Literature reviews  >  Articles for review > Vuylsteke et al. Assessment of the validity of... 

 

About SDI
Mission
Diagnostic
Priorities
Workplan
Activities
Newsletters
Grants
Publications
Journal articles
Guidelines
Manuals
Reports
Literature reviews
Contact us

The sensitivity and positive predictive value of STI algorithms in use at a female sex worker clinic in Abidjan, Côte d'Ivoire, have decreased since they were originally validated.

Assessment of the validity of and adherence to sexually transmitted infection algorithms at a female sex worker clinic in Abidjan, Côte D'Ivoire.
Vuylsteke BL, Ettiegne-Traore V, Anoma CK, Bandama C, Ghys PD, Maurice CE, Van Dyck E, Wiktor SZ, Laga M.
Sexually Transmitted Diseases 2003;30;284-291

 

Summary:

Question
How well do the algorithms used at a female sex worker clinic in Abidjan, Côte d'Ivoire, which were designed in 1993, currently perform for the diagnosis of vaginal and cervical infections when applied to returning clients, and how accurately are they used by the health workers?

Design
The performance of algorithms designed in 1993 and used for sexually transmitted infection (STI) case management at a female sex worker (FSW) clinic in Abidjan, Côte d'Ivoire, were evaluated in a cross-sectional study conducted from 1999 to 2000 among FSWs attending as returning clients. The adherence of health workers to the application of the algorithms was also assessed.

Participants
Eight hundred forty-two female sex workers attending the Clinique de Confiance in Abidjan, Côte d'Ivoire, as returning clients were tested. Women younger than 18 years, attending for the first time, or who had already participated once were excluded. The median age was 25 years (range = 18-53 years), the median duration of sex work was 16 months, and 94% reported using a condom with all their clients during the past working day.

Description of Tests and Diagnostic Standard
Physicians applied one of three STI algorithms to women who spontaneously declared an STI symptom, including 1) women with vaginal discharge, dysuria, or itching, 2) women with lower abdominal pain, and 3) women with both symptoms. A gynecological examination with speculum and vaginal and/or cervical sampling were performed according to the algorithm. Cervical smears were examined for the number of leukocytes per microscopic field, and vaginal smears for the presence of T. vaginalis and candida. Sociodemographic, behavioral, and other information were collected on a standardized questionnaire and used to calculate a risk score based on age, money received for last sex act, and duration of sex work.

A first-void urine sample and two self-collected vaginal swabs were obtained for laboratory testing. The urine was tested by PCR for N. gonorrhoeae and C. trachomatis DNA (Amplicor, Roche Diagnostic Systems, Branchburg, NJ). A Gram stain was prepared from one of the vaginal swabs and examined for the presence of yeast and clue cells, and scored for bacterial vaginosis organisms according to the Nugent method. The same swab was used to inoculate medium for culture of T. vaginalis. The second swab was shipped dry and frozen to a laboratory in Belgium and tested for T. vaginalis using two in-house PCR assays. Women were considered positive for C. trachomatis or N. gonorrhoeae if the PCR assay was positive; for T. vaginalis if the culture or if both of the PCR assays were positive; for yeast infection if mycelia were seen on the vaginal smear and abnormal vaginal discharge was observed; for bacterial vaginosis if the Nugent score was >6 or clue cells were present on the vaginal smear.

Main Outcome Measures
The sensitivity, specificity, and positive predictive value (PPV) of the algorithms were determined by comparing the outcome of the algorithm as noted by the physician with the gold standard laboratory diagnosis. Adherence of the health staff to the algorithm was evaluated by calculating the proportion of women for whom all steps of the algorithms were followed correctly.

Main Results
The rates of STI determined by laboratory diagnosis were 8.2% N. gonorrhoeae and/or C. trachomatis, 16.7% T. vaginalis, 62.3% bacterial vaginosis, and 6.2% yeast. An alternative risk assessment, taking into account age, prompted symptoms, and time since last visit was significantly associated with and highly predictive of gonococcal and/or chlamydial infection. Vaginal discharge was predictive of yeast infection and was the only symptom predictive of any infection. The performance of the algorithms for diagnosis of STI as determined by the laboratory analyses is shown in the table. Correct case management by health workers using the algorithms was lowest at the first step and highest at the last step of the algorithms. The overall rate of correct case management was 30%.

Authors' Conclusions
The sensitivity and PPV of the algorithms currently in use in a FSW clinic in Abidjan decreased over time. The sensitivity and PPV for N. gonorrhoeae and/or C. trachomatis were 79% and 48% five years ago compared to 20% and 14% in the current study. Several factors could explain the difference including a change in sociodemographic and risk behavior, the use of dynamic rather than static factors in the risk assessment, a lower prevalence of N. gonorrhoeae and C. trachomatis, the restriction of subjects to returning clients, and the restricted criteria for entry into the algorithm. Poor adherence to the algorithms further reduced the validity. Although the performance of the algorithms was poor, they remain the only practical tool available for the diagnosis of STI in FSWs in Abidjan, and should be periodically evaluated and adapted to the changing characteristics of the population.

Source of funding: Wellcome Trust, London, UK and the Belgian International Cooperation (DGCI).

For correspondence: Bea Vuylsteke, Project RETRO-CI, BP 1712 Abidjan 01, Côte d'Ivoire. E-mail address: bbv1@cdc.gov.

   

about SDI | newsletters | grants | publications | literature reviews

WHO Home - WHO Search - TDR Home - SDI Home - SDI Contact us
(c) WHO/OMS 2001