Man Adeboye, M B Abdulkadir, O A Adegboye, A O Saka, P D Oladele, D M Oladele, E C Eze, O O Adeyemi, U Abubakar, A Grace, B F Rotimi
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A detailed examination was also performed and abnormalities documented. The data was analyzed using Epi-info version 6 (Atlanta, USA). The Chi-square was used to identify significant differences for categorical variables. Mid-P and Fisher's exact tests were utilized as appropriate. A <i>P</i> < 0.05 was considered to be significant.</p><p><strong>Results: </strong>A total of 46 children with congenital anomalies were seen during the study period, all which were recruited into the study. The hospital based prevalence amongst neonates was 111/1000 neonates. The most common system affected was the digestive system(50.0%) followed by the central nervous system and head and neck anomalies. There was no significant difference in distribution of anomalies amongst the various ethnic groups. About 22% of families were consanguineous, all being first cousins and 8.7% of mothers were greater than 35 years of age. The case fatality rate for congenital malformations was 2.2%, while 60.9% were referred to other hospitals for further care.</p><p><strong>Conclusion: </strong>The study has demonstrated a wide variety of congenital anomalies in Bida, North-Central Nigeria with the digestive system anomalies being the most frequent. 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引用次数: 8
摘要
背景:先天性疾病是出生时就存在的结构、代谢、行为和功能障碍。它们的表现是多种多样的,从轻微的异常到危及生命的情况。目的:本研究的目的是描述在比达联邦医疗中心12个月期间所见的先天性异常儿童,确定与这些异常相关的可能因素;以及他们的短期结果。研究对象和方法:连续招募临床确诊的先天性畸形患儿12个月,获取社会人口学、病因学等相关临床资料。还进行了详细的检查并记录了异常情况。使用Epi-info version 6 (Atlanta, USA)分析数据。使用卡方来确定类别变量的显著差异。适当时使用Mid-P和Fisher精确试验。P < 0.05为差异有统计学意义。结果:研究期间共发现46例先天性异常患儿,全部纳入研究。以医院为基础的新生儿患病率为111/1000。最常见的系统是消化系统(50.0%),其次是中枢神经系统和头颈部异常。不同族群间的异常分布无显著差异。大约22%的家庭是近亲,都是表兄弟姐妹,8.7%的母亲年龄超过35岁。先天性畸形病死率为2.2%,60.9%转诊至其他医院接受进一步治疗。结论:该研究表明,在尼日利亚中北部的比达市存在多种先天性异常,其中消化系统异常最为常见。这项研究的结果加强了在适当管理这些疾病方面赋予机构权力的必要性。
A Prospective Study of Spectrum, Risk Factors and Immediate Outcome of Congenital Anomalies in Bida, North Central Nigeria.
Background: Congenital disorders are structural, metabolic, behavioral and functional disorders that are present at birth. Their manifestations are protean ranging from mild anomalies to life-threatening conditions.
Aim: The objectives of this study were to describe the congenital anomalies in children seen at Federal Medical Center, Bida over a 12 month period, determine possible factors associated with these anomalies; and their short term outcome.
Subjects and methods: Children with clinically recognized congenital malformations were recruited consecutively over a 12 month period and socio-demographic, etiologic and other relevant clinical data were obtained. A detailed examination was also performed and abnormalities documented. The data was analyzed using Epi-info version 6 (Atlanta, USA). The Chi-square was used to identify significant differences for categorical variables. Mid-P and Fisher's exact tests were utilized as appropriate. A P < 0.05 was considered to be significant.
Results: A total of 46 children with congenital anomalies were seen during the study period, all which were recruited into the study. The hospital based prevalence amongst neonates was 111/1000 neonates. The most common system affected was the digestive system(50.0%) followed by the central nervous system and head and neck anomalies. There was no significant difference in distribution of anomalies amongst the various ethnic groups. About 22% of families were consanguineous, all being first cousins and 8.7% of mothers were greater than 35 years of age. The case fatality rate for congenital malformations was 2.2%, while 60.9% were referred to other hospitals for further care.
Conclusion: The study has demonstrated a wide variety of congenital anomalies in Bida, North-Central Nigeria with the digestive system anomalies being the most frequent. The findings of this study strengthen the need for empowerment of the institution in appropriate management of these disorders.