Literature DB >> 7481937

Acceptability of prenatal diagnosis of sickle cell anaemia (SCA) by female patients and parents of SCA patients in Nigeria.

M A Durosinmi1, A I Odebiyi, I A Adediran, N O Akinola, D E Adegorioye, M A Okunade.   

Abstract

The acceptability of prenatal diagnosis (PND) of sickle cell anaemia (SCA) as a means of controlling sickle cell disorder in Nigeria was examined using a structured questionnaire. The respondents were comprised of 92 adult female patients with SCA, aged 15-20 (23 +/- 6) years; 53 HbAS mothers, aged 20-61 (37 +/- 11) years and 48 HbAS fathers, aged 33-65 (46 +/- 8) years. More than 85% of the respondents would like PND to be offered in Nigeria and 92% of the HbAS mothers as well as 86% of the fathers would like to have the investigation or allow their wives to go through the procedure, respectively. Only 35% of the patients as compared to 63% of the mothers and 51% of the fathers would opt for termination of an affected pregnancy. Fear of the complications of abortion and religious convictions were the two most frequently cited reasons for opposing pregnancy termination. The high percentage of parents who would opt for termination of an affected pregnancy was associated with the societal emphasis on perfection and on previous experience in management of SCA patients. It is interesting that most of the respondents still favoured effective genetic counselling as the best means of controlling SCA.

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Year:  1995        PMID: 7481937     DOI: 10.1016/0277-9536(94)00361-v

Source DB:  PubMed          Journal:  Soc Sci Med        ISSN: 0277-9536            Impact factor:   4.634


  15 in total

1.  Acceptability of prenatal diagnosis by a sample of parents of sickle cell anemia patients in Cameroon (sub-Saharan Africa).

Authors:  Ambroise Wonkam; Alfred K Njamnshi; Dora Mbanya; Jeanne Ngogang; Caryl Zameyo; Fru F Angwafo
Journal:  J Genet Couns       Date:  2011-05-21       Impact factor: 2.537

2.  A call for policy action in sub-Saharan Africa to rethink diagnostics for pregnancy affected by sickle cell disease: differential views of medical doctors, parents and adult patients predict value conflicts in Cameroon.

Authors:  Ambroise Wonkam; Samia Hurst
Journal:  OMICS       Date:  2014-04-22

3.  Decisions about testing and termination of pregnancy for different fetal conditions: a qualitative study of European White and Pakistani mothers of affected children.

Authors:  Shenaz Ahmed; Jenny Hewison; Josephine M Green; Howard S Cuckle; Janet Hirst; Jim G Thornton
Journal:  J Genet Couns       Date:  2008-10-09       Impact factor: 2.537

4.  Types of anaemic crises in paediatric patients with sickle cell anaemia seen in Enugu, Nigeria.

Authors:  A I Juwah; E U Nlemadim; W Kaine
Journal:  Arch Dis Child       Date:  2004-06       Impact factor: 3.791

5.  Ethical, social, and cultural issues related to clinical genetic testing and counseling in low- and middle-income countries: a systematic review.

Authors:  Adrina Zhong; Benedict Darren; Bethina Loiseau; Li Qun Betty He; Trillium Chang; Jessica Hill; Helen Dimaras
Journal:  Genet Med       Date:  2018-08-03       Impact factor: 8.822

6.  Perspectives in Genetics and Sickle Cell Disease Prevention in Africa: Beyond the Preliminary Data from Cameroon.

Authors:  Ambroise Wonkam; Valentina Josiane Ngo Bitoungui; Jeanne Ngogang
Journal:  Public Health Genomics       Date:  2015-06-04       Impact factor: 2.132

7.  Public perceptions and attitudes toward thalassaemia: Influencing factors in a multi-racial population.

Authors:  Li Ping Wong; Elizabeth George; Jin-Ai Mary Anne Tan
Journal:  BMC Public Health       Date:  2011-03-30       Impact factor: 3.295

Review 8.  Sickle cell disease: new opportunities and challenges in Africa.

Authors:  J Makani; S F Ofori-Acquah; O Nnodu; A Wonkam; K Ohene-Frempong
Journal:  ScientificWorldJournal       Date:  2013-09-19

9.  The role of religious leaders and faith organisations in haemoglobinopathies: a review.

Authors:  Thelma K Toni-Uebari; Baba P D Inusa
Journal:  BMC Blood Disord       Date:  2009-08-15

10.  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
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