Skip to main content
Cell Transplantation logoLink to Cell Transplantation
. 2019 Sep 24;28(12):1465–1471. doi: 10.1177/0963689719878380

Substance Use Disorder, Intravenous Injection, and HIV Infection: A Review

Shao-Cheng Wang 1,2,, Brion Maher 2
PMCID: PMC6923556  PMID: 31547679

Abstract

DSM-V-defined substance use disorder comprises four groups of symptoms: impaired control, social impairment, risky use, and pharmacological reactions. Behavioral patterns of impaired control, including impulsivity and risk taking, are associated with HIV risk behaviors. Substance users with stronger craving symptoms are more likely to use drugs via intravenous injection than other routes because of the faster drug effect and the higher bioavailability; thus, they are at high risk of HIV infection. HIV risk behaviors such as unprotected sex and intravenous injection facilitate HIV disease spread. Public health policies such as Needle and Syringe Exchange Programs and medication-assisted treatment are proven to reduce HIV risk behaviors such as the frequency of intravenous injection and even the incidence of HIV infection, but both of them have limitations. While intravenous injection is a frequently discussed issue in public policies and the HIV-related literature, it is a much less frequent topic in the addiction literature. We believed that understanding the mental substrate behind impulsivity/risk taking and the possible biological mechanism of intravenous injection may help in creating more effective strategies to slow down HIV infection.

Keywords: substance use disorder, HIV risk behavior, intravenous drug injection

Introduction

Substance use disorder is a complex phenotype, and is the result of a series of causal influences such as genetic factors, diverse environmental factors, and predicted drug-induced effects14. Several behavior patterns such as impulsivity, risk taking, and stress response resulting from specific personality and physiological traits are considered to contribute to the vulnerability or liability to addictive disease, partially accounting for the influence of genetic variation, indexed as heritability, on addiction. Moreover, different personality and physiological traits may affect different stages of addiction, chronologically defined as initiation of drug use, continued regular drug use, and subsequent abuse/dependence and relapse5.

Substance use disorder is complicated in its symptoms and signs, which involve several domains such as cognition, behavior, and physiology. Persistent substance use changes brain reward circuits and causes specific behavior patterns such as craving. According to DSM-V, the criteria of substance use disorder can be grouped into four groups: impaired control, risky use, biological reactions, and social impairment caused by substances. Impaired control includes taking larger amounts than originally intended, multiple unsuccessful efforts to decrease or discontinue use, spending a great deal of time on substance use, and craving. Using substances in a physically hazardous situation and/or using substances despite the knowledge of its physical or psychological consequences belong to the risky use category. The development of substance tolerance and withdrawal comprise the biological reactions6.

DSM-V defines symptoms such as tolerance, withdrawal, and uncontrolled increasing intake as the basic elements of substance use disorders, and these symptoms are associated with intravenous drug use. As a result of tolerance development, the longer these symptoms persist, the greater the amount of drug the user needs to consume to have the same effect. Among the most frequent (and tolerant) drug users, injection is more common, because injection causes an immediate and strong drug effect, leading to frequent reuse of contaminated needles and needle sharing. DSM-V also defines impaired control and risky use as the other two basic elements of substance use disorders, which are also associated with intravenous drug use. When severe substance abusers exhibit strong craving and impaired self-control, there is a desire to experience the drug effect immediately, ignoring the hazard of blood-borne diseases, such as HIV, hepatitis B, and hepatitis C. Impulsivity is an internal mental urge and impaired self-control is associated with poor judgment. Impulsivity and impaired self-control are the tendency to act without forethought, leading to increased external risky behaviors such as unsafe intravenous drug use. In brief, several symptoms of substance use disorders such as the increasing drug use with tolerance and impulsivity/poor self-control are obviously associated with intravenous drug use. Though intravenous drug use is highly associated with severe forms of substance use disorder and persons who inject drugs (PWID) are at high risk of blood-borne disease such as HIV/AIDS and hepatitis, the biological, psychological, and molecular mechanisms underlying the liability to intravenous drug use are less frequently discussed. In this article, we reviewed the literature related to the symptoms of substance use disorder, the mechanisms of intravenous drug use, and the public approaches to HIV/AIDS infection prevention. We hope this review may provide insight into all possible avenues that can be explored in current and future public health approaches to reducing the spread of HIV infection by reducing injection rates.

Symptoms and Signs of Substance Use Disorder: DSM-IV and DSM-V Diagnosis

According to DSM-IV, the criteria of substance use disorder include tolerance, withdrawal, uncontrolled increasing intake, spending more time and money on substances, and impaired social, occupational, or recreational function, and use that continues in spite of knowledge of the impact of substance on physical and psychological health7. In 2013, DSM-V was published and revealed the criteria change of substance-related disorders. DSM-V removed the criterion of recurrent substance use resulting in legal problems and added the criterion of craving to use substance, and kept all other criteria from DSM-IV. Furthermore, the criteria of DSM-V substance use disorder can be used to specify current severity, with mild, moderate, and severe6.

This change between DSM-IV and DSM-V in substance-related disorders means the movement from a categorical view to dimensional approach. A categorical view is used by clinicians to meet the needs of reporting for health care planners; on the other hand, a dimensional approach conceptualizes a quantitative disorder that is more useful for the purpose of research8.

Intravenous Injection

Injection and Other Routes of Drug Administration

Several routes of drug administration are commonly used by substance abusers: oral, sniffing or intranasal using, and injection. Injection is the act of putting a drug into a person’s body using a needle and a syringe, delivering drugs by parenteral administration, including subcutaneous, intramuscular, intraperitoneal, intracardiac, intraarticular, and intravenous injection. Injection can cause several side effects, including high fever, pain over the injection site, swelling or hardness under the injection site, and anaphylaxis. In addition, injection can cause skin and soft tissue infections (SSTIs) such as abscesses and cellulitis; PWID are at high risk of SSTIs, especially those with high injecting frequency9. Compared with the other administration routes, intravenous injection results in the fastest drug effect because the drug reaches the brain through the circulatory system almost immediately. Bioavailability is the fraction of an administered dose of unchanged drug reaching the systemic circulation, and the bioavailability of intravenous administration was defined as 100%; the bioavailability of other administration routes such as oral, sniffing or intranasal use, subcutaneous, intramuscular, intraperitoneal, intracardiac, and intraarticular injection generally decreases due to incomplete absorption and/or first-pass metabolism10. In brief, compared with other drug administration routes, substances have the strongest and fastest effect via intravenous injection.

Intravenous injection and needle sharing are a consequence of severe forms of drug addiction. For example, it is common for PWID to inject heroin multiple times per day, thereby reusing or sharing needles due to limited resources. Because of the fast drug effect on the brain, the highest bioavailability, and cost, intravenous injection and sharing of needles are more among the PWID with the most severe craving symptoms. With more severe craving symptoms, substance abusers are at higher risk of risky behaviors and are more likely to use drugs impulsively, regardless of the hazard of blood-borne diseases6.

Impact of Injection and Drug Addiction

Injection behavior is very common among severe substance abusers. Drug addiction is associated with several psychiatric conditions including psychosis, mood disorders, depression, suicide, violence, and aggression; consequently, many PWID suffer from multiple morbidities and lose family support and occupational functioning. As a result, drug addiction causes serious social problems, with a substantial human and financial cost. In 2009, worldwide, an estimate showed that 271 million people have used at least one illicit drug, 39 million opioid, amphetamine, or cocaine users, and 21 million people who inject drugs11. This estimate excluded several kinds of illicit drug—3,4-methylenedioxy-N-methylamphetamine (MDMA or ecstasy), hallucinogens, and inhalants—so the true numbers of illicit drug users may be higher. Opioid overdose and opioid dependence are potentially lethal; injection of opioids, cocaine, or amphetamine is a substantial risk factor for transmission of HIV, hepatitis C, and hepatitis B12. According to the results from the National Epidemiologic Survey on Alcohol and Related Condition (NESARC) in 2004, the 12-month prevalence in the United States of substance use disorder and any drug use disorders were 9.35% and 2.00%, respectively. The prevalence of opioid use disorder, amphetamine use disorder and cocaine use disorder were 0.35, 0.16, and 0.27, respectively13. Based on the result of the Monitoring the Future study, the number of injecting heroin users has fluctuated in recent years, with the annual prevalence rising from 0.3% in 2009 to 0.7% in 2010, and then went back to 0.5% or less in 201514,15. In Western countries, almost 3.5% of gross domestic product was consumed by both alcohol abuse and drug addictions16. In 2007, in the United States, $55.7 billion (USD in 2009) were lost due to prescription opioid abuse. Workplace, health care, and criminal justice costs accounted for $25.6 billion, $25.0 billion, and $5.1 billion, respectively.

Over the past decades, the high prevalence of HIV/AIDS among substance abusers drew the attention of many infectious disease physicians and epidemiologists, so several evidence-based approaches have been developed to reduce the frequency of risky injection behavior among those substance abusers who are at high risk of HIV infection. In the next paragraph, we review the previous studies which link HIV infection and PWID, and the related approaches to reduce the frequency of injection behavior.

Impact of HIV

AIDS was first reported within a small group of homosexual men with opportunistic infections and Kaposi’s sarcoma17,18. Two years later, HIV was identified as the cause of AIDS. The transmission pathway was identified as spreading through certain body fluids such as blood, semen, vaginal secretions, and breast milk. Several preventive measures were implemented such as risk reduction programs, condom distribution, and needle exchange programs. Since the last decade, the number of HIV infections has increased rapidly, and the public’s concern has been aroused. According to a UNAIDS estimate, in 2011, 34.2 million persons were infected by HIV, as compared with 29.1 million in 2001, and 2.5 million persons were newly infected and 1.7 million persons died19. In 2015, the number of people living with HIV/AIDS reached 38.8 million20. The infection trend decreased from 1990 but then steadily increased from 2002 to 2015. Based on the CDC fact sheet, in the United States there are 1.2 million people with HIV infection and 20% of them are unaware of their infection21. Currently, highly active antiretroviral therapy (HAART), which combines at least three drugs from two classes of antiretroviral agents, is used to treat HIV22. However, this virus is highly mutable so drug resistance may develop. Prevention is a good alternative to reduce HIV transmission.

Ten years after HIV was first described, three main transmission routes were identified: blood-to-blood, sexual, and perinatal. Transmission by blood included transfusion of blood and blood products, needle sharing among intravenous drug users, and injection with unsterilized needles. Though sexual transmission plays an important role in PWID, in this article, we focus on needle sharing and unsterilized needles among PWID23. A host of behavioral risk patterns, now defined as HIV risk behaviors, are observed in those at highest risk of HIV infection, including injection drug use and sexual behaviors including multiple partners, sex trade, and sex without using condom24,25. Injection drug use, which is becoming increasingly associated with severe substance dependence, is also a well-known transmission pathway for HIV infection2628. Rosenberg et al. showed that substance use disorder and sexual orientation is directly associated with HIV risk behaviors such as needle sharing and intravenous injection29.

Psychosocial Interventions and Public Policies Related to Drug Injection Behavior and HIV Infection

Psychosocial Interventions and Public Policies

Dutra et al. reviewed psychosocial interventions for substance use disorders and concluded that psychosocial interventions have low-moderate to high-moderate treatment effect for illicit drugs30. Carroll and Onken reviewed the literature and found support for behavioral and pharmacological treatment effects on drug abuse, and that combinations of behavioral and pharmacological treatments have better potency than either one alone31. Two randomized clinical trials found that the Holistic Harm Reduction Program with behavioral therapy reduced HIV risk behaviors and improved adherence to medical treatment among intravenous drug users32,33.

A systematic review by Mathers et al. finds PWID have increased in several countries over the last decade and are reported with a high prevalence of HIV34. The high HIV incidence among PWID in many developing countries can be controlled by key harm reduction and treatment interventions such as needle and syringe programs, medication-assisted therapy (MAT), HIV counseling and testing, and antiretroviral therapy35. In addition, opioid substitution is being used to reduce the prevalence of HIV infection, thereby causing modest reduction in HIV transmission rates36.

Needle and Syringe Exchange Program (NSEP)

NSEP is a public health innovation which provides clean needles and syringes to reduce the time that contaminated needles are in circulation. NSEP also offers legal, social and health counseling, sex education, and referrals to medical services as part of comprehensive approaches37,38. While the range of NSEP practices varies broadly by country, needles and syringes are available for free from vending machines and pharmacies in some countries in Europe and Australia39. The theory behind NSEP is that the less time the contaminated needles and syringes are in use; the less likely they are to be used by uninfected drug users. There is strong evidence that NSEP reduces the frequency of injection behavior with contaminated devices. Separate reviews by Drucker et al. and Palmateer et al. showed a positive association between NSEP and the reduction of injection risk behavior39,40. The relationship between NSEP and the incidence of HIV is controversial. Two reviews support the idea that NSEP reduces HIV41,42; however, a review by Degenhardt et al. also claimed that NSEP is negatively associated with HIV36. MacArthur et al. found that NSEP can reduce the injection risk behavior, but the effectiveness in preventing blood-borne disease is insufficient43. A review by Sawangjit et al. also showed that pharmacy-based NSEPs are effective for injection risk behaviors, although the effectiveness on blood-borne disease is still unclear44. Noroozi et al. conducted a multilevel analysis in Iran and found that NSEPs might reduce HIV risk behavior, as well as injection-related risk behaviors, among PWID45,46. Fernandes et al. conducted a systematic review and found that NSEP was effective in reducing HIV and injection risk behaviors among PWID43.

Medication-Assisted Therapy

Heroin, cocaine, and amphetamine are the three most commonly injected drugs, but only heroin agonist pharmacotherapy is available for treating heroin addiction. Hence, this review only focuses on heroin agonist pharmacotherapy, also called substitution or maintenance pharmacotherapy. The best-known heroin substitution treatment, methadone maintenance therapy, is the standard protocol for treating heroin addiction47. Methadone is a long-acting synthetic opiate agonist. It is initially administered in low doses to prevent respiratory depression and the dose is gradually raised to a maximum and maintain at that level in order to minimize withdrawal symptoms. Methadone doses at a high level can block the superimposed effects of heroin, so the PWID does not experience euphoria when they inject heroin under this treatment48,49. In addition, methadone can be taken orally, thus reducing cues associated with injection behaviors in PWID50. Methadone maintenance treatment has proven effective in reducing heroin use after 24 months of treatment, and the longer patients remain in the treatment program the better the results51. Remaining in a treatment program longer can bring about a range of positive outcomes, for example, improved family relationships, more stable employment, and fewer legal problems40. The Three Cities Study by Ball and Ross and The Treatment Outcome Evaluation Study (TOPS) both showed a reduction in injection behaviors among the PWID with methadone treatment52,53. There is strong evidence that methadone maintenance treatment decreases HIV seroconversion rates among PWID because fewer people engage in HIV risk behaviors such as drug injection and/or needle sharing40. Dutta et al. found consistently lower rates of AIDS among PWID in methadone treatment programs. HIV seroconversion is associated with the length of time in methadone maintenance treatment35. In addition to methadone, buprenorphine and naltrexone are currently two other medications for opioid addiction54. Buprenorphine is a partial agonist for the μ opioid receptor; thus, buprenorphine has a ceiling effect when it binds to and activates the μ opioid receptor, providing less euphoric feelings, as well as respiratory depression, making it a safer alternative to methadone55. Long-acting injectable naltrexone can block opioid receptors and decrease the feeling of craving, as well as the risk of overdose56. Naltrexone implants also had a lower mortality rate than buprenorphine57, and a randomized clinical trial supported that long-acting injectable naltrexone was as safe and effective as buprenorphine with naloxone58.

Discussion

The Possible Mechanism behind Intravenous Drug Use

Intravenous injection is strongly associated with HIV infection. PWID become infected with HIV when they share needles with other infected PWID; consequently, they become HIV carriers and transmitters through HIV risk behaviors such as needle sharing and having unprotected sex. This global spread of HIV infection ultimately results in dramatic loss of health and financial productivity. Intravenous injection is very common among PWID with severe craving symptoms as it has the fastest drug effect on brain and the highest bioavailability. Thus, PWID with more severe craving symptoms are more likely to use intravenous injection, regardless of the legal problems and the hazard of blood-borne diseases; in other words, they are more likely to take risks and are more impulsive, which are also associated with other HIV risk behaviors.

As mentioned above, intravenous injection can cause local pain, swelling, or hardness over injection sites, and possible anaphylaxis. Intravenous injection, with the fastest drug effect on brain and the highest bioavailability, can relieve craving symptoms. While intravenous injection is a frequently discussed risk factor in the HIV-related literature, it is a much less frequent topic in the addiction literature. In particular, the causal relationship between impulsivity/risk taking and intravenous injection is still unclear, as is the biological mechanism behind the liability to intravenous injection.

The Alternative Approach to Reduce HIV/AIDS Distribution

In the past decade, NSEP and MAT have succeeded in reducing the rate of HIV infection; meanwhile, there is strong evidence that HAART is effective in reducing HIV transmission rates and prolonging life59. However, as there is no proven cure for HIV, the best way to reduce infection rates is to prevent its spread. More effectively identifying those at a high risk of HIV infection is the key. NSEP is a widely used public health innovation which is significantly reducing contaminated needle distribution, but the relationship between NSEP and the incidence of HIV is controversial. Only heroin agonist pharmacotherapy is available for treating heroin addiction in MAT, despite other substance such as cocaine and amphetamine being injectable.

While intravenous injection is a frequently discussed target in the public policies, it is a much less frequent topic in the addiction literature. We believed that understanding the mental malfunction behind impulsivity/risk taking and the possible biological mechanism of intravenous injection will provide new information about more effective preventives. Several key findings are suggested. First, PWID use drugs intravenously because their effects kick in immediately; however, intravenous drug users and those who share needles are at risk of blood-borne diseases. This suggests that PWID will more likely take risks when they become severe substance abusers with stronger craving, needing more drugs to reach the same effect and having impaired self-control. Second, individual personal traits such as impulsivity/risk taking are symptoms of severe substance use disorder. This review supports that impulsivity/risk taking are associated with HIV risk behavior, especially using intravenous drugs and sharing needles. Finally, there is evidence that substance use disorders are associated with HIV risk behaviors directly and indirectly through impulsivity/risk taking, and psychosocial interventions are beneficial to substance abusers. In two small randomized controlled trials, psychosocial interventions also had an effect on reducing the frequency of HIV risk behaviors such as intravenous injection. NSEP and the MAT both showed a reduction in HIV risk behaviors, but they have their own limitations. In this review, we suggest that interventions to reduce the severity of substance use disorder and the frequency of intravenous injection could be beneficial to reducing HIV infection. However, more research is needed to illuminate the biological mechanisms behind intravenous injection and the casual relationship between drug addiction and intravenous injection, so that we can provide more effective strategies for prevention.

Footnotes

Declaration of Conflicting Interests: The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Funding: The author(s) received no financial support for the research, authorship, and/or publication of this article.

ORCID iD: Shao-Cheng Wang Inline graphic https://orcid.org/0000-0002-7009-5338

References

  • 1. Kreek MJ, Nielsen DA, LaForge KS. Genes associated with addiction: alcoholism, opiate, and cocaine addiction. Neuromol Med. 2004;5(1):85–108. [DOI] [PubMed] [Google Scholar]
  • 2. Tsuang MT, Lyons MJ, Meyer JM, Doyle T, Eisen SA, Goldberg J, True W, Lin N, Toomey R, Eaves L. Co-occurrence of abuse of different drugs in men: the role of drug-specific and shared vulnerabilities. Arch Gen Psychiat. 1998;55(11):967–972. [DOI] [PubMed] [Google Scholar]
  • 3. Kendler KS, Jacobson KC, Prescott CA, Neale MC. Specificity of genetic and environmental risk factors for use and abuse/dependence of cannabis, cocaine, hallucinogens, sedatives, stimulants, and opiates in male twins. Am J Psychiat. 2003;160(4):687–695. [DOI] [PubMed] [Google Scholar]
  • 4. Pickens RW, Svikis DS, McGue M, Lykken DT, Heston LL, Clayton PJ. Heterogeneity in the inheritance of alcoholism. A study of male and female twins. Arch Gen Psychiat. 1991;48(1):19–28. [DOI] [PubMed] [Google Scholar]
  • 5. Kreek MJ, Nielsen DA, Butelman ER, LaForge KS. Genetic influences on impulsivity, risk taking, stress responsivity and vulnerability to drug abuse and addiction. Nat Neurosci. 2005;8(11):1450–1457. [DOI] [PubMed] [Google Scholar]
  • 6. American Psychiatric Association. Diagnostic and Statistical Manual of Mental Disorders, 5th ed (DSM-V). Virginia (US): American Psychiatric Association; 2013. [Google Scholar]
  • 7. American Psychiatric Association. Diagnostic and Statistical Manual, 4th edn, Text Revision (DSM-IV-TR). Virginia (US): American Psychiatric Association; 2000. [Google Scholar]
  • 8. Saunders JB, Schuckit MA, Sirovatka PJ, Regier DA. Diagnostic issues in substance use disorders: refining the research agenda for DSM-V Virginia (US): 2007. [Google Scholar]
  • 9. Moradi-Joo M, Ghiasvand H, Noroozi M, Armoon B, Noroozi A, Karimy M, Rostami A, Mirzaee MS, Hemmat M. Prevalence of skin and soft tissue infections and its related high-risk behaviors among people who inject drugs: a systematic review and meta-analysis. J Substance Use. 2019;24(4):350–360. [Google Scholar]
  • 10. Griffin JP, O’Grady J. The Textbook of Pharmaceutical Medicine. New York (US): Wiley Online Library; 2006. [Google Scholar]
  • 11. United Nations Office on Drugs and Crime. World drug report 2011. 2011. https://www.unodc.org/unodc/en/data-and-analysis/WDR-2011.html [accessed 2018 Feb 1].
  • 12. Degenhardt L, Hall W. Extent of illicit drug use and dependence, and their contribution to the global burden of disease. Lancet. 2012;379(9810):55–70. [DOI] [PubMed] [Google Scholar]
  • 13. Grant BF, Stinson FS, Dawson DA, Chou SP, Dufour MC, Compton W, Pickering RP, Kaplan K. Prevalence and co-occurrence of substance use disorders and independent mood and anxiety disorders: results from the national epidemiologic survey on alcohol and related conditions. Arch Gen Psychiat. 2004;61(8):807–816. [DOI] [PubMed] [Google Scholar]
  • 14. Johnston LD, O’Malley PM, Bachman JG, Schulenberg JE. Monitoring the Future National Survey Results on Drug use, 1975-2010. Institute for Social Research, The University of Michigan (US); 2011. [Google Scholar]
  • 15. Johnston LD, O’Malley PM, Bachman JG, Schulenberg JE, Miech RA. Monitoring the future national survey results on drug use, 1975-2015: Volume ii, college students and adults ages 19-55 United States; 2016. [Google Scholar]
  • 16. Pouletty P. Drug addictions: towards socially accepted and medically treatable diseases. Nat Rev Drug Discov. 2002;1(9):731–736. [DOI] [PubMed] [Google Scholar]
  • 17. Centers for Disease Control, Prevention. Pneumocystis pneumonia-Los Angeles. MMWR Morbid Mortal W. 1981;30:250–252. [PubMed] [Google Scholar]
  • 18. Friedman-Kien A, Laubenstein L, Marmor M, Hymes K, Green J, Ragaz A, Gottleib J, Muggia F, Demopoulos R, Weintraub M. Kaposi’s sarcoma and Pneumocystis pneumonia among homosexual men—New York City and California. MMWR Morbid Mortal W. 1981;30(25);305–308. [PubMed] [Google Scholar]
  • 19. WHO UNAIDS, Unicef. Global HIV/AIDS Response: Epidemic Update and Health Sector Progress Towards Universal Access. WHO UNAIDS, Geneva, Switzerland: Unicef; 2011. [Google Scholar]
  • 20. Wang H, Wolock TM, Carter A, Nguyen G, Kyu HH, Gakidou E, Hay SI, Mills EJ, Trickey A, Msemburi W. Estimates of global, regional, and national incidence, prevalence, and mortality of HIV, 1980–2015: the global burden of disease study 2015. The Lancet HIV. 2016;3(8):e361–e387. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21. Centers for Disease Control, Prevention. CDC fact sheet: HIV in the United States. 2011. http://www.Cdc.Gov/nchhstp/newsroom/docs/cdc-hiv+aids-in-america-081211-508c.Pdf [accessed 2018 Nov 2].
  • 22. Panel on Antiretroviral Guidelines for Adults and Adolescents. Guidelines for the use of Antiretroviral Agents in HIV-1-Infected Adults and Adolescents. California (US): Department of Health and Human Services; 2009. [Google Scholar]
  • 23. Sherman SG. The role of sexual transmission of HIV infection among injection and non-injection drug users. J Urban Health. 2003;80(3):iii7–iii14. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24. Carey MP, Carey KB, Kalichman SC. Risk for human immunodeficiency virus (HIV) infection among persons with severe mental illnesses. Clin Psychol Rev. 1997;17(3):271–291. [DOI] [PubMed] [Google Scholar]
  • 25. Patrick ME, O’Malley PM, Johnston LD, Terry-McElrath YM, Schulenberg JE. HIV/AIDS risk behaviors and substance use by young adults in the United States. Prev Sci. 2012;13(5):532–538. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26. Hou QF, Li SB. Potential association of drd2 and dat1 genetic variation with heroin dependence. Neurosci Lett. 2009;464(2):127–130. [DOI] [PubMed] [Google Scholar]
  • 27. Haerian BS, Haerian MS. Oprm1 rs1799971 polymorphism and opioid dependence: evidence from a meta-analysis. Pharmacogenomics. 2013;14(7):813–824. [DOI] [PubMed] [Google Scholar]
  • 28. Horwath E, Cournos F, McKinnon K, Guido JR, Herman R. Illicit-drug injection among psychiatric patients without a primary substance use disorder. Psychiatr Serv. 1996;47(2):181–185. [DOI] [PubMed] [Google Scholar]
  • 29. Rosenberg SD, Trumbetta SL, Mueser KT, Goodman LA, Osher FC, Vidaver RM, Metzger DS. Determinants of risk behavior for human immunodeficiency virus/acquired immunodeficiency syndrome in people with severe mental illness. Compr Psychiat. 2001;42(4):263–271. [DOI] [PubMed] [Google Scholar]
  • 30. Dutra L, Stathopoulou G, Basden SL, Leyro TM, Powers MB, Otto MW. A meta-analytic review of psychosocial interventions for substance use disorders. Am J Psychiat. 2008;165(2):179–187. [DOI] [PubMed] [Google Scholar]
  • 31. Carroll KM, Onken LS. Behavioral therapies for drug abuse. Am J Psychiat. 2005;162(8):1452–1460. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32. Margolin A, Avants SK, Warburton LA, Hawkins KA, Shi J. A randomized clinical trial of a manual-guided risk reduction intervention for HIV-positive injection drug users. Health Psychol. 2003;22(2):223. [PubMed] [Google Scholar]
  • 33. Avants SK, Margolin A, Usubiaga MH, Doebrick C. Targeting HIV-related outcomes with intravenous drug users maintained on methadone: a randomized clinical trial of a harm reduction group therapy. J Subst Abuse Treat. 2004;26(2):67–78. [DOI] [PubMed] [Google Scholar]
  • 34. Mathers BM, Degenhardt L, Phillips B, Wiessing L, Hickman M, Strathdee SA, Wodak A, Panda S, Tyndall M, Toufik A, Mattick RP. Global epidemiology of injecting drug use and HIV among people who inject drugs: a systematic review. Lancet. 2008;372(9651):1733–1745. [DOI] [PubMed] [Google Scholar]
  • 35. Dutta A, Wirtz AL, Baral S, Beyrer C, Cleghorn FR. Key harm reduction interventions and their impact on the reduction of risky behavior and HIV incidence among people who inject drugs in low-income and middle-income countries. Curr Opin HIV AIDS. 2012;7(4):362–368. [DOI] [PubMed] [Google Scholar]
  • 36. Degenhardt L, Mathers B, Vickerman P, Rhodes T, Latkin C, Hickman M. Prevention of HIV infection for people who inject drugs: why individual, structural, and combination approaches are needed. Lancet. 2010;376(9737):285–301. [DOI] [PubMed] [Google Scholar]
  • 37. Kaplan EH, Heimer R. A model-based estimate of HIV infectivity via needle sharing. J Acq Immun Def Synd. 1992;5(11):1116–1118. [PubMed] [Google Scholar]
  • 38. Kaplan EH. Needles that kill: modeling human immunodeficiency virus transmission via shared drug injection equipment in shooting galleries. Rev Infect Dis. 1989;11(2):289–298. [DOI] [PubMed] [Google Scholar]
  • 39. Palmateer N, Kimber J, Hickman M, Hutchinson S, Rhodes T, Goldberg D. Evidence for the effectiveness of sterile injecting equipment provision in preventing hepatitis c and human immunodeficiency virus transmission among injecting drug users: a review of reviews. Addiction. 2010;105(5):844–859. [DOI] [PubMed] [Google Scholar]
  • 40. Drucker E, Lurie P, Wodak A, Alcabes P. Measuring harm reduction: the effects of needle and syringe exchange programs and methadone maintenance on the ecology of HIV. AIDS. 1998;12(suppl A):S217–S230. [PubMed] [Google Scholar]
  • 41. Gibson DR, Flynn NM, Perales D. Effectiveness of syringe exchange programs in reducing HIV risk behavior and HIV seroconversion among injecting drug users. AIDS. 2001;15(11):1329–1341. [DOI] [PubMed] [Google Scholar]
  • 42. WHO. Effectiveness of Sterile Needle and Syringe Programming in Reducing HIV/AIDS Among Injecting Drug Users. Geneva, Switzerland: WHO; 2004. [Google Scholar]
  • 43. Fernandes RM, Cary M, Duarte G, Jesus G, Alarcão J, Torre C, Costa S, Costa J, Carneiro AV. Effectiveness of needle and syringe programmes in people who inject drugs–an overview of systematic reviews. BMC Public Health. 2017;17(1):309. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 44. Sawangjit R, Khan TM, Chaiyakunapruk N. Effectiveness of pharmacy-based needle/syringe exchange programme for people who inject drugs: a systematic review and meta-analysis. Addiction. 2017;112(2):236–247. [DOI] [PubMed] [Google Scholar]
  • 45. Noroozi M, Marshall BD, Noroozi A, Armoon B, Sharifi H, Farhoudian A, Ghiasvand H, Vameghi M, Rezaei O, Sayadnasiri M. Do needle and syringe programs reduce risky behaviours among people who inject drugs in Kermanshah City, Iran? A coarsened exact matching approach. Drug Alcohol Rev. 2018;37:S303–S308. [DOI] [PubMed] [Google Scholar]
  • 46. Noroozi M, Noroozi A, Sharifi H, Harouni GG, Marshall BD, Ghisvand H, Qorbani M, Armoon B. Needle and syringe programs and HIV-related risk behaviors among men who inject drugs: a multilevel analysis of two cities in Iran. Int J Behav Med. 2019;26(1):50–58. [DOI] [PubMed] [Google Scholar]
  • 47. Dole VP, Nyswander ME, Kreek MJ. Narcotic blockade. Arch Intern Med. 1966;118(4):304–309. [PubMed] [Google Scholar]
  • 48. Kreek MJ, LaForge KS, Butelman E. Pharmacotherapy of addictions. Nat Rev Drug Discov. 2002;1(9):710–726. [DOI] [PubMed] [Google Scholar]
  • 49. Wang S. Historical review: opiate addiction and opioid receptors. Cell Transplant. 2019;28(3):233–238. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 50. Dole VP, Nyswander ME. Methadone maintenance treatment. A ten-year perspective. JAMA. 1976;235(19):2117–2119. [PubMed] [Google Scholar]
  • 51. Gerstein DR, Lewin LS. Treating drug problems. New Engl J Med. 1990;323(12):844–848. [DOI] [PubMed] [Google Scholar]
  • 52. Hubbard RL, Rachal JV, Craddock SG, Cavanaugh ER. Treatment Outcome Prospective Study (TOPS): client characteristics and behaviors before, during, and after treatment. NIDA Res MG. 1984;51:42–68. [PubMed] [Google Scholar]
  • 53. Ball JC, Ross A. The Effectiveness of Methadone Maintenance Treatment: Patients, Programs, Services, and Outcome. New York (US): Springer-Verlag Publishing; 1991. [Google Scholar]
  • 54. Volkow ND, Frieden TR, Hyde PS, Cha SS. Medication-assisted therapies—tackling the opioid-overdose epidemic. N Engl J Med. 2014;370(22):2063–2066. [DOI] [PubMed] [Google Scholar]
  • 55. Kimber J, Larney S, Hickman M, Randall D, Degenhardt L. Mortality risk of opioid substitution therapy with methadone versus buprenorphine: a retrospective cohort study. Lancet Psychiatry. 2015;2(10):901–908. [DOI] [PubMed] [Google Scholar]
  • 56. Kelty E, Hulse G. Examination of mortality rates in a retrospective cohort of patients treated with oral or implant naltrexone for problematic opiate use. Addiction. 2012;107(10):1817–1824. [DOI] [PubMed] [Google Scholar]
  • 57. Reece AS. Favorable mortality profile of naltrexone implants for opiate addiction. J Addict Dis. 2010;29(1):30–50. [DOI] [PubMed] [Google Scholar]
  • 58. Lee JD, Nunes EV, Jr, Novo P, Bachrach K, Bailey GL, Bhatt S, Farkas S, Fishman M, Gauthier P, Hodgkins CC. Comparative effectiveness of extended-release naltrexone versus buprenorphine-naloxone for opioid relapse prevention (x: Bot): a multicentre, open-label, randomised controlled trial. Lancet. 2018;391(10118):309–318. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 59. Vereczkei A, Demetrovics Z, Szekely A, Sarkozy P, Antal P, Szilagyi A, Sasvari-Szekely M, Barta C. Multivariate analysis of dopaminergic gene variants as risk factors of heroin dependence. Plos One. 2013;8(6):e66592. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Cell Transplantation are provided here courtesy of SAGE Publications

RESOURCES