Objective To examine factors associated with HIV infection among transgender women in Cambodia.
Design Cross-sectional study.
Settings HIV high-burden sites including the capital city and 12 provinces.
Participants This study included 1375 sexually active transgender women with a mean age of 25.9 years (SD 7.1), recruited by using respondent-driven sampling for structured questionnaire interviews and rapid finger-prick HIV testing.
Primary outcome measure HIV infection detected by using Determine antibody test.
Results HIV prevalence among this population was 5.9%. After adjustment for other covariates, participants living in urban areas were twice as likely to be HIV infected as those living in rural areas. Participants with primary education were 1.7 times as likely to be infected compared with those with high school education. HIV infection increased with age; compared with those aged 18–24 years, the odds of being HIV infected were twice as high among transgender women aged 25–34 years and 2.8 times higher among those aged ≥35 years. Self-injection of gender affirming hormones was associated with a fourfold increase in the odds of HIV infection. A history of genital sores over the previous 12 months increased the odds of HIV infection by threefold. Transgender women with stronger feminine identity, dressing as a woman all the time, were twice as likely to be HIV infected compared with those who did not dress as a woman all the time. Having never used online services developed for transgender women in the past six months was also associated with higher odds of being HIV infected.
Conclusions Transgender women in Cambodia are at high risk of HIV. To achieve the goal of eliminating HIV in Cambodia, effective combination prevention strategies addressing the above risk factors among transgender women should be strengthened.
- transgender women
- HIV infection
- risk factors
- integrated biological and behavioral survey
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- transgender women
- HIV infection
- risk factors
- integrated biological and behavioral survey
Strengths and limitations of this study
This is a rare and the second ever Integrated Biological and Behavioral Survey among transgender women—one of the most vulnerable and understudied populations in Cambodia and globally.
This study covered HIV high-burden sites including the capital city and 12 provinces, thus providing more nationally generalisable results.
This study identified important risk factors for HIV infection among transgender women, which require being addressed in order to reduce HIV infection among this key population.
Limitations of the study included potential bias of self-reported measures, participant sampling, the cross-sectional nature of the data that limits causation inferences and the backward selection of variables in multivariable analysis.
Globally, transgender women are at high risk for HIV infection, and little is known about the burden of HIV infection and its related factors in this population. A 2013 systematic review showed that the global HIV prevalence among transgender women was 19%, with low-income and middle-income countries having a slightly lower prevalence of 18% compared with 22% in high-income countries.1 The probability of being infected with HIV among transgender women was approximately 49 times higher than among the general adult population.1 Epidemiologically, transgender women share some HIV risk factors with other populations, such as ulcerative sexually transmitted infections (STIs),2 3 multiple substance use, victimisation, intimate partner violence,4 unprotected sex,5 multiple sex partners6 and injecting drug use.5–7
However, transgender women encounter additional and unique biological, social, cultural, legal and economic issues, which increase their vulnerability to HIV. Transgender women are marginalised legally and economically through discriminative legislation and practice, which accelerates their vulnerability to HIV infection by confining their job options to sex work. Sex work in turn exacerbates their stigmatisation and alienation,8 and further increases their HIV risk.9 10Stigmatisation and discrimination further increase the risk of HIV infection by preventing transgender women from seeking essential health information and services.11 Depression and low self-esteem, which are common psychological consequences of stigma, further weaken the bargaining power for condom use in sexual relationships, resulting in heightened vulnerability to HIV infection.5 12–15 Transgender women who have sex with men often engage in receptive anal intercourse, which increases their risk of HIV acquisition, compared with insertive sexual partners.2 Syndemics of illicit drug use, abuse by family members and mental health often occur together16 and are often associated with less likelihood of transgender women to use condoms during sex with commercial partners.17 In addition, the confluence of arbitrary arrests,18 19 violence,16 20 economic pressures21 and other social problems further aggravates mental health risks among transgender women, causing them to engage in risky sexual behaviours.6 17
In Southeast Asia, a systematic review of studies from Indonesia, Thailand and Vietnam demonstrated that transgender women are particularly at high HIV risk, with an estimated HIV prevalence of 26.1%, 12.2% and 6.7%, respectively.1 In Cambodia, up to 2012, transgender women were traditionally included in HIV prevention programmes targeting men who have sex with men (MSM). As a result, their unique needs were not reflected in HIV programmes’ goals.22 There was also a lack of transgender women-specific data to quantify the number reached by outreach programmes and services. In 2012, the first Integrated Biological and Behavioral Survey (IBBS) that specifically included transgender women in Cambodia found an HIV prevalence of 4.2% among this population,22 which was six times higher than the 0.7% prevalence among the general adult population aged 15–45 years,23 and about twice higher than the 2.1% among MSM.24 This 2012 study also found that older age (>35 years), residing in Siem Reap province (a major tourist site), having sex during or after drug use, not using a condom during the last anal sex and low self-esteem were associated with HIV infection among transgender women.22
Recognising the differences in HIV vulnerability and prevention needs between transgender women and MSM, in 2013 the National Center for HIV/AIDS, Dermatology and STD (NCHADS) separated these two populations in its revised Standard Operating Procedure known as Boosted Continuum of Prevention, Care and Treatment (B-CoPCT).25 Transgender women have since been considered a distinct at-risk group for HIV surveillance and programming. The National B-CoPCT approach aims to increase the uptake of HIV testing and counselling and other related services, ensure the quality of outreach and strengthen service delivery to meet specific needs of key populations, including transgender women, in-order to achieve Cambodia’s 3.0 goal (ie, zero new HIV infection, zero discrimination and zero AIDS-related deaths) by 2020.
This study was conducted to explore the HIV prevalence and identify risk factors associated with HIV infection among transgender women in Cambodia. The study findings will help determine ways in which services and policies can be tailored for this key population.
Study design and sites
Between December 2015 and February 2016, a cross-sectional study was conducted in the capital city of Phnom Penh and 12 provinces, namely Battambang, Banteay Meanchey, Kampong Cham, Kandal, Koh Kong, Kampong Chhnang, Kampong Speu, Prey Veng, Preah Sihanouk, Siem Reap, Svay Rieng and Tbong Khmum. These sites were purposively selected from the 23 HIV high-burden operational districts identified by NCHADS.26 27 The study was a combination of a biological (blood test) and behavioural (face-to-face interview) survey using Respondent-Driven Sampling method to reach the target population.
Sample size and sampling procedures
The sample size calculation was based on an assumption that HIV prevalence would have changed between the first and the current IBBS. The minimum sample size required for this study was 1380, which would result in sufficient power to detect a priori significant difference in HIV prevalence, as expressed in the following null and alternative hypotheses. The hypothesis test was that of one-sample proportion compared with the null hypothesis.
The null hypothesis (H0): HIV prevalence among transgender women remains constant at 4.2%, similar to that found in the 2012 IBBS.
The alternative hypothesis (Ha): HIV prevalence among transgender women has decreased by 1.2% from 4.2% in 2012 to 3.0% in the present IBBS.
The sample size was calculated using the following formula and assumptions:
P0 = estimated proportion in H0. (In the most recent survey, HIV prevalence among transgender women was 4.2% in 2012).
P1 = estimated proportion in Ha. (The expected HIV prevalence among transgender women in the current study is about 3.0%).
Z(1-α)⁄) = significance level at 5% in response to one-sided test (Z score=1.645).
Z(1- β) = power level of 80% (Z score=0.83).
Refusal rate of 10%.
Design effect is assumed to be one.
This sample size was stratified by study site. Roughly half of the estimated transgender women in each study site were recruited. However, in five provinces where the estimated number of transgender women was <100, all transgender women were recruited. Potential participants were included in the study if they (1) were biologically male at birth and self-identified as a woman or third gender, (2) were Khmer-speaking, (3) were at least 18 years of age at the time of screening, (4) reported having had sex with at least one man within the past 12 months and (5) were able and willing to provide an informed consent.
Among the 13 study sites, data collection was conducted in 20 locations (6 locations in Phnom Penh and 14 locations in the remaining provinces). The number of the selected locations was determined based on the required sample size in each study site. Our participants, including the seeds and the people the seeds referred, had to meet the eligibility criteria. These participants were recruited from the entire transgender population in the study sites. However, the initial seeds at each site were recruited through our implementing partners. First, four ‘seeds’ (two seeds aged 18–24 and two seeds 25 or older) who were well connected with other transgender women in each location were selected by outreach workers from implementing partners (local non-governmental organisations (NGOs)) based in the selected locations. These seeds had to meet the above-mentioned eligibility criteria for participation and have an established and large social network consisting of ≥10 other transgender women in their given location. Eligibility to participate as a seed was determined by the leader of the data collection team, using a paper-based eligibility form.
Second, each seed was given a personal identity number and enrolled in the study. Third, each seed was given three coupons and asked to refer three additional transgender women. US$2 was given to each seed for a successful referral. Each seed was expected to extend to 3–6 ‘recruitment waves’ in each location. If the initial seeds did not recruit participants, or if enrolment was halted because all recruitment chains had ‘dried up’ (ie, stopped recruiting), additional seeds were selected. In total, 80 seeds were selected by the outreach workers, and a total of 1375 transgender women were enrolled in the study. Referred participants were initially screened by the data collectors for eligibility.
Data collection training
Data were collected by three teams; each team comprised one field supervisor, five interviewers, one lab technician and one counsellor. Lab technicians and counsellors were from the Municipal or Provincial AIDS and STI Program of the study sites. Data collection teams were trained for 3 days on study protocol, research ethics, interview techniques and data collection procedures provided by the principal investigators and research coordinators.
Data collection procedures
Biological data collection
To determine HIV prevalence, all participants received onsite rapid finger-prick testing. Pre-test counselling was provided by qualified, well-trained counsellors working for voluntary confidential counselling and testing (VCCT) centres. Participants could receive their HIV test result verbally after the questionnaire interview. A blood sample was obtained from each participant by a trained laboratory technician through finger-prick and tested for HIV using Determine test, in keeping with the national protocol.28 Post-test counselling was provided for each participant regardless of their HIV test result by the same counsellor who conducted the pre-test counselling in accordance with NCHADS HIV testing guidelines.28 Participants who were HIV reactive and did not know their HIV status were referred by the counsellor for confirmatory testing at the nearest VCCT centre. The quality of HIV tests was monitored using quality control samples. Discordant results between the screening and confirmatory tests were investigated to elucidate potential causes and minimise potential erroneous results. In the case of human error, individuals performing screening tests were retrained before resuming their involvement in the study.
After HIV testing, the participant was interviewed by a well-trained interviewer using a computer-assisted survey instrument. The questionnaire was set up in Qualtrics, a web-based application, and run on an Android tablet. HIV testing and interviews were conducted in the selected 20 locations including drop-in centres, private houses and offices of implementing partners, depending on participants’ convenience.
Questionnaire development and measures
The questionnaire was developed using standardised and validated tools adapted from TGIBBS-2012,22 FHI 360’s guideline for Behavioral Surveillance Survey29 and NCHADS’s Boosted-CoPCT25 to measure key variables related to the objectives of the study. The questionnaire was initially drafted in English and translated into Khmer, the national language of Cambodia. Consultative meetings to improve the draft questionnaire were held with representatives of transgender women, communities and NGOs working with transgender women, as well as researchers and practitioners working on HIV and AIDS in Cambodia. The questionnaire was pre-tested with 20 transgender women in Phnom Penh and finalised based on findings.
The questionnaire collected information on socioeconomic characteristics, transgender identity and related experiences, sexual behaviours and condom use with different types of sexual partners, HIV/STI screening and care seeking behaviours, substance use and exposure to HIV programmes. For details of the questionnaire, please see online supplementary file 1.
HIV prevalence was calculated by dividing the total number of participants with HIV reactive test results with the total number of participants. To examine the associated factors of HIV infection, we conducted both bivariate and multivariable analyses. In the bivariate analyses, we compared all characteristics and behavioural variables of participants with a reactive test result to those of participants with a non-reactive test result. Among participants who tested HIV positive, additional analyses were conducted to assess whether there was a significant difference in sexual behaviours of those who were aware of their HIV-positive status and of those who were not. χ2 test or Fisher’s exact test (for an expected cell value of ≤5) was used for categorical variables, while Student’s t-test was used for continuous variables. To facilitate the model, some continuous variables, such as age, were transformed to categorical variables. A multivariable logistic regression model was constructed to examine independent factors associated with HIV infection. Variables with a significance level of p<0.05 in the bivariate analyses were simultaneously included in the model. Backward elimination method was then used to eliminate variables with the highest p-value one-by-one from the model. STATA V.12.0 for Windows was used to conduct the data analyses.
Participation in this study was voluntary, and a written informed consent was obtained from each study participant after a detailed description of the study objective and procedures was explained to them. Participants were informed that they could stop responding to questions and discontinue their participation at any time. Interviews were conducted at a private place, and confidentiality was enhanced by assigning a unique and anonymous code to each participant. No personal identifiers were contained in the questionnaires or dataset.
Of 1375 participants tested, 81 (5.9%) had an HIV reactive test; of whom, 42 (52%) were not aware of their HIV status prior to the study. Out of the 39 cases who already knew their status, 37 (94.9%) were currently on HIV treatment, with the other two reporting having dropped out of the treatment.
As shown in table 1, the majority of the participants (83.4%) were recruited from urban communities; 53.0% were younger than 25 years and 97.2% had never been married. More than two-thirds of participants (68.6%) had completed high school and 9.1% had a higher education. The most common main occupations reported by the participants were hair dressers/beauticians (35.1%), labourers/farmers (17.5%) and entertainment workers (14.8%). More than one-third of participants (38.6%) reported an average monthly income in the past six months of US$100–199, while 16.5% reported it to be >US$300. Regarding gender identity, 42.2% identified themselves as female, while 57.2% identified themselves as third gender. Almost half (48.0%) of the participants reported dressing as a woman all the time; 45% ever used hormone/non-hormone substance; and 14.0% ever injected hormones.
HIV prevalence was significantly higher among participants living in urban communities compared with participants living in rural communities (6.5% vs 2.6%, p=0.02). The HIV prevalence was also significantly different by age group: 3.0% of participants in the age group of 18–24 years, 8.2% in 25–34 years, 13.1% in 35–44 years and 11.4% in 45 years or older (p<0.001). HIV prevalence was also significantly higher among those who never attended school or dropped out of primary school compared with those who at least attended high school or higher (10.4% vs 8.0%, p<0.001). In addition, HIV prevalence was significantly higher among transgender women who were NGO staff (mainly HIV-focused NGOs) (20.6%) and those who were unemployed (9.4%) (p=0.03). HIV prevalence was significantly higher among transgender women who reported dressing as women all the time (8.5% vs 3.5%, p=0.001), among those who ever used female hormones (8.1% vs 4.1%, p=0.02) and among those who ever injected hormones (9.1% vs 5.2%, p=0.002). Moreover, HIV prevalence was significantly higher among transgender women who reported never using online services developed specifically for MSM or transgender women, such as Facebook group pages or various websites (9.5% vs 3.9%, p<0.001).
Sexual behaviours among transgender women with reactive and non-reactive HIV test are shown in table 2. An overwhelming majority of study participants (87.5%) reported only having had receptive anal sex in the past 12 months. Of the total, 86.0% reported having had anal sex with at least one man within the previous three months, with the median number of male sex partners in the past three months being three (IQR 1–9). Of those who were sexually active with men in the past three months, 61.9% reported having used a condom at last sex with a man.
A total of 94.8% of participants who had anal sex in the prior three months reported having at least one non-transactional male sex partner within the past three months; of which, 62.1% reported always using condoms with their non-transactional male sex partners. Of participants who had sex in the past three months, 41.8% reported having sex with at least one man in exchange for money or gift; of whom 60.0% reported always using condoms with the partners.
Table 2 also shows that HIV prevalence was significantly higher among participants who reported having had anal sex with a man in the past three months (6.5% vs 2.1%, p=0.02) and among those who reported having had sex with at least one man in exchange for money or gift in the prior three months (8.1% vs 5.4%, p=0.04) compared with participants who did not report these sexual behaviours.
Sexual behaviours and awareness of HIV status
Among the participants who had HIV reactive tests, additional analyses were conducted to see if there were differences in sexual behaviours among those who self-reported a positive status and those who did not. Participants who did not report or were unaware of their positive status were significantly less likely to report using a condom at last sexual intercourse (52.4% vs 79.0%, p=0.01). No other significant differences were found.
Sexually transmitted infections
Overall, 14.0% of participants reported having had at least one STI symptom in the past 12 months. Anal and perianal symptoms were most commonly reported (6.1%). As shown in table 3, HIV prevalence was significantly higher among participants who reported having had an STI symptom compared with that among participants who did not have an STI symptom in the past 12 months (11.4% vs 5.0%, p<0.001). HIV prevalence was also significantly higher among participants who reported having had an ulceration or sore in the genital area in the past 12 months compared with that among participants who did not have it (15.2% vs 5.6%, p<0.001).
As shown in table 5, the majority (75.9%) of participants reported drinking at least one can of beer or a glass of wine in the past three months, while 10.1% reported using amphetamine-type stimulants (Yama, Crystal Ice, Ecstasy) and 0.9% reported using other drugs (marijuana, heroin) in the previous 12 months. Of total, 1.5% reported having injected any illicit drugs in the past three months.
Table 4 also shows that HIV prevalence was significantly higher among participants who did not drink alcohol when compared with that among participants who reported drinking at least one can of beer or a glass of wine in the past three months (8.5% vs 5.1%, p=0.02). Moreover, HIV prevalence was significantly higher among participants who reported injecting any illicit drugs in the past three months compared with participants who did not (15.0% vs 5.8%, p=0.01).
Factors associated with HIV infection
Table 5 presents independent factors associated with HIV infection in multivariable logistic regression analyses. After adjustment for other covariates, participants living in urban areas were twice as likely to be HIV infected as those living in rural areas (adjusted OR (AOR) 2.7, 95% CI 1.1 to 6.5). Participants with primary education were 1.7 times as likely to be infected compared with those with high school education (AOR 1.7, 95% CI 1.0 to 2.9). HIV infection increased with age; compared with those aged 18–24 years, the odds of being HIV infected were twice as high among transgender women aged 25–34 years (AOR 2.1, 95% CI 1.2 to 3.6) and 2.8 times higher among those aged ≥35 years (AOR 2.8, 95% CI 1.3 to 6.1). Self-injection of gender affirming hormones was associated with a fourfold increase in the odds of HIV infection (AOR 4.4, 95% CI 1.1 to 17.3). A history of genital sores over the previous 12 months increased the odds of HIV infection by threefold (AOR 3.0, 95% CI 1.2 to 7.8). Transgender women with stronger feminine identity, dressing as a woman all the time, were twice as likely to be HIV infected compared with those who did not dress as a woman all the time (AOR 2.1, 95% CI 1.2 to 3.8). Having never used online services developed for transgender women in the past six months was also associated with higher odds of being HIV infected (AOR 1.9, 95% CI 1.2 to 3.2).
This study reveals an HIV prevalence of 5.9% among transgender women in Cambodia. This prevalence was about 20 times higher than the 0.3% among women attending antenatal care clinics in 2014 who represent the general adult population aged 15–45 years,30 and about 2.5 times higher than the 2.3% among MSM in 2014.26 This observed prevalence emphasises that transgender women in Cambodia are at high risk of HIV and is consistent with global literature regarding the high burden of HIV among this transgender population.1
Although statistically non-significant (p=0.13), the prevalence found in this study was higher than the prevalence of 4.2% reported in the smaller (n=891) TGIBBS conducted in 201222 and was therefore contrary to our hypothesised expectations of reduction in HIV prevalence among this population. Recent progress in Cambodia, where 73% of all estimated HIV-positive people or 93% of those who have been aware of their positive status are in care,31 had prompted us to hypothesise the lower prevalence. Although we have no concrete evidence regarding the non-significant increase of HIV prevalence, we suggest that it may be related to the sampling variation in the two surveys. The previous study recruited participants only from the capital city and five provinces (Phnom Penh, Battambang, Banteay Meanchey, Kampong Cham, Siem Reap and Preah Sihanouk),22 whereas our study expanded to additional eight provinces.
More than half (52%) of those who had HIV reactive tests reported that they had never learnt about their HIV-positive status before they participated in the study. We believe that this self-reporting of the HIV status is realistic. Since we were concerned that those who were already aware of their HIV status may be unwilling to report their status, we decided to use well-trained counsellors who all were from the government’s VCCT centres. These counsellors had many years of experience in providing VCCT services and were better equipped to cope with difficult situations. In Cambodia, we believe people are more likely to trust their counsellors, as opposed to interviewers. However, as in all self-reported measures, the potential for response bias cannot be entirely ruled out.
This study also reports important findings related to factors associated with HIV infection among transgender women in Cambodia. First, the HIV prevalence among transgender women residing in urban communities was twice as high compared with that among transgender women living in rural communities. This finding is similar to that in a previous study that found a higher HIV prevalence in transgender women living in urban areas of Siem Reap and Phnom Penh compared with that among transgender women living in other provinces.22 Findings from our study suggest that these differences may not necessarily be attributable to common sexual risk practices. The mean number of sexual partners (8.4 vs 7.9, p=0.70) and the mean number of male commercial sexual partners (0.7 vs 0.7, p=0.48) in the past three months among transgender women living in urban and rural communities were not significantly different. In addition, the rates of inconsistent condom use with male non-commercial sexual partners in the past three months were also similar in the two groups (58.0% vs 62%, p=0.32).
Given the failure of sexual risk behaviours to sufficiently account for the difference in HIV prevalence, these data suggest that a higher HIV prevalence among sexual partners of transgender women in urban communities may possibly explain the higher probability of urban transgender women to get infected, although this may not be stated with certainty. This is particularly relevant given that previous studies among all transgender women found a higher prevalence of HIV in urban areas.22 Studies among MSM in Cambodia have also found a higher prevalence of HIV in urban areas.24 32 In addition, a recent national sentinel survey among women attending antenatal care clinics found that HIV prevalence among women in urban areas was consistently high,30 implying that HIV prevalence in urban areas among most populations, who potentially include transgender women and their partners, is high. It is also possible that transgender population in urban communities face unique or additional risks compared with other members of this population in rural areas,22 which could also contribute to the difference in HIV prevalence between urban and rural communities. Still, it is possible that those who knew they were positive may have moved to urban centres for care and treatment, which unfortunately cannot be examined further in this cross-sectional study. Further research is needed with regard to this observation.
Second, HIV prevalence among older transgender women (≥25 years) was significantly higher compared with that among their younger counterparts. This finding is similar to those of previous studies in Cambodia22 and Thailand.3 A possible explanation is that older transgender women had been exposed to risks for a longer period of time; the number of their sexual partners accumulated over time and thus increased cumulative probability of HIV acquisition.22
Third, our study suggests that more overt feminine expression (eg, those who dressed as a woman all the time) was associated with a higher HIV prevalence. A study in the USA found that transgender women who disclosed their female gender identity possessed a higher HIV prevalence.33 In our study, these transgender women who dressed as a woman all the time had higher numbers of both male non-commercial (mean=8.1 vs 5.1, p=0.004) and male commercial sexual partners (mean=3.7 vs 1.6, p<0.001), compared with those who did not. Making their female status visible could render more chances to meet with men. However, it could make them difficult to find a decent job due to stigmatisation and discrimination, thus leading them to engage in sex work. This finding is in line with existing literature showing that transgender women try to have sex with men—both casual and paid sex—to prove or validate their female gender identity.34–36 In these contexts, ‘sex work provides both desired gender affirmation and economic stability, often with greater financial rewards for sex without a condom’.34 The desire to affirm their gender identity and attractiveness to men also incentivises them to engage in casual sex with multiple partners.15 This sexual behaviour may make them more prone to HIV infection.
There is a tendency to self-inject gender-affirming hormones, often with shared needles, among transgender women in Cambodia.37 This risky practice was associated with an increased risk of HIV infection, implying that self-injecting was performed through unsafe means, and that injecting by a trained health or other professional might mitigate the likelihood of HIV infection. Although hormone injection to augment femininity is becoming more common, it can potentially cause adverse health effects among transgender women.3 38 A Thai study also found that transgender women who injected hormone to make them more feminine had a higher HIV prevalence.3
Fourth, transgender women who completed or dropped out of primary school had a higher HIV prevalence than those with high school education. This finding confirms results of the TGIBBS 2012 in Cambodia22 and other studies6 39 that associated low education with high HIV prevalence among transgender women. This has important implications for HIV programmes to ensure that poorly educated transgender women are reached with education, information, communication and skills related to HIV prevention and other health-related services.
Fifth, transgender women with self-reported STI symptoms (having ulcerations or sores in the genital area in the past 12 months) had a greater HIV prevalence. This is in line with existing evidence showing that STIs promote HIV transmission via a variety of biological mechanisms.40 Transgender women with high rates of STIs, particularly ulcerative genital diseases, are at high risk of HIV acquisition.2 3
Finally, transgender women who reported never using online services developed for transgender women or MSM had an increased risk of HIV infection. Low use of online services by key populations in Cambodia is iterated in other studies.41 Non-users of online services, which tend to provide HIV information, education and communication, might have riskier sexual behaviours. Our data suggest that transgender women who did not use online services had higher numbers of overall male sexual partners (10.2 vs 6.3, p=0.002) and male commercial sexual partners (0.8 vs 0.6, p=0.001) in the past three months. Also, they had a higher rate of inconsistent condom use with male commercial sexual partners in the past three months (48.5% vs 34.4%, p=0.004). Unfortunately, in this study, we did not collect the details about the type of the online services, which could refer to dating, health and social services, or another type of online service. Studies in other settings confirm that transgender women with multiple sexual partners are exposed to a riskier level of HIV infection.6 15 This finding suggests that access to community-based services tailored to transgender population can reduce their vulnerability to HIV as demonstrated in other settings.42 Sustaining and increasing the coverage of internet and peer-led community-based services for this population is particularly important, given that they are often unable to access health services due to stigmatisation and discrimination,16 41 even in healthcare settings.18 As in other settings globally,9 only half of those who were infected with HIV were aware of their status, demonstrating the need to intensify HIV testing, including self-testing at the community level, which transgender women in Cambodia are willing to use.43 Our study also found that once diagnosed the coverage of antiretroviral therapy was high in this population.
Limitations of the study
Our study covered only the capital city and 12 provinces, which contain the highest numbers of transgender women. Since cities and provinces with fewer transgender women were left out, these results may not be generalised to all transgender women nationally. Second, the initial participant seeds were identified and recruited by outreach workers of community-based organisations, which could introduce bias towards transgender women under their programmes, leading to a recruitment bias. This problem could be exacerbated by outreach workers interviewing some participants who had received services from their NGO, which could have induced the participants’ responses. Third, this study employed a self-reporting questionnaire on sensitive health and sexual behaviours, which may have been limited by social desirability bias. Fourth, although minimal, the monetary incentive given to the participants to recruit seeds may have affected their genuine motivation to partake in the study, which could influence their responses. Fifth, we used the backward selection of variables in the multivariable analysis. By using this method, we possibly dropped one or more variables that could be significant if we kept them until the final model. Finally, as this study was cross-sectional, it reports associations at a given time and may not be construed to be reporting causal relationships.
This study demonstrates that HIV prevalence among transgender women in Cambodia remains persistently high. With the prevalence rate at 5.9%, higher prevalence was observed among transgender women who resided in urban areas, of older age, with low education levels, with previous genital sores, with a history of self-injected hormone and those who had never used online services developed for transgender women or MSM. Therefore, to eliminate new HIV infections among transgender women, tailored interventions need to focus on these subpopulations and attendant risk factors.
This study was conducted in collaboration between the consortium partners of the HIV/AIDS Flagship Project including KHANA, FHI360, PSI/PSK and the 13 Municipal and Provincial Health Departments under the leadership of National Center for HIV/AIDS, Dermatology and STD (NCHADS). The authors thank all implementing partners, data collection teams and participants in the study who fully supported during the study design and data collection.
Contributors SC, ST, PM, CL, PC and SY designed the study, developed the research protocol and tools. SC, CN and SY analysed the data, interpreted the results and wrote the manuscript. PC, SC, CL, KP, ST and PM were responsible for training and data collection. JM, JD and GB supported findings analyses and manuscript writing. All authors read and approved the final manuscript.
Funding This study was conducted as part of the HIV/AIDS Flagship Project funded by President's Emergency Plan For AIDS Relief (PEPFAR) through the United States Agency for International Development (USAID).
Disclaimer Content of this paper is the responsibility of the authors and does not reflect the view of USAID or our respective institutions.
Competing interests None declared.
Ethics approval National Ethics Committee for Health Research (NECHR) of the Ministry of Health, Cambodia (no. 420 NECHR) and FHI 360’s Protection of Human Subjects Committee (PHSC no. 713897).
Provenance and peer review Not commissioned; externally peer reviewed.
Data sharing statement Data used for this study cannot be made available in the manuscript, the supplemental files, or a public repository due to the ethical restriction stated in the agreement with the ethical committees. However, they can be accessed upon request from the principal investigator (SY) at firstname.lastname@example.org.
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