Literature DB >> 84163

Discrimination between iron-deficiency and heterozygous-thalassaemia syndromes in differential diagnosis of microcytosis.

J M England, P Fraser.   

Abstract

Three formulae have been advocated for interpreting the blood-count when differentiating between iron deficiency and heterozygous thalassaemia: the discriminant function. M.C.V.-R.B.C.-(5 X Hb)-k, the M.C.V/R.B.C. ratio, and the (M.C.V.)2 X M.C.H. product. In a comparison of their diagnostic accuracy in microcytic adults from several countries, the discriminant function was the most satisfactory. 417 of 455 uncomplicated cases (91.6%) of iron deficiency, heterozygous alpha1- and beta- thalassaemia were correctly identified. The function was not able to distinguish heterozygous alpha2-thalassaemia from iron deficiency. A flow chart illustrates how the discriminant function can be used in haematological practice.

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Year:  1979        PMID: 84163     DOI: 10.1016/s0140-6736(79)90532-4

Source DB:  PubMed          Journal:  Lancet        ISSN: 0140-6736            Impact factor:   79.321


  8 in total

1.  Guidelines for investigation of the alpha and beta thalassaemia traits. The Thalassaemia Working Party of the BCSH General Haematology Task Force.

Authors: 
Journal:  J Clin Pathol       Date:  1994-04       Impact factor: 3.411

2.  Thalassemia in Vietnamese refugees.

Authors:  R G Chaytors; M J Woolgar
Journal:  Can Med Assoc J       Date:  1981-05-15       Impact factor: 8.262

3.  NESTROFT - A Valuable, Cost Effective Screening Test for Beta Thalassemia Trait in North Indian Punjabi Population.

Authors:  Sanjay Piplani; Rahul Manan; Monika Lalit; Mridu Manjari; Tajinder Bhasin; Jasmine Bawa
Journal:  J Clin Diagn Res       Date:  2013-11-20

4.  Inadequate utilization of routine electronic RBC counts to identify beta thalassemia carriers.

Authors:  O Shalev; E Yehezkel; E A Rachmilewitz
Journal:  Am J Public Health       Date:  1988-11       Impact factor: 9.308

5.  Evaluation of low red blood cell mean corpuscular volume in an apheresis donor population.

Authors:  Barbara J Bryant; Julie A Hopkins; Sarah M Arceo; Susan F Leitman
Journal:  Transfusion       Date:  2009-05-11       Impact factor: 3.157

6.  Comparison of haemoglobin H inclusion bodies with embryonic zeta globin in screening for alpha thalassaemia.

Authors:  L C Chan; J C So; D H Chui
Journal:  J Clin Pathol       Date:  1995-09       Impact factor: 3.411

7.  Detection of β-Thalassemia Carriers by Red Cell Parameters Obtained from Automatic Counters using Mathematical Formulas.

Authors:  Idit Lachover Roth; Boaz Lachover; Guy Koren; Carina Levin; Luci Zalman; Ariel Koren
Journal:  Mediterr J Hematol Infect Dis       Date:  2018-01-01       Impact factor: 2.576

8.  Effect of heterozygous beta-thalassaemia trait on coronary atherosclerosis via coronary artery disease risk factors: a preliminary study.

Authors:  M Hashemi; E Shirzadi; Z Talaei; L Moghadas; I Shaygannia; M Yavari; N Amiri; H Taheri; H Montazeri; H Shamsolkottabi
Journal:  Cardiovasc J Afr       Date:  2007 May-Jun       Impact factor: 1.167

  8 in total

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