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1
Editorial: Research challenges of drug utilization, data collection, data validation, and adverse drug reactions in neonates.社论：新生儿药物利用、数据收集、数据验证及药物不良反应的研究挑战
Front Pharmacol. 2024 Mar 12;15:1376770. doi: 10.3389/fphar.2024.1376770. eCollection 2024.
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Newborn hearing screening: effectiveness, importance of high-risk factors, and characteristics of infants in the neonatal intensive care unit and well-baby nursery.新生儿听力筛查：有效性、高危因素的重要性以及新生儿重症监护病房和健康婴儿护理室中婴儿的特征
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本文引用的文献

1
Development of a neonatal adverse event severity scale through a Delphi consensus approach.通过德尔菲共识方法制定新生儿不良事件严重程度量表。
Arch Dis Child. 2019 Dec;104(12):1167-1173. doi: 10.1136/archdischild-2019-317399. Epub 2019 Sep 19.
2
Safety, dosing, and pharmaceutical quality for studies that evaluate medicinal products (including biological products) in neonates.评估新生儿药品（包括生物制品）的研究中的安全性、剂量和药品质量。
Pediatr Res. 2017 May;81(5):692-711. doi: 10.1038/pr.2016.221. Epub 2016 Nov 3.
3
Drug labeling and exposure in neonates.新生儿的药物标签和暴露情况。
JAMA Pediatr. 2014 Feb;168(2):130-6. doi: 10.1001/jamapediatrics.2013.4208.

Editorial: Research challenges of drug utilization, data collection, data validation, and adverse drug reactions in neonates.

作者信息

Ward Robert M

机构信息

Department of Pediatrics, University of Utah, Salt Lake City, UT, United States.

出版信息

Front Pharmacol. 2024 Mar 12;15:1376770. doi: 10.3389/fphar.2024.1376770. eCollection 2024.

DOI:10.3389/fphar.2024.1376770
PMID:38533255
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10964945/
Abstract
摘要