Literature DB >> 22078432

Birth prevalence of congenital heart disease worldwide: a systematic review and meta-analysis.

Denise van der Linde1, Elisabeth E M Konings, Maarten A Slager, Maarten Witsenburg, Willem A Helbing, Johanna J M Takkenberg, Jolien W Roos-Hesselink.   

Abstract

Congenital heart disease (CHD) accounts for nearly one-third of all major congenital anomalies. CHD birth prevalence worldwide and over time is suggested to vary; however, a complete overview is missing. This systematic review included 114 papers, comprising a total study population of 24,091,867 live births with CHD identified in 164,396 individuals. Birth prevalence of total CHD and the 8 most common subtypes were pooled in 5-year time periods since 1930 and in continent and income groups since 1970 using the inverse variance method. Reported total CHD birth prevalence increased substantially over time, from 0.6 per 1,000 live births (95% confidence interval [CI]: 0.4 to 0.8) in 1930 to 1934 to 9.1 per 1,000 live births (95% CI: 9.0 to 9.2) after 1995. Over the last 15 years, stabilization occurred, corresponding to 1.35 million newborns with CHD every year. Significant geographical differences were found. Asia reported the highest CHD birth prevalence, with 9.3 per 1,000 live births (95% CI: 8.9 to 9.7), with relatively more pulmonary outflow obstructions and fewer left ventricular outflow tract obstructions. Reported total CHD birth prevalence in Europe was significantly higher than in North America (8.2 per 1,000 live births [95% CI: 8.1 to 8.3] vs. 6.9 per 1,000 live births [95% CI: 6.7 to 7.1]; p < 0.001). Access to health care is still limited in many parts of the world, as are diagnostic facilities, probably accounting for differences in reported birth prevalence between high- and low-income countries. Observed differences may also be of genetic, environmental, socioeconomical, or ethnic origin, and there needs to be further investigation to tailor the management of this global health problem. Copyright Â
© 2011 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.

Entities:  

Mesh:

Year:  2011        PMID: 22078432     DOI: 10.1016/j.jacc.2011.08.025

Source DB:  PubMed          Journal:  J Am Coll Cardiol        ISSN: 0735-1097            Impact factor:   24.094


  674 in total

1.  Parental and peer support in adolescents with a chronic condition: a typological approach and developmental implications.

Authors:  Leen Oris; Inge Seiffge-Krenke; Philip Moons; Liesbet Goubert; Jessica Rassart; Eva Goossens; Koen Luyckx
Journal:  J Behav Med       Date:  2015-09-14

2.  Detecting maternal-fetal genotype interactions associated with conotruncal heart defects: a haplotype-based analysis with penalized logistic regression.

Authors:  Ming Li; Stephen W Erickson; Charlotte A Hobbs; Jingyun Li; Xinyu Tang; Todd G Nick; Stewart L Macleod; Mario A Cleves
Journal:  Genet Epidemiol       Date:  2014-03-02       Impact factor: 2.135

3.  A parent-of-origin analysis of paternal genetic variants and increased risk of conotruncal heart defects.

Authors:  Wendy N Nembhard; Xinyu Tang; Jingyun Li; Stewart L MacLeod; Joseph Levy; Gerald B Schaefer; Charlotte A Hobbs
Journal:  Am J Med Genet A       Date:  2018-02-05       Impact factor: 2.802

4.  Pulmonic regurgitation and management challenges in the adult with tetralogy of fallot.

Authors:  Emily Ruckdeschel; Joseph D Kay
Journal:  Curr Treat Options Cardiovasc Med       Date:  2014-06

5.  Transcriptional atlas of cardiogenesis maps congenital heart disease interactome.

Authors:  Xing Li; Almudena Martinez-Fernandez; Katherine A Hartjes; Jean-Pierre A Kocher; Timothy M Olson; Andre Terzic; Timothy J Nelson
Journal:  Physiol Genomics       Date:  2014-05-06       Impact factor: 3.107

6.  Endothelial deletion of murine Jag1 leads to valve calcification and congenital heart defects associated with Alagille syndrome.

Authors:  Jennifer J Hofmann; Anais Briot; Josephine Enciso; Ann C Zovein; Shuxun Ren; Zhen W Zhang; Freddy Radtke; Michael Simons; Yibin Wang; M Luisa Iruela-Arispe
Journal:  Development       Date:  2012-10-24       Impact factor: 6.868

7.  Beyond Gene Panels: Whole Exome Sequencing for Diagnosis of Congenital Heart Disease.

Authors:  Sharon L Paige; Priyanka Saha; James R Priest
Journal:  Circ Genom Precis Med       Date:  2018-03

8.  Atrial Septal Defect as Unexpected Cause of Pulmonary Artery Hypertension.

Authors:  Rushi V Parikh; Jack Boyd; David P Lee; Ronald Witteles
Journal:  Tex Heart Inst J       Date:  2018-02-01

9.  Caval to pulmonary 3D flow distribution in patients with Fontan circulation and impact of potential 4D flow MRI error sources.

Authors:  Kelly Jarvis; Susanne Schnell; Alex J Barker; Michael Rose; Joshua D Robinson; Cynthia K Rigsby; Michael Markl
Journal:  Magn Reson Med       Date:  2018-09-15       Impact factor: 4.668

10.  Management of pulmonic regurgitation and right ventricular dysfunction in the adult with repaired tetralogy of fallot.

Authors:  Elisa Zaragoza-Macias; Karen K Stout
Journal:  Curr Treat Options Cardiovasc Med       Date:  2013-10
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.