TY - JOUR
T1 - The reinstatement model and relapse prevention
T2 - A clinical perspective
AU - Epstein, David H.
AU - Preston, Kenzie L.
N1 - Funding Information:
Most of the questions and issues raised in this commentary could be resolved by increased “crosstalk” between clinical and preclinical researchers. At an institutional level, there are instances of support for bench-to-bedside research. For example, in the US, the National Institute on Drug Abuse has established a funding mechanism called SPIRCAP (Strategic Program for Innovative Research on Cocaine Addiction Pharmacotherapy), and the National Institutes of Health have an intramural initiative called, fittingly, Bench to Bedside. However, recent Bench to Bedside awards do not appear to include any studies of addiction (Gallin et al. 2003). A brief search of the CRISP database of federally funded biomedical research projects (CRISP 2003) revealed no relapse studies of the kind we have suggested here, except for some studies of the natural history of cocaine dependence and predictors of relapse (which do not appear to include EMA) and some clinical trials of bupropion or nicotine replacement for prevention of smoking relapse in postpartum women. Although there is justification for testing those agents for smoking relapse, that justification does not come from the reinstatement model, where neither agent has apparently been tested.
Copyright:
Copyright 2008 Elsevier B.V., All rights reserved.
PY - 2003/7
Y1 - 2003/7
N2 - Objectives: This commentary assesses the degree to which the reinstatement model is homologous to the human experience of relapse. Results: A review of the literature suggests that the relationship is less clear than is often assumed, largely due to a lack of prospective data on the precipitants and process of relapse (especially relapse to heroin or cocaine abuse). However, reinstatement does not need to resemble relapse to have immediate clinical value; predictive validity as a medication screen would be sufficient. Whether the model has predictive validity is unknown, because, to date, very few clinical trials have tested medications that are effective in the reinstatement model, and even fewer have used designs comparable to those of reinstatement experiments. A clinical trial comparable to a reinstatement experiment would enroll participants who are already abstinent, and its main outcome measure would be propensity to undergo a specific type of relapse (e.g., relapse induced by stress or cues). Conclusions: Until clinical and preclinical work are more comparable, criticisms of the reinstatement model's presumed shortcomings are premature.
AB - Objectives: This commentary assesses the degree to which the reinstatement model is homologous to the human experience of relapse. Results: A review of the literature suggests that the relationship is less clear than is often assumed, largely due to a lack of prospective data on the precipitants and process of relapse (especially relapse to heroin or cocaine abuse). However, reinstatement does not need to resemble relapse to have immediate clinical value; predictive validity as a medication screen would be sufficient. Whether the model has predictive validity is unknown, because, to date, very few clinical trials have tested medications that are effective in the reinstatement model, and even fewer have used designs comparable to those of reinstatement experiments. A clinical trial comparable to a reinstatement experiment would enroll participants who are already abstinent, and its main outcome measure would be propensity to undergo a specific type of relapse (e.g., relapse induced by stress or cues). Conclusions: Until clinical and preclinical work are more comparable, criticisms of the reinstatement model's presumed shortcomings are premature.
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U2 - 10.1007/s00213-003-1470-6
DO - 10.1007/s00213-003-1470-6
M3 - Review article
C2 - 12721778
AN - SCOPUS:0038163567
VL - 168
SP - 31
EP - 41
JO - Psychopharmacology
JF - Psychopharmacology
SN - 0033-3158
IS - 1-2
ER -