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. Author manuscript; available in PMC: 2020 Jun 10.
Published in final edited form as: Int J Drug Policy. 2018 Oct 31;61:44–51. doi: 10.1016/j.drugpo.2018.07.001

Peer-to-peer injection: Demographic, drug use, and injection-related risk factors

Shona Lamb a, Alex H Kral b, Karina Dominguez-Gonzalez c, Lynn D Wenger b, Ricky N Bluthenthal c,*
PMCID: PMC7285620  NIHMSID: NIHMS1597121  PMID: 30388569

Abstract

Background:

Peer-to-peer injection (either providing or receiving an injection to/from a person who injects drugs [PWID]) is common (19%–50%) among PWID. Most studies of peer-to-peer injection have focused on receiving injection assistance, with fewer examining providing injection assistance and none considering characteristics of PWID who do both. We examined characteristics of PWID by peer-to-peer injection categories (receiving, providing, both, and neither) and determined if these behaviors were associated with receptive and distributive syringe sharing.

Methods:

Los Angeles and San Francisco PWID (N = 777) were recruited using targeted sampling methods and interviewed during 2011–2013. Multinomial logistic regression was used to determine characteristics associated with peer-to-peer injection categories and logistic regression was used to examine if peer-to-peer categories were independently associated with distributive and receptive syringe sharing.

Results:

Recent peer-to-peer injection was reported by 42% of PWID (18% provider; 14% recipient; 10% both). In multinomial regression analysis, PWID reporting any peer-to-peer injection were more likely to inject with others than those who did neither. Injection providers and those who did both were associated with more frequent injection, illegal income source, and methamphetamine injection while injection recipients were associated with fewer years of injection. Injection providers were younger, had more years of injecting, and were more likely to inject heroin than PWID who did neither. In multivariate analyses, we found that providers and PWID who did both were significantly more likely to report receptive and distributive syringe sharing than PWID who did neither.

Conclusion:

Peer-to-peer injection is associated with HIV/HCV risk. Current prevention strategies may not sufficiently address these behaviors. Modification of existing interventions and development of new interventions to better respond to peer-to-peer injection is urgently needed.

Keywords: HIV/HCV injection risk, Injecting others, Receiving injections, PWID

Introduction

Injection drug use is a significant global public health issue (Degenhardt et al., 2017; Mathers et al., 2008; Nelson et al., 2011). People who inject drugs (PWID) face elevated risk for a variety of health problems including HIV, HCV, skin and soft tissue infections (SSTIs), overdose, sexually transmitted infections, and mental health disorders (Aceijas & Rhodes, 2007; Aceijas, Stimson, Hickman, & Rhodes, 2004; Degenhardt et al., 2017; Ebright & Pieper, 2002; Khan et al., 2013; Kral, Bluthenthal, Booth, & Watters, 1998; Mackesy-Amiti, Donenberg, & Ouellet, 2012; Nelson et al., 2011). As a consequence, premature mortality among PWID is elevated throughout the world (Mathers et al., 2013). A significant portion of the risks associated with drug injection arise from unsanitary injection and shared use of injection equipment.

Theory, ethnographic research, and observational epidemiology suggest that multi-level factors contribute to unsanitary injection by PWID including setting (Rhodes et al., 2006), time pressures (Ti et al., 2015), law enforcement contact (Booth et al., 2013), and interactions with other PWID to name a few (Harris & Rhodes, 2013). Among PWID interactions, peer-to-peer injection or the practice of giving (provider) or receiving injection assistance (recipient) from another PWID, is an important contributor to health outcomes in this population. Both forms of peer-to-peer injection have been associated with infectious disease risk and other harms related to drug injection including syringe sharing (Carlson, 2000; Fairbairn et al., 2006; Friedman et al., 2002; Kral, Bluthenthal, Erringer, Lorvick, & Edlin, 1999; Lee et al., 2013; Pedersen et al., 2016; Wood et al., 2001), abscesses and soft tissue infections (Lee et al., 2013; Lloyd-Smith et al., 2008), drug overdose (Fairbairn, Small, Van Borek, Wood, & Kerr, 2010), and HIV incidence (Lappalainen, Kerr, Hayashi, Dong, & Wood, 2015; O’Connell et al., 2005; Spittal et al., 2002).

Peer-to-peer injection is common among PWID. Studies from a variety of settings have reported recent (i.e., last 6 months) peer-to-peer injection ranging from 19% to 50% (Cheng et al., 2016; Kral et al., 1999; Lee et al., 2013). Peer-to-peer injection arises from diverse circumstances and motivations. For injection recipients, lack of knowledge on how to inject has been reported, along with shorter length of injection career (Epele, 2001; Fairbairn et al., 2010; Lee et al., 2013; O’Connell et al., 2005). For women, poor vein availability, as well as wanting to reducing scarring and damage have been documented as reasons for needing injection assistance (Epele, 2001; Wood, Spittal et al., 2003). PWID wanting jugular injection and those in the midst of withdrawal have also report needing assistance injecting (Hoda, Kerr, Li, Montaner, & Wood, 2008; Wood, Spittal et al., 2003). Providing injection assistance can be associated with exchanges of money or drugs (Epele, 2001; Fairbairn et al., 2010; Parkin & Coomber, 2009), although qualitative research has found that some providers take pride in assisting others and do so because they have had their own troubles self-injecting (Carlson, 2000; Murphy & Waldorf, 1991).

To date, much of the published research on peer-to-peer injection has focused on people who receive injection assistance (Cheng et al., 2016; Fairbairn et al., 2010; Lee et al., 2013; McElrath & Harris, 2013; O’Connell et al., 2005; Robertson et al., 2010; Wood, Spittal et al., 2003), although a few have also examined the risk profiles of those who provide injections (Carlson, 2000; Fairbairn et al., 2006; Friedman et al., 2002; Kral et al., 1999). It is important to note that some proportion of PWID engage in both behaviors (Kral et al., 1999), yet no published studies have examined this group in relationship to PWID who do not engage in peer-to-peer injection. Nor have studies examined if engaging in both are associated with distributive and receptive syringe sharing. Therefore, in the following, we present three multivariate models: 1) drug use and demographic factors associated with injection receiving, providing, both, or neither; 2) factors associated with distributive syringe sharing; and 3) factors associated with receptive syringe sharing among PWID in California.

Methods

Study sampling and recruitment

Targeted sampling and community outreach methods were used to recruit a cross-sectional sample of PWID in Los Angeles and San Francisco, California between April 2011 and April 2013 (Bluthenthal & Watters, 1995; Kral et al., 2010; Lopez et al., 2013; Watters & Biernacki, 1989). Eligible participants were 18 years of age or older and self-reported injection drug use in the last 30 days, which was verified by visual inspection for signs of recent venipuncture or track marks (Cagle, Fisher, Senter, Thurmond, & Kastar, 2002). Following an informed consent process prior to enrollment, trained interviewers administered a computer-assisted personal interview (Questionnaire Development System, NOVA Research, Bethesda, MD). Participants were compensated $20 for completing the survey. This analysis includes data from 777 PWID, of which 397 participants were recruited in Los Angeles and 380 in San Francisco. All study procedures were approved by the Institutional Review Boards at RTI International and the University of Southern California.

Study measures

For these analyses, we classified participants into one of four categories based on their response to the following two questions: “In the last 30 days, did you inject another person?” (referred to as an “injection provider” from here on). And, “In the last 30 days, were you injected by another person?” (referred to as an “injection recipient”). Response options for both were yes or no. Comparing responses to these two items resulted in 4 classifications: recipient, provider, both or neither.

We also considered variables related to peer-to-peer injection as indicated by prior research. These items included injection frequency, types of drugs used, years of injection, public injection, and any injecting with other PWID (as opposed to always injecting alone). These variables were created by using the following items. Injection frequency was the sum of self-reported injection episodes with the following drugs: cocaine, crack cocaine, methamphetamine, heroin, speedball (admixture of cocaine and heroin), goofball (admixture of heroin and methamphetamine), prescription opiates, stimulants, sedatives, tranquilizers, methadone, and buprenorphine in the last 30 days. Injection frequency in last 30 days was considered as a continuous variable and as a categorical variable with the following classifications: less than daily use (< 30 injections), once or twice a day (30–89 injections), and three or more times a day (≥90). Any injection and non-injection use of the drugs listed above was also considered, along with reported multi-route drug use (injection and non-injection use of any drugs), and polysubstance use (reported 2 or more drugs used in the last 30 days). Years of injection was calculated by subtracting current age from age at first injection. Public injection was assessed using the following item: “How often do you inject in public places (e.g. a park, alley, parking lot)?” (Response options: “Always,” “Often,” “Sometimes,” “Rarely,” and “Never”). To facilitate interpretation, this variable was recoded to any public injection (Always to Rarely) versus never injecting in public. Injecting with others was assessed by asking, “How often do you inject with other people?” Response options (“Always,” “Often,” “Sometimes,” “Rarely,” and “Never”) were recoded to never injection with others versus rarely to always injection with others.

We also examined if peer-to-peer classification was associated with distributive and receptive syringe sharing. Data for distributive and receptive syringe sharing were collected in the following manner: “In the last 30 days, how many times did you give or loan syringes/needles that you had used to someone else (including a close friend or lover) who then used them?” and “In the last 30 days, how many times did you inject using a syringe/needle that you know had been used by someone else (including a close friend or lover)?” For the syringe sharing items, the number of sharing episodes was re-coded as 0 equals ‘no’ and 1 or more equals ‘yes.’

Questions in the following domains were treated as potential covariates in all analyses: socio-demographic (e.g. age, gender, race/ethnicity, sexual partner types, sexual orientation), socioeconomic characteristics (e.g. housing status, monthly income, income sources [options were: job, unemployment and veterans benefits, welfare, disability, supplemental security income (SSI), spouse, family, friends, recycling, panhandling, and illegal or possibly illegal sources]), and contact with police, including arrest, legal status (on probation or parole), and concern with arrest for drug paraphernalia.

Statistical analyses

Descriptive statistics (e.g. frequencies, means, standard deviations, among others) were examined for all study variables. Bivariate analysis was conducted to determine factors correlated with peer-to-peer injection behaviors. Statistical significance of bivariate comparisons was set at p < 0.05 and was tested using chi-square test for categorical variables and t-test for continuous variables. Variables significant (p < 0.05) in bivariate analysis were assessed for collinearity. Collinear variables were removed from the final analysis based on strength of association with the dependent variable. Correlations were assessed using multinomial logistic regression with peer-to-peer injection category as the dependent variable. Variables found to be significant at the p < 0.05 were considered to be independently associated with peer-to-peer injection group. Variables that were not collinear but found to be non-significant in regression analyses were dropped from the final model. We implemented a similar procedure for constructing separate logistic regression models for distributive and receptive syringe sharing for purposes of determining if peer-to-peer injection was associated independently with these important injection-related HIV and HCV risk behaviors

Results

Sample characteristics were as follows: 26% female, 50% ≥50 years old, 34% white, 30% African American, 25% Latino, 15% gay, lesbian, or bisexual, 7% HIV positive. Study participants had low income with 81% reporting a total monthly income of less than $1350, and 62% considered themselves homeless.

Factors associated with peer-to-peer injection categories

Any peer-to-peer injection was reported by 41% of participants with 18% being injection providers, 14% being injection recipients, and 10% reporting both behaviors in the last 30 days. In bivariate analysis of factors associated with peer-to-peer injection (Table 1), a wide range of variables were found to correlate with these categories including race, age, sexual orientation, sexual partner type, homelessness, income, injection behaviors, recent drugs used, drug use frequency, years of use, and law enforcement contact.

Table 1.

Bivariate analysis of peer to peer injection by selected characteristics (N = 777).

Characteristic Total
N = 777
100%
Neither
N = 455
59%
Injection provider
N = 140
18%
Both
N = 76
10%
Injection recipient
N = 107
14%
Socio-demographics
Gender
 Female 203 (26%) 117 (26%) 30 (22%) 24 (32%) 32 (30%)
 Male 572 (74%) 338 (74%) 108 (78%) 51 (68%) 75 (70%)
Race*
 White 265 (34%) 129 (29%) 70 (50%) 29 (39%) 37 (35%)
 African American 233 (30%) 146 (32%) 28 (20%) 24 (32%) 35 (33%)
 Latino 192 (25%) 131 (29%) 23 (17%) 16 (21%) 22 (21%)
 Other 82 (11%) 46 (10%) 18 (13%) 6 (8%) 12 (11%)
Study site*
 Los Angeles 397 (51%) 257 (56%) 54 (39%) 37 (49%) 49 (46%)
 San Francisco 380 (49%) 198 (44%) 86 (61%) 38 (51%) 58 (54%)
Age*
 Less than 30 80 (10%) 32 (7%) 24 (17%) 8 (11%) 16 (15%)
 30–39 86 (11%) 35 (8%) 29 (21%) 10 (13%) 12 (11%)
 40–49 223 (29%) 129 (28%) 33 (24%) 25 (33%) 36 (34%)
 50 or more 388 (50%) 259 (57%) 54 (38%) 32 (43%) 43 (40%)
Gay, lesbian or bisexual*
 Yes 118 (15%) 52 (11%) 29 (21%) 19 (25%) 18 (17%)
Casual sex partner in the last 6 months*
 Yes 236 (30%) 117 (26%) 47 (34%) 37 (49%) 35 (33%)
Paying sex partner in the last 6 months*
 Yes 90 (12%) 40 (9%) 17 (12%) 19 (25%) 14 (13%)
Steady sex partner is an PWID*
 Yes 212 (27%) 96 (21%) 50 (36%) 33 (44%) 33 (31%)
Casual sex partner is an PWID*
 Yes 139 (18%) 60 (13%) 28 (20%) 26 (35%) 25 (23%)
Paying sex partner is an PWID*
 Yes 56 (7%) 27 (6%) 13 (9%) 11 (15%) 5 (5%)
Homeless*
 Yes 484 (62%) 264 (58%) 94 (67%) 57 (76%) 69 (65%)
Any mental health diagnosis*
 Yes 363 (47%) 188 (42%) 81 (58%) 38 (51%) 56 (53%)
Income source
 Government assistance* 273 (35%) 141 (31%) 65 (46%) 28 (37%) 39 (36%)
 Other family/friends* 122 (16%) 54 (12%) 29 (21 %0 19 (25%) 20 (19%)
 Spouse* 60 (8%) 26 (6%) 15 (11%) 12 (16%) 7 97%)
 Panhandling* 203 (26%) 102 (22%) 52 (37%) 22 (29%) 27 (25%)
 Illegal or possibly illegal income* 286 (37%) 142 (31%) 68 (49%) 42 (56%) 34 (32%)
Monthly income*
 < $1350 627 (81%) 381 (84%) 103 (74%) 54 (72%) 89 (83%)
 $1,350 or more 150 (19%) 74 (16%) 37 (26%) 21 (28%) 18 (17%)
Injection behaviors
Any public injection, last 30 days*
 Yes 392 (51%) 192 (42%) 93 (66%) 55 (73%) 52 (49%)
Inject with others*
 Yes 628 (81%) 325 (71%) 132 (94%) 73 (97%) 98 (92%)
Drug use items
Non-injection drug use, last 30 days
 Methamphetamine* 192 (25%) 76 (17%) 41 (29%) 29 (39%) 46 (43%)
 Marijuana* 416 (54%) 220 (48%) 94 (67%) 41 (55%) 61 (57%)
Prescription
 Opiates* 189 (24%) 90 (20%) 46 (33%) 23 (31%) 30 (28%)
 Tranquilizer* 192 (25%) 94 (21%) 46 (33%) 25 (33%) 27 (25%)
 Methadone* 162 (21%) 85 (19%) 34 (24%) 26 (35%) 17 (16%)
Injected drug use, last 30 days
 Crack Cocaine* 70 (9%) 31 (7%) 21 (15%) 13 (17%) 5 (5%)
 Powder cocaine* 83 (11%) 38 (8%) 24 (17%) 14 (19%) 7 (7%)
 Heroin* 613 (79%) 369 (81%) 114 (81%) 60 (80%) 70 (65%)
 Methamphetamine* 290 (37%) 124 (27%) 69 (49%) 44 (59%) 53 (50%)
 Speedball* 128 (17%) 57 (13%) 35 (25%) 21 (28%) 15 (14%)
 Goofball* 93 (12%) 27 (6%) 34 (24%) 23 (31%) 9 (8%)
Prescription drugs
 Opiates* 93 (12%) 28 (6%) 38 (27%) 15 (20%) 12 (11%)
Injection frequency, last 30 days*
 < 30 362 (47%) 227 (50%) 47 (34%) 25 (33%) 63 (59%)
 30–89 214 (27%) 121 (27%) 47 (34%) 25 (33%) 32 (20%)
 90 or more 201 (26%) 107 (23%) 46 (33%) 25 (33%) 29 (21%)
Poly injection drug use, last 30 days*
 Yes 290 (37%) 121 (27%) 88 (63%) 43 (57%) 38 (36%)
Multi-route drug use*
 Yes 552 (71%) 293 (64%) 110 (79%) 58 (77%) 91 (85%)
Years of injection use*
 < 10 126 (16%) 61 (13%) 27 (19%) 13 (17%) 25 (23%)
 10–19 128 (17%) 56 (12%) 37 (26%) 11 (15%) 24 (22%)
 20 or more 523 (67%) 338 (74%) 76 (54%) 51 (68%) 58 (54%)
Law enforcement
Any contact
 Police* 399 (52%) 193 (43%) 91 (65%) 55 (74%) 60 (56%)
 Arrest* 206 (27%) 98 (22%) 41 (29%) 35 (47%) 32 (30%)
 Security guard* 167 (22%) 61 (13%) 51 (36%) 26 (35%) 29 (27%)
 Probation* 172 (22%) 83 (18%) 39 (28%) 26 (35%) 24 (23%)
*

Chi-square p < 0.05.

In multinomial logistic regression modelling (Table 2) with “neither” type of peer-to-peer injection as the referent category, we found that being an injection provider was independently associated with any injecting with other PWID (Adjusted odds ratio [AOR] = 5.71; 95% Confidence Interval [CI] = 2.66, 12.20) as opposed to injecting alone, any methamphetamine injection in the last 30 days (AOR = 2.75; 95% CI = 1.64, 4.61), any heroin injection (AOR = 2.14; 95% CI = 1.14, 4.02), illegal or possibly illegal income source (AOR = 1.55; 95% CI = 1.03, 2.35), injection frequency (AOR = 1.00; 95% CI = 1.00, 1.01), years of injection (AOR = 1.03; 95% CI = 1.00, 1.06), and age (AOR = 0.94; 95% CI = 0.91, 0.97). Engaging in both peer-to-peer behaviors was associated with injecting with other PWID (AOR = 12.35; 95% CI = 2.92, 52.63), any methamphetamine injection (AOR = 5.38; 95% CI = 2.83, 10.20), illegal income source (AOR = 2.38; 95% CI = 1.40, 4.03) and injection frequency (AOR = 1.01; 95% CI = 1.00, 1.01). For injection recipients, only injecting with other PWID (AOR = 3.95; 95% CI = 1.92, 8.13) and years of injection (AOR = 0.98; 95% CI = 0.95, 1.00) were significantly associated with this peer-to-peer injection behavior. It is worth noting that the overlapping confidence intervals amongst the peer-to-peer injection categories indicates that there are no significant differences amongst them with regard to these demographic and drug use behaviors.

Table 2.

Multinomial logistic regression of peer to peer injection.

No Peer
Injection
Injection
provider β 95% Confidence Interval
Both
β 95% Confidence Interval
Injection recipient
β 95% Confidence Interval
Injection frequency, 30 days referent 1.00 (1.00, 1.01)* 1.01 (1.00, 1.01)* 1.00 (1.00, 1.01)
Age referent 0.94 (0.91, 0.97)* 1.00 (0.96, 1.04) 1.00 (0.97, 1.03)
Years of injecting referent 1.03 (1.00, 1.06)* 1.00 (0.97, 1.03) 0.98 (0.95, 1.00)*
Any illegal income, last 30d referent 1.55 (1.03, 2.35)* 2.38 (1.40, 4.03)* 0.89 (0.56, 1.44)
Any meth injection, last 30d referent 2.75 (1.64, 4.61)* 5.38 (2.83, 10.20)* 1.77 (0.95, 3.29)
Any heroin injection, last 30d referent 2.14 (1.14, 4.02)* 2.12 (0.99, 4.52) 0.78 (0.40, 1.52)
Inject with others, last 30 days referent 5.71 (2.66, 12.20)* 12.35 (2.92, 52.63)* 3.95 (1.92, 8.13)*

β=point estimate.

*

p < 0.05.

Factors associated with distributive and receptive syringe sharing

To determine if peer-to-peer behaviors were independently associated with critical injection-related HIV and HCV risk, we constructed multivariate models of distributive and receptive syringe sharing. Bivariate factors associated with distributive and receptive syringe sharing are presented in Table 3. In the multivariate distributive syringe sharing model (Table 4), being an injection provider (AOR = 1.88; 95% CI = 1.02, 3.45) and doing both (AOR = 3.71; 95% CI = 1.87, 7.36) were associated with this type of sharing, but not being an injection recipient. This model included African American race, public injection, unauthorized syringe source, paying sex partner in the last 6 months, steady sex partner is a PWID, concern about arrest for drug paraphernalia, and being HIV positive. In the multivariate receptive syringe sharing model (Table 4), being an injection provider (AOR = 1.84; 95% CI = 1.01, 3.35) and doing both (AOR = 2.29; 95% CI = 1.14, 4.59) were associated with this type of sharing, but not being an injection recipient. This model included income over $1351 per month, public injection, injects with others, syringe coverage of 100% or more, paying sex partner is a PWID, any police contact in the last 6 months, and being concerned with being arrested for possessing drug paraphernalia. Overlapping confidence intervals on the peer-to-peer behaviors indicate that differences between the categories are not significant.

Table 3.

Bivariate analysis of distributive and receptive syringe sharing by selected characteristics (N = 777).

Characteristics Distributive syringe
sharing
N (%)
Receptive syringe
sharing
N (%)
Socio-demographics
Gender
 Female (n = 203) 38 (19%) 28 (14%)
 Male (n = 572) 76 (13%) 78 (14%)
Race * *
 White (n = 265) 53 (20%) 43 (16%)
 African American (n = 233) 18 (8%) 17 (7%)
 Latino (n = 192) 33 (17%) 35 (18%)
 Other (n = 82) 10 (12%) 11 (13%)
Study site * *
 Los Angeles (n = 397) 74(19%) 66 (17%)*
 San Francisco (n = 380) 40 (11%) 40 (11%)
Age * *
 Less than 30 (n = 80) 21 (26%) 16 (20%)
 30–39 (n = 86) 11 (13%) 10 (12%)
 40–49 (n = 223) 36 (16%) 39 (18%)
 50 or more (n = 388) 46 (12%) 41 (11%)
Paying sex partner in the last 6 months * *
 Yes (n = 90) 25 (22%) 24 (27%)
Steady sex partner is an PWID * *
 Yes (n = 212) 49 (23%) 42 (20%)
Casual sex partner is an PWID
 Yes (n = 139) 27 (19%) 25 (18%)
Paying sex partner is an PWID * *
 Yes (n = 56) 16 (29%) 18 (32%)
Homeless
 Yes (n = 484) 86 (18%)* 84 (17%)*
Income source
 Government assistance (n = 273) 52 (19%)* 46 (17%)
 Family (n = 122) 24 (20%) 23 (19%)
 Spouse (n = 60) 15 (25%)* 13 (22%)
 Panhandling (n = 203) 48 (24%)* 46 (23%)*
 Recycling (n = 202) 33 (16%) 37 (18%)*
 Illegal or possibly illegal (n = 286) 47 (16%) 48 (17%)*
 SSI benefits (n = 267) 30 (11%) 29 (11%)
Income in the last 30 days * *
 < $1350 (n = 627) 90 (14%) 97 (16%)
 $1350 or more (n = 150) 24 (15%) 9 (6%)
HIV positive *
 Yes (n = 53) 1 (2%) 5 (9%)
Injection behaviors
Any public injection, last 30 days * *
 Yes (n = 392) 90 (23%) 83 (21%)
Inject with others * *
 Yes (n = 628) 107 (17%) 103 (16%)
Peer to peer injection * *
 Neither (n = 455) 43 (10%) 43 (10%)
 Injection provider (n = 140) 31 (22%) 28 (20%)
 Both (n = 75) 25 (33%) 21 (28%)
 Injection recipient (n = 107) 15 (14%) 14 (13%)
Syringe coverage of 100% or more *
 Yes (n = 472) 53 (11%) 48 (10%)
Pharmacy syringe access * *
 Yes (n = 245) 51 (21%) 48 (20%)
Unauthorized syringe access * *
 Yes (n = 270) 59 (22%) 57 (21%)
Shooting gallery use * *
 Yes (n = 84) 20 (24%) 21 (25%)
Drug use items
Non-injection drug use, last 30 days
 Methamphetamine (n = 192) 38 (20%)* 36 (19%)*
  Prescription
 Opiates (n = 189) 36 (19%)* 37 (20%)*
 Tranquilizer (n = 192) 48 (25%)* 37 (19%)*
 Methadone (n = 162) 31 (19%) 30 (19%)*
Injected drug use, last 30 days
 Heroin (n = 613) 98 (16%)* 90 (15%)
 Goofball (n = 93) 25 (27%)* 29 (31%)*
Prescription drugs
 Opiates (n = 93) 21 (22%)* 13 (14%)
Injection frequency, last 30 days * *
 < 30 (n = 362) 33 (9%) 39 (11%)
 30–89 (n = 214) 37 (17%) 29 (14%)
 90 or more (n = 201) 44 (22%) 38 (19%)
Years of injection use *
 < 10 (n = 126) 31 (25%) 21 (17%)
 10–19 (n = 128) 15 (12%) 14 (11%)
 20 or more (n = 523) 68 (13%) 71 (14%)
Law enforcement
Any contact
 Police (n = 399) 76 (19%)* 79 (20%)*
 Arrest (n = 206) 43 (21%)* 39 (19%)*
 Security guard (n = 167) 37 (22%)* 29 (17%)
 Concerned with arrest for paraphernalia (n = 344) 75 (22%)* 66 (19%)*
 Probation (n = 172) 28 (16%)* 32 (19%)*
*

Chi-square p < 0.05.

Table 4.

Logistic regression analysis of distributive and receptive syringe sharing.

Variables Distributive syringe sharing
(1)
Receptive syringe sharing
(2)
Adjusted Odds Ratio, (95%
CI) +
Adjusted Odds Ratio (95%
CI) +
Peer to Peer injecting
 Neither Referent Referent
 Injection provider 1.88 (1.02, 3.45) 1.84 (1.01, 3.35)
 Both 3.71 (1.87, 7.36) 2.29 (1.14, 4.59)
 Injection recipient 1.53 (0.76, 3.10) 1.11 (0.54, 2.28)
+

Confidence interval.

(1)

Controlling for African American race, public injection, unauthorized syringe source, paying sex partner in the last 6 months, steady sex partner is a PWID, concern about arrest for drug paraphernalia, and being HIV positive.

(2)

Controlling for income, any public injection, injecting with others, syringe coverage, paying sex partner is a PWID, any police contact, and concern about arrest for drug paraphernalia.

Discussion

Peer-to-peer injection remains common among PWID and is associated with important injection-related HIV/HCV risk behaviors. Specifically, PWID who are injection providers and those who engage in both behaviors were associated with both distributive and receptive syringe sharing as compared to those who reported no peer-to-peer injection. This poses a challenge for existing syringe-related prevention strategies. For instance, operational policies of many safer injection facilities (SIFs) do not permit assisted injection despite this being a persistent need for a significant proportion of PWID (Gagnon, 2017; Kerr, Mitra, Kennedy, & McNeil, 2017). One potential response to this need was the development of injection support teams - teams where peer outreach workers would provide advice, education, and injection assistance for PWID who used in public settings (Callon, Charles, Alexander, Small, & Kerr, 2013; Small et al., 2012). The injection support teams were developed by the Vancouver Area Network of Drug Users (VANDU) organization and represented a logical extension of the unsanctioned, nighttime syringe access program and the unsanctioned SIF that VANDU had initiated several years prior (Kerr, Oleson, Tyndall, Montaner, & Wood, 2005; Wood, Kerr et al., 2003). The VANDU unsanctioned SIF did permit assisted injection but was closed down by government officials after 6 months of operation (Kerr et al., 2005). An unsanctioned SIF in the United States is also allowing assisted injection (Davidson, Lopez, & Kral, 2017). According to one report, assisted injection has been permitted at a few SIFs, typically when a participant has a severe disability (Kimber, Dolan, & Wodak, 2005). Data from this study underscore the need to permit assisted injection in SIFs (Fast, Small, Wood, & Kerr, 2008; Wood et al., 2008).

Nonetheless, other intervention strategies are needed to address assisted injection. The literature suggests at least two promising approaches. One is the deployment of combined, multi-level interventions such as expanded medication-assisted treatment, syringe exchange programs, and HIV and HCV treatment enrollment and adherence support. Combined approaches have been found to reduce HIV incidence among PWID (Des Jarlais, Arasteh, & Friedman, 2011; Van Den Berg, Smit, Van Brussel, Coutinho, & Prins, 2007) as well as maintain low HIV seroprevalence in areas where this approach has been taken (Des Jarlais et al., 1995). While this approach may not directly impact peer-to-peer injection practices, by reducing HIV and HCV seroprevalence in PWID populations, they reduce an important harm of this practice. Another approach is to consider engaging directly with PWID involved in peer-to-peer injection to support behavior changes that reduce potential harms associated with this practice. Peer interventions among PWID have been successful in the area of overdose reversals (Wheeler et al., 2015), reducing syringe sharing (Roux et al., 2016), and navigation of services including entering medication assisted treatment and HIV care (Des Jarlais et al., 2016). Consideration on how to engage injection providers and recipients in risk reduction related to peer-to-peer injection is needed.

We also found that receiving injection assistance alone was not significantly associated with either distributive or receptive syringe sharing. This finding differs significantly from prior studies where receiving injection assistance was associated with syringe sharing (Cheng et al., 2016; Lee et al., 2013; Pedersen et al., 2016; Robertson et al., 2010; Wood, Spittal et al., 2003), HIV infection, and HCV and HIV incidence (Lappalainen et al., 2015; Miller et al., 2002; Spittal et al., 2002). The lack of an association between receiving injection assistance and syringe sharing behaviors could be the result of three things. First, in most prior studies on risk behaviors, injection recipients were regarded as the dependent variable. This approach reverses the causal direction of this association since the interpretation is typically that receiving injection assistance leads to syringe sharing. In our study, we treat injection receipt as the independent variable in relationship to syringe sharing. Second, other studies have classified injection recipients as a dichotomous variable. This has the consequence of including PWID who are not engaged in peer-to-peer injection with those who provided injections. This seems inappropriate since multiple studies have found that providing injections is also associated with syringe sharing (Fairbairn et al., 2006; Kral et al., 1999). And third, acknowledging that peer-to-peer injection behaviors might be distinct, we constructed models that classified PWID based on their involvement in all three types of peer-to-peer injection involvement (provider, recipient, or both). We believe this leads to a more accurate assessment of the risk of each behavior as compared to those who do not engage in either behavior.

Drug use and demographic differences were also found. Specifically, being a recipient was associated only with years of injecting, where more years was protective against this behavior, and injecting with other PWID, a necessary prerequisite for receiving injections. Meanwhile, doing both and providing injections was associated with income from illegal sources and likely reflects greater involvement in the drug economy as observed elsewhere (Carlson, 2000; Friedman et al., 2002; Parkin & Coomber, 2009). PWID who did both and provided injections were also found to inject more frequently and to have used methamphetamine in the last 30 days. More frequent injection has been associated with injection providers in other studies (Fairbairn et al., 2006; Friedman et al., 2002), although our finding that methamphetamine use predicts this behavior is novel. This likely reflects the relatively high portion of PWID who inject methamphetamine in Los Angeles and San Francisco (Corsi et al., 2012; Gonzales, Mooney, & Rawson, 2010). Lastly, injection providers were associated with more years of injection and younger age as compared to those who had no peer-to-peer injection behaviors. We suspect the positive association with longer injection career reflects injection skill, while the inverse association with age is surprising since age can also be an indicator of injecting skill. However, looking at the bivariate proportions (Table 2), PWID under the age of 40 were significantly more likely to report providing injection assistance. Injection assistance may be a behavior that PWID “age out” of. More research on age differences among PWID engaged in peer-to-peer injection is necessary to understand this phenomenon.

Limitations

Study results should be interpreted with the following limitations in mind. Given our cross-sectional study design, causality cannot be inferred. Study data are derived from participant self-reports and are subject to recall and social desirability biases. However, the reliability and validity of items used in this study have been established in prior studies (Dowling-Guyer et al., 1994; Needle et al., 1995; Weatherby et al., 1994). Different time frames were used to measure variables. For example, a thirty-day time frame was used for peer-to-peer injection but sex-related variables were assessed over 6 months. Lastly, data were collected in 2011 to 2013. It is possible that temporal changes have made these data obsolete. In the United States, there have been two significant drug use transitions since 2013. First, is the growing use of heroin by former prescription opioid users. The second, is the contamination of the heroin supply with fentanyl and other synthetic opioids. Neither of these changes are likely to change the prevalence of peer-to-peer injection in our minds. In fact, California for the most part appears to have missed the second trend as measured by overdose deaths, which have remained stable for the last 5 years. As a consequence, we believe this data from 2011/13 is still relevant.

Conclusions

Future research on peer-to-peer injection should use longitudinal cohort study designs and consistent time frames for data collection. Also, we have little quantitative data on motivations for providing or receiving injection assistance including frequency of such behaviors. Obtaining information on frequency of peer-to-peer injection will help prioritize the need to amend existing SIF policies and inform the operational policies for new SIFs. Further, we know little about the relative importance of different motivations to receive injection assistance. That is, whether it is related mostly to withdrawal symptoms, vein loss, or desire to inject in difficult-to-reach locations. On this latter point, at least three studies have found that PWID who engage in neck or jugular injection were more likely to receive injection assistance (Hoda et al., 2008; Pedersen et al., 2016; Rafful et al., 2015). Establishing frequency, motivations, demographic, and drug use characteristics of PWID who receive injection assistance is essential for ensuring that prevention activities reach high-need subgroups among PWID.

There is also a need for more qualitative research on peer-to-peer injection. This could uncover other intervention approaches that address enduring infectious disease risk related to this behavior. In addition, geographic differences in recent peer-to-peer injection have been found but the causes of these differences are not well understood. More qualitative and ethnographic research is needed to explore and describe peer-to-peer behaviors in varied settings and by different drug use patterns and preferences.

The risk profiles of PWID who engage in peer-to-peer injection suggest that these individuals are at the intersection of syndemics related to blood borne infectious diseases and chronic ailments common to those who inject drugs (Mizuno et al., 2015; Singer & Clair, 2003). Interventions that engage PWID involved in peer-to-peer injection behaviors are few (e.g. injection teams, assisted injection within SIFs), but preliminary results suggest promise (Callon et al., 2013; Small et al., 2012). Implementation of these existing strategies and development of new approaches are needed in the face of what appears to be increases in diseases associated with drug injection in the US and elsewhere (Bruneau, Roy, Arruda, Zang, & Justras-Aswad, 2012; Global Commission on Drug Policy, 2017; Zibbell et al., 2015, 2017).

Acknowledgements

We thank the participants who took part in this study. The following research staff and volunteers also contributed to the study and are acknowledged here: Sonya Arreola, Vahak Bairamian, Philippe Bourgois, Soo Kin Byun, Jose Collazo, Jacob Curry, David-Preston Dent, Jahaira Fajardo, Richard Hamilton, Frank Levels, Luis Maldonado, Askia Muhammad, Brett Mendenhall, Stephanie Dyal-Pitts, and Michele Thorsen.

Role of the funding source

The research was supported by NIDA (grant # R01DA027689: Program Official Elizabeth Lambert and grant # R01DA038965: Program Official Richard Jenkins). The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.

Footnotes

Conflict of interest

The authors have no financial relationships that are related to the topic of this manuscript and no conflicts of interest.

References

  1. Aceijas C, & Rhodes T (2007). Global estimates of prevalence of HCV infection among injecting drug users. International Journal on Drug Policy, 18(5), 352–358. 10.1016/j.drugpo.2007.04.004S0955-3959(07)00091-6 [pii]. [DOI] [PubMed] [Google Scholar]
  2. Aceijas C, Stimson GV, Hickman M, & Rhodes T (2004). Global overview of injecting drug use and HIV infection among injecting drug users. AIDS, 18(17), 2295–2303. [DOI] [PubMed] [Google Scholar]
  3. Bluthenthal RN, & Watters JK (1995). Multimethod research from targeted sampling to HIV risk environments. NIDA Research Monograph, 157, 212–230 1995/01/01 ed. [PubMed] [Google Scholar]
  4. Booth RE, Dvoryak S, Sung-Joon M, Brewster JT, Wendt WW, Corsi KF, … Strathdee SA (2013). Law enforcement practices associated with HIV infection among injection drug users in Odessa, Ukraine. AIDS and Behavior, 17(8), 2604–2614. 10.1007/s10461-013-0500-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Bruneau J, Roy E, Arruda N, Zang G, & Justras-Aswad D (2012). The rising prevalence of prescription opioid injection and its association with hepatitis C incidence among street-drug users. Addiction, 107, 1318–1327. [DOI] [PubMed] [Google Scholar]
  6. Cagle HH, Fisher DG, Senter TP, Thurmond RD, & Kastar AJ (2002). Classifying skin lesions of injection drug users: A method for corroborating disease risk. Rockville, MD: Substance Abuse and Mental Health Services Administration. [Google Scholar]
  7. Callon C, Charles G, Alexander R, Small W, & Kerr T (2013). ‘On the same level’: Facilitators’ experiences running a drug user-led safer injecting education campaign. Harm Reduction Journal, 10(1), 4 10.1186/1477-7517-10-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Carlson RG (2000). Shooting galleries, dope houses, and injection doctors: Examining the social ecology of HIV risk behaviors among drug injectors in Dayton, Ohio. Human Organization, 59(3), 325–333. [Google Scholar]
  9. Cheng T, Kerr T, Small W, Dong H, Montaner J, Wood E, … DeBeck K (2016). High prevalence of assisted injection among street-involved youth in a Canadian setting. AIDS and Behavior, 20(2), 377–384. 10.1007/s10461-015-1101-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Corsi KF, Lehman WE, Min SJ, Lance SP, Speer N, Booth RE, … Shoptaw S (2012). The feasibility of interventions to reduce HIV risk and drug use among heterosexual methamphetamine users. Journal of AIDS and Clinical Research, S1(10), 10.4172/2155-6113.S1-010. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Davidson PJ, Lopez AM, & Kral AH (2017). Using drugs in un/safe spaces: Impact of perceived illegality on an underground supervised injecting facility in the United States. International Journal on Drug Policy, 53, 37–44. 10.1016/j.drugpo.2017.12.005. [DOI] [PubMed] [Google Scholar]
  12. Degenhardt L, Peacock A, Colledge S, Leung J, Grebely J, Vickerman P, … Larney S (2017). Global prevalence of injecting drug use and sociodemographic characteristics and prevalence of HIV, HBV, and HCV in people who inject drugs: A multistage systematic review. Lancet Global Health, 5(12), e1 192–el 207. 10.1016/s2214-109x(17)30375-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Des Jarlais D, Duong HT, Pham Minh K, Khuat OH, Nham TT, Arasteh K, … Nagot N (2016). Integrated respondent-driven sampling and peer support for persons who inject drugs in Haiphong, Vietnam: A case study with implications for interventions. Aids Care, 28(10), 1312–1315. 10.1080/09540121.2016.1178698. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Des Jarlais DC, Arasteh K, & Friedman SR (2011). HIV among drug users at Beth Israel Medical Center, New York City, the first 25 years. Substance Use and Misuse, 46(2–3), 131–139. 10.3109/10826084.2011.521456. [DOI] [PubMed] [Google Scholar]
  15. Des Jarlais DC, Hagan H, Friedman SR, Friedman P, Goldberg D, Frischer M, … Myers T (1995). Maintaining low HIV seroprevalence in populations of injecting drug users. Journal of the American Medical Association, 274, 1226–1231. [DOI] [PubMed] [Google Scholar]
  16. Dowling-Guyer S, Johnson ME, Fisher DG, Needle R, Watters JK, Andersen M, … Tortu S (1994). Reliability of drug users’ self-reported HIV risk behaviors and validity of self-reported recent drug use. Assessment, 1, 383–392. [Google Scholar]
  17. Ebright JR, & Pieper B (2002). Skin and soft tissue infectious in injection drug users. Infectious Disease Clinics of North America, 16(3), 697–712. [DOI] [PubMed] [Google Scholar]
  18. Epele ME (2001). Scars, harm and pain. Journal of Ethnicity in Substance Abuse, 1(1), 47–69. 10.1300/J233v01n01_04. [DOI] [Google Scholar]
  19. Fairbairn N, Small W, Van Borek N, Wood E, & Kerr T (2010). Social structural factors that shape assisted injecting practices among injection drug users in Vancouver, Canada: A qualitative study. Harm Reduction Journal, 7, 20. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Fairbairn N, Wood E, Small W, Stoltz JA, Li K, & Kerr T (2006). Risk profile of individuals who provide assistance with illicit drug injection. Drug and Alcohol Dependence, 82(1), 41–46. [DOI] [PubMed] [Google Scholar]
  21. Fast D, Small W, Wood E, & Kerr T (2008). The perspectives of injection drug users regarding safer injecting education delivered through a supervised injecting facility. Harm Reduction Journal, 5(1), 32 10.1186/1477-7517-5-32. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Friedman SR, Kang S-Y, Deren S, Robles RR, Colon HM, Andia J, … Finlinson A (2002). Drug-scene roles and HIV risk among Puerto Rican injection drug users in East Harlem, New York and Bayaman, Puerto Rico. Journal of Psychoactive Drugs, 34(4), 363–369. [DOI] [PubMed] [Google Scholar]
  23. Gagnon M (2017). It’s time to allow assisted injection in supervised injection sites. CMAJ, 189(34), E1083–e1084. 10.1503/cmaj.170659. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Global Commission on Drug Policy (2017). The opioid crisis in North America. Retrieved from Geneva, Switzerland: http://www.globalcommissionondrugs.org/position-papers/opioid-crisis-north-america-position-paper/. [Google Scholar]
  25. Gonzales R, Mooney L, & Rawson RA (2010). The methamphetamine problem in the United States. Annual Review of Public Health, 31(1), 385–398. 10.1146/annurev.publhealth.012809.103600. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Harris M, & Rhodes T (2013). Injecting practices in sexual partnerships: Hepatitis C transmission potentials in a ‘risk equivalence’ framework. Drug and Alcohol Dependence, 132(3), 617–623. 10.1016/j.drugalcdep.2013.04.012. [DOI] [PubMed] [Google Scholar]
  27. Hoda ZIA, Kerr T, Li K, Montaner JSG, & Wood E (2008). Prevalence and correlates of jugular injections among injection drug users. Drug and Alcohol Review, 27(4), 442–446. 10.1080/09595230802089701. [DOI] [PubMed] [Google Scholar]
  28. Kerr T, Mitra S, Kennedy MC, & McNeil R (2017). Supervised injection facilities in Canada: Past, present, and future. Harm Reduction Journal, 14(1), 28 10.1186/s12954-017-0154-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Kerr T, Oleson M, Tyndall MW, Montaner J, & Wood E (2005). A description of a peer-run supervised injection site for injection drug users. Journal of Urban Health, 82(2), 267–275. 10.1093/jurban/jti050. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Khan MR, Berger A, Hemberg J, O’Neill A, Dyer TP, & Smyrk KK (2013). Non-injection and injection drug use and STI/HIV risk in the United States: The degree to which sexual risk behaviors versus sex with an STI-infected partner account for infection transmission among drug users. AIDS and Behavior, 17(3), 1185–1194. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Kimber J, Dolan K, & Wodak A (2005). Survey of drug consumption rooms: Service delivery and perceived public health and amenity impact. Drug and Alcohol Review, 24(1), 21–24. 10.1080/09595230500125047. [DOI] [PubMed] [Google Scholar]
  32. Kral AH, Bluthenthal RN, Booth RE, & Watters JK (1998). HIV seroprevalence among street-recruited injection drug and crack cocaine users in 16 US municipalities. American Journal of Public Health, 88(1), 108–113. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Kral AH, Bluthenthal RN, Erringer EA, Lorvick J, & Edlin BR (1999). Risk factors among IDUs who give injections to or receive injections from other drug users. Addiction, 94(5), 675–683. [DOI] [PubMed] [Google Scholar]
  34. Kral AH, Malekinejad M, Vaudrey J, Martinez AN, Lorvick J, McFarland W, … Raymond HF (2010). Comparing respondent-driven sampling and targeted sampling methods of recruiting injection drug users in San Francisco. Journal of Urban Health, 87(5), 839–850. 10.1007/s11524-010-9486-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Lappalainen L, Kerr T, Hayashi K, Dong H, & Wood E (2015). Decreasing impact of requiring assistance injecting on HIV incidence. Journal of Acquired Immune Deficiency Syndromes, 69(1), e40–e42. 10.1097/QAI.0000000000000554. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Lee WK, Ti L, Hayashi K, Kaplan K, Suwannawong P, Wood E, … Kerr T (2013). Assisted injection among people who inject drugs in Thailand. Substance Abuse Treatment, Prevention, and Policy, 8, 32 10.1186/1747-597X-8-32. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Lloyd-Smith E, Wood E, Zhang R, Tyndall MW, Montaner JS, & Kerr T (2008). Risk factors for developing a cutaneous injection-related infection among injection drug users: A cohort study. BMC Public Health, 8, 405 10.1186/1471-2458-8-405. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Lopez AM, Bourgois P, Wenger LD, Lorvick J, Martinez AN, & Kral AH (2013). Interdisciplinary mixed methods research with structurally vulnerable populations: Case studies of injection drug users in San Francisco. International Journal on Drug Policy, 24(2), 101–109. 10.1016/j.drugpo.2012.12.004. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. Mackesy-Amiti ME, Donenberg GR, & Ouellet LJ (2012). Prevalence of psychiatric disorders among young injection drug users. Drug And Alcohol Dependence, 124(1-2), 70–78. 10.1016/j.drugalcdep.2011.12.012S0376-8716(11)00545-X [pii]. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Mathers B, Degenhardt L, Bucello C, Lemon J, Wiessing L, & Hickman M (2013). Mortality among people who inject drugs: A systematic review and meta-analysis. Bulletin of the World Health Organization, 91(2), 102–123. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. Mathers BM, Degenhardt L, Phillips B, Wiessing L, Hickman M, Strathdee SA, … Mattick RP (2008). Global epidemiology of injecting drug use and HIV among people who inject drugs: A systematic review. Lancet, 372(9651), 1733–1745. 10.1016/S0140-6736(08)61311-2S0140-6736(08)61311-2 [pii]. [DOI] [PubMed] [Google Scholar]
  42. McElrath K, & Harris J (2013). Peer injecting: Implications for injecting order and bloodborne viruses among men and women who inject heroin. Journal of Substance Use, 18, 31–45. [Google Scholar]
  43. Miller CL, Johnston C, Spittal PM, Li K, Laliberte N, Montaner JS, … Schechter, M. T. (2002). Opportunities for prevention: Hepatitis C prevalence and incidence in a cohort of young injection drug users. Hepatology, 36(3), 737–742. 10.1053/jhep.2002.35065. [DOI] [PubMed] [Google Scholar]
  44. Mizuno Y, Purcell DW, Knowlton AR, Wilkinson JD, Gourevitch MN, & Knight KR (2015). Syndemic vulnerability, sexual and injection risk behaviors, and HIV continuum of care outcomes in HIV-positive injection drug users. AIDS and Behavior, 19(4), 684–693. 10.1007/s10461-014-0890-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  45. Murphy S, & Waldorf D (1991). ‘Kickin’ down to the street doc: Shooting galleries in the San Francisco Bay Area. Contemporary Drug Problems, 18, 9–29. [Google Scholar]
  46. Needle RN, Fisher DG, Weatherby N, Chitwood D, Brown B, Cesari H, … Braunsterin M (1995). Reliability of self-reported HIV risk behaviors of drug users. Psychology of Addictive Behaviors, 9, 242–250. [Google Scholar]
  47. Nelson PK, Mathers BM, Cowie B, Hagan H, Des Jarlais D, Horyniak D, … Degenhardt L (2011). Global epidemiology of hepatitis B and hepatitis C in people who inject drugs: Results of systematic reviews. Lancet, 378(9791), 571–583. [DOI] [PMC free article] [PubMed] [Google Scholar]
  48. O’Connell JM, Kerr T, Li K, Tyndall MW, Hogg RS, Montaner JS, … Wood E (2005). Requiring help injecting independently predicts incident HIV infection among injection drug users. Journal of Acquired Immune Deficiency Syndromes, 40(1), 83–88. [DOI] [PubMed] [Google Scholar]
  49. Parkin S, & Coomber R (2009). Informal ‘Sorter’ houses: A qualitative insight of the ‘shooting gallery’ phenomenon in a UK setting. Health & Place, 15(4), 981–989. 10.1016/j.healthplace.2009.03.004. [DOI] [PubMed] [Google Scholar]
  50. Pedersen JS, Dong H, Small W, Wood E, Nguyen P, Kerr T, … Hayashi K (2016). Declining trends in the rates of assisted injecting: A prospective cohort study. Harm Reduction Journal, 13(2), 10.1186/s12954-016-0092-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  51. Rafful C, Wagner KD, Werb D, González-Zúñiga PE, Verdugo S, Rangel G, … Strathdee SA (2015). Prevalence and correlates of neck injection among people who inject drugs in Tijuana, Mexico. Drug and Alcohol Review, 34(6), 630–636. 10.1111/dar.12264. [DOI] [PMC free article] [PubMed] [Google Scholar]
  52. Rhodes T, Kimber J, Small W, Fitzgerald J, Kerr T, Hickman M, … Holloway G (2006). Public injecting and the need for ‘safer environment interventions’ in the reduction of drug-related harm. Addiction, 101 (10), 1384–1393. 10.1111/j.1360-0443.2006.01556.x. [DOI] [PubMed] [Google Scholar]
  53. Robertson AM, Vera AY, Gallardo M, Pollini RA, Patterson TL, Case P, … Strathdee SA (2010). Correlates of seeking injection assistance among injection drug users in Tijuana, Mexico. American Journal on Addictions, 19(4), 357–363. 10.1111/j.1521-0391.2010.00053.x AJAD53 [pii]. [DOI] [PMC free article] [PubMed] [Google Scholar]
  54. Roux P, Rojas Castro D, Ndiaye K, Debrus M, Protopopescu C, Le Gall JM, … Carrieri P (2016). Increased uptake of HCV testing through a community-based educational intervention in difficult-to-reach people who inject drugs: Results from the ANRS-AERLI study. PLoS One, 11(6), e0157062 10.1371/journal.pone.0157062. [DOI] [PMC free article] [PubMed] [Google Scholar]
  55. Singer M, & Clair S (2003). Syndemics and public health: Reconceptualizing disease in bio-social context. Medical Anthropology Quarterly, 17(4), 423–441. 10.1525/maq.2003.17.4.423. [DOI] [PubMed] [Google Scholar]
  56. Small W, Wood E, Tobin D, Rikley J, Lapushinsky D, & Kerr T (2012). The injection support team: A peer-driven program to address unsafe injecting in a Canadian setting. Substance Use and Misuse, 47(5), 491–501. 10.3109/10826084.2012.644107. [DOI] [PubMed] [Google Scholar]
  57. Spittal PM, Craib KJ, Wood E, Laliberte N, Li K, Tyndall MW, … Schechter MT (2002). Risk factors for elevated HIV incidence rates among female injection drug users in Vancouver. CMAJ, 166(7), 894–899. [PMC free article] [PubMed] [Google Scholar]
  58. Ti L, Hayashi K, Kaplan K, Suwannawong P, Wood E, & Kerr T (2015). Contextual factors associated with rushed injecting among people who inject drugs in Thailand. Prevention Science, 16(2), 313–320. 10.1007/s11121-014-0477-z. [DOI] [PubMed] [Google Scholar]
  59. Van Den Berg C, Smit C, Van Brussel G, Coutinho R, & Prins M (2007). Full participation in harm reduction programmes is associated with decreased risk for human immunodeficiency virus and hepatitis C virus: Evidence from the Amsterdam Cohort Studies among drug users. Addiction, 102(9), 1454–1462. 10.1111/j.1360-0443.2007.01912.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  60. Watters JK, & Biernacki P (1989). Targeted sampling: Options for the study of hidden populations. Social Problems, 36, 416–430. [Google Scholar]
  61. Weatherby N, Needle RH, Cesari H, Booth R, McCoy CB, Watters JK, … Chitwood DD (1994). Validity of self-reported drug use among injection drug users recruited through street outreach. Evaluation and Program Planning, 17, 347–355. [Google Scholar]
  62. Wheeler E, Jones TS, Gilbert MK, Davidson PJ, Centers for Disease, C., & Prevention (2015). Opioid overdose prevention programs providing naloxone to laypersons—United States, 2014. MMWR Morbidity and Mortality Weekly Report, 64(23), 631–635. [PMC free article] [PubMed] [Google Scholar]
  63. Wood E, Tyndall MW, Spittal PM, Li K, Kerr T, Hogg RS, … Schechter MT (2001). Unsafe injection practices in a cohort of injection drug users in Vancouver: Could safer injecting rooms help? Canadian Medical Association Journal, 165(4), 405–410. [PMC free article] [PubMed] [Google Scholar]
  64. Wood RA, Wood E, Lai C, Tyndall MW, Montaner JSG, & Kerr T (2008). Nurse-delivered safer injection education among a cohort of injection drug users: Evidence from the evaluation of Vancouver’s supervised injection facility. International Journal of Drug Policy, 19(3), 183–188. 10.1016/j.drugpo.2008.01.003. [DOI] [PubMed] [Google Scholar]
  65. Wood E, Kerr T, Spittal PM, Small W, Tyndall MW, O’Shaughnessy MV, … Schechter MT (2003). An external evaluation of a peer-run “unsanctioned” syringe exchange program. Journal of Urban Health, 80(3), 455–464. 10.1093/jurban/jtg052. [DOI] [PMC free article] [PubMed] [Google Scholar]
  66. Wood E, Spittal PM, Kerr T, Small W, Tyndall MW, O’Shaughnessy MV, … Schechter MT (2003). Requiring help injecting as a risk factor for HIV infection in the Vancouver epidemic: Implications for HIV prevention. Canadian Journal of Public Health, 94(5), 355–359. [DOI] [PMC free article] [PubMed] [Google Scholar]
  67. Zibbell J, Iqbal K, Patel RC, Suryaprasad AG, Sanders KJ, Moore-Moravian L, … Holtzman D (2015). Increases in hepatitis C virus infection related to injection drug use among persons aged < 30 years—Kentucky, Tennessee, Virginia, and West Virginia, 2006–2012. Morbidity and Mortality Weekly Report: MMWR, 64(17), 453–458. [PMC free article] [PubMed] [Google Scholar]
  68. Zibbell JE, Asher AK, Patel RC, Kupronis B, Iqbal K, Ward JW, … Holtzman D (2017). Increases in acute hepatitis C virus infection related to a growing opioid epidemic and associated injection drug use, United States, 2004 to 2014. American Journal of Public Health, e1–e7. 10.2105/ajph.2017.304132. [DOI] [PMC free article] [PubMed] [Google Scholar]

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