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  1. The Ethics of Randomised Controlled Trials: A Matter of Statistical Belief?Jane L. Hutton - 1996 - Health Care Analysis 4 (2):95-102.
    This paper outlines the approaches of two apparently competing schools of statistics. The criticisms made by supporters of Bayesian statistics about conventional Frequentist statistics are explained, and the Bayesian claim that their method enables research into new treatments without the need for clinical trials is examined in detail. Several further important issues are considered, including: the use of historical controls and data routinely collected on patients; balance in randomised trials; the possibility of giving information to patients; patient choice and patient (...)
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  • Some Popular Versions of Uninformed Consent.Jane L. Hutton & Richard E. Ashcroft - 2000 - Health Care Analysis 8 (1):41-53.
    A patient's informed consent is required by the Nuremberg code, and its successors, before she can be entered into a clinical trial. However, concern has been expressed by both patients and professionals about the beneficial or detrimental effect on the patient of asking for her consent. We examine advantages and drawbacks of popular variations on consent, which might reduce the stress on patients at the point of illness. Both informed and uninformed responses to particular trials, and trials in general, are (...)
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  • Efficiency and Health.Trevor Hussey - 1997 - Nursing Ethics 4 (3):181-190.
    Efficiency has become of central importance in health care and is seen as wholly laudable. It appears to offer a precise and objective means of evaluating and comparing institutions, practices and individuals, and is a principle that underlies techniques of cost-benefit analysis and other methods of option appraisal. However, there is a need to examine the concept of efficiency and explore the problems of its application within health care. Efficiency is a value laden notion and it cannot be used as (...)
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