Literature DB >> 30784072

First report of the rare RhCE-depleted D--phenotype in sixteen people of Iranian origin.

Ehsan Shahverdi1,2, Mostafa Moghaddam1, Hassan Abolghasemi3.   

Abstract

BACKGROUND AND OBJECTIVES: In transfusion medicine, it may be a challenge to acquire compatible blood for patients who have clinically important alloantibodies to high-prevalence antigens. The aim of this study was to study prevalence of rare D-- phenotype in samples from patients and their relatives referred to the Immunohematology reference laboratory of the Iranian Blood Transfusion Organization and the detection and identification of the phenotype and associated antibodies, particularly in an antenatal setting. This is the first report of the cases evaluated by the IBTO and family studies of the D-- proposita in Iran and possibly the first attempted comprehensive study in the current transfusion-related literatures.
MATERIALS AND METHODS: This retrospective cross-sectional study was carried out on 6720 pregnant women and individuals with difficult positive pretransfusion testing referred for ABO/Rh(D) typing and antibody screening during a period of 8 years from 2008 to December 2016 in the Immunohematology Reference Laboratory of the Iranian Blood Transfusion Organization, Tehran, Iran.
RESULTS: During 2008 to December 2016, 16 persons from ten families were detected to have rare D-- phenotype. Anti-Rh17 and anti-c were identified in plasma of the 11 persons, including 10 females with a history of multiple unsuccessful pregnancy and the total number of 24 abortions and one male with history of blood transfusion vs. 5 individuals, including an unmarried single woman, 1 person with a history of first-time pregnancy and 3 persons with a history of multiple pregnancy, who showed no alloimmunization. Based on these collective findings, we interpreted these results as being confirmed as D-- phenotype (0.23%).
CONCLUSION: Irrespective of Rh (D) group a serological antibody screening test is recommended to be required in a National prenatal testing guideline.
© 2019 International Society of Blood Transfusion.

Entities:  

Keywords:  Anti-Rh17 (anti-Hro); D-- phenotype; haemolytic disease of the fetus and newborn

Mesh:

Substances:

Year:  2019        PMID: 30784072     DOI: 10.1111/vox.12738

Source DB:  PubMed          Journal:  Vox Sang        ISSN: 0042-9007            Impact factor:   2.144


  1 in total

1.  Ethical Issues and Management of Fetal Hemolytic Anemia Caused by Anti-Rh17 in a Multipara with Rare -D- Phenotype.

Authors:  Patrick P Torreiter; Susanne Macher; Eva-Maria Matzhold; Bernhard Resch; Philipp Klaritsch; Günther F Körmöczi; Helene Polin; Leopold Neuhold; Marlies Schönbacher; Peter Schlenke; Thomas Wagner
Journal:  Transfus Med Hemother       Date:  2021-01-05       Impact factor: 3.747

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.