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Baseline survey
of sexually transmitted infections in a cohort of female bar workers in
Mbeya Region, Tanzania
G Riedner1, M Rusizoka2,
O Hoffmann3, F Nichombe4, E Lyamuya5, D
Mmbando2, L Maboko2, P Hay6, J Todd1,
R Hayes1, M Hoelscher3 and H Grosskurth1
1
London School of Hygiene and Tropical Medicine, London, UK
2 Regional Medical Office, Mbeya, Tanzania
3 Department of Infectious Diseases and Tropical Medicine,
Ludwig-Maximilians-University, Munich, Germany
4 Mbeya Consultant Hospital, Mbeya, Tanzania
5 Muhimbili University College of Health Sciences, Dar es
Salaam, Tanzania
6 St George’s Hospital, London, UK
Correspondence to:
Gabriele Riedner, Department of Infectious and Tropical Diseases, London
School of Hygiene and Tropical Medicine, Keppel Street, London WC1E 7HT,
UK;
gabriele.riedner@lshtm.ac.uk
Accepted for
publication 14 April 2003
ABSTRACT
Objectives: To determine baseline prevalence of sexually
transmitted infections (STI) and other reproductive tract
infections (RTI) and their association with HIV as well as
sociodemographic and behavioural characteristics in a newly
recruited cohort of female bar workers in Mbeya Region,
Tanzania
Methods:
600 female bar workers were recruited from 17 different
communities during September to November 2000 and underwent
gynaecological examination, laboratory testing for HIV/STI,
and interviews using structured questionnaires.
Results:
HIV-1 seroprevalence was 68%. Prevalences of STI/RTI were
high titre syphilis (TPPA/RPR 1/8),
9%; herpes simplex virus 2 antibodies, 87%; chlamydia, 12%;
gonorrhoea, 22%; trichomoniasis, 24%; and bacterial
vaginosis, 40%. HIV infection was associated with TPPA and
HSV-2 seropositivity, bacterial vaginosis and clinically
diagnosed genital ulcers, blisters, and warts. Reported high
risk sexual behaviour during the past year (having multiple
casual partners) was associated with prevalent STI.
Conclusion:
Female bar workers in Mbeya are at high risk of STI and HIV
infection. Targeted STI/HIV prevention interventions for
these women and their sexual partners need to be reinforced.
Methods should be sought to improve healthcare seeking and to
provide easily accessible and affordable STI care services.
Keywords:
STIs; female bar workers; Tanzania
In Tanzania, as in
other countries of sub-Saharan Africa, trading centres along
the major highways have facilitated the spread of HIV from
urban to rural areas. These settlements are characterised by
frequent transit of short term visitors with ample opportunities
for social interactions and casual sexual contact between
travellers and local inhabitants. In particular, women
working in the trading, hotel, and catering businesses in
such communities together with their sexual partners may form
part of a sexual network of individuals at increased risk of
HIV and sexually transmitted infections (STI). Though sex
work is illegal in Tanzania, the nature of the sexual
relationships is often commercial, involving the exchange of
gifts or money. Regarding payment women are usually totally
dependent on the generosity of their client. This type of
informal and unprotected sex work renders women especially
vulnerable to demands for unsafe sex by their clients and to
violence.
In 1991, a cross
sectional survey among 106 sex workers in Moshi, Tanzania
reported high prevalences of HIV (73%), syphilis (27%), and
gonorrhoea (51%).1
Since the mid 1990s little information has been published on
the extent, trends, and determinants of HIV and STI among
women engaging in sex work and their clients in Tanzania.
In the context of
a study of HIV superinfection with different viral subtypes,
an open cohort of 600 women working in bars, hotels, and
guesthouses was established in late 2000 in roadside
settlements in Mbeya Region, Tanzania. In addition to investigations
on the immunological, behavioural, and clinical correlates of
HIV superinfections, several studies of STI and their
interrelation with HIV infection and of interventions to
control them are under way.
The objectives of
the present study were: (1) to assess baseline prevalences of
STI and reproductive tract infections (RTI), (2) to determine
sociodemographic and behavioural risk factors for prevalent
STI, and (3) to investigate associations between HIV
infection and STI/RTI among bar workers recruited to the
cohort.
METHODOLOGY
Study population and design
In late 2000, a cohort of 600 women working in modern and traditional
bars, guesthouses and hotels, was established in Mbeya Region,
south west Tanzania. The region is well connected with other
parts of Tanzania and with neighbouring Malawi and Zambia through
international highways. Women were recruited from 17 sites located
in Mbeya town, trading centres along the main roads, and one
gold mining area. Distances between these sites were in the
order of 20–240 km. Eligibility criteria for cohort participants
included (1) age between 18 and 35 years, and (2) presence at
the project site during the past 6 months. On the days of
recruitment at each site, one group (and at three sites two
groups) of 30 women fulfilling these criteria was enrolled
consecutively.
Interviews
and clinical examinations
All 600 women were interviewed in Swahili, using a structured
questionnaire. Information collected included sociodemographic
characteristics, living conditions, sexual behaviour, lifetime
history of genital ulcers and vaginal discharge, contraceptive
use, and pregnancy.
At each site,
clinical examinations were carried out in a suitable
locality, usually a local government health facility, ensuring
privacy and confidentiality. Consenting women were interviewed,
a blood sample was taken and a gynaecological examination
performed, during which genital specimens were collected for
laboratory diagnosis. Women with signs or symptoms suggestive
of STI were treated on the spot by study clinicians following
the Tanzanian national syndromic STI case management
guidelines.
Laboratory
methods
Swabs from the vaginal fornix were immediately inoculated onto
a culture medium for Trichomonas vaginalis (InPouch TV;
Biomed Diagnostics, San Jose, CA, USA), which was read
according to manufacturer’s instructions after 3 and 5 days.
Smears obtained from the vaginal wall were examined
microscopically for bacterial vaginosis using the Nugent
score criteria.2
Cervical swabs were tested with the Amplicor C trachomatis
and N gonorrhoeae polymerase chain reaction (PCR)
(Roche Diagnostics, Branchburg, NJ, USA). Ulcer swabs were
examined by Multiplex PCR3
for T pallidum (TP), H ducreyi (HD), and HSV
(Roche Diagnostics, Branchburg, NJ, USA).
Syphilis serology
was assessed by means of the Serodia Treponema pallidum
particle agglutination assay (TPPA; Fujirebio Inc, Tokyo,
Japan) and with the rapid plasma reagin test (RPR; VD25,
Murex Diagnostics Ltd, Cambridge, UK). RPR/TPPA positive results
were categorised into high titre RPR ( 1/8),
suggestive of early latent, untreated syphilis, and low titre
RPR ( 1/4),
suggestive of late latent, and/or treated syphilis.
All sera were
tested with a dual ELISA strategy (HIV-Determine, Abbott
Laboratories, USA and Enzygnost HIV1+2 plus, Behring,
Germany).
Statistical methods
Data were entered in Microsoft Access 2000 (Microsoft Inc, USA)
and statistical analysis was performed using STATA 6.0 (Stata
Inc, 1999).
The association of
STI prevalence with increasing age (grouped as <20 years;
20–24 years; 25–29 years, and 30+ years) was examined using
the Mantel-Haenszel test for trend controlling for site of
recruitment. Adjusting for age and site of recruitment,
logistic regression was used to calculate odds ratios (ORs)
for the association between (1) STI pathogens and selected
sociodemographic and behavioural variables, and (2) HIV
serostatus and STI. To analyse independent effects of sociodemographic
and behavioural variables on STI risk logistic regression was
used to adjust ORs for all variables that were statistically
significant (p<0.05) in the age and site adjusted model.
RESULTS
General characteristics of the study population
At recruitment the mean age of the 600 women was 25.4 years.
All 583 women, who reported on their educational status, had
some formal education, 433 (74%) had completed primary education
and 54 (9%) had attended secondary school for some time. In
all, 127 of 600 women (21%) were married or living with a partner,
264 (44%) were widowed or divorced, and 209 (35%) were single;
289 (48%) worked in modern bars, 169 (28%) in traditional bars
(vilabu), 113 (19%) in restaurants/guesthouses, and 29 (5%)
in kiosks serving drinks; 408 (68%) had been working in their
current profession less than 2 years. Mobility was high, and
one fifth of the women had changed residence during the past
year.
Prevalence
of STI/RTI symptoms, signs and pathogens
Prevalences of symptoms and signs of STI/RTI are shown in table
1 .
Table 1 Prevalence of STI/RTI symptoms and
signs among 600 female bar workers
|
STI/RTI symptom or sign |
No (%) |
|
|
|
Reported current STI/RTI
symptoms |
|
Any STI/RTI symptom |
181 (30.2) |
|
Genital discharge |
56 (9.3) |
|
Genital ulcer |
18 (3.0) |
|
Genital warts |
61 (10.2) |
|
Genital itching |
80 (13.3) |
|
Lower abdominal pain |
45 (7.5} |
|
Swollen inguinal lymph nodes |
14 (2.3) |
|
Clinically diagnosed STI/RTI
signs |
|
Any STI/RTI sign |
326 (54.3) |
|
Abnormal genital discharge |
213 (35.5) |
|
Cervicitis |
113 (18.8) |
|
Genital ulcer(s) |
52 (8.7) |
|
Genital blister(s) |
12 (2.0) |
|
Genital warts |
39 (6.5) |
|
Inguinal lymphadenopathy |
62 (10.3) |
|
Lower abdominal tenderness |
38 (6.3} |
|
Reported lifetime STI/RTI
symptoms |
|
Ulcer |
106 (17.7) |
|
Discharge |
141 (23.5) |
|
There was a poor
correlation between reported symptoms and clinically
diagnosed signs. For example, 56% of clinically diagnosed STI
signs were not reported by the women, while about 20% of symptoms
women complained of could not be verified upon clinical
examination. Out of 181 women complaining of STI symptoms, 33
(18%) had already sought treatment.
Prevalence of
infection with HIV and STI pathogens by age is shown in table
2 .
Table 2 Prevalence of STI/RTI pathogens and
STI/HIV seromarkers by age
|
Pathogen |
Prevalence of positive laboratory
test result by age group
|
Test for trend |
|
Age <20 (n=52) |
Age 20–24 (n=210) |
Age 25–29 (n=222) |
Age 30+ (n=116) |
All ages (n=600) |
|
|
|
Genital swabs |
|
N gonorrhoeae (NG) |
21.2% |
30.0% |
19.4% |
13.8% |
22.2% |
(p<0.01) |
|
C trachomatis (CT) |
17.3% |
15.7% |
9.9% |
9.5% |
12.5% |
(p<0.01) |
|
NG/CT |
36.5% |
37.6% |
26.1% |
20.7% |
30.0% |
(p<0.01) |
|
T vaginalis |
32.7% |
24.3% |
22.1% |
21.5% |
23.7% |
(p=0.12) |
|
C albicans |
63.5% |
61.6% |
61.9% |
56.9% |
60.5% |
(p=0.64) |
|
Bacterial vaginosis |
42.3% |
45.2% |
39.4% |
31.9% |
40.2% |
(p=0.04) |
|
T pallidum (ulcer) |
|
|
|
|
0.8% |
|
|
H ducreyi (ulcer) |
|
|
|
|
0.0% |
|
|
HSV (ulcer or blister) |
|
|
|
|
1.7% |
|
|
Serology |
|
HIV |
46.2% |
71.9% |
68.0% |
70.7% |
68.0% |
(p<0.01) |
|
TPPA+ve |
26.9% |
41.9% |
46.4% |
50.0% |
44.2% |
(p<0.01) |
|
TPPA+/RPR+ (all titres) |
17.3% |
16.7% |
18.0% |
16.4% |
17.2% |
(p=1.0) |
|
TPPA+/RPR+ (titre 1:8) |
11.5% |
10.5% |
6.8% |
5.2% |
8.2% |
(p=0.07) |
|
HSV-2 |
59.6% |
88.1% |
90.1% |
89.7% |
86.8% |
(p<0.001) |
|
At least one classic STI pathogen (T
vaginalis, N gonorrhoeae, C trachomatis,
H ducreyi, T pallidum, HSV) was detected in 282/600
(47.0%) women. Including women with bacterial vaginosis and
candidosis and women with high titre active syphilis, 89% of
all women were diagnosed with one or more STI and/or RTI.
Of pathogens
causing cervicitis or colpitis, N gonorrhoeae was
present in 133 (22.2%) of the women, C trachomatis in 75 (12.5%),
concurrent C trachomatis and N gonorrhoeae in 28
(4.7%), and T vaginalis in 142 (23.7%); 8.7% had a
syphilis serology suggestive of current untreated syphilis
(RPR 1/8/TPPA+ve).
The prevalence of
C trachomatis and syphilis (RPR 1:8)
decreased with increasing age. The prevalence of N
gonorrhoeae peaked in the age group 20–24 years and
decreased thereafter. In contrast, antibodies to HIV-1,
HSV-2, and T pallidum were more prevalent among older
women. The highest relative increase of the latter infections
occurred between the youngest age group (<20 years) and the
second youngest (20–24 years): HIV-1 prevalence increased
from 46% to 72%, HSV-2 seropositivity from 60% to 88%, and
TPPA seropositivity from 27% to 42%.
HSV and T
pallidum were detected in 13.5% and 9.6% and H ducreyi
in none of specimens of 52 women with genital ulcerative/erosive
lesions respectively.
Among women with
clinically diagnosed vaginal discharge and/or cervicitis, the
prevalence of T vaginalis (25.8%), C albicans
(59.6%), N gonorrhoeae (23.5%), and C trachomatis (13.2%)
was not significantly higher than among those without
discharge.
Sociodemographic and behavioural risk factors for STI
Detailed data on self reported risk behaviour and their analysis
will be published elsewhere.4
In the present analysis only selected behavioural variables
have been included. The majority of the women (90%) currently
had a sexual partner, whom they perceived as a "regular" as
opposed to a "casual" partner; 57% reported "casual" partners
besides their regular partner during the past year. In 75% of
these casual sexual relationships some payment was involved.
"Ever condom use" was as low as 50% with both regular and
casual partners. The reported age at first sexual intercourse
ranged between 9 and 26 years (mean 16 years).
In the
multivariate analysis no association was found between any
STI and the following characteristics: frequency of condom
use with regular and casual partners, age when first working
as bar worker, duration of work as bar worker, and mobility.
Associations were found with some variables and these data are
shown in table 3 .
After adjusting for age and site of recruitment, lifetime
infection with syphilis (TPPA+ve) was significantly
associated with a lower educational level (p<0.001). Women
working in "modern bars"—in contrast with other establishments—were
at higher risk of lifetime syphilis as well as HSV-2 infection
(p<0.01), while current infection with N gonorrhoeae/C
trachomatis occurred most frequently in women working in
traditional bars (0.01). N gonorrhoeae/C
trachomatis infections were associated with partner
change (p<0.001) and with the receipt of money for sexual
favours (data not shown). There was a statistically
non-significant association between early age at first sex and
lifetime risk of syphilis or HSV-2 infection (data not shown).
Table 3 Association of STI with
sociodemographic and behavioural characteristics
|
|
|
Lifetime syphilis infection
(TPPA+ve)
|
Lifetime HSV-2 infection (HSV-2
+ve)
|
Current infection with N
gonorrhoeae/C trachomatis
|
|
Variable |
(n) |
% +ve |
OR* (95% CI) |
% +ve |
OR** (95% CI) |
% +ve |
OR*** (95% CI) |
|
|
|
Age (years) |
|
|
p=0.01 |
|
p=0.0004 |
|
p=0.0001 |
|
<20 |
(52) |
26.9 |
1.00 |
59.6 |
1.00 |
36.5 |
1.00 |
|
20–24 |
(210) |
41.9 |
2.28 (1.11 to 4.69) |
88.1 |
4.54 (2.04 to 10.13) |
37.6 |
0.93 (0.47 to 1.85) |
|
25–29 |
(222) |
46.4 |
2.76 (1.34 to 5.66) |
90.1 |
6.03 (2.54 to 14.29) |
26.1 |
0.40 (0.19 to 0.81) |
|
30+ |
(116) |
50.0 |
3.41 (1.54 to 7.58) |
89.7 |
5.29 (1.94 to 14.39) |
20.7 |
0.34 (0.14 to 0.86) |
|
Education (17 missing values) |
|
|
p=0.002 |
|
p=0.08 |
|
p=0.5 |
|
primary incomplete |
(96) |
58.3 |
1.00 |
90.6 |
1.00 |
34.0 |
1.00 |
|
primary complete |
(433) |
41.6 |
0.47 (0.29 to 0.77) |
84.7 |
0.55 (0.24 to 5.65) |
28.6 |
1.02 (0.60 to 1.70) |
|
secondary |
(54) |
31.5 |
0.31 (0.14 to 0.66) |
92.6 |
1.47 (0.39 to 5.52) |
30.3 |
1.50 (0.68 to 3.27) |
|
Marital status |
|
|
p=0.5 |
|
p=0.02 |
|
p=0.6 |
|
single |
(209) |
37.8 |
1.00 |
78.9 |
1.00 |
34.4 |
1.00 |
|
cohabiting/married |
(127) |
47.2 |
0.48 (0.70 to 2.20) |
87.4 |
1.47 (0.66 to 3.23) |
22.8 |
0.70 (0.37 to 1.36) |
|
widowed/divorced |
(264) |
47.7 |
1.28 (0.83 to 1.96) |
92.4 |
2.55 (1.30 to 4.98) |
30.3 |
0.88 (0.55 to 1.38) |
|
Workplace |
|
|
p=0.04 |
|
p=0.009 |
|
p=0.01 |
|
Modern bar |
(289) |
45.7 |
1.00 |
90.3 |
1.00 |
33.9 |
1.00 |
|
Traditional bar |
(169) |
52.7 |
1.29 (0.70 to 2.37) |
89.3 |
0.52 (0.19 to 1.37) |
32.5 |
1.88 (0.96 to 3.67) |
|
Guesthouse/hotel |
(113) |
25.7 |
0.57 (0.33 to 0.98) |
74.3 |
0.31 (0.15 to 0.63) |
14.2 |
0.52 (0.27 to 0.99) |
|
Kiosk (minibar) |
(29) |
51.7 |
1.38 (0.61 to 3.11) |
82.8 |
0.34 (0.09 to 1.14) |
27.9 |
1.21 (0.51 to 2.82) |
|
Number of casual partners |
|
|
p=0.7 |
|
p=0.3 |
|
p=0.0007 |
|
No casual partner past year |
(255) |
42.0 |
1.00 |
84.3 |
1.00 |
23.9 |
1.00 |
|
One
casual partners past year
|
(205) |
45.4 |
1.19 (0.78 to 1.82) |
85.8 |
1.32 (0.72 to 2.44) |
30.2 |
1.82 (1.14 to 2.92) |
|
Any new partner past month |
(140) |
46.4 |
1.16 (0.71 to 1.87) |
92.1 |
1.90 (0.83 to 4.32) |
40.7 |
2.63 (1.56 to 4.43) |
|
|
|
*p Value and OR adjusted for site
of recruitment, age, education and workplace; **p value
and OR adjusted for site of recruitment, age, marital
status and workplace; ***p value and OR adjusted for
site of recruitment, age, workplace, and number of
casual partners. |
|
Association of STI with HIV infection
A total of 408 (68.0%) of the 600 women were HIV positive (table
4 ).
HIV positive women had a significantly higher prevalence of
markers of lifetime infection with T pallidum (50% v 33%)
and HSV-2 (91% v 77%) and of current bacterial vaginosis
(44% v 32%) than HIV negative women. More HIV positive
than HIV negative women were clinically diagnosed with
genital ulcers (11% v 4%), enlarged inguinal lymph
nodes (13% v 4%), and warts (10% v 0%) and they
also reported higher numbers of lifetime STI. Adjusting for
the effect of age and site of recruitment, these associations
were independent of the coexistence of other STI and other
sociodemographic and behavioural variables.
Table 4 Association of HIV status with
STI/RTI pathogens, clinical STI/RTI signs, and reported lifetime STI/RTI
syndromes
|
STI/RTI pathogens, signs and
symptoms |
HIV+ve (n=408)
|
HIV-ve (n=192)
|
OR*
|
|
No (%) |
No (%) |
(95% CI) |
|
|
|
Genital swabs |
|
N gonorrhoeae |
102 (25.0%) |
31 (16.1%) |
1.33 (0.83 to 2.14) |
|
C trachomatis |
52 (12.5%) |
23 (12.4%) |
1.00 (0.56 to 1.76) |
|
N gonorrhoeae/C trachomatis |
132 (32.4%) |
48 (25%) |
1.22 (0.80 to 1.88) |
|
T vaginalis |
98 (24.0%) |
45 (23.5%) |
1.01 (0.65 to 1.57) |
|
C albicans |
245 (60.0%) |
119 (62.0%) |
0.83 (0.55 to 1.24) |
|
Bacterial vaginosis |
179 (43.9%) |
62 (32.3%) |
1.65 (1.12 to 2.45) |
|
Serology |
|
TPPA+ve |
202 (49.5%) |
63 (32.8%) |
1.60 (1.09 to 2.35) |
|
TPPA/RPR+ve (all titres) |
71 (17.4%) |
32 (16.7%) |
0.81 (0.49 to 1.33) |
|
TPPA/RPR+ve ( 1/8) |
35 (8.6%) |
17 (8.9%) |
0.74 (0.37 to 1.47) |
|
HSV-2 |
372 (91.2%) |
148 (77.1%) |
2.77 (1.62 to 4.73) |
|
STI/RTI signs (clinically
diagnosed) |
|
Abnormal genital discharge |
147 (36.0%) |
66 (34.4%) |
1.26 (0.85 to 1.88) |
|
Cervicitis |
84 (20.6%) |
29 (15.1%) |
1.63 (0.97 to 2.73) |
|
Genital ulcer(s) |
44 (10.8%) |
8 (4.2%) |
3.54 (1.52 to 8.26) |
|
Genital blister(s) |
11 (2.7%) |
1 (0.5%) |
3.70 (0.44 to 30.91) |
|
Genital warts |
39 (9.6%) |
None |
|
|
Inguinal lymphadenopathy |
54 (13.2%) |
8 (4.2%) |
4.66 (1.95 to 11.12) |
|
Lower abdominal tenderness |
29 (7.1%) |
9 (4.7%) |
1.38 (0.59 to 3.23) |
|
Reported lifetime STI/RTI
syndrome |
|
Ulcer |
84 (20.6%) |
22 (11.5%) |
2.31 (1.34 to 3.98) |
|
Discharge |
109 (26.7%) |
32 (16.7%) |
1.85 (1.16 to 2.96) |
|
|
|
*OR adjusted for age and site of
recruitment. |
|
DISCUSSION
This cross
sectional study collected baseline information on a newly
recruited cohort of 600 women working in modern and
traditional bars, restaurants, and guesthouses/hotels at settlements
along the highways in Mbeya Region. The study found high infection
rates with HIV and other STI, comparable to rates reported in
other studies of female sex workers in sub-Saharan Africa during
recent years.5–7
Women
participating in the cohort are clearly working in a high
risk environment, although not all of them report that they
engage in sex work. For instance, only 58% of the women reported
having had one or more casual partners during the past 12 months
and approximately 45% reported having received money for sexual
favours.
HIV and
STI/RTI prevalence
The prevalence of HIV infection was high (68%), indicating a
high exposure to infected sexual partners during their lifetime.
In fact, many HIV infections may have occurred before women
started working in their current profession, as the duration
of work in the profession was not associated with increased
HIV risk.8
In comparison, rates among antenatal care attenders in this
region are significantly lower (21.7% in Mbeya town and 17.4%
in roadside settlements).9
In such a situation, even though Tanzania experiences a
generalised HIV epidemic, male clients of female bar workers
may function as a bridging group for HIV transmission in the
general population.10,11
The prevalence of
STI among the women in the cohort generally lies within the
range of prevalences reported from studies among sex workers
in other countries in sub-Saharan Africa in recent years. For
example, in Nairobi, Kenya,5
and Kwa Zulu Natal, South Africa7
genital ulcers have been observed in 2.7% and 12.7% of sex
workers respectively, active syphilis in 8.8% and 12.7%, N
gonorrhoeae in 10.5% and 14.3%, C trachomatis in 9.1%
and 16.7%, T vaginalis in 13% and 40.8%, and bacterial
vaginosis in 46% and 71%. HSV-2 antibodies were found in
around 80% of sex workers in Zimbabwe,12
Eritrea,13
and Nigeria.14
These STI prevalences indicate a high rate of exposure to STI
and inadequate treatment. In our study, only few women
complaining of STI symptoms had sought treatment. Data on
obstacles to treatment seeking were not systematically
collected, but "lack of money" was frequently mentioned in
this context to study clinicians. These findings indicate
that the regionwide introduction in the late 1990s of free
STI services in public health facilities has so far failed to
adequately reach this highly vulnerable group. Further
investigations into the availability and quality of these STI
services, and their accessibility to high risk groups, might
shed light on existing constraints and ways to overcome them.
Association between STI and HIV
Current infection with N gonorrhoeae, C trachomatis, T
vaginalis, C albicans, or active syphilis
(TPPA/RPR+ve) was not associated with prevalent HIV infection
in this cross sectional study. However, different findings
were obtained for some clinical signs of STI. There was a
strong correlation between HIV infection and the following
STI signs: genital warts, genital ulcers (including those not
associated with an identifiable causative agent), inguinal
lymphadenopathy, and genital blisters. This confirms findings
from other studies that HIV infection may exacerbate
symptomatic HPV and HSV infection and directly cause an enlargement
of inguinal lymph glands and possibly genital ulcerations.15,16
Women with
bacterial vaginosis, a recurrent imbalance of the vaginal
microbial flora, were more likely to be HIV infected. The
reasons for this correlation, which has also been found in
other studies,17,18
remain unclear and warrant further investigation. The altered
vaginal milieu with a high pH and a lack of H2O2,
may predispose to HIV infection.19
Bacterial vaginosis also occurs together with other STI/RTI.20,21
In our study bacterial vaginosis was associated with vaginal
discharge, with cervicitis, with N gonorrhoeae, T
vaginalis, and with HIV seropositivity. Alternatively,
HIV infection may predispose to bacterial vaginosis, as
concluded in a study of HIV positive women in Thailand.22
Sociodemographic and behavioural characteristics and STI
In the present study few sociodemographic and behavioural variables
correlated with STI risk. This may partly reflect methodological
limitations, as information on risk behaviour obtained in
interviews is known to be inaccurate.23
It is possible that women under-reported risk behaviours, as
observed in other studies on AIDS related risk behaviours,24
especially in a situation (baseline survey), where
interviewers and cohort participants were not yet familiar
with each other. In addition, women may not have been able to
recall accurate numbers and types of sexual partners, or frequency
of condom use over periods longer than a few days or weeks.
In the
multivariate analysis a weak, though recognisable pattern
emerges regarding the relation between STI risk and sociodemographic
and behavioural characteristics. We found an association of
relatively "acute" infections (N gonorrhoeae, C
trachomatis) with variables reflecting current/recent
exposure (for example, multiple causal partners during past
12 months; receipt of money in exchange for sexual favours).
On the other hand serological markers of lifetime infection
with STI (TPPA+ve, HSV2+ve) were associated with variables
reflecting cumulative exposure to STI (for example, age or
marital status).
Correlation between STI infection and clinical signs and symptoms
Clinical STI signs and self reported symptoms showed little
correlation with the presence of causative STI pathogens. Because
of the low sensitivity of "vaginal discharge" as a sign to detect
bacterial vaginosis (46.5%), T vaginalis (38.5%), and C
albicans (34.9%) and of "cervicitis" as a sign to detect
infections with N gonorrhoeae (21%) and C
trachomatis (24%), between 50% and 80% of the women with
these infections were not treated on the spot. Conversely,
because of the low specificity of these signs, approximately
one third of the women diagnosed with vaginal discharge and
one fifth of the women with cervicitis were treated, although
they did not carry the respective causative agents. Since 83%
of women were found to be affected by T vaginalis,
C albicans, or bacterial vaginosis, while 30% were infected
with either N gonorrhoeae and/or C trachomatis, and
in the absence of practicable rapid tests for STI, it may be
appropriate to consider periodic presumptive treatment
together with condom promotion and treatment of partners as
measures to reduce the burden of STI in this group. Periodic
presumptive treatment of STIs among sex workers has recently
been introduced in several South African mining communities
and found to be highly effective in reducing STIs among both
sex workers and the male mining population residing in the
same communities.25
CONCLUSION
Our study shows that prevalences of STI and HIV are very high
among female bar workers in Mbeya Region. Taken together with
the data on high risk behaviours—for example, low prevalence
of reported condom use with both regular and casual partners,
these findings reveal a largely unmet need for interventions
supporting behaviour change and effective STI care for female
bar workers and their male clients in order to reduce the transmissions
of STI and HIV and the negative health and social impact of
untreated infection.
|
Key
messages
Prevalence
of HIV, clinically and laboratory diagnosed STI was
high among 600 female bar workers who were recruited
into an open cohort in late 2000 in Mbeya Region, Tanzania.
Taken
together with the data on high risk behaviours—for
example, low prevalence of reported condom use, these
findings reveal a largely unmet need for
interventions supporting behaviour change and
effective STI care for female bar workers and their
male partners. |
ACKNOWLEDGEMENTS
We wish to acknowledge the contributions of our collaborators
from various institutions, including Fred Mhalu and Judica Mbwana
of the Muhimbili University College of Health Sciences in Dar
es Salaam, Tanzania; Titus Nkulila and Eleuter Samki of the
Mbeya Consultant Hospital, Mbeya, Tanzania; John Changalucha
of the National Institute of Medical Research in Mwanza, Tanzania;
David Mabey, Brent Wolff, Tamara Hurst, John Williams, Aura
Beltran, and Dean Everett of the Department of Infectious and
Tropical Diseases at the London School of Hygiene and Tropical
Medicine (LSHTM) in London, UK; Frank von Sonnenburg of the
Department of Infectious Diseases and Tropical Medicine,
Ludwig-Maximilians-University, Munich, Germany; and Ian
MacLean and Faye Kingyens of the Department of Microbiology
of the University of Manitoba. Further, we are grateful to
those who were involved in the field and laboratory work in
Mbeya, in particular Joshua Mwakyelu, Leonard Ndeki, Immanuel
Burton, Oliver Mwamanga, Yohana Fungo, Triphonia Mbena, and
Azania Ntakije. Our special thanks go to the women who participated
in the study.
This study was
funded in part by the Wellcome Trust, UK, by the European
Commission and the Department for International Development
(DFID), UK.
CONTRIBUTORS
All co-authors commented on draft versions of the paper. GR
designed the study, developed data collection instruments,
supervised field work, analysed the data and prepared the manuscript;
MR assisted in the development of data collection instruments
and was responsible for field work; OH was responsible for the
cohort recruitment and the sociobehavioural data collection;
FN was responsible for laboratory testing in Mbeya; EL and PH
co-designed the study, supported the quality assurance of
laboratory work in Mbeya and assisted in manuscript
preparation; DN and LM co-designed the study and assisted in
the supervision of the field work; JT, RH, and HG co-designed
the study and advised on the implementation and the analysis;
MH designed and implemented the cohort study on HIV
superinfections in the context of which this baseline survey
took place and assisted in the manuscript preparation.
REFERENCES
Nkya WM,
Gillespie SH, Howlett W, et al. Sexually transmitted diseases in
prostitutes in Moshi and Arusha, northern Tanzania. Int J STD AIDS
1991;2:432–5.
Nugent RP,
Krohn MA, Hillier SL. Reliability of diagnosing bacterial vaginosis is
improved by a standardized method of gram stain interpretation. J
Clin Microbiol 1991;29:297–301.
Orle KA,
Gates CA, Martin DH, et al. Simultaneous PCR detection of
Haemophilus ducreyi, Treponema pallidum and herpes simplex virus types 1
and 2 from genital ulcers. J Clin Micorbiol 1996;1:49–54.
Hoffmann O,
Wolff B, Maboko L, et al, and the HISIS Mbeya Study Group. Can
self-reported risk factors predict HIV status in cross-sectional studies
of high risk populations? First results of a cohort of female
bar-workers in Tanzania. AIDS (in press).
Fonck K,
Kaul R, Kimani J, et al. A randomised, placebo-controlled trial
of monthly azithromycin prophylaxis to prevent sexually transmitted
infection and HIV-1 in Kenyan sex workers: study design and baseline
findings. Int J STD AIDS 2000;11:804–11.
Lankoande S,
Meda N, Sangare L, et al. Prevalence and risk of HIV infection
among female sex workers in Burkina Faso. Int J STD AIDS 1998;9:146–50.
Ranjee G,
Abdool Karim SS, Sturm AW. Sexually transmitted infections among sex
workers in KwaZulu-Natal, South Africa. Sex Transm Dis 1998;25:346–9.
Hoffmann O,
Maboko L, Wolff B, Herbinger K, Riedner G, Mhalu F, v. Sonnenburg F,
Hoelscher M, and the HISIS Mbeya Study Group. Correlates of HIV status
among women in a high risk environment in Tanzania. Presentation at the
7th German AIDS Conference 2001.
The United
Republic of Tanzania.
National AIDS Control Programme HIV/AIDS/STI Surveillance Report.
January-December 2000. Report No 15.
Morris M,
Podhisita C, Wawer MJ, et al. Bridge populations in the spread of
HIV/AIDS in Thailand. AIDS 1996;11:1265–71.
Lowndes CM,
Alary M, Meda H, et al. Role of core and bridging groups in the
transmission dynamics of HIV and STIs in Cotonou, Benin, West Africa.
Sex Transm Infect 2002;78:i68–i77.
Cowan F,
Langhaug L, Swarthout T, et al. Are rural women who have sex in
exchange for gifts or money part of the core group? Int J STD AIDS
2001;12(Suppl 2): 53.
Ghebrekidan H,
Ruden U, Cox S, et al. Prevalence of herpes simplex virus types 1
and 2, cytomegalovirus, and varicella-zoster virus infections in
Eritrea. J Clin Virol 1999;12:53–64.
Dada AJ,
Ajayi AO, Diamondstone L, et al. A serosurvey of Haemophilus
ducreyi, syphilis and herpes simplex virus type 2 and their association
with human immunodeficiency virus among female sex workers in Lagos,
Nigeria. Sex Transm Dis 1998;25:237–2.
Ghys PD,
Diallo MO, Ettiegne-Traore V, et al. Genital ulcers associated
with human immunodeficiency virus-related immunosuppression in female
sex workers in Abidjan, Ivory Coast. J Infect Dis 1995;172:1371–4.
Kaul R,
Kimani J, Nagelkerke NJ, et al. Risk factors for genital
ulcerations in Kenyan sex workers. The role of HIV-1 infection. Sex
Transm Infect 1997;24:387–92.
Martin HL Jr,
Nyange PM, Richardson BA, et al. Hormonal contraception, sexually
transmitted diseases, and risk of human immunodeficiency virus type 1.
J Infect Dis 1998;178:1063–59.
Taha TE,
Hoover DR, Dallabetta GA, et al. Bacterial vaginosis and
disturbances of vaginal flora: association with increased acquisition of
HIV. AIDS 1998;12:1699–706.
Hillier SL.
The vaginal microbial ecosystem and resistance to HIV. AIDS Res Hum
Retroviruses 1998;14(Suppl 1): S17–S21.
Moi H.
Prevalence of bacterial vaginosis and its association with genital
infections, inflammation and contraceptive methods in women attending
sexually transmitted disease and primary health care clinics. Int J
STD AIDS 1990;1:86–94.
Schwebke JR,
Weiss HL. Interrelationship of bacterial vaginosis and cervical
inflammation. Sex Transm Dis 2002;29:59–64.
Rugpao S,
Nagachinta T, Wanapirak C, et al. Gynaecological conditions
associated with HIV infection in women who are partners of HIV-positive
Thai blood donors. Int J STD AIDS 1998;9:677–82.
Lee R,
Renzetti CM. The Problems of Researching Sensitive Topics. American
Behavioural Scientist 1990;33:510–28.
Weinhardt LS,
Forsyth AD, Carey MP, et al. Reliability and validity of
self-report measures of HIV-related sexual behavior: progress since 1990
and recommendations for research and practice. Arch Sex Behav
1998;27:155–80.
Steen R,
Vuylsteke B, DeCoito T, et al. Evidence of declining STD
prevalence in a South African Mining population community following a
core-group intervention. Sex Transm Dis 2000;27:1–8.
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