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HIV testing among United States high school students at the state and national level, Youth Risk Behavior Survey 2005–2011



Human immunodeficiency virus (HIV) remains an important public health issue and CDC recommends routine HIV screening for Americans aged 13–64. Adolescents and young adults are disproportionately affected compared to the overall population. We analyzed self-reported HIV testing and related risk behaviors at the state and national level among youths who had sexual intercourse, with a focus on state level differences.


This study used the state and national Youth Risk Behaviors Surveys 2005–2011. It included a total of 59,793 national-level observations and 39,421 state-level observations of US high school students, of which respectively 28,177 and 13,916 reported ever having sexual intercourse.

The outcome of interest was having ever been tested for HIV. The risk behaviors were condom use at last intercourse, number of sexual partners in lifetime, age at first intercourse, ever forced sexual intercourse, and ever illegal injection drug use. Analyses performed included logistic regression and t-test analyses.


HIV testing was positively associated with HIV-related risk behaviors among sexually active high school students. However, HIV testing remained relatively low (22%) between 2005 and 2011, even for those engaging in risk behaviors. Results differed among the only 7 states that monitored HIV testing through YRBS, most commonly with respect to HIV testing and condom use.


Routine HIV testing is critical for early identification of HIV, which was set as a priority in a recent Executive Order. Our data suggest further efforts are needed to achieve widespread uptake of HIV testing among high school students. Furthermore, differences observed across states likely reflect different needs and should be followed up closely by states. Finally, having accurate data that reflects the reality of youths’ lives is crucial for efficient prevention planning. Thus, more states should consider collecting HIV testing data to evaluate uptake of HIV testing among youth.


Human Immunodeficiency Virus (HIV) remains an important public health issue among young people in the United States. Compared to the overall population, adolescents and young adults are disproportionately affected by HIV. Youth aged 13–24 represented 4% of all diagnosed cases by the end of 2010, but 21% of new diagnoses in 2011 (CDC 2011).

As recommendations have moved toward earlier treatment, early testing is getting more attention as a gateway to care. Benefits of early diagnosis of HIV infection are multiple (CDC 2013b). It provides patients with timely access to treatment and thus improves their quality of life and survival time. People, who initiate antiretroviral therapy before getting to a CD4 count below 350 cells per μL, have a significantly reduced risk for AIDS-related events or death (Sterne et al. 2009). Early HIV diagnosis is also crucial in limiting the spread of the disease in the general population. Infected patients becoming aware of their positive HIV status can adapt their behavior to avoid infecting others, and engage in HIV treatment, which substantially reduces their infectiousness (Branson et al. 2013).

It is now clear that control and elimination of HIV will be possible only with widespread testing, prompt and accurate diagnosis, and universal access to antiviral therapy (Branson et al. 2013). Also, as patients are likely to be asymptomatic at early stage of HIV infection, prompt diagnosis implies routine screening.

In 2006, the Center for Disease Control and Prevention (CDC) recommended routine voluntary HIV screening in all individuals aged 13 to 64 regardless of recognized risk factors (Branson et al. 2006). In line with these recommendations, the United States Preventive Services Task Force now recommends that clinicians screen all individuals aged 15–65 for HIV (Moyer 2013). This implies that an important proportion of adolescents should be routinely tested for HIV infection, regardless of their risk level. Recently, the President issued an Executive Order emphasizing the national priority of improving all phases of the HIV care continuum, including early HIV diagnosis (Gardner et al. 2011; The White House 2013).

Still, at the end of 2009, one in five (18%) US adults and adolescents living with HIV infection was unaware of its status. Youth aged 13–24 are estimated to be the age group with the highest share of people unaware about their HIV infection. In 2009, 76,400 aged 13–24 were estimated to be living with HIV and six out of ten were undiagnosed (CDC 2010). Many adolescents still have a limited knowledge about HIV/AIDS and underestimate their personal infection risk (Gurvey et al. 2005). One of the main limitations to self-initiated testing among adolescents is the concern about confidentiality (Hyden et al. 2014). The inadequate access to HIV prevention and treatment services was also identified as a major barrier, as some adolescents have only limited contact with the health care system (Irwin et al. 2009). Finally, the implementation of routine HIV testing in the real-life can remain challenging and in some locations it is still sometimes only offered to patients perceived at high risk (Jain et al. 2009).

Moreover, diagnosis often occurs late in the course of the disease. During 2010, people aged 13–24 represented 12.7% of persons with stage 3 (AIDS) classification at the time of HIV diagnosis. Furthermore, additional efforts are needed to systematically link newly diagnosed individuals to treatment and reduce drop offs across the continuum of HIV care (Gardner et al. 2011). Thus, legislation changes under the Affordable Care Act aiming at extending HIV care coverage represent an important step forward (The White House 2013).

Understanding testing patterns of youth is essential in better scaling up HIV testing. The National HIV Behavioral Surveillance System enrolls people aged 18 or more who are in identified high risk groups, and thereby does not reflect testing patterns of younger people (Gallagher et al. 2007). Thus, the Youth Risk Behavioral Survey (YRBS), which collects data from a representative sample of high school students, can be used as an alternative to understand current patterns of HIV testing among youths.

A previous report demonstrated the association of HIV testing with some risk behaviors using the 2009 national YRBS (Balaji et al. 2012). To update this previous report and further address gaps in knowledge, we analyzed YRBS over the period 2005–2011, at the state and national levels. We explored further the association between HIV testing and HIV-related risk behaviors, including state level differences, because such differences may reflect different testing needs across states. The present report includes, (i) estimates of HIV testing and selected risk behaviors among youths who had sexual intercourse, (ii) associations between HIV testing and selected behaviors associated with HIV acquisition (HIV risk behaviors), (iii) comparison of state and national estimates of HIV testing and risk behaviors.


Of 59,793 high school student observations from the national YRBS for the period 2005–2011, 28,177 reported prior sexual intercourse. The distributions of sexually active students across sex and grade levels were similar for each survey year. Only one out of five students reported ever testing for HIV. Most students did not engage in studied HIV-related risk behaviors (Table 1).

Table 1 Characteristics of High School Students Who Had Sexual Intercourse, National YRBS 2005–2011

Crude analysis showed that the odds of HIV testing were higher for females compared to males, for students in 12th grade compared to students in lower grades and for Black or African American students compared to other race and ethnicity groups. Moreover, the odds of HIV testing were higher for students engaging in HIV-related risk behaviors (Table 2).

Table 2 Characteristics Associated With HIV Testing Among Students Who Had Sexual Intercourse, National YRBS 2005–2011

In the logistic regression model, four interaction terms were significant. First, although HIV testing was more prevalent among students with 4 or more sexual partners for all race and ethnicity groups, it was associated with higher odds of testing among White and Other race students than among Black/African American or Hispanic students. Second, males with first sexual intercourse before 13 had higher odds of HIV testing compared to males with first sexual intercourse at 13 or later. No significant difference was found for females. Third, females who did not use a condom at last intercourse were more likely to be tested for HIV compared to females who used a condom at last sex. No significant difference was found for males. Fourth, the odds of HIV testing were the highest among 11th graders, when comparing students ever forced to have intercourse to those never forced (Table 2).

Of 39,421 high school student observations from the states’ YRBS for the period 2005–2011, 13,916 reported prior sexual intercourse. For each of the seven states with available data, the distribution of high school students who had sexual intercourse was comparable across sex and grade levels. Still, Connecticut, New Jersey, and North Dakota had slightly greater proportions of students in 12th grade compared to 9th grade. Racial and ethnic composition varied substantially across states. Most students had never been tested for HIV and never engaged in HIV-related risk behaviors but with cross-state differences (Table 3).

Table 3 Characteristics of High School Students Who Had Sexual Intercourse by State, State YRBS 2005–2011

The comparison of state and national prevalence of HIV testing and engagement in risk behaviors among high school students who had sexual intercourse, while controlling for sex, grade, race and ethnicity, revealed some significant differences (Figure 1). The prevalence of HIV testing among sexually active students in Arkansas was higher than the national average, as opposed to New Jersey and South Carolina, where it was below the national average. Compared to the national level, Arkansas and North Carolina had a higher prevalence of students who did not use condom at last intercourse. Also, Arkansas had a higher prevalence of students who had four or more partners in life and of students who had their first sexual intercourse before 13. Finally, Massachusetts had a higher prevalence of students with forced intercourse. Conversely, compared to the national average, New Jersey had significantly lower prevalence of students who did not use condom at last intercourse and Connecticut had a significantly lower prevalence of students who had four or more partners in life.

Figure 1

State and National Prevalence Comparison of HIV Testing and HIV-Risk Behaviors, State and National YRBS. The comparison of state and national prevalence of HIV testing and engagement in risk behaviors among high school students who had sexual intercourse, while controlling for sex, grade, and race and ethnicity are presented in this figure. Abbreviations: HIV, human immunodeficiency virus; MA, Massachusetts; CT, Connecticut; NJ, New Jersey; AR, Arkansas; NC, North Carolina; ND, North Dakota; SC, South Carolina. aHIV testing estimates for the period 2007–2011.


This study showed that HIV testing among students who had sexual intercourse remained relatively low (22%) and stable (data not shown) between 2005 and 2011, despite CDC’s 2006 recommendations for making HIV testing a standard part of the medical care for individuals aged 13–64 (Branson et al. 2006). These results were consistent with the literature (CDC 2012). Furthermore, this study highlighted that HIV testing and risk behavior profiles differ across states. HIV testing differences could be interpreted in the context of risk behaviors. This new piece of information is important for future prevention interventions among youths.

Our results confirmed that HIV testing was more common among females, Black or African Americans, 12th graders, and students engaging in HIV-related risk behaviors (Balaji et al. 2012). The three risk factors most strongly associated with HIV testing were having four or more lifetime sexual partners, lifetime illegal injection drug use, and ever having been forced to have sexual intercourse. This was consistent with previous studies (Arrington-Sanders et al. 2008; Balaji et al. 2012; Decker et al. 2005,2014; Miller 2010; Samet et al. 1997; Talib et al. 2013). However, Swenson reported higher odds of rapid HIV testing among those with only one sex partner in the past 90 days than those with multiple partners, using a sample of 81 adolescents (Swenson et al. 2011). Observed differences are likely due to smaller sample size (Swenson et al. 2011). The association of HIV testing with lifetime illegal injection drug use and ever having been forced to have intercourse were also reported among young adults (Decker et al. 2009; Kellerman et al. 2002; Williams-Roberts et al. 2010).

Several interaction terms were found to be significant in this study, adding nuance to previous findings (Balaji et al. 2012). Large size in YRBS provides more statistical power for the detection of interactions.

Interaction between race and number of sexual partners

Although number of sexual partners was significantly associated with testing for all students, it was particularly important for White students. One possible explanation could be the higher level of HIV testing among Black or African American students with less than 4 partners compared to White and Hispanic. This could also be explained by the lower use of condom among high school students with higher numbers of sexual partners, in particular among White, as reported by Richter et al. (1993).

Interaction between sex and age at first intercourse

Having first intercourse before 13 was associated with higher odds of HIV testing among males. One possible explanation could be that the share of black students is higher among males who had sex before 13 compared to males who had sex after 13, whereas it is similar for females who had sex either before or after 13 (Cavazos-Rehg et al. 2009). As Black students have higher rates of HIV testing, this could drive the difference between the two male subgroups.

Interaction between sex and use of condom

Not using a condom at last intercourse was associated with higher odds of HIV testing among females compared to males. Young women, who use condoms as contraception and did not use one at last sex, are likely to get tested for pregnancy at a care provider (Daley et al. 2005) and should receive HIV testing, given efforts for integrating pregnancy and STIs prevention among teens (Tran et al. 2010). Besides, young women who did not use condom at last sex, but use oral contraception, are likely to receive counseling and HIV testing from the doctor who prescribes their contraceptive (American College of Obstetricians and Gynecologists (ACOG) 2008).

The comparison between states and the national sample highlighted geographic differences in HIV testing and risk behavior profiles, with the most common difference in prevalence use of condom at last sex. This reinforces previous observations of risk profile variations across locations among older adolescents (Moore et al. 2013).

These geographic differences are very informative for State Health Departments as they point toward areas that need further investments in programs. They can also inform state education agencies and school districts about local adaptations needed in HIV/AIDS educational curriculum (National Association of State Boards of Education 2013). For example, currently, only 33 states and the district of Columbia mandate HIV education and only 13 states require the inclusion of information on the possible negative outcomes of teen sex and pregnancy (Guttmacher Institute 2014). Thus, states could gain great benefits from reinforcing their programs according to the sexual risk behaviors patterns of their local youth populations.

Forty-eight states plus District of Columbia now have HIV testing laws that are consistent with the key features of the CDC’s 2006 recommendations: opt-out HIV testing, no written consent required, and no pretest counseling required (CDC 2013c). Still, some differences remain across states (e.g., minimum age required to consent, availability of anonymous testing, reporting policies of positive HIV tests) and can sometimes limit widespread HIV testing among adolescents (National HIV/AIDS Clinicians’ Consultation Center 2014). Additionally, rapidly aligning practices with new HIV testing laws can be a real challenge in itself (Hyden et al. 2014; Kelley et al. 2011). For example, some HIV locations lack a clear and consistent communication of their confidentiality policies for HIV testing due to a lack of training (Hyden et al. 2014).

This study also highlights the missed opportunity to collect HIV testing information through YRBS. Although weighted data were available for 43 states, only 7 monitored HIV testing for at least one of the years within 2005–2011. National and state use the same standard questionnaire, but state and local officials responsible for the coordination of YRBS can add or delete questions to meet their policy or programmatic needs (CDC 2013a). This can result in gaps in knowledge. Controlling HIV/AIDS epidemic requires measuring progress in HIV testing and prioritizing interventions accordingly. The comprehensive monitoring of HIV testing across all states through YRBS would be an important step forward in terms of HIV prevention among youths. Furthermore, systematic monitoring of sexual preferences would be of great value in targeting populations at increased risk of transmission, such as male having sex with male (CDC 2013d).

This study has some limitations. The cross-sectional design of YRBS prevents identification of temporal order between HIV testing and risk behaviors. Additionally, the self-reported nature of YRBS can introduce bias (e.g., recall, non-response, social desirability) (Sackett 1979). However, several studies evaluated YRBS validity and concluded to its reliability (Brener et al. 2002). Additionally, YRBS is limited to students attending high school; this results in selection bias. Finally, higher dropouts among Hispanics and Black or African American ethnicities can also raise bias issue (National Center for Education Statistics 2012).


Routine HIV testing is an efficient strategy for early identification of HIV. It allows early linkage to care of HIV positive adolescents and reduces the rate of new HIV infections. Although early HIV identification became a national priority, HIV testing among high school students remains low, even for those at increased risk of HIV infection.

Moreover, state action is critical to enhance routine HIV testing among youth. Differences in patterns across states observed, are meant to be exploratory and hypothesis generating. They should be followed up by states and try to be correlated with knowledge of programs. Finally, all states should participate in YRBS to monitor accurately HIV testing and should ensure that testing laws in place are prone to the rapid and full implementation of routine HIV testing among youths.


Participants and procedure

This study used national and state YRBS 2005–2011. YRBS measures the prevalence of health risk behaviors among high school students, through an anonymous paper-and-pencil survey administered every other year in randomly selected public and private high schools. National and state levels are representative of high school students in the United States and states considered. They come from separate scientific samples of schools and students, follow the same survey methodology and use the same core questionnaire, to which state and local agencies can add or delete questions (CDC 2013a). National YRBS data are publicly accessible and state data are available upon request. After IRB (Emory University) approval, data were retrieved for 43 states. Data were not available for the seven remaining states due to either absence of weighted data (California, Oregon), no YRBS participation (Minnesota, Washington), or no data sharing policy (Hawaii, Indiana, and Vermont). Out of the 43 states, seven collected the information related to HIV testing through their YRBS questionnaire for at least one year in the studied period (Massachusetts: 2005–2011; Connecticut: 2007–2011; New Jersey: 2005, 2009, and 2011; Arkansas, North Carolina, North Dakota: 2009–2011; South Carolina: 2009). This study used 59,793 observations at the national level and 39,421 observations at the state level.


Population of interest

The subpopulation of interest was high school students who had sex and was defined by positive answer to the question “Have you ever had sex?”.

Outcome variable

HIV testing was assessed through the question “Have you ever been tested for HIV, the virus that causes AIDS?”.

Independent variables

The five HIV-related risk behaviors selected were assessed through the questions: (i) “The last time you had sexual intercourse, did you or your partner use a condom?”; (ii) “During your life, with how many people have you had sexual intercourse?”; (iii) “How old were you when you had sexual intercourse for the first time?”; (iv) “Have you ever been physically forced to have sexual intercourse when you did not want to?”; (v) “During your life, how many times have you used a needle to inject any illegal drug into your body?”.

Controlling variables

Sex and grade were classified through the questions: “What is your sex?” and “In what grade are you?”. Race/ethnicity was computed from the questions “Are you Hispanic or Latino?” and “What is your race?”, and had four categories: White, Black/African Americans, Hispanic, and Other (American Indian or Native Alaskan, Asian, Native Hawaiian or other Pacific Islander, and multiracial).

Statistical analysis

All analyses were conducted using SAS-callable SUDAAN version 9.3, accounted for the complex sampling design, and used a significant level α = 0.05. Domain analyses were used to perform calculation on the subpopulation of high school students who had sexual intercourse. Less than 10% of data were missing across all variables, except for: HIV testing in the 2011 national survey (24%) and in North Carolina (12% for 2009–2011); and lifetime illegal injection drug use in North Carolina (29% for 2009–2011). Missing data were accounted for by using the “not missing completely at random” option.

Descriptive analyses were conducted at national and state levels for the period 2005–2011. Testing prevalence, risk behavior prevalence and demographic characteristics were calculated among students who ever had sex. Finite population correction was applied for the calculation of state prevalence due to the smaller size of state samples (<5,000).

The association of HIV testing with risk behaviors at the national level for the 2005–2011 period was modeled using logistic regression. First, logistic regression was used to assess the crude association between HIV testing and each risk behavior and demographic. Multivariable logistic regression model was then used to assess the adjusted association between HIV testing and each independent variable, controlling for sex, grade, and race/ethnicity. Effect modification by sex, race/ethnicity, grade level, and year of survey was assessed through backward elimination. The Bonferroni method was used to correct multiple testing (Bland and Altman 1995). Four interaction terms were significant at the level 0.05, with k = α/4, and remained in the final model: Race/ethnicity and Number of sexual partner in life (p-value = 0.004), Sex and Age at first sexual intercourse (p-value = 0.004), Sex and Use of condom at last intercourse (p-value = 0.007), and Grade and Ever forced intercourse (p-value = 0.012). No multicolinearity was found between covariates.

State HIV testing and risk behavior prevalence were compared to national estimates. Significant differences were assessed using t-test controlling for sex, grade, and race/ethnicity. Multiple-testing was accounted for through a statewide significance α = 0.05 (k = α/6).



Acquired immunodeficiency syndrome




Center for disease control and prevention


Confidence interval




Human immunodeficiency virus


Institutional review board




North Carolina


North Dakota


New Jersey


Odds ratio


South Carolina


Youth risk behavior survey.


  1. American College of Obstetricians and Gynecologists (ACOG): Routine human immunodeficiency virus screening. Obstet Gynecol 2008, 112(2 Pt 1):401-403.

    Google Scholar 

  2. Arrington-Sanders R, Ellen J, Trent M: HIV testing in adolescents and young adults receiving STI testing in an urban primary care setting. Sex Transm Dis 2008, 35(7):686-688. 10.1097/OLQ.0b013e31816b1f9b

    Article  Google Scholar 

  3. Balaji AB, Eaton DK, Voetsch AC, Wiegand RE, Miller KS, Doshi SR: Association between HIV-related risk behaviors and HIV testing among high school students in the United States, 2009. Arch Pediatr Adolesc Med 2012, 166(4):331-336. 10.1001/archpediatrics.2011.1131

    Article  Google Scholar 

  4. Bland JM, Altman DG: Multiple significance tests: the Bonferroni method. BMJ 1995, 310(6973):170. 10.1136/bmj.310.6973.170

    Article  Google Scholar 

  5. Branson BM, Handsfield HH, Lampe MA, Janssen RS, Taylor AW, Lyss SB, Clark JE: Revised recommendations for HIV testing of adults, adolescents, and pregnant women in health-care settings. Morb Mortal Wkly Rep 2006, 55: 1-17.

    Google Scholar 

  6. Branson BM, Viall A, Marum E: Expanding HIV testing: back to the future. J Acquir Immune Defic Syndr 2013, 63(Suppl 2):S117-S121.

    Article  Google Scholar 

  7. Brener ND, Kann L, McManus TL, Kinchen S, Sundberg EC, Ross JG: Reliability of the 1999 Youth Risk Behavior Survey Questionnaire. J Adolesc Health 2002, 31: 336-342. 10.1016/S1054-139X(02)00339-7

    Article  Google Scholar 

  8. Cavazos-Rehg PA, Krauss MJ, Spitznagel EL, Schootman M, Bucholz KK, Peipert JF, Sanders-Thompson V, Cottler LB, Bierut LJ: Age of sexual debut among US adolescents. Contraception 2009, 80(2):158-162. 10.1016/j.contraception.2009.02.014

    Article  Google Scholar 

  9. CDC: Monitoring selected national HIV prevention and care objectives by using HIV surveillance data–United States and 6 U.S. dependent areas–2010. HIV Surveillance Supplemental Report 2010, 17(3):Part A.

    Google Scholar 

  10. CDC: Diagnoses of HIV infection in the United States and dependent areas. HIV Surveillance Report 23. 2011. . Accessed 03/13/2014

    Google Scholar 

  11. CDC: Vital signs: HIV infection, testing, and risk behaviors among youths–United States. MMWR Morb Mortal Wkly Rep 2012, 61(47):971-976.

    Google Scholar 

  12. CDC: Adolescent and school health. 2013a. . Accessed 03/13/2014

    Google Scholar 

  13. CDC: Brief on the prevention benefits of HIV treatment. 2013b. . Accessed 03/13/2014

    Google Scholar 

  14. CDC: HIV and the laws. Fast facts. 2013c. . Accessed 02/19/2014

    Google Scholar 

  15. CDC: HIV testing and risk behaviors among gay, bisexual, and other men who have sex with men–United States. MMWR Morb Mortal Wkly Rep 2013d, 62(47):958-962.

    Google Scholar 

  16. Daley AM, Sadler LS, Leventhal JM, Cromwell PF, Reynolds HD: Negative pregnancy tests in urban adolescents: an important and often missed opportunity for clinicians. Pediatr Nurs 2005, 31(2):87-89.

    Google Scholar 

  17. Decker MR, Silverman JG, Raj A: Dating violence and sexually transmitted disease/HIV testing and diagnosis among adolescent females. Pediatrics 2005, 116(2):e272-e276. 10.1542/peds.2005-0194

    Article  Google Scholar 

  18. Decker MR, Seage GR, Hemenway D, Gupta J, Raj A, Silverman JG: Intimate partner violence perpetration, standard and gendered STI/HIV risk behaviour, and STI/HIV diagnosis among a clinic-based sample of men. Sex Transm Infect 2009, 85(7):555-560. 10.1136/sti.2009.036368

    Article  Google Scholar 

  19. Decker MR, Miller E, McCauley HL, Tancredi DJ, Anderson H, Levenson RR, Silverman JG: Recent partner violence and sexual and drug-related STI/HIV risk among adolescent and young adult women attending family planning clinics. Sex Transm Infect 2014, 90(2):145-149. doi:10.1136/sextrans-2013-051288 10.1136/sextrans-2013-051288

    Article  Google Scholar 

  20. Gallagher KM, Sullivan PS, Lansky A, Onorato IM: Behavioral surveillance among people at risk for HIV infection in the U.S.: the National HIV Behavioral Surveillance System. Public Health Rep 2007, 122(Suppl 1):32-38.

    Google Scholar 

  21. Gardner EM, McLees MP, Steiner JF, Del Rio C, Burman WJ: The spectrum of engagement in HIV care and its relevance to test-and-treat strategies for prevention of HIV infection. Clin Infect Dis 2011, 52: 793-800. 10.1093/cid/ciq243

    Article  Google Scholar 

  22. Gurvey JE, Adler N, Ellen JM: Factors associated with self-risk perception for sexually transmitted diseases among adolescents. Sex Transm Dis 2005, 32(12):742-744. 10.1097/01.olq.0000175385.23447.27

    Article  Google Scholar 

  23. Guttmacher Institute: State policies in brief. Sex and HIV education. 2014. Available at: . Accessed 3/13/2014 Available at: . Accessed 3/13/2014

    Google Scholar 

  24. Hyden C, Allegrante JP, Cohall AT: HIV testing sites’ communication about adolescent confidentiality: potential barriers and facilitators to testing. Health Promot Pract 2014, 15(2):173-180. 10.1177/1524839913499347

    Article  Google Scholar 

  25. Irwin CE Jr, Adams SH, Park MJ, Newacheck PW: Preventive care for adolescents: few get visits and fewer get services. Pediatrics 2009, 123(4):e565-e572. doi:10.1542/peds.2008-2601 10.1542/peds.2008-2601

    Article  Google Scholar 

  26. Jain CL, Wyatt CM, Burke R, Sepkowitz K, Begier EM: Knowledge of the Centers for Disease Control and Prevention’s 2006 routine HIV testing recommendations among New York City internal medicine residents. AIDS Patient Care STDS 2009, 23: 167-176. 10.1089/apc.2008.0130

    Article  Google Scholar 

  27. Kellerman SE, Lehman JS, Lansky A, Stevens MR, Hecht FM, Bindman AB, Wortley PM: HIV testing within at-risk populations in the United States and the reasons for seeking or avoiding HIV testing. J Acquir Immune Defic Syndr 2002, 31(2):202-210. 10.1097/00126334-200210010-00011

    Article  Google Scholar 

  28. Kelley CE, Paul SM, Vali FM, Caruso JM, Martin RM, Fleming PL: Toward elimination of perinatal HIV transmission: New Jersey hospital barriers to rapid HIV testing in labor and delivery, 2005. Public Health Rep 2011, 126(1):145-152.

    Google Scholar 

  29. Miller E: Intimate partner violence and health care-seeking patterns among female users of urban adolescent clinics. Matern Child Health J 2010, 14(6):910-917. 10.1007/s10995-009-0520-z

    Article  Google Scholar 

  30. Moore MJ, Barr EM, Johnson TM: Sexual behaviors of middle school students: 2009 Youth Risk Behavior Survey results from 16 locations. J Sch Health 2013, 83: 61-68. 10.1111/j.1746-1561.2012.00748.x

    Article  Google Scholar 

  31. Moyer VA: Screening for HIV: U.S. Preventive Services Task Force recommendation statement. Ann Intern Med 2013, 159(1):51-60.

    Google Scholar 

  32. National Association of State Boards of Education: State school health policy database. 2013. . Accessed 3/13/2014

    Google Scholar 

  33. National Center for Education Statistics: Percentage of high school dropouts among persons 16 through 24 years old (status dropout rate), by sex and race/ethnicity: selected years, 1960 through 2011. 2012. Available at: . Accessed February 19, 2014 Available at: . Accessed February 19, 2014

    Google Scholar 

  34. National HIV/AIDS Clinicians’ Consultation Center: Compendium of state HIV testing laws. 2014. Available at: . Accessed April 15 Available at: . Accessed April 15

    Google Scholar 

  35. Richter DL, Valois RF, McKeown RE, Vincent ML: Correlates of condom use and number of sexual partners among high school adolescents. J Sch Health 1993, 63(2):91-96. 10.1111/j.1746-1561.1993.tb06087.x

    Article  Google Scholar 

  36. Sackett DL: Bias in analytic research. J Chronic Dis 1979, 32(1–2):51-63.

    Article  Google Scholar 

  37. Samet JH, Winter MR, Grant L, Hingson R: Factors associated with HIV testing among sexually active adolescents: a Massachusetts survey. Pediatrics 1997, 100(3 Pt 1):371-377.

    Article  Google Scholar 

  38. Sterne JA, May M, Costagliola D, de Wolf F, Phillips AN, Harris R, Funk MJ, Geskus RB, Gill J, Dabis F, Miró JM, Justice AC, Ledergerber B, Fätkenheuer G, Hogg RS, Monforte AD, Saag M, Smith C, Staszewski S, Egger M, Cole SR: Timing of initiation of antiretroviral therapy in AIDS-free HIV-1-infected patients: a collaborative analysis of 18 HIV cohort studies. Lancet 2009, 373(9672):1352-1363.

    Article  Google Scholar 

  39. Swenson RR, Hadley WS, Houck CD, Dance SK, Brown LK: Who accepts a rapid HIV antibody test? The role of race/ethnicity and HIV risk behavior among community adolescents. J Adolesc Health 2011, 48(5):527-529. 10.1016/j.jadohealth.2010.08.013

    Article  Google Scholar 

  40. Talib HJ, Silver EJ, Coupey SM, Bauman LJ: The influence of individual, partner, and relationship factors on HIV testing in adolescents. AIDS Patient Care STDS 2013, 27(11):637-645. 10.1089/apc.2013.0218

    Article  Google Scholar 

  41. The White House: Executive order–the HIV care continuum initiative. Accelerating improvements in HIV prevention and care in the United States through the HIV care continuum initiative. 2013. . Accessed 3/13/2014

    Google Scholar 

  42. Tran NT, Hallerdin JM, Flowers-Maple C, Moskosky SB: Collaboration for the integration of HIV prevention at Title X family planning service delivery sites. Public Health Rep 2010, 125(Suppl 1):47-54.

    Google Scholar 

  43. Williams-Roberts H, Chang Y, Losina E, Freedberg KA, Walensky RP: Frequent HIV testing among participants of a routine HIV testing program. Virulence 2010, 1(2):68-71. 10.4161/viru.1.2.10570

    Article  Google Scholar 

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Correspondence to Karen Coeytaux.

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Competing interests

The authors declare that they have no competing interests.

Authors’ contributions

KC had full access to all the data in the study. She participated in conceiving and designing the study, performed the statistical analyses, contributed to data interpretation, and drafted the manuscript. MRK participated in conceiving and designing the study, contributed to statistical analyses and data interpretation, and helped draft the manuscript. PSS participated in conceiving and designing the study, contributed to data interpretation, and helped draft the manuscript. All authors read and approved the final manuscript.

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Coeytaux, K., Kramer, M.R. & Sullivan, P.S. HIV testing among United States high school students at the state and national level, Youth Risk Behavior Survey 2005–2011. SpringerPlus 3, 202 (2014).

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  • HIV testing
  • Adolescent
  • High school
  • Risk behavior
  • YRBS