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September 15, 2024Canadian Journal of Cardiology15 citationsOpen Access

Meta-Analysis of Risk Factors for Congenital Heart Disease: Part 2, Maternal Medication, Reproductive Technologies, and Familial and Fetal Factors

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ALAlyssia LemieuxSKS. KhalilipalandiJLJonathan Lauzon-Schnittka

Key Result

Prenatal risk factors including increased nuchal translucency (OR 6.87), extracardiac anomalies (OR 3.41), and family history (OR 2.90) were strongly associated with congenital heart disease.

Study Design

Type

Meta-Analysis

Structured PICO

Are maternal medications, reproductive technologies, and familial and fetal factors associated with an increased risk of congenital heart disease?

P
Population
Meta-analysis of 131 peer-reviewed articles published between 1989 and 2022 quantifying the effects of prenatal risk factors on congenital heart disease.
E
Exposure
Maternal medication (antidepressants, antihypertensives, lithium, anticonvulsants, retinoids), assisted reproductive technologies (ART), and familial and fetal factors (extracardiac anomalies, increased nuchal translucency, family history of CHD)
C
Comparator
Absence of these risk factors
O
Outcome
Congenital heart disease (CHD)hard clinical

Increased nuchal translucency, extracardiac anomalies, and family history of CHD are strongly associated with congenital heart disease, while maternal medications and assisted reproductive technologies have modest effects.

Main Result

Odds Ratio: 3.41 (95% CI 1.72–6.77)

Limitations

  • Data were scarce and sometimes inconclusive for some risk factors commonly cited as being associated with CHD such as lithium, anomalies of the umbilical cord, anticonvulsants, and retinoid medication.
  • Insufficient data for anomalies of the umbilical cord, anticonvulsants, and retinoid medication
  • Very wide CI encompassing the null effect for lithium

Abstract

BACKGROUND: The quantitative effects of congenital heart disease (CHD) risk factors are not fully understood. We conducted a meta-analysis of all CHD risk factors. This report explores maternal medication, assisted reproductive technologies (ART), and familial and fetal factors. METHODS: Relevant studies were identified using a search strategy encompassing the concepts of CHD and prenatal risk factors with the following inclusion criteria: (1) peer-reviewed articles, (2) quantifying the effects of CHD risk factors, and (3) between 1989 and 2022. Pooled odds ratios (OR) and 95% confidence intervals (CIs) were calculated using a random effect model. RESULTS: There were 131 articles that met the inclusion criteria. Associations were found between CHDs and extracardiac anomalies (OR, 3.41; 95% CI, 1.72-6.77), increased nuchal translucency (OR, 6.87; 95% CI, 2.42-19.53), family history of CHD (OR, 2.90; 95% CI, 2.25-3.75), maternal antidepressants (OR, 1.23; 95% CI, 1.09-1.38), and antihypertensives (OR, 2.07; 95% CI, 1.80-2.38). A positive association was observed between severe CHDs and lithium, but with a very wide CI encompassing the null effect. A positive association was observed between severe CHDs and ARTs (OR, 1.98; 95% CI, 1.30-3.02). The data were insufficient for anomalies of the umbilical cord, anticonvulsants, and retinoid medication. CONCLUSIONS: There were strong associations among CHDs and increased nuchal translucency, extracardiac anomalies, and family history of CHD. Effect sizes were modest for maternal medication and ART. Data were scarce and sometimes inconclusive for some risk factors commonly cited as being associated with CHD such as lithium, anomalies of the umbilical cord, anticonvulsants, and retinoid medication.

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Cite This Study

Lemieux et al. (2024) conducted a meta-analysis in Congenital heart disease. Prenatal risk factors (maternal medication, ART, familial and fetal factors) was evaluated on Congenital heart disease (OR 3.41, 95% CI 1.72-6.77). Prenatal risk factors including increased nuchal translucency (OR 6.87), extracardiac anomalies (OR 3.41), and family history (OR 2.90) were strongly associated with congenital heart disease.

synapsesocial.com/papers/6aa292878adb575768fdce17https://doi.org/10.1016/j.cjca.2024.09.011
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