Regional Distribution of Congenital Heart Disease in Iran; A Study on 1000 Iranian Hospitalized Patients in Three Years

authors:

avatar Samira Kalayinia ORCID 1 , avatar Mohammad Mahdavi ORCID 1 , avatar Majid Maleki ORCID 1 , avatar Saeideh Mazloumzadeh 2 , avatar Bahareh Rabbani 1 , 3 , avatar Nejat Mahdieh ORCID 1 , 3 , *

Cardiogenetic Research Center, Rajaie Cardiovascular Medical and Research Center, Iran University of Medical Sciences, Tehran, IR Iran
Rajaie Cardiovascular Medical and Research Center, Iran University of Medical Sciences, Tehran, IR Iran
Growth and Development Research Center, Tehran University of Medical Sciences, Tehran, IR Iran

how to cite: Kalayinia S, Mahdavi M, Maleki M , Mazloumzadeh S, Rabbani B, et al. Regional Distribution of Congenital Heart Disease in Iran; A Study on 1000 Iranian Hospitalized Patients in Three Years. Int Cardiovasc Res J. 2020;14(4):e108858. 

Abstract

Background:
Congenital Heart Disease (CHD) is a major health problem around the world. Several maternal and fetal risk factors have been mentioned to be associated with development of CHD. However, the epidemiological pattern is different in various parts of the world. Thus, the present study aimed to demonstrate the descriptive characteristics of a group of Iranian children with CHD.
Objectives:
The present study aimed to determine the regional distribution of CHD among 1000 Iranian hospitalized children during three years.
Methods:
This cross-sectional study was conducted on 1000 Iranian children with CHD who were hospitalized in Rajaie Cardiovascular, Medical and Research Center, as a tertiary cardiovascular hospital (2017 - 2019). The participants were selected via convenience sampling. Clinical data were extracted from the patients' medical records and questionnaires and then, a comprehensive evaluation was performed.
Results:
The median (IQR) age of the children was 18 (8 - 60) months. In addition, the mean ± SD of maternal age at pregnancy was 27.3 ± 5.92 years. Ventricular Septal Defect (VSD) was the most frequent CHD. Most of the patients were Fars (35.7%), Azeri (18.4%), and Kurd (10.7%). Besides, 58.7% of the patients lived in rural areas. The family history of CHD was present in 23.9% of the patients. Additionally, 41.4% of the patients’ parents had consanguineous marriages. Spotting was the most common (48.7%) complication during pregnancy followed by infectious disease (24.2%), toothache (12.9%), and diabetes mellitus (7.8%).
Conclusions:
The present study demonstrated the baseline neonatal and maternal characteristics of the patients with CHD, which revealed that some risk factors were common in these individuals. Hence, it is necessary to provide preventive strategies for modifiable risk factors, monitor high-risk pregnant women at shorter intervals, raise awareness in the general population, and perform genetic counselling, as appropriated. This was the first report of the CHD frequency in Iran.
 

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