Skip to main content
Log in

Measuring the quality of life: Why, how and what?

  • Published:
Theoretical Medicine Aims and scope Submit manuscript

Abstract

In this paper three questions concerning quality of life in medicine and health care are analysed and discussed: the motives for measuring the quality of life, the methods used in assessing it, and the definition of the concept. The purposes of the study are to find an ethically acceptable motive for measuring the quality of life; to identify the methodological advantages and disadvantages of the most prevalent current methods of measurement; and to present an approach towards measuring and defining the quality of life which evades the difficulties encountered and discussed. The analysis comprises measurements both in the clinical situation concerning individual patients and in research concerning whole populations.

Three motives are found for evaluating the quality of human life: allocation of scarce medical resources, facilitating clinical decision making, and assisting patients towards autonomous decision making. It is argued that the third alternative is the only one which does not evoke ethical problems.

As for the methods of evaluation, several prevalent alternatives are presented, ranging from scales of physical performance to more subtle psychological questionnaires. Clinical questionnaires are found to fail to provide a scientific foundation for universally measuring the quality of life.

Finally, the question of definition is tackled. The classical distinction between need-based and want-based theories of human happiness is presented and discussed. The view is introduced and defended that neither of these approaches can be universally preferred to the other. The difficulty with the need approach is that it denies the subjective aspects of human life; whereas the problem of the want approach is that it tends to ignore some of the objective realities of the human existence.

In conclusion, it is argued that the choice of methods as well as definitions should be left to the competent patients themselves — who are entitled, if they so wish, to surrender the judgement to the medical personnel. Technical factors as well as the requirements of respect for autonomy and informed consent support this conclusion.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

Similar content being viewed by others

References

  1. Clark A, Fallowfield LJ. Quality of life measurements in patients with malignant disease: a review. J R Soc Med 1986;79:165–9.

    Google Scholar 

  2. Daughton DM, Fix AJ, Kass I, Bell CW, Patil KD. Maximum oxygen consumption and the ADAPT quality-of-life scale. Arch Phys Med Rehabil 1982;63:620–2.

    Google Scholar 

  3. Hörnquist JO. The concept of quality of life. Scand J Soc Med 1982;10:57–61.

    Google Scholar 

  4. Siegrist J, Junge A. Conceptual and methodological problems in research on the quality of life in clinical medicine. Soc Sci Med 1989;29:463–8.

    Google Scholar 

  5. Harris J. QALYfying the value of life. J Med Ethics 1987;13:117–23.

    Google Scholar 

  6. Lohr KN, Ware JE Jr, eds. Proceedings of the advances in health assessment conference. J Chronic Dis 1987;40 (Suppl 1).

  7. Neuhausser D. Advances in health status assessment: conference proceedings. Med Care 1989;27 (Suppl).

  8. Callahan D. Setting Limits: Medical Goals in an Aging Society. New York: Simon and Schuster, 1987.

    Google Scholar 

  9. Daniels N. Am I My Parents' Keeper? New York: Oxford University Press, 1988.

    Google Scholar 

  10. Häyry M, Häyry H. Health care as a right, fairness and medical resources. Bioethics 1990;4:1–21.

    Google Scholar 

  11. Carr-Hill RA. Assumptions of the QALY procedure. Soc Sci Med 1989;29:469–77.

    Google Scholar 

  12. Williams A. The economics of coronary artery bypass grafting. Br Med J 1985;291:326–9.

    Google Scholar 

  13. Duff RS, Campbell AGM. Moral and ethical dilemmas in the special-care nursery. N Engl J Med 1973;289:890–4.

    Google Scholar 

  14. Shaw A. Dilemmas of ‘informed consent’ in children. N Engl J Med 1973;289:885–90.

    Google Scholar 

  15. Kirby MD. Informed consent: what does it mean? J Med Ethics 1983;9:69–75.

    Google Scholar 

  16. Gillon R. Consent. Br Med J 1985;291:1700–1.

    Google Scholar 

  17. Hakama M, Holli K. Millainen on oikea rintasyövän hoito? Duodecim 1990;106:907–9.

    Google Scholar 

  18. Kuhse H. The Sanctity-of-Life Doctrine in Medicine: A Critique. Oxford: Oxford University Press, 1987.

    Google Scholar 

  19. Clark B. Whose Life Is It Anyway? London: Samuel French Ltd, 1978.

    Google Scholar 

  20. Fayers PM, Jones DR. Measuring and analysing quality of life in cancer clinical trials: a review. Stat Med 1983;2:429–46.

    Google Scholar 

  21. Drettner B, Ahlbom A. Quality of life and state of health for patients with cancer in the head and neck. Acta Otolaryngol 1983;96:307–14.

    Google Scholar 

  22. Haes JCJM de, Knippenberg FCE van. The quality of life of cancer patients: a review of the literature. Soc Sci Med 1985;20:809–17.

    Google Scholar 

  23. Priestman TJ, Baum M. Evaluation of quality of life in patients receiving treatment for advanced breast cancer. Lancet 1976;i:899–901.

    Google Scholar 

  24. Spitzer WO, Dobson AJ, Hall J, et al. The QL-index. J Chronic Dis 1981;34:585–97.

    Google Scholar 

  25. Heinrich RL, Schag CC, Ganz PA. Living with cancer: the cancer inventory of problem situations. J Clin Psychol 1984;40:972–80.

    Google Scholar 

  26. Morrow GR, Chiarello RJ, Derogatis LR. A new scale for assessing patients' psychosocial adjustment to medical illness. Psychol Med 1978;8:605–10.

    Google Scholar 

  27. Zigmond AS, Snaith RP. The hospital anxiety and depression scale. Acta Psychiatr Scand 1983;67:361–70.

    Google Scholar 

  28. Campbell A, Converse PE, Rodgers WL. Quality of American Life Perceptions, Evaluations and Satisfaction. New York: Russell Sage Foundation, 1976.

    Google Scholar 

  29. Lanham RJ, DiGiannantonio AF. Quality-of-life in cancer patients. Oncology 1988;45:1–7.

    Google Scholar 

  30. Torrance GW. Measurement of health state activities for economic appraisal: a review. Journal of Health Economics 1986;5:1–30.

    Google Scholar 

  31. Wright SJ. Age, Sex and Health: A Summary of the Findings from the York Health Evaluation Survey. York: University of York, 1986.

    Google Scholar 

  32. Pörn I. An equilibrium model of health. In: Nordenfelt L, Lindahl BIB, eds. Health, Disease, and Causal Explanations in Medicine. Dordrecht: D Reidel Publishing Co, 1984:3–9.

    Google Scholar 

  33. Nordenfelt L. On the circle of health. In: Nordenfelt L, Lindahl BIB, eds. Health, Disease, and Causal Explanations in Medicine. Dordrecht: D Reidel Publishing Co, 1984:15–23.

    Google Scholar 

  34. Nordenfelt L. On the Nature of Health: An Action-Theoretic Approach. Dordrecht: D Reidel Publishing Co, 1987.

    Google Scholar 

  35. More T. Utopia. London: Chatto & Windus Publishers, 1908.

    Google Scholar 

  36. Calman KC. Quality of life in cancer patients — an hypothesis. J Med Ethics 1984;10:124–7.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Häyry, M. Measuring the quality of life: Why, how and what?. Theor Med Bioeth 12, 97–116 (1991). https://doi.org/10.1007/BF00489791

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00489791

Key words

Navigation