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Efficacy assessed in follow-ups of clinical trials: methodological conundrum

Increasingly, we see papers describing the long-term follow-up results of randomised clinical trials. Sometimes, like the article by Rantalaiho and colleagues in the previous issue of Arthritis Research & Therapy, the follow-up extends to more than 10 years. It is not uncommon that authors of su...

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Autor principal: Landewé, Robert BM
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2945032/
https://www.ncbi.nlm.nih.gov/pubmed/20723206
http://dx.doi.org/10.1186/ar3080
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author Landewé, Robert BM
author_facet Landewé, Robert BM
author_sort Landewé, Robert BM
collection PubMed
description Increasingly, we see papers describing the long-term follow-up results of randomised clinical trials. Sometimes, like the article by Rantalaiho and colleagues in the previous issue of Arthritis Research & Therapy, the follow-up extends to more than 10 years. It is not uncommon that authors of such articles describe their results as a comparison of the original treatment groups in the original randomised clinical trial. Methodologically, such a comparison is fallible for several reasons. In this editorial, two important sources of bias that may jeopardise the results of such follow-up studies are discussed: confounding by indication and confounding by trial completion.
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spelling pubmed-29450322011-01-30 Efficacy assessed in follow-ups of clinical trials: methodological conundrum Landewé, Robert BM Arthritis Res Ther Editorial Increasingly, we see papers describing the long-term follow-up results of randomised clinical trials. Sometimes, like the article by Rantalaiho and colleagues in the previous issue of Arthritis Research & Therapy, the follow-up extends to more than 10 years. It is not uncommon that authors of such articles describe their results as a comparison of the original treatment groups in the original randomised clinical trial. Methodologically, such a comparison is fallible for several reasons. In this editorial, two important sources of bias that may jeopardise the results of such follow-up studies are discussed: confounding by indication and confounding by trial completion. BioMed Central 2010 2010-07-30 /pmc/articles/PMC2945032/ /pubmed/20723206 http://dx.doi.org/10.1186/ar3080 Text en Copyright ©2010 BioMed Central Ltd
spellingShingle Editorial
Landewé, Robert BM
Efficacy assessed in follow-ups of clinical trials: methodological conundrum
title Efficacy assessed in follow-ups of clinical trials: methodological conundrum
title_full Efficacy assessed in follow-ups of clinical trials: methodological conundrum
title_fullStr Efficacy assessed in follow-ups of clinical trials: methodological conundrum
title_full_unstemmed Efficacy assessed in follow-ups of clinical trials: methodological conundrum
title_short Efficacy assessed in follow-ups of clinical trials: methodological conundrum
title_sort efficacy assessed in follow-ups of clinical trials: methodological conundrum
topic Editorial
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2945032/
https://www.ncbi.nlm.nih.gov/pubmed/20723206
http://dx.doi.org/10.1186/ar3080
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