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Program - International Chinese Statistical Association

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ICSA 2010 SYMPOSIUM ABSTRACTS<br />

ABSTRACTS BY PRESENTER’S LAST NAME<br />

Presenter: Abowd, John Affiliation: Cornell University<br />

Abstract Title: Measurement Error in Large-scale Administrative Record <strong>Statistical</strong> Systems<br />

Author(s): John M. Abowd*<br />

Abstract:<br />

Session: M17<br />

Regency B<br />

Monday, June 21<br />

10:20 a.m.–12:10 p.m.<br />

Building frames, preparing summary tabulations, and sourcing some survey information<br />

from administrative data has a long history in statistics. Constructing entire statistical<br />

systems from integrated, multi-source administrative data is a much more recent<br />

phenomenon. Population coverage, source data quality, linkage management, edit<br />

procedures, imputation, and privacy protection all interact in such systems. The paper<br />

provides examples of the importance of each of these sources of potential error in the context<br />

of the U.S. Census Bureau's Longitudinal Employer-Household Dynamics program<br />

infrastructure file system. This longitudinally integrated employer-employee database is the<br />

source for multiple detailed public-use data products (Quarterly Workforce Indicators,<br />

OnTheMap), survey data integration (Survey of Income and <strong>Program</strong> Participation), and<br />

restricted access studies based on the confidential micro-data.<br />

Presenter: Alosh, Mohamed Affiliation: FDA<br />

Abstract Title: A general approach for testing a prespecifeid subgroup in clinical trials<br />

Author(s): Mohamed Alosh* and Mohammad Huque<br />

Abstract:<br />

Subgroup analyses are commonly used in clinical trials with the objective of learning about<br />

differential treatment effect across subgroups. Due to power consideration among other<br />

Session: W12 factors, clinical trials are seldom considered for establishing an efficacy claim for a subgroup<br />

Regency B in case the trial fails to establish an efficacy claim for the total population. However, through<br />

Wednesday, June 23<br />

8:00 a.m.–9:50 a.m.<br />

proper study design and analysis the clinical trial can be designed to establish efficacy claim<br />

for the total population as well as for the subgroup, thus increasing the chance of a positive<br />

trial. The concern that clinical trials are underpowered for subgroups can be relaxed<br />

somewhat through enrichment of the patient population for a priori identified subgroup and<br />

by using statistical testing strategies which spend the overall Type I error rate more<br />

efficiently than many traditional methods. In this presentation we consider a multiple testing<br />

strategy for the total population and the subgroup with the following features: (i) ensuring<br />

consistency of efficacy findings of the total population and that of the subgroup so that the<br />

results of the study overall are interpretable and (ii) allowing the significance level for testing<br />

the subgroup to adapt to the efficacy findings of the total population in a general form. We<br />

consider application of the proposed methodology to clinical trial data.<br />

Presenter: Andrieu, Christophe Affiliation: University of Bristol<br />

Abstract Title: On the computation of normalizing constants<br />

Author(s): C. Andrieu*, joint with N. Whiteley<br />

Abstract:<br />

The estimation of normalizing constants is central to numerous inference procedure. We<br />

review some techniques, provide novel theoretical results as well as new methods which aim<br />

Session: M26<br />

Cosmopolitan C<br />

Monday, June 21<br />

to achieve optimality in a sense to be made precise during the presentation.<br />

1:30 p.m.–3:20 p.m.<br />

Presenter: Austin, Peter Affiliation: Institute for Clinical Evaluative Sciences<br />

Abstract Title: Optimal estimation of risk differences using propensity-score matching<br />

Author(s): Peter Austin*<br />

Abstract: Propensity-score matching allows one to create a sample of treated and untreated subjects<br />

49

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