Literature DB >> 8308877

Ethics and statistical methodology in clinical trials.

C R Palmer1.   

Abstract

Statisticians in medicine can disagree on appropriate methodology applicable to the design and analysis of clinical trials. So called Bayesians and frequentists both claim ethical superiority. This paper, by defining and then linking together various dichotomies, argues there is a place for both statistical camps. The choice between them depends on the phase of clinical trial, disease prevalence and severity, but supremely on the ethics underlying the particular trial. There is always a tension present between physicians primarily obligated to their own patients (the weight of 'individual ethics') and ethical committees responsible for the scientific merit of the trial and its long-term implications ('collective ethics'). Individual ethics, it is proposed, favour the Bayesian approach; collective ethics, the frequentist. Though in some situations the choice appears clear-cut, there remain other where both methodologies can be appropriate.

Entities:  

Keywords:  Biomedical and Behavioral Research; Empirical Approach

Mesh:

Year:  1993        PMID: 8308877      PMCID: PMC1376342          DOI: 10.1136/jme.19.4.219

Source DB:  PubMed          Journal:  J Med Ethics        ISSN: 0306-6800            Impact factor:   2.903


  1 in total

1.  At what level of collective equipoise does a clinical trial become ethical?

Authors:  N Johnson; R J Lilford; W Brazier
Journal:  J Med Ethics       Date:  1991-03       Impact factor: 2.903

  1 in total
  3 in total

Review 1.  Study design in medical research: part 2 of a series on the evaluation of scientific publications.

Authors:  Bernd Röhrig; Jean-Baptist du Prel; Maria Blettner
Journal:  Dtsch Arztebl Int       Date:  2009-03-13       Impact factor: 5.594

2.  A comparison of two worlds: How does Bayes hold up to the status quo for the analysis of clinical trials?

Authors:  Alice R Pressman; Andrew L Avins; Alan Hubbard; William A Satariano
Journal:  Contemp Clin Trials       Date:  2011-03-29       Impact factor: 2.226

3.  Informed consent and research design in critical care medicine.

Authors: 
Journal:  Crit Care       Date:  1999       Impact factor: 9.097

  3 in total

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