The ASAM National Practice Guideline for the Use of Medications in the Treatment of Addiction Involving Opioid Use
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Pressoffice@Cityhal
From: Mayor's Press Office <[email protected]> Sent: Monday, December 7, 2015 3:54 PM To: Mayor's Press Office Subject: DE BLASIO ADMINISTRATION LAUNCHES COMPREHENSIVE EFFORT TO REDUCE OPIOID MISUSE AND OVERDOSE DEATHS ACROSS THE CITY THE CITY OF NEW YORK OFFICE OF THE MAYOR NEW YORK, NY 10007 FOR IMMEDIATE RELEASE: December 7, 2015 CONTACT: [email protected], (212) 788-2958 DE BLASIO ADMINISTRATION LAUNCHES COMPREHENSIVE EFFORT TO REDUCE OPIOID MISUSE AND OVERDOSE DEATHS ACROSS THE CITY City to make naloxone, overdose-reversing medication, available without a prescription at participating pharmacies in New York City New data shows 56 percent increase in unintentional opioid overdose deaths since 2010 NEW YORK—Mayor Bill de Blasio and First Lady Chirlane McCray today announced that beginning immediately, naloxone, a safe medication that can prevent death from opioid overdose, is available in pharmacies without a prescription. “Last year, this city experienced the equivalent of more than one fatal opioid overdose a day,” said Mayor Bill de Blasio. “These are people whose lives, once filled with promise, have been upended, leaving families to struggle with deep, lasting pain. We won’t accept this as our fate as a city – and we’ve resolved to do something about it.” “For any New Yorker who has ever worried about a loved one struggling with opioid dependency, today's announcement is an enormous relief. Anyone who fears they will one day find their child, spouse or sibling collapsed on the floor and not breathing now has the power to walk into a neighborhood pharmacy and purchase the medication that can reverse that nightmare. -
Medications for Opioid Use Disorder Save Lives
HEALTH AND MEDICINE DIVISION BOARD ON HEALTH SCIENCES POLICY Case and Comments on “Medications for Opioid Use Disorder Save Lives” Scott Steiger, MD, FACP, FASAM UCSF Associate Clinical Professor of Medicine and Psychiatry Deputy Medical Director, Opiate Treatment Outpatient Program Committee on Medication- Assisted Treatment for Opioid Use Disorder Sponsors • National Institute on Drug Abuse (NIDA) • Substance Abuse and Mental Health Services Administration (SAMHSA) Charge to the committee • Review current knowledge and gaps on the effectiveness of medications for OUD • Examine how medications can be effectively delivered, and in what settings and populations • Identify challenges in implementation and uptake • Identify additional research needed Committee members Alan Leshner, Ph.D. (Chair) Traci Green, Ph.D., M.Sc. American Associaon for the Advancement of Brown University/Boston University Science (ret.) Huda Akil, Ph.D. Alan Je=e, Ph.D. University of Michigan MGH Ins,tute of Health Professions Colleen Barry, Ph.D. Laura R. Lander, M.S.W. Johns Hopkins School of Public Health West Virginia University Kathleen Carroll, Ph.D. David Paerson Silver Wolf, Ph.D. Yale School of Medicine Washington University Chinazo Cunningham, M.D. Seun Ross, D.N.P. Albert Einstein College of Medicine American Nurses Associaon Walter Ginter Sco= Steiger, M.D. MARS Statewide Network University of California San Francisco Yasmin Hurd, Ph.D. David Vlahov, Ph.D., RN, FAAN, Icahn School of Medicine at Mount Sinai Yale School of Nursing The Opioid Crisis in the U.S. • > 2 million people with OUD • > 47,000 people died from opioid overdose in 2017 alone • Tied to reemerging public health crisis of infectious disease • Socioeconomic consequences include health care costs, loss of productivity, criminal involvement, housing insecurity, impact on families Anna’s Story Opioid Use Disorder • Compulsive or uncontrolled use of prescription or illicit opioids in the face of negative consequences. -
Medications to Treat Opioid Use Disorder Research Report
Research Report Revised Junio 2018 Medications to Treat Opioid Use Disorder Research Report Table of Contents Medications to Treat Opioid Use Disorder Research Report Overview How do medications to treat opioid use disorder work? How effective are medications to treat opioid use disorder? What are misconceptions about maintenance treatment? What is the treatment need versus the diversion risk for opioid use disorder treatment? What is the impact of medication for opioid use disorder treatment on HIV/HCV outcomes? How is opioid use disorder treated in the criminal justice system? Is medication to treat opioid use disorder available in the military? What treatment is available for pregnant mothers and their babies? How much does opioid treatment cost? Is naloxone accessible? References Page 1 Medications to Treat Opioid Use Disorder Research Report Discusses effective medications used to treat opioid use disorders: methadone, buprenorphine, and naltrexone. Overview An estimated 1.4 million people in the United States had a substance use disorder related to prescription opioids in 2019.1 However, only a fraction of people with prescription opioid use disorders receive tailored treatment (22 percent in 2019).1 Overdose deaths involving prescription opioids more than quadrupled from 1999 through 2016 followed by significant declines reported in both 2018 and 2019.2,3 Besides overdose, consequences of the opioid crisis include a rising incidence of infants born dependent on opioids because their mothers used these substances during pregnancy4,5 and increased spread of infectious diseases, including HIV and hepatitis C (HCV), as was seen in 2015 in southern Indiana.6 Effective prevention and treatment strategies exist for opioid misuse and use disorder but are highly underutilized across the United States. -
How to Select Pharmacologic Treatments to Manage Recidivism Risk in Sex Off Enders
How to select pharmacologic treatments to manage recidivism risk in sex off enders Consider patient factors when choosing off -label hormonal and nonhormonal agents ® Dowden Healthex offenders Media traditionally are managed by the criminal justice system, but psychiatrists are fre- Squently called on to assess and treat these indi- CopyrightFor personalviduals. use Part only of the reason is the overlap of paraphilias (disorders of sexual preference) and sexual offending. Many sexual offenders do not meet DSM criteria for paraphilias,1 however, and individuals with paraphil- ias do not necessarily commit offenses or come into contact with the legal system. As clinicians, we may need to assess and treat a wide range of sexual issues, from persons with paraphilias who are self-referred and have no legal involvement, to recurrent sexual offenders who are at a high risk of repeat offending. Successfully managing sex offenders includes psychological and pharmacologic interven- 2009 © CORBIS / TIM PANNELL 2009 © CORBIS / tions and possibly incarceration and post-incarceration Bradley D. Booth, MD surveillance. This article focuses on pharmacologic in- Assistant professor terventions for male sexual offenders. Department of psychiatry Director of education Integrated Forensics Program University of Ottawa Reducing sexual drive Ottawa, ON, Canada Sex offending likely is the result of a complex inter- play of environment and psychological and biologic factors. The biology of sexual function provides nu- merous targets for pharmacologic intervention, in- cluding:2 • endocrine factors, such as testosterone • neurotransmitters, such as serotonin. The use of pharmacologic treatments for sex of- fenders is off-label, and evidence is limited. In general, Current Psychiatry 60 October 2009 pharmacologic treatments are geared toward reducing For mass reproduction, content licensing and permissions contact Dowden Health Media. -
Pharmacological Interventions with Adult Male Sexual Offendersi
Pharmacological Interventions with Adult Male Sexual Offendersi Adopted by the ATSA Executive Board of Directors on August 30, 2012 Introduction The treatment of sexual offending behaviors is complex and involves multiple etiologies, individualized risk reduction and risk management needs, and heterogeneous biopsychosocial, interpersonal, and legal factors. Clinicians and researchers have attempted to identify approaches which promise the greatest success in addressing these behaviors. Findings from a meta-analysis examining the effectiveness of various treatment interventions for adult sex offenders indicated that, when used in combination with other treatment approaches, biological interventions like testosterone-lowering hormonal treatments may be linked to greater reductions in recidivism for some offenders than the use of psychosocial treatments alone (Losel and Schmucker, 2005). Other data, described below, suggest that non- hormonal psychotropic medications can also be effective supplements to standard therapeutic interventions for sex offenders as well. This document is designed to provide an overview of key issues pertaining to the use of hormonal and non- hormonal agents to reduce or inhibit sexual arousal and recidivism in some sexual offenders.ii Mechanism-of- action, anticipated results of medication administration, side effects, ethical considerations, and empirical evidence regarding efficacy of pharmacological interventions will be highlighted. It should be noted that pharmacological interventions are not typically used for all sexual offenders, but are often applied to those with paraphilias or offense-specific patterns of sexual arousal which could be altered through the use of such interventions. Further, such interventions should be integrated into a comprehensive treatment program that addresses other static and dynamic risk factors that contribute to sexual offending. -
Combining a Candidate Vaccine for Opioid Use Disorders with Extended-Release Naltrexone Increases Protection Against Oxycodone-Induced Behavioral Effects and Toxicity
Title page Combining a candidate vaccine for opioid use disorders with extended-release naltrexone increases protection against oxycodone-induced behavioral effects and toxicity. Michael D. Raleigha, Claudia Accetturob, and Marco Pravetonia,c,d*. aUniversity of Minnesota, School of Medicine, Department of Pharmacology, 6-120 Jackson Hall, 321 Church St. SE, Minneapolis MN 55455, USA. bUniversita’ degli Studi di Milano, Socrates Program, 20 Via Giovanni Celoria, 18, 20133 Milano, Italy. cUniversity of Minnesota, School of Medicine, Department of Medicine, 420 Delaware Street SE, MMC 194 Suite 14-110 Phillips- Wangensteen Building Minneapolis, MN 55455, USA. dHennepin Healthcare Research Institute, 701 Park Avenue, Minneapolis, MN 55415, USA. Running Title Page Combination of opioid vaccine and naltrexone Corresponding author: Marco Pravetoni University of Minnesota Department of Pharmacology 3-108 Nils Hasselmo Hall 312 Church St SE, Minneapolis, MN 55455 612-625-6243, [email protected] Number of text pages: 39 Number of tables: 0 Number of figures: 5 Number of references: 62 Number of words in the Abstract: 232 Number of words in the Introduction: 722 Number of words in the Discussion: 1498 Abbreviations: arterial oxygen saturation (SaO2), enzyme-linked immunosorbent assay (ELISA), extended release naltrexone (XR-NTX), good manufacturing practice (GMP), keyhole limpet hemocyanin (KLH), opioid use disorder (OUD), oxycodone (OXY), ovalbumin (OVA), percent maximum possible effect (%MPE) Recommended section assignment: Drug Discovery and Translational Medicine 2 Abstract Opioid use disorders (OUD) and opioid-related fatal overdoses are a significant public health concern in the United States and worldwide. To offer more effective medical interventions to treat or prevent OUD, anti-opioid vaccines are in development that reduce the distribution of the targeted opioids to brain and subsequently reduce the associated behavioral and toxic effects. -
ASAM National Practice Guidelines
NATIONAL PRACTICE GUIDELINE National Practice Guideline for the Use of Medications in the Treatment of Addiction Involving Opioid Use ASAM National Practice Guideline for the Use of Medi- Robert J. Roose, MD, MPH cations in the Treatment of Addiction Involving Opioid Alexis Geier-Horan, ASAM Staff Use Beth Haynes, ASAM Staff Guideline Committee Members (alpha order): Penny S. Mills, MBA, ASAM, Executive Vice President Sandra Comer, PhD Special External Reviewer: Chinazo Cunningham, MD, MS Michael M. Miller, MD, FASAM, FAPA Marc J. Fishman, MD, FASAM Adam Gordon, MD, MPH, FASAM Treatment Research Institute Technical Team Mem- Kyle Kampman, MD, Chair bers (alpha order): Daniel Langleben, MD Amanda Abraham, PhD Ben Nordstrom, MD, PhD Karen Dugosh, PhD David Oslin, MD David Festinger, PhD George Woody, MD Kyle Kampman, MD, Principal Investigator Tricia Wright, MD, MS Keli McLoyd, JD Stephen Wyatt, DO Brittany Seymour, BA Abigail Woodworth, MS ASAM Quality Improvement Council (alpha order): John Femino, MD, FASAM Disclosure information for Guideline Committee Members, Margaret Jarvis, MD, FASAM, Chair the ASAM Quality Improvement Council, and External Margaret Kotz, DO, FASAM Reviewers is available respectively in Appendices III, IV, Sandrine Pirard, MD, MPH, PhD and V. Table of Contents EXECUTIVE SUMMARY ........................................................03 Purpose .....................................................................03 Background . 03 Scope of Guideline . 04 Intended Audience . 04 Qualifying Statement . 04 Overview of Methodology . 04 Summary of Recommendations . 05 Abbreviations and Acronyms . 10 National Practice Guideline Glossary . 10 INTRODUCTION . 14 Purpose .....................................................................14 Background on Opioid Use Disorder . 14 Scope of Guideline . 15 Intended Audience . 15 Qualifying Statement . 16 METHODOLOGY . 16 Overview of Approach . 16 Task 1: Review of Existing Guidelines . -
Cohort 7 RAM Scholars (2018-20)
RESEARCH IN ADDICTION MEDICINE SCHOLARS PROGRAM 2018-2020 Scholars Scholars Mentors Miriam Harris, MD Christine Gunn, PhD Dr. Harris is an Addiction Medicine Fellow at Boston University. She is Dr. Gunn is a Research Assistant Professor in the Department of Addiction Medicine a General Internist and completed her training at the University of Medicine at Boston University and in the Department of Health Law, British Columbia and fellowship at McGill University. Her research Policy and Management at the School of Public Health. Dr. Gunn has Boston University Boston University School interests are in women's health and addiction. In particular, she hopes extensive experience in qualitative research methods, surveys, and School of of Medicine to examine communication strategies that will engage women who use mixed methods approaches to studying risk and prevention behaviors. Medicine NAC Mentor: Patrick O’Connor, MD, MPH heroin and fentanyl in harm reduction and assess how to expand Her current research focuses on understanding age- and gender-based reproductive health service access within addiction health services. perceptions of overdose risk related to fentanyl use and preferences for risk communication in this setting. Shakevia Johnson, MD, MS Michael Hoefer, MD, MS Dr. Johnson is an Addiction Psychiatry Fellow at the University of Dr. Hoefer is an Assistant Clinical Professor of Psychiatry at the Addiction Psychiatry California, San Francisco. Her clinical and research interests include University of California San Francisco (UCSF) and the Medical Director University of the treatment of opioid use disorder during pregnancy, quality of the San Francisco VA Medical Center Opioid Treatment Program. University of California California San improvement, maximizing access to care and minimizing barriers to He is also the Program Director of the UCSF Addiction Psychiatry San Francisco Francisco treatment for those with substance use disorders. -
Using Low Dose Naltrexone (LDN)
J Neuroimmune Pharmacol DOI 10.1007/s11481-013-9451-y PERSPECTIVE Treatment of Complex Regional Pain Syndrome (CRPS) Using Low Dose Naltrexone (LDN) Pradeep Chopra & Mark S. Cooper Received: 7 November 2012 /Accepted: 4 March 2013 # The Author(s) 2013. This article is published with open access at Springerlink.com Abstract Complex Regional Pain Syndrome (CRPS) is a dysfunctions. One of the characteristic symptoms of this neuropathic pain syndrome, which involves glial activation condition is that the pain is out of proportion to the initial and central sensitization in the central nervous system. Here, injury. Diagnoses of CRPS are often delayed because it is we describe positive outcomes of two CRPS patients, after under recognized (Binkley 2012). If effective treatments are they were treated with low-dose naltrexone (a glial attenu- given early enough in progression of the disease, there is ator), in combination with other CRPS therapies. Prominent reduced chance for the spread of regional pain, autonomic CRPS symptoms remitted in these two patients, including dysfunction, motor changes, and negative sensory symptoms, dystonic spasms and fixed dystonia (respectively), following such as hypoalgesia (Marinus et al. 2011). As CRPS treatment with low-dose naltrexone (LDN). LDN, which is progresses, it becomes refractory to sympathetic nerve known to antagonize the Toll-like Receptor 4 pathway and blocks, conventional analgesics, anticonvulsants and attenuate activated microglia, was utilized in these patients antidepressants. after conventional CRPS pharmacotherapy failed to suppress During neuroimmune activation, TLR4 (Toll-Like their recalcitrant CRPS symptoms. Receptor 4) is upregulated in microglia, resident immune cells of the central nervous system (Watkins et al. -
ASAM National Practice Guideline for the Treatment of Opioid Use Disorder: 2020 Focused Update
The ASAM NATIONAL The ASAM National Practice Guideline 2020 Focused Update Guideline 2020 Focused National Practice The ASAM PRACTICE GUIDELINE For the Treatment of Opioid Use Disorder 2020 Focused Update Adopted by the ASAM Board of Directors December 18, 2019. © Copyright 2020. American Society of Addiction Medicine, Inc. All rights reserved. Permission to make digital or hard copies of this work for personal or classroom use is granted without fee provided that copies are not made or distributed for commercial, advertising or promotional purposes, and that copies bear this notice and the full citation on the fi rst page. Republication, systematic reproduction, posting in electronic form on servers, redistribution to lists, or other uses of this material, require prior specifi c written permission or license from the Society. American Society of Addiction Medicine 11400 Rockville Pike, Suite 200 Rockville, MD 20852 Phone: (301) 656-3920 Fax (301) 656-3815 E-mail: [email protected] www.asam.org CLINICAL PRACTICE GUIDELINE The ASAM National Practice Guideline for the Treatment of Opioid Use Disorder: 2020 Focused Update 2020 Focused Update Guideline Committee members Kyle Kampman, MD, Chair (alpha order): Daniel Langleben, MD Chinazo Cunningham, MD, MS, FASAM Ben Nordstrom, MD, PhD Mark J. Edlund, MD, PhD David Oslin, MD Marc Fishman, MD, DFASAM George Woody, MD Adam J. Gordon, MD, MPH, FACP, DFASAM Tricia Wright, MD, MS Hendre´e E. Jones, PhD Stephen Wyatt, DO Kyle M. Kampman, MD, FASAM, Chair 2015 ASAM Quality Improvement Council (alpha order): Daniel Langleben, MD John Femino, MD, FASAM Marjorie Meyer, MD Margaret Jarvis, MD, FASAM, Chair Sandra Springer, MD, FASAM Margaret Kotz, DO, FASAM George Woody, MD Sandrine Pirard, MD, MPH, PhD Tricia E. -
508C, Naltrexone Medication Assisted Treatment (MAT) Program
Naltrexone Medication Assisted Treatment (MAT) Program Description Division of TennCare BCBST Tracking #: 18-091 Overview of the Opioid Use Disorder Medication Assisted Treatment Program The Division of TennCare along with the contracted Managed Care Organizations (Amerigroup, BlueCare and United Healthcare) has determined the need for a comprehensive network of providers who offer specific treatment for members with opioid use disorder. These providers may be agencies or licensed independent practitioners, but all must attest to provide treatment as outlined in this program description to be included in this network. Medication Assisted Treatment (MAT) for persons diagnosed with opioid-use disorder is the use of medications, in combination with counseling and behavioral therapies, to provide a whole-patient approach to the treatment of substance use disorders. Research shows that when treating substance- use disorders, a combination of medication and behavioral therapies is most successful. The duration of treatment should be based on the needs of the persons served. The Food and Drug Administration (FDA) has approved several medications for the use in treatment of opioid-use disorder (OUD) which include buprenorphine containing products and naltrexone products Treatment with buprenorphine and naltrexone for opioid use disorders is considered an evidence-based best practice by the Substance Abuse and Mental Health Services Administration (SAMHSA) Center and the American Society of Addiction Medicine (ASAM) for substance abuse treatment. This naltrexone MAT Program Description outlines treatment and clinical care activities expected of providers who prescribe naltrexone products and professionals who provide therapy, care coordination or other ancillary services for those members who are being treated with naltrexone products. -
SUD,OUD and MAT: Epidemiology, Stigma, Misconceptions, and Myths
SUD,OUD and MAT: Epidemiology, Stigma, Misconceptions, and Myths Kelly S. Ramsey, MD, MPH, MA, FACP Medical Director of Substance Use Disorders HRHCare HOPE Conference November 1, 2019 DISCLOSURES Dr. Ramsey has no relevant disclosures LEARNING OBJECTIVES 1. Discuss substance use disorder (SUD), the opioid epidemic and opioid use disorder (OUD) 2. Discuss stigma related to SUD/OUD/people who use drugs (PWUD) 3. Discuss medication assisted treatment (MAT) for OUD 4. Discuss the misconceptions and myths surrounding MAT Epidemiology of SUD Epidemiology of SUD Epidemiology of SUD Epidemiology of SUD Epidemiology of SUD Epidemiology of SUD Epidemiology of SUD Epidemiology of SUD Epidemiology of SUD Epidemiology of SUD Epidemiology of SUD Epidemiology of SUD Epidemiology of SUD Adverse Childhood Experiences Adverse Childhood Experiences and Outcomes Vulnerability Factors for SUD ✚ Genetic predisposition ✚ Concomitant mental health diagnoses: bipolar disorder, anxiety (GAD, PTSD, social anxiety), depression, ADD/ADHD, personality disorders (borderline, antisocial), antisocial conduct disorder (especially in adolescence); undiagnosed or undertreated or untreated or treated inappropriately ✚ History of trauma and/or abuse ✚ Poor coping mechanisms/escapism ✚ Impulsivity ✚ Sensation/novelty seeking (initially) ✚ Environmental triggers/cues ✚ Lack of homeostatic reward regulation; reward “deficiency”: orientation towards pleasurable rewards Why Are We Here? Let’s Discuss Opioids… Opiate v. Opioid ● Opiate: a term that refers to drugs or medications