A US perspective on newborn screening: a powerful tool for prevention
被引:0
|
作者:
DeBarber, Andrea E.
论文数: 0引用数: 0
h-index: 0
机构:
Oregon Hlth & Sci Univ, Dept Physiol & Pharmacol, Portland, OR 97201 USAOregon Hlth & Sci Univ, Dept Physiol & Pharmacol, Portland, OR 97201 USA
DeBarber, Andrea E.
[1
]
Steiner, Robert D.
论文数: 0引用数: 0
h-index: 0
机构:
Marshfield Clin Res Fdn, Marshfield, WI USA
Marshfield Clin Res Fdn, Madison, WI USAOregon Hlth & Sci Univ, Dept Physiol & Pharmacol, Portland, OR 97201 USA
Steiner, Robert D.
[2
,3
]
机构:
[1] Oregon Hlth & Sci Univ, Dept Physiol & Pharmacol, Portland, OR 97201 USA
[2] Marshfield Clin Res Fdn, Marshfield, WI USA
[3] Marshfield Clin Res Fdn, Madison, WI USA
来源:
EXPERT OPINION ON ORPHAN DRUGS
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2014年
/
2卷
/
11期
基金:
美国国家卫生研究院;
关键词:
addition of new conditions to the RUSP;
newborn screening;
rare conditions;
Recommended Uniform Screening Pane;
TANDEM MASS-SPECTROMETRY;
DRIED BLOOD SPOTS;
SEVERE COMBINED IMMUNODEFICIENCY;
COA DEHYDROGENASE-DEFICIENCY;
LYSOSOMAL STORAGE DISORDERS;
YORK-STATE MODEL;
KRABBE-DISEASE;
FILTER-PAPER;
DIRECT ASSAY;
ENZYMATIC DIAGNOSIS;
D O I:
10.1517/21678707.2014.978857
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
This article describes the rise of newborn screening in the USA, where it has become a powerful tool to prevent the mortality, morbidity and disability otherwise associated with many undetected rare conditions. In an effort to improve harmonization of newborn screening across the USA, a Recommended Uniform Screening Panel (RUSP) of core conditions was proposed in 2005 that is now near universally screened for. An evidence-based procedure has been developed to assess candidate conditions nominated for addition to the RUSP. Multiple stakeholders must play a role to generate the high-quality evidence required to support successful nomination of a condition for addition to the RUSP. The nomination, and potential addition, of conditions to the RUSP, can be a difficult and lengthy process. Screening newborns for new conditions requires significant effort not only on the part of researchers to develop screening tests and treatments but also on the part of newborn screening programs to implement new testing methodologies, in quality management, follow up, diagnosis and education. Continued advances in newborn screening methodologies and development of new treatments for rare conditions not currently screened for in newborns offer exciting new avenues to prevent mortality, morbidity and disability in newborns affected with rare conditions.