High rates of reinfection and incidence of bacterial sexually transmitted infections in a cohort of female sex workers from two Indian cities: need for different STI control strategies?
- Anjana Das1,
- Anupam Khungar Pathni2,
- Prakash Narayanan1,
- Bitra George3,
- Guy Morineau4,
- Tobi Saidel2,
- Parimi Prabhakar1,
- Gururaj Rao Deshpande5,
- Raman Gangakhedkar5,
- Sanjay Mehendale6,
- Arun Risbud5
- 1STI Capacity Raising, FHI 360, New Delhi, India
- 2Independent Consultant, New Delhi, India
- 3India Country Office, FHI 360, New Delhi, India
- 4Asia Pacific Regional Office, FHI 360, Bangkok, Thailand
- 5Department of Microbiology, National AIDS Research Institute, Pune, Maharashtra, India
- 6National Institute of Epidemiology, Chennai, Tamil Nadu, India
- Correspondence to Anjana Das, STI Capacity Raising, FHI 360, H-5 Ground Floor, Green Park Extension, New Delhi 110016, India;
- Received 6 January 2012
- Revised 12 October 2012
- Accepted 28 October 2012
- Published Online First 29 November 2012
Background Female sex workers (FSWs) in India are provided a standardised package of clinical interventions for management of sexually transmitted infections (STIs). A study was conducted among FSWs at known high STI prevalence sites to determine the effectiveness of the service package.
Methods A cohort of FSW clinic attendees in two cities, Hyderabad and Mumbai, were enrolled and followed up from October 2008 to November 2009. At each visit, behavioural and clinical data were obtained and vaginal swabs collected for laboratory testing of cervical infections (gonorrhoea and chlamydia).
Results 417 participants were enrolled, of whom 360 attended at least a follow-up visit. Prevalence of cervical infections did not change between the baseline and final visits (27.7% and 21.3% respectively, p=0.08) in spite of presumptive treatment at baseline and syndromic management at all visits. The proportion of asymptomatic cervical infections increased from 36% at baseline to 77% at the final visit. Incidence rate of cervical infections was high (85.6/100 person years) and associated with a prevalent cervical infection at baseline (HR=2.7, p<0.001) and inconsistent condom use with non-commercial partners (HR=2.5, p=0.014).
Conclusions High rates of STIs persisted despite the interventions due to poor condom use, minimal partner treatment, and high prevalence and incidence of STIs with a large proportion of asymptomatic infections. High-prevalence FSW sites in India need to design more effective partner treatment strategies and consider increasing the frequency of presumptive treatment as a temporary measure for quickly reducing STI prevalence, with renewed emphasis on consistent condom use with all partners.
India is a large country with marked geographical heterogeneity in the prevalence of sexually transmitted infections (STIs), including HIV.1 ,2 The HIV epidemic is mainly core group driven with a wide heterogeneity of HIV prevalence and stages of the epidemic across the country.3 ,4 Predictably, the prevalence of classical STIs also varies across states and districts.1 However, the current state of knowledge is limited to primarily clinic-based studies, certain geographical areas and a wide variety of methods used for laboratory diagnosis. In the general population, various studies have shown that reactive syphilis serology ranged from 0 to 4.7% among women and from 1% to 10.1% among men. In female sex workers (FSWs), the range for reactive syphilis serology was 1.7–39.7%, gonorrhoea 0–16.9%, chlamydia 0.9–22.6% and trichomoniasis 2–54.1%.1
The Indian national STI control programme advocates syndromic management for the general population.5 In addition to syndromic management for symptomatic infections, FSWs are provided a package of services for managing asymptomatic infections, which includes one-time presumptive treatment for gonorrhoea and chlamydia at the first clinic visit, quarterly STI check-ups and biannual syphilis screening.5 In addition, risk reduction counselling, free provision of condoms, client-initiated partner notification and motivation for periodic HIV testing are integral parts of the standardised package of services for FSWs.6 However, these strategies were developed based on limited data from India and international best practices.
Avahan is a large-scale HIV prevention programme for high-risk groups (HRGs) which has been implemented since 2004 in 83 out of a total of 130 districts in six states of India with a high prevalence of HIV. Avahan works either alongside government or other donor-supported NGOs, or as the sole HIV prevention service provider for these groups in a district. Under this programme, approximately 221 000 FSWs are currently provided the STI service package as per national guidelines in conjunction with peer outreach to promote service uptake.7 To date, two rounds of community-based, district-wise surveys, the Integrated Biological and Behavioural Assessments (IBBA), have been carried out to evaluate the programme. The first round of the IBBA (IBBA-1) conducted in 2005–2007 showed an overall low prevalence of cervical infections in most districts; however, a higher prevalence was seen at FSW sites in Hyderabad (gonorrhoea 6.4%, chlamydia 6.5%) and Mumbai brothels (gonorrhoea 9.3%, chlamydia 8.5%).8 Since STI interventions for FSWs at all districts had been initiated about a year prior to IBBA-1, the disparity in STI prevalence needed further investigation. An Avahan-supported operations research study was carried out among a cohort of FSWs in these two cities to determine the effectiveness of the standardised STI service package in controlling common bacterial STIs at known high prevalence sites. This paper analyses the findings and suggests additional STI management strategies for FSWs.
The study design is depicted in figure 1. After written/oral witnessed consent at the baseline visit, trained female investigators administered a behavioural questionnaire covering demographics, sexual practices, condom use, symptoms and STI treatment seeking. Clinicians trained in study procedures carried out detailed history-taking and clinical examination of the ano-genital area. Vaginal swabs were collected during speculum examination. Study participants were asked to return for follow-ups at 1, 2, 3 and 6 months after their initial visit. At follow-up visits during months 1, 2 and 3, a shortened version of the behavioural questionnaire pertaining only to risk behaviour was administered, clinical examination was performed and vaginal swabs were collected. The behavioural questionnaire and laboratory testing done at the final visit were the same as at the baseline visit. The study interventions included the Indian national STI service package for FSWs (mentioned earlier) and treatment for gonorrhoea and chlamydia for all at the baseline visit, either for the relevant syndrome (vaginal discharge (VD) or lower abdominal pain (LAP)) or presumptively. Presumptive treatment consisted of a single dose of cefixime 400 mg and azithromycin 1 g. Syndromic management was provided at all visits. Those with VD syndrome were treated for gonorrhoea (cefixime 400 mg), chlamydia (azithromycin 1 g), candidiasis (fluconazole 150 mg), trichomoniasis and bacterial vaginosis (metronidazole 2 g); those with LAP syndrome were treated for gonorrhoea (cefixime 400 mg), chlamydia (doxycycline 100 mg twice daily for 14 days) and anaerobic infections (metronidazole 400 mg twice daily for 14 days). Cefixime and azithromycin were administered under direct observation at the clinic. The treatment for other STI syndromes was as per the Avahan Clinic Operation Guidelines and Standards.9
Two study clinics were located in different parts of Hyderabad, providing services mainly to street and home-based sex workers. A third study site was located in a large brothel at Mumbai at a dedicated clinic for FSWs. The funding support for the outreach and clinical services varied across sites—while one of the Hyderabad sites was fully supported by Avahan, the other site was supported by Avahan for the clinical services and the National AIDS Control Program (NACP) for the outreach activities. The Mumbai site was supported by the NACP for the outreach services and the clinical services were provided through a local government clinic. From October 2008 to May 2009, all eligible and consenting attendees at these FSW clinics were recruited. Data collection of follow-up visits continued up to November 2009. The eligibility criteria for enrolment included at least two clients in the previous week and/or eight in the last month and age between 18 and 40 years. Additionally, pregnant women or those under the influence of alcohol/drugs at the time of consent were excluded from the study. Peer educators who were oriented about the study raised awareness during routine field visits and encouraged eligible FSWs to attend the clinic. Participants were given a card with their unique study number at enrolment on which the date of the next follow-up was written and explained to them at every visit. If participants provided a phone number, they were reminded about their appointments by a phone call from the study staff.
Infections with Neisseria gonorrhoeae (GC) and Chlamydia trachomatis (CT) were detected in vaginal swab samples using transcription mediated amplification (Gen-Probe APTIMA Combo-2 Assay, Gen-Probe Inc, San Diego, CA, USA). Vaginal swabs were tested by the nucleic acid amplification technique using the PCR method published by Van Der Pol et al10 for Trichomonas vaginalis (TV). Sera from all participants were screened for syphilis by rapid plasma reagin (RPR, Span Diagnostics, Surat, India) and confirmation of all RPR-reactive sera was done by Treponema pallidum haemagglutination assay (TPHA) using Syphagen-TPHA (Biokit, Barcelona, Spain). An RPR titre of >1:8 with a positive TPHA was considered as an active syphilis infection.
The study was approved by the Ethics Committee of the National AIDS Research Institute, Pune, India and the Protection of Human Subjects Committee of Family Health International, North Carolina, USA.
The questionnaire and clinical data of participants were entered into CSPro 3.3 (US Bureau of Census, USA). Participants with complete behavioural and biological data at baseline were included in the analysis. Analysis was performed using STATA V.12.0. The characteristics of participants lost to follow-up were compared with those retained in the cohort. Differences in behavioural characteristics and STI prevalence were assessed using the Wald test or the Fisher-exact test when cell size was less than 5. The means of continuous variables were compared using the Student t test. All tests were double sided and p values <0.05 were considered significant. Prevalence of GC, CT, TV and syphilis were compared at baseline and final visits among participants who attended the final visit (as per month 6 of figure 1). Asymptomatic infections were defined as laboratory-confirmed infections among individuals who did not complain of VD (TV, GC, CT) and/or LAP (GC, CT).
The principal outcome was the incidence of gonorrhoea and chlamydia. Lost to follow-up were those who were enrolled at baseline but did not attend any follow-up visits; they were excluded from the incidence analysis. Participants who had attended at least one follow-up visit with data on laboratory testing of GC and CT were included for the calculation of incidence of cervical infections. Incident cases were defined as GC and/or CT infections (by laboratory test) at the current visit among participants either uninfected or treated at the previous visit. Person years (PYs) for incidence rate (IR) calculations were measured by the time since the previous visit, assuming that the infection occurred at the mid-point between the visits. In addition, individuals who had received a single dose of azithromycin 1 g were considered to be protected against GC/CT for 7 days (because of the long half life of the drug) which was deducted from the person time.
Incidence of GC, CT, GC and/or CT was computed and comparison between those infected and those uninfected at baseline was assessed using Cox regression; hazard ratios (HRs) were presented. Predictors of GC/CT incidence were assessed using Cox regression. All variables associated with incidence of GC/CT in bivariate analysis with p values <0.2 were included in a proportional hazard model. The final model was obtained using backward, stepwise elimination.
Of the 517 individuals screened during the recruitment period, 468 were eligible; 455 individuals consented to participate in the study, and of these, 417 completed all baseline study procedures. The demographic characteristics for those who refused to participate were not available. Among those who consented and completed (n=417) and those who did not complete (n=38) all baseline study procedures, there was no significant difference in socio-demographic characteristics except for the mean duration of sex work (4.6 and 6.3 years respectively, p=0.047). Of the 417 individuals with complete data at baseline, 360 attended at least one follow-up visit. A total of 282 individuals attended the final visit (month 6 in figure 1).
The socio-demographic and behavioural characteristics, and STI prevalence were measured among all participants (n=417) at baseline. Table 1 compares the baseline characteristics between those who attended at least one follow-up visit and those lost to follow-up. Those lost to follow-up were more likely to be brothel-based sex workers than those who attended follow-up (23% vs 6%, p<0.001). Among all enrolled participants, the mean age was 30.4 years, the majority were street-based sex workers (71%), consistent condom use was low with both clients and non-commercial partners (70% and 17% respectively), and TV was the most common STI (31%). Further details about the baseline characteristics are discussed elsewhere.11
At baseline, of a total of 417 participants, 270 (64.7%) presented with complaints of VD and/or LAP, 234 (56.1%) were treated for VD syndrome, while 59 (14.1%) were treated for LAP syndrome. During 1089 follow-up visits, 198 episodes of VD and 44 episodes of LAP syndromes were treated.
Among 255 participants who made a follow-up visit within 90 days of baseline (when all were treated for GC and CT), the prevalence of GC and/or CT decreased from 25.5% to 14.4% (p=0.002). For the 282 participants who attended the final visit, the mean number of days between the baseline and final visits was 217 days (SD 60). Between these visits, there was a significant increase in consistent condom use with clients from 69.5% to 80.9% (p=0.002) and a significant reduction in the mean number of clients in the last week from 4.7 (SD 3.4) to 3.4 (SD 2.5, p<0.001). However, consistent condom use with non-commercial partners remained low (18.6% and 14.2% at baseline and final visits respectively, p=0.214). The prevalence of STIs based on laboratory investigations at the baseline and final visits is shown in table 2. Between the first and last visit, the prevalence of GC and/or CT reduced insignificantly from 27.7% to 21.3% (OR 0.71, p=0.078), while TV increased from 30.3% to 45.7% (OR 1.94, p<0.001). The proportion of asymptomatic infections was higher at the final visit than at baseline for GC, CT and TV (all p values <0.001). Seven incident cases of syphilis were observed at the final visit.
Of a total of 1089 follow-up visits, the intervals between consecutive visits were as follows: the majority (81%) were within 90 days, 9.8% were within 180 days, while 8.5% were after 180 days. A total of 137 incident GC and/or CT infections were observed among 360 participants followed up for a period of 160.0 PYs. Accordingly, the IR for GC and/or CT infections was 85.6/100 PYs; calculated separately for GC and CT, it was 51.7/100 PYs and 56.8/100 PYs respectively. Higher IRs were observed among participants who had a cervical infection at baseline than those who were uninfected (table 3).
In multivariate analysis, the risk factors associated with incidence of GC and/or CT were presence of infection at baseline (HR 2.8, p<0.001), having a larger number of clients in the past week (HR=1.1 per additional client, p=0.012), inconsistent condom use with non-commercial partners (HR=2.5, p=0.014), follow-up visit to the clinic within 45 days compared with >90 days (HR=3.5, p<0.001), and follow-up visit to clinic within 46–90 days compared with >90 days (HR=2.3, p=0.002).
The study was conducted with a cohort of primarily street-based FSWs who were provided standardised STI interventions. Among those who made a follow-up visit within 90 days of the baseline (when all were treated for GC and CT), the prevalence of GC and/or CT decreased from 25.5% to 14.4% (p=0.002). However, owing to high IRs of GC and/or CT (85.6/100 PYs), there was no significant change in prevalence at baseline and final visits (27.7% and 21.3% respectively, p=0.08). Higher IRs were associated with a prevalent cervical infection at baseline, inconsistent condom use with non-commercial partners and shorter duration between follow-up visits. The prevalence of TV increased between the baseline and final visits (from 30.1% to 45.7%, p<0.001) The proportion of asymptomatic GC, CT and TV infections increased to 80% at the final visit compared with 30–35% at baseline (p<0.001).
To the best of our knowledge, evaluation of the effectiveness of a package of STI services among a cohort of FSWs in India has not been reported in the literature. However, the study had several limitations. It was conducted with a single group, which is not an optimal design for evaluating an intervention. More reliable conclusions would have been obtained from a randomised control trial. The study was conducted at sites with known high prevalence of GC/CT based on results of IBBA-1 (2005–2007). Hence the study findings may not be generalisable. As this was a clinic-based survey, the study group is likely to be biased towards symptomatic clients as against the general population of FSW. Collection of rectal and oral swabs for STI tests was not feasible, though 18.7% and 14.6% of participants at baseline did report oral and anal sex respectively in the preceding 3 months. Molecular tests for TV were performed only at the baseline and final visits; the incidence pattern of this common STI could have been determined if the tests were done at all follow-up visits.
High rates of STIs persisted despite the standardised intervention package (one-time presumptive treatment at baseline, clinical screening and syndromic management at all visits, risk reduction counselling, free condom provision and client-initiated partner notification). This was possibly due to poor rates of condom use, particularly with non-commercial partners; high baseline prevalence and incidence of cervical infections and trichomoniasis; and a high proportion of asymptomatic infections at follow-up visits. Although we did not track partner treatment in the study, inadequate partner treatment may have been a contributory factor to the high re-infection rates.
We compared our clinic-based findings on condom use with non-commercial partners and STI prevalence with other FSW studies from India. The IBBA-2 (2009–2010), performed after our study, also showed overall low rates of consistent condom use with regular partners ranging from 0.7% to 42% across districts. The prevalence of GC and CT in Hyderabad was 11.5% and 8.2%, and among Mumbai brothel-based FSWs 5.9% and 4.1% respectively.12 The IBBA results show that some pockets of high prevalence persist in large cities like Hyderabad and Mumbai. Low condom use with regular, non-commercial partners has also been reported from other studies in India.13 ,14 A high prevalence of TV has been reported by several FSW studies in India.15 ,16 The current WHO global estimates show that TV constitutes more than half of all curable STIs.17
Our study showed a high incidence of GC and/or CT infections at the study sites (85.6/100 PYs), with two to three times higher IRs among those with a prevalent infection compared with those uninfected at baseline. FSW studies from Kenya, Guatemala and Melbourne have reported lower IRs, ranging from 11.30 to 12.7/100 PYs for gonorrhoea and from 7.32 to 14.5/100 PYs for chlamydia.18–20 Two FSW studies from Madagascar and China have reported very high IRs for gonorrhoea (0.09/person/month in Madagascar) and chlamydia (0.05/person/month in Madagascar and 65.91/PYs in China).21 ,22 Our findings are also similar to a study from Madagascar which reported that FSWs with a prevalent chlamydial, gonococcal or trichomonal infection at baseline were two to four times more likely to become infected during follow-up compared with those without STIs at baseline.23
The study showed an increasing trend of asymptomatic GC, CT and TV infections between the baseline and final visits. As this was a clinic-based study, the study group was likely to be biased towards symptomatic FSWs attending the clinic for treatment and recruited at baseline. In fact, about 65% of all participants recruited at baseline had symptoms of VD and/or LAP. A recent study carried out in five countries including a cohort of FSWs in India also showed an increasing trend of incident asymptomatic chlamydial infections over a period of 2 years (31.2% from baseline to 12 months and 66.7% at 12–24 months).24 Thus, STI syndromic management would miss most cervical infections at follow-up visits owing to lack of symptoms, and laboratory facilities are unavailable at most FSW clinics.
The current practice in India for partner management is client-initiated partner notification.6 Although we did not track partner treatment in the study, the low condom use and early, high re-infection rates indicate that treatment for regular partners needs to be improved.
To examine the effectiveness of cefixime for the treatment of gonorrhoea, we searched for recent studies from India. A study of antimicrobial susceptibility of GC from India from 2002 to 2006 using ceftriaxone did not report resistance, but about 3% of the isolates did show reduced susceptibility.25 All cases were given either ceftriaxone or cefixime and there were no treatment failures observed among those with the less susceptible strains. However, other countries have reported treatment failures with oral third-generation cephalosporin, which is a matter of concern.26
Based on our study, we have the following recommendations for the national STI programme in India. In addition to continuing efforts to promote consistent condom use, there is a need for designing more effective partner treatment strategies. Further studies are required, including expedited partner therapy, which has been proven to be useful in managing partners of heterosexual men and women with GC, CT and, to some extent, TV infections.27 One-off presumptive treatment may be inadequate at places with continuing poor STI control such as the study sites and proven active transmission dynamics, as shown by the high incidence. An increased frequency of presumptive treatment should be considered as a temporary measure for quickly reducing STI prevalence.28–31 This could be tapered off once the thresholds of <10% combined GC/CT prevalence and >70% reported condom use (with clients) have been met, as suggested by the 2005 WHO consultation.32 Addition of presumptive treatment for trichomoniasis, implemented elsewhere, may be considered.33 The availability of rapid, point-of care tests for GC/CT/TV would be very useful for screening of asymptomatic infections among FSWs at their initial clinic visit. This would enable the programme to intensify interventions, including retesting for those at high risk with a prevalent infection.
The female sex worker study was conducted at known high sexually transmitted infection (STI) prevalence sites to evaluate the effectiveness of a clinical service package for controlling STIs.
The results showed a high incidence of cervical infections associated with a prevalent infection at baseline and inconsistent condom use with non-commercial partners.
More effective partner treatment strategies need to be designed.
High prevalence sites should consider increasing the frequency of presumptive treatment as a temporary measure.
Contributors AD and AKP were primarily responsible for drafting and revising the manuscript. AD, PN and PP were responsible for the field research, oversaw data collection and management. GD and PP were responsible for the laboratory tests. PN, GM and TS contributed to the data analysis. AD, PP, BG, TS, SM, RG and AR participated in developing the concept and design of the study, data interpretation and manuscript review.
Funding This work was supported by the Bill & Melinda Gates Foundation, grant number OPP31280. The views expressed herein are those of the authors and do not necessarily reflect the official policy or position of the Bill & Melinda Gates Foundation.
Disclaimer The views expressed herein are those of the authors and do not necessarily reflect the official policy or position of the Bill & Melinda Gates Foundation.
Competing interests None.
Patient consent Obtained.
Provenance and peer review Commissioned; externally peer reviewed.
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