Back to Search Start Over

Foetal haemoglobin (HbF) status in adult sickle cell anaemia patients in Ibadan, Nigeria

Authors :
A. B. Odetunde
J. A. Olaniyi
O. G Arinola
Source :
Annals of Ibadan Postgraduate Medicine; Vol 8, No 1 (2010); 30-33, Annals of Ibadan Postgraduate Medicine
Publication Year :
2011
Publisher :
Annals of Ibadan Postgraduate Medicine, 2011.

Abstract

Aim: - Elevated HbF, among other biological and environmental factors, is responsible for decrease in mortality in sickle cell anaemia (SCA). This study determined the levels of HbF in adult SCA patients in steady state compared with HbAA controls. HbF was discussed in line with the clinical course of the disease so as to emphasize the relevance of hydroxyurea in the management of adult SCA patients.Materials and methods: - The HbF levels of 66 confirmed SCA patients and 31 HbAA controls were estimated using Betke method and HbF percentage was calculated using formula: %HbF percentage = A413 filtrate x 100A413 standard x 20.Result: - A statistical significant difference in the mean of the levels of HbF in patients (5.16±4.04) compared to controls (1.04±0.44) (p = 0.000) was observed. The mean levels of HbF for males (4.71±3.49) compared to that of females (4.99) were statistically similar (p =0.773). It was also observed that the mean HbF level appears to be declining as age advances. SCA patients were classified to three categories viz: HbF

Details

Language :
English
ISSN :
15971627
Database :
OpenAIRE
Journal :
Annals of Ibadan Postgraduate Medicine
Accession number :
edsair.doi.dedup.....6fdf47e018c06729b06acde8dbe5c936