Adane Fentahun, Afework Mekbeb, Seyoum Girma, Gebrie Alemu
Department of Anatomy, College of Health Sciences, Addis Ababa University, Addis Ababa, Ethiopia.
Department of Biomedical Science, School of Medicine, Debre Markos University, Debre Markos, Ethiopia.
Pan Afr Med J. 2020 May 14;36:19. doi: 10.11604/pamj.2020.36.19.19411. eCollection 2020.
Birth defects are the most serious causes of infant mortality and disability in sub-Saharan African countries with variable magnitude. Hence, this study was aimed to determine the pooled prevalence of birth defects and its associated risk factors among newborn infants in sub-Saharan African countries.
A total of 43 eligible studies were identified through literature search from Medline (PubMed), EMBASE, HINARI, Google scholar, Science Direct, Cochrane Library and other sources. Extracted data were analyzed using STATA 15.0 statistical software. A random effect meta-analysis model was used.
Twenty-five studies in 9 countries showed that the pooled prevalence of birth defects was 20.40 per 1,000 births (95% CI: 17.04, 23.77). In the sub-group analysis, the highest prevalence was observed in southern Africa region with a prevalence of 43 per 1000 (95% CI: 14.89, 71.10). The most prevalent types of birth defects were musculo-skeletal system defects with a pooled prevalence of 3.90 per 1000 (95% CI: 3.11, 4.70) while the least was Down syndrome 0.62 per 1000 (95% CI: 0.40, 0.84). Lack of folic acid supplementation (95% CI: 1.95, 7.88), presence of chronic disease (95% CI: 2.00, 6.07) and intake of drugs (95% CI: 3.88, 14.66) during pregnancy were significantly associated with the birth defects.
The prevalence of birth defects is relatively high with high degree of regional variabilities. The most common types of birth defects were musculoskeletal defects. Lack of folic acid supplementation, presence of chronic disease and intake of drugs during pregnancy were significantly associated with birth defects.
出生缺陷是撒哈拉以南非洲国家婴儿死亡和残疾的最严重原因,其严重程度各不相同。因此,本研究旨在确定撒哈拉以南非洲国家新生儿出生缺陷的合并患病率及其相关危险因素。
通过文献检索,从Medline(PubMed)、EMBASE、HINARI、谷歌学术、科学Direct、Cochrane图书馆和其他来源共识别出43项符合条件的研究。使用STATA 15.0统计软件对提取的数据进行分析。采用随机效应荟萃分析模型。
9个国家的25项研究表明,出生缺陷的合并患病率为每1000例出生20.40例(95%CI:17.04,23.77)。在亚组分析中,南部非洲地区的患病率最高,为每1000例43例(95%CI:14.89,71.10)。最常见的出生缺陷类型是肌肉骨骼系统缺陷,合并患病率为每1000例3.90例(95%CI:3.11,4.70),而最低的是唐氏综合征,每1000例0.62例(95%CI:0.40,0.84)。孕期缺乏叶酸补充(95%CI:1.95,7.88)以及患有慢性病(95%CI:2.00,6.07)和孕期服药(95%CI:3.88,14.66)与出生缺陷显著相关。
出生缺陷的患病率相对较高,且存在高度的地区差异。最常见的出生缺陷类型是肌肉骨骼缺陷。孕期缺乏叶酸补充、患有慢性病和孕期服药与出生缺陷显著相关。