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Risk-benefit decisions in patient care

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Medicines and Risk/Benefit Decisions

Part of the book series: CMR Workshop Series ((CMRWS))

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Abstract

Various authors have discussed risk-benefit decisions in relation to their predictive aspect for patient care1-3. However, they are not always discussing the same thing, some being concerned most with averaged risks and benefits and others with their impact on individuals. Thus it would appear that there is very little sound information available to help a physician when trying to reach a risk-benefit decision on behalf of, or with, an individual patient.

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References

  1. Brimblecombe, R.W. and Dayan, A.D. (1985). Preclinical toxicity testing. In Burley, D.M. and Binns, T.B. (eds.) Pharmaceutical Medicine, p. 18 (London: Arnold)

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  2. Teeling-Smith, G. (1983). In Teeiing-Smith, G. (ed.). Measuring the Social Benefits of Medicine, pp. 163–6 (London: Office of Health Economics.)

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  3. Ford, A.R., Aronson, J.K., Grahame-Smith, D.G. and Carver, J.G. (1979). The acute changes seen in cardiac glycoside receptor sites during the early phases of digoxin therapy are not found during chronic therapy. Br. J. Clin. Pharmacol., 8, 135–42

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© 1987 MTP Press Limited

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Vere, D.W. (1987). Risk-benefit decisions in patient care. In: Walker, S.R., Asscher, A.W. (eds) Medicines and Risk/Benefit Decisions. CMR Workshop Series. Springer, Dordrecht. https://doi.org/10.1007/978-94-009-3221-0_17

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  • DOI: https://doi.org/10.1007/978-94-009-3221-0_17

  • Publisher Name: Springer, Dordrecht

  • Print ISBN: 978-94-010-7946-4

  • Online ISBN: 978-94-009-3221-0

  • eBook Packages: Springer Book Archive

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