Midwives’ Knowledge and Readiness to Practice Antenatal Screening and Genetic Testing in selected Hospitals in Lagos, Nigeria

Kafayat Asafa, C. Ndikom, Adewale Adelanwa
{"title":"Midwives’ Knowledge and Readiness to Practice Antenatal Screening and Genetic Testing in selected Hospitals in Lagos, Nigeria","authors":"Kafayat Asafa, C. Ndikom, Adewale Adelanwa","doi":"10.22038/JMRH.2021.56759.1690","DOIUrl":null,"url":null,"abstract":"Background & aim: The case fatality rate for most severe abnormalities such as anencephaly, trisomy 13, trisomy 18 and severe heart defects are virtually 100% by the child’s first birthday. The burden of congenital malformation can be decreased through two major approaches- primary preventions among those at risk through antenatal screening and improving survival among those who are affected. This study was conducted to investigate the knowledge and readiness of midwives to practice antenatal screening and genetic testing for congenital abnormalities. \nMethods: A cross-sectional study among 245 midwives who were selected across five (5) maternal and child health government hospitals within Lagos metropolis using simple random sampling method. The validated self-administered questionnaire, with 0.74 reliability coefficient, was used to obtain information within a period of Five weeks, after obtaining ethical approval. The obtained information was analysed using SPSS version 22 and the result was presented on frequency-percentage tables and charts while the hypotheses were tested at p = 0.05 using chi-square test. \nResults: The study findings revealed that most of the midwives sampled (37.6%) were aged between 31 and 40years. Some (56.3%) of the respondents were Registered Nurses/Registered Midwives only. The highest category of year of experience was 6 to 10years with 32.7%. 62.9% of the midwives had inadequate knowledge of antenatal screening and genetic testing for congenital abnormalities. Nonetheless, up to, 82.4% were ready to practice antenatal screening and genetic testing for congenital abnormalities. The midwives’ level of knowledge was not significantly associated with their readiness to practice antenatal screening and genetic testing for congenital abnormalities (p=0.74), meanwhile, professional qualification (p = 0.003) and years of experience (p < 0.001) were significantly associated with readiness to practice antenatal screening and genetic testing. \nConclusion: The study recommends that midwives should improve their knowledge and skills in genetic testing by attending both local and international training workshops/seminars. Government/employers of midwives should provide the screening devices to facilitate the practice of antenatal screening and genetic testing for congenital abnormalities during antenatal clinic.","PeriodicalId":283698,"journal":{"name":"Journal of midwifery and reproductive health","volume":"2106 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2021-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of midwifery and reproductive health","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.22038/JMRH.2021.56759.1690","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

Abstract

Background & aim: The case fatality rate for most severe abnormalities such as anencephaly, trisomy 13, trisomy 18 and severe heart defects are virtually 100% by the child’s first birthday. The burden of congenital malformation can be decreased through two major approaches- primary preventions among those at risk through antenatal screening and improving survival among those who are affected. This study was conducted to investigate the knowledge and readiness of midwives to practice antenatal screening and genetic testing for congenital abnormalities. Methods: A cross-sectional study among 245 midwives who were selected across five (5) maternal and child health government hospitals within Lagos metropolis using simple random sampling method. The validated self-administered questionnaire, with 0.74 reliability coefficient, was used to obtain information within a period of Five weeks, after obtaining ethical approval. The obtained information was analysed using SPSS version 22 and the result was presented on frequency-percentage tables and charts while the hypotheses were tested at p = 0.05 using chi-square test. Results: The study findings revealed that most of the midwives sampled (37.6%) were aged between 31 and 40years. Some (56.3%) of the respondents were Registered Nurses/Registered Midwives only. The highest category of year of experience was 6 to 10years with 32.7%. 62.9% of the midwives had inadequate knowledge of antenatal screening and genetic testing for congenital abnormalities. Nonetheless, up to, 82.4% were ready to practice antenatal screening and genetic testing for congenital abnormalities. The midwives’ level of knowledge was not significantly associated with their readiness to practice antenatal screening and genetic testing for congenital abnormalities (p=0.74), meanwhile, professional qualification (p = 0.003) and years of experience (p < 0.001) were significantly associated with readiness to practice antenatal screening and genetic testing. Conclusion: The study recommends that midwives should improve their knowledge and skills in genetic testing by attending both local and international training workshops/seminars. Government/employers of midwives should provide the screening devices to facilitate the practice of antenatal screening and genetic testing for congenital abnormalities during antenatal clinic.
助产士的知识和准备在尼日利亚拉各斯选定的医院进行产前筛查和基因检测
背景与目的:大多数严重的畸形,如无脑畸形、13三体、18三体和严重的心脏缺陷,到孩子一周岁时病死率几乎为100%。可以通过两种主要方法减少先天性畸形的负担:通过产前筛查对高危人群进行初级预防,以及提高受影响人群的生存率。本研究旨在调查助产士在产前筛查和先天性异常基因检测方面的知识和准备情况。方法:采用简单随机抽样的方法,对拉各斯市区5所公立妇幼保健医院的245名助产士进行横断面研究。经验证的自填问卷,信度系数为0.74,在获得伦理批准后,在五周内获取信息。所得资料采用SPSS 22进行分析,结果以频率百分比表格和图表呈现,假设采用卡方检验,p = 0.05。结果:调查结果显示,接生员年龄在31 ~ 40岁之间占37.6%。约56.3%的回答者只属注册护士/注册助产士。6 - 10年工作经验最多,占32.7%。62.9%的助产士对先天性异常的产前筛查和基因检测知识不足。尽管如此,高达82.4%的人准备进行先天性异常的产前筛查和基因检测。助产士的知识水平与从事产前筛查和先天性异常基因检测的意愿无显著相关(p=0.74),而专业资格(p= 0.003)和经验年限(p < 0.001)与从事产前筛查和基因检测的意愿有显著相关。结论:该研究建议助产士应该通过参加本地和国际培训讲习班/研讨会来提高他们在基因检测方面的知识和技能。政府/助产士的雇主应提供筛查设备,以便在产前诊所进行产前筛查和先天性异常基因测试。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
1.10
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信