A validated NICU database: recounting 50 years of clinical growth, quality improvement and research.

IF 3.1 3区 医学 Q1 PEDIATRICS
Kikelomo Babata, Charles R Rosenfeld, Mambarambath Jaleel, Patti J Burchfield, Marina Santos Oren, Riya Albert, L Steven Brown, Lina Chalak, Luc P Brion
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Abstract

The importance of a Neonatal Intensive Care Unit (NICU) database lies in its critical role in improving the quality of care for very preterm neonates and other high-risk newborns. These databases contain extensive information regarding maternal exposures, pregnancy complications, and neonatal care. They support quality improvement (QI) initiatives, facilitate clinical research, and track health outcomes in order to identify best practices and improve clinical guidelines. The Parkland Memorial Hospital NICU database was originally part of the Maternal and Neonatal Data Acquisition, Transmission and Evaluation project funded by the Robert Wood Johnson Foundation to assess perinatal-neonatal care in Dallas County Texas, 1977-1982. Clinical data points were defined, transcribed and validated in 1977; revalidation has occurred multiple times. Data are prospectively extracted from health records of high-risk neonates among >11,000 births annually. The database contains clinical information on >50,000 neonates, including all initially admitted to the NICU regardless of gestational age or birthweight and since 10/03/2011, all neonates admitted for observation and transferred to the term newborn nursery. The database has provided the basis for QI studies and research designed to assess and improve neonatal care. We discuss the history, evolution, administration, impact on neonatal outcomes, and future directions of our database. IMPACT: A single neonatal intensive care unit (NICU) database was designed for prospective data collection, validated and maintained for 46yrs. This database has supported quality improvement assessment, original clinical research, education and administrative requirements and impacted clinical neonatal care.

经过验证的新生儿重症监护室数据库:回顾 50 年的临床发展、质量改进和研究历程。
新生儿重症监护室(NICU)数据库的重要性在于它在提高早产新生儿和其他高危新生儿的护理质量方面起着至关重要的作用。这些数据库包含有关产妇暴露、妊娠并发症和新生儿护理的大量信息。它们支持质量改进 (QI) 计划、促进临床研究并跟踪健康结果,以确定最佳实践并改进临床指南。帕克兰纪念医院新生儿重症监护室数据库最初是罗伯特-伍德-约翰逊基金会资助的产妇和新生儿数据采集、传输和评估项目的一部分,该项目旨在评估 1977-1982 年德克萨斯州达拉斯县的围产期新生儿护理情况。临床数据点是在 1977 年定义、转录和验证的,并经过多次重新验证。数据是从每年 >11,000 例新生儿中高风险新生儿的健康记录中提取的。该数据库包含超过 5 万名新生儿的临床信息,其中包括所有最初进入新生儿重症监护室的新生儿,无论其胎龄或出生体重如何;自 2011 年 3 月 10 日起,还包括所有进入新生儿重症监护室接受观察并转入足月新生儿室的新生儿。该数据库为旨在评估和改善新生儿护理的 QI 研究提供了基础。我们将讨论该数据库的历史、演变、管理、对新生儿预后的影响以及未来发展方向。影响:我们设计了一个单一的新生儿重症监护室(NICU)数据库,用于前瞻性数据收集、验证和维护长达 46 年之久。该数据库支持质量改进评估、原始临床研究、教育和管理要求,并对新生儿临床护理产生了影响。
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来源期刊
Pediatric Research
Pediatric Research 医学-小儿科
CiteScore
6.80
自引率
5.60%
发文量
473
审稿时长
3-8 weeks
期刊介绍: Pediatric Research publishes original papers, invited reviews, and commentaries on the etiologies of children''s diseases and disorders of development, extending from molecular biology to epidemiology. Use of model organisms and in vitro techniques relevant to developmental biology and medicine are acceptable, as are translational human studies
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