How do we define congenital heart defects for scientific studies?

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Standard

How do we define congenital heart defects for scientific studies? / Danish Register of Congenital Heart Disease.

I: Congenital Heart Disease, Bind 7, Nr. 1, 21.10.2011, s. 46-9.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Danish Register of Congenital Heart Disease 2011, 'How do we define congenital heart defects for scientific studies?', Congenital Heart Disease, bind 7, nr. 1, s. 46-9. https://doi.org/10.1111/j.1747-0803.2011.00581.x

APA

Danish Register of Congenital Heart Disease (2011). How do we define congenital heart defects for scientific studies? Congenital Heart Disease, 7(1), 46-9. https://doi.org/10.1111/j.1747-0803.2011.00581.x

Vancouver

Danish Register of Congenital Heart Disease. How do we define congenital heart defects for scientific studies? Congenital Heart Disease. 2011 okt. 21;7(1):46-9. https://doi.org/10.1111/j.1747-0803.2011.00581.x

Author

Danish Register of Congenital Heart Disease. / How do we define congenital heart defects for scientific studies?. I: Congenital Heart Disease. 2011 ; Bind 7, Nr. 1. s. 46-9.

Bibtex

@article{6650e871216c4cd3b73b3417d305799f,
title = "How do we define congenital heart defects for scientific studies?",
abstract = "Estimates of the prevalence of congenital heart defects (CHD) have been published over many years and from many regions. As they are based on different definitions of which cases to include in the CHD prevalence, published prevalence estimates vary substantially. With the increasing use of echocardiography in neonatal intensive care, a patent ductus arteriosus (PDA) or flow over the atrial septum will often be visible. These findings may be coded as CHD at discharge and in this way falsely increase the CHD prevalence in the population. There are several purposes for which population-based data on CHD may be used: etiology, planning of treatment, or obtain information on outcome, including mortality. For etiology studies, it is important to include terminations of pregnancy as well as all births with CHD. For mortality studies in live births, inclusion of preterm born infants with PDA will increase overall mortality of CHD. The Danish Register of Congenital Heart Disease is based on hospital discharge diagnoses and diagnoses from outpatient visits. To increase the validity of these data, extensive data cleaning has been carried out based on record review and knowledge on the discharge coding practice. We include PDA and atrial septal defects as CHD cases if these defects are still open 2 months after birth. International consensus on how to define CHD would improve the validity and comparability of epidemiological studies on CHD.",
keywords = "Denmark/epidemiology, Epidemiologic Research Design, Female, Heart Defects, Congenital/classification, Humans, Infant, Infant, Newborn, International Classification of Diseases, Male, Patient Discharge/statistics & numerical data, Pregnancy, Prevalence, Quality Indicators, Health Care/statistics & numerical data, Registries, Terminology as Topic, Time Factors",
author = "Ester Garne and Olsen, {Morten Smaerup} and Johnsen, {S{\o}ren Paaske} and Vibeke Hjortdal and Andersen, {Henrik {\O}rbaek} and Henrik Nissen and Lars S{\o}ndergaard and J{\o}rgen Videbaek and {Danish Register of Congenital Heart Disease}",
note = "{\textcopyright} 2011 Wiley Periodicals, Inc.",
year = "2011",
month = oct,
day = "21",
doi = "10.1111/j.1747-0803.2011.00581.x",
language = "English",
volume = "7",
pages = "46--9",
journal = "Congenital Heart Disease",
issn = "1747-079X",
publisher = "Wiley-Blackwell",
number = "1",

}

RIS

TY - JOUR

T1 - How do we define congenital heart defects for scientific studies?

AU - Garne, Ester

AU - Olsen, Morten Smaerup

AU - Johnsen, Søren Paaske

AU - Hjortdal, Vibeke

AU - Andersen, Henrik Ørbaek

AU - Nissen, Henrik

AU - Søndergaard, Lars

AU - Videbaek, Jørgen

AU - Danish Register of Congenital Heart Disease

N1 - © 2011 Wiley Periodicals, Inc.

PY - 2011/10/21

Y1 - 2011/10/21

N2 - Estimates of the prevalence of congenital heart defects (CHD) have been published over many years and from many regions. As they are based on different definitions of which cases to include in the CHD prevalence, published prevalence estimates vary substantially. With the increasing use of echocardiography in neonatal intensive care, a patent ductus arteriosus (PDA) or flow over the atrial septum will often be visible. These findings may be coded as CHD at discharge and in this way falsely increase the CHD prevalence in the population. There are several purposes for which population-based data on CHD may be used: etiology, planning of treatment, or obtain information on outcome, including mortality. For etiology studies, it is important to include terminations of pregnancy as well as all births with CHD. For mortality studies in live births, inclusion of preterm born infants with PDA will increase overall mortality of CHD. The Danish Register of Congenital Heart Disease is based on hospital discharge diagnoses and diagnoses from outpatient visits. To increase the validity of these data, extensive data cleaning has been carried out based on record review and knowledge on the discharge coding practice. We include PDA and atrial septal defects as CHD cases if these defects are still open 2 months after birth. International consensus on how to define CHD would improve the validity and comparability of epidemiological studies on CHD.

AB - Estimates of the prevalence of congenital heart defects (CHD) have been published over many years and from many regions. As they are based on different definitions of which cases to include in the CHD prevalence, published prevalence estimates vary substantially. With the increasing use of echocardiography in neonatal intensive care, a patent ductus arteriosus (PDA) or flow over the atrial septum will often be visible. These findings may be coded as CHD at discharge and in this way falsely increase the CHD prevalence in the population. There are several purposes for which population-based data on CHD may be used: etiology, planning of treatment, or obtain information on outcome, including mortality. For etiology studies, it is important to include terminations of pregnancy as well as all births with CHD. For mortality studies in live births, inclusion of preterm born infants with PDA will increase overall mortality of CHD. The Danish Register of Congenital Heart Disease is based on hospital discharge diagnoses and diagnoses from outpatient visits. To increase the validity of these data, extensive data cleaning has been carried out based on record review and knowledge on the discharge coding practice. We include PDA and atrial septal defects as CHD cases if these defects are still open 2 months after birth. International consensus on how to define CHD would improve the validity and comparability of epidemiological studies on CHD.

KW - Denmark/epidemiology

KW - Epidemiologic Research Design

KW - Female

KW - Heart Defects, Congenital/classification

KW - Humans

KW - Infant

KW - Infant, Newborn

KW - International Classification of Diseases

KW - Male

KW - Patient Discharge/statistics & numerical data

KW - Pregnancy

KW - Prevalence

KW - Quality Indicators, Health Care/statistics & numerical data

KW - Registries

KW - Terminology as Topic

KW - Time Factors

U2 - 10.1111/j.1747-0803.2011.00581.x

DO - 10.1111/j.1747-0803.2011.00581.x

M3 - Journal article

C2 - 22010848

VL - 7

SP - 46

EP - 49

JO - Congenital Heart Disease

JF - Congenital Heart Disease

SN - 1747-079X

IS - 1

ER -

ID: 247872284