One‐to‐many propensity score matching in cohort studies

Pharmacoepidemiology and Drug Safety - Tập 21 Số S2 - Trang 69-80 - 2012
Jeremy A. Rassen1,2, Abhi Shelat3, Jessica A. Myers1,2, Robert J. Glynn1,2, Kenneth J. Rothman4, Sebastian Schneeweiß1,2
1Division of Pharmacoepidemiology and Pharmacoeconomics,
2Division of Pharmacoepidemiology and Pharmacoeconomics, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA
3Department of Computer Science, University of Virginia, Charlottesville, VA, USA
4RTI International Research Triangle Park NC USA

Tóm tắt

ABSTRACTBackgroundAmong 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.ObjectiveTo evaluate several methods of propensity score matching in cohort studies through simulation and empirical analyses.MethodsWe 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.ResultsIncreasing 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.Conclusions1: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 © 2012 John Wiley & Sons, Ltd.

Từ khóa


Tài liệu tham khảo

Rothman KJ, 2008, Modern Epidemiology

10.7326/0003-4819-127-8_Part_2-199710151-00064

10.1093/biomet/70.1.41

10.1002/(SICI)1097-0258(19981015)17:19<2265::AID-SIM918>3.0.CO;2-B

10.1093/oxfordjournals.aje.a112339

10.2307/2683903

10.1162/003465304323023651

10.1002/pst.433

10.1093/aje/kwq198

Reducing bias in a propensity score matched‐pair sample using greedy matching techniques.2001. (Accessed atwww2.sas.com/proceedings/sugi26/p214‐26.pdf.)

10.1002/sim.2781

10.1002/bimj.200810488

10.1093/aje/kwq224

10.1111/j.0006-341X.2000.00118.x

Performing a 1:N case–control match on propensity score.2004. (Accessed athttp://www2.sas.com/proceedings/sugi29/165‐29.pdf.)

SAS Macros. (Accessed December 15 2011 athttp://mayoresearch.mayo.edu/mayo/research/biostat/sasmacros.cfm.)

10.1016/j.jclinepi.2005.07.004

10.1002/sim.3150

MatchIt: nonparametric preprocessing for parametric causal inference.2011. (Accessed athttp://gking.harvard.edu/matchit.)

10.1002/sim.3245

Cormen TH, 2009, Introduction to Algorithms

10.1097/MLR.0b013e318070c057

10.1002/art.22219

10.1097/01.ede.0000193606.58671.c5

10.1016/j.jclinepi.2008.12.006

RassenJA DohertyM HuangW SchneeweissS.Pharmacoepidemiology Toolbox version 2. In. Boston MA;2011.