Department of Pediatrics, University of North Carolina, Chapel Hill, North Carolina 27599-7596, USA.
Am J Respir Crit Care Med. 2011 Jun 15;183(12):1715-22. doi: 10.1164/rccm.201101-0055OC. Epub 2011 Mar 4.
Benefits of identifying risk factors for bronchopulmonary dysplasia in extremely premature infants include providing prognostic information, identifying infants likely to benefit from preventive strategies, and stratifying infants for clinical trial enrollment.
To identify risk factors for bronchopulmonary dysplasia, and the competing outcome of death, by postnatal day; to identify which risk factors improve prediction; and to develop a Web-based estimator using readily available clinical information to predict risk of bronchopulmonary dysplasia or death.
We assessed infants of 23-30 weeks' gestation born in 17 centers of the Eunice Kennedy Shriver National Institute of Child Health and Human Development Neonatal Research Network and enrolled in the Neonatal Research Network Benchmarking Trial from 2000-2004.
Bronchopulmonary dysplasia was defined as a categorical variable (none, mild, moderate, or severe). We developed and validated models for bronchopulmonary dysplasia risk at six postnatal ages using gestational age, birth weight, race and ethnicity, sex, respiratory support, and Fi(O(2)), and examined the models using a C statistic (area under the curve). A total of 3,636 infants were eligible for this study. Prediction improved with advancing postnatal age, increasing from a C statistic of 0.793 on Day 1 to a maximum of 0.854 on Day 28. On Postnatal Days 1 and 3, gestational age best improved outcome prediction; on Postnatal Days 7, 14, 21, and 28, type of respiratory support did so. A Web-based model providing predicted estimates for bronchopulmonary dysplasia by postnatal day is available at https://neonatal.rti.org.
The probability of bronchopulmonary dysplasia in extremely premature infants can be determined accurately using a limited amount of readily available clinical information.
识别极早产儿支气管肺发育不良的风险因素具有重要意义,包括提供预后信息、识别可能从预防策略中获益的婴儿,以及为临床试验入组分层。
确定支气管肺发育不良的风险因素及死亡这一竞争结局的发生时间;确定哪些风险因素能改善预测;并开发一个基于网络的预测器,使用易于获得的临床信息来预测支气管肺发育不良或死亡的风险。
我们评估了 2000-2004 年在 Eunice Kennedy Shriver 国家儿童健康与人类发展研究所新生儿研究网络的 17 个中心出生、胎龄为 23-30 周且纳入新生儿研究网络基准试验的婴儿。
支气管肺发育不良定义为分类变量(无、轻度、中度或重度)。我们使用胎龄、出生体重、种族和民族、性别、呼吸支持和 Fi(O(2))在六个出生后年龄开发和验证了支气管肺发育不良风险模型,并使用 C 统计量(曲线下面积)评估了这些模型。共有 3636 名婴儿符合本研究条件。随着出生后天数的增加,预测结果得到改善,出生后第 1 天的 C 统计量为 0.793,出生后第 28 天达到最大的 0.854。在出生后第 1 天和第 3 天,胎龄对改善结局预测的效果最好;在出生后第 7、14、21 和 28 天,呼吸支持的类型则有此效果。一个提供按出生后天数预测支气管肺发育不良概率的网络模型可在 https://neonatal.rti.org 获得。
使用有限的易于获得的临床信息可以准确确定极早产儿支气管肺发育不良的发生概率。