Joseph J. Zilber School of Public Health, University of Wisconsin-Milwaukee, 1240 N 10th St, Milwaukee, WI, 53205, USA.
School of Public Health, Division of Biostatistics, University of Minnesota, 420 Delaware St. SE, MMC 303, Minneapolis, MN, 55455, USA.
BMC Med Res Methodol. 2018 Dec 18;18(1):170. doi: 10.1186/s12874-018-0635-2.
Missing data are common in tobacco studies. It is well known that from the observed data alone, it is impossible to distinguish between missing mechanisms such as missing at random (MAR) and missing not at random (MNAR). In this paper, we propose a sensitivity analysis method to accommodate different missing mechanisms in cessation outcomes determined by self-report and urine validation results.
We propose a two-stage imputation procedure, allowing survey and urine data to be missing under different mechanisms. The motivating data were from a tobacco cessation trial examining the effects of the extended vs. standard Quit and Win contests and counseling vs. no counseling under a 2-by-2 factorial design. The primary outcome was 6-month biochemically verified tobacco abstinence.
Our proposed method covers a wide spectrum of missing scenarios, including the widely adopted "missing = smoking" imputation by assuming a perfect smoking-missing correlation (an extreme case of MNAR), the MAR case by assuming a zero smoking-missing correlation, and many more in between. The analysis of the data example shows that the estimated effects of the studied interventions are sensitive to the different missing assumptions on the survey and urine data.
Sensitivity analysis has played a crucial role in assessing the robustness of the findings in clinical trials with missing data. The proposed method provides an effective tool for analyzing missing data introduced at two different stages of outcome assessment, the self-report and validation time. Our methods are applicable to trials studying biochemically verified abstinence from alcohol and other substances.
在烟草研究中,数据缺失很常见。仅从观察到的数据来看,不可能区分随机缺失(MAR)和非随机缺失(MNAR)等缺失机制,这是众所周知的。在本文中,我们提出了一种敏感性分析方法,以适应通过自我报告和尿液验证结果确定的戒烟结果中不同的缺失机制。
我们提出了一种两阶段插补程序,允许在不同机制下调查和尿液数据缺失。主要数据来自一项评估扩展与标准戒烟比赛以及咨询与不咨询在 2×2 析因设计下对戒烟效果的影响的戒烟试验。主要结局是 6 个月生化验证的烟草戒断。
我们提出的方法涵盖了广泛的缺失情况,包括假设完美的吸烟缺失相关性的广泛采用的“缺失=吸烟”插补(MNAR 的极端情况)、假设零吸烟缺失相关性的 MAR 情况以及更多的情况。对数据示例的分析表明,研究干预措施的估计效果对调查和尿液数据的不同缺失假设很敏感。
敏感性分析在评估缺失数据临床试验结果的稳健性方面发挥了关键作用。所提出的方法为分析自我报告和验证时间两个不同阶段的结果评估中引入的缺失数据提供了有效的工具。我们的方法适用于研究生物化学验证的酒精和其他物质戒断的试验。