Hutcheon Jennifer A, Bodnar Lisa M
From the Department of Obstetrics and Gynaecology, University of British Columbia, Vancouver, Canada (JAH), and the Departments of Epidemiology and Obstetrics, Gynecology, and Reproductive Sciences, Graduate School of Public Health and School of Medicine, University of Pittsburgh, Pittsburgh, PA (LMB).
Am J Clin Nutr. 2014 Aug;100(2):701-7. doi: 10.3945/ajcn.114.085258. Epub 2014 Jun 25.
Current approaches for establishing public health guidelines on the recommended range of weight gain in pregnancy are subjective and nonsystematic.
In this article, we outline how decision-making on gestational weight-gain guidelines could be aided by quantitative approaches used in noninferiority trials.
We reviewed the theoretical application of noninferiority margins to pregnancy weight-gain guidelines. A worked example illustrated the selection of the recommended range of pregnancy weight gain in women who delivered at the Magee-Womens Hospital, Pittsburgh, PA, in 2003-2010 by identifying weight-gain z scores in which risk of unplanned cesarean delivery, preterm birth, small-for-gestational-age infant, and large-for-gestational-age infant were not meaningfully increased (based on noninferiority margins of 10% and 20%).
In normal-weight women, lowest risk of adverse perinatal outcome was observed at a weight-gain z score of -0.2 SDs. With a noninferiority margin of 20%, risks of adverse outcome were not meaningfully increased from the -0.2-SD reference value between z scores of -0.97 and +0.33 SDs (which corresponded to 11.3-18.4 kg). In overweight women, the recommended range was much broader: -2.11 to +0.29 SDs (4.4-18.1 kg).
The new approach illustrated in this article has a number of advantages over current methods for establishing pregnancy weight-gain guidelines because it is systematic, it is reproducible, and it provides a tool for policy makers to derive guidelines that explicitly reflect values at which risk of adverse outcome becomes meaningfully increased.
目前制定孕期推荐体重增加范围公共卫生指南的方法主观且缺乏系统性。
在本文中,我们概述了非劣效性试验中使用的定量方法如何有助于孕期体重增加指南的决策制定。
我们回顾了非劣效性界值在孕期体重增加指南中的理论应用。一个实例说明了通过确定计划外剖宫产、早产、小于胎龄儿和大于胎龄儿风险未显著增加的体重增加z分数(基于10%和20%的非劣效性界值),来选择2003 - 2010年在宾夕法尼亚州匹兹堡市梅杰妇女医院分娩的女性孕期体重增加的推荐范围。
在体重正常的女性中,体重增加z分数为 -0.2标准差时观察到不良围产期结局风险最低。以20%的非劣效性界值,在z分数 -0.97至 +0.33标准差(对应11.3 - 18.4千克)之间,不良结局风险与 -0.2标准差的参考值相比未显著增加。在超重女性中,推荐范围更广: -2.11至 +0.29标准差(4.4 - 18.1千克)。
本文阐述的新方法相较于目前制定孕期体重增加指南的方法具有诸多优势,因为它具有系统性、可重复性,并且为政策制定者提供了一种工具,以得出明确反映不良结局风险显著增加时数值的指南。