Literature DB >> 10895231

Acceptability of prenatal diagnosis of sickle cell anaemia by a sample of the Nigerian population.

M A Durosinmi1, A I Odebiyi, N O Akinola, L A Adediran, Y Aken'Ova, M A Okunade, N K Halim, K E Onwukeme, P O Olatunji, D E Adegoroye.   

Abstract

The acceptability of prenatal diagnosis (PND) as a means of controlling sickle cell anaemia (SCA) in Nigeria was examined using a semi-structured questionnaire. The aim of the study was to examine the attitudes of well-informed, educated Nigerians to the use of PND and abortion of confirmed HbSS pregnancies in the control of SCA. There were 433 respondents comprising 204 males and 210 females (gender was not recorded for 19 respondents). They were aged 15-50 (31 +/- 18) years. Forty percent had HbAA, 15% HbAS, 1.6% HbAC, 2% HbSS, and 0.2% HbSC; 153 (35%) had no knowledge of their haemoglobin electrophoretic patterns "genotypes". The majority of the respondents (69.5%) appreciated the role of both parents in the transmission of the disease. Only 45 (18%) of the respondents heard of SCA for the first time through sickle cell counsellors, 23% through newsmedia, 29% through friends and relations, 21% obtained the information through health workers, while 5% had never heard of sickle cell disease before the interview. As many as 192 (44%) of the respondents were aware that SCA could be diagnosed in pregnancy; 45% would opt for termination of the affected pregnancies. Avoidance of the problems associated with managing SCA children was the most important reason for approving pregnancy termination, whereas 73% of those rejecting pregnancy termination did so for religious and moral reasons. Seventy-eight percent of those interviewed would want PND started in Nigeria. The two approved control measure for SCA by most of the respondents were genetic counselling and PND; both should, therefore, be considered in implementing control measures for SCA in this country.

Entities:  

Keywords:  Empirical Approach; Genetics and Reproduction

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Substances:

Year:  1997        PMID: 10895231

Source DB:  PubMed          Journal:  Afr J Med Med Sci        ISSN: 0309-3913


  5 in total

1.  Hepatobiliary Ultrasonographic Abnormalities in Adult Patients with Sickle Cell Anaemia in Steady State in Ile-Ife, Nigeria.

Authors:  Oluwatosin O Oguntoye; Dennis A Ndububa; Musah Yusuf; Rahman A Bolarinwa; Oluwagbemiga O Ayoola
Journal:  Pol J Radiol       Date:  2017-01-03

2.  Medical genetics and genomic medicine in Nigeria.

Authors:  Adebowale A Adeyemo; Olukemi K Amodu; Ekanem E Ekure; Olayemi O Omotade
Journal:  Mol Genet Genomic Med       Date:  2018-06-05       Impact factor: 2.183

3.  Successful pregnancy outcome after in vitro fertilisation following Pre-implantation Genetic Diagnosis/Polymerase Chain Reaction screening for single gene disorder (sickle cell anaemia) before embryo transfer: The clinical experience of an in vitro fertilisation clinic in Nigeria.

Authors:  Chizara Okeke; Kemi Ailoje-Ibru; Kemi Olukoya; Rose Ogbeche; Abiola Adewusi; Ebele Iloabachie; Oladapo Ashiru
Journal:  Niger Med J       Date:  2014-01

4.  Some ethical issues in the prenatal diagnosis of sickle cell anaemia.

Authors:  Joseph O Fadare
Journal:  Ann Ib Postgrad Med       Date:  2009-12

5.  A Multi-centre Survey of Acceptability of Newborn Screening for Sickle Cell Disease in Nigeria.

Authors:  Obiageli E Nnodu; Samuel A Adegoke; Osita U Ezenwosu; Ifeoma I Emodi; Ngozi I Ugwu; Chinatu N Ohiaeri; Biobele J Brown; John A Olaniyi; Hezekiah Isa; Chinedu C Okeke; Benard A Bene; Modupe T Balogun; Emmanuel C Okocha; John C Aneke; Juliana Olufunke J Lawson; Abjah M Usman; Ijeoma N Diaku-Akinwumi; Angela A Okolo; Yetunde T Israel-Aina; Mustapha Jamda; Oladapo W Aworanti; Frédéric B Piel; Adekunle D Adekile
Journal:  Cureus       Date:  2018-03-21
  5 in total

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