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New methodologies for faster study of new psychoactive substances: A proposal

Published online by Cambridge University Press:  23 March 2020

P. Quintana Mathé*
Affiliation:
Hospital del Mar Medical Research Institute, Grup de Recerca en Addiccions, Barcelona, Spain Associació Benestar i Desenvolupament, Energy Control, Barcelona, Spain
M. Grifell
Affiliation:
Hospital del Mar Medical Research Institute, Grup de Recerca en Addiccions, Barcelona, Spain Associació Benestar i Desenvolupament, Energy Control, Barcelona, Spain Parc de Salut Mar, Institut de Neuropsiquiatria i Addiccions, Barcelona, Spain
*
* Corresponding author.

Abstract

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Introduction

New psychoactive substances (NPS) are substances that have recently become available, and are not worldwide regulated. They often intend to mimic the effect of controlled drugs, becoming a public health concern. In 2014, 101 substances were reported for the first time in the EU, which may require to be studied and risk-assessed by the scientific community. The EMCDDA recognizes it as an emerging topic where research is most needed, as the scientific community is struggling to keep pace with the speed at which new substances appear. On the one hand, case reports and internet-based surveys are quickly published but do not provide enough evidence to guide clinical decisions. On the other hand, classical high-reliability methodologies such as Cohort and Clinical studies take too long and their cost is too high to be of much use for the study of NPS. We propose an intermediate methodology to tackle this unmet need.

Rationale

González and colleagues described a set of highly educated, experimental users of NPS with extensive knowledge and consumption of substances. These users usually look for drug checking of the substances they intend to consume. We suggest we could benefit from the collaboration of such users, and the possibility of obtaining analytical confirmation, to retrieve information about NPS in a quick and reliable fashion.

Outline of methodology

Recluting of subjects that submit NPS to a drug checking facility. Analysis of the samples for analytical confirmation. Check inclusion criteria and propose inclusion in the study. Give structured forms for reporting effects and adverse events.

Disclosure of interest

The authors have not supplied their declaration of competing interest.

Type
EV1131
Copyright
Copyright © European Psychiatric Association 2016
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