Evidence map›Paper›PMID 20527011›Full record

ArticleStatistics in medicine2010

Improving cost-effectiveness of epidemiological studies via designed missingness strategies.

Warren J Strauss, Louise Ryan, Michele Morara, Nicole Iroz-Elardo, Mark Davis, Matthew Cupp, Marcia G Nishioka, James Quackenboss, Warren Galke, Haluk Ozkaynak and 1 more

Abstract read
In one paragraph

Article in Statistics in medicine, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.6field-weighted citation impact, top 29% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. On Enrichment Strategies for Biomarker Stratified Clinical Trials.Journal of biopharmaceutical statistics · 2018
    Article
  5. Brief Report: Rethinking Data Collection for HIV Prevention Trials.Journal of acquired immune deficiency syndromes (1999) · 2016
    Review
  6. Time-dependent classification accuracy curve under marker-dependent sampling.Biometrical journal. Biometrische Zeitschrift · 2016
    Article
  7. Statistical Design Features of the Healthy Communities Study.American journal of preventive medicine · 2015
    Article
  8. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 1 institution in 1 country.

Warren J StraussBattelle Memorial Institute, 505 King Avenue, Columbus, OH 43201, USA. strauss@battelle.org
Louise Ryan
Michele Morara
Nicole Iroz-Elardo
Mark Davis
Matthew Cupp
Marcia G Nishioka
James Quackenboss
Warren Galke
Haluk Ozkaynak
Peter Scheidt
Battelle · US

Funding

Texas Tech Center for Translational Research and Rural Health - Research Capacity CoreU54MD020892 · NIMHD · TEXAS TECH UNIVERSITY HEALTH SCIS CENTER · PI Lance R. McMahon, Naima Moustaid-Moussa · 2026 to 2026
$10.0M
INCYTE MICROARRAY SERV IN SUPPORT OF THE PRBN01HD003311 · NICHD · INCYTE PHARMACEUTICALS, INC. · PI REISS, MICHAEL · 2000 to 2000
$204k
NICHD NIH HHS Y01 HD003311NIMHD NIH HHS U54 MD020892PHS HHS 282-98-0019
6 · The paper itself

Abstract

Modern epidemiological studies face opportunities and challenges posed by an ever-expanding capacity to measure a wide range of environmental exposures, along with sophisticated biomarkers of exposure and response at the individual level. The challenge of deciding what to measure is further complicated for longitudinal studies, where logistical and cost constraints preclude the collection of all possible measurements on all participants at every follow-up time. This is true for the National Children's Study (NCS), a large-scale longitudinal study that will enroll women both prior to conception and during pregnancy and collect information on their environment, their pregnancies, and their children's development through early adulthood-with a goal of assessing key exposure/outcome relationships among a cohort of approximately 100 000 children. The success of the NCS will significantly depend on the accurate, yet cost-effective, characterization of environmental exposures thought to be related to the health outcomes of interest. The purpose of this paper is to explore the use of cost saving, yet valid and adequately powered statistical approaches for gathering exposure information within epidemiological cohort studies. The proposed approach involves the collection of detailed exposure assessment information on a specially selected subset of the study population, and collection of less-costly, and presumably less-detailed and less-burdensome, surrogate measures across the entire cohort. We show that large-scale efficiency in costs and burden may be achieved without making substantive sacrifices on the ability to draw reliable inferences concerning the relationship between exposure and health outcome. Several detailed scenarios are provided that document how the targeted sub-sampling design strategy can benefit large cohort studies like the NCS, as well as other more focused environmental epidemiologic studies.

Indexed as

Child DevelopmentData Interpretation, StatisticalEpidemiologic Research DesignChildCohort StudiesCost-Benefit AnalysisFemaleHumansPregnancyUnited States

Identifiers

PMID20527011
PMCPMC2882677
OpenAlexW2043936336

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.