The Journal of Pediatrics
Volume 156, Issue 5 , Pages 782-785, May 2010

Prevalence of Congenital Heart Disease at Live Birth in Taiwan

  • Mei-Hwan Wu, MD, PhD

      Affiliations

    • Department of Pediatrics, National Taiwan University Hospital, Taipei, Taiwan
    • Corresponding Author InformationReprint requests: Dr Mei-Hwan Wu, Division of Pediatric Cardiology, Department of Pediatrics, National Taiwan University Hospital, No 7, Chung-Shan South Road, Taipei 100, Taiwan.
  • ,
  • Hui-Chi Chen, PhD

      Affiliations

    • The Genomics Research Center, Academia Sinica, Taipei, Taiwan
  • ,
  • Chun-Wei Lu, MD

      Affiliations

    • Department of Pediatrics, National Taiwan University Hospital, Taipei, Taiwan
  • ,
  • Jou-Kou Wang, MD, PhD

      Affiliations

    • Department of Pediatrics, National Taiwan University Hospital, Taipei, Taiwan
  • ,
  • Shin-Chung Huang, MS

      Affiliations

    • Taiwan Bureau of National Health Insurance, Taipei, Taiwan
  • ,
  • San-Kuei Huang, MD

      Affiliations

    • Taiwan Bureau of National Health Insurance, Taipei, Taiwan

Received 28 July 2009; received in revised form 1 October 2009; accepted 20 November 2009. published online 08 February 2010.

Objectives

To investigate the prevalence at live birth of congenital heart disease (CHD) in Taiwan.

Study design

Patients with CHD born from 2000 to 2006 were identified from National Health Insurance databases.

Results

CHD prevalence was 13.08 per 1000 live births: 12.05 (simple, 10.53; severe, 1.51) in male infants and 14.21 (simple, 12.90; severe, 1.32) in female infants. Ventricular septal defect (VSD; 4.0) was the most common defect, followed by secundum atrial septal defect (ASDII; 3.2), patent ductus arteriosus (PDA; 2.0), pulmonary stenosis (PS; 1.2), tetralogy of Fallot (TOF; 0.63), coarctation of aorta (CoA; 0.25), transposition of great arteries (TGA; 0.21), endocardial cushion defect (ECD; 0.20), double outlet of right ventricle (DORV; 0.15), total anomalous pulmonary venous return (TAPVR; 0.11), aortic stenosis (0.09), hypoplastic left heart syndrome (HLHS; 0.062), Ebstein anomaly (0.047), and tricuspid atresia (0.046). Female predominance was observed in VSD, ASDII, PDA, and ECD; and male predominance was observed in TGA and TOF. Ratios of western prevalence to our Asian prevalence were high for HLHS (3.68-4.5), CoA (1.13-1.96), TGA (1.09-1.83), and tricuspid atresia (1.09-2.57), but low for PS (0.15-0.99), TOF (0.41-0.92), and possibly ASDII.

Conclusions

In this Asian population, the prevalence of CHD was at the high end of the reported range, with more PS and TOF, but fewer left-sided obstructions, TGA, and tricuspid atresia.

ASDII, Secundum atrial septal defect, CHD, Congenital heart disease, CoA, Coarctation of aorta, DORV, Double outlet of right ventricle, ECD, Endocardial cushion defect, HLHS, Hypoplastic left heart syndrome, ICD-9-CM, International Classification of Diseases, Ninth Revision, Clinical Modification, NHI, National Health Insurance, PDA, Patent ductus arteriosus, PS, Pulmonary stenosis, TAPVR, Total anomalous pulmonary venous return, TCPC, Total cavopulmonary connection, TGA, Transposition of great arteries, TOF, Tetralogy of Fallot, VSD, Ventricular septal defect

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 The authors declare no conflicts of interest.

PII: S0022-3476(09)01197-4

doi:10.1016/j.jpeds.2009.11.062

The Journal of Pediatrics
Volume 156, Issue 5 , Pages 782-785, May 2010