Drug Checking As a Harm Reduction Tool for Recreational Users
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Bridging the Gap: a Practitioner's Guide to Harm Reduction in Drug
Bridging the Gap A Practitioner’s Guide to Harm Reduction in Drug Courts by Alejandra Garcia and Dave Lucas a Author Alejandra Garcia, MSW Center for Court Innovation Dave Lucas, MSW Center for Court Innovation Acknowledgements Bridging the Gap: A Practitioners Guide to Harm Reduction in Drug Courts represents an ambitious reimagining of drug court practices through a harm reduction lens. It was born of two intersecting health emergencies—COVID-19 and the overdose crisis—and a belief that this moment calls for challenging conversations and bold change. Against this backdrop, Bridging the Gap’s first aim is plain: to elevate the safety, dignity, and autonomy of current and future drug court participants. It is also an invitation to practitioners to revisit and reflect upon drug court principles from a new vantage point. There are some who see the core tenets of drug courts and harm reduction as antithetical. As such, disagreement is to be expected. Bridging the Gap aspires to be the beginning of an evolving discussion, not the final word. This publication would not have been possible without the support of Aaron Arnold, Annie Schachar, Karen Otis, Najah Magloire, Matt Watkins, and Julian Adler. We are deeply grateful for your thoughtful advice, careful edits, and encouraging words. A special thanks also to our designers, Samiha Amin Meah and Isaac Gertman. Bridging the Gap is dedicated to anyone working to make the world a safer place for people who use drugs. Thanks to all who approach this document with an open mind. For more information, email [email protected]. -
Raphael Bossong, LSE
Challenge Working Paper July 2007 The politics of subterfuge and EU JHA governance capacity Raphael Bossong, LSE This paper starts out from a puzzle: Why is EU JHA characterized by frustrations and blockades, while it is at the same time one of the most dynamic policy-areas?1 Posed in such general terms, this question is almost impossible to answer: Not only is EU JHA policy2 a highly diverse, but has also seen phases of ambitious agenda-setting contrasted by periods of stagnation.3 Therefore, a convincing answer to the above puzzle would require an extensive historical exposition of this policy area, which is beyond the scope of this paper. Here I only intend to review some general factors that inform EU’s current governance capacity in JHA,4 giving particular emphasis to the problems posed by unanimous decision- making in the Third Pillar.5 This structuralist approach cannot explain any particular instances of EU JHA policy-making on its own,6 but it aims to inform subsequent case studies. The paper proceeds in four steps. In a first part, I will discuss the EU’s structural obstacles to unanimous decision-making from a rationalist perspective. For this purpose I draw heavily on the work of Fritz Scharpf (1997) and Adrianne Héritier (1999) who have introduced many useful insights from comparative politics and policy analysis into EU studies. In the second part, I will survey different strategies for successful policy-making under extensive structural constraints to account for the dynamic development of EU JHA policy in recent years. This overview will be broken down into the classic dimensions of policy, polity and politics. -
NMR Project Proposal
www.ssoar.info National minority 'regions' in the enlarged European Union: mobilizing for third level politics? Malloy, Tove H. Arbeitspapier / working paper Empfohlene Zitierung / Suggested Citation: Malloy, T. H. (2005). National minority 'regions' in the enlarged European Union: mobilizing for third level politics? (ECMI Working Paper, 24). Flensburg: European Centre for Minority Issues (ECMI). https://nbn-resolving.org/ urn:nbn:de:0168-ssoar-63119 Nutzungsbedingungen: Terms of use: Dieser Text wird unter einer Deposit-Lizenz (Keine This document is made available under Deposit Licence (No Weiterverbreitung - keine Bearbeitung) zur Verfügung gestellt. Redistribution - no modifications). We grant a non-exclusive, non- Gewährt wird ein nicht exklusives, nicht übertragbares, transferable, individual and limited right to using this document. persönliches und beschränktes Recht auf Nutzung dieses This document is solely intended for your personal, non- Dokuments. Dieses Dokument ist ausschließlich für commercial use. All of the copies of this documents must retain den persönlichen, nicht-kommerziellen Gebrauch bestimmt. all copyright information and other information regarding legal Auf sämtlichen Kopien dieses Dokuments müssen alle protection. You are not allowed to alter this document in any Urheberrechtshinweise und sonstigen Hinweise auf gesetzlichen way, to copy it for public or commercial purposes, to exhibit the Schutz beibehalten werden. Sie dürfen dieses Dokument document in public, to perform, distribute or otherwise use the nicht in irgendeiner Weise abändern, noch dürfen Sie document in public. dieses Dokument für öffentliche oder kommerzielle Zwecke By using this particular document, you accept the above-stated vervielfältigen, öffentlich ausstellen, aufführen, vertreiben oder conditions of use. anderweitig nutzen. Mit der Verwendung dieses Dokuments erkennen Sie die Nutzungsbedingungen an. -
2017 Global Drug Survey
Prepared by the GDS Core Research Team Dr Adam Winstock, Dr Monica Barratt, Dr Jason Ferris & Dr Larissa Maier Global overview and highlights N > 115,000 Global Drug Survey GDS2017 © Not to be reproduced without authors permission Hi everyone On behalf of the GDS Core Research Team and everyone of our amazing international network partners and supportive media organisations we’d like to share our headline report deck. I know it won’t have everything that everyone wants but we are hopeful it will give people an idea of how the world of drugs is changing and highlight some of the key things that we think people can better engage with to keep themselves and those they care for safe. Once we cleaned the data from 150,000 people we chose to use data from just under 120,000 people this year for these reports. We have data reports addressing 18 different areas for over 25 countries. We can only share a fraction of what we have here on the site. However, we are very open to sharing the other findings we have and would ask researchers and public health groups to contact us so we can discuss funding and collaboration. We have almost completed designing GDS2018 so that we can start piloting early and give countries where we have not yet found friends to reach out to us. We particularly want to hear from people in Japan, Eastern Europe, Africa and the Middle East. Dr Adam R Winstock Founder and CEO Global Drug Survey Consultant Psychiatrist and Addiction Medicine Specialist Global Drug Survey GDS2017 © Not to be reproduced without authors permission We think this will be interesting. -
Adverse Reactions to Hallucinogenic Drugs. 1Rnstttutton National Test
DOCUMENT RESUME ED 034 696 SE 007 743 AUTROP Meyer, Roger E. , Fd. TITLE Adverse Reactions to Hallucinogenic Drugs. 1rNSTTTUTTON National Test. of Mental Health (DHEW), Bethesda, Md. PUB DATP Sep 67 NOTE 118p.; Conference held at the National Institute of Mental Health, Chevy Chase, Maryland, September 29, 1967 AVATLABLE FROM Superintendent of Documents, Government Printing Office, Washington, D. C. 20402 ($1.25). FDPS PRICE FDPS Price MFc0.50 HC Not Available from EDRS. DESCPTPTOPS Conference Reports, *Drug Abuse, Health Education, *Lysergic Acid Diethylamide, *Medical Research, *Mental Health IDENTIFIEPS Hallucinogenic Drugs ABSTPACT This reports a conference of psychologists, psychiatrists, geneticists and others concerned with the biological and psychological effects of lysergic acid diethylamide and other hallucinogenic drugs. Clinical data are presented on adverse drug reactions. The difficulty of determining the causes of adverse reactions is discussed, as are different methods of therapy. Data are also presented on the psychological and physiolcgical effects of L.S.D. given as a treatment under controlled medical conditions. Possible genetic effects of L.S.D. and other drugs are discussed on the basis of data from laboratory animals and humans. Also discussed are needs for futher research. The necessity to aviod scare techniques in disseminating information about drugs is emphasized. An aprentlix includes seven background papers reprinted from professional journals, and a bibliography of current articles on the possible genetic effects of drugs. (EB) National Clearinghouse for Mental Health Information VA-w. Alb alb !bAm I.S. MOMS Of NAM MON tMAN IONE Of NMI 105 NUNN NU IN WINES UAWAS RCM NIN 01 NUN N ONMININI 01011110 0. -
Neuroreceptor Activation by Vibration-Assisted Tunneling
OPEN Neuroreceptor Activation by SUBJECT AREAS: Vibration-Assisted Tunneling BIOPHYSICAL CHEMISTRY Ross D. Hoehn1, David Nichols2, Hartmut Neven3 & Sabre Kais4,5,6 MECHANISM OF ACTION 1Department of Chemistry, Purdue University, West Lafayette, IN 47907, USA, 2Department of Medicinal Chemistry and Molecular Pharmacology, Purdue University, West Lafayette, IN 47907, USA,3 Google, Venice, CA 90291, USA,4 Department of Received 5 20 October 2014 Chemistry, Purdue University, West Lafayette, IN 47907, USA, Departments of Physics, Purdue University, West Lafayette, IN 47907, USA,6 Qatar Environment and Energy Research Institute, Qatar Foundation, Doha, Qatar. Accepted 20 March 2015 G protein-coupled receptors (GPCRs) constitute a large family of receptor proteins that sense molecular Published signals on the exterior of a cell and activate signal transduction pathways within the cell. Modeling how an 24 April 2015 agonist activates such a receptor is fundamental for an understanding of a wide variety of physiological processes and it is of tremendous value for pharmacology and drug design. Inelastic electron tunneling spectroscopy (IETS) has been proposed as a model for the mechanism by which olfactory GPCRs are activated by a bound agonist. We apply this hyothesis to GPCRs within the mammalian nervous system Correspondence and using quantum chemical modeling. We found that non-endogenous agonists of the serotonin receptor share requests for materials a particular IET spectral aspect both amongst each other and with the serotonin molecule: a peak whose should be addressed to intensity scales with the known agonist potencies. We propose an experiential validation of this model by S.K. (kais@purdue. utilizing lysergic acid dimethylamide (DAM-57), an ergot derivative, and its deuterated isotopologues; we also provide theoretical predictions for comparison to experiment. -
Evaluation of a Drug Checking Service at a Large Scale Electronic Music Festival in Portugal
International Journal of Drug Policy 73 (2019) 88–95 Contents lists available at ScienceDirect International Journal of Drug Policy journal homepage: www.elsevier.com/locate/drugpo Research Paper Evaluation of a drug checking service at a large scale electronic music festival in Portugal T ⁎ Helena Valentea,b,c, , Daniel Martinsb,d, Helena Carvalhoe,f, Cristiana Vale Piresb,g,h, Maria Carmo Carvalhob,h, Marta Pintoa,c,i, Monica J. Barrattj,k a Faculty of Psychology and Educational Sciences of the Porto University, Portugal b Kosmicare Association, Portugal c CINTESIS. Centre for Health Technology and Services Research, Portugal d CIQUP. Department of Chemistry and Biochemistry, Faculty of Sciences of the Porto Univsersity of Porto, Portugal e CPUP. Centre for Psychology of the University of Porto, Portugal f inED. Centre for Research and Innovation in Education, Portugal g Faculty of Education and Psychology of the Portuguese Catholic University, Portugal h CRIA. Centre for Research in Anthropology, Portugal i Faculty of Medicine of the Porto University, Portugal j Social and Global Studies Centre, RMIT University, Australia k National Drug and Alcohol Research Centre, Australia ARTICLE INFO ABSTRACT Keywords: Background: Drug checking services are being implemented in recreational settings across the world, however Harm reduction these projects are frequently accused of a lack of evidence concerning their impact on people who use drugs. This Program evaluation paper describes the implementation of a drug checking service at the Boom Festival 2016 and explores the Drug checking impact of this service on its users’ behavioural intentions. Boom festival Methods: 753 drug samples were submitted to the drug checking service for chemical analysis. -
Year End Report 2019 Year End Report 2019
Vancouver Island Drug Checking Project Year End Report 2019 Year End Report 2019 The Vancouver Island Drug Checking Project delivers drug checking services in Victoria, BC. We currently operate at SOLID Outreach, AVI Health and Community Services, and Lantern Services as well as festivals and community events. This free and confidential service provides information on composition of substances and harm reduction infor- mation. We employ five instruments as follows: Fentanyl Strip Tests Fourier Transformed Infrared Spectroscopy (FTIR) Raman Spectroscopy 935 Surface Enhanced Raman Spectroscopy (SERS) Samples Tested Gas Chromatography – Mass Spectrometry (GC-MS) in 2019 What were people bringing to be tested? We asked people what drug they were bringing to be tested. The majority of substances were expected to be heroin or fentanyl (362), a stimulant (234), or a psychedelic (139). Further, many brought unknown samples for testing (73) or did not provide information (56). This may be due in part to people testing for others and bringing multiple samples or hav- ing found substances. The remaining substances were expected to be dissociatives (31), benzodiazepines (16) or other depressants (5), other opioids (5), polysubstance (3) or other (11). Opioid-Down: heroin and/or Stimulant: methampheta- Psychedelic: LSD, MDMA, 362362 fentanyl 234234 mine, cocaine HCl, cocaine base 139139 MDA, 2CB, DMT Unknown Missing Dissociative: ketamine, DXM, 7373 5656 3131 methoxetamine, PCP Depressant- Other Depressant-Other: GHB, 1616 Benzodiazepines 1111 5 GBL, barbiturates, methaqualone, phenibut Opioid-Other: morphine, phar- Polysubstance 55 maceutical opioids 33 Data are not finalized and subject to change. There were missing data for some samples. Vancouver Island Drug Checking Project Year End Report 2019 How many samples tested positive for fentanyl? We tested all samples using Fentanyl Test Strips to determine whether they contained fentanyl. -
Molecular Mechanisms of Addiction
Molecular Mechanisms of Addiction Eric J. Nestler Nash Family Professor The Friedman Brain Institute Medical Model of Addiction • Pathophysiology - To identify changes that drugs produce in a vulnerable brain to cause addiction. • Individual Risk - To identify specific genes and non-genetic factors that determine an individual’s risk for (or resistance to) addiction. - About 50% of the risk for addiction is genetic. Only through an improved understanding of the biology of addiction will it be possible to develop better treatments and eventually cures and preventive measures. Scope of Drug Addiction • 25% of the U.S. population has a diagnosis of drug abuse or addiction. • 50% of U.S. high school graduates have tried an illegal drug; use of alcohol and tobacco is more common. • >$400 billion incurred annually in the U.S. by addiction: - Loss of life and productivity - Medical consequences (e.g., AIDS, lung cancer, cirrhosis) - Crime and law enforcement Diverse Chemical Substances Cause Addiction • Opiates (morphine, heroin, oxycontin, vicodin) • Cocaine • Amphetamine and like drugs (methamphetamine, methylphenidate) • MDMA (ecstasy) • PCP (phencyclidine or angel dust; also ketamine) • Marijuana (cannabinoids) • Tobacco (nicotine) • Alcohol (ethanol) • Sedative/hypnotics (barbiturates, benzodiazepines) Chemical Structures of Some Drugs of Abuse Cocaine Morphine Ethanol Nicotine ∆9-tetrahydrocannabinol Drugs of Abuse Use of % of US population as weekly users 100 25 50 75 0 Definition of Drug Addiction • Loss of control over drug use. • Compulsive drug seeking and drug taking despite horrendous adverse consequences. • Increased risk for relapse despite years of abstinence. Definition of Drug Addiction • Tolerance – reduced drug effect after repeated use. • Sensitization – increased drug effect after repeated use. -
Annual Report 2019
Annual Report 2019 Who we are What we want How we work Table of Contents Foreword ................................................................................................................................................................. 1 Climate justice – now! ...................................................................................................................................... 2 Shaping a new energy system ........................................................................................................................ 4 For a responsible infrastructure and raw materials policy ................................................................ 6 Promoting sustainable agriculture and development .......................................................................... 8 Strengthening democracy and human rights .........................................................................................10 Strengthening women’s and LGBTI rights .............................................................................................12 Towards a sustainable and humane migration policy ........................................................................14 For European solidarity in times of crisis ...............................................................................................16 30th anniversary of the Peaceful Revolution – promoting a strong democracy! ...................18 A just society needs intact public spaces .................................................................................................19 -
Licensing and Differential Object Marking: the View from Neo-Aramaic Laura Kalin
Syntax 21:2, June 2018, 112–159 DOI: 10.1111/synt.12153 Licensing and Differential Object Marking: The View from Neo-Aramaic Laura Kalin Abstract. I propose a novel analysis of differential object marking (DOM) that revolves around nominal licensing and, unlike most previous accounts, does not appeal to object visibility (e.g., Danon 2006, Lyutikova & Pereltsvaig 2015), object raising (e.g., Bhatt & Anagnostopoulou 1996, Baker & Vinokurova 2010), or object differentiation or identification (e.g., Aissen 2003, De Hoop & Malchukov 2008). I argue (i) that not all nominals need abstract licensing (following Massam 2001, Danon 2006, Ormazabal & Romero 2013), but also that all nominals have the potential to be licensed, that is, all nominals are visible to case and agreement processes; (ii) that the set of objects that are overtly marked (e.g., by case or agreement) can reveal the set of nominals that require licensing in a language, and (iii) that clauses typically have one obligatory nominal licenser, with secondary licensers merging only when needed for convergence (following Levin & Massam 1985; Bobaljik 1993; Laka 1993, 2000; Rezac 2011). Taken together, I show that variation in the types of nominals that need licensing and the location/identity of obligatory and secondary licensers can derive crosslinguistic differences in case, agreement, and DOM patterns. This unified account simplifies our understanding of nominal licensing within and across languages, as it does not require objects to have special properties as compared to subjects, nor does it fundamentally differentiate DOM languages from non-DOM languages. The motivating data come largely from the Neo-Aramaic language Senaya, which clearly illustrates that certain nominals can occupy a position where abstract licensing is unavailable. -
Vol. 85 Tuesday, No. 67 April 7, 2020 Pages 19375–19640
Vol. 85 Tuesday, No. 67 April 7, 2020 Pages 19375–19640 OFFICE OF THE FEDERAL REGISTER VerDate Sep 11 2014 21:02 Apr 06, 2020 Jkt 250001 PO 00000 Frm 00001 Fmt 4710 Sfmt 4710 E:\FR\FM\07APWS.LOC 07APWS khammond on DSKJM1Z7X2PROD with FR-1WS II Federal Register / Vol. 85, No. 67 / Tuesday, April 7, 2020 The FEDERAL REGISTER (ISSN 0097–6326) is published daily, SUBSCRIPTIONS AND COPIES Monday through Friday, except official holidays, by the Office PUBLIC of the Federal Register, National Archives and Records Administration, under the Federal Register Act (44 U.S.C. Ch. 15) Subscriptions: and the regulations of the Administrative Committee of the Federal Paper or fiche 202–512–1800 Register (1 CFR Ch. I). The Superintendent of Documents, U.S. Assistance with public subscriptions 202–512–1806 Government Publishing Office, is the exclusive distributor of the official edition. Periodicals postage is paid at Washington, DC. General online information 202–512–1530; 1–888–293–6498 Single copies/back copies: The FEDERAL REGISTER provides a uniform system for making available to the public regulations and legal notices issued by Paper or fiche 202–512–1800 Federal agencies. These include Presidential proclamations and Assistance with public single copies 1–866–512–1800 Executive Orders, Federal agency documents having general (Toll-Free) applicability and legal effect, documents required to be published FEDERAL AGENCIES by act of Congress, and other Federal agency documents of public Subscriptions: interest. Assistance with Federal agency subscriptions: Documents are on file for public inspection in the Office of the Federal Register the day before they are published, unless the Email [email protected] issuing agency requests earlier filing.