Literature DB >> 23918815

Would you terminate a pregnancy affected by sickle cell disease? Analysis of views of patients in Cameroon.

Ambroise Wonkam1, Jantina de Vries2, Charmaine D Royal3, Raj Ramesar4, Fru F Angwafo5.   

Abstract

Sickle cell disease (SCD) is a debilitating illness that affects quality of life and life expectancy for patients. In Cameroon, it is now possible to opt for termination of an affected pregnancy (TAP) where the fetus is found to be affected by SCD. Our earlier studies found that, contrary to the views of Cameroonian physicians, a majority of parents with their children suffering from SCD would choose to abort if the fetuses were found to be affected. What have not yet been investigated are the views of people suffering from/living with SCD. We used a quantitative sociological method, with administered structured questionnaires, to study the attitudes of adult patients suffering from SCD on prenatal genetic diagnosis (PND) and possible TAP. The majority of the 89 participants were urban dwellers (84.3%), women (57.3%), Christian (95.5%) and single (90.9%), with a secondary/tertiary education (79.5%). The majority (89.2%) would consider PND for SCD; almost half (48.5%) would reject TAP while 40.9% would consider it. Respondents who rejected TAP claimed mostly ethical reasons (78.1%) while those who found TAP acceptable cited fear of having an affected child (88.9%) and the poor quality of the affected child's health (81.5%). Cameroonian patients with SCD are generally supportive of PND and a remarkably high number of patients living with SCD reported that they would consider terminating a pregnancy based on their assessment of the future well-being of the child. Research is required to investigate the burden of SCD on families and their quality of life. Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.

Entities:  

Keywords:  Abortion; Abortion Counselling; Clinical Ethics; Genetic Counselling/Prenatal Diagnosis; Genetic Screening/Testing

Mesh:

Year:  2013        PMID: 23918815     DOI: 10.1136/medethics-2013-101392

Source DB:  PubMed          Journal:  J Med Ethics        ISSN: 0306-6800            Impact factor:   2.903


  12 in total

Review 1.  The current state of sickle cell trait: implications for reproductive and genetic counseling.

Authors:  Lydia H Pecker; Rakhi P Naik
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2018-11-30

Review 2.  The current state of sickle cell trait: implications for reproductive and genetic counseling.

Authors:  Lydia H Pecker; Rakhi P Naik
Journal:  Blood       Date:  2018-11-29       Impact factor: 22.113

Review 3.  Beta-globin gene haplotypes among cameroonians and review of the global distribution: is there a case for a single sickle mutation origin in Africa?

Authors:  Valentina J Ngo Bitoungui; Gift D Pule; Neil Hanchard; Jeanne Ngogang; Ambroise Wonkam
Journal:  OMICS       Date:  2015-03

4.  It's complicated - Factors predicting decisional conflict in prenatal diagnostic testing.

Authors:  Cécile Muller; Linda D Cameron
Journal:  Health Expect       Date:  2015-04-13       Impact factor: 3.377

5.  Relation Between Religious Perspectives and Views on Sickle Cell Disease Research and Associated Public Health Interventions in Ghana.

Authors:  Jemima A Dennis-Antwi; Kwaku Ohene-Frempong; Kofi A Anie; Helen Dzikunu; Veronica A Agyare; Richard Okyere Boadu; Joseph Sarfo Antwi; Mabel K Asafo; Oboshie Anim-Boamah; Augustine K Asubonteng; Solomon Agyei; Ambroise Wonkam; Marsha J Treadwell
Journal:  J Genet Couns       Date:  2018-09-01       Impact factor: 2.537

6.  Perception of Genetic Testing for Deafness and Factors Associated with Interest in Genetic Testing Among Deaf People in a Selected Population in Sub-Saharan Africa.

Authors:  Babatunde O Adedokun; Bidemi O Yusuf; J Taye Lasisi; A A Jinadu; M T Sunmonu; A F Ashanke; O Akeem Lasisi
Journal:  J Genet Couns       Date:  2015-05-19       Impact factor: 2.537

7.  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

8.  Psychosocial stressors of sickle cell disease on adult patients in Cameroon.

Authors:  Ambroise Wonkam; Caryl Zameyo Mba; Dora Mbanya; Jeanne Ngogang; Raj Ramesar; Fru F Angwafo
Journal:  J Genet Couns       Date:  2014-02-21       Impact factor: 2.537

9.  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

Review 10.  Knowledge gaps in reproductive and sexual health in girls and women with sickle cell disease.

Authors:  Lydia H Pecker; Deva Sharma; Alecia Nero; Michael J Paidas; Russell E Ware; Andra H James; Kim Smith-Whitley
Journal:  Br J Haematol       Date:  2021-07-07       Impact factor: 8.615

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