Survival analysis using auxiliary variables via multiple imputation, with application to AIDS clinical trial data

被引:48
|
作者
Faucett, CL
Schenker, N
Taylor, JMG
机构
[1] Univ Calif Los Angeles, Sch Publ Hlth, Dept Biostat, Los Angeles, CA 90095 USA
[2] Natl Ctr Hlth Stat, Off Res & Methodol, Hyattsville, MD 20782 USA
[3] Univ Michigan, Sch Publ Hlth, Dept Biostat, Ann Arbor, MI 48109 USA
关键词
AIDS; change-point model; dependent censoring; longitudinal data; missing data; random effects;
D O I
10.1111/j.0006-341X.2002.00037.x
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
We develop an approach, based on multiple imputation, to using auxiliary variables to recover information from censored observations in survival analysis. We apply the approach to data from an AIDS clinical trial comparing ZDV and placebo, in which CD4 count is the time-dependent auxiliary variable. To facilitate imputation, a joint model is developed for the data, which includes a hierarchical change-point model for CD4 counts and a tune-dependent proportional hazards model for the time to AIDS. Markov chain Monte Carlo methods are used to multiply impute event times for censored cases. The augmented data are then analyzed and the results combined using standard multiple-imputation techniques. A comparison of our multiple-imputation approach to simply analyzing the observed data indicates that multiple imputation leads to a small change in the estimated effect of ZDV and smaller estimated standard errors. A sensitivity analysis suggests that the qualitative findings are reproducible under a variety of imputation models. A simulation study indicates that improved efficiency over standard analyses and partial corrections for dependent censoring can result. An issue that arises with our approach, however, is whether the analysis of primary interest and the imputation model axe compatible.
引用
收藏
页码:37 / 47
页数:11
相关论文
共 50 条
  • [41] MULTIPLE IMPUTATION OF INCOMPLETE CATEGORICAL DATA USING LATENT CLASS ANALYSIS
    Vermunt, Jeroen K.
    van Ginkel, Joost R.
    van der Ark, L. Andries
    Sijtsma, Klaas
    SOCIOLOGICAL METHODOLOGY, VOL 38, 2008, 38 : 369 - 397
  • [42] Missing Data Analysis Using Multiple Imputation Getting to the Heart of the Matter
    He, Yulei
    CIRCULATION-CARDIOVASCULAR QUALITY AND OUTCOMES, 2010, 3 (01): : 98 - U145
  • [43] Statistical Analysis of Noise-Multiplied Data Using Multiple Imputation
    Klein, Martin
    Sinha, Bimal
    JOURNAL OF OFFICIAL STATISTICS, 2013, 29 (03) : 425 - 465
  • [44] EVALUATION OF MISSING DATA IMPUTATION STRATEGIES IN CLINICAL TRIAL AND EMR DATA USING STANDARDIZED DATA MODELS
    McLean, C.
    Ransom, J.
    Galaznik, A.
    VALUE IN HEALTH, 2019, 22 : S520 - S520
  • [45] Clustering-Based Multiple Imputation via Gray Relational Analysis for Missing Data and Its Application to Aerospace Field
    Tian, Jing
    Yu, Bing
    Yu, Dan
    Ma, Shilong
    SCIENTIFIC WORLD JOURNAL, 2013,
  • [46] The analysis of record-linked data using multiple imputation with data value priors
    Goldstein, Harvey
    Harron, Katie
    Wade, Angie
    STATISTICS IN MEDICINE, 2012, 31 (28) : 3481 - 3493
  • [47] SENSITIVITY ANALYSIS FOR NOT-AT-RANDOM MISSING DATA IN TRIAL-BASED COST-EFFECTIVENESS ANALYSIS USING MULTIPLE IMPUTATION
    Leurent, B.
    Gomes, M.
    Faria, R.
    Morris, S.
    Grieve, R.
    Carpenter, J.
    VALUE IN HEALTH, 2018, 21 : S14 - S14
  • [48] ANALYSIS OF DOUBLY-CENSORED SURVIVAL-DATA, WITH APPLICATION TO AIDS
    DEGRUTTOLA, V
    LAGAKOS, SW
    BIOMETRICS, 1989, 45 (01) : 1 - 11
  • [49] Sensitivity analysis for clinical trials with missing continuous outcome data using controlled multiple imputation: A practical guide
    Cro, Suzie
    Morris, Tim P.
    Kenward, Michael G.
    Carpenter, James R.
    STATISTICS IN MEDICINE, 2020, 39 (21) : 2815 - 2842
  • [50] Clinical and multiple gene expression variables in survival analysis of breast cancer: Analysis with the hypertabastic survival model
    Mohammad A Tabatabai
    Wayne M Eby
    Nadim Nimeh
    Hong Li
    Karan P Singh
    BMC Medical Genomics, 5