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DOI 10.1093/pubmed/fdv150

Медицинская библиотека · Journal of public health (Oxford, England) · 2015

Addressing misuse and diversion of opioid substitution medication: guidance based on systematic evidence review and real-world experience.

Wright Nat, D'Agnone Oscar, Krajci Peter, Littlewood Richard, Alho Hannu, Reimer Jens, Roncero Carlos, Somaini Lorenzo, Maremmani Icro

СтатьяСистематический обзорПеревод в очереди

Аннотация

BACKGROUND

Opioid dependence treatment, comprising opioid substitution treatment (OST) and psychosocial intervention, is accepted to improve outcomes in opioid addiction for both the individual and public health. OST medication such as methadone or buprenorphine may be misused or diverted. This results in failure to recover from addiction, increased crime and the spread of blood-borne viruses. Worldwide, attempts to address misuse and diversion have been proposed and implemented with varying impact.

METHODS

A structured, expert-led process recommended the most impact. As an initial step, a broad range of strategies were defined, and a systematic review of published literature identified 37 highly relevant sources of evidence. Experts reviewed this evidence and ranked the list of strategies for effectiveness and ease of implementation, based on their clinical experience.

RESULTS/

CONCLUSIONS

Three groups of strategies to address misuse or diversion are defined, depending on impact (effectiveness and ease of implementation). Preferred strategies include the promotion of access to treatment and the use of product formulations less likely to be misused. However, additional data and innovative approaches to address this complex problem are needed.

Для цитирования: Wright Nat, D'Agnone Oscar, Krajci Peter, Littlewood Richard, Alho Hannu, Reimer Jens, Roncero Carlos, Somaini Lorenzo, Maremmani Icro. Addressing misuse and diversion of opioid substitution medication: guidance based on systematic evidence review and real-world experience.. Journal of public health (Oxford, England). 2015. DOI: 10.1093/pubmed/fdv150.

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