Journal Home
Search for

Volume 20, Issue 6, Pages 480-487 (November 2009)


View previous. 6 of 12 View next.

Optimal timing of use reduction vs. harm reduction in a drug epidemic model

Jonathan P. Caulkinsab, Gernot Traglerc, Dagmar WallnercCorresponding Author Informationemail address

Received 23 June 2008; received in revised form 23 December 2008; accepted 26 February 2009. published online 10 April 2009.

Abstract 

Background

Opponents of harm reduction fear that reducing harmfulness might increase use, and opponents of use reduction fear that efforts to reduce use can increase harmfulness. We raise the possibility that both strategies have a role but at different points in a drug “epidemic”.

Methods

We present a stylized two-state, one-control policy simulation model of the use vs. harm reduction choice when initiation stems from susceptible non-users interacting with current users.

Results

Within this model, whether harm reduction is a good strategy can depend on the particular drug and/or country, the social cost structure, and the stage of the epidemic. The dynamic solutions also involve indifference curves, consisting of points where the decision maker is indifferent between two transients that will approach the same steady state in the long run. Depending on how overall prevalence feeds back to affect the likelihood a susceptible non-user will initiate after interacting with a current user, the model can have tipping points where small shocks can have amplified long-run effects. For most epidemic states, harm reduction reduces the present value of future social costs, but not near such tipping points.

Conclusion

To the extent that drug use patterns involve feedback effects, any shock to initiation – from harm reduction or any other source – can produce changes in use that are more than proportional, or less than proportional, to the shock. Hence, advocates in the use vs. harm reduction debate may wish to explain why their preferred policy is particularly appropriate at the current stage of a country's drug use trajectory, rather than arguing for universal applicability of their preferred programme.

a Carnegie Mellon University, H. John Heinz III School of Public Policy and Management, 5000 Forbes Ave., Pittsburgh, PA 15213, USA

b Carnegie Mellon University in Qatar, PO Box 24866, Doha, Qatar

c Department of Mathematical Methods in Economics, Vienna University of Technology, Argentinierstrasse 8/105/4, A-1040 Vienna, Austria

Corresponding Author InformationCorresponding author. Tel.: +43 1 58801 11929; fax: +43 1 58801 11999.

PII: S0955-3959(09)00053-X

doi:10.1016/j.drugpo.2009.02.010


View previous. 6 of 12 View next.