The prevalence of an elevated F cell population in a maternal and gynaecology cohort

SUMMARY Objectives This study aimed to determine F cell prevalence in a cohort of maternal and gynaecology specimens using QuikQuant anti‐HbF flow cytometry (FC) kit and to investigate if the presence of maternal F cells can lead to fetomaternal haemorrhage (FMH) overestimation. Background The gold...

Full description

Saved in:
Bibliographic Details
Published in:Transfusion medicine (Oxford, England) Vol. 29; no. 5; pp. 369 - 373
Main Authors: Cormack, O. M., Guilfoyle, F., Flynn, C. M.
Format: Journal Article
Language:English
Published: Oxford, UK Blackwell Publishing Ltd 01-10-2019
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:SUMMARY Objectives This study aimed to determine F cell prevalence in a cohort of maternal and gynaecology specimens using QuikQuant anti‐HbF flow cytometry (FC) kit and to investigate if the presence of maternal F cells can lead to fetomaternal haemorrhage (FMH) overestimation. Background The gold standard to estimate FMH is the Kleihauer–Betke test (KBT). The KBT has proved to be insufficiently sensitive to detect low numbers of circulating fetal cells due to the presence of maternal F cells. At present, the prevalence of false positive KBT results due to raised maternal F cell population, defined as >5%, is poorly characterised. Methods A total of 120 specimens were tested for the presence of F cells and fetal cells by KBT and anti‐HbF FC. The results calculated were compared to determine FMH overestimation. Results Of our cohort, 32% showed an elevated F cell population, of which 69% (27 of 39) were clinically significant according to KBT (>2 mL FMH). The mean FMH volumes by KBT and anti‐HbF FC were 3·90 mL (0·20–35·40 mL) and 4·09 mL (0·20–9·70 mL), respectively. Conclusion The study highlighted that an elevated F cell level could be found in the cohort tested, with an F cell level of >10% causing significant FMH overestimation by KBT.
Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ISSN:0958-7578
1365-3148
DOI:10.1111/tme.12625