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1.
Sex Transm Dis ; 25(10): 533-8, 1998 Nov.
Article in English | MEDLINE | ID: mdl-9858349

ABSTRACT

BACKGROUND AND OBJECTIVES: Culture, the conventional method for detection of Neisseria gonorrhoeae, requires invasive sampling and stringent specimen transport conditions. The recently developed ligase chain reaction test (LCR; Abbott Laboratories; North Chicago, IL) allows noninvasive sampling and stable transport conditions, but has not been evaluated with specimens from adolescent populations. GOAL OF THIS STUDY: To perform a comparative evaluation of a commercial LCR test and culture for the diagnosis of N. gonorrhoeae in adolescent women. STUDY DESIGN: Urine and endocervical swab specimens from 330 teenage women seen in two public health adolescent clinics were tested by LCR and culture. For resolution of discordant results, a polymerase chain reaction (PCR) test was developed that directly amplifies N. gonorrhoeae DNA from urine samples processed for LCR. RESULTS: Thirty-one of 330 (9.4%) cervical specimens were culture-positive for N. gonorrhoeae, and 30 of 330 (9.1%) urine specimens were positive by LCR. After resolution of 13 discordant results, the sensitivity, specificity, and positive and negative predictive values of LCR for urine were 88.2%, 100%, 100%, 98.7%, respectively, and for culture of endocervical specimens were 82.3%, 98.9%, 90.3% and 98%, respectively. CONCLUSIONS: Although more expensive than culture, LCR offers a sensitive means for the detection of N. gonorrhoeae in urine samples and may be useful for this purpose in settings where pelvic examinations are difficult to perform and simultaneous detection of N. gonorrhoeae and Chlamydia trachomatis is advantageous.


Subject(s)
Chlamydia Infections/complications , DNA Ligases , DNA, Bacterial/urine , Gonorrhea/diagnosis , Neisseria gonorrhoeae/isolation & purification , Adolescent , Adult , Cervix Uteri/microbiology , Chlamydia Infections/diagnosis , Chlamydia trachomatis/genetics , Chlamydia trachomatis/isolation & purification , DNA Primers , Female , Gonorrhea/complications , Gonorrhea/urine , Humans , Neisseria gonorrhoeae/genetics , Polymerase Chain Reaction , Predictive Value of Tests , Sensitivity and Specificity
2.
J Infect Dis ; 178(6): 1795-8, 1998 Dec.
Article in English | MEDLINE | ID: mdl-9815237

ABSTRACT

To determine the etiology of genital ulcers and to assess the prevalence of human immunodeficiency virus (HIV) infection in ulcer patients in 10 US cities, ulcer and serum specimens were collected from approximately 50 ulcer patients at a sexually transmitted disease clinic in each city. Ulcer specimens were tested using a multiplex polymerase chain reaction assay to detect Haemophilus ducreyi, Treponema pallidum, and herpes simplex virus (HSV); sera were tested for antibody to HIV. H. ducreyi was detected in ulcer specimens from patients in Memphis (20% of specimens) and Chicago (12%). T. pallidum was detected in ulcer specimens from every city except Los Angeles (median, 9% of specimens; range, 0%-46%). HSV was detected in >/=50% of specimens from all cities except Memphis (42%). HIV seroprevalence in ulcer patients was 6% (range by city, 0%-18%). These data suggest that chancroid is prevalent in some US cities and that persons with genital ulcers should be a focus of HIV prevention activities.


Subject(s)
Genital Diseases, Female/complications , Genital Diseases, Male/complications , HIV Infections/complications , HIV Infections/epidemiology , HIV Seroprevalence , Sexually Transmitted Diseases/complications , Ulcer/complications , Urban Population , Female , Genital Diseases, Female/epidemiology , Genital Diseases, Female/microbiology , Genital Diseases, Male/epidemiology , Genital Diseases, Male/microbiology , HIV Antibodies/blood , Haemophilus ducreyi/isolation & purification , Humans , Male , Polymerase Chain Reaction , Prevalence , Sexually Transmitted Diseases/epidemiology , Sexually Transmitted Diseases/microbiology , Simplexvirus/isolation & purification , Treponema pallidum/isolation & purification , Ulcer/epidemiology , Ulcer/microbiology , United States/epidemiology
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