One-to-many propensity score matching in cohort studies

被引:398
作者
Rassen, Jeremy A. [1 ]
Shelat, Abhi A. [2 ]
Myers, Jessica [1 ]
Glynn, Robert J. [1 ]
Rothman, Kenneth J. [3 ]
Schneeweiss, Sebastian [1 ]
机构
[1] Harvard Univ, Sch Med, Div Pharmacoepidemiol & Pharmacoecon, Dept Med,Brigham & Womens Hosp, Boston, MA 02120 USA
[2] Univ Virginia, Dept Comp Sci, Charlottesville, VA 22903 USA
[3] RTI Int, Res Triangle Pk, NC USA
基金
美国医疗保健研究与质量局; 美国国家科学基金会;
关键词
propensity scores; confounding factors (epidemiology); epidemiologic methods; comparative effectiveness research; MEDICAL LITERATURE; CRITICAL-APPRAISAL; BIAS REDUCTION; PERFORMANCE; NUMBER;
D O I
10.1002/pds.3263
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Background Among the large number of cohort studies that employ propensity score matching, most match patients 1:1. Increasing the matching ratio is thought to improve precision but may come with a trade-off with respect to bias. Objective To evaluate several methods of propensity score matching in cohort studies through simulation and empirical analyses. Methods We simulated cohorts of 20 000 patients with exposure prevalence of 10%50%. We simulated five dichotomous and five continuous confounders. We estimated propensity scores and matched using digit-based greedy (greedy), pairwise nearest neighbor within a caliper (nearest neighbor), and a nearest neighbor approach that sought to balance the scores of the comparison patient above and below that of the treated patient (balanced nearest neighbor). We matched at both fixed and variable matching ratios and also evaluated sequential and parallel schemes for the order of formation of 1:n match groups. We then applied this same approach to two cohorts of patients drawn from administrative claims data. Results Increasing the match ratio beyond 1:1 generally resulted in somewhat higher bias. It also resulted in lower variance with variable ratio matching but higher variance with fixed. The parallel approach generally resulted in higher mean squared error but lower bias than the sequential approach. Variable ratio, parallel, balanced nearest neighbor matching generally yielded the lowest bias and mean squared error. Conclusions 1:n matching can be used to increase precision in cohort studies. We recommend a variable ratio, parallel, balanced 1:n, nearest neighbor approach that increases precision over 1:1 matching at a small cost in bias. Copyright (C) 2012 John Wiley & Sons, Ltd.
引用
收藏
页码:69 / 80
页数:12
相关论文
共 26 条
[1]  
[Anonymous], 2011, MATCHIT NONPARAMETRI
[2]  
[Anonymous], 2004, Performing a 1: N case-control match on propensity score [computer program]
[3]  
[Anonymous], 2001, REDUCING BIAS PROPEN
[4]  
Austin PC, 2008, STAT MED, V27, P2037, DOI 10.1002/sim.3150
[5]   The performance of different propensity score methods for estimating marginal odds ratios [J].
Austin, Peter C. .
STATISTICS IN MEDICINE, 2007, 26 (16) :3078-3094
[6]   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
[7]   Statistical Criteria for Selecting the Optimal Number of Untreated Subjects Matched to Each Treated Subject When Using Many-to-One Matching on the Propensity Score [J].
Austin, Peter C. .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 2010, 172 (09) :1092-1097
[8]   Some Methods of Propensity-Score Matching had Superior Performance to Others: Results of an Empirical Investigation and Monte Carlo simulations [J].
Austin, Peter C. .
BIOMETRICAL JOURNAL, 2009, 51 (01) :171-184
[9]   Evaluating the validity of an instrumental variable study of neuroleptics - Can between-physician differences in prescribing patterns be used to estimate treatment effects? [J].
Brookhart, M. Alan ;
Rassen, Jeremy A. ;
Wang, Philip S. ;
Dormuth, Colin ;
Mogun, Helen ;
Schneeweiss, Sebastian .
MEDICAL CARE, 2007, 45 (10) :S116-S122
[10]   Evaluating short-term drug effects using a physician-specific prescribing preference as an instrumental variable [J].
Brookhart, MA ;
Wang, PS ;
Solomon, DH ;
Schneeweiss, S .
EPIDEMIOLOGY, 2006, 17 (03) :268-275