Literature DB >> 25220118

U.S. international efforts on critical congenital heart disease screening: can we have a uniform recommendation for Europe?

Lisa A Hom1, Gerard R Martin2.   

Abstract

An estimated 90% of births or more in the United States will be screened for critical congenital heart disease (CCHD) by the end of 2014. Europe has made less progress despite providing the population-based studies that were critical in driving support for efforts within the United States. Congenital Heart Disease (CHD) advocacy groups, investigators in screening for CCHD and international health organizations have been meeting with health care providers and government officials on a country by country basis. Countries that are implementing or have pilot projects have been identified to track global implementation. The Nordic countries, the United States, Switzerland and the United Arab Emirates are closest to universal screening for CCHD in newborns. Significant pilot projects tailored to unique care delivery systems screen through the use of midwives in the Netherlands, on maternity wards in the United Kingdom and while developing newborn care infrastructure in China. In Africa, South and Central America, individual countries are in the early stages of organization. Screening for CCHD is spreading across the globe. Early recognition has the ability to improve care in countries providing CHD treatment and prepare parents for adverse events in countries where care is not accessible. Impact of screening in regions with less access to intervention will be important to track.
Copyright © 2014 Elsevier Ireland Ltd. All rights reserved.

Entities:  

Keywords:  CCHD; Congenital heart disease; Neonate; Pulse oxymetry; Screening

Mesh:

Year:  2014        PMID: 25220118     DOI: 10.1016/S0378-3782(14)50004-7

Source DB:  PubMed          Journal:  Early Hum Dev        ISSN: 0378-3782            Impact factor:   2.079


  3 in total

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Authors:  Mohammed A Chamsi-Pasha; Hassan Chamsi-Pasha
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2.  Maternal acceptability of pulse oximetry screening at home after home birth or very early discharge.

Authors:  Ilona C Narayen; Adrian A Kaptein; Janine A Hogewoning; Nico A Blom; Arjan B Te Pas
Journal:  Eur J Pediatr       Date:  2017-03-09       Impact factor: 3.183

3.  Newborn blood DNA epigenetic variations and signaling pathway genes associated with Tetralogy of Fallot (TOF).

Authors:  Uppala Radhakrishna; Sangeetha Vishweswaraiah; Avinash M Veerappa; Rita Zafra; Samet Albayrak; Prajna H Sitharam; Nazia M Saiyed; Nitish K Mishra; Chittibabu Guda; Ray Bahado-Singh
Journal:  PLoS One       Date:  2018-09-13       Impact factor: 3.240

  3 in total

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