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Classifying radiographic progression status in early rheumatoid arthritis patients using propensity scores to adjust for baseline differences.

Classifying radiographic progression status in early rheumatoid arthritis patients using propensity scores to adjust for baseline differences. Research Abstract Details 

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  • Classifying radiographic progression status in early rheumatoid arthritis patients using propensity scores to adjust for baseline differences. Abstract Text:

    grace s parkGrace S Park,weng kee wongWeng Kee Wong,myungshin ohMyungShin Oh,dinesh khannaDinesh Khanna,richard h goldRichard H Gold,john t sharpJohn T Sharp,harold e paulusHarold E Paulus,

    Various methods are used to measure radiographic joint damage in patients with rheumatoid arthritis (RA), but determining proportions of responsive patients is difficult. A key problem in observational studies when assessing damage outcomes is incorporating time to treatment initialization and adjusting for observed baseline differences. We examined five different definitions to select an appropriate index to classify radiographic damage in RA patients as progressive or nonprogressive. In addition, we compared different times from symptom onset to treatment and their effects on patient radiographic categorization. Propensity scores to adjust for baseline differences, including time since symptom onset, were used to match those treated early with those treated later using the stratification, radius, nearest neighbor and kernel methods. The mean effect of treatment on the treated was computed for each matching method. Observational data were analyzed for 185 early RA patients from the Western Consortium study followed six to sixty months (mean thirty-one months). For the selected index, 75 patients were categorized as nonprogressors; they had significantly lower disease activity, more clinical improvement and were treated earlier than the progressors. Of those treated within three months of symptom onset, 57% were classified as radiographically progressive versus 35% of those treated later (P = 0.0058). However, after propensity score adjustment for baseline differences, we noticed nonsignificant (P > 0.05) nonprogression in patients given earlier treatment. We conclude that propensity score analysis reduced but did not remove all bias.

    Classifying radiographic progression status in early rheumatoid arthritis patients using propensity scores to adjust for baseline differences. Publishing Authors By Initials

    gs parkGS Park,wk wongWK Wong,m ohM Oh,d khannaD Khanna,rh goldRH Gold,jt sharpJT Sharp,he paulusHE Paulus,

    For similar geographic locations: americas: north america: united states research abstracts see: geographic locations: americas: north america: united states research

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    Classifying radiographic progression status in early rheumatoid arthritis patients using propensity scores to adjust for baseline differences. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Statistical methods in medical research

    VOLUME: 16

    Page Numbers: 13-29

    Journal Abbreviation:

    ISSN: 0962-2802

    DAY: 3

    MONTH: Feb

    YEAR: 2007

    Classifying radiographic progression status in early rheumatoid arthritis patients using propensity scores to adjust for baseline differences. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 9212457

    Classifying radiographic progression status in early rheumatoid arthritis patients using propensity scores to adjust for baseline differences. Keywords Mesh Terms:

    KEYWORDS: United States

    MESH TERMS: statistics & numerical data

    Chemical & Substance for Abstract: Classifying radiographic progression status in early rheumatoid arthritis patients using propensity scores to adjust for baseline differences. Information

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    Grant and Affiliation Information for Classifying radiographic progression status in early rheumatoid arthritis patients using propensity scores to adjust for baseline differences.

    AFFILIATION: Department of Biostatistics, School of Public Health, University of California, Los Angeles, CA 90095-1772, USA. gspark@mednet.ucla.edu

    Country: England

    England Research PublicationEngland Research Publication

    AGENCY: United States NIGMS

    GRANT: R01GM072876

    ACRONYM: GM

    MEDLINETA: Stat Methods Med Res

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