0
We're unable to sign you in at this time. Please try again in a few minutes.
Retry
We were able to sign you in, but your subscription(s) could not be found. Please try again in a few minutes.
Retry
There may be a problem with your account. Please contact the AMA Service Center to resolve this issue.
Contact the AMA Service Center:
Telephone: 1 (800) 262-2350 or 1 (312) 670-7827  *   Email: subscriptions@jamanetwork.com
Error Message ......
Article |

Self-obtained Vaginal Swabs for Diagnosis of Treatable Sexually Transmitted Diseases in Adolescent Girls FREE

Kim Smith, MT(ASCP); Kathy Harrington, MAEd, MPH; Gina Wingood, ScD, MPH; M. Kim Oh, MD; Edward W. Hook III, MD; Ralph J. DiClemente, PhD
[+] Author Affiliations

From the Division of Infectious Diseases, Department of Medicine (Ms Smith and Dr Hook), and the Department of Pediatrics (Ms Harrington and Dr Oh), University of Alabama at Birmingham; Rollins School of Public Health, Emory University, Atlanta, Ga (Drs Wingood and DiClemente); and Emory/Atlanta Center for AIDS Research (Drs Wingood and DiClemente).


Arch Pediatr Adolesc Med. 2001;155(6):676-679. doi:10.1001/archpedi.155.6.676.
Text Size: A A A
Published online

Objective  To ascertain the acceptability of testing and prevalence of 3 readily treatable sexually transmitted diseases (STDs) (infections with Neisseria gonorrhoeae, Chlamydia trachomatis, and Trichomonas vaginalis) with the use of patient-obtained vaginal swabs.

Study Design  Study participants at each initial session were asked to provide self-obtained vaginal swabs for ligase chain reaction testing to detect N gonorrhoeae and C trachomatis, and for culture of T vaginalis.

Setting  Behavioral intervention sessions with African American adolescent girls in a nonclinical program to reduce risk of STDs, human immunodeficiency virus infection, and pregnancy.

Results  All study participants were offered their choice of STD screening in the context of a traditional pelvic examination or using self-obtained vaginal swabs. All eligible participants chose self-administered vaginal swabs. Of the 512 participants examined at their initial study visit, 28.7% were found to be infected with 1 or more treatable STDs (5.3% with N gonorrhoeae, 17.8% with C trachomatis, and 12.9% with T vaginalis).

Conclusions  With the use of newer detection systems, STDs can be readily detected in nonclinical settings with the use of self-obtained vaginal swabs, providing new opportunities for efforts to control STDs.

Figures in this Article

TREATABLE sexually transmitted diseases (STDs) caused by Trichomonas vaginalis, Chlamydia trachomatis, and Neisseria gonorrhoeae are relatively common among sexually active young women and may lead to serious complications and sequelae. Infections with C trachomatis and N gonorrhoeae are the 2 most common reportable bacterial STDs in the United States,1 and vaginal trichomoniasis2 is more common than chlamydial and gonococcal infection. Each of these infections is also an important contributor to the STD-related morbidity in women. Gonococcal and chlamydial infections cause pelvic inflammatory disease, ectopic pregnancy, infertility, and perinatal and congenital infections, and cost millions of dollars in health care costs.2,3Trichomonas vaginalis infection is a common cause of symptomatic vaginal discharge and has been implicated in preterm birth.2,4 Moreover, recent studies have demonstrated increased efficiency of transmission of human immunodeficiency virus (HIV) in the presence of coinfection with bacterial STDs or trichomoniasis.57 However, each of these infections often remains undiagnosed because many infected women have mild, nonspecific symptoms or are asymptomatic.2 As a result, screening for bacterial STDs and trichomoniasis is a critical component of control efforts.

Until recently, diagnosis of these STDs required a pelvic examination. The development of diagnostic nucleic acid amplification technology has made chlamydial and gonococcal diagnoses in women possible in circumstances in which the usual endocervical specimen collection is difficult. Self-obtained vaginal specimens for diagnosis of genital infections have been used successfully in research settings810; however, few data have been published on patient-obtained vaginal specimens for STD diagnosis in teenage girls.11

This article reports the utility of patient-obtained vaginal swabs as tools for STD diagnosis in a nonclinical setting where they are collected without a pelvic examination according to instruction by nonclinicians. Questions we sought to address were 2-fold: (1) Are sexually active adolescent girls willing and able to obtain their own vaginal specimens? (2) Can the specimens obtained in a nonclinical setting be processed for delivery to the laboratory for appropriate assays for the identification of C trachomatis, N gonorrhoeae, and T vaginalis infections?

SUBJECT POPULATION

From December 1996 through April 1999, project recruiters screened 1130 teenage girls in adolescent and school-based primary care clinics and in health education classes at local high schools to assess eligibility for STD/HIV prevention intervention. Recruiters presented a brief description of a young women's health study, then assessed the eligibility of those expressing an interest in participating by means of a short questionnaire. Adolescents were eligible to participate in the study if they were African American girls, were between the ages of 14 and 18 years at the time of enrollment, had been sexually active (vaginal or anal sex) in the previous 6 months, and provided written informed consent. In this study, African American female teenagers were selected as the target population because of reports of high escalating risk for HIV and STD.1214 The recruitment sites were in neighborhoods characterized by high rates of unemployment, substance abuse, violence, and STDs.

STUDY DESIGN

Subjects recruited from a variety of settings were informed, via telephone and mailed brochure, about the methods of the study, including surveys, interviews, specimen collection, incentives, workshops, and follow-up. These adolescents were then invited to ask questions about the study and to sign a consent form to participate. For the study, 4 intervention workshops and data collection sessions were held in a local clinic facility on Saturdays. For baseline data collection and each workshop, participants received a $20 cash incentive. The study protocol was reviewed by the university's Institutional Review Board Committee on Human Research before implementation of the study.

SPECIMEN COLLECTION METHODS

During the baseline data information collection session and before randomization to a behavioral STD/HIV risk-reduction intervention, each adolescent was instructed by a nonclinician research assistant to obtain 2 vaginal swabs for STD testing by means of a written protocol. Research assistants instructed adolescents in appropriate procedures for collecting vaginal specimens. During a preliminary 2-hour training session, research assistants were instructed on the methods used in obtaining self-obtained vaginal swabs, the efficacy of this procedure for STD analysis relative to pelvic examination, and how to address questions posed by participants.

The research assistant explained the purpose of collecting the vaginal specimens, presenting a discussion biased toward self-obtained vaginal specimen collection rather than specimen collection by a clinician on a pelvic examination table. The discussion included the relative advantages of self-obtained vaginal specimens, such as being under their control, less painful, not as invasive, and more convenient. For participants preferring not to collect vaginal swabs, free pelvic examination appointments for specimen collection were available for girls the following week at a local adolescent clinic. Choosing the pelvic examination option would still allow for study entry and receipt of the $20 incentive. After research assistants described the insertion procedure to the adolescents and answered any questions regarding it, participants were asked about their willingness to collect self-obtained vaginal swabs. Adolescents completed specimen collection within 3 to 4 minutes in a private clinical examination room. Vaginal swabs were not collected from adolescents in their third trimester of pregnancy or 6 weeks postpartum; these adolescents provided a first-void urine specimen for ligase chain reaction testing.

For specimen collection, each participant was asked to obtain 2 vaginal specimens by sequentially inserting 2 sterile Dacron-tipped swabs about 2.5 in or as far as comfortable into the vagina, rotating them for 15 to 30 seconds, and removing them. After specimen collection, the first swab was placed in a specimen transport tube for subsequent ligase chain reaction testing (LCx Probe System for N gonorrhoeae and C trachomatis assays; Abbott Laboratories, Diagnostics Division, Abbott Park, Ill), and the second swab was used to inoculate culture medium for T vaginalis (InPouch TV Test; BioMed Diagnostics Inc, Santa Clara, Calif).

Ligase chain reaction specimens were stored at 4°C until delivered to the laboratory. Pouches for T vaginalis culture were immediately incubated at 37°C. All specimens were transported to the laboratory in insulated containers within 48 hours.

LABORATORY METHODS

Study participants were examined for 3 prevalent sexually transmitted organisms: N gonorrhoeae, C trachomatis, and T vaginalis.810 On receipt in the laboratory, cultures for T vaginalis were incubated at 37°C and read daily until the fifth day after inoculation. Cultures were considered positive on the basis of identification of motile trichomonads within the pouch.8 Swab specimens for ligase chain reaction were processed immediately on receipt in the laboratory. Ligase chain reaction assays for C trachomatis and N gonorrhoeae were performed according to the manufacturer's instructions.9,10

Of the 609 eligible adolescents referred to intervention workshops, 522 (85.7%) attended and agreed to participate in the study. Of the 522 adolescents, 512 were asked to collect vaginal swabs. Ten (2.0%) were excluded because they were known to be in their third trimester of pregnancy and were not asked to provide vaginal swabs. Of the 87 recruited teens (14.3%) who did not participate, 31% (27 subjects) could not be reached because of incorrect contact information given at screening, 29% (25) stated that they were not interested in taking part in the health promotion program, 22% (19) had employment or child care conflicts, 9% (8) expressed interest but never showed up to enroll, 3% (3) declined because of chronic illness, 3% (3) were incarcerated after the initial referral, and 2% (2) were not permitted to participate by their parents. No participant cited vaginal swab screening as a specific reason for not participating. Of the 512 participants asked to provide vaginal swabs, none declined.

As shown in Table 1, participants were at high risk for STD acquisition and pregnancy: 39.3% reported at least 1 previous pregnancy, and 9.4% reported multiple partners in the 6 months before enrollment. Overall, 147 participants (28.7%) had at least 1 treatable STD detected, and 28 (5.5%) were coinfected with 2 or more pathogens (Table 2). Infection rates were 17.8% for C trachomatis, 5.3% for N gonorrhoeae, and 12.9% for T vaginalis. Age distribution of subjects with infections is shown in Figure 1.

Table Graphic Jump LocationTable 2. Laboratory Test Results of Subjects at Enrollment (Baseline) Visit*
Place holder to copy figure label and caption

Prevalence of sexually transmitted diseases by participant age (N = 512).

Graphic Jump Location

In this study, sexually active teens were willing to obtain their own vaginal swab specimens for STD diagnosis. No participant declined to obtain the vaginal swabs or reported difficulty in doing so. Some aspects of the study methods may have influenced participants in favor of the self-obtained specimen collection over the traditional pelvic examination collection. The convenience of immediate swab collection as opposed to having to make another trip to a clinic for specimen collection on a pelvic examination table, as well as presenting the self-obtained method first with all of the relative advantages, may have influenced some participants to prefer the self-obtained method. Perhaps, given a choice of an immediate pelvic examination or immediate self-obtained swabs, some girls may have chosen the pelvic examination. However, with no participants opting for the pelvic examination or refusing specimen collection, collection of vaginal swab specimens for STD screening appears to be readily acceptable to this group of high-risk adolescents.

Nearly all participants were asymptomatic at the time of enrollment, yet unsuspected gonorrhea, Chlamydia, and Trichomonas infections were common. Since we did not compare the prevalence of infection detected by means of patient-obtained specimens with the results of testing with specimens collected by clinicians in the context of a speculum-guided genital examination, it is possible that some infections were missed by allowing participants to collect their own specimens. On the basis of our own earlier work comparing performance of patient-obtained vaginal swabs with that of clinician-obtained specimens, as well as the work of others,810,15,16 we suspect that the diminution of sensitivity was slight, if any.

These data add to growing literature that suggests that, for women, patient-obtained vaginal swabs are adequate and appropriate specimens for STD screening at sites or in situations where pelvic examinations are not otherwise required.

In some situations, urine may be a favored analyte for gonococcal and chlamydial screening; however, the sensitivity of urine culture for T vaginalis is poor.17 In addition, transport and laboratory processing of swab specimens for STD diagnosis is simpler (no aliquoting or centrifugation is required) than for urine. Thus, patient-obtained vaginal swab specimens, analyzed by newly developed nucleic acid amplification assays, enhance the likelihood that individuals will provide a specimen and increase the potential for detecting asymptomatic infection. This method should be evaluated further as a potential tool for STD screening and control efforts.

Accepted for publication January 8, 2001.

This study was supported by grants R01 MH 54412 from the Center for Mental Health Research on AIDS, National Institute of Mental Health, and U AI 38514 from the National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Md.

We thank Jane Schwebke, MD, and her laboratory for performing Trichomonas cultures for this study.

Corresponding author and reprints: Kim Smith, MT(ASCP), Division of Infectious Diseases, Department of Medicine, University of Alabama at Birmingham, 229 Tinsley Harrison Tower, 1900 University Blvd, Birmingham, AL 35294-0006 (e-mail: krs@uab.edu).

Division of STD Prevention, Sexually Transmitted Diseases Surveillance 1997.  Atlanta, Ga Public Health Service, Centers for Disease Control and Prevention, US Dept of Health and Human Services September1998;
American Social Health Association, Sexually Transmitted Disease in America: How Many Cases and at What Cost?  Menlo Park, Calif Kaiser Family Foundation1998;
Mangiore-Smith  RO'Leary  JMcGlynn  EA Health and cost-benefits of chlamydia screening in young women. Sex Transm Dis. 1999;26309- 316
Link to Article
Coth  MFPastorek  JGNugent  RP  et al.  Demographic and behavioral predictors of Trichomonas vaginalis infection among pregnant women. Obstet Gynecol. 1991;781087- 1092
Greenblatt  RMBacchetti  PBarkan  S  et al.  Lower genital tract infections among HIV-infected and high-risk uninfected women. Sex Transm Dis. 1999;26143- 151
Link to Article
Parazzini  FD'Oro  LCNaldi  L  et al.  Sexually transmitted diseases and risk of HIV infection. Acta Derm Venereol. 1996;76147- 149
Rotchford  KStrum  AWWilkinson  D Effect of coinfection with STDs and of STD treatment on HIV shedding in genital-tract secretions: systematic review and data synthesis. Sex Transm Dis. 2000;27243- 248
Link to Article
Schwebke  JRMorgan  SCPinson  GB Validity of self-obtained vaginal specimens for diagnosis of trichomoniasis. J Clin Microbiol. 1997;351618- 1619
Hook III  EWChing  SFStephens  JHardy  KFSmith  KRLee  HH Diagnosis of Neisseria gonorrhoeae infections in women by using the ligase chain reaction on patient-obtained vaginal swabs. J Clin Microbiol. 1997;352129- 2132
Hook III  EWSmith  KMullen  C  et al.  Diagnosis of genitourinary Chlamydia trachomatis infections by using the ligase chain reaction on patient-obtained vaginal swabs. J Clin Microbiol. 1997;352133- 2135
Polaneczky  MQuigley  CPollock  LDulko  DWitkin  SS Use of self-collected vaginal specimens for detection of Chlamydia trachomatis infection. Obstet Gynecol. 1998;91375- 378
Link to Article
Division of STD Prevention, Sexually Transmitted Disease Surveillance, 1998.  Atlanta, Ga Centers for Disease Control and Prevention, US Dept of Health and Human Services September1999;
Eng  TButler  W The Hidden Epidemic: Confronting Sexually Transmitted Diseases.  Washington, DC National Academy Press1997;
Wasserheit  JN Effects of changes in human ecology and behavior on patterns for sexually transmitted diseases, including human immunodeficiency virus infection. Proc Natl Acad Sci U S A. 1994;912430- 2435
Link to Article
Blake  DRDuggan  AQuinn  TZenilman  JJoffe  A Evaluation of vaginal infections in adolescent women: can it be done without a speculum? Pediatrics. 1998;102939- 944
Link to Article
Gray  RHWawer  MJGirdner  J  et al.  Use of self-collected vaginal swabs for detection of Chlamydia trachomatis infection [letter]. Sex Transm Dis. 1998;25450
Link to Article
Lawing  LFHedges  SRSchwebke  JR Detection of trichomonosis in vaginal and urine specimens from women by culture and PCR. J Clin Microbiol. 2000;383585- 3588

Figures

Place holder to copy figure label and caption

Prevalence of sexually transmitted diseases by participant age (N = 512).

Graphic Jump Location

Tables

Table Graphic Jump LocationTable 2. Laboratory Test Results of Subjects at Enrollment (Baseline) Visit*

References

Division of STD Prevention, Sexually Transmitted Diseases Surveillance 1997.  Atlanta, Ga Public Health Service, Centers for Disease Control and Prevention, US Dept of Health and Human Services September1998;
American Social Health Association, Sexually Transmitted Disease in America: How Many Cases and at What Cost?  Menlo Park, Calif Kaiser Family Foundation1998;
Mangiore-Smith  RO'Leary  JMcGlynn  EA Health and cost-benefits of chlamydia screening in young women. Sex Transm Dis. 1999;26309- 316
Link to Article
Coth  MFPastorek  JGNugent  RP  et al.  Demographic and behavioral predictors of Trichomonas vaginalis infection among pregnant women. Obstet Gynecol. 1991;781087- 1092
Greenblatt  RMBacchetti  PBarkan  S  et al.  Lower genital tract infections among HIV-infected and high-risk uninfected women. Sex Transm Dis. 1999;26143- 151
Link to Article
Parazzini  FD'Oro  LCNaldi  L  et al.  Sexually transmitted diseases and risk of HIV infection. Acta Derm Venereol. 1996;76147- 149
Rotchford  KStrum  AWWilkinson  D Effect of coinfection with STDs and of STD treatment on HIV shedding in genital-tract secretions: systematic review and data synthesis. Sex Transm Dis. 2000;27243- 248
Link to Article
Schwebke  JRMorgan  SCPinson  GB Validity of self-obtained vaginal specimens for diagnosis of trichomoniasis. J Clin Microbiol. 1997;351618- 1619
Hook III  EWChing  SFStephens  JHardy  KFSmith  KRLee  HH Diagnosis of Neisseria gonorrhoeae infections in women by using the ligase chain reaction on patient-obtained vaginal swabs. J Clin Microbiol. 1997;352129- 2132
Hook III  EWSmith  KMullen  C  et al.  Diagnosis of genitourinary Chlamydia trachomatis infections by using the ligase chain reaction on patient-obtained vaginal swabs. J Clin Microbiol. 1997;352133- 2135
Polaneczky  MQuigley  CPollock  LDulko  DWitkin  SS Use of self-collected vaginal specimens for detection of Chlamydia trachomatis infection. Obstet Gynecol. 1998;91375- 378
Link to Article
Division of STD Prevention, Sexually Transmitted Disease Surveillance, 1998.  Atlanta, Ga Centers for Disease Control and Prevention, US Dept of Health and Human Services September1999;
Eng  TButler  W The Hidden Epidemic: Confronting Sexually Transmitted Diseases.  Washington, DC National Academy Press1997;
Wasserheit  JN Effects of changes in human ecology and behavior on patterns for sexually transmitted diseases, including human immunodeficiency virus infection. Proc Natl Acad Sci U S A. 1994;912430- 2435
Link to Article
Blake  DRDuggan  AQuinn  TZenilman  JJoffe  A Evaluation of vaginal infections in adolescent women: can it be done without a speculum? Pediatrics. 1998;102939- 944
Link to Article
Gray  RHWawer  MJGirdner  J  et al.  Use of self-collected vaginal swabs for detection of Chlamydia trachomatis infection [letter]. Sex Transm Dis. 1998;25450
Link to Article
Lawing  LFHedges  SRSchwebke  JR Detection of trichomonosis in vaginal and urine specimens from women by culture and PCR. J Clin Microbiol. 2000;383585- 3588

Correspondence

CME
Meets CME requirements for:
Browse CME for all U.S. States
Accreditation Information
The American Medical Association is accredited by the Accreditation Council for Continuing Medical Education to provide continuing medical education for physicians. The AMA designates this journal-based CME activity for a maximum of 1 AMA PRA Category 1 CreditTM per course. Physicians should claim only the credit commensurate with the extent of their participation in the activity. Physicians who complete the CME course and score at least 80% correct on the quiz are eligible for AMA PRA Category 1 CreditTM.
Note: You must get at least of the answers correct to pass this quiz.
You have not filled in all the answers to complete this quiz
The following questions were not answered:
Sorry, you have unsuccessfully completed this CME quiz with a score of
The following questions were not answered correctly:
Commitment to Change (optional):
Indicate what change(s) you will implement in your practice, if any, based on this CME course.
Your quiz results:
The filled radio buttons indicate your responses. The preferred responses are highlighted
For CME Course: A Proposed Model for Initial Assessment and Management of Acute Heart Failure Syndromes
Indicate what changes(s) you will implement in your practice, if any, based on this CME course.
Submit a Comment

Multimedia

Some tools below are only available to our subscribers or users with an online account.

Web of Science® Times Cited: 45

Related Content

Customize your page view by dragging & repositioning the boxes below.

Articles Related By Topic
Related Collections
PubMed Articles
JAMAevidence.com

The Rational Clinical Examination
Testing for STIs