日本新生儿研究网络与新生儿数据库

S. Kusuda
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引用次数: 0

摘要

2004年,日本新生儿研究网络启动了日本高危婴儿数据库登记系统。目前,65%的极低出生体重婴儿或妊娠<32周出生的婴儿都登记在数据库中。每年登记的新病例约为4000例。该数据库的一个独特之处在于,它包括新生儿重症监护室出院后1.5年、3年和6年的结果数据。所有登记的数据每年都会反馈给参与的医院,并用于衡量新生儿护理的基准。该数据库的结果也发表在许多国际期刊上。随着这个数据库的发展,日本的新生儿医学取得了进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Neonatal Research Network of Japan and Neonatal Database
In 2004, the Neonatal Research Network of Japan initiated a database registration system for high-risk infants in Japan. Currently, 65% of all very low the birth weight infants or infants born at <32 weeks of gestation are registered in the database. Approximately 4,000 new cases are registered annually. A unique feature of the database is that it includes outcome data at 1.5, 3, and 6 years after discharge from neonatal intensive care units. All registered data are fed back annually to the participating hospitals and used to benchmark neonatal care. Results from this database have also been published in many international journals. With the development of this database, neonatal medicine in Japan has progressed.
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