Prevalence of congenital anomalies and related factors in live births in Zahedan, Southeast of Iran: A cross-sectional study.

IF 1.6 Q3 OBSTETRICS & GYNECOLOGY International Journal of Reproductive Biomedicine Pub Date : 2023-09-20 eCollection Date: 2023-08-01 DOI:10.18502/ijrm.v21i8.14020
Azam Asemi-Rad, Zahra Heidari, Hamidreza Mahmoudzadeh-Sagheb, Yousef Mehdipour, Bita Moudi, Nadia Sheibak, Saeid Ebrahimi
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Abstract

Background: The term congenital anomalies (CAs) refers to structural or functional abnormalities at the time of conception. Approximately 12 deaths related to congenital disabilities occur in every 10,000 babies born.

Objective: This study aimed to evaluate the prevalence and associated factors of single and multiple CAs in live births in Zahedan, Southeast Iran.

Materials and methods: This cross-sectional study was conducted on 59,087 live births in a referral hospital in Zahedan located in the southeast of Iran from 2009 to 2019. All live births were examined by pediatricians and the CAs and categorized based on the international classification of diseases.

Results: Of 59,085 live births, at least 883 had a significant anomaly, and the prevalence rate of CAs was about 149 per 10,000. Anomalies of the nervous (24.1%) and cardiovascular systems (21.10%) were the most frequent, occurring in 213 and 187 of the live births, respectively. Spina bifida is the most common anomaly of the central nervous system. The most common anomalies in the cardiovascular system were unspecified heart malformations (17.1%), cardiovascular malformations (18.7%), and patent ductus arteriosus (11.7%). Significant correlations were found between the parent's consanguinity marriage, the mother's age, an existing anomaly in the family, and relatives in single and multiple CAs (p = 0.02, p = 0.02, p < 0.001, p = 0.01, respectively).

Conclusion: The prevalence of CAs was 149 per 10,000 live births. The highest prevalence of CAs was related to the central nervous system. Increasing the public's knowledge about fetal defects can reduce the prevalence of CAs.

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伊朗东南部扎黑丹活产先天性畸形的患病率及相关因素:一项横断面研究。
背景:先天性畸形是指受孕时的结构或功能异常。每出生10000名婴儿中,约有12人死于先天性残疾。目的:本研究旨在评估伊朗东南部扎黑丹地区活产中单个和多个CA的患病率及其相关因素。材料和方法:本横断面研究于2009年至2019年在伊朗东南部扎黑丹的一家转诊医院对59087例活产进行了研究。所有活产都由儿科医生和CA进行检查,并根据国际疾病分类进行分类。结果:在59085例活产中,至少883例有明显异常,CA的患病率约为万分之149。神经系统异常(24.1%)和心血管系统异常(21.10%)最为常见,分别发生在213例和187例活产中。脊柱裂是最常见的中枢神经系统异常。心血管系统中最常见的异常是未指明的心脏畸形(17.1%)、心血管畸形(18.7%)和动脉导管未闭(11.7%)。父母的血亲婚姻、母亲的年龄、家庭中存在的异常之间存在显著相关性,以及单胎和多胎CAs的亲属(分别为p=0.02,p=0.02,p=0.001,p=0.01)。结论:CAs的患病率为149/10000活产。CAs的最高患病率与中枢神经系统有关。增加公众对胎儿缺陷的了解可以降低CA的患病率。
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来源期刊
CiteScore
2.40
自引率
7.70%
发文量
93
审稿时长
16 weeks
期刊介绍: The International Journal of Reproductive BioMedicine (IJRM), formerly published as "Iranian Journal of Reproductive Medicine (ISSN: 1680-6433)", is an international monthly scientific journal for who treat and investigate problems of infertility and human reproductive disorders. This journal accepts Original Papers, Review Articles, Short Communications, Case Reports, Photo Clinics, and Letters to the Editor in the fields of fertility and infertility, ethical and social issues of assisted reproductive technologies, cellular and molecular biology of reproduction including the development of gametes and early embryos, assisted reproductive technologies in model system and in a clinical environment, reproductive endocrinology, andrology, epidemiology, pathology, genetics, oncology, surgery, psychology, and physiology. Emerging topics including cloning and stem cells are encouraged.
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