The commencement of congenital heart diseases registry in Isfahan, Iran: Methodology and design

BACKGROUND: Reported prevalence of congenital heart diseases (CHDs) varies widely among studies worldwide. The incidence of CHD, total number of pediatric and adult grown-up congenital heart disease (GUCH), is not determined in Iran. Therefore, we have designed a system to register the information o...

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Main Authors: Bahar Dehghan, Mohammad Reza Sabri, Mohsen Hosseinzadeh, Alireza Ahmadi, Mehdi Ghaderian, Nizal Sarrafzadegan, Hamidreza Roohafza
Format: Article
Language:English
Published: Vesnu Publications 2020-10-01
Series:ARYA Atherosclerosis
Subjects:
Online Access:https://arya.mui.ac.ir/article_10749_ac1bc645e02305cb46a85144d93e188a.pdf
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author Bahar Dehghan
Mohammad Reza Sabri
Mohsen Hosseinzadeh
Alireza Ahmadi
Mehdi Ghaderian
Nizal Sarrafzadegan
Hamidreza Roohafza
author_facet Bahar Dehghan
Mohammad Reza Sabri
Mohsen Hosseinzadeh
Alireza Ahmadi
Mehdi Ghaderian
Nizal Sarrafzadegan
Hamidreza Roohafza
author_sort Bahar Dehghan
collection DOAJ
description BACKGROUND: Reported prevalence of congenital heart diseases (CHDs) varies widely among studies worldwide. The incidence of CHD, total number of pediatric and adult grown-up congenital heart disease (GUCH), is not determined in Iran. Therefore, we have designed a system to register the information of patients with CHD for the first time in our country.METHODS: CHD registry is a database in which the patients' data are collected by five pediatric cardiologists from three referral hospitals affiliated to Isfahan University of Medical Sciences, Isfahan, Iran, and five outpatient clinics. We enrolled patients with CHD either as new cases who were referred for evaluation of potential CHD or those who were being followed within the outpatient clinics and entered their whole information in a website specifically designed for it. All the information was collected from checklist by those pediatric cardiologistsRESULTS: From April 2017 to April 2020, after developing the forms and website, the Quality Control Committee evaluated the first 558 files. 73 files (13%) needed major revisions. Among them, 34 (46%) files were omitted totally and the 39 remaining files were revised and completed. After that revision, we changed our checklist and gathered about 1600 patients accordingly.CONCLUSION: Registry of CHDs not only improves epidemiologic studies but also assists researchers to understand how much a disease management is useful and how to raise the quality of cares and outcomes. Moreover, this provides a better insight for policymakers to understand the extent of health-related problems as well as the issues related to the prevention and management of CHDs all around the world.
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spelling doaj.art-1438b7893cca43dda17f224baf322a952023-03-11T12:58:52ZengVesnu PublicationsARYA Atherosclerosis1735-39552251-66382020-10-0116524424710.22122/arya.v16i5.191310749The commencement of congenital heart diseases registry in Isfahan, Iran: Methodology and designBahar Dehghan0Mohammad Reza Sabri1Mohsen Hosseinzadeh2Alireza Ahmadi3Mehdi Ghaderian4Nizal Sarrafzadegan5Hamidreza Roohafza6Assistant Professor, Pediatric Cardiovascular Research Center, Cardiovascular Research Institute, Isfahan University of Medical Sciences, Isfahan, IranProfessor, Pediatric Cardiovascular Research Center, Cardiovascular Research Institute, Isfahan University of Medical Sciences, Isfahan, IranAssistant Professor, Department of Pediatric Cardiology, School of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, IranAssociate Professor, Pediatric Cardiovascular Research Center, Cardiovascular Research Institute, Isfahan University of Medical Sciences, Isfahan, IranAssociate Professor, Pediatric Cardiovascular Research Center, Cardiovascular Research Institute, Isfahan University of Medical Sciences, Isfahan, IranProfessor, Isfahan Cardiovascular Research Center, Cardiovascular Research Institute, Isfahan University of Medical Sciences, Isfahan, IranAssistant Professor, Cardiac Rehabilitation Research Center, Cardiovascular Research Institute, Isfahan University of Medical Sciences, Isfahan, IranBACKGROUND: Reported prevalence of congenital heart diseases (CHDs) varies widely among studies worldwide. The incidence of CHD, total number of pediatric and adult grown-up congenital heart disease (GUCH), is not determined in Iran. Therefore, we have designed a system to register the information of patients with CHD for the first time in our country.METHODS: CHD registry is a database in which the patients' data are collected by five pediatric cardiologists from three referral hospitals affiliated to Isfahan University of Medical Sciences, Isfahan, Iran, and five outpatient clinics. We enrolled patients with CHD either as new cases who were referred for evaluation of potential CHD or those who were being followed within the outpatient clinics and entered their whole information in a website specifically designed for it. All the information was collected from checklist by those pediatric cardiologistsRESULTS: From April 2017 to April 2020, after developing the forms and website, the Quality Control Committee evaluated the first 558 files. 73 files (13%) needed major revisions. Among them, 34 (46%) files were omitted totally and the 39 remaining files were revised and completed. After that revision, we changed our checklist and gathered about 1600 patients accordingly.CONCLUSION: Registry of CHDs not only improves epidemiologic studies but also assists researchers to understand how much a disease management is useful and how to raise the quality of cares and outcomes. Moreover, this provides a better insight for policymakers to understand the extent of health-related problems as well as the issues related to the prevention and management of CHDs all around the world.https://arya.mui.ac.ir/article_10749_ac1bc645e02305cb46a85144d93e188a.pdfregistriescongenitalheart diseasesdata collection
spellingShingle Bahar Dehghan
Mohammad Reza Sabri
Mohsen Hosseinzadeh
Alireza Ahmadi
Mehdi Ghaderian
Nizal Sarrafzadegan
Hamidreza Roohafza
The commencement of congenital heart diseases registry in Isfahan, Iran: Methodology and design
ARYA Atherosclerosis
registries
congenital
heart diseases
data collection
title The commencement of congenital heart diseases registry in Isfahan, Iran: Methodology and design
title_full The commencement of congenital heart diseases registry in Isfahan, Iran: Methodology and design
title_fullStr The commencement of congenital heart diseases registry in Isfahan, Iran: Methodology and design
title_full_unstemmed The commencement of congenital heart diseases registry in Isfahan, Iran: Methodology and design
title_short The commencement of congenital heart diseases registry in Isfahan, Iran: Methodology and design
title_sort commencement of congenital heart diseases registry in isfahan iran methodology and design
topic registries
congenital
heart diseases
data collection
url https://arya.mui.ac.ir/article_10749_ac1bc645e02305cb46a85144d93e188a.pdf
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