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image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Pharmacoepidemiology...arrow_drop_down
image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao
Pharmacoepidemiology and Drug Safety
Article . 2004 . Peer-reviewed
License: Wiley Online Library User Agreement
Data sources: Crossref
image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao
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Application of a propensity score to adjust for channelling bias with NSAIDs

Authors: Morant, Steve V.; Pettitt, D.; MacDonald, T. M.; Burke, T. A.; Goldstein, J. L.;

Application of a propensity score to adjust for channelling bias with NSAIDs

Abstract

AbstractPurposeTo compare the relative risks of upper GI haemorrhage (UGIH) in users of Newer versus Older, non‐specific NSAIDs when adjusted for channelling bias by regression on individual covariates, a propensity score and both.MethodsCohort study of patients prescribed NSAIDs between June 1987 and January 2000. Exposure to Newer and Older non‐specific NSAIDs was identified, and risk factors evaluated for each patient. Results of multiple covariate analyses and the propensity scoring technique to assess potential channelling bias in comparisons between Newer and Older non‐specific NSAIDs were compared.ResultsThis study included 7.1 thousand patient years (tpy) exposure to meloxicam, 1.6 tpy exposure to coxibs, and 628 tpy exposure to Older non‐specific NSAIDs. Patients receiving Newer NSAIDs were older, more likely to have a history of GI symptoms, and at higher risk for GI complications. Adjusting for these risk factors reduced the relative risks of UGIH on meloxicam and coxibs versus Older non‐specific NSAIDs to 0.84 (95%CI 0.60, 1.17) and 0.36 (0.14, 0.97) respectively.ConclusionsChannelling towards high GI risk patients occurred in the prescribing of Newer NSAIDs. Propensity scores highlighted the markedly different risk profiles of users of Newer and Older non‐specific NSAID. Correcting for channelling bias, coxib exposure, but not meloxicam exposure, was associated with less UGIH than Older non‐specific NSAID exposure. In the present study, corrections made by regression on a propensity score and on individual covariates were similar. Copyright © 2004 John Wiley & Sons, Ltd.

Country
United Kingdom
Related Organizations
Keywords

Adult, Male, Propensity score, Databases, Factual, 610, Gastrointestinal haemorrhage, name=Pharmacology, Meloxicam, General practice research database, 618, Cohort Studies, Drug Utilization Review, Risk Factors, /dk/atira/pure/subjectarea/asjc/3000, Osteoarthritis, Coxibs, Humans, Cyclooxygenase Inhibitors, Aged, Aged, 80 and over, Pharmacoepidemiology, Nonsteroidal anti-inflammatory drugs, Anti-Inflammatory Agents, Non-Steroidal, Age Factors, Middle Aged, name=Pharmacology (medical), Toxicology and Pharmaceutics(all), /dk/atira/pure/subjectarea/asjc/2700/2736, Regression Analysis, Female, Family Practice, Gastrointestinal Hemorrhage

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
12
Average
Top 10%
Top 10%
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