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1.
PLoS One ; 13(4): e0194986, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-29621304

RESUMO

BACKGROUND: Surveillance of congenital anomalies is important to identify potential teratogens. METHODS: This study analysed the prevalence of 61 congenital anomaly subgroups (excluding chromosomal) in 25 population-based EUROCAT registries (1980-2012). Live births, fetal deaths and terminations of pregnancy for fetal anomaly were analysed with multilevel random-effects Poisson regression models. RESULTS: Seventeen anomaly subgroups had statistically significant trends from 2003-2012; 12 increasing and 5 decreasing. CONCLUSIONS: The annual increasing prevalence of severe congenital heart defects, single ventricle, atrioventricular septal defects and tetralogy of Fallot of 1.4% (95% CI: 0.7% to 2.0%), 4.6% (1.0% to 8.2%), 3.4% (1.3% to 5.5%) and 4.1% (2.4% to 5.7%) respectively may reflect increases in maternal obesity and diabetes (known risk factors). The increased prevalence of cystic adenomatous malformation of the lung [6.5% (3.5% to 9.4%)] and decreased prevalence of limb reduction defects [-2.8% (-4.2% to -1.5%)] are unexplained. For renal dysplasia and maternal infections, increasing trends may be explained by increased screening, and deceases in patent ductus arteriosus at term and increases in craniosynostosis, by improved follow up period after birth and improved diagnosis. For oesophageal atresia, duodenal atresia/stenosis and ano-rectal atresia/stenosis recent changes in prevalence appeared incidental when compared with larger long term fluctuations. For microcephaly and congenital hydronephrosis trends could not be interpreted due to discrepancies in diagnostic criteria. The trends for club foot and syndactyly disappeared once registries with disparate results were excluded. No decrease in neural tube defects was detected, despite efforts at prevention through folic acid supplementation.


Assuntos
Anormalidades Congênitas/epidemiologia , Anormalidades Congênitas/diagnóstico , Anormalidades Congênitas/etiologia , Anormalidades Congênitas/história , Europa (Continente)/epidemiologia , Feminino , História do Século XX , História do Século XXI , Humanos , Masculino , Vigilância da População , Gravidez , Prevalência , Sistema de Registros
2.
Cent Eur J Public Health ; 22(1): 42-7, 2014 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-24844106

RESUMO

The aim of this study was to assess the risk factors in the origin of lethal or surgically corrected isolated atrial septal defect secundum. The population-based Hungarian Case-Control Surveillance of Congenital Abnormalities (conducted between 1980 and 1996) comprised 472 atrial septal defect secundum cases, 678 matched controls and 38,151 available controls without any defects; in addition, 21,022 malformed controls with other isolated defects. Medically recorded chronic disorders in the prenatal maternity logbook were evaluated, while acute maternal diseases, drug treatments and pregnancy supplements were analyzed on the basis of both prospective medically recorded data and retrospective maternal information. Acute pelvic inflammatory disease, paroxysmal supraventricular tachycardia and phenolphthalein treatment due to severe constipation of mothers were shown to contribute to the development of atrial septal defect secundum of their children. High doses of folic acid in early pregnancy had positively influenced a minor part of isolated atrial septal defect secundum in foetuses. In conclusion, the obvious genetic predisposition for atrial septal defect secundum is connected with maternal paroxysmal supraventricular tachycardia and triggered by acute pelvic inflammatory diseases and phenolphthalein treatment, while the manifestation of atrial septal defect secundum can be reduced by high doses of folic acid supplementation in early pregnancy.


Assuntos
Ácido Fólico/administração & dosagem , Comunicação Interatrial/etiologia , Comunicação Interatrial/prevenção & controle , Complicações na Gravidez , Viés , Estudos de Casos e Controles , Feminino , Humanos , Hungria , Recém-Nascido , Rememoração Mental , Mães , Doença Inflamatória Pélvica/complicações , Fenolftaleína/efeitos adversos , Vigilância da População , Gravidez , Fatores de Risco , Autorrelato , Taquicardia Paroxística/complicações , Taquicardia Supraventricular/complicações
3.
Pediatr Cardiol ; 35(1): 108-20, 2014 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-23843102

RESUMO

The aim of our project was to study possible etiological factors in the origin of congenital heart defects (CHDs) because in the majority of patients the underlying causes are unclear. Cases with different CHD entities as homogeneously as possible were planned for evaluation in the population-based large data set of the Hungarian Case Control Surveillance of Congenital Abnormalities. Dead or surgically corrected 302 live-born cases with different types of left-ventricular outflow tract obstructive defects (LVOT, i.e., valvular aortic stenosis 76, hypoplastic left heart syndrome 76, coarctation of the aorta 113, and other congenital anomalies of aorta 32) were compared with 469 matched controls, 38,151 controls without any defects, and 20,750 malformed controls with other isolated defects. Medically recorded pregnancy complications and chronic diseases were evaluated based on prenatal maternity logbooks, whereas acute diseases, drug treatments, and folic acid/multivitamin supplementation were analyzed both on the basis of retrospective maternal information and medical records. The results of the study showed the role of maternal diabetes in the origin of LVOT in general, while panic disorder was associated with a higher risk of hypoplastic left heart syndrome and ampicillin treatment with a higher risk of coarctation of the aorta (COA). High doses of folic acid had a protective effect regarding the manifestation of LVOT, particularly COA. In conclusion, only a minor portion of causes was shown in our study; thus, further studies are needed to understand better the underlying causal factors in the origin of LVOT.


Assuntos
Diabetes Mellitus/epidemiologia , Cardiopatias Congênitas , Transtorno de Pânico/epidemiologia , Complicações na Gravidez , Obstrução do Fluxo Ventricular Externo , Estudos de Casos e Controles , Feminino , Ácido Fólico/uso terapêutico , Cardiopatias Congênitas/complicações , Cardiopatias Congênitas/diagnóstico , Cardiopatias Congênitas/epidemiologia , Cardiopatias Congênitas/prevenção & controle , Humanos , Hungria/epidemiologia , Masculino , Bem-Estar Materno , Gravidez , Complicações na Gravidez/classificação , Complicações na Gravidez/tratamento farmacológico , Complicações na Gravidez/epidemiologia , Cuidado Pré-Natal/estatística & dados numéricos , Sistema de Registros/estatística & dados numéricos , Medição de Risco , Fatores de Risco , Análise de Sobrevida , Ultrassonografia Pré-Natal/estatística & dados numéricos , Obstrução do Fluxo Ventricular Externo/congênito , Obstrução do Fluxo Ventricular Externo/diagnóstico , Obstrução do Fluxo Ventricular Externo/epidemiologia , Obstrução do Fluxo Ventricular Externo/etiologia , Obstrução do Fluxo Ventricular Externo/prevenção & controle
4.
Am J Med Genet A ; 161A(10): 2444-52, 2013 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-23950097

RESUMO

Congenital heart defect (CHD) cases have been evaluated together as a group in some previous epidemiological studies. However, different CHD entities have different etiologies, and the underlying causes are unclear in the vast majority of patients. Thus the aim of this study was to analyze the possible association of different maternal diseases with the risk of four types of conotruncal defects (CTD), that is, truncus arteriosus, d-transposition of the great arteries, tetralogy of Fallot, and double-outlet right ventricle based on autopsy or surgical report diagnosis. Acute and chronic diseases with related drug treatments and peri-conceptual folic acid or multivitamin supplementations were compared in mothers of 598 CTD cases, of 902 matched controls, and 38,151 population controls without any defects, and with 20,896 malformed controls with other isolated non-cardiac defects in the population-based large dataset of the Hungarian Case-Control Surveillance of Congenital Abnormalities. Mothers who had medically recorded influenza and the common cold with secondary complications in the prenatal maternity logbook during the second and/or third gestational months were associated with a higher risk of CTD (OR with 95% CI: 2.22, 1.19-3.88). The common denominator of these maternal diseases may be high fever, which could be prevented by antifever therapies. On the other hand, high doses of medically recorded folic acid in early pregnancy were able to reduce the birth prevalence of CTD (OR with 95% CI: 0.54, 0.39-0.73), and this reduction was significant in transposition of the great arteries (0.46, 0.29-0.71) as well. In conclusion, high fever related maternal diseases may have a role in the origin of CTD, while high doses of folic acid in early pregnancy were able to reduce of CTD, particularly transposition of great vessels.


Assuntos
Cardiopatias Congênitas/epidemiologia , Cardiopatias Congênitas/etiologia , Adulto , Estudos de Casos e Controles , Suplementos Nutricionais , Feminino , Humanos , Incidência , Vigilância da População , Gravidez , Prevalência , Sistema de Registros , Risco
5.
Birth Defects Res A Clin Mol Teratol ; 97(4): 217-24, 2013 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-23554238

RESUMO

BACKGROUND: The role of possible environmental factors in the origin of congenital heart defects is unclear in the vast majority of patients. The objective of this study was to describe the birth outcomes and risk factors in isolated atrioventricular canal defect (AVCD) cases. METHODS: Medically recorded birth outcomes, maternal age, parity, acute and chronic maternal diseases with related drug treatments and folic acid/multivitamin supplementation were evaluated in isolated AVCD cases. The diagnosis of AVCD was based on the autopsy report or surgical description in the population-based Hungarian Case-Control Surveillance of Congenital Abnormalities, between 1980 and 1996. RESULTS: The birth outcomes and exposures of 77 isolated AVCD cases were compared with 38,151 controls without defect. Mean gestational age at delivery (38.6 week) and birth weight (2992 g), rate of preterm birth (20.8%) and low birthweight (23.4%) of cases with a female excess (59.7%) differed significantly from the controls. Mothers of cases had higher parity, higher prevalence of conduction disorders/cardiac dysrhythmias and chronic hypertension. The high doses of folic acid in early pregnancy associated with a reduced rate of AVCD. CONCLUSIONS: Conduction disorders/cardiac dysrhythmias and chronic hypertension of mothers may have a role in the origin of AVCD, while high doses of folic acid in early pregnancy may reduce the risk of the development of AVCD. Birth Defects Research (Part A) 97:217-224, 2013. © 2013 Wiley Periodicals, Inc.


Assuntos
Comunicação Atrioventricular/epidemiologia , Vigilância da População/métodos , Resultado da Gravidez/epidemiologia , Arritmias Cardíacas/epidemiologia , Estudos de Casos e Controles , Doença Crônica , Feminino , Ácido Fólico/administração & dosagem , Defeitos dos Septos Cardíacos , Humanos , Hungria , Hipertensão/epidemiologia , Recém-Nascido , Idade Materna , Gravidez , Nascimento Prematuro/epidemiologia , Fatores de Risco
6.
J Matern Fetal Neonatal Med ; 26(8): 738-47, 2013 May.
Artigo em Inglês | MEDLINE | ID: mdl-23205869

RESUMO

OBJECTIVE: In general, the analytical epidemiological studies evaluated cases with congenital heart defects (CHDs) together. However, different CHD entities have different etiology, and in the vast majority of patients the underlying causes are unclear. Thus the objective of the study was to evaluate the possible etiological factors in the origin of single ventricular septal defect (VSD) after surgical intervention or lethal outcome, i.e. as homogeneous as possible. METHOD: In the population-based large dataset of the Hungarian Case-Control Surveillance of Congenital Abnormalities acute and chronic maternal diseases with related drug treatments and pregnancy supplements in early pregnancy were evaluated in the mothers of 1661 cases with isolated/single VSD and their 2534 matched and 38,151 all controls without defect, and 19,833 malformed controls with other isolated non-cardiac defect. RESULTS: There was a higher risk of VSD in the children of mothers with high fever related influenza during the critical period of VSD and this risk was limited by antifever therapy. In addition paroxysmal supraventricular tachycardia and epilepsy treated with anticonvulsant drugs associated with higher risk of VSD. Finally, the high doses of folic acid alone in early pregnancy. CONCLUSIONS: High-fever-related maternal diseases may have a role in the origin of VSD which is preventable with antifever drug therapy, and the high doses of folic acid in early pregnancy reduced the risk of VSD.


Assuntos
Comunicação Interventricular/etiologia , Complicações Infecciosas na Gravidez , Estudos de Casos e Controles , Feminino , Ácido Fólico/uso terapêutico , Comunicação Interventricular/epidemiologia , Comunicação Interventricular/prevenção & controle , Humanos , Hungria/epidemiologia , Vigilância da População , Gravidez , Complicações Infecciosas na Gravidez/tratamento farmacológico , Complicações Infecciosas na Gravidez/epidemiologia , Taquicardia Paroxística/complicações , Taquicardia Supraventricular/complicações
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