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. Author manuscript; available in PMC: 2013 Jul 22.
Published in final edited form as: AIDS. 2011 Oct 23;25(16):2009–2018. doi: 10.1097/QAD.0b013e32834b005d

A Prospective Study of Frequency and Correlates of Intimate Partner Violence among African Heterosexual HIV Serodiscordant Couples

Edwin Were 1, Kathryn Curran 2,4, Sinead Delany-Moretlwe 5, Edith Nakku-Joloba 6, Nelly R Mugo 7, James Kiarie 7, Elizabeth A Bukusi 2,7,8, Connie Celum 2,3,4, Jared M Baeten 2,3,4; for the Partners in Prevention HSV/HIV Transmission Study Team
PMCID: PMC3718250  NIHMSID: NIHMS483724  PMID: 21811146

Abstract

Background

Intimate partner violence (IPV) is common worldwide and is an important consideration in couples HIV voluntary counseling and testing (CVCT), especially for HIV serodiscordant couples (i.e., in which only one member is HIV infected).

Design

Prospective study of 3408 HIV serodiscordant couples (2299 in which the HIV infected partner was female) from 7 countries from East and Southern Africa.

Methods

At quarterly visits during up to 2 years of follow-up, participants were asked, separately, about IPV perpetrated against them by their partner during the prior 3 months. Correlates of IPV were determined by generalized estimating equations.

Results

The majority of couples were married and living together, with an average duration of partnership of approximately 5 years. More than 39,000 quarterly visits were recorded. IPV was reported in 2.7% of visits by HIV infected women, 2.2% by HIV uninfected women, 0.9% by HIV infected men, and 0.7% by HIV uninfected men. The majority of IPV reports were verbal or a combination of verbal and physical violence. Those who were HIV infected were more likely to report IPV (for women adjusted odds ratio [AOR] 1.33, p=0.043; for men AOR 2.20, p=0.001), but IPV was not significantly associated with risk of HIV seroconversion in HIV uninfected participants. IPV incidence decreased during follow-up (p<0.001).

Conclusions

During up to 2 years of prospective follow-up, most persons in stable HIV serodiscordant partnerships who had undergone CVCT did not report IPV. A modest increased risk of IPV was seen for HIV infected partners, both female and male.

Keywords: intimate partner violence, HIV serodiscordant couples, women, Africa

Introduction

Intimate partner violence (IPV), including physical, emotional and sexual abuse perpetrated by an intimate partner, has been documented frequently in populations worldwide. In sub-Saharan Africa, studies have reported high lifetime experience of IPV [13]. For example, one study from South Africa found that 32% of young men reported having perpetrated some form of abuse on their partner [4] and a study from Kenya found a lifetime prevalence of physical violence was 26% in women, of which 74% was perpetrated by intimate partners [3]. A number of studies have found a correlation between IPV and risk of HIV infection in African women [2, 57].

One group in which HIV risk from IPV could be especially important is HIV serodiscordant couples (i.e., in which one member is HIV infected and the other is HIV uninfected). In sub-Saharan Africa, the likelihood that the stable partner of an HIV-infected person will be HIV uninfected is approximately 50%, with women as likely as men to be the infected partner in a serodiscordant couple [8]. Moreover, HIV risk is high in serodiscordant couples, ranging from 2–6% per year when partner status is known to the couple [9] to 10–15% per year in couples unaware of their serodiscordant status [10, 11]. A substantial fraction of new HIV infections in Africa have been estimated to occur among HIV serodiscordant married or cohabiting couples [12].

Becoming aware of being in a serodiscordant relationship itself could lead to IPV, and knowledge of serodiscordancy could contribute to ongoing IPV risk in couples. Prevention of blame and IPV is an important consideration in HIV voluntary counseling and testing, especially in the setting of couples voluntary counseling and testing (CVCT). Higher uptake of HIV prevention strategies, such as safer sex practices and antiretrovirals for prevention of mother-to-child HIV transmission, by persons undergoing CVCT compared to those using only individual VCT have made CVCT a priority strategy for HIV prevention [1315]. However, few data on IPV have been reported among HIV serodiscordant couples who have undergone CVCT.

CVCT and facilitated disclosure of results offers an important opportunity to prevent HIV transmission. Efforts to expand CVCT as an HIV prevention strategy need to be informed by data on possible consequences of knowledge of serodiscordant HIV status, especially potential increased risk of IPV. We assessed the frequency and correlates of IPV by partners in a multinational prospective study of HIV serodiscordant African couples.

Methods

Population and Procedures

Between November 2004 and May 2007, 3408 HIV serodiscordant couples from seven African countries in East (Kenya, Rwanda, Tanzania, Uganda) and Southern Africa (Botswana, South Africa, Zambia) were enrolled in the Partners in Prevention HSV/HIV Transmission Study, a randomized, double-blind, placebo-controlled, clinical trial of acyclovir herpes simplex virus type 2 (HSV-2) suppressive therapy for the prevention of HIV transmission [9, 16, 17]. All couples were aware of their HIV serodiscordant status; most became aware at the time of screening for the study, during the month prior to enrollment. Eligible couples were those in which both members were ≥18 years of age, sexually active, and intended to remain as a couple for the duration of the study. HIV infected partners were also seropositive for HSV-2 and had a CD4 count above national cut-offs for antiretroviral therapy initiation at the time (i.e., ≥250 cells/mm3); CD4 counts were monitored every 6 months and those who came to meet national criteria for antiretroviral therapy were referred to HIV treatment clinics. HIV infected partners visited the study clinic monthly and HIV uninfected partners had visits scheduled quarterly. Couples were encouraged to attend study visits together, as often as they found possible, to allow ongoing counseling together and to address any emerging challenges related to living together as an HIV serodiscordant couple. Follow-up was for up to a maximum of 24 months, with earlier completion of follow-up for some couples as a result of site closure at the end of the study (October 2008). HSV-2 suppressive therapy with acyclovir did not decrease the risk of HIV transmission [9].

Laboratory procedures included serology for HIV (at baseline and then quarterly for HIV uninfected participants), serology for HSV-2 (baseline), and nucleic acid amplification for sexually transmitted infections (STIs, Chlamydia trachomatis, Neisseria gonorrhoeae, and Trichomonas vaginalis) from samples collected at study enrollment, as described previously [16]. CD4 counts were measured by standard flow cytometry.

All participants received pre- and post-test HIV counseling, risk reduction counseling (both individual and couple), free condoms, and management of STIs according to World Health Organization guidelines at each study visit. The study protocol was approved by the University of Washington Human Subjects Review Committee and ethics review boards at each study site. All participants provided written informed consent.

Assessment of IPV

The present report is a secondary analysis of the Partners in Prevention HSV/HIV Transmission Study dataset, evaluating the frequency of IPV at enrollment into the study and incidence of IPV during study prospective follow-up. At enrollment and at quarterly follow-up visits thereafter, all HIV infected and uninfected participants were asked, separately and in the setting of a private counseling room, about any abuse – verbal or physical – against them by their study partner during the prior 3 months. Study staff were provided with examples of verbal (“yelling, name calling, or threatening”) and physical abuse (“hitting, slapping, or forcing someone to have sex against their wishes”) to facilitate data collection. The question about IPV was asked in local languages and in a manner considered culturally appropriate for each study site. Interviewers were experienced in couples counseling and were trained through multiple role plays to ask the question as a part of a risk-reduction counseling process. If IPV was reported, a standard data collection form was completed by the interviewer, detailing the nature of the abuse. In addition, if other reports of IPV were made by participants at interim visits occurring between the quarterly visits, the same data form was collected. Information about IPV was obtained from the participant who reported the abuse (i.e., the survivor) rather than the perpetrator; those accused of being perpetrators of IPV were not asked about abuse reported by their partner.

Statistical Analysis

Medians and inter-quartile ranges (IQR) were provided for continuous variables. Counts and percentages were provided for categorical variables. IPV incidence during follow-up was calculated by dividing the number of IPV reports by person-time in follow-up. The cumulative proportion of persons ever reporting IPV, including at enrollment and follow-up, was determined using Kaplan-Meier analysis. Univariate and multivariate generalized estimating equations with robust standard errors were used to assess correlates of IPV. Variables statistically significant in univariate analyses at p<0.10 were included in multivariate adjusted models. For analyses of correlates of IPV, HIV uninfected participants who seroconverted to HIV during follow-up were censored thereafter; separate descriptions of IPV after HIV seroconversion were then calculated. Data were analyzed using Intercooled STATA version 11.0.

Results

Participant characteristics and prevalence of IPV at study enrollment

Of 3408 HIV serodiscordant couples enrolled, 2299 were couples in which the HIV infected partner was female and 1109 were couples in which the HIV infected partner was male (Table 1). Two-thirds of the couples were from the East Africa region. The majority were married and living together. The average duration of the partnerships was 4.9 years for couples in which the HIV-infected partner was female and 6.7 years for couples in which the HIV-infected partner was male. The average age was in the mid-30s, with male partners on average older than female partners. Most couples had at least one child together. Most participants had attended school for ≥8 years and were either low or no income earners. Couples reported a median of 4 sex acts (IQR 2 – 8) in the month prior to enrollment with about one quarter reporting unprotected sex.

Table 1.

Enrollment Characteristics

Median (IQR) or number (%)
Couples with HIV infected women (n=2299) Couples with HIV infected men (n=1109)
HIV infected
woman
HIV uninfected
man
HIV infected
man
HIV uninfected
woman
Couple Characteristics*
East Africa (vs. Southern Africa) 1487 (64.7%) 763 (68.8%)
Married 1691 (73.6%) 895 (80.7%)
Living together 2050 (89.2%) 1032 (93.1%)
Duration of partnership, years 4.9 (2.1, 9.4) 6.7 (2.9, 13.8)
Number of living children with study partner 1 (0, 2) 2 (1, 3)
Number of sex acts, prior month 4 (2, 8) 4 (2, 8)
Any unprotected sex with study partner, prior month 700 (30.5%) 294 (26.5%)
Demographic characteristics
Age, years 30 (25.2, 34.7) 35.1 (29.6, 42.1) 37.2 (32.0, 44.9) 30.6 (25.4, 37.7)
Education, years 8 (6, 10) 9 (7, 12) 8 (7, 11) 8 (6, 10)
Monthly income
  None 1734 (75.4%) 923 (40.2%) 444 (40.0%) 821 (74.0%)
  < median income for the study site 343 (14.9%) 576 (25.1%) 266 (24.0%) 170 (15.3%)
  >= median income for the study site 221 (9.6%) 800 (34.8%) 399 (36.0%) 118 (10.6%)
Health characteristics
Any STI 416 (18.1%) 220 (9.6%) 73 (6.6%) 144 (13.0%)
Current hormonal contraceptive use 455 (19.8%) N/A N/A 197 (17.8%)
Other sexual partners in past month 32 (1.4%) 89 (3.9%) 85 (7.7%) 6 (0.5%)
Verbal or physical abuse by study partner, past 3 months 65 (2.8%) 23 (1.0%) 22 (2.0%) 34 (3.1%)
*

Couple characteristics based on data reported by the HIV uninfected partner.

IQR, interquartile range; STI, sexually transmitted infection (Chlamydia trachomatis, Neisseria gonorrhea, and Trichomonas vaginalis)

At the enrollment visit, 2.8% and 3.1% of HIV infected and uninfected women and 2.0% and 1.0% of HIV infected and uninfected men, respectively, reported having experienced IPV during the prior 3 months. Approximately 36.9% of IPV reports at enrollment in HIV infected women were assessed by the study staff as definitely or probably related to the couples’ learning their of serodiscordant HIV serostatus, compared to only 14.7% of IPV reports from HIV uninfected women. Similar percentages were observed in men: 36.4% of reports were probably/definitely related to discovery of serodiscordancy in HIV infected men compared to 13.0% in HIV uninfected men.

IPV during follow-up

Median follow-up was 18 months (IQR 15–24) for HIV infected and 18 months (IQR 12–24) for HIV uninfected participants. During follow-up, women completed a total of 19,985 assessments of IPV (13,392 HIV infected, 6593 HIV uninfected) and men completed a total of 19,813 assessments (6674 HIV infected, 13,139 HIV uninfected).

IPV was reported at 2.7% of quarterly visits by HIV infected women, 2.2% of visits by HIV uninfected women, 0.9% of visits by HIV infected men, and 0.7% of visits by HIV uninfected men (Table 2). By Kaplan-Meier analysis, the cumulative proportion of persons ever reporting IPV by 24 months of follow-up was 18.0% in HIV infected women, 14.4% in HIV uninfected women, 7.1% in HIV infected men, and 5.0% in HIV uninfected men (Figure 1). For both HIV infected and uninfected participants, women had a higher cumulative risk of IPV than men (log-rank p<0.0001). In addition, report of IPV at enrolment was strongly and significantly associated with reporting IPV during follow-up, for both women (odds ratio [OR] 5.75, 95% confidence interval [CI] 4.19–7.89, p<0.001) and men (OR 7.90, 95% CI 4.41–14.14, p<0.001).

Table 2.

Incidence of Intimate Partner Abuse during Follow-up Visits by Gender, HIV status, Region & Type of Abuse*

WOMEN MEN
HIV-infected HIV-uninfected HIV-infected HIV-uninfected
Intimate
Partner
abuse
reports /
visits
% of
visits
Incidence
per 100
py**
Intimate
partner
abuse
reports
% of
visits
Incidence
per 100
py**
Intimate
partner
abuse
reports
% of
visits
Incidence
per 100
py**
Intimate
partner
abuse
reports
% of
visits
Incidence
per 100
py**
East Africa 231 / 9397 2.5% 9.7 89 / 4829 1.8% 7.1 37 / 4938 0.7% 3.0 42 / 9248 0.5% 1.7
Verbal only 100 1.1% 4.2 38 0.8% 3.0 32 0.6% 2.6 31 0.3% 1.3
Physical only 22 0.2% 0.9 10 0.2% 0.8 1 0.0% 0.1 2 0.0% 0.1
Both 108 1.1% 4.5 40 0.8% 3.2 4 0.1% 0.3 9 0.1% 0.4
Southern Africa 137 / 3995 3.4% 13.5 53 / 1764 3.0% 11.4 21 / 1715 1.2% 4.8 53 / 3891 1.4% 5.1
Verbal only 55 1.4% 5.4 17 1.0% 3.6 16 0.9% 3.7 39 1.0% 3.8
Physical only 11 0.3% 1.1 11 0.6% 2.4 0 0.0% 0.0 1 0.0% 0.1
Both 71 1.8% 7.0 25 1.4% 5.4 5 0.3% 1.1 12 0.3% 1.2
TOTAL 368 / 13392 2.7% 10.8 142 / 6593 2.2% 8.3 58 / 6653 0.9% 3.4 95 / 13139 0.7% 2.7
Verbal only 155 1.2% 15.3 55 0.8% 3.2 48 0.7% 2.8 70 0.5% 2.0
Physical only 33 0.2% 3.3 21 0.3% 1.2 1 0.0% 0.1 3 0.0% 0.1
Both 179 1.3% 17.7 65 1.0% 3.8 9 0.1% 0.5 21 0.2% 0.6
*

Type of abuse was unknown for 3 IPV reports, thus columns may not add up to totals.

**

Person years (PY): HIV infected women (2383 East Africa [EA], 1012 Southern Africa [SA]), HIV uninfected women (1253 EA, 467 SA), HIV infected men (1250 EA, 437 SA), HIV uninfected men (2427 EA, 1040 SA).

Figure 1. Cumulative probability of reporting IPV, by gender and HIV status.

Figure 1

Cumulative proportion of persons reporting IPV during study follow-up, by HIV status and gender, as calculated by Kaplan-Meier analysis. At 24 months, the cumulative probability of any IPV report was 18.0% for HIV infected women, 14.4% for HIV uninfected women, 7.1% for HIV infected men, and 5.0% for HIV uninfected men.

For both men and women, the majority of the IPV reports were verbal or a combination of verbal and physical abuse. For women, 41.2% of IPV reports were verbal only, 47.8% were both verbal and physical, and this distribution was similar for both HIV infected and HIV uninfected women. For men, about three-quarters of reports were verbal abuse only. Compared to men, women were significantly more likely to report physical abuse only (10.6% vs. 2.6% of reports, p=0.002) or a combination of verbal and physical abuse (47.8% vs. 19.6% of reports, p<0.001).

In total, there were 536 couples (15.7% of 3408 couples) in which one or both members ever reported IPV during the study (at enrollment or during follow-up). Among couples who reported IPV, 369 (68.8%) had reports by the woman only, 71 (13.2%) had reports by the man only, and 96 (17.9%) had reports by both the man and the woman. Overall, for 64 (66.7%) of the 96 couples in which both members ever reported IPV, both members had at least one IPV report from the same study visit, demonstrating that IPV was bidirectional during that study time interval.

Correlates of IPV

Correlates of IPV during the study were assessed, separately for women and men, in multivariate models.

Among women (Table 3), IPV was significantly more frequent in those who were HIV infected (AOR 1.33, p=0.043), those who were unmarried (AOR 1.42, p=0.026), and those living with their partner (AOR 2.57, p<0.001). Notably, IPV was also reported more commonly at visits at which women reported unprotected sex with their partner (AOR 1.86, p<0.001). There were statistical trends (p<0.1) for younger women (<45 years, AOR 1.6–1.7), individuals whose duration of relationship with their serodiscordant partner was <10 years (AOR 1.2–1.6), and those from Southern Africa sites (AOR 1.28, p=0.068) to be more likely to report IPV. There was no statistically significant relationship between pregnancy and risk of IPV, and women who had sex partners in addition to their study partner were no more likely to report IPV. For HIV infected women, IPV was less frequently reported by those with CD4 counts <350 (AOR 0.72, p=0.027, compared to those with CD4 counts ≥500) and those who were on antiretroviral therapy (AOR 0.42, p=0.091).

Table 3.

Correlates of IPV among Women

Study visits
n=23393
Visits IPV
reported
n=609
Correlates n(%)* n(%) OR (95%CI) P AOR (95%CI) P
Socio-Demographic Characteristics

Age (years)
<25 5021 (21.5) 147 (2.9) 1.87 (1.12, 3.14) 0.017 1.63 (0.86, 3.08) 0.134
25–34 11266 (48.2) 306 (2.7) 1.73 (1.05, 2.84) 0.030 1.71 (0.96, 3.05) 0.069
35–44 5509 (23.6) 129 (2.3) 1.51 (0.89, 2.56) 0.131 1.64 (0.92, 2.92) 0.095
45+ 1592 (6.8) 26 (1.6) Reference Reference
Region
East Africa 16476 (70.4) 368 (2.2) Reference Reference
Southern Africa 6917 (29.6) 241 (3.5) 1.58 (1.30, 1.93) <0.001 1.28 (0.98, 1.66) 0.068
Education (years)
None 1269 (5.4) 47 (3.7) 1.4 (0.92, 2.13) 0.117
1–8 12839 (54.9) 318 (2.5) 0.95 (0.77, 1.16) 0.594
>8 9285 (39.7) 244 (2.6) Reference
Monthly income
None 17386 (74.3) 463 (2.7) 1.32 (0.92, 1.89) 0.138
< median site income 3619 (15.5) 94 (2.6) 1.30 (0.84, 2.01) 0.243
≥median site income 2377 (10.2) 48 (2.0) Reference

Couple Characteristics

Age difference (years , man’s age –woman’s age)
≤−5 761 (3.3) 27 (3.6) 1.63 (0.94, 2.84) 0.084 1.53 (0.84, 2.78) 0.166
−5 to 5 10437 (44.6) 283 (2.7) 1.21 (0.93, 1.57) 0.149 1.14 (0.86, 1.51) 0.351
5 to 10 6513 (27.8) 157 (2.4) 1.08 (0.81, 1.44) 0.609 1.14 (0.84, 1.54) 0.407
10+ 5641 (24.1) 127 (2.3) Reference Reference
Married
Yes 18322 (78.3) 434 (2.4) Reference Reference
No 5071 (21.7) 175 (3.5) 1.47 (1.18, 1.82) <0.001 1.42 (1.04, 1.92) 0.026
Living together
Yes 21323 (91.2) 573 (2.7) 1.55 (1.03, 2.33) 0.035 2.57 (1.59, 4.15) <0.001
No 2070 (8.9) 36 (1.7) Reference Reference
Partnership duration (years)
<2 4701 (20.1) 123 (2.6) 1.41 (1.03, 1.93) 0.032 1.22 (0.82, 1.81) 0.326
2 to 5 5998 (25.6) 211 (3.5) 1.93 (1.45, 2.56) <0.001 1.59 (1.12, 2.26) 0.010
5 to 10 6239 (26.7) 153 (2.5) 1.35 (1.00, 1.82) 0.054 1.26 (0.90, 1.77) 0.186
10+ 6226 (26.6) 115 (1.9) Reference Reference
Children together
Yes 16470 (70.4) 410 (2.5) Reference
No 6914 (29.6) 199 (2.9) 1.14 (0.92, 1.40) 0.230

Self-reported Sexual Behavior

Unprotected sex with study partner, prior month
Yes 2775 (11.9) 132 (4.8) 1.98 (1.59, 2.45) <0.001 1.86 (1.46, 2.37) <0.001
No 20593 (88.0) 463 (2.3) Reference Reference
Other sex partners, prior month
Yes 765 (3.3) 26 (3.4) 1.11 (0.69, 1.79) 0.674
No 22060 (94.3) 548 (2.5) Reference

Medical Characteristics

STI at enrollment
Yes 3523 (15.1) 111 (3.2) 1.29 (1.01, 1.67) 0.045 1.14 (0.88, 1.48) 0.326
No 17636 (75.4) 432 (2.5) Reference Reference
Pregnant during study
Yes 5809 (24.8) 171 (2.9) 1.22 (0.98, 1.52) 0.072 1.21 (0.94, 1.56) 0.135
No 17569 (75.1) 424 (2.4) Reference Reference
Hormonal contraceptive use
Yes 5016 (21.4) 148 (3.0) 1.15 (0.93, 1.43) 0.201
No 18362 (78.5) 447 (2.4) Reference

HIV Characteristics

HIV infected 15691 (67.1) 433 (2.8) 1.22 (0.98, 1.53) 0.081 1.33 (1.01, 1.76) 0.043
HIV uninfected 7702 (32.9) 176 (2.3) Reference Reference
CD4 count**
<350 4450 (28.4) 92 (2.1) 0.64 (0.49, 0.84) 0.001 0.72 (0.54, 0.96) 0.027
350–499 4493 (28.6) 113 (2.5) 0.79 (0.62, 1.01) 0.058 0.81 (0.63, 1.05) 0.116
≥500 6712 (42.8) 214 (3.2) Reference Reference
WHO stage of disease**
I & II 14898 (95.0) 398 (2.7) Reference
III & IV 757 (4.8) 21 (2.8) 1.05 (0.69, 1.60) 0.812
ART***
Yes 616 (3.9) 4 (0.7) 0.24 (0.09, 0.61) 0.003 0.42 (0.16, 1.15) 0.091
No 15039 (95.8) 415 (2.8) Reference Reference
Seroconverted to HIV during study***
Yes 260 (3.4) 13 (5.0) 2.71 (1.26, 5.82) 0.011 1.62 (0.59, 4.47) 0.348
No 7442 (96.6) 163 (2.2) Reference Reference

Time in study

Enrollment 3408 (14.6) 99 (2.9) Reference Reference
1–6 months 6502 (27.8) 237 (3.7) 1.27 (1.01, 1.58) 0.039 1.53 (1.17, 1.97) 0.002
7–12 months 5993 (25.6) 153 (2.6) 0.88 (0.69, 1.13) 0.318 1.14 (0.86, 1.51) 0.360
13–18 months 4610 (19.7) 80 (1.7) 0.61 (0.46, 0.80) <0.001 0.70 (0.50, 0.97) 0.031
19–24 months 2880 (12.3) 40 (1.4) 0.47 (0.32, 0.67) <0.001 0.63 (0.42, 0.96) 0.031
*

Column totals may not add up to total number of study visits due to missing data.

**

Limited to 15,691 study visits by 2,299 HIV-infected women.

***

Limited to 1,109 initially HIV-uninfected participants (61 women seroconverted).

OR, odds ratio; AOR, adjusted odds ratio; STI, sexually transmitted infection; IPV, intimate partner violence; WHO, World Health Organization; ART, antiretroviral therapy

In men (Table 4), HIV seropositivity (AOR 2.20, p=0.001), younger age (<45 years, AOR ∼1.9), being from the Southern African region (AOR 2.19, p<0.001), and having other sexual partners (AOR 2.57, p<0.001) were associated with increased likelihood of reporting IPV. Men who had an STI diagnosed at enrollment were at decreased likelihood of reporting IPV (AOR 0.45, p=0.04). Marital status and other couple characteristics were not associated with IPV in men. For HIV infected men, CD4 count and ART use were not significantly associated with IPV.

Table 4.

Correlates of IPV Among Men

Study visits
n=23221
Visits IPV
reported
n=198
Correlates n(%)* n(%) OR (95%CI) P AOR (95%CI) P

Socio �Demographic Characteristics

Age (years)
<25 1260 (5.4) 14 (1.1) 2.47 (1.12, 5.45) 0.025 1.99 (0.77, 5.14) 0.154
25–34 8350 (36.0) 86 (1.0) 2.30 (1.36, 3.90) 0.002 1.85 (0.96, 3.55) 0.065
35–44 8270 (35.6) 74 (0.9) 2.01 (1.18, 3.42) 0.010 1.90 (1.04, 3.45) 0.036
45+ 5325 (22.9) 24 (0.5) Reference Reference
Region
East Africa 16436 (70.8) 99 (0.6) Reference Reference
Southern Africa 6785 (29.2) 99 (1.5) 2.40 (1.74, 3.31) <0.001 2.19 (1.46, 3.28) <0.001
Education (years)
None 805 (3.5) 8 (1.0) 0.98 (0.45, 2.14) 0.955 1.21 (0.52, 2.83) 0.655
1–8 10577 (45.6) 75 (0.7) 0.72 (0.51, 1.00) 0.048 0.88 (0.62, 1.25) 0.482
>8 11832 (51.0) 115 (1.0) Reference Reference
Monthly income
None 9166 (39.5) 68 (0.7) 0.80 (0.54, 1.18) 0.265
< median site income 5900 (25.4) 52 (0.9) 0.95 (0.65, 1.41) 0.807
≥ median site income 8153 (35.1) 77 (0.9) Reference

Couple Characteristics

Age difference (years, man’s age –woman’s age)
≤−5 738 (3.2) 9 (1.2) 2.00 (0.90, 4.43) 0.087 1.32 (0.55, 3.16) 0.540
−5 to 5 10272 (44.2) 102 (1.0) 1.65 (1.06, 2.59) 0.028 1.23 (0.74, 2.07) 0.426
5 to 10 6484 (27.9) 50 (0.8) 1.27 (0.78, 2.08) 0.331 1.04 (0.62, 1.76) 0.874
10+ 5703 (24.6) 35 (0.6) Reference Reference
Married
Yes 18275 (78.7) 125 (0.7) Reference Reference
No 4945 (21.3) 73 (1.5) 2.19 (1.57, 3.06) <0.001 1.25 (0.78, 2.01) 0.351
Living together
Yes 21223 (91.4) 186 (0.9) 1.51 (0.81, 2.82) 0.191
No 1997 (8.6) 12 (0.6) Reference
Partnership Duration (years)
<2 4611 (19.9) 51 (1.1) 1.87 (1.14, 3.05) 0.013 1.36 (0.69, 2.69) 0.378
2 to 5 5926 (25.5) 56 (0.9) 1.57 (0.98, 2.51) 0.059 1.22 (0.64, 2.34) 0.546
5 to 10 6090 (26.2) 51 (0.8) 1.40 (0.85, 2.29) 0.182 1.45 (0.80, 2.62) 0.217
10+ 6342 (27.3) 38 (0.6) Reference Reference
Children together
Yes 16322 (70.3) 138 (0.9) Reference
No 6894 (26.7) 60 (0.9) 1.05 (0.74, 1.49) 0.779

Self-reported Sexual Behavior

Unprotected sex with partner, prior month
Yes 2754 (11.9) 30 (1.1) 1.26 (0.81, 1.98) 0.305
No 20454( 88.1) 166 (0.8) Reference
Other sex partners, prior month
Yes 2271 (9.8) 32 (1.4) 1.75 (1.11, 2.76) 0.016 2.57 (1.61, 4.10) <0.001
No 19723 (84.9) 147 (0.8) Reference Reference

Medical Characteristics

STI at enrollment
Yes 1854 (8.0) 8 (0.4) 0.48 (0.22, 1.04) 0.063 0.45 (0.21, 0.97) 0.041
No 20947 (90.2) 184 (0.9) Reference Reference

HIV Characteristics

HIV infected 7783 (33.5) 80 (1.0) 1.34 (0.97, 1.85) 2.20 (1.40, 3.44) 0.001
HIV uninfected 15438 (66.48) 118 (0.8) Reference Reference
CD4 count**
<350 2,793 (35.9) 22 (0.8) 0.59 (0.33, 1.06) 0.076 0.66 (0.37, 1.18) 0.164
350–499 2,456 (31.6) 23 (0.9) 0.69 (0.39, 1.22) 0.202 0.66 (0.36, 1.19) 0.166
≥500 2526 (32.5) 33 (1.3) Reference Reference
WHO stage of disease**
I & II 7373 (94.7) 75 (1.0) Reference
III & IV 402 (5.2) 3 (0.8) 0.69 (0.19, 2.50) 0.571
ART***
Yes 422 (5.4) 2 (0.5) 0.46 (0.13, 1.69) 0.243
No 7353 (94.5) 76 (1.0) Reference
Seroconverted to HIV during study***
Yes 371 (2.4) 6 (1.6) 2.09 (0.93, 4.69) 0.070 1.69 (0.62, 4.64) 0.305
No 15067 (97.6) 112 (0.7) Reference Reference

Time in study

Enrollment 3408 (14.7) 45 (1.3) Reference Reference
1–6 months 6429 (27.7) 81 (1.3) 0.95 (0.67, 1.35) 0.776 0.99 (0.65, 1.52) 0.981
7–12 months 5937 (25.6) 42 (0.7) 0.52 (0.35, 0.79) 0.002 0.52 (0.32, 0.83) 0.006
13–18 months 4547 (19.6) 18 (0.4) 0.29 (0.17, 0.52) <0.001 0.29 (0.16, 0.55) <0.001
19–24 months 2900 (12.5) 12 (0.4) 0.28 (0.13, 0.59) 0.001 0.31 (0.14, 0.69) 0.004
*

Column totals may not add up to total number of study visits due to missing data.

**

Limited to 7,783 study visits by HIV-infected men.

***

Limited to 2,299 initially-HIV uninfected participants (90 men seroconverted).

OR, odds ratio; AOR, adjusted odds ratio; STI, sexually transmitted infection; IPV, intimate partner violence; WHO, World Health Organization; ART, antiretroviral therapy

For both women and men, those who experienced HIV seroconversion did not have statistically significant increased risk of IPV prior to acquiring HIV (AOR 1.62, p=0.348 for women and AOR 1.69, p=0.305 for men). Similarly, IPV was not reported significantly more often at visits at which HIV seroconversion was detected (data not shown). During 497 post-seroconversion visits by 146 HIV seroconverters, a total of eight (1.6% of visits) reports of IPV were obtained, by 7 women: 4 had not reported IPV and 3 had reported IPV before seroconversion. No men reported IPV after HIV seroconversion.

Finally, for both women and men, the incidence of IPV decreased significantly during study follow-up (test for trend p<0.001).

Consequences of IPV

Relationship dissolution was the most common consequence of IPV during the follow-up period, occurring in 31.3% and 22.5% of HIV infected and uninfected women and 20.7% and 35.8% of HIV infected and uninfected men reporting IPV. The second most common consequence associated with IPV was change of residence, also occurring in slightly over 20% of cases. Other consequences included loss of economic support (18.8% of HIV infected women, <10% of others) and loss of custody of children (6.3% of HIV uninfected men, <5% of others). For 24.5% and 47.2% of IPV reports by HIV infected and uninfected women, and 34.5% and 31.6% of reports by HIV infected and uninfected men, participants reported that there were no consequences to the relationship or the individual as a result of IPV.

Discussion

In this large prospective study of HIV serodiscordant couples from East and Southern Africa who were aware of their serodiscordant status, we found less than 20% of women and less than 10% of men experienced verbal or physical IPV over up to 24 months of prospective follow-up. IPV was reported at less than 3% of quarterly follow-up visits by women and less than 1% of visits by men; the frequency of IPV decreased during follow-up. Thus, among HIV serodiscordant couples who had recently become aware of their serodiscordant serostatus and who received frequent couples counseling, frequency of IPV was similar to or lower than background levels in the general population in the region [13, 7, 1820].

We had hypothesized that IPV might be common among HIV serodiscordant couples, particularly couples in which the HIV infected partner was female. Other studies have recorded higher vulnerability to abuse of women who are HIV infected [20, 21], and one Nigerian study reported a 3-fold rise in reports of partner abuse after HIV diagnosis among pregnant HIV infected women who had an uninfected partner [22]. In our study, women more frequently reported IPV than men, and HIV infected women had a 33% higher risk of IPV compared with uninfected women and had the highest cumulative risk of IPV (18.0% ever reporting by 24 months).

IPV has been associated with increased HIV risk in some [2], but not all studies [23], with the strongest associations likely reflecting physical abuse accompanied by forced sex [3, 6, 7, 24]. Much of this literature points at the role of partner violence in transmission of HIV through concurrent partnerships, transactional sex, and coercive sex without condoms [2, 25, 26]. For HIV uninfected women, risk of HIV acquisition could be increased due to reduced capacity to negotiate condom use in an abusive partnership [27, 28]. We found that women were more prone to report partner violence that included physical abuse than men, and that IPV was more common among women reporting recent sex unprotected by condoms. However, we found no statistically significant relationship between IPV and subsequent HIV seroconversion, for women or for men.

Among women in HIV serodiscordant partnerships, not being married to the partner was associated with a 44% higher risk of IPV report and living together was associated with a 62% higher risk. For unmarried couples, the relative instability of the relationship may lead to greater risk of IPV; couples living together may have more frequent opportunity for IPV. For both women and men, we found those from Southern African sites were more likely to report IPV than those from East Africa, which may reflect differences in gender power or relationship stability on a regional level.

Our data are unique in documenting the frequency of IPV against men by their female partners. Similar to findings for women, men also had increased risk of intimate partner abuse report if they were HIV infected. There may have been underreporting of IPV among men due to social desirability bias in the patriarchal societies of Africa [29].

Our study had several strengths. First, it analyzed data from a large prospective cohort. Many of the available published works are either from cross-sectional studies, such as national demographic and health surveys. Second, we recorded intimate partner abuse reports over relatively short recall periods (3 months), which likely increased the accuracy of our data compared to reports recalled over longer periods. Third, we examined the role of both HIV status and the gender in IPV incidents. Finally, our data were from 14 study sites in East and Southern Africa, which may increase the generalizability of our findings. We did not collect data on alcohol use, which is a limitation as alcohol has been associated with IPV in other settings [30, 31]. Our clinical trial population may not be fully representative of HIV serodiscordant couples, particularly those unaware of their serodiscordant status and those who do not receive ongoing couples counseling and support services. Ongoing individual and couples counseling, by experienced staff, may have maximized condom use and other risk reductions in the study population, and decreased the frequency of IPV.

In summary, we found that most members of known HIV serodiscordant couples followed for up to two years do not report IPV. Overall, the rate of IPV was lower than or similar to that expected in the general population of the countries in which this study was done; HIV infected partners, both women and men, were at modest increased IPV risk. Men and women experienced IPV differently, with women reporting physical and verbal abuse compared to men who generally reported verbal abuse alone. The decrease in IPV incidence with follow-up could also be an indicator of the effectiveness of ongoing counseling in addressing couples’ need for support and thereby reducing the risk of IPV report over time. Further studies are warranted to determine the frequency and focus of counseling for HIV serodiscordant couples in order to reduce HIV transmission and minimize IPV.

Acknowledgments

We gratefully acknowledge the invaluable contributions of the HIV serodiscordant couples who participated in this study. We thank the teams at the study sites and at the University of Washington for work on data collection and management.

Funding source: This study was supported through research grants from the Bill & Melinda Gates Foundation (grant ID # 26469) and the US National Institutes of Health (National Institute of Allergy and Infectious Diseases grant R01 AI083034).

Role of the Funding Source: The authors designed and executed the study, had full access to the raw data, performed all analyses, wrote the manuscript, and had final responsibility for the decision to submit for publication. The funder had no role in design, data collection, analysis, interpretation, or writing of the report.

Partners in Prevention HSV/HIV Transmission Study Team

University of Washington Coordinating Center and Central Laboratories, Seattle, USA: Connie Celum (principal investigator), Anna Wald (protocol co-chair), Jairam Lingappa (medical director), Jared M. Baeten, Mary Campbell, Lawrence Corey, Robert W. Coombs, James P. Hughes, Amalia Magaret, M. Juliana McElrath, Rhoda Morrow, James I. Mullins

Study sites and site principal investigators:

Cape Town, South Africa (University of Cape Town): David Coetzee; Eldoret, Kenya (Moi University, Indiana University): Kenneth Fife, Edwin Were; Gaborone, Botswana (Botswana Harvard Partnership): Max Essex, Joseph Makhema; Kampala, Uganda (Infectious Disease Institute, Makerere University): Elly Katabira, Allan Ronald; Kigali, Rwanda (Rwanda Zambia HIV Research Group, and Emory University): Susan Allen, Kayitesi Kayitenkore, Etienne Karita; Kisumu, Kenya (Kenya Medical Research Institute, University of California San Francisco): Elizabeth Bukusi, Craig Cohen; Kitwe, Zambia (Rwanda Zambia HIV Research Group, and Emory University): Susan Allen, William Kanweka; Lusaka, Zambia (Rwanda Zambia HIV Research Group, and Emory University): Susan Allen, Bellington Vwalika; Moshi, Tanzania (Kilimanjaro Christian Medical College, Harvard University): Saidi Kapiga, Rachel Manongi; Nairobi, Kenya (University of Nairobi, University of Washington): Carey Farquhar, Grace John-Stewart, James Kiarie; Ndola, Zambia (Rwanda Zambia HIV Research Group, and Emory University): Susan Allen, Mubiana Inambao; Orange Farm, South Africa (Reproductive Health Research Unit, University of the Witwatersrand): Sinead Delany-Moretlwe, Helen Rees; Soweto, South Africa (Perinatal HIV Research Unit, University of the Witwatersrand): Guy de Bruyn, Glenda Gray, James McIntyre; Thika, Kenya (University of Nairobi, University of Washington): Nelly Rwamba Mugo Data management was provided by DF/Net Research, Inc. (Seattle, USA) and site laboratory oversight was provided by Contract Lab Services (University of the Witwatersrand, Johannesburg, South Africa).

Footnotes

Conflict of interest: No authors report conflicts of interest regarding content for this manuscript.

Author contributions: EW conceived the study, with EN-J, and wrote the first draft of the manuscript, along with KC and JMB. KC and JMB performed the statistical analysis. SD-M, EN-J, NRM, JK, EB, and CC contributed critical revisions to the analysis and interpretation. All authors contributed to the writing of the final draft.

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