Actions in Support of Newborn Screening for Critical Congenital Heart Disease - United States, 2011-2018

被引：32

作者：

Glidewell, Jill ^{[1
]}

Grosse, Scott D. ^{[1
]}

Riehle-Colarusso, Tiffany ^{[1
]}

Pinto, Nelangi ^{[2
]}

Hudson, Jeff ^{[2
]}

Daskalov, Rachel ^{[2
]}

Gaviglio, Amy ^{[3
]}

Darby, Erin ^{[4
]}

Singh, Sikha

Sontag, Marci ^{[5
]}

机构：

[1] CDC, Natl Ctr Birth Defects & Dev Disabil, Atlanta, GA 30333 USA

[2] Amer Acad Pediat, Itasca, IL USA

[3] Minnesota Dept Hlth, Minneapolis, MN 55414 USA

[4] Assoc Publ Hlth Labs, Silver Spring, MD USA

[5] Univ Colorado, Colorado Sch Publ Hlth, Aurora, CO USA

来源：

MMWR-MORBIDITY AND MORTALITY WEEKLY REPORT | 2019年 / 68卷 / 05期

关键词：

DEFECTS; ROLES;

D O I：

10.15585/mmwr.mm6805a3

中图分类号：

R1 [预防医学、卫生学];

学科分类号：

1004 ; 120402 ;

摘要：

What is already known about this topic? Critical congenital heart disease (CCHD) occurs in two of every 1,000 births and might be undetected at birth. Affected infants are at risk for substantial morbidity and death early in life. In 2011, the U.S. Department of Health and Human Services Secretary endorsed the Advisory Committee on Heritable Disorders in Newborns and Children’s recommendation to add CCHD to the recommended universal newborn screening panel. What is added by this report? By 2018, all U.S. states and the District of Columbia had implemented newborn CCHD screening policies. Opportunities for program improvement, particularly around data collection, persist. Not all jurisdictions collect screening data or share data among relevant programs. What are the implications for public health practice? All U.S. newborns, regardless of which state they are born in, now have the opportunity to be screened for CCHD. © 2019, Department of Health and Human Services. All rights reserved.

引用

页码：107 / 111

页数：5

共 9 条

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