是国家卫生负担,因此有必要在产前查明这些疾病,以便采取适当措施。方法:一项前瞻性研究,筛查血红蛋白变异产前患者由于低血红蛋白和评估其他原因进行了1年的570个样本。对低Hb患者的CBC进行网织红细胞染色和镰状红细胞试验。血红蛋白分析采用HPLC BIO RAD VARIANT II。缺铁性贫血(IDA)测定血清铁蛋白和血清铁水平,巨幼细胞性贫血(MA)测定维生素B12水平。结果:产前患者贫血患病率为90.25%;其中IDA占84.21%,MA占4.73%,二型贫血占1.27%。本研究中血红蛋白病的患病率为9.75%;其中β地中海贫血5.08%,镰状细胞性状4.03%,旁遮普Hb D 0.52%,印度Hb Q 0.17%。结论:产前筛查遗传疾病,如β地中海贫血、镰状细胞性贫血,旨在通过向极有可能生育受影响婴儿的个人提供信息,并为父母在生育决定方面提供更多选择,从而减轻这些疾病的负担。为此,应强制进行婚前和产前检查,以防止产生受影响的后代。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
POSTCOVID-19 WAR era, remarkable accelerated hemato-immunologic processes affecting patients disease progression toward excess mortality POSTCOVID-19 WAR era, remarkable accelerated hemato-immunologic processes affecting patients disease progression toward excess mortality Von willebrand disease and gastrointestinal bleeding: case presentation Von willebrand disease and gastrointestinal bleeding: case presentation Prevalence and associated factors of anemia among elderly patients at a tertiary hospital in Estern Ethiopia: a cross-sectional study
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1