Skip to main content
Log in

Do economic evaluations have a role in decision-making in Medicine Management Committees? A qualitative study

  • Research Article
  • Published:
Pharmacy World & Science Aims and scope Submit manuscript

Abstract

Objective

To explore pharmacists’ perceptions on the use of economic evaluations in decision-making within Medicine Management Committees (MMCs), identify factors that influence the uptake of economic evidence and examine the usefulness of different presentations of economic evidence.

Method

This two-stage qualitative study was carried out in July and August 2004 in two hospitals in northwest England. First, a researcher observed the decision-making process at two MMCs. Handwritten notes were made during observation, which were later transcribed. Subsequently, in-depth semi-structured interviews were conducted with a purposive sample of pharmacists involved in the MMCs. The interviews explored pharmacists’ views on the usefulness of economic evaluations in decision-making, the factors influencing the uptake of economic evidence by the MMCs, and the optimal presentation of economic results. The interviews were audiotaped and transcribed verbatim. All the transcribed data were thematically analysed using the constant comparison approach.

Results

In all, six new drug applications were observed and ten pharmacists were interviewed. Pharmacists were observed to play an important role in decisions about drug formularies in hospitals. Although interviewees considered that timely economic evaluations would be useful in reviewing new medicines, the actual use of economic evidence in decision-making within MMCs was limited. The barriers to using economic evaluations included pharmacists’ lack of initiative to search for and difficulty in understanding economic evaluations, and the perceived availability, credibility and transferability of economic studies. However, the main barrier to implementing economic evidence was the decision makers’ concern about the impact of the medicines on the hospitals’ drug budgets. Interviewees felt that they understood and trusted disaggregated economic results better than aggregated ones.

Conclusion

This study found the use of economic evidence in decision-making at both MMCs was limited. To improve the usefulness of economic evaluations in MMCs, members of MMCs will need more training in accessing, understanding and appraising economic evidence; researchers need to improve the credibility and transferability of economic studies, and present the results in clear and understandable ways. However, due to the restricted focus of local, short-term drug budgets, evidence-based decision-making remains a challenge for local MMCs.

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.

Fig. 1

Similar content being viewed by others

Notes

  1. The outcome for the point estimate table (−3) means parecoxib caused fewer GI bleeding episodes than ketorolac, but the effectiveness of the ICER (+3) is the number of GI bleeding being avoided. Therefore, the negative ICER shows the new treatment is less expensive and more effective (i.e. dominant).

References

  1. Duthie T, Trueman P, Chancellor J, Diez L. Research into the use of health economics in decision making in the United Kingdom–Phase II. Is health economics ‘for good or evil’? Health Policy 1999;46(2):143–57.

    Article  PubMed  CAS  Google Scholar 

  2. National Institute for Clinical Excellence (NICE). Guide to the methods of technology appraisal. Reference N0515. London: National Institute for Clinical Excellence; 2004.

  3. Commonwealth Department of Human Services and Health. Guidelines for the pharmaceutical industry on preparation of submissions to the Pharmaceutical Benefits Advisory Committee including major submissions involving economic analysis. Canberra: Australian Government Publishing Services; 2002.

  4. Ontario Ministry of Health. Ontario guidelines for economic analysis of pharmaceutical products. Ontario: Ministry of Health; 1994.

  5. Johannesson M. Economic evaluation of drugs and its potential uses in policy making. Pharmacoeconomics 1995;8(3):190–8.

    PubMed  CAS  Google Scholar 

  6. Drummond M, Cooke J, Walley T. Economic evaluation under managed competition: evidence from the U.K Soc Sci Med 1997;45(4):583–95.

    Article  PubMed  CAS  Google Scholar 

  7. Wise J. Report lays out strategy to end “postcode prescribing”. Brit Med J 2000;320(7241):1027a.

    Article  Google Scholar 

  8. Jenkings KN, Barber N. What constitutes evidence in hospital new drug decision-making? Soc Sci Med 2004;58(9):1757–66.

    Article  PubMed  Google Scholar 

  9. Walley T, Barton S, Cooke J, Drummond M. Economic evaluations of drug therapy: attitudes of primary care prescribing advisers in Great Britain. Health Policy 1997;41(1):61–72.

    Article  PubMed  CAS  Google Scholar 

  10. Lavis JN, Ross SE, Stoddart GL, Hohenadel JM, McLeod CB, Evans RG. Do Canadian civil servants care about the health of populations? Am J Public Health 2003;93(4):658–63.

    Article  PubMed  Google Scholar 

  11. Lavis JN, Robertson D, Woodside JM, McLeod CB, Abelson J. How can research organizations more effectively transfer research knowledge to decision makers? Milbank Q 2003;81(2):221–2.

    Article  PubMed  Google Scholar 

  12. Coyle D. Increasing the impact of economic evaluation on health-care decision-making. Centre for Health Economic Discussion Paper 108 ed. England: University of York; 1993.

  13. Mays N, Pope C. Qualitative research: observational methods in health care settings. BMJ 1995;311(6998):182–4.

    PubMed  CAS  Google Scholar 

  14. Britten N. Qualitative interview in health care research. In: Pope C, Mays N, editors. Qualitative research in health care. 2nd ed. London: BMJ Books; 2000. p. 11–8.

    Google Scholar 

  15. Pope C, Ziebland S, Mays N. Qualitative research in health care. Analysing qualitative data. BMJ 2000;320(7227):114–6.

    Article  PubMed  CAS  Google Scholar 

  16. Ritchie J, Spencer L. Qualitative data analysis for applied policy research. In: Bryman A, Burgess RG, editors. Analyzing qualitative data. London: Routledge; 1994. p. 174–94.

    Google Scholar 

  17. Thorne S. Data analysis in qualitative research. ENB Notebook 2000;3:68–70.

    Google Scholar 

  18. Taylor RS, Drummond MF, Salkeld G, Sullivan SD. Inclusion of cost effectiveness in licensing requirements of new drugs: the fourth hurdle. BMJ 2004;329(7472):972–5.

    Article  PubMed  CAS  Google Scholar 

  19. Lexchin J, Bero LA, Djulbegovic B, Clark O. Pharmaceutical industry sponsorship and research outcome and quality: systematic review. BMJ 2003;326(7400):1167–70.

    Article  PubMed  Google Scholar 

  20. Hillman A, Eisenberg JM, Pauly MV. Avoiding bias in the conduct of cost-effectiveness research sponsored by pharmaceutical companies. N Engl J Med 1991;324:1362–5.

    Article  PubMed  CAS  Google Scholar 

  21. Friedberg M, Saffron B, Stinson TJ, Nelson W, Bennett CL. Evaluation of conflict of interest in economic analyses of new drugs used in oncology. JAMA 1999;282(15):1453–7.

    Article  PubMed  CAS  Google Scholar 

  22. Drummond M, Sculpher M. Common methodological flaws in economic evaluations. Med Care 2005;43(7 Suppl):5–14.

    PubMed  Google Scholar 

  23. Drummond MF, McGuire A. Economic evaluation in health care: merging theory with practice. Oxford: Oxford University Press; 2001.

    Google Scholar 

  24. Bryan S, Brown J. Extrapolation of cost-effectiveness information to local settings. J Health Serv Res Policy 1998;3(2):108–12.

    PubMed  CAS  Google Scholar 

  25. UKPDS Group. Cost effectiveness analysis of improved blood pressure control in hypertensive patients with type 2 diabetes: UKPDS 40. UK Prospective Diabetes Study Group. BMJ 1998;317(7160):720–6.

  26. Sculpher MJ, Poole L, Cleland J, Drummond M, Armstrong PW, Horowitz JD, et al. Low doses vs. high doses of the angiotensin converting-enzyme inhibitor lisinopril in chronic heart failure: a cost-effectiveness analysis based on the Assessment of Treatment with Lisinopril and Survival (ATLAS) study. The ATLAS Study Group. Eur J Heart Fail 2000;2(4):447–54.

    Article  PubMed  CAS  Google Scholar 

Download references

Acknowledgements

The authors would like to thank all the participants who took part in this study, Miss Penny Lewis for attending the ethics committees’ meeting, Mr. Wayne Boyle and Dr. Liz Seston for comments on the manuscript.

Financial support University of Manchester, UK; Ministry of Education, Taiwan, ROC

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Li-Chia Chen.

Appendix 1 The five-level outcome presentation of a cost-effectiveness analysis

Appendix 1 The five-level outcome presentation of a cost-effectiveness analysis

 

figure a1

At this stage of interview, the principal researcher briefly explained the hypothetical scenarios of a cost-effectiveness analysis to individual participants using the above framework.

Point estimate

 

figure b2

This table shows that compared to ketorolac, parecoxib cost £31,359 less to treat 1,000 patients, and resulted in 3 fewer patients having GI bleeding.

Point estimate with 2.5th and 97.5th percentile

 

figure c3

Compared to ketorolac, parecoxib causes 1–5 fewer patients to have GI bleeding, and costs in a range from £72,964 less to £8,286 more to treat 1,000 patients.

Incremental cost-effectiveness ratio

 

figure d4

The incremental cost effectiveness ratio (ICER) is the cost of achieving an extra unit of outcome, i.e. the cost per GI bleeding averted. The ICER was calculated as:

$$ {\hbox{ICER}}\, = \,\frac{{\Delta \,{\hbox{cost}}}} {{\Delta \,{\hbox{effectiveness}}}}\, = \,\frac{{ - \pounds{\hbox{30,937}}}} {3}\, = \, - \pounds{\hbox{10,312}} $$

Where ‘Δ costs’ refers to the difference in costs between the two alternatives, and ‘Δ effectiveness’ is the difference in effectiveness between the two alternatives.Footnote 1

Cost-effectiveness plane

 

figure e5

Compared parecoxib against ketorolac, if the ICERs fall in the four quadrants (see the following figure) of cost-effectiveness plane indicates parecoxib is: (I) more expensive, more effective; (II) more expensive, less effective; (III) less expensive, less effective; and (IV) less expensive, more effective.

figure f6

The cost-effectiveness of parecoxib not only depends on the uncertainty in the estimated values of cost and outcome, but also a decision maker’s willingness-to-pay for preventing one gastrointestinal bleed. The decision maker’s maximum willingness-to-pay can be presented as the slope (λ) of a price line on the cost-effectiveness plane. If the ICERs are less than λ, i.e. the dots lie below the price line, then it shows that parecoxib is cost-effective.

Cost-effectiveness acceptability curve

 

figure g7

The cost-effectiveness acceptability curve is an estimate of the proportion of the sampling distribution of costs and effects that lie below the price line (willingness to pay for each GI bleeding avoided) in the cost-effectiveness plane. This figure shows there is 66% probability that parecoxib is cost-effective even if the decision-maker is not willing to pay anything for preventing one extra GI bleeding. There is 95% probability that parecoxib is cost-effective when a decision maker is willing to pay up to £23,100 to avoid one extra GI bleeding.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Chen, LC., Ashcroft, D.M. & Elliott, R.A. Do economic evaluations have a role in decision-making in Medicine Management Committees? A qualitative study. Pharm World Sci 29, 661–670 (2007). https://doi.org/10.1007/s11096-007-9125-z

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11096-007-9125-z

Keywords

Navigation