Literature DB >> 25501660

Comparison and evaluation of three screening tests of hereditary spherocytosis in Chinese patients.

Yi-feng Tao1, Zeng-fu Deng, Lin Liao, Yu-ling Qiu, Wen-qiang Chen, Fa-quan Lin.   

Abstract

The objective of this study is to compare and evaluate the diagnostic value of hereditary spherocytosis (HS) by three screening tests, comparing mean spherical corpuscular volume (MSCV) to mean corpuscular volume (MCV), mean corpuscular hemoglobin concentration (MCHC), and flow cytometric osmotic fragility test. Peripheral blood was collected from 237 participators diagnosed at the First Affiliated Hospital of Guangxi Medical University, including 56 hereditary spherocytosis patients, 86 thalassemia patients, and 95 healthy people. The samples were examined by three tests, and the three screening tests were evaluated by the sensitivity and specificity of tests. The sensitivity was only 41.07%, and specificity was 94.47% when using MCHC >355 g/L as diagnostic criteria. The sensitivity was 89.28%, and specificity was 96.14% when using MSCV < MCV as the optimum cutoff point. When using the residual red cell percentage <23.6% as the diagnostic threshold in flow cytometric osmotic fragility test, the sensitivity was 85.71% and the specificity was 97.24%. Flow cytometry osmotic fragility test or comparing MSCV to MCV combined with smear examination of peripheral red blood cells morphology can be a simple, practical, and accurate hereditary spherocytosis (HS) laboratory screening method.

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Year:  2014        PMID: 25501660     DOI: 10.1007/s00277-014-2270-2

Source DB:  PubMed          Journal:  Ann Hematol        ISSN: 0939-5555            Impact factor:   3.673


  8 in total

1.  Usefulness of Reticulocyte Parameters for Diagnosis of Hereditary Spherocytosis in Children.

Authors:  Olga Ciepiela; Anna Adamowicz-Salach; Andżelika Radgowska; Katarzyna Żbikowska; Iwona Kotuła
Journal:  Indian J Hematol Blood Transfus       Date:  2016-05-24       Impact factor: 0.900

Review 2.  Old and new insights into the diagnosis of hereditary spherocytosis.

Authors:  Olga Ciepiela
Journal:  Ann Transl Med       Date:  2018-09

3.  Identification of a De Novoc.1000delA ANK1 mutation associated to hereditary spherocytosis in a neonate with Coombs-negative hemolytic jaundice-case reports and review of the literature.

Authors:  Lichun Xie; Zhihao Xing; Si-Xi Liu; Fei-Qiu Wen; Changgang Li
Journal:  BMC Med Genomics       Date:  2021-03-11       Impact factor: 3.063

4.  Cryohemolysis, erythrocyte osmotic fragility, and supplementary hematimetric indices in the diagnosis of hereditary spherocytosis.

Authors:  Ledesma Achem Miryam Emilse; Haro Cecilia; Terán Magdalena María; Mónaco María Eugenia; Issé Blanca Alicia; Sandra Stella Lazarte
Journal:  Blood Res       Date:  2018-03-27

5.  Blood cell parameters for screening and diagnosis of hereditary spherocytosis.

Authors:  Lin Liao; Yuchan Xu; Hongying Wei; Yuling Qiu; Wenqiang Chen; Jian Huang; Yifeng Tao; Xuelian Deng; Zengfu Deng; Hui Tao; Faquan Lin
Journal:  J Clin Lab Anal       Date:  2019-04-03       Impact factor: 2.352

Review 6.  The diagnostic protocol for hereditary spherocytosis-2021 update.

Authors:  Yangyang Wu; Lin Liao; Faquan Lin
Journal:  J Clin Lab Anal       Date:  2021-10-24       Impact factor: 2.352

7.  Study on Management of Blood Transfusion Therapy in Patients with Hereditary Spherocytosis.

Authors:  Shiyue Ma; Lingjian Tang; Chaoli Wu; Hui Tang; Xue Pu; Jinhong Niu
Journal:  Appl Bionics Biomech       Date:  2022-01-28       Impact factor: 1.781

8.  Novel SPTB frameshift mutation in a Chinese neonatal case of hereditary spherocytosis type 2: A case report.

Authors:  Cunxin Xu; Ya Wu; Dujuan Wang; Xuemin Zhang; Ningling Wang
Journal:  Exp Ther Med       Date:  2022-07-28       Impact factor: 2.751

  8 in total

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