Sexually Transmitted Diseases:
Chlamydia Screening Strategies and Outcomes in Educational Settings: A Systematic Review
Jamil, Muhammad Shahid MPH, MHM, MBBS*; Bauer, Heidi M. MD, MS, MPH†; Hocking, Jane S. PhD‡; Ali, Hammad MPH, MBBS*; Wand, Handan PhD*; Walker, Jennifer PhD§; Douglas, Laura MPH¶; Donovan, Basil MD*∥; Kaldor, John M. PhD*; Guy, Rebecca J. PhD*
From the *The Kirby Institute, University of New South Wales, Sydney, NSW, Australia; †Division of Epidemiology, School of Public Health, University of California, Berkeley, CA; ‡Center for Women’s Health, Gender and Society, Melbourne School of Population Health, and §Department of General Practice and Primary Health Care Academic Centre, University of Melbourne, Melbourne, Victoria, Australia; ¶Department of Obstetrics, Gynecology, and Reproductive Sciences, University of California, San Francisco, CA; and ∥Sydney Sexual Health Centre, Sydney Hospital, Sydney, NSW, Australia
Conflict of interest: None declared.
Correspondence: Muhammad Shahid Jamil, MPH, MHM, MBBS, The Kirby Institute, University of New South Wales, Sydney NSW 2052, Australia. E-mail: Mjamil@kirby.unsw.edu.au.
Received for publication June 4, 2013, and accepted December 18, 2013.
Abstract: Chlamydia trachomatis (CT) screening programs have been established in educational settings in many countries during the past 2 decades. However, recent evidence suggests that high uptake of screening and management (treatment, partner notification, and retesting for reinfection) improves program effectiveness. We conducted a systematic review to understand the screening strategies, the extent of screening conducted, and uptake of management strategies in educational settings. Screening studies in educational settings were identified through a systematic search of published literature from 2005 to 2011. We identified 27 studies describing 30 screening programs in the United States/Canada (n = 10), Europe (n = 8), Australia/New Zealand (n = 5), and Asia (n = 4). Most studies targeted both male and female students (74%). Classroom-based strategies resulted in 21,117 testes overall (4 programs), followed by opportunistic screening during routine health examination (n = 13,470; 5 programs) and opportunistic screening at school-based health centers (n = 13,006; 5 programs). The overall median CT positivity was 4.7% (range, 1.3%–18.1%). Only 5 programs reported treatment rates (median, 100%; range, 86%–100%), 1 partner notification rate (71%), 1 retesting rate within a year of an initial CT diagnosis (47%), and 2 reported repeat positivity rates (21.1% and 26.3%). In conclusion, this systematic review shows that a variety of strategies have been used to screen large numbers of students in educational settings; however, only a few studies have reported CT management outcomes.
Adolescents and young adults are major risk groups for Chlamydia trachomatis (CT) and Neisseria gonorrhoea (NG) infections.1–3 Clinical guidelines in many countries recommend annual CT screening for all sexually active young women4–6 and extend to young men in some countries.7 Also, it is recommended that any person diagnosed as having CT infection should be retested within 3 months of treatment.5,6,8 The conventional approach to opportunistically screen people attending primary care clinics for nonsexual health reasons has often failed to achieve high coverage,9–11 and retesting rates are also low in many clinical settings.12–15
The advent of nucleic acid amplification tests, which detect CT/NG infection with self-collected vaginal swab and urine specimens, has encouraged screening programs outside conventional clinical settings, including educational settings, with numerous programs established in various countries.16–19 However, in recent years, mathematical modeling studies have suggested that to achieve population level impact on CT transmission, screening programs need to achieve high testing coverage and also high rates of partner notification and retesting for reinfection after treatment.20–22
Mathematical modeling in Australia has predicted that screening 40% of men and women younger than 25 years annually would decrease CT prevalence rapidly for 10 years in all age groups.20 Other mathematical modeling also suggests that treating symptomatic men and women and screening 38% of women aged 15 to 24 years annually would significantly reduce the average number of secondary infections and that screening men and women aged up to 29 years may affect CT transmission.21 Modeling by Althaus et al.22 also estimated that in a population-wide screening program, the treatment for current partners is the most effective strategy for reducing CT transmission at the population level.
Despite screening programs being implemented in educational institutions (school, college, universities) for many years, the screening strategies used and other program components that improve effectiveness have not been studied in a systematic manner. In this context, we systematically reviewed the published literature on CT/NG screening programs in educational settings to explore the screening strategies used, the extent of screening conducted, and the uptake of treatment, partner notification, and retesting after treatment.
The review was conducted according to the PRISMA guidelines.23 The electronic bibliographic databases, PubMed and EMBASE, were searched for English-language studies published between January 1, 2005, and January 28, 2011, with the following search terms: Chlamydia, or Chlamydia infections, or Chlamydia trachomatis, OR Gonorrhea, AND Screening, or Mass Screening, or testing. The reference lists of selected studies were also screened to identify other eligible studies. A study was included if it reported on a CT or CT and NG screening program in an educational setting (school, college, university, technical institution) using self-collected specimens and reported the number of tests.
The articles were reviewed by 2 authors (M.S.J. and R.J.G.) independently, and disagreements were resolved by discussion and consensus. One author (M.J.) extracted the data from each article, and a second author (R.G.) double checked the data. The following information was extracted: demographics; screening strategy (location, recruitment, advertisement, incentive, etc); number screened; CT/NG positivity; notification of results; treatment, retesting, and reinfection rate; and partner notification. The authors were contacted to collect additional information, if required.
Programs were classified into 7 groups (hereafter called program type) based on screening strategy and location. All analyses were conducted in STATA 12 (StataCorp, College Station, TX).
Of 3219 articles identified through the literature search, 27 articles were included in the review (Fig. 1).24–50 Of these, 3 articles described programs using 2 different screening strategies29,31,46 and were thus classified into different program types, giving a total of 30 programs that formed the basis of analysis.
Overview of Programs
Programs involved classroom-based screening (n = 4), opportunistic screening at school-based health centers (SBHCs; n = 5), opportunistic screening during routine health/sports physical examinations (n = 6), voluntary screening at SBHC (n = 3), screening at other on-campus locations (n = 4), event-based screening (n = 4), and other strategies (n = 5; Table 1). Programs were conducted in the United States/Canada (37.0%), Europe (29.6%), Australia/New Zealand (18.5%), and Asia (14.8%). Most targeted both male and female students (74.1%). The specimens consisted of urine only (77.8%), vaginal swab only (7.4%), and urine for men and vaginal swab for women (14.8%).
Across all programs, 53,935 tests were conducted (median, 515). The overall median CT positivity was 4.7% (n = 28), and NG positivity was 0.2% (n = 12). Five programs reported the treatment rate with a median of 100% (range, 86%–100%).
Findings by Program Type
Classroom-Based Screening. In these 4 programs, students were approached in the classrooms for screening.25,27,38,44 In 2 programs, every grade 9 to 12 student was scheduled to attend an education/screening session25 or students viewed a brief presentation in classrooms.27 Every student received a test kit and returned it with or without a specimen at stalls near bathrooms.25,27 The entire class was escorted to the testing area, and students were individually counseled for an opportunity to screen in the third program.44 In the fourth program, female students were provided with screening information and test kits during lectures or lecture breaks, and specimens were returned on the next day.38 In 2 of these programs, screening was part of ongoing annual programs in New Orleans44 and Philadelphia25 high schools.
Across these programs, 21,117 tests were conducted (median, 535), but most of these tests (93.3%) were done in one program.25 The median CT positivity was 5.4% (n = 4). Test results were accessible through a Web site in one program.38 Two programs reported treatment rates of 99.9%25 and 100%.27
Opportunistic Screening at SBHC. In these programs, students attending SBHCs were screened opportunistically.24,26,33,45,46 Detailed screening method was not available from all programs but included the following: receptionist approaching every second or third clinic attendee,26 advertisement at SBHC and on-campus with receptionist offering flyers to consecutive students attending for nonsexual health reasons,24 nurse/doctor offering screening after consultation, nurse referring students to doctors, or receptionists offering information leaflets to students.45
Across these programs, 13,006 tests were conducted (median, 715). The median CT positivity was 4.9% (n = 5). In one program where screening was routinely offered to sexually active female students attending SBHCs, 47% of those with CT diagnosis were retested within 1 to 12 months (mean, 4.3 months), and the repeat positivity rate was 26.3%.33
Voluntary Screening at SBHC. In these programs, students were encouraged to get voluntarily screened at SBHC by promoting screening through: e-mails, flyers, and student radio37; newsletter, school Web site, nurse visits to classes, and information session in school assembly39; and education sessions for students enrolled in an intervention study.32 In one program, test packs could be picked up and dropped off in the SBHC waiting room.39 Across these programs, 1691 tests were conducted (median, 789), and the median CT positivity was 9.7% (n = 3).
Opportunistic Screening During Health/Sports Physical Examination. In 5 programs, students were opportunistically screened during routine/annual health examination,35,36,43 sports physical examination,34 and adolescent health check.49 None of the programs mentioned whether these examinations were carried out at SBHCs. Screening strategies varied across programs and included the following: information leaflet distribution,43 recruitment by research/school staff,35 information sessions for student athletes with a station added to usual sports examination rotation for specimen collection,34 sexually transmitted infection (STI) testing within sexual health component of adolescent health checkup,49 and posting notices with oral and written invitations by staff before screening and lectures at health checkup site, in lecture hall, or in classrooms on screening days with specimens dropped off in boxes.36
Across these programs, 13,470 tests were conducted (median, 993), and one program disproportionately contributed to the number of tests (79.3%).36 The median CT positivity was 2.5% (n = 4). In a program that conducted screening in 2 consecutive school years, 53% of participants in the first year were retested in the next year, and the repeat CT positivity was 21.1%.35 In one program, tests results were available through a Web site.36
Event-Based Screening. These 4 programs used various student events for screening such as orientation week29; sexual health awareness and guidance week48; school health fair46; orientation week; market stalls; band and bar nights; sporting events; scavenger hunts; and Halls of Residence.31 Screening was promoted through advertisements including posters29; posters, student media, SMS, Web sites, and education sessions31; and posters, leaflets, media, radio, e-mail, and newspapers.48 In one program, test packs were available in bathrooms as well as distributed by volunteers with specimen collection boxes placed inside toilet areas.48
Across these programs, 1861 tests were conducted (median, 564). The median CT positivity was 2.8% (n = 4). Treatment rate was 86% in one program48 and 100% in another.29 In one program, of the students diagnosed as having CT, partner notification was conducted with 71% (15/21), with patient referral being the most preferred method (n = 13).48
Screening at Other On-Campus Locations. These programs offered screening at on-campus locations other than SBHC and classrooms.28,30,31,41 Screening was offered in canteens in one program,41 whereas in another program, test packs were available in the lavatories of university restaurant and students were informed through presentations, flyers, posters, and e-mails.30 In the third program, clinicians recruited students in offices after being informed through advertisements, presentation in school assemblies, and peer recruiters.28 In one school, students were given appointments, whereas screening was conducted on a “drop-in” basis in the second school with specimen collection in nearby toilets.28 In the fourth study, a station was set up and 183 students were sent an SMS inviting them to screen and receive $10 cash incentive.31 Students were encouraged to forward SMS to other students.
Across these programs, 1189 tests were conducted (median, 348), and the median CT positivity was 2.9% (n = 3).
Other Strategies. In 5 studies, sufficient screening details were not provided to allow classification.29,40,42,47,50 Program details are contained in Table 1.
This systematic review shows that CT/NG screening in educational settings is a feasible approach to screen large numbers of young people and to identify and treat new infections. Screening programs have been conducted in many countries and in a range of educational facilities including schools, colleges, and universities. A variety of screening strategies were used, but the number of students screened seemed to be higher in classroom-based programs and programs offering opportunistic screening at SBHC and during routine health examinations. The CT management outcomes such as treatment, partner notification, and retesting at 3 months after treatment were only reported in a few studies.
The review has a few limitations. First, we did not search the gray literature and thus may not have included other relevant unpublished studies. Second, we purposely selected a literature search period of January 2005 to January 2011 to provide a current perspective on CT screening in educational settings; however, we acknowledge that we may have excluded programs published before this time, which may have had different outcomes to those included in our review. Other eligible articles may also have been published after the cutoff date for literature search. Third, the duration of programs varied, most were of a short duration but some were more than a year, which would influence the number of students screened. Finally, any comparison of CT/NG positivity across the programs is limited by different age groups, ethnic composition, and proportion of sexually active students in the target population as well as prevalence in the underlying populations.
One of the main objectives of this review is to understand the strategies that result in more people being screened. The programs that targeted entire classes of students25 and conducted opportunistic screening at SBHC33,46 and opportunistic screening during routine/annual health examination36,43 appeared to screen the most number of students. However, the decision of what strategy to use may be dependent on resources available, availability of SBHCs, and whether the schools conduct annual health and/or sports physical examinations. School-based health centers are present only in 6.4% of US public schools.51 A survey of 736 US colleges/universities found that STI services were available in 66% of institutions with a SBHC, and only 48% and 67% of these screened sexually active men and women, respectively.52
Education facilities are ideal to reach adolescents and young adults for screening because it is mandatory for students to remain in school in many countries. However, in addition to screening coverage, the success of screening programs depends on treatment, partner management, and retesting after treatment. Overall, there was a lack of quantitative data on these outcomes. A number of programs noted the presence of partner notification strategies, but the outcomes were only reported in one program in the review.48 The presence of SBHCs seems to facilitate the treatment for students and their same-school partners32,37,39,45; however, partner treatment can be challenging when they are not students at the same school. One of the programs in the review reported retesting rates at 1 year after a positive CT diagnosis with higher rates achieved (47%; median time to retest, 4.3 months33) compared with clinical settings.12–14
A key aim of STI screening is to reduce population prevalence. However, it may not be realistic for school-based screening programs alone to achieve this because of sexual mixing of students with outside partners who are not participating in screening.53 It may also take some time for screening programs to achieve prevalence reductions, even if coverage is high, as suggested by mathematical modeling.20 Two school-based screening programs included in our review25,44 were part of annual programs that achieved high testing coverage over many years, but only demonstrated a transient decline in prevalence for boys in one program53,54 and girls in the other.55,56 School-based screening programs can, nevertheless, represent an important component of an overall population-based screening program, by improving access for a subgroup of the population with high CT prevalence,1,3 yet lower access to testing, especially in young men.57–59
This is the first systematic review, to our knowledge, to synthesize the findings of CT screening programs in educational settings based on strategies, coverage, and outcomes. The review demonstrated that screening programs have been conducted in a range of educational facilities in a number of countries and screened a large number of both male and female students, although some strategies seemed to reach a greater number of students than others. However, only a few programs reported on important screening outcomes such as treatment, partner notification, and retesting after treatment. Future evaluations of school-based program should also focus on collection and reporting of these important program outcomes.
1. Adams EJ, Charlett A, Edmunds WJ, et al. Chlamydia trachomatis
in the United Kingdom: A systematic review and analysis of prevalence studies. Sex Transm Infect 2004; 80: 354–362.
2. Centers for Disease Control and Prevention. Sexually Transmitted Disease Surveillance 2010. Atlanta, GA: U.S. Department of Health and Human Services; 2011.
3. Vajdic CM, Middleton M, Bowden FJ, et al. The prevalence of genital Chlamydia trachomatis
in Australia 1997–2004: A systematic review. Sex Health 2005; 2: 169–183.
5. Lanjouw E, Ossewaarde J, Stary A, et al. 2010 European guideline for the management of Chlamydia trachomatis
infections. Int J STD AIDS 2010; 21: 729–737.
6. Workowski KA, Berman S. Sexually transmitted diseases treatment guidelines, 2010. MMWR Recomm Rep 2010; 59: 1–110.
7. European Centre for Disease Prevention and Control. Chlamydia Control in Europe. Stockholm: ECDC; 2009.
9. Johnson SA, Simms I, Sheringham J, et al. The implementation of chlamydia screening: A cross-sectional study in the South East of England. Sex Transm Infect 2010; 86: 217–221.
10. Kong F, Guy RJ, Hocking JS, et al. Australian general practitioner chlamydia testing rates among young people. Med J Aust 2011; 194: 249–252.
11. Levine WC, Dicker LW, Devine O, et al. Indirect estimation of chlamydia screening coverage using public health surveillance data. Am J Epidemiol 2004; 160: 91–96.
12. Bowring AL, Gouillou M, Guy R, et al. Missed opportunities—Low levels of chlamydia retesting at Australian general practices, 2008–2009. Sex Transm Infect 2012; 88: 330–334.
13. Caggiano ME, Dumas W, Bertrand T, et al. Re-testing for Chlamydia trachomatis
infection in Massachusetts family planning clinics. Presented at: National STD Prevention Conference; 2008; Chicago, IL.
14. Guy R, Wand H, Franklin N, et al. Re-testing for chlamydia at sexual health services in Australia, 2004–08. Sex Health 2011; 8: 242–247.
15. Hoover KW, Tao G, Nye MB, et al. Suboptimal adherence to repeat testing recommendations for men and women with positive chlamydia tests in the United States, 2008–2010. Clin Infect Dis 2013; 56: 51–57.
16. Bauer HM, Chartier M, Kessell E, et al. Chlamydia screening of youth and young adults in non-clinical settings throughout California. Sex Transm Dis 2004; 31: 409–414.
17. Cohen DA, Kanouse DE, Iguchi MY, et al. Screening for sexually transmitted diseases in non-traditional settings: A personal view. Int J STD AIDS 2005; 16: 521–527.
18. Ford CA, Viadro CI, Miller WC. Testing for chlamydial and gonorrheal infections outside of clinic settings: A summary of the literature. Sex Transm Dis 2004; 31: 38–51.
19. Jamil M, Hocking J, Bauer H, et al. Home-based chlamydia and gonorrhoea screening: A systematic review of strategies and outcomes. BMC Public Health 2013; 13: 189.
20. Regan DG, Wilson DP, Hocking JS. Coverage is the key for effective screening of Chlamydia trachomatis
in Australia. J Infect Dis 2008; 198: 349–358.
21. Glasser JW, Owusu-Edusei K, Glick SN, et al. Controlling chlamydia: population modeling to assess promising interventions. Sex Transm Infect 2013; 89 (suppl 1): A57.
22. Althaus CL, Heijne JCM, Herzog SA, et al. Individual and population level effects of partner notification for Chlamydia trachomatis
. PLoS One 2012; 7: e51438.
23. Ottawa Hospital Research Institute. PRISMA: Transparent Reporting of Systematic Reviews and Meta-Analyses. Available at: http://www.prisma-statement.org
. Accessed December 1, 2010.
24. Aldeen T, Jacobs J, Powell R. Screening university students for genital chlamydial infection: Another lesson to learn. Sex Health 2010; 7: 491–494.
25. Asbel LE, Newbern EC, Salmon M, et al. School-based screening for Chlamydia trachomatis
and Neisseria gonorrhoeae
among Philadelphia public high school students. Sex Transm Dis 2006; 33: 614–620.
26. Baker M, Ortega-Benito J, Garret N, et al. Prevalence and risk factors for Chlamydia trachomatis
infection in female New Zealand university students. N Z Med J 2005; 118: U1607.
27. Barry PM, Scott KC, McCright J, et al. Stay in school? Results of a sexually transmitted diseases screening program in San Francisco high schools—2007. Sex Transm Dis 2008; 35: 550–552.
28. Bowden FJ, O’Keefe EJ, Primrose R, et al. Sexually transmitted infections, blood-borne viruses and risk behaviour in an Australian senior high school population—the SHLiRP study. Sex Health 2005; 2: 229–236.
29. Buhrer-Skinner M, Muller R, Menon A, et al. Novel approach to an effective community-based chlamydia screening program within the routine operation of a primary healthcare service. Sex Health 2009; 6: 51–56.
30. Colliers A, Verster A, Van Puyenbroeck K, et al. Screening Belgian university students for Chlamydia trachomatis
infection: A feasibility study. Int J Adolesc Med Health 2009; 21: 343–346.
31. Currie MJ, Schmidt M, Davis BK, et al. ‘Show me the money’: Financial incentives increase chlamydia screening rates among tertiary students: A pilot study. Sex Health 2010; 7: 60–65.
32. Gaydos CA, Hsieh YH, Galbraith JS, et al. Focus-on-teens, sexual risk-reduction intervention for high-school adolescents: Impact on knowledge, change of risk-behaviours, and prevalence of sexually transmitted diseases. In J STD AIDS 2008; 19: 704–710.
33. Gaydos CA, Wright C, Wood BJO, et al. Chlamydia trachomatis
reinfection rates among female adolescents seeking rescreening in school-based health centers. Sex Transm Dis 2008; 35: 233.
34. Hennrikus E, Oberto D, Linder JM, et al. Sports preparticipation examination to screen college athletes for Chlamydia trachomatis
. Med Sci Sports Exerc 2010; 42: 683–688.
35. Hsieh YH, Shih TY, Lin HW, et al. High-risk sexual behaviours and genital chlamydial infections in high school students in Southern Taiwan. Int J STD AIDS 2010; 21: 253–259.
36. Imai H, Nakao H, Shinohara H, et al. Population-based study of asymptomatic infection with Chlamydia trachomatis
among female and male students. Int J STD AIDS 2010; 21: 362–366.
37. James AB, Simpson TY, Chamberlain WA. Chlamydia prevalence among college students: Reproductive and public health implications. Sex Transm Dis 2008; 35: 529–532.
38. Kucinskiene V, Juseviciute V, Valiukeviciene S, et al. Home sampling and pooling of vaginal samples are effective tools for genetic screening of Chlamydia trachomatis
among high school female students in Lithuania. Scand J Infect Dis 2008; 40: 88–93.
39. Langille DB, Proudfoot K, Rigby J, et al. A pilot project for chlamydia screening in adolescent females using self-testing: Characteristics of participants and non-participants. Can J Public Health 2008; 99: 117–120.
40. Lee SJ, Cho YH, Ha US, et al. Sexual behavior survey and screening for chlamydia and gonorrhea in university students in South Korea. Int J Urol 2005; 12: 187–193.
41. Lorimer K, Reid ME, Hart GJ. Willingness of young men and women to be tested for Chlamydia trachomatis
in three non-medical settings in Glasgow, UK. J Fam Plann Reprod Health Care 2009; 35: 21–26.
42. Morris SR, Bauer HM, Chartier M, et al. Relative efficiency of chlamydia screening in non-clinical settings in two California counties. Int J STD AIDS 2010; 21: 52–56.
43. Mossong J, Muller M, Majery N, et al. Screening for Chlamydia trachomatis
in secondary schools, family planning and occupational health centres in Luxembourg. Sex Transm Infect 2009; 85: 455–458.
44. Nsuami MJ, Taylor SN, Smith BS, et al. Increases in gonorrhea among high school students following hurricane Katrina. Sex Transm Infect 2009; 85: 194–198.
45. O’Connell E, Brennan W, Cormican M, et al. Chlamydia trachomatis
infection and sexual behaviour among female students attending higher education in the Republic of Ireland. BMC Public Health 2009; 9: 397.
46. Schillinger JA, Dunne EF, Chapin JB, et al. Prevalence of Chlamydia trachomatis
infection among men screened in 4 U.S. cities. Sex Transm Dis 2005; 32: 74–77.
47. Takahashi S, Takeyama K, Miyamoto S, et al. Incidence of sexually transmitted infections in asymptomatic healthy young Japanese men. J Infect Chemother 2005; 11: 270–273.
48. Vaughan D, O’Connell E, Cormican M, et al. “Pee-in-a-Pot”: Acceptability and uptake of on-site chlamydia screening in a student population in the Republic of Ireland. BMC Infect Dis 2010; 10: 325.
49. Vogler CM, Russell D, Wenitong M, et al. Providing quality sexual health care to at risk indigenous youth in a north Queensland school. Sex Health 2009; 6: 379–380.
50. Williamson LM, Scott G, Carrick-Anderson K, et al. Chlamydia trachomatis
testing among 13-25-year-olds in non-genitourinary medicine settings. J Fam Plann Reprod Health Care 2007; 33: 177–182.
51. Kann L, Brener ND, Wechsler H. Overview and summary: School health policies and programs study 2006. J Sch Health 2007; 77: 385–397.
52. Koumans EH, Sternberg MR, Motamed C, et al. Sexually transmitted disease services at US colleges and universities. J Am Coll Health 2005; 53: 211.
53. Nsuami MJ, Nsa M, Brennan C, et al. Chlamydia positivity in New Orleans public high schools, 1996–2005: Implications for clinical and public health practices. Acad Pediatr 2013; 13: 308–315.
54. Cohen DA, Nsuami M, Martin DH, et al. Repeated school-based screening for sexually transmitted diseases: A feasible strategy for reaching adolescents. Pediatrics 1999; 104: 1281–1285.
55. Fisman DN, Spain CV, Salmon ME, et al. The Philadelphia high-school STD screening program: Key insights from dynamic transmission modeling. Sex Transm Dis 2008; 35: S61–S65.
56. Salmon M. The more you look, the more you find—Results from the Philadelphia high school STD screening program, 2002–2011. Presented at: National STD Prevention Conference; 2012; Minneapolis, MN.
57. Booth ML, Bernard D, Quine S, et al. Access to health care among Australian adolescents young people’s perspectives and their sociodemographic distribution. J Adolesc Health 2004; 34: 97–103.
58. Ford CA, Bearman PS, Moody J. Foregone health care among adolescents. JAMA 1999; 282: 2227–2234.
59. Marcell AV, Klein JD, Fischer I, et al. Male adolescent use of health care services: Where are the boys? J Adolesc Health 2002; 30: 35–43.
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