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Cardiac malformations in children with congenital hypothyroidism
M Scavone1, V Tallarico1, E Stefanelli1
1Pediatric Unit, Department of Science of Health, University Magna Graecia of Catanzaro, Catanzaro, Italy.
Insights
Congenital hypothyroidism (CH) in infants is linked to a high rate of congenital heart defects (CD). Routine echocardiography is crucial for early diagnosis and management of these cardiac issues in CH patients.
Area of Science:
- Pediatric Endocrinology
- Cardiology
- Genetics
Background:
- Congenital hypothyroidism (CH) is a common endocrine disorder in children.
- Infants with CH have a higher incidence of congenital malformations (CM), particularly cardiac defects (CD).
Purpose of the Study:
- To determine the prevalence of cardiac defects (CD) in infants diagnosed with congenital hypothyroidism (CH).
- To assess the necessity of routine echocardiography for early detection of CD in CH patients.
Main Methods:
- Retrospective analysis of medical records for 255 infants screened for CH between 1991 and 2016.
- Clinical examination for heart murmurs and dysmorphic features, alongside echocardiography and cardiological evaluation.
- Final analysis included 191 patients, examining thyroid gland status (eutopic vs. dysgenesis) and presence of CD.
Main Results:
- 13.6% (26/191) of infants with CH presented with cardiac defects (CD).
- Atrial septal defect (ASD) was the most common anomaly (65.4% of CD cases), followed by VSD, PDA, and others.
- No significant association was found between CD frequency and sex, CH type, or TSH levels.
Conclusions:
- There is a high prevalence of cardiac defects (CD) in infants with congenital hypothyroidism (CH).
- Routine echocardiography is recommended for all infants with CH to facilitate early diagnosis and management of associated cardiac anomalies.
Abstract:
Congenital hypothyroidism (CH) is the most common endocrine disease in children, according to literature, infants with CH have an increased risk of associated congenital malformations (CM), especially cardiac defects (CD), compared to the general population. We retrospectively analyzed medical records of 255 patients with a positive screening result for CH in the period 1991-2016 followed at our Center. At the time of enrollment, the clinical examination included looking for the presence of heart murmurs and dysmorphic features. In all patients an echocardiography with cardiological evaluation were performed. Of all patients, 191 were included in the final analysis. Of these, 51.3% (98/191) presented an eutopic normally sized thyroid gland while 48.7% (93/191) showed a thyroid dysgenesis. Among the studied infants, 13.6% (26/191) presented CD. The most frequent cardiac anomaly was atrial septal defect (ASD) which was found in 65.4% (17/26) of patients with CD. Other defects were ventricular septal defect (VSD), patent ductus arteriosus (PDA), pulmonary valve stenosis (PvS), transposition of the great vessels (TGV), aortic valve stenosis (AvS). Six patients had multiple defects. In the analysed group, there was no significant relation with sex, type of CH, median blood-TSH (b-TSH) and serum-TSH (s-TSH) values and frequency of CD. There is a high prevalence of CD in CH, indicating the need of routine echocardiography in these patients to achieve an early diagnosis and management of CD.
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