Double propensity-score adjustment: A solution to design bias or bias due to incomplete matching

被引:69
作者
Austin, Peter C. [1 ,2 ,3 ]
机构
[1] Inst Clin Evaluat Sci, G1 06,2075 Bayview Ave, Toronto, ON M4N 3M5, Canada
[2] Univ Toronto, Inst Hlth Management Policy & Evaluat, Toronto, ON, Canada
[3] Sunnybrook Res Inst, Schulich Heart Res Program, Toronto, ON, Canada
基金
加拿大健康研究院;
关键词
propensity score; matching; optimal matching; Monte Carlo simulations; observational studies; bias; MODEL; PERFORMANCE; BALANCE; NUMBER;
D O I
10.1177/0962280214543508
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Propensity-score matching is frequently used to reduce the effects of confounding when using observational data to estimate the effects of treatments. Matching allows one to estimate the average effect of treatment in the treated. Rosenbaum and Rubin coined the term bias due to incomplete matching to describe the bias that can occur when some treated subjects are excluded from the matched sample because no appropriate control subject was available. The presence of incomplete matching raises important questions around the generalizability of estimated treatment effects to the entire population of treated subjects. We describe an analytic solution to address the bias due to incomplete matching. Our method is based on using optimal or nearest neighbor matching, rather than caliper matching (which frequently results in the exclusion of some treated subjects). Within the sample matched on the propensity score, covariate adjustment using the propensity score is then employed to impute missing potential outcomes under lack of treatment for each treated subject. Using Monte Carlo simulations, we found that the proposed method resulted in estimates of treatment effect that were essentially unbiased. This method resulted in decreased bias compared to caliper matching alone and compared to either optimal matching or nearest neighbor matching alone. Caliper matching alone resulted in design bias or bias due to incomplete matching, while optimal matching or nearest neighbor matching alone resulted in bias due to residual confounding. The proposed method also tended to result in estimates with decreased mean squared error compared to when caliper matching was used.
引用
收藏
页码:201 / 222
页数:22
相关论文
共 37 条
[1]   Bias-Corrected Matching Estimators for Average Treatment Effects [J].
Abadie, Alberto ;
Imbens, Guido W. .
JOURNAL OF BUSINESS & ECONOMIC STATISTICS, 2011, 29 (01) :1-11
[2]   The performance of different propensity score methods for estimating marginal odds ratios [J].
Austin, Peter C. .
STATISTICS IN MEDICINE, 2007, 26 (16) :3078-3094
[3]   A comparison of the ability of different propensity score models to balance measured variables between treated and untreated subjects: a Monte Carlo study [J].
Austin, Peter C. ;
Grootendorst, Paul ;
Anderson, Geoffrey M. .
STATISTICS IN MEDICINE, 2007, 26 (04) :734-753
[4]   Conditioning on the propensity score can result in biased estimation of common measures of treatment effect: A Monte Carlo study (p n/a) [J].
Austin, Peter C. ;
Grootendorst, Paul ;
Normand, Sharon-Lise T. ;
Anderson, Geoffrey M. .
STATISTICS IN MEDICINE, 2007, 26 (16) :3208-3210
[5]   The use of bootstrapping when using propensity-score matching without replacement: a simulation study [J].
Austin, Peter C. ;
Small, Dylan S. .
STATISTICS IN MEDICINE, 2014, 33 (24) :4306-4319
[6]   A comparison of 12 algorithms for matching on the propensity score [J].
Austin, Peter C. .
STATISTICS IN MEDICINE, 2014, 33 (06) :1057-1069
[7]   The performance of different propensity score methods for estimating marginal hazard ratios [J].
Austin, Peter C. .
STATISTICS IN MEDICINE, 2013, 32 (16) :2837-2849
[8]   A Tutorial and Case Study in Propensity Score Analysis: An Application to Estimating the Effect of In-Hospital Smoking Cessation Counseling on Mortality [J].
Austin, Peter C. .
MULTIVARIATE BEHAVIORAL RESEARCH, 2011, 46 (01) :119-151
[9]   Optimal caliper widths for propensity-score matching when estimating differences in means and differences in proportions in observational studies [J].
Austin, Peter C. .
PHARMACEUTICAL STATISTICS, 2011, 10 (02) :150-161
[10]   A Data-Generation Process for Data with Specified Risk Differences or Numbers Needed to Treat [J].
Austin, Peter C. .
COMMUNICATIONS IN STATISTICS-SIMULATION AND COMPUTATION, 2010, 39 (03) :563-577