Abstract
Washington, DC has among the highest HIV/AIDS rates in the US. Gender differences among injection drug users (IDUs) may be associated with adoption of prevention opportunities including needle exchange programs, HIV testing, psychosocial support, and prevention programming. National HIV Behavioral Surveillance data on current IDUs aged ≥18 were collected from 8/09 to 11/09 via respondent-driven sampling in Washington, DC. HIV status was assessed using oral OraQuick with Western Blot confirmation. Weighted estimates were derived using RDSAT. Stata was used to characterize the sample and differences between male and female IDU, using uni-, bi-, and multivariable methods. Factors associated with HIV risk differed between men and women. Men were more likely than women to have had a history of incarceration (86.6 % vs. 66.8 %, p < 0.01). Women were more likely than men to have depressive symptoms (73.9 % vs. 47.4 %, p < 0.01), to have been physically or emotionally abused (66.1 % vs. 16.1 %, p < 0.0001), to report childhood sexual abuse (42.7 % vs. 4.7 %, p < 0.0001), and pressured or forced to have sex (62.8 % vs. 4.0 %, p < 0.0001); each of these differences was significant in the multivariable analysis. Despite a decreasing HIV/AIDS epidemic among IDU, there remain significant gender differences with women experiencing multiple threats to psychosocial health, which may in turn affect HIV testing, access, care, and drug use. Diverging needs by gender are critical to consider when implementing HIV prevention strategies.
Keywords: HIV/AIDS, Behavioral surveillance, Gender, IDU, HIV/AIDS prevention
Background
Centers for Disease Control and Prevention (CDC) surveillance data reveal that at the end of 2008, 16,513 persons were living with a diagnosis of HIV infection in the District of Columbia (DC), making it one of the cities with the highest prevalence of HIV/AIDS cases in the US.1 While the epidemic among injecting drug users (IDU) has slowed, there remains a concentrated epidemic of HIV among IDU; recent DC surveillance data reveal that 21.4 % of all new AIDS cases are attributed to injection drug use, and it is the second leading cause of new AIDS cases among women.1 In DC, half (47.5 %) of all persons acquiring HIV through injection drug use are considered late testers, those who progress to AIDS within 12 months of their HIV diagnosis, and the largest proportion of deaths attributable to HIV was among IDU (30.7 %).1 Despite effective prevention methods available to IDU including needle exchange programs (NEP),2–5 HIV among IDU does not appear to be moving towards elimination.
Previous literature suggests consistent differences between men and women IDU in behaviors as well as HIV-prevalence.6–17 In DC, IDU, especially women IDU, are poorly characterized, contributing to difficulties in addressing their HIV prevention needs. For example, NEPs provide one of the most important methods of HIV prevention among IDU,2–5 yet barriers to their utilization by women in DC have not yet been described in the literature. Locally, recent changes in the law allow for NEPs to be supported by federal funds,18 providing a new opportunity in DC for HIV prevention when funds are available,18–20 and organizations are operational.21 Gender differences among IDU may affect access to other prevention opportunities as well, including HIV testing, and ancillary support such as mental health and domestic violence care. The paucity of information available surrounding experiences of women IDU with regard to HIV prevention strategies makes it difficult to predict how well these strategies can be implemented among them or remove barriers to their uptake. The purpose of this analysis was to assess the constellation of behavioral and psychosocial risk factors associated with gender among IDU to inform development of novel HIV prevention strategies.
Methods
Data were obtained through the Centers for Disease Control and Prevention (CDC)-funded National HIV Behavioral Surveillance (NHBS) DC site. NHBS methods have been described elsewhere.22–24 Briefly, cross-sectional behavioral and HIV testing data from men who have sex with men, IDU, and heterosexuals at increased risk of HIV infection are collected in repeated, annual community-based surveys. For NHBS-IDU-2, a sample of IDU was recruited between August and November 2009 via respondent-driven sampling (RDS), a chain-referral method which accesses hard to reach populations and provides estimates generalizable to the population of networks from which they are drawn; this method has been used in populations of IDU by other authors.25–36 Non-randomly identified “seeds” are given coupons to recruit three people from their social and/or sexual networks to join the study, and each subsequent eligible person completing the interview is provided with up to three coupons with which to recruit their network members. Eligible individuals lived in the metropolitan DC area, were 18 years old and older, and injected drugs in the past 12 months based on verification of injection sites or successful completion of a knowledge screener specific to IDU. All subjects met eligibility criteria, had a coupon, completed the survey in English, and provided informed consent. Following administration of an anonymous, interviewer-administered questionnaire on sexual, drug use, and health care utilization behaviors, a rapid oral HIV screening test (OraQuick Rapid 1/2 ADVANCE®, Bethlehem, PA) was conducted; those who screened positive or self-reported positive provided a sample of oral fluid for OraSure Western Blot confirmation of HIV status. Participants received $25.00 for the interview, $10.00 for the HIV screening, and $10.00 for each eligible participant referred. Subjects screening HIV-positive were immediately referred into care. All activities were overseen by the CDC, approved by DC Department of Health (DOH) and The George Washington University (GWU) Institutional Review Boards, and guided by the GWU HIV Research Community Advisory Board.
Analytic Methods
Provided that RDS assumptions are met,27,29,30,37 RDS allows for a final sample independent from the seeds, and for calculation of sampling probabilities that provide population-based estimates of variables under study. Chi-square tests were used to compare demographic and behavioral characteristics between men and women. Variables that were significantly associated upon weighted bivariable analysis were tested for inclusion in the logistic regression models to describe HIV-related and psychosocial characteristics associated with gender. Demographic confounders remained if they were statistically significant or if addition or removal resulted in a change of ±5 % in the estimates. All data reported were weighted for RDS using RDSAT, version 5.6.0 (Ithaca, NY). SAS version 9.1 (Cary, NC), and Stata 10.0se (College Station, TX) were used for analysis.
Results
Overall Sample Characteristics
Of 553 participants, the majority was male (62.7 %), over 50 years of age (57.9 %), self-identified as heterosexual (94.3 %), a high school graduate or less (76.6 %), unemployed (52.8 %), and had an annual income of under $10,000 (65.3 %). Five were transgender and eliminated from the gender comparison due to small sample size. The majority of the sample (96.4 %) identified as black. Most participants had health insurance (87.9 %), and of those who did, most had Medicaid (83.2 %). A large proportion of the population (49.1 %) had ever been homeless, and 79.6 % had ever been in prison, juvenile detention, or jail, with 22.6 % having been arrested in the past year. Thirteen percent of the participants were confirmed HIV-positive, and 30.3 % of those were unaware of their status.
Demographic Differences Associated with Gender
As shown in Table 1, of the 548 participants eligible for the gender comparison, men were significantly older than women (p < 0.01), with the largest proportion of men found in the 51–60 year old group (52.6 %), and the largest proportion of women in the 41–50 year old group (48.4 %). Although nearly all study participants were black, men were more likely to be black than women (99.3 % vs. 91.1 %, p < 0.0001). Women were more likely to report being bisexual or homosexual than men (12.7 % vs. 1.2 %, p < 0.0001). Women were more likely than men to currently have health insurance (93.1 % vs. 84.4 %, p < 0.05), yet among those who were insured, females were more likely than males to have Medicaid (92.7 % vs. 76.0 %, p < 0.001; data not shown in table).
Table 1.
Male n = 342 n ( %) | Female n = 206 n ( %) | Adjusted behavioral factors associated with being femalea | |
---|---|---|---|
NHBS HIV screening test positive | 13.1 | 12.7 | 1.75 (1.02–3.03)* |
Ever tested for HIV | 97.1 | 98.7 | – |
Demographic characteristics | |||
Age (years)** | |||
18–40 | 6.4 | 5.4 | – |
41–50 | 30.3 | 48.4 | – |
51–60 | 52.6 | 45.2 | – |
61+ | 10.6 | 1.0 | – |
Black race*** | 99.3 | 91.1 | – |
Sexual orientation*** | |||
Heterosexual | 98.7 | 87.3 | – |
Homosexual or bisexual | 1.2 | 12.7 | – |
High school graduate or less | 74.2 | 80.7 | – |
Unemployed | 51.1 | 52.5 | – |
Homeless last 12 months*** | 15.2 | 10.5 | 0.83 (0.58–1.18) |
Ever been to jail, prison, or juvenile detention** | 86.6 | 66.8 | 0.40 (0.25–0.63)*** |
Psychosocial characteristics | |||
Depressive symptoms within the last week (CES-D ≥16)** | 47.4 | 73.9 | 3.38 (2.20–5.20)*** |
Ever physically or emotionally abused*** | 16.1 | 66.1 | 4.50 (3.03–6.78)*** |
Ever pressured/forced to have sex*** | 4.0 | 62.8 | 0.72 (0.19–2.66) |
Ever experienced child abuse*** | 4.7 | 42.7 | 5.94 (3.57–9.91)*** |
Characteristics of last sex partner | |||
Type of partner at last sex** | |||
Main | 72.0 | 79.9 | 0.91 (0.48–1.71) |
Casual | 23.2 | 8.5 | – |
Exchange | 4.8 | 11.6 | – |
Partner ever injected drugs*** | 39.1 | 87.4 | 5.11 (3.12–8.37)*** |
Drug use behaviors (not mutually exclusive) | |||
Injection drug use, last 12 months | |||
Heroin | 99.6 | 99.2 | – |
Speedballs | 51.5 | 50.1 | – |
Powdered Cocaine | 31.4 | 26.6 | – |
Crack Cocaine | 14.0 | 16.5 | – |
Non-injection drug use, last 12 months | 1.16 (0.81–1.66) | ||
Heroin | 68.4 | 73.6 | – |
Crack Cocaine | 70.0 | 72.4 | – |
Marijuana* | 70.7 | 50.7 | – |
Pain Killers | 37.8 | 50.4 | – |
Downers* | 24.7 | 45.3 | – |
Powdered Cocaine | 44.5 | 40.9 | – |
Ecstasy | 13.4 | 9.1 | – |
Needle sharing behaviors | |||
Shared needles with last injecting partner* | 10.7 | 26.6 | 1.91 (1.02–3.59)* |
Last shared needles with sex partner* | 9.7 | 25.5 | 2.39 (1.35–4.23)** |
Although transgender individuals are allowed in NHBS-IDU, not all behavioral information is collected for them and the very small sample size limits their analysis; thus for the purpose of this analysis, they were excluded. All bivariable estimates are adjusted using RDSAT. OR and 95 % CI are unweighted, given no significant differences being found on comparison of weighted and unweighted bivariable proportions
*p < 0.05; **p < 0.01; ***p < 0.001
aFactors associated with being female after adjustment for age, race, incarceration history, employment status, and condom use at last sex except for evaluation of incarceration as an outcome, which is adjusted for age, race, employment status, and condom use at last sex
HIV and Risk Factor Differences Associated with Gender
Factors associated with HIV risk differed between men and women. Men were more likely to be currently homeless compared to women (42.7 % vs. 23.1 %, p < 0.001) and more likely to have had a history of incarceration (86.6 % vs. 66.8 %, p < 0.01), including being arrested and booked in the past 12 months (30.1 % vs. 10.2 %, p < 0.001; data not shown in table). Women were more likely than men to have depressive symptoms defined by a Center for Epidemiologic Studies Depression Scale (CES-D) score ≥16 (73.9 % vs. 47.4 %, p < 0.01), and to have ever been physically or emotionally abused by someone close to them (66.1 % vs. 16.1 %, p < 0.0001). Women were also more likely to report having experienced childhood sexual abuse (42.7 % vs. 4.7 %, p < 0.0001) and having been pressured or forced to have sex (62.8 % vs. 4.0 %, p < 0.0001), although if they were abused, men were more likely than women to report that this occurred within the past 12 months (58.2 % vs. 14.1 %, p < 0.01) (data not shown in table). Characteristics of sexual partners differed between men and women as well. Men were more likely than women to have a casual partner as their last sex partner (23.2 % vs. 8.5 %, p < 0.007), where a higher proportion of women reported having an exchange partner at last sex (11.6 % vs. 4.8 %, p < 0.007). Women were more likely to have a last sex partner who injected drugs, ever used crack, ever been in prison or jail for more than 24 h, and was older (p < 0.01 for all variables). There were no unadjusted differences by gender with regard to HIV status or HIV testing behaviors.
As shown in Table 1, although heroin, cocaine, and speedball (combination of heroin and cocaine) use did not differ by gender, women were significantly more likely to report using injected oxycontin, downers, and other club drugs, such as ketamine, gamma-hydroxybutyric acid, and poppers (amyl nitrite). However, men were more likely than females to report using marijuana. Men were younger at their first injection and had a longer injection career than females [median years 18 (IQR 16–22) vs. median 21 (IQR 17–28), p < 0.0001] (data not shown in table). In terms of needle acquisition, women were more likely than men to report getting their needles from a friend or partner (73.9 % vs. 59.5 %, p < 0.05); women were less likely to utilize sterile needles or cookers, cotton, or water from a NEP than men, although these differences were not statistically significant (p < 0.11 and p < 0.08, respectively) (data not shown in table). Women were significantly more likely to report needle sharing with the last injection compared to men (31.5 % vs. 26.6 %, p < 0.05). In addition, a higher proportion of women reported that their last injection partner was also a sex partner (25.5 % vs. 9.7 %, p < 0.05), while a higher proportion of men reported their last injection partner to be a friend or acquaintance (84.7 % vs. 68.9 %, p < 0.05; data not shown in table).
Multivariable Associations with Gender
In multivariable logistic regression, women had significantly different risk factors and psychosocial lifetime experiences than men. As shown in Table 1, for confounders, being a woman was independently associated with being HIV-positive [adjusted odds ratio (AOR) 1.75 (95 % CI 1.02–3.03)], reduced odds of having a history of incarceration [AOR 0.40 (95 % CI 0.25–0.63)], depressive symptoms [AOR 3.38 (95 % CI 2.20–5.20)], physical/emotional [AOR 4.50 (95 % CI 3.03–6.78)], and sexual child abuse [AOR 5.94 (95 % CI 3.57–9.91), having a last sex partner who injected drugs [AOR 5.11 (95 % CI 3.12–8.37)] or used crack [AOR 1.77 (95 % CI 1.11–2.83)], had a history of incarceration [AOR 5.78 (95 % CI 3.50–9.54)], or was older than the participant [AOR 5.75 (95 % CI 3.46–9.57)], sharing needles in the last 12 months [AOR 2.25 (95 % CI 1.50–3.39)] and with last injecting partner [AOR 1.91 (95 % CI 1.02–3.59)], and sharing needles at last injection with a sex partner [AOR 2.39 (95 % CI 1.35–4.23)].
Discussion
This study of IDU in the District of Columbia provides the first community-based estimate of behaviors among this population, with a focus on the key differences between men and women. In this study, we found women IDU were more likely to have depressive symptoms, be younger, and have experienced abuse than men IDU. Women had greater odds of having HIV-related risk factors including needle sharing and high-risk sex partners. After adjustment for confounders, women were more likely to be HIV-positive. The elevated prevalence of psychosocial correlates of HIV including depressive symptoms, having high-risk sexual partners, and needle sharing behaviors after adjustment for confounders, suggest that the constellation of factors affecting women IDU differ substantially from men.
Like other authors, we found that injection behaviors differ substantially by gender,6–11,13–15,17,38–43 with women more likely to be injected by a sexual partner than friends or acquaintances, share needles, and use a greater variety of drugs than men. We found that men experienced HIV risk behaviors as well, with increased homelessness and incarceration relative to women, though these differences were attenuated after adjustment for confounders; indeed, the constellation of psychosocial issues including depression was greater among women than men, as other authors have found.7,41,44–46 Other authors have noted differences in injection rituals, practices, and injection partner selection between men and women7,10,14,15,17,39; identification of needs that are fulfilled by such practices and that drive their selection, may inform development of innovative prevention approaches developed specifically for women. Our findings echo those of other authors, with some differences: in a convenience sample of younger IDU, Doherty et al.15,16 found women had elevated risk of HIV and while they had similar patterns of injection initiation, women were no more likely to be injected by sex partners at injection initiation. Evans et al.17 found no significant differences between men and women with respect to education, race, housing, yet, as we also found, had increased odds of being injected by a sex partner relative to men. These findings suggest that—especially in view of overlapping epidemics among IDU and heterosexual populations23,24—identifying new ways to reach women and provide services to address overall as well as HIV prevention needs is a critical step in slowing the HIV epidemic in the District of Columbia.
There are several limitations to this study. As with most studies of sexual and drug use risk behaviors, the majority of information is obtained via self-report and participants may have had difficulty recalling information or may have underreported socially undesirable behaviors. As an interviewer-administered questionnaire, it is possible that there were inter- and/or intra-interviewer differences in the reading of questions or the recording of answers, although extensive training and ongoing quality assurance were performed to avoid these errors. Although there is a possibility that some non-IDUs enrolled in the study, participants were screened for physical signs of recent injection. RDS has been shown to be an effective recruitment strategy for hidden populations including IDU47–51; despite concerns that RDS could negatively impact data collection or interpretation of analysis, we found no untoward effect of RDS on the participants. Finally, cross-sectional studies are not able to demonstrate causality.
This study suggests that women IDU have diverging needs, risk factors, and behaviors from their male counterparts. Future studies are needed to develop improved prevention strategies for women IDU, even in the presence of a slowing IDU epidemic. The high prevalence of abuse, depressive symptoms, and needle sharing among women highlight the need for gender-specific prevention approaches to slow HIV among IDU; given the overlapping nature of the epidemics in DC, this has implications for the overall population as well as the IDU population. By focusing not only on HIV-related injection and sexual behaviors, this study adds to the dialogue regarding gender differences by characterizing differences with respect to other service needs and potential barriers to NEP uptake. Future studies to evaluate women IDU continue to be necessary to more fully expand on our knowledge of this population.
Acknowledgments
For their assistance and expertise throughout the study, the authors acknowledge Dr. Amanda Castel of GWU SPHHS; Dr. Amy Lansky, Dr. Elizabeth DiNenno, Ms. Tricia Martin, and Dr. Isa Miles of CDC; and the WORD UP Community Advisory Board Members. Interviewers Luz Montanez, Julie Archer, Ashley Clegg, Megan Condrey, Daniel Choi, Keith Egan, and Mariel Marlow. This study could not have been conducted without the enormous support of our many community partners. For their participation in and support of NHBS, the study team would like to acknowledge the participants of the study and the citizens of the District of Columbia, without whom this study would not have been possible.
Funding source
This study was funded by District of Columbia, Department of Health/HIV/AIDS, Hepatitis, STD and Tuberculosis Administration (DC DOH/HAHSTA), Contract Number POHC-2006-C-0030, funded in part by Grant Number PS000966-01, from the US Department of Health and Human Services (DHHS)/Centers for Disease Control and Prevention (CDC). All co-authors have reviewed and approved of the final draft of the paper including those from DC DOH/HAHSTA. Under the Partnership contract, DC DOH/HAHSTA had the right to review and approve the manuscript. The content of this publication does not necessarily reflect the views or policies of DHHS/CDC and responsibility for the content rests solely with the authors.
References
- 1.DC Department of Health HIV/AIDS, Hepatitis, STD, and TB Administration. District of Columbia HIV/AIDS, Hepatitis, STD, and TB Epidemiology 2009 Annual Report Update, 2010.
- 2.Vlahov D, Des Jarlais DC, Goosby E, et al. The role of epidemiology in needle exchange programs. Am J Public Health. 2000;90(9):1390–2. doi: 10.2105/AJPH.90.9.1390. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Holtzman D, Barry V, Ouellet LJ, et al. The influence of needle exchange programs on injection risk behaviors and infection with hepatitis C virus among young injection drug users in select cities in the United States, 1994–2004. Prev Med. 2009;49(1):68–73. doi: 10.1016/j.ypmed.2009.04.014. [DOI] [PubMed] [Google Scholar]
- 4.Vlahov D, Des Jarlais DC, Goosby E, et al. Needle exchange programs for the prevention of human immunodeficiency virus infection: epidemiology and policy. Am J Epidemiol. 2001;154(12 Suppl):S70–7. doi: 10.1093/aje/154.12.S70. [DOI] [PubMed] [Google Scholar]
- 5.Vlahov D, Junge B, Brookmeyer R, et al. Reductions in high-risk drug use behaviors among participants in the Baltimore needle exchange program. J Acquir Immune Defic Syndr Hum Retrovirol. 1997;16(5):400–6. doi: 10.1097/00042560-199712150-00014. [DOI] [PubMed] [Google Scholar]
- 6.Absalon J, Fuller CM, Ompad DC, et al. Gender differences in sexual behaviors, sexual partnerships, and HIV among drug users in New York City. AIDS Behav. 2006;10(6):707–15. doi: 10.1007/s10461-006-9082-x. [DOI] [PubMed] [Google Scholar]
- 7.Riehman KS, Kral AH, Anderson R, Flynn N, Bluthenthal RN. Sexual relationships, secondary syringe exchange, and gender differences in HIV risk among drug injectors. J Urban Health. 2004;81(2):249–59. doi: 10.1093/jurban/jth111. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Garcia de la Hera M, Ferreros I, del Amo J, et al. Gender differences in progression to AIDS and death from HIV seroconversion in a cohort of injecting drug users from 1986 to 2001. J Epidemiol Community Health. 2004;58(11):944–50. doi: 10.1136/jech.2003.017475. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Spijkerman IJ, Langendam MW, van Ameijden EJ, Coutinho RA, van den Hoek A. Gender differences in clinical manifestations before AIDS diagnosis among injecting drug users. Eur J Epidemiol. 1998;14(3):213–8. doi: 10.1023/A:1007416920420. [DOI] [PubMed] [Google Scholar]
- 10.Gollub EL, Rey D, Obadia Y, Moatti JP. Gender differences in risk behaviors among HIV+ persons with an IDU history. The link between partner characteristics and women’s higher drug-sex risks. The Manif 2000 Study Group. Sex Transm Dis. 1998;25(9):483–8. doi: 10.1097/00007435-199810000-00008. [DOI] [PubMed] [Google Scholar]
- 11.Singh BK, Koman JJ, 3rd, Williams JS, Catan VM, Souply KL. Sex differences in self-report of physical health by injection drug users. Int J Addict. 1994;29(2):275–83. doi: 10.3109/10826089409047381. [DOI] [PubMed] [Google Scholar]
- 12.McDonald C, Loxley W, Marsh A. A bridge too near? Injecting drug users’ sexual behaviour. AIDS Care. 1994;6(3):317–26. doi: 10.1080/09540129408258643. [DOI] [PubMed] [Google Scholar]
- 13.Dwyer R, Richardson D, Ross MW, Wodak A, Miller ME, Gold J. A comparison of HIV risk between women and men who inject drugs. AIDS Educ Prev. 1994;6(5):379–89. [PubMed] [Google Scholar]
- 14.Montgomery SB, Hyde J, De Rosa CJ, et al. Gender differences in HIV risk behaviors among young injectors and their social network members. Am J Drug Alcohol Abuse. 2002;28(3):453–75. doi: 10.1081/ADA-120006736. [DOI] [PubMed] [Google Scholar]
- 15.Doherty MC, Garfein RS, Monterroso E, Latkin C, Vlahov D. Gender differences in the initiation of injection drug use among young adults. J Urban Health. 2000;77(3):396–414. doi: 10.1007/BF02386749. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Latkin CA, Mandell W, Knowlton AR, et al. Gender differences in injection-related behaviors among injection drug users in Baltimore, Maryland. AIDS Educ Prev. 1998;10(3):257–63. [PubMed] [Google Scholar]
- 17.Evans JL, Hahn JA, Page-Shafer K, et al. Gender differences in sexual and injection risk behavior among active young injection drug users in San Francisco (the UFO Study) J Urban Health. 2003;80(1):137–46. doi: 10.1093/jurban/jtg137. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Frears D. House passes bill that lifts ban on using federal money for needle exchanges. Washington Post 2009.
- 19.Pershing B. Spending bill spares D.C. needle exchange, Chesapeake cleanup plan. Washington Post 2011.
- 20.Opinion EB. Bargaining away the District’s rights. Washington Post 2011.
- 21.Dvorak P. End of needle exchange marks loss of a bulwark in D.C.’s AIDS fight. Washington Post 2011;2/24/11.
- 22.Magnus M, Kuo I, Phillips G, 2nd, et al. Elevated HIV prevalence despite lower rates of sexual risk behaviors among black men in the District of Columbia who have sex with men. AIDS Patient Care STDS. 2010;24(10):615–22. doi: 10.1089/apc.2010.0111. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23.Magnus M, Kuo I, Shelley K, et al. Risk factors driving the emergence of a generalized heterosexual HIV epidemic in Washington, District of Columbia networks at risk. Aids. 2009;23(10):1277–84. doi: 10.1097/QAD.0b013e32832b51da. [DOI] [PubMed] [Google Scholar]
- 24.Kuo I, Greenberg AE, Magnus M, et al. High prevalence of substance use among heterosexuals living in communities with high rates of AIDS and poverty in Washington, DC. Drug Alcohol Depend. 2011;117:139–44. [DOI] [PubMed]
- 25.Abdul-Quader AS, Heckathorn DD, McKnight C, et al. Effectiveness of respondent-driven sampling for recruiting drug users in New York City: findings from a pilot study. J Urban Health. 2006;83(3):459–76. doi: 10.1007/s11524-006-9052-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 26.Abdul-Quader AS, Heckathorn DD, Sabin K, Saidel T. Implementation and analysis of respondent driven sampling: lessons learned from the field. J Urban Health. 2006;83(6 Suppl):i1–5. doi: 10.1007/s11524-006-9108-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27.Abdul-Quader AS, Heckathorn DD, Sabin K, Saidel T, Ramirez-Valles J, Heckathorn DD, Vázquez R, Diaz RM, Campbell RT. From networks to populations: the development and application of respondent-driven sampling among IDUs and Latino gay men. AIDS Behav. 2005;9(4):387–402. doi: 10.1007/s10461-005-9012-3. [DOI] [PubMed] [Google Scholar]
- 28.Deiss RG, Brouwer KC, Loza O, Lozada RM, Ramos R, FirestoneCruz MA, Patterson TL, Heckathorn DD, Frost SD, Strathdee SA. High-risk sexual and drug using behaviors among male injection drug users who have sex with men in 2 Mexico–US border cities. Sex Transm Dis. 2008;35:243–249. doi: 10.1097/OLQ.0b013e31815abab5. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 29.Heckathorn D. Respondent-driven sampling: a new approach to the study of hidden populations. Social Problems. 1997;44(2):174–99. doi: 10.2307/3096941. [DOI] [Google Scholar]
- 30.Heckathorn D. Respondent-driven sampling II: deriving valid population estimates from chain-referral samples of hidden populations. Social Problems. 2002;49(1):11–34. doi: 10.1525/sp.2002.49.1.11. [DOI] [Google Scholar]
- 31.Heckathorn D. Extensions of respondent-driven sampling: analyzing continuous variables and controlling for differential recruitment. Sociological Methodology 2007;37:151–207.
- 32.Magnani R, Sabin K, Saidel T, Heckathorn D. Review of sampling hard-to-reach and hidden populations for HIV surveillance. Aids. 2005;19(Suppl 2):S67–72. doi: 10.1097/01.aids.0000172879.20628.e1. [DOI] [PubMed] [Google Scholar]
- 33.McKnight C, Des Jarlais D, Bramson H, et al. Respondent-driven sampling in a study of drug users in New York City: notes from the field. J Urban Health. 2006;83(6 Suppl):i54–9. doi: 10.1007/s11524-006-9102-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 34.Ramirez-Valles J, Heckathorn DD, Vazquez R, Diaz RM, Campbell RT. From networks to populations: the development and application of respondent-driven sampling among IDUs and Latino gay men. AIDS Behav. 2005;9(4):387–402. doi: 10.1007/s10461-005-9012-3. [DOI] [PubMed] [Google Scholar]
- 35.Semaan S, Santibanez S, Garfein RS, Heckathorn DD, Des Jarlais DC. Ethical and regulatory considerations in HIV prevention studies employing respondent-driven sampling. Int J Drug Policy 2008. Am J Public Health. 2010;100:582–3. [DOI] [PubMed]
- 36.Stormer A, Tun W, Guli L, et al. An analysis of respondent driven sampling with Injection Drug Users (IDU) in Albania and the Russian Federation. J Urban Health. 2006;83(6 Suppl):i73–82. doi: 10.1007/s11524-006-9105-y. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 37.Lansky A, Drake A, DiNenno E, Lee CW. HIV behavioral surveillance among the U.S. general population. Public Health Rep. 2007;122(Suppl 1):24–31. doi: 10.1177/00333549071220S105. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 38.Woods WJ, Lindan CP, Hudes ES, Boscarino JA, Clark WW, Avins AL. HIV infection and risk behaviors in two cross-sectional surveys of heterosexuals in alcoholism treatment. J Stud Alcohol. 2000;61(2):262–6. doi: 10.15288/jsa.2000.61.262. [DOI] [PubMed] [Google Scholar]
- 39.Unger JB, Kipke MD, De Rosa CJ, Hyde J, Ritt-Olson A, Montgomery S. Needle-sharing among young IV drug users and their social network members: the influence of the injection partner’s characteristics on HIV risk behavior. Addict Behav. 2006;31(9):1607–18. doi: 10.1016/j.addbeh.2005.12.007. [DOI] [PubMed] [Google Scholar]
- 40.Bennett GA, Velleman RD, Barter G, Bradbury C. Gender differences in sharing injecting equipment by drug users in England. AIDS Care. 2000;12(1):77–87. doi: 10.1080/09540120047495. [DOI] [PubMed] [Google Scholar]
- 41.Wisniewski AB, Apel S, Selnes OA, Nath A, McArthur JC, Dobs AS. Depressive symptoms, quality of life, and neuropsychological performance in HIV/AIDS: the impact of gender and injection drug use. J Neurovirol. 2005;11(2):138–43. doi: 10.1080/13550280590922748. [DOI] [PubMed] [Google Scholar]
- 42.Cruz MF, Mantsios A, Ramos R, et al. A qualitative exploration of gender in the context of injection drug use in two US-Mexico border cities. AIDS Behav. 2007;11(2):253–62. doi: 10.1007/s10461-006-9148-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 43.Strathdee SA, Galai N, Safaiean M, et al. Sex differences in risk factors for hiv seroconversion among injection drug users: a 10-year perspective. Arch Intern Med. 2001;161(10):1281–8. doi: 10.1001/archinte.161.10.1281. [DOI] [PubMed] [Google Scholar]
- 44.Mandell W, Kim J, Latkin C, Suh T. Depressive symptoms, drug network, and their synergistic effect on needle-sharing behavior among street injection drug users. Am J Drug Alcohol Abuse. 1999;25(1):117–27. doi: 10.1081/ADA-100101849. [DOI] [PubMed] [Google Scholar]
- 45.Latkin CA, Mandell W. Depression as an antecedent of frequency of intravenous drug use in an urban, nontreatment sample. Int J Addict. 1993;28(14):1601–12. doi: 10.3109/10826089309062202. [DOI] [PubMed] [Google Scholar]
- 46.Purcell DW, Mizuno Y, Metsch LR, et al. Unprotected sexual behavior among heterosexual HIV-positive injection drug using men: associations by partner type and partner serostatus. J Urban Health. 2006;83(4):656–68. doi: 10.1007/s11524-006-9066-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 47.Burt RD, Hagan H, Sabin K, Thiede H. Evaluating respondent-driven sampling in a major metropolitan area: comparing injection drug users in the 2005 Seattle area national HIV behavioral surveillance system survey with participants in the RAVEN and Kiwi studies. Ann Epidemiol. 2005;20(2):159–67. doi: 10.1016/j.annepidem.2009.10.002. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 48.Abramovitz D, Volz EM, Strathdee SA, Patterson TL, Vera A, Frost SD. Using respondent-driven sampling in a hidden population at risk of HIV infection: who do HIV-positive recruiters recruit? Sex Transm Dis. 2009;36(12):750–6. doi: 10.1097/OLQ.0b013e3181b0f311. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 49.Lansky A, Abdul-Quader AS, Cribbin M, et al. Developing an HIV behavioral surveillance system for injecting drug users: the National HIV Behavioral Surveillance System. Public Health Rep. 2007;122(Suppl 1):48–55. doi: 10.1177/00333549071220S108. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 50.Platt L, Wall M, Rhodes T, et al. Methods to recruit hard-to-reach groups: comparing two chain referral sampling methods of recruiting injecting drug users across nine studies in Russia and Estonia. J Urban Health. 2006;83(6 Suppl):i39–53. doi: 10.1007/s11524-006-9101-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 51.Robinson WT, Risser JM, McGoy S, et al. Recruiting injection drug users: a three-site comparison of results and experiences with respondent-driven and targeted sampling procedures. J Urban Health. 2006;83(6 Suppl):i29–38. doi: 10.1007/s11524-006-9100-3. [DOI] [PMC free article] [PubMed] [Google Scholar]