A dynamic model of drug initiation: implications for treatment and drug control

被引:33
作者
Behrens, DA
Caulkins, JP
Tragler, G
Haunschmied, JL
Feichtinger, G
机构
[1] Vienna Tech Univ, Dept Operat Res & Operat Management, A-1040 Vienna, Austria
[2] Carnegie Mellon Univ, H John Heinz III Sch Publ Policy & Management, Pittsburgh, PA 15213 USA
[3] Rand Corp, Drug Policy Res Ctr, Pittsburgh, PA 15213 USA
基金
美国国家科学基金会;
关键词
non-linear dynamic systems; Hopf bifurcation; illicit drugs;
D O I
10.1016/S0025-5564(99)00016-4
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
We set up a time-continuous version of the first-order difference equation model of cocaine use introduced by Everingham and Rydell [S.S. Everingham, C.P. Rydell, Modeling the Demand for Cocaine, MR-332-ONDCP/A/DPRC, RAND, Santa Monica, CA, 1994] and extend it by making initiation an endogenous function of prevalence. This function reflects both the epidemic spread of drug use as users 'infect' non-users and Musto's [D.F. Musto, The American Disease: Origins of Narcotic Control, Oxford University, New York, 1987] hypothesis that drug epidemics die out when a new generation is deterred from initiating drug use by observing the ill effects manifest among heavy users. Analyzing the model's dynamics suggests that drug prevention can temper drug prevalence and consumption, but that drug treatment's effectiveness depends critically on the stage in the epidemic in which it is employed. Reducing the number of heavy users in the early stages of an epidemic can be counter-productive if it masks the risks of drug use and, thereby, removes a disincentive to initiation. This strong dependence of an intervention's effectiveness on the state of the dynamic system illustrates the pitfalls of applying a static control policy in a dynamic context. (C) 1999 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:1 / 20
页数:20
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