- Research article
- Open Access
- Open Peer Review
Risk factors, healthcare-seeking and sexual behaviour among patients with genital ulcers in Zambia
© Makasa et al.; licensee BioMed Central Ltd. 2012
- Received: 7 February 2012
- Accepted: 18 May 2012
- Published: 6 June 2012
Genital ulcers (GU) are associated with an increased risk of HIV transmission. Understanding risk factors for genital ulcers and sexual behaviour patterns after onset of symptoms and health seeking behaviour among GU-patients can provide useful information to aid design effective prevention strategies for genital ulcers. We investigated risk factors of self-reported GUs and care-seeking in the general population, and assessed GU patients regarding past care-seeking, recent sexual behaviour and partner awareness of the disease.
We analysed national data on genital ulcers from the 2007 Zambia Demographic and Health Survey, and data from a cross-sectional survey of genital ulcer patients from primary health care facilities in Lusaka, Zambia.
The prevalence of GU in 2007 in the general population of Lusaka was 3.6%. Important predictors for genital ulcers were age 25–29 years, being widowed/separated/divorced and having a high number of life-time sexual partners. No differences in care-seeking were observed by residence, wealth and gender, and 60% of the respondents sought care from public health facilities. Among patients with GUs in Lusaka, 14% sought care >2 weeks after symptom onset. Forty-two percent were not aware of their HIV status, 57% reported sex after onset of symptoms and only 15% reported consistent condom use.
Low awareness of HIV status despite high probability of being infected and low condom use after onset of genital ulcer symptoms leads to a high potential for transmission to sexual partners. This, combined with the fact that many patients with GUs delayed seeking care, shows a need for awareness campaigns about GUs and the importance of abstinence or use of condoms when experiencing such symptoms.
- Genital ulcers (GUs)
- Inconsistent condom use
Sexually transmitted Infections (STIs) remain a public health problem in developing countries . The common causes of genital ulcers (GUs) include Herpes Simplex Virus type 2 (HSV-2), Treponema pallidum, which causes syphilis, and Haemophilus ducreyi which causes chancroid [2–7]. Genital ulcers are particularly associated with increased risk of Human Immuno-deficiency Virus (HIV) acquisition and transmission , but may also lead to complications of their own, such as chronic infection, still-births and congenital infection with syphilis . A meta-analysis showed a 3–4fold increase in susceptibility to HIV infection among women and men with Genital Ulcer Disease (GUD) . In a Ugandan cohort of HIV discordant couples, the probability of HIV transmission per coital act increased 2fold in the presence of GUD, whereas there was no increased risk of transmission for non-ulcer syndromes . Biologically the disrupted genital mucosa or skin provides a port of entry for transmission for the virus, increasing the susceptibility or infectiousness of HIV [8, 12, 13].
Transmission dynamics in a population are dependent upon the rate of new infections of STIs (the reproductive rate), which is a function of the probability of transmission of a pathogen, the rate of partner change, and the duration of infectiousness . The probability of transmission depends on individual factors such as risky sexual behaviour, virulence and efficiency of the organism and the duration of infection . Based on mathematical models, the transmission probabilities of chlamydial infection, syphilis, chancroid and HSV-2 per unprotected sexual act (in a long-term relationship involving uncircumcised men) are estimated at 0.16, 0.18, 0.2 and 0.0009 for male-to-female transmission, and 0.12, 0.15, 0.2 and 0.00015, for female-to-male transmission, respectively, if neither partner is immuno-compromised . The rate at which partners are changed and the probability of transmission can be targeted partly through preventive campaigns and partner notification. Since many STIs are easily curable, onward transmission can be prevented by prompt treatment of the infected (source) patient, tracing of partner(s) within a short period, and treatment of infected or exposed partners.
Not all individuals with an STI are aware of their infection, and an asymptomatic presentation is one of the reasons for the lack of awareness . Amongst those aware of the STI, some seek treatment whilst others do not . A cross-sectional study of residents in Lusaka in the 1990s showed diverse preferences when seeking care for STIs. These included traditional healers, chemists, and public and private health facilities . Stigma, lack of privacy and confidentiality, the availability of other care options, and perceived poor quality of care, were among the factors impeding care-seeking for STIs from public facilities [18, 19]. Early diagnosis and treatment of STIs is important for comprehensive management  and prevents further spread. Delayed care prolongs the duration of infection [14, 21] and thus increases the likelihood of its secondary transmission and the occurrence of complications, such as still births or congenital infections (associated with a high mortality) .
We found no recent studies in Zambia examining sexual behaviour and care-seeking among patients with GUs. This paper examines the risk factors of self-reported GUs and care-seeking in the general population, and assesses GU-patients regarding their past care-seeking, recent sexual behaviour and partner awareness of the disease.
Two data sources were used; data from a GU aetiological study (referred to as the “GUD study”), and data from the 2007 Zambia Demographic and Health Survey (DHS). The primary objective of the GUD study was to ascertain the aetiological pattern of GUs among patients in primary health care facilities in Lusaka. Ten health centres in Lusaka district with the highest STI incidence during the year preceding the study were conveniently selected. Incidence was measured as diagnosed STI cases per 1000 inhabitants in each catchment area in 2009 according to the District Health Management Information System. Consenting patients aged 16 and above presenting with GUs were recruited consecutively between April and May 2010. A structured questionnaire which included questions on demographic data, sexual behaviour and partner’s awareness of the ulcer was administered by the research assistants. A physical examination of the genitalia was done and in addition, women had a speculum examination. Swabs obtained from the GUs were sent for Polymerase Chain Reaction (PCR) testing to detect the aetiological agent. Specimen handling and testing are described elsewhere (paper in press). In addition, consenting patients were given an Oral Mucosal Transudate (OMT) HIV test, using the Oraquick® rapid HIV 1/2 antibody test.
The DHS data was based on 2-stage random cluster sampling. The sampling frame from the census of population and housing of Zambia for the year 2000 was used, which consists of >16,000 Standard Enumeration Areas (SEAs). A SEA is a small geographic unit consisting of 130 households on average. An urban–rural stratification was done for each of the 9 provinces of Zambia, making a total of 18 strata. In the first stage, 320 SEAs were sampled from these strata with proportional probability. In the second stage, 25 households were randomly picked from each selected SEA using equal probability systematic sampling. Men aged 15–59 and women aged 15–49 years of permanent residence or visiting the night before were eligible for interview. The overall response rate was 98%. The interviews included various questions, however of interest to our study were the questions on demographic, socioeconomic position factors, episodes of genital ulcer in the previous year, and healthcare seeking related to these episodes. The socioeconomic position indicators included were education and wealth index. Wealth index was recorded from 5 to 3 categories i.e. poorest/poorer, middle and richer/richest. All respondents were asked to consent to HIV testing and one third to syphilis testing. Serial testing using 2 ELISA tests, Vironostika® HIV Uni-Form II Plus O, Biomerieux and Anti-HIV 1/2 Plus, by Enzygnost® Dade Behring, was done and Western Blot 2.2, Abbott Labs, as a tie breaker. For syphilis testing, Rapid Plasma Reagin was used for screening, and Treponema Pallidum Haemagluttination Assay as a confirmatory test. Further details are described elsewhere .
All analyses were conducted using the statistical software for social sciences, PASW for Windows version 18.0. The design effect (stratified cluster sampling) and weighting for differential selection and response probabilities were taken into account by using complex sample analyses for the DHS data. Associations were assessed for predictors of genital ulcers, care-seeking in general and late care-seeking using logistic regression models. Late care-seeking among patients in the GUD study was defined as having an ulcer for >2 weeks before care was sought. Since there was interaction between the effect of sex and the sexual behaviour variables on the risk of reported genital ulcer in the preceding year, stratified risk factor analyses for GU by sex were done. Factors that were associated (p-value <0.2) with reported genital ulcers in either men or women were included in a multivariate regression model. The proximate determinants conceptual framework was used to guide the analysis of predictors of genital ulcers and a hierarchical multiple regression model was built. In model I, we included socio-demographic factors, i.e. age, marital status, socioeconomic position indicated by educational attainment and wealth index which are considered underlying determinants of STIs. In model II, we added the proximate determinants (“recent sexual activity”, “type of relationship with the previous sexual partner”, “use of condom at the previous sexual intercourse”, “age at first sex” and “total number of life-time sex partners”). Only factors that were significant (p < 0.1) in model II were included in the final model III.
In the GUD study, there was no direct question on sex after onset of symptoms. A new variable was formed by combining information on the duration of the ulcer with the time since the most recent sexual intercourse. Both these questions had the following responses “1–6 days”, “1–2 weeks”, “>2 weeks”, “>1 month”, or “>2 months”. A person was considered to have had sex after onset of symptoms if he/she reported sex within the same period that the ulcer occurred. The question on patients` awareness of the cause of the genital ulcer was open-ended. We re-coded it into a dichotomous variable and grouped all responses that indicated attribution to having had unprotected sex with a partner who was supposedly unwell as being aware of the cause of genital ulceration. A common response for those categorised as unaware of the cause of the ulcer was witchcraft.
The protocol for the GUD study was cleared by the Biomedical Research and Ethics Committee of the University of Zambia and the regional ethical committee of Western Norway. The Ministry of Health in Zambia gave authority to carry out the study in the designated health facilities. The patients were seen by a clinician and treated according to the national treatment guidelines for STIs based on syndromic management, before being recruited into the study. All the patients were counselled and referred for HIV testing based on an opt-out principle. Written informed consent to participate and separate written consent for HIV testing were obtained from all patients prior to participation.
Approval for the serial DHS was given in 1992 by the government through Ministry of Finance. The anonymous linked protocol developed by Measure DHS was used for HIV specimen collection and analysis, which allows linking of the results to socio-demographic data if information that potentially identifies an individual is destroyed. Information on testing, storage and further testing of the DBS was provided to all participants. Results of the HIV test were not provided, but print material was availed to all on HIV/AIDS and the available fixed points for HIV testing . A single injection of the standard treatment in Zambia, Benzathine penicillin, was given to respondents that tested positive for syphilis. Alternative treatment for pregnant women and patients allergic to penicillin was provided, and referral to the nearest health facility for those who did not wish to be treated at home .
Predictors of genital ulcer symptoms among men in the general population
Age in years
0.9 (0.43, 1.72)
1.6 (0.59, 4.33)
Married / Cohabiting
Widowed /Separated / Divorced
Poorest / Poorer
Richer / Richest
Recent sexual activity
Active last 4 weeks
Not active last 4 weeks
Used condom last sex
Relationship with last partner
Casual acquaintance /Girl friend
Age at first sex (in years)
Life-time sex partners
11 and above
Circumcised (men only)
Predictors of genital ulcer symptoms among women in the general population
Age in years
Married / Cohabiting
Widowed /Separated / Divorced
Poorest / Poorer
Richer / Richest
Recent sexual activity
Active last 4 weeks
Not active last 4 weeks
Used condom last sex
Relationship with last partner
Casual acquaintance /Girl friend
Age at first sex (in years)
Life-time sex partners
11 and above
Most respondents (78%) had sought care for their ulcers. Of these, 60% had sought care at a public health facility, 10% at a private and 30% at another kind of facility. There was no association between residence, socio-economic position or sex and seeking care for GU symptoms in the general population. (Additional file 1: Table S1).
Findings from the GUD study
Characteristics of patients with GUD attending government clinics in Lusaka, Zambia
Overall no. of patients (%)
Males n (%)
Females n (%)
Age Mean, in years (SD)
Education: (n = 201)
Primary / no education
84 (41.8 )
Secondary / tertiary
117 (58.2 )
Duration of ulcer
more than 2 weeks
more than 1 month
more than 2 months
When last did you have an ulcer? (n = 96)
Last 3 months
Last 6 months
Last 1 year
More than 1 year
Partner aware of your genital ulcer (n = 195)
Knowledge on cause of genital ulcers (n = 184)
Do not have knowledge
Aware of their HIV status (n = 125)
HIV Status (n = 128)
Sought treatment previously for present ulcer (n = 177)
Where (n = 101)
Government hospital/health centre
Private hospital/health centre
Sex since onset of symptoms
Condom-use since ulcer developed
We also found that patients with bilateral nodes and recent experience of ulcers were less likely to have postponed care-seeking than those with unilateral nodes (7 vs. 21%) and first occurrence of an ulcer (9 vs. 16%), respectively. The differences were however non-significant. The data showed no association between education or severe symptoms of genital ulcers such as bleeding, pain, or genital swelling and late care-seeking (results not shown).
Probability of GUD patients reporting that partners are aware of their STI
Sex after onset of symptoms
Knowledge on causes of genital ulcers
The data from the Zambia DHS 2007 indicated a low annual prevalence of genital ulcers in the general population. We found that the majority of the respondents sought care in public health facilities in contrast to earlier studies from the late 1990s, that showed a preference for private over public facilities [18, 19]. There were no differences by residence or socioeconomic position indicators in care-seeking among respondents in the general population. The data from the GUD study in Lusaka indicated that most patients with genital ulcers were sexually active after the onset of symptoms and that consistent condom use was very low. This indicates a great potential for further transmission of the disease, while partner awareness had a disappointingly limited impact on condom use.
The age category with the highest estimate of GU symptoms in both men and women in the general population was 25–29 years. This could reflect higher sexual activity in this age group although the risk remained significantly higher even after adjusting for some sexual behaviour characteristics. Some factors such as concurrency, frequency of sex or consistent use of condoms, however could not be adjusted for as they were not available, and thus could explain the persistent association.
Widowhood, separation or being divorced was also associated with GU symptoms in men, although this was not the case in women. It is possible that the widowed and separated/divorced engage in more risky sexual behaviour, putting them at risk of GUD, as seen in a Zimbabwean study where widows and widowers had more partners, a higher partner change rate and were likely to engage in transactional sex, compared to the non-widowed . We also found that HIV prevalence was significantly higher among this group, which is in line with other studies [24–26]. This could be due to higher risky sexual behaviour among them or could arise from the fact that the most common cause of adult mortality in Sub-Saharan Africa is HIV. If the deceased spouse died of HIV, the widowed respondent would obviously be at increased risk of being infected too [24, 27].
The prevalence of GUD was the same irrespective of education status. This does not correspond with the findings from 5 rounds of syphilis surveillance among pregnant women in Zambia between 1994–2008 which showed consistently lower risk of syphilis in higher educated women . It is likely that GUD is substantially under-reported in this population-based survey, and therefore this lack of association could be explained by differential reporting bias, i.e. that under-reporting is negatively associated with level of education due to a higher level of awareness among the higher educated. Under-reporting could also be due to both recall and social desirability biases, and may result in no apparent associations, especially for small samples and rare conditions, as in this case.
In this study, the majority of the respondents from the general population sought care from a public health facility, but 40% sought care from private or “other” unspecified facilities. “Other” facilities comprised of a shop or pharmacy and the non-biomedical sector. Alternative sources for STI care reported previously in Zambia and other African countries include chemists/pharmacies and traditional healers [18, 19, 29, 30]. Reasons cited in literature, why patients seek care outside the public sector, include long waiting time at the health facilities, lack of privacy, lack of drugs and insistence on bringing the sexual partner(s) for treatment [18, 19, 31, 32]. Although the quality of services varies in both private and public health facilities, there are reports that suggest that the latter provide better STI services [17, 33–35]. Public facilities may be better placed in providing good services if a functional national STI programme is in existence, which involves in-service trainings, provision of treatment guidelines and ensuring constant drug supplies for syndromic management of STIs. Literature shows that many private facilities fall short of standardised care  as seen in a South African study in Hlabisa, which compared STI therapeutic practices of private doctors with standard guidelines from the provincial health department. The treatment of STIs by the private doctors was not in line with provincial guidelines. In that study, patients were inadequately treated and a variation was observed in the type of treatment prescribed for any single syndrome among the doctors . In Zambia, periodic performance appraisals are conducted for all public facilities by supervising authorities. Public facilities also benefit from capacity building programmes organised by the national control programme, while private facilities are often not included in these quality assurance mechanisms. Considering the different players involved in care for STIs, standardised STI care in both public and private facilities should be an important strategy in reducing STI morbidity. Another key strategy is to increase awareness among the traditional healers on STIs, their consequences, and the need to refer patients to health facilities where effective treatment can be obtained. Encouragingly, only a minority of the patients from the GUD study in Lusaka sought care >2 weeks after symptom onset. It was however surprising that the DHS data showed that there were only minor differences in care seeking by residence and socioeconomic position indicators. Considering that only 50% of the rural population in Zambia live within 5 km of a health facility, compared to >90% of the urban population, one would have expected a difference in the likelihood of seeking care between urban and rural residents . The data suggest that there are no substantial inequities to care seeking in this setting. This finding should be interpreted with caution since the association might be affected by the likely substantial under-reporting of symptoms.
In the GUD study, almost half the patients had partners who were aware of their STI. The association found between partner awareness and higher likelihood of engaging in sex after onset of symptoms may indicate that the ulcer had become visible during intercourse. However, it is surprising that only 16% of those who had partners who were aware of the ulcer used condoms consistently. Condom use in Africa is still generally low [34, 38] and having sex while having symptoms of an STI also seem to be common as seen in other studies too [30, 39, 40]. These findings indicate that partner notification may only stop transmission if the partner is successfully treated, since awareness of an ulcer may not result in preventive precautions. Partner notification and treatment, and patient counselling and advice to inform their partners to seek care are all included in the Zambian STI guidelines. However, there is no legal framework-backing for this, and the notification system does not function optimally . Although notification and referral to facilities for treatment may deter some patients from seeking care at government facilities , it remains important for reducing secondary spread and re-infections. However, patients` unwillingness to disclose all partners, can impede such notification programmes, and tracing partners without the assistance of the source patient is time-consuming . Of concern was also the high proportion of GUD patients who did not know their HIV status, considering the increased risk of such patients to acquire or transmit HIV to their partners. This is compounded by low condom use and tendency to continue having unprotected sex while symptomatic. Control programmes must attempt to ensure that most GUD patients are tested for HIV and risk reduction messages are re-enforced.
In addition to the previously discussed weakness of reporting bias in self-reporting of STIs in the population-based surveys, some other important limitations of our study are worth considering. The sample for the GUD study was small and designed for another study to ascertain microbiological etiologies of genital ulcers in Lusaka using molecular techniques. The small sample therefore limited the ability to establish significant differences between the sub-populations. The study was facility-based, thus representing GUD patients who seek care in primary healthcare facilities and do not necessarily represent all STI patients and those who sought care elsewhere. On the other hand, a strength worth noting is the representativeness of the DHS surveys at national, provincial, and rural/urban levels of the country and the overall high response rate of the 2007 survey. Non-response in the DHS was mainly due to absence, while refusal to participate was low . However, the low number of people reporting GU symptoms meant that only a small sample was available when examining predictors of care-seeking, resulting in few significant associations, although the percentages indicated important differences between subgroups.
In conclusion, public awareness needs to be raised on the importance of early treatment seeking at public facilities, long-term consequences of STIs and sexual risk reduction as strategies for reducing STIs. Intensification of health campaigns on abstinence and promoting condom-use when there is ulceration are key to stopping further transmission of infections. Partnering with providers in the private sector ought to be considered to ensure referral where appropriate, and standardised patient care.
We thank the Central Statistical Office, the implementers of the DHS, in partnership with Ministry of Health, Topical Diseases Research Centre, and the Demography Division, University of Zambia. Technical support was provided by Macro International through the Measure DHS programme. Funding for the DHS was provided by USAID, Ministry of Health, Ministry of Finance, CDC, PEPFAR, MACEPA, EU, World Bank, ZANARA, WHO, UNAIDS, UNFPA, UNDP, UNICEF, JICA, SIDA, DFID, DCI. We also thank the data collectors and the respondents of the DHS and the GUD study.
The GUD study was funded by the University of Bergen, Norway.
- Buve A, Carael M, Hayes RJ, Auvert B, Ferry B, Robinson NJ, Anagonou S, Kanhonou L, Laourou M, Abega S, et al: Multicentre study on factors determining differences in rate of spread of HIV in sub-Saharan Africa: methods and prevalence of HIV infection. AIDS. 2001, 15 (Suppl 4): S5-14.View ArticlePubMedGoogle Scholar
- Ahmed HJ, Mbwana J, Gunnarsson E, Ahlman K, Guerino C, Svensson LA, Mhalu F, Lagergård T: Etiology of genital ulcer disease and association with human immunodeficiency virus infection in Two Tanzanian Cities. Sex Transm Dis. 2003, 30 (2): 114-119. 10.1097/00007435-200302000-00004.View ArticlePubMedGoogle Scholar
- Bruisten SM, Cairo I, Fennema H, Pijl A, Bruimer M, Peerbooms PGH, Van Dyk E, Meijer A, Ossewaarde JM, van Doornum GJJ: Diagnosing genital ulcer disease in a clinic for sexually transmitted disease in Amsterdam, The Netherlands. J Microbiol. 2001, 39 (2): 601-605.Google Scholar
- Pickering JM, Whitworth JAG, Hughes P, Kasse M, Morgan D, Mayanja B, Van der Paal L, Mayaud P: Aetiology of sexually transmitted infections and response to syndromic treatment in southwest Uganda. Sex Transm Infect. 2005, 81: 488-493. 10.1136/sti.2004.013276.View ArticlePubMedPubMed CentralGoogle Scholar
- Risbud A, Chan-Tack K, Gadkari D, Gangakhedkar RR, Shepherd ME, Bollinger R, Mehendale S, Gaydos C, Divekar A, Rompalo A, et al: The etiology of genital ulcer disease by multiplex polymerase chain reaction and relationship to HIV infection among patients attending sexually transmitted disease clinics in Pune, India. Sex Transm Dis. 1999, 26 (1): 55-62. 10.1097/00007435-199901000-00009.View ArticlePubMedGoogle Scholar
- Sanchez JJ, Volquez CC, Totten PAP, Campos PEP, Ryan CC, Catlin MM, Hasbun JJ, Rosado De Quiñones MM, Sanchez CC, De Lister MBM, et al: The etiology and management of genital ulcers in the Dominican Republic and Peru. Sex Transm Dis. 2002, 29 (10): 559-567. 10.1097/00007435-200210000-00001.View ArticlePubMedGoogle Scholar
- Sunkote TR, Hardick A, Tobian AAA, Mpoza B, Laeyendecker O, Serwadda D, Opendi P, Gaydos CA, Gray RH, Wawer MJ, et al: Evaluation of multiplex real-time PCR for detection of Haemophilus ducreyi, Treponema pallidum, herpes simplexvirus type 1and 2 in the diagnosis of genital ulcer disease in the Rakai District, Uganda. Sex Transm Infect. 2008, 85: 97-101. 10.1136/sti.2008.034207.View ArticleGoogle Scholar
- Cohen MS: Sexually transmitted diseases enhance HIV transmission: no longer a hypothesis. Lancet. 1998, 351 (Suppl 3): 5-7.View ArticlePubMedGoogle Scholar
- World Health Organization: Sexually Transmitted and Other Reproductive Tract Infections. Intergrating STI/RTI Care for Reproductive Health. 2005, Geneva, Switzerland: World Health OrganizationGoogle Scholar
- Rottingen JA, Cameron DW, Garnett GP: A systematic review of the epidemiologic interactions between classic sexually transmitted diseases and HIV: how much really is known?. Sex Transm Dis. 2001, 28 (10): 579-597. 10.1097/00007435-200110000-00005.View ArticlePubMedGoogle Scholar
- Gray RH, Wawer MJ, Brookmeyer R, Sewankambo NK, Serwadda D, Wabwire Mangen F, Lutalo T, Li X, Cott T, vanQuinn TC: Probability of HIV-1 transmission per coital act in monogamous, heterosexual, HIV-1-discordant couples in Rakai, Uganda. Lancet. 2001, 357 (9263): 1149-1153. 10.1016/S0140-6736(00)04331-2.View ArticlePubMedGoogle Scholar
- Vernazza PL, Eron JJ, Fiscus SA, Cohen MS: Sexual transmission of HIV: infectiousness and prevention. AIDS. 1999, 13 (2): 155-166. 10.1097/00002030-199902040-00003.View ArticlePubMedGoogle Scholar
- Wawer MJ, Sewankambo NK, Serwadda D, Quinn TC, Paxton LA, Kiwanuka N, Wabwire-Mangen F, Li C, Lutalo T, Nalugoda F, et al: Control of sexually transmitted diseases for AIDS prevention in Uganda: a randomised community trial. Rakai Project Study Group. Lancet. 1999, 353 (9152): 525-535. 10.1016/S0140-6736(98)06439-3.View ArticlePubMedGoogle Scholar
- Aral SO: Determinants of STD epidemics: implications for phase appropriate intervention strategies. Sex Transm Infect. 2002, 78 (Suppl 1): i3-13.View ArticlePubMedPubMed CentralGoogle Scholar
- Low N, Broutet N, Adu-Sarkodie Y, Barton P, Hossain M, Hawkes S: Global control of sexually transmitted infections. Lancet. 2006, 368 (9551): 2001-2016. 10.1016/S0140-6736(06)69482-8.View ArticlePubMedGoogle Scholar
- Wawer MJ, Gray RH, Sewankambo NK, Serwadda D, Li X, Laeyendecker O, Kiwanuka N, Kigozi G, Kiddugavu M, Lutalo T, et al: Rates of HIV-1 Transmission per Coital Act, by Stage of HIV-1 Infection, in Rakai, Uganda. J Infect Dis. 2005, 191 (9): 1403-1409. 10.1086/429411.View ArticlePubMedGoogle Scholar
- Moses S, Ngugi EN, Bradley JE, Njeru EK, Eldridge G, Muia E, Olenja J, Plummer FA: Health care-seeking behavior related to the transmission of sexually transmitted diseases in Kenya. Am J Public Health. 1994, 84 (12): 1947-1951. 10.2105/AJPH.84.12.1947.View ArticlePubMedPubMed CentralGoogle Scholar
- Msiska R, Nangawe E, Mulenga D, Sichone M, Kamanga J, Kwapa P: Understanding Lay Perspectives: Care Options for STD Treatment in Lusaka, Zambia. Health Policy Plan. 1997, 12 (3): 248-252. 10.1093/heapol/12.3.248.View ArticlePubMedGoogle Scholar
- Ndulo J, Faxelid E, Tishelman C, Krantz I: "Shopping" for Sexually Transmitted Disease Treatment: Focus Group Discussions Among Lay Persons in Rural and Urban Zambia. Sex Transm Dis. 2000, 27 (9): 496-503. 10.1097/00007435-200010000-00002.View ArticlePubMedGoogle Scholar
- Meyer-Weitz A, Reddy P, Van den Borne H, Kok G, Pietersen J: Health care seeking behaviour of patients with sexually transmitted diseases: determinants of delay behaviour. Patient Educ Couns. 2000, 41: 263-274. 10.1016/S0738-3991(99)00103-2.View ArticlePubMedGoogle Scholar
- Fonck KK: Healthcare-Seeking Behavior and Sexual Behavior of Patients With Sexually Transmitted Diseases in Nairobi, Kenya. Sex Transm Dis. 2001, 28 (7): 367-371. 10.1097/00007435-200107000-00002.View ArticlePubMedGoogle Scholar
- World Health Organization: Global prevalence and incidence of selected curable sexually transmitted infections: overview and estimates World Health Organization. 2001, Geneva: World Health Organization, 52-Google Scholar
- Central Statistical Office (CSO), Ministry of Health (MOH), Tropical Diseases Research Centre (TDRC), University of Zambia, Macro International Inc: Zambia Demographic and Health Survey. 2009, Claverton, Maryland: CSO and Macro International IncGoogle Scholar
- Lopman BA, Nyamukapa C, Hallett TB, Mushati P, Preez NS-d, Kurwa F, Wambe M, Gregson S: Role of widows in the heterosexual transmission of HIV in Manicaland, Zimbabwe, 1998–2003. Sex Transm Infect. 2009, 85 (Suppl 1): i41-i48. 10.1136/sti.2008.033043.View ArticlePubMedPubMed CentralGoogle Scholar
- Dzekedzeke K, Siziya S, Fylkesnes K: The impact of HIV infection on adult mortality in some communities in Zambia: a cohort study. Trop Med Int Health. 2008, 13 (2): 152-161. 10.1111/j.1365-3156.2007.01985.x.View ArticlePubMedGoogle Scholar
- Porter L, Hao L, Bishai D, Serwadda D, Wawer M, Lutalo T, Gray R, Team TRP: HIV status and union dissolution in Sub-saharan Africa: The case of Rakai, Uganda. Demography. 2004, 41 (3): 465-482. 10.1353/dem.2004.0025.View ArticlePubMedGoogle Scholar
- Mekonnen YY, Sanders EE, Messele TT, Wolday DD, Dorigo Zestma WW, Schaap AW, Mekonnen WW, Meless HH, Mihret WW, Fontanet AA, et al: Prevalence and incidence of, and risk factors for, HIV-1 infection among factory workers in Ethiopia, 1997–2001. J Health Popul Nutr. 2005, 23 (4): 358-368.PubMedGoogle Scholar
- Makasa M, Fylkesnes K, Michelo C, Kayeyi N, Chirwa B, Sandoy I: Declining syphilis trends in concurrence with HIV declines among pregnant women in Zambia: observations over 14 years of national surveillance. Sex Transm Dis. 2012, 39 (3): 173-181. 10.1097/OLQ.0b013e31823b23a4.View ArticlePubMedGoogle Scholar
- Nuwaha FF: Determinants of choosing public or private health care among patients with sexually transmitted infections in Uganda. Sex Transm Dis. 2006, 33 (7): 422-427. 10.1097/01.olq.0000204574.78135.9f.View ArticlePubMedGoogle Scholar
- Zachariah R, Nkhoma W, Harries AD, Arendt V, Chantulo A, Spielmann MP, Mbereko MP, Buhendwa L: Health seeking and sexual behaviour in patients with sexually transmitted infections: the importance of traditional healers in Thyolo, Malawi. Sex Transm Infect. 2002, 78 (2): 127-129. 10.1136/sti.78.2.127.View ArticlePubMedPubMed CentralGoogle Scholar
- Mayaud P, Mabey D: Approaches to the control of sexually transmitted infections in developing countries: old problems and modern challenges. Sex Transm Infect. 2004, 80 (3): 174-182. 10.1136/sti.2002.004101.View ArticlePubMedPubMed CentralGoogle Scholar
- Ndubani P, Hojer B: Sexual behaviour and sexually transmitted diseases among young men in Zambia. Health Policy Plan. 2001, 16 (1): 107-112. 10.1093/heapol/16.1.107.View ArticlePubMedGoogle Scholar
- Fonck KK, Mwai CC, Ndinya Achola JJ, Bwayo JJ, Temmerman MM: Health-seeking and sexual behaviors among primary healthcare patients in Nairobi, Kenya. Sex Transm Dis. 2002, 29 (2): 106-111. 10.1097/00007435-200202000-00007.View ArticlePubMedGoogle Scholar
- O`Farrell N: Genital ulcers, stigma, HIV and STI control in sub-Saharan Africa. Sex Transm Infect. 2002, 78: 143-146. 10.1136/sti.78.2.143.View ArticleGoogle Scholar
- Voeten H: Gender differences in health care-seeking behavior for sexually transmitted diseases: a population-based study in Nairobi, Kenya. Sex Transm Dis. 2004, 31 (5): 265-272. 10.1097/01.OLQ.0000124610.65396.52.View ArticlePubMedGoogle Scholar
- Connolly AM, Wilkinson D, Harrison A, Lurie M, Abdool Karim SS: Inadequate treatment for sexually transmitted diseases in the South African private health sector. Int J STD AIDS. 1999, 10 (5): 324-10.1258/0956462991914195.View ArticlePubMedGoogle Scholar
- Chankova S, Sulzbach S: Human Resources For Health Occassional Paper. 2006, Abt Associates Inc, Bathesaida: Health Services and Systems Program, 37-Google Scholar
- Sandoy IF, Michelo C, Siziya S, Fylkesnes K: Associations between sexual behaviour change in young people and decline in HIV prevalence in Zambia. BMC Public Health. 2007, 7: 60-10.1186/1471-2458-7-60.View ArticlePubMedPubMed CentralGoogle Scholar
- Morrison CS, Sunkutu MR, Musaba E, Glover LH: Sexually transmitted disease among married Zambian women: the role of male and female sexual behaviour in prevention and management. Genitourin Med. 1997, 73 (6): 555-557.PubMedPubMed CentralGoogle Scholar
- O'Farrell N, Hoosen AA, Coetzee KD, van den Ende J: Sexual behaviour in Zulu men and women with genital ulcer disease. Genitourin Med. 1992, 68 (4): 245-248.PubMedPubMed CentralGoogle Scholar
- Faxelid EA, Ramstedt KM: Partner notification in context: Swedish and Zambian experiences. Soc Sci Med. 1997, 44 (8): 1239-1243. 10.1016/S0277-9536(96)00312-7.View ArticlePubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2458/12/407/prepub
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