This presentation, to an international web audience, was presented alongside one by Dr Wilson Compton, Deputy Director of the National Institute on Drug Abuse. Sponsored by NDEWS, it explores the structural reasons for the emerging heroin overdose epidemic and ways to address it.
National Academies of Science and Medicine: Intertwined Epidemics: Opioid and...Dan Ciccarone
This presentation explores the current heroin overdose epidemic;how it evolved out of the prescription pill epidemic and how changes in heroin supply are creating regional differences in heroin overdose.
This presentation describes the forces behind the opioid pill to heroin to fentanyl "Triple Wave" epidemic. Policy issues and harm reduction measures needed to address this unprecedented crisis are discussed
This research paper focuses on prescription opioids and its effects on the African American community. The author discusses the background, best treatment intervention, and ethical considerations associated with prescription opioids and their use within the African American population.
Kana Enomoto, Acting Administrator, Substance Abuse and Mental Health Services Administration, keynote presentation at the National Rx Drug Abuse & Heroin Summit March 29, 2016
National Academies of Science and Medicine: Intertwined Epidemics: Opioid and...Dan Ciccarone
This presentation explores the current heroin overdose epidemic;how it evolved out of the prescription pill epidemic and how changes in heroin supply are creating regional differences in heroin overdose.
This presentation describes the forces behind the opioid pill to heroin to fentanyl "Triple Wave" epidemic. Policy issues and harm reduction measures needed to address this unprecedented crisis are discussed
This research paper focuses on prescription opioids and its effects on the African American community. The author discusses the background, best treatment intervention, and ethical considerations associated with prescription opioids and their use within the African American population.
Kana Enomoto, Acting Administrator, Substance Abuse and Mental Health Services Administration, keynote presentation at the National Rx Drug Abuse & Heroin Summit March 29, 2016
Dr. Tom Frieden, Director of the Centers for Disease Control and Prevention, keynote presentation at the National Rx Drug Abuse & Heroin Summit on March 30, 2016.
This critical analysis explores the impact of substance abuse in America at both a global and local level. Topics of societal stigma, personal bias and drug decriminalization are among the topics explored.
A study published in the American Journal of Preventive Medicine today finds that more than 2 million Americans who misused opioids between 2012 and 2014 also identified as binge drinkers. Overall, binge drinkers had nearly twice the odds of misusing opioids compared to non-drinkers.
The finding alarmed researchers, who noted that one in five prescription opioid deaths in recent years also involved alcohol. "Combining alcohol and opioids can significantly increase the risk of overdoses and deaths," CDC Director Robert Redfield said in a statement.
Dr. Andrew Kolodny: "Reporting on America’s Opioid Drug Crisis" 4.11.17reportingonhealth
Dr. Andrew Kolodny's slides from the Center for Health Journalism webinar, "Reporting on America’s Opioid Drug Crisis," 4.11.17
More info: http://www.centerforhealthjournalism.org/content/after-obamacare-future-us-health-care
Dr. Tom Frieden, Director of the Centers for Disease Control and Prevention, keynote presentation at the National Rx Drug Abuse & Heroin Summit on March 30, 2016.
This critical analysis explores the impact of substance abuse in America at both a global and local level. Topics of societal stigma, personal bias and drug decriminalization are among the topics explored.
A study published in the American Journal of Preventive Medicine today finds that more than 2 million Americans who misused opioids between 2012 and 2014 also identified as binge drinkers. Overall, binge drinkers had nearly twice the odds of misusing opioids compared to non-drinkers.
The finding alarmed researchers, who noted that one in five prescription opioid deaths in recent years also involved alcohol. "Combining alcohol and opioids can significantly increase the risk of overdoses and deaths," CDC Director Robert Redfield said in a statement.
Dr. Andrew Kolodny: "Reporting on America’s Opioid Drug Crisis" 4.11.17reportingonhealth
Dr. Andrew Kolodny's slides from the Center for Health Journalism webinar, "Reporting on America’s Opioid Drug Crisis," 4.11.17
More info: http://www.centerforhealthjournalism.org/content/after-obamacare-future-us-health-care
Lisa Girion: "Reporting on America’s Opioid Drug Crisis" 4.11.17reportingonhealth
Lisa Girion's slides from the Center for Health Journalism webinar, "Reporting on America’s Opioid Drug Crisis," 4.11.17
More info: https://www.centerforhealthjournalism.org/content/reporting-americas-opioid-drug-crisis
Jill Blumenthal MD of UC San Diego presents "Free to Be You and Me: Providing Culturally-Sensitive Patient Care to Transgender Individuals" at AIDS Clinical Rounds
The purpose of the Idaho’s Response to the Opioid Crisis (IROC) sub-grant is to promote the national best practice of connecting individuals seeking recovery from addiction with Recovery Coaches who assist them during the beginning stages of recovery and throughout their journey.
#IROC #HopeandRecovery #RecoveryIdaho
Knee anatomy and clinical tests 2024.pdfvimalpl1234
This includes all relevant anatomy and clinical tests compiled from standard textbooks, Campbell,netter etc..It is comprehensive and best suited for orthopaedicians and orthopaedic residents.
ABDOMINAL TRAUMA in pediatrics part one.drhasanrajab
Abdominal trauma in pediatrics refers to injuries or damage to the abdominal organs in children. It can occur due to various causes such as falls, motor vehicle accidents, sports-related injuries, and physical abuse. Children are more vulnerable to abdominal trauma due to their unique anatomical and physiological characteristics. Signs and symptoms include abdominal pain, tenderness, distension, vomiting, and signs of shock. Diagnosis involves physical examination, imaging studies, and laboratory tests. Management depends on the severity and may involve conservative treatment or surgical intervention. Prevention is crucial in reducing the incidence of abdominal trauma in children.
Muktapishti is a traditional Ayurvedic preparation made from Shoditha Mukta (Purified Pearl), is believed to help regulate thyroid function and reduce symptoms of hyperthyroidism due to its cooling and balancing properties. Clinical evidence on its efficacy remains limited, necessitating further research to validate its therapeutic benefits.
share - Lions, tigers, AI and health misinformation, oh my!.pptxTina Purnat
• Pitfalls and pivots needed to use AI effectively in public health
• Evidence-based strategies to address health misinformation effectively
• Building trust with communities online and offline
• Equipping health professionals to address questions, concerns and health misinformation
• Assessing risk and mitigating harm from adverse health narratives in communities, health workforce and health system
- Video recording of this lecture in English language: https://youtu.be/kqbnxVAZs-0
- Video recording of this lecture in Arabic language: https://youtu.be/SINlygW1Mpc
- Link to download the book free: https://nephrotube.blogspot.com/p/nephrotube-nephrology-books.html
- Link to NephroTube website: www.NephroTube.com
- Link to NephroTube social media accounts: https://nephrotube.blogspot.com/p/join-nephrotube-on-social-media.html
micro teaching on communication m.sc nursing.pdfAnurag Sharma
Microteaching is a unique model of practice teaching. It is a viable instrument for the. desired change in the teaching behavior or the behavior potential which, in specified types of real. classroom situations, tends to facilitate the achievement of specified types of objectives.
DISSERTATION on NEW DRUG DISCOVERY AND DEVELOPMENT STAGES OF DRUG DISCOVERYNEHA GUPTA
The process of drug discovery and development is a complex and multi-step endeavor aimed at bringing new pharmaceutical drugs to market. It begins with identifying and validating a biological target, such as a protein, gene, or RNA, that is associated with a disease. This step involves understanding the target's role in the disease and confirming that modulating it can have therapeutic effects. The next stage, hit identification, employs high-throughput screening (HTS) and other methods to find compounds that interact with the target. Computational techniques may also be used to identify potential hits from large compound libraries.
Following hit identification, the hits are optimized to improve their efficacy, selectivity, and pharmacokinetic properties, resulting in lead compounds. These leads undergo further refinement to enhance their potency, reduce toxicity, and improve drug-like characteristics, creating drug candidates suitable for preclinical testing. In the preclinical development phase, drug candidates are tested in vitro (in cell cultures) and in vivo (in animal models) to evaluate their safety, efficacy, pharmacokinetics, and pharmacodynamics. Toxicology studies are conducted to assess potential risks.
Before clinical trials can begin, an Investigational New Drug (IND) application must be submitted to regulatory authorities. This application includes data from preclinical studies and plans for clinical trials. Clinical development involves human trials in three phases: Phase I tests the drug's safety and dosage in a small group of healthy volunteers, Phase II assesses the drug's efficacy and side effects in a larger group of patients with the target disease, and Phase III confirms the drug's efficacy and monitors adverse reactions in a large population, often compared to existing treatments.
After successful clinical trials, a New Drug Application (NDA) is submitted to regulatory authorities for approval, including all data from preclinical and clinical studies, as well as proposed labeling and manufacturing information. Regulatory authorities then review the NDA to ensure the drug is safe, effective, and of high quality, potentially requiring additional studies. Finally, after a drug is approved and marketed, it undergoes post-marketing surveillance, which includes continuous monitoring for long-term safety and effectiveness, pharmacovigilance, and reporting of any adverse effects.
These lecture slides, by Dr Sidra Arshad, offer a quick overview of the physiological basis of a normal electrocardiogram.
Learning objectives:
1. Define an electrocardiogram (ECG) and electrocardiography
2. Describe how dipoles generated by the heart produce the waveforms of the ECG
3. Describe the components of a normal electrocardiogram of a typical bipolar lead (limb II)
4. Differentiate between intervals and segments
5. Enlist some common indications for obtaining an ECG
6. Describe the flow of current around the heart during the cardiac cycle
7. Discuss the placement and polarity of the leads of electrocardiograph
8. Describe the normal electrocardiograms recorded from the limb leads and explain the physiological basis of the different records that are obtained
9. Define mean electrical vector (axis) of the heart and give the normal range
10. Define the mean QRS vector
11. Describe the axes of leads (hexagonal reference system)
12. Comprehend the vectorial analysis of the normal ECG
13. Determine the mean electrical axis of the ventricular QRS and appreciate the mean axis deviation
14. Explain the concepts of current of injury, J point, and their significance
Study Resources:
1. Chapter 11, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 9, Human Physiology - From Cells to Systems, Lauralee Sherwood, 9th edition
3. Chapter 29, Ganong’s Review of Medical Physiology, 26th edition
4. Electrocardiogram, StatPearls - https://www.ncbi.nlm.nih.gov/books/NBK549803/
5. ECG in Medical Practice by ABM Abdullah, 4th edition
6. Chapter 3, Cardiology Explained, https://www.ncbi.nlm.nih.gov/books/NBK2214/
7. ECG Basics, http://www.nataliescasebook.com/tag/e-c-g-basics
Title: Sense of Smell
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the primary categories of smells and the concept of odor blindness.
Explain the structure and location of the olfactory membrane and mucosa, including the types and roles of cells involved in olfaction.
Describe the pathway and mechanisms of olfactory signal transmission from the olfactory receptors to the brain.
Illustrate the biochemical cascade triggered by odorant binding to olfactory receptors, including the role of G-proteins and second messengers in generating an action potential.
Identify different types of olfactory disorders such as anosmia, hyposmia, hyperosmia, and dysosmia, including their potential causes.
Key Topics:
Olfactory Genes:
3% of the human genome accounts for olfactory genes.
400 genes for odorant receptors.
Olfactory Membrane:
Located in the superior part of the nasal cavity.
Medially: Folds downward along the superior septum.
Laterally: Folds over the superior turbinate and upper surface of the middle turbinate.
Total surface area: 5-10 square centimeters.
Olfactory Mucosa:
Olfactory Cells: Bipolar nerve cells derived from the CNS (100 million), with 4-25 olfactory cilia per cell.
Sustentacular Cells: Produce mucus and maintain ionic and molecular environment.
Basal Cells: Replace worn-out olfactory cells with an average lifespan of 1-2 months.
Bowman’s Gland: Secretes mucus.
Stimulation of Olfactory Cells:
Odorant dissolves in mucus and attaches to receptors on olfactory cilia.
Involves a cascade effect through G-proteins and second messengers, leading to depolarization and action potential generation in the olfactory nerve.
Quality of a Good Odorant:
Small (3-20 Carbon atoms), volatile, water-soluble, and lipid-soluble.
Facilitated by odorant-binding proteins in mucus.
Membrane Potential and Action Potential:
Resting membrane potential: -55mV.
Action potential frequency in the olfactory nerve increases with odorant strength.
Adaptation Towards the Sense of Smell:
Rapid adaptation within the first second, with further slow adaptation.
Psychological adaptation greater than receptor adaptation, involving feedback inhibition from the central nervous system.
Primary Sensations of Smell:
Camphoraceous, Musky, Floral, Pepperminty, Ethereal, Pungent, Putrid.
Odor Detection Threshold:
Examples: Hydrogen sulfide (0.0005 ppm), Methyl-mercaptan (0.002 ppm).
Some toxic substances are odorless at lethal concentrations.
Characteristics of Smell:
Odor blindness for single substances due to lack of appropriate receptor protein.
Behavioral and emotional influences of smell.
Transmission of Olfactory Signals:
From olfactory cells to glomeruli in the olfactory bulb, involving lateral inhibition.
Primitive, less old, and new olfactory systems with different path
Ozempic: Preoperative Management of Patients on GLP-1 Receptor Agonists Saeid Safari
Preoperative Management of Patients on GLP-1 Receptor Agonists like Ozempic and Semiglutide
ASA GUIDELINE
NYSORA Guideline
2 Case Reports of Gastric Ultrasound
NVBDCP.pptx Nation vector borne disease control programSapna Thakur
NVBDCP was launched in 2003-2004 . Vector-Borne Disease: Disease that results from an infection transmitted to humans and other animals by blood-feeding arthropods, such as mosquitoes, ticks, and fleas. Examples of vector-borne diseases include Dengue fever, West Nile Virus, Lyme disease, and malaria.
Integrating Ayurveda into Parkinson’s Management: A Holistic ApproachAyurveda ForAll
Explore the benefits of combining Ayurveda with conventional Parkinson's treatments. Learn how a holistic approach can manage symptoms, enhance well-being, and balance body energies. Discover the steps to safely integrate Ayurvedic practices into your Parkinson’s care plan, including expert guidance on diet, herbal remedies, and lifestyle modifications.
Integrating Ayurveda into Parkinson’s Management: A Holistic Approach
National Drug Early Warning (NDEWS) webinar: A more dangerous heroin: Emerging patterns in the heroin overdose epidemic
1. Dan Ciccarone, MD, MPH
Professor, Family and Community Medicine
University of California, San Francisco
A MORE DANGEROUS “HEROIN”:
EMERGING PATTERNS IN THE
HEROIN OVERDOSE EPIDEMIC
2. OBJECTIVES
EPIDEMIOLOGY
• Describe demographic differences in prescription opioid- and
heroin-related overdose
• Describe regional differences in prescription opioid- and
heroin-related overdose
• Describe changes in heroin supply
• Evidence for contamination/adulteration
QUALITATIVE
• Relate stories of heroin adulteration:
• National
• Case study: Baltimore (preliminary)
3. HEROIN IN TRANSITION (“HIT”) STUDY
NIH: National Institute of Drug Abuse
• DA037820
• Multi-methodological study: quantitative and qualitative
aims
• New heroin source-forms and how they are perceived and
used
• Emerging patterns in consequences of use
• Heroin supply flows
4. HEROIN IN TRANSITION (“HIT”) STUDY
DATA ANALYZED:
• Nationwide Inpatient Survey (NIS)
• Stratified sample of approximately 20% of US community
hospitals representing 5 to 8 million hospital admissions
annually?
• States included in the NIS represent about 95% of the US
population
• All payer data (Medicaid, Medicare, Private Insurance and
uninsured)
• Years 1993 to 2013
• ICD-9 codes for opiate (not heroin) and heroin overdoses
• Jay Unick, U. of Maryland, lead
5. HEROIN IN TRANSITION (“HIT”) STUDY
QUALITATIVE:
• Rapid Assessment Project
• “Hot spot” study with ethnographic and qualitative
methodologies
• 3-4 cities per year
• Preliminary findings: Baltimore
• Sarah Mars, PhD, lead
SUPPLY:
• Data sources: DEA: STRIDE (FOIA), Heroin Signature
Program, Domestic Monitoring Program, NFLIS
7. Unfortunately:
• Heroin use and
consequences are up
• Rise is concurrent with the
later stages of the opioid
misuse epidemic
TRENDS IN HEROIN USE AND
CONSEQUENCES
9. ARE THESE THE SAME EPIDEMICS?
• Opioid ”push”:
• Intertwining of population at risk1
• Stories of initiation: “Every never…”2
• How does the heroin epidemic differ from the
earlier opioid misuse epidemic?
• Comparisons by age, ethnicity, gender and region
1UNICK, ET AL. INTERTWINED EPIDEMICS: NATIONAL DEMOGRAPHIC TRENDS IN
HOSPITALIZATIONS FOR HEROIN- AND OPIOID-RELATED OVERDOSES. PLOS ONE 2012
2MARS, ET AL. “EVERY ‘NEVER’ I EVER SAID CAME TRUE”: TRANSITIONS FROM OPIOID PILLS
TO HEROIN INJECTING. IJDP 2013
10. NIS: OVERDOSE RATES (1993-2012)
BY AGE GROUP:
HOD: 20-34 y.o. OPOD: 45-59 y.o.
13. NIS: OVERDOSE RATES (1993-2012)
BY ETHNICITY:
HOD: White and
African American
OPOD: White and Native
American
14. AGE AND GENDER DISPARITIES
Opioid at-
risk
Heroin at-risk
15. NIS: OVERDOSE RATES (1993-2012)
BY GEOGRAPHIC REGION:
HOD: Northeast and
Midwest!!
OPOD: Even – South
Good News: West
16. • Timing of opioid and heroin curves: +/-
• Key convergences by ethnicity
• Symmetrical converging curves in 20-34
yo age groups
• Surveys of recent heroin initiates report
prior opioid dependency
• Demographic differences can be
explained by risker sub-population
• Exception: Midwest
Summary:
Opioid “Push”
17.
18. Heroin patients in
treatment: first opiate
of abuse
• 75% of the 2000 cohort
of heroin tx pts started
with an prescription
opioid
Cicero TJ, Ellis MS; Surratt HL; Kurtz SP. The Changing Face of Heroin Use in the United States: A
Retrospective Analysis of the Past 50 Years. JAMA Psychiatry. Published online May 28, 2014.
19. Heroin “Pull”
• US heroin seizures
are up ~ 100%,
2009-14
Source: EPIC National Seizure System. Reported in the 2015 National Drug
Threat Assessment Summary; DOJ, DEA, 2015
21. Heroin Seizures,
Southwest Border:
2000-2013
• SW heroin seizures up
4-fold
Source: National Seizure System. Reported in the 2014 National Drug
Threat Assessment Summary; DOJ, DEA, 2014
24. HEROIN SOURCES OVER TIME
Source: Heroin Signature Program. Reported in the 2015 National Drug
Threat Assessment Summary; DOJ, DEA, 2015
25. HEROIN OF UNKNOWN SOURCE
Source: Domestic Monitoring Program. Reported in the 2015 National Drug Threat
Assessment Summary; DOJ, DEA, 2015
26. A MORE DANGEROUS “HEROIN”
• Fentanyl laced heroin
• Novel Mexican heroin?
• Other synthetic opioids
• Case study: Baltimore
27. FENTANYL LACED HEROIN
• Fentanyl laced heroin and heroin laced fentanyl and
just plain fentanyl (and fentanyl analogues):
• NFLIS (2015): Fentanyl reports increased by 300% from
the late 2013 to early 2014
• Clandestinely-produced fentanyl, not diverted
pharmaceutical fentanyl*
• 30-40x stronger than heroin by weight
• DEA and CDC 2015 warnings
• Sources: Mexico and China (fentanyl analogues)
• Analogous: Levamistole as adulterant for cocaine
*National Heroin Threat Assessment Summary, DEA, 2015
28. NFLIS: Fentanyl
• Testing seized drugs
• Highest rise in rates in
NE and MW
• Recent relative to
earlier rises in
heroin overdose
NATIONAL FORENSIC LABORATORY INFORMATION SYSTEM.
Special Report: Opiates and Related Drugs Reported in NFLIS, 2009–2014. Office
of Diversion Control, DOJ, DEA. 2015
29. MEXICAN-SOURCED HEROIN: CHANGES
• Mexican opium/heroin production has grown while Colombian production is
down 40%
• Explanations for rising HOD in Midwest (in addition to fentanyl):
• Strong suspicion of more purified product coming from Mexico
• Rise in heroin with unknown DEA “signature”
• Colombian mimic?
• DEA: Mexican white heroin
• Explanation for rising HOD in New England:
• Distribution innovations: Dispatch*
• A market is any place with lower competition (think Vermont)
• High purity heroin going to small cities: Gary, Madison, Memphis,
Minneapolis, Cleveland
* Sam Quinones: Dreamland: The true tale of America’s opiate epidemic (2015)
30. SYNTHETICS
• In addition to fentanyl there are reports of:
• Fentanyl analogues:
• Acetyl fentanyl
• Butyryl fentanyl
• Furanyl-fentanyl
• Parafluoro-fentanyl
• Novel synthetics:
• M-15, M-18
• U47700
• Others…
Sources: various. National Drug Early Warning System (NDEWS) listserve
alerts
32. BALTIMORE: HEROIN
• Estimated number of injection drug users: ~19,000
• Doubling of heroin overdose deaths 2010-2014
• Dramatic rise in fentanyl-related deaths late 2013 to
2014
Source: Drug and Alcohol-Related Intoxication Deaths in Maryland, 2014.
Maryland Department of Health and Mental Hygiene. May 2015
33. ETHNOGRAPHIC WORK
• Heroin scene:
• “Old school:” Open street dealing, branded heroin,
free samples(“tastes”!)
• Two types: “raw” and “scramble”
• Decayed infrastructure:
• City on the mend but…
• Abandoned buildings, deserted streets and
alleyways make convenient venues for drug
injection
35. BALTIMORE: “HEROIN” (FIELD WORK 11/15, 3/16)
• High quality:
“The best stuff I've ever used is the stuff I’m using now“
- 28 yo from Ohio, using heroin x 8 years
• Chemical feel/”taste”
Q: How does the heroin you are using now feel?
A: “Its kinda like [heroin]. It gets me well. But it is also tastes chemically”
- 60+ yo using over 30 years
• Fentanyl contamination: likely; other synthetics possible
• Sometimes sold as is; sometimes desired; however effect short-
lasting and users know this
• Some fear/concern; some old-timers are doing “tester shots” which
is unusual
37. BALTIMORE: “SCRAMBLE”
• Old term but a new form
• White powder heroin – unique
• Mixed locally;
• contains multiple powders; mixing problem!
• in contrast to “raw” heroin: not as powerful but better “rush”
• Highly variable:
• Wide range in price, volume
• Color changes: white to concrete grey, colored speckles or white
sparkles
• In solution: clear to ice-tea colored
• Effect: good rush, duration of effect 0.5 – 12 hours
• Unpredictable!
• Growing in popularity and market share
40. • The novel entry of
Colombian-sourced
heroin increased HOD
rates; 1993-1999
• New increases:
• New forms of Mexican-
sourced heroin?
• Fentanyl(+) adulteration
• Wider distribution models
• Intertwined with opioid pill
epidemic
FINAL THOUGHTS: HEROIN IN
EVOLUTION
41. FINAL THOUGHTS: MULTIPLE PATHWAYS
• Opioid to heroin transitions:
• High dependency
• Opioid restrictions?
• Heroin as initial drug of choice:
• New England, Mid-Atlantic and Midwest: New market
strategies; expanded supply;
• New products that we don’t understand
• Fentanyl but it cant explain everything as it hits later
than the rises seen in heroin OD
• Testing bias?
43. FINAL THOUGHTS: CHALLENGES
• Better surveillance:
• Public health forensics: “contaminated lettuce”
• Heroin and fentanyl products
• Synthetics are the new reality eg NPS, cannabinoids
• Use patterns and consequences
• Harm reduction responses:
• Naloxone: 2 decades of community peer use
• Technological and policy innovations
• Expanding MAT:
• Only 3% of DEA registered physicians are buprenorphine
prescribers
44. FINAL THOUGHTS: CHALLENGES
• Supervised injection facilities:
• Growing intervention worldwide
• Best evidence from “Insite” in Vancouver:
• Decreased: OD, hospitalizations, infections
• Increased: uptake of medical and substance treatment
• Stem out of crises – like the one we have now
• Challenges:
• Wrap-around services
• Canada and Europe not like US:
• Stigma may bedevil
• Persons at risk may not use, communities may not allow; culture
at large may not be ready
• Legal and political issues
47. ACKNOWLEDGEMENTS
Heroin in Transition study:
Jay Unick, PhD, University of Maryland
Sarah Mars, PhD, UCSF
Jeff Ondoscin
NIH/NIDA funding: R01DA037820
Jon E. Zibbell, PhD, CDC
Baltimore City Health Dept.
Mishka Terplan
Derrick Hunt, Jeffrey Long and NEP staff
NDEWS: Erin, Kathy and Marwa. - Eric Wish
Maryland Department of Health and Mental Hygiene
Michael Baier
Philippe Bourgois, PhD
Drug Enforcement Administration
Photo credits: Fernando Castillo,
Dan Ciccarone