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本文引用的文献

1
Directed acyclic graphs: a tool for causal studies in paediatrics.有向无环图:儿科因果研究的工具。
Pediatr Res. 2018 Oct;84(4):487-493. doi: 10.1038/s41390-018-0071-3. Epub 2018 Jun 4.
2
Let's Require the "T-Word".让我们使用“T 字”。 (由于原文简短且含义不明,此译文仅基于字面翻译,可能需要更多上下文来准确理解其确切意思。)
Am J Public Health. 2018 May;108(5):624. doi: 10.2105/AJPH.2018.304365.
3
Bias from restricting to live births when estimating effects of prescription drug use on pregnancy complications: A simulation.估计处方药使用对妊娠并发症的影响时因局限于活产而产生的偏倚:一项模拟研究。
Pharmacoepidemiol Drug Saf. 2018 Mar;27(3):307-314. doi: 10.1002/pds.4387. Epub 2018 Jan 17.
4
Only some questions of cause and effect can be evaluated in highly selected populations.只有一些因果问题能够在经过高度筛选的人群中进行评估。
BJOG. 2018 May;125(6):647-648. doi: 10.1111/1471-0528.15001. Epub 2017 Dec 6.
5
Causal inference in studies of preterm babies: a simulation study.早产儿研究中的因果推断:一项模拟研究。
BJOG. 2018 May;125(6):686-692. doi: 10.1111/1471-0528.14942. Epub 2017 Oct 30.
6
The fetuses-at-risk approach: survival analysis from a fetal perspective.高危胎儿法:从胎儿角度进行的生存分析。
Acta Obstet Gynecol Scand. 2018 Apr;97(4):454-465. doi: 10.1111/aogs.13194. Epub 2017 Aug 29.
7
An introduction to g methods.G方法简介。
Int J Epidemiol. 2017 Apr 1;46(2):756-762. doi: 10.1093/ije/dyw323.
8
A Simulation Platform for Quantifying Survival Bias: An Application to Research on Determinants of Cognitive Decline.一种用于量化生存偏差的模拟平台:在认知衰退决定因素研究中的应用。
Am J Epidemiol. 2016 Sep 1;184(5):378-87. doi: 10.1093/aje/kwv451. Epub 2016 Aug 30.
9
Outdoor air pollution and human infertility: a systematic review.户外空气污染与人类不孕:系统综述。
Fertil Steril. 2016 Sep 15;106(4):897-904.e1. doi: 10.1016/j.fertnstert.2016.07.1110. Epub 2016 Aug 8.
10
Three alternative methods to resolve paradoxical associations of exposures before term.解决产前暴露悖论关联的三种替代方法。
Eur J Epidemiol. 2016 Oct;31(10):1011-1019. doi: 10.1007/s10654-016-0175-1. Epub 2016 Jun 20.

围产期流行病学家的诅咒:在选择中推断因果关系。

The curse of the perinatal epidemiologist: inferring causation amidst selection.

作者信息

Snowden Jonathan M, Bovbjerg Marit L, Dissanayake Mekhala, Basso Olga

机构信息

School of Public Health, Oregon Health and Science University-Portland State University, 3181 SW Sam Jackson Park Rd, Mail Code: CB-669, Portland, OR 97239-3098, USA.

Department of Obstetrics and Gynecology, Oregon Health and Science University, 3181 SW Sam Jackson Park Rd, Mail Code: L-466, Portland, OR 97239-3098, USA.

出版信息

Curr Epidemiol Rep. 2018 Dec;5(4):379-387. doi: 10.1007/s40471-018-0172-x. Epub 2018 Sep 27.

DOI:10.1007/s40471-018-0172-x
PMID:31086756
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6510491/
Abstract

PURPOSE OF REVIEW

Human reproduction is a common process and one that unfolds over a relatively short time, but pregnancy and birth processes are challenging to study. Selection occurs at every step of this process (e.g., infertility, early pregnancy loss, and stillbirth), adding substantial bias to estimated exposure-outcome associations. Here we focus on selection in perinatal epidemiology, specifically, how it affects research question formulation, feasible study designs, and interpretation of results.

RECENT FINDINGS

Approaches have recently been proposed to address selection issues in perinatal epidemiology. One such approach is the ongoing pregnancies denominator for gestation-stratified analyses of infant outcomes. Similarly, bias resulting from left truncation has recently been termed "live birth bias," and a proposed solution is to control for common causes of selection variables (e.g., fecundity, fetal loss) and birth outcomes. However, these approaches have theoretical shortcomings, conflicting with the foundational epidemiologic concept of populations at risk for a given outcome.

SUMMARY

We engage with epidemiologic theory and employ thought experiments to demonstrate the problems of using denominators that include units not "at risk" of the outcome. Fundamental (and commonsense) concerns of outcome definition and analysis (e.g., ensuring that all study participants are at risk for the outcome) should take precedence in formulating questions and analysis approach, as should choosing questions that stakeholders care about. Selection and resulting biases in human reproductive processes complicate estimation of unbiased exposure- outcome associations, but we should not focus solely (or even mostly) on minimizing such biases.

摘要

综述目的

人类生殖是一个常见过程,且在相对较短的时间内展开,但怀孕和分娩过程很难进行研究。在这个过程的每一步都会发生选择(例如,不孕、早期流产和死产),这给估计暴露-结果关联带来了很大的偏差。在这里,我们关注围产期流行病学中的选择,具体而言,它如何影响研究问题的提出、可行的研究设计以及结果的解释。

最新发现

最近有人提出了一些方法来解决围产期流行病学中的选择问题。其中一种方法是在对婴儿结局进行妊娠分层分析时,将正在进行的妊娠作为分母。同样,左截断导致的偏差最近被称为“活产偏差”,一种建议的解决方案是控制选择变量(如生育力、胎儿丢失)和出生结局的共同原因。然而,这些方法存在理论缺陷,与给定结局的风险人群这一基础流行病学概念相冲突。

总结

我们运用流行病学理论并通过思想实验来证明使用包含无结局“风险”个体的分母所存在的问题。在提出问题和分析方法时,结局定义和分析的基本(且符合常识)关注点(例如,确保所有研究参与者都有结局风险)应优先考虑,选择利益相关者关心的问题也应如此。人类生殖过程中的选择及由此产生的偏差使无偏暴露-结局关联的估计变得复杂,但我们不应仅仅(甚至主要)关注将此类偏差最小化。