Sickle cell disease awareness and perception among Christian religious leaders in Accra Metropolis: a qualitative study.

IF 1.5 Q4 GENETICS & HEREDITY Journal of Community Genetics Pub Date : 2024-10-02 DOI:10.1007/s12687-024-00738-3
Rebecca Okyere, Menford Owusu Ampomah, Gloria Achempim-Ansong, Luke Laari, Lillian Akorfa Ohene, Karl Atkin
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Abstract

Sickle Cell Disease (SCD) is a severe hemoglobin gene mutation disorder inherited from both parents. 2% of Ghanaian newborns are affected by SCD; one in three Ghanaians has the hemoglobin S gene. Christian religious leaders may play a role in the prevention of SCD through the promotion of genetic counseling, genotype screening for premarital couples, and offering counseling to couples on prenatal screening and diagnosis for SCD. However, little is known about the awareness and perception of SCD among Christian religious leaders in Ghana, and this study aims to explore these. This study adopted a qualitative descriptive design to explore the awareness and perception of SCD among Christian religious leaders in the capital city of Ghana. A purposive sampling technique selected 16 participants from churches under the main Christian groups. The participants were chosen based on their roles and responsibilities within their respective churches. Data was collected using a semi-structured interview guide, which included open-ended questions to encourage participants to share their thoughts and experiences. The interviews were conducted in a private setting to ensure confidentiality. The data was then analyzed using a thematic analysis approach, which involved identifying recurring themes and patterns in the participants' responses. The study's findings are crucial. They reveal a high awareness of SCD among Christian religious leaders, but also some misconceptions. Most of the religious leaders knew SCD was a genetic disease, although a few associated SCD with superstitious beliefs, poor dietary intake, and lifestyle. Some also stated that SCD was a disease of the blood group instead of the defective haemoglobin gene. They perceived SCD to be burdensome, disruptive, and draining, and they associated the disease with burnout in Persons Living with SCD (PLWSCD) and their families. The religious leaders had a good social network with PLWSCD, including family, friends, colleagues, and congregants. These findings underscore the need for intense education about SCD, especially among Christian religious leaders. It is crucial to engage all stakeholders to intensify public awareness and education about SCD while improving the management and social support systems available to PLWSCD and families. This includes the religious institution's leadership, PLWSCD and families, the Ministry of Health, Ghana Health Service, and the Ghana Education Service. As active stakeholders, religious leaders can play a vital role in supporting PLWSCD if they are equipped with the necessary knowledge about the condition. .

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阿克拉市基督教宗教领袖对镰状细胞病的认识和看法:一项定性研究。
镰状细胞病(SCD)是一种严重的血红蛋白基因突变疾病,遗传自父母双方。2% 的加纳新生儿受到 SCD 的影响;每三个加纳人中就有一人带有 S 型血红蛋白基因。基督教宗教领袖可以通过推广遗传咨询、为婚前夫妇进行基因型筛查以及为夫妇提供产前筛查和 SCD 诊断方面的咨询,在预防 SCD 方面发挥作用。然而,人们对加纳基督教宗教领袖对 SCD 的认识和看法知之甚少,本研究旨在探讨这些问题。本研究采用了定性描述设计,以探讨加纳首都基督教宗教领袖对 SCD 的认识和看法。研究采用目的性抽样技术,从主要基督教团体下属的教堂中选出了 16 名参与者。这些参与者是根据他们在各自教会中的角色和职责选出的。数据收集采用了半结构化访谈指南,其中包括开放式问题,以鼓励参与者分享他们的想法和经验。访谈在私人环境中进行,以确保保密性。然后采用主题分析方法对数据进行了分析,包括从参与者的回答中找出重复出现的主题和模式。研究结果至关重要。它们揭示了基督教宗教领袖对 SCD 的高度认识,但也存在一些误解。大多数宗教领袖都知道 SCD 是一种遗传疾病,但也有少数人将 SCD 与迷信、不良饮食习惯和生活方式联系起来。有些人还说 SCD 是一种血型疾病,而不是血红蛋白基因缺陷疾病。他们认为 SCD 是一种负担、破坏性和耗费精力的疾病,并将这种疾病与 SCD 患者(PLWSCD)及其家人的职业倦怠联系在一起。宗教领袖们与 PLWSCD 有着良好的社会网络,包括家人、朋友、同事和教徒。这些发现强调了加强 SCD 相关教育的必要性,尤其是在基督教宗教领袖中。让所有利益相关者参与进来,加强公众对 SCD 的认识和教育,同时改善为 PLWSCD 及其家庭提供的管理和社会支持系统,这一点至关重要。这其中包括宗教机构的领导层、残疾人及其家庭、卫生部、加纳卫生服务机构和加纳教育服务机构。作为积极的利益相关者,宗教领袖如果掌握了有关 PLWSCD 的必要知识,就可以在支持 PLWSCD 方面发挥重要作用。.
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来源期刊
Journal of Community Genetics
Journal of Community Genetics GENETICS & HEREDITY-
CiteScore
3.30
自引率
5.30%
发文量
54
期刊介绍: The Journal of Community Genetics is an international forum for research in the ever-expanding field of community genetics, the art and science of applying medical genetics to human communities for the benefit of their individuals. Community genetics comprises all activities which identify persons at increased genetic risk and has an interest in assessing this risk, in order to enable those at risk to make informed decisions. Community genetics services thus encompass such activities as genetic screening, registration of genetic conditions in the population, routine preconceptional and prenatal genetic consultations, public education on genetic issues, and public debate on related ethical issues. The Journal of Community Genetics has a multidisciplinary scope. It covers medical genetics, epidemiology, genetics in primary care, public health aspects of genetics, and ethical, legal, social and economic issues. Its intention is to serve as a forum for community genetics worldwide, with a focus on low- and middle-income countries. The journal features original research papers, reviews, short communications, program reports, news, and correspondence. Program reports describe illustrative projects in the field of community genetics, e.g., design and progress of an educational program or the protocol and achievement of a gene bank. Case reports describing individual patients are not accepted.
期刊最新文献
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