Diagnostic Performance of 10 Mathematical Formulae for Identifying Blood Donors with Thalassemia Trait

Author:

Noulsri Egarit1ORCID,Lerdwana Surada2,Palasuwan Duangdao3,Palasuwan Attakorn3

Affiliation:

1. Research Division

2. Biomedical Research Incubator Unit, Faculty of Medicine Siriraj Hospital, Mahidol University , Bangkok , Thailand

3. Oxidation in Red Cell Disorders Research Unit, Department of Clinical Microscopy, Faculty of Allied Health Sciences, Chulalongkorn University , Bangkok , Thailand

Abstract

Abstract Objective To compare the diagnostic performance of 10 mathematical formulae for identifying thalassemia trait in blood donors. Methods Compete blood counts were conducted on peripheral blood specimens using the UniCel DxH 800 hematology analyzer. Receiver operating characteristic curves were used to evaluate the diagnostic performance of each mathematical formula. Results In the 66 donors with thalassemia and 288 subjects with no thalassemia analyzed, donors with thalassemia trait had lower values for mean corpuscular volume and mean corpuscular hemoglobin than subjects without thalassemia donors (77 fL vs 86 fL [P < .001]; 25 pg vs 28 pg [P < .001]). The formula developed by Shine and Lal in 1977 showed the highest area under the curve value, namely, 0.9. At the cutoff value of <1812, this formula had maximum specificity of 82.35% and sensitivity of 89.58%. Conclusions Our data indicate that the Shine and Lal formula has remarkable diagnostic performance in identifying donors with underlying thalassemia trait.

Funder

Chulalongkorn University

Publisher

Oxford University Press (OUP)

Subject

Biochemistry (medical),Clinical Biochemistry

Reference40 articles.

1. Thalassemia and malaria: new insights into an old problem;Clegg;Proc Assoc Am Physicians.,1999

2. Hb E/beta-thalassaemia: a common & clinically diverse disorder;Olivieri;Indian J Med Res.,2011

3. β-Thalassemia distribution in the Old World: an ancient disease seen from a historical standpoint;De Sanctis;Mediterr J Hematol Infect Dis,2017

4. Beta-thalassemia in Iran: new insight into the role of genetic admixture and migration;Rezaee;Sci. World J.,2012

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3