Abstract
Many adolescents living with or without HIV are sexually active and in need of continuous free access to a variety of contraceptive methods. Dual contraception, condom use together with reversible effective contraception (hormonal contraception [HC] or intrauterine device), seems to be the most effective option for female adolescents for protection from unintended pregnancy and sexually transmitted infections. When counselling on specific contraceptive choice, healthcare providers should be aware about possible interactions of some types of HC with the immune system, with possible changes in infectivity, as well as about drug interactions between mainly efavirenz and some types of progestins. Adding HC to HIV-positive status and antiretroviral therapy could have additive effects on metabolism. At the same time, the possible disadvantages of using HC in women living with HIV should be balanced against the advantages of very reliable methods of preventing unintended pregnancies. To reach and deliver a contraceptive service to more young women, it has proven effective to organise adolescent-friendly clinics and/or integrate them with HIV services. Diverse approaches, including community-based contraceptive service provision and the use of modern technologies, can complement the effort of providing contraceptive services to this target group of female adolescents living with HIV or at risk of HIV.
Keywords: adolescents, HIV, contraceptive choice, contraceptive programmes
Introduction
This review gives an update on the challenges over the last 5 years related to contraceptive use by female adolescents who are living with, or at risk for, HIV and aged between 12 and 24 years of age. About one-third of perinatally HIV-infected children worldwide have reached adolescence [1,2] and half of them are female [1]. Additionally, about one-third of all new infections in sub-Saharan Africa, the region with the highest HIV prevalence in the world, are in young women 15–24 years of age [3,4]. Antiretroviral therapy (ART) gives young people with HIV a chance to live, grow up and enjoy life, including sex. Behaviourally infected, and in smaller numbers perinatally infected, HIV-positive adolescents are sexually active [2,5,6]. Many engage in unprotected sex and experience an unintended pregnancy [7–9]. In Thailand for instance, the median age of sexual debut in perinatally HIV-infected adolescents is 15 years, and about 20% of these sexually active female adolescents became pregnant [2]. Up to 80% of pregnancies in HIV-positive adolescents are reported as unintended [10].
Effective contraception (EC) can reduce the number of unintended pregnancies, and thus improve the quality of life of young women, socially and physically. Pregnancy in HIV-positive women is in general safe; however, adolescent pregnancy is usually viewed as more risky. Additionally, perinatally HIV-infected adolescents seem to be exposed to a higher risk of disease progression and death postpartum in comparison to those who are behaviourally infected [11] as a result of the complex inter-relation of reproductive health, adherence and mental health issues [8]. EC can also reduce vertical transmission of HIV from mother to child, by reducing the number of pregnancies. It might also reduce horizontal transmission as well, as HIV-negative pregnant women might have increased risk for HIV acquisition, while HIV-positive women may have increased infectivity [12].
Delaying the start of sexual life and using dual contraception thereafter, condom use together with reversible EC, seems to be the most effective option for female adolescents for protection from unintended pregnancy and sexually transmitted infections (STI) [13]. Here, we focus on two areas of challenge related to the use of EC. The first area is related to the best choice of reversible EC for female adolescents living with or at risk of HIV; the second to the most effective ways to deliver EC to this target group.
Challenges related to the choice of reversible EC
The use of EC, has been widely promoted in HIV-positive women in the last few years [14,15]. Adolescents, due to their young age, can only be offered reversible methods of EC. The choice of reversible EC methods is limited to hormonal contraception (HC) or intrauterine device (IUD), which could be hormonal or non-hormonal, such as the copper IUD. HC can be progestin-only or combined progestin and oestrogen, and the hormones can be delivered in various ways to the body, including pills, injection, rings, patches and implants. Depending on the frequency with which reversible EC has to be re-administered, it is divided into short-acting (most HC) and long-acting reversible contraception (LARC), including the hormonal implant and the IUD, with re-administration every 3–10 years. Being independent of adherence issues, LARC is currently recommended as first-line contraception, especially for adolescents [16].
Hormonal contraception in adolescents living with HIV
The World Health Organization (WHO) states that there are no restrictions on the use of any hormonal contraceptive method for women living with HIV or at high risk of HIV [15]. Nevertheless, there are issues to be considered when offering HC to adolescents living with HIV, or at risk for HIV infection, related to disease progression and infectivity, pharmacokinetic (PK) interactions, as well as further metabolic changes.
Infectivity and disease progression with HC
The question of HC affecting immunity and thus influencing HIV infectivity and disease progression has been broadly discussed. A number of studies have looked at the topic, suggesting that the use of progestin-only HC, especially depot medroxyprogesterone acetate (DMPA) injection, can lead to increased genital viral shedding in HIV-positive women, and therefore increased infectivity [17–19], as well as to an increased risk of HIV acquisition, especially in young women below 24 years of age [20–22]. Pregnancy, a naturally high-progesterone state, has also been associated with an increased risk of HIV acquisition for HIV-negative women and increased infectivity of HIV-positive women [12,20]. Oestrogens and progesterone/progestins have an effect on the structure of the vaginal epithelial wall and microbiome, and they influence the immune system [23]. Progesterone can have a suppressive effect whereas oestrogens can have the reverse. The exact mechanisms are not clearly understood; however, some underlying reasons are starting to be found. A recent study found an association between DMPA use and higher pro-inflammatory and lower anti-inflammatory protein levels [20]. The genital tract microenvironment can also impact the effects of HC on cervical immunity [20,24]. HIV-uninfected women who used progestin-only contraceptives had an increase in the frequencies of cervical CCR5+CD4+ T cells that are targets for HIV [25]. Some authors have raised the question of whether there should be complete withdrawal of DMPA [19], or rather accept the more moderate approach of the WHO, which strongly advises to always use condoms and other preventive measures [15] together with an effective HC method.
If the use of HC can affect the immune system with possible clinical implications in HIV-positive adolescents, it is important to study and gain a good understanding of the underlying causes in order to maintain the balance between effectively preventing unintended pregnancies and causing no harm in relation to HIV, and possibly other diseases.
PK interactions between HC and ART
Sex steroid hormones (ethinyl oestradiol [EE2] and progestins) and some antiretrovirals (ARVs), have common metabolic pathways, mainly via the cytochrome P450 enzyme system (CYP450) [26,27]. As a result of using both at the same time, the levels of either can be reduced with possible compromises in effectiveness, or increased with possible enhanced toxicities. In addition, the activity of drug-metabolising enzymes in adolescents is influenced by physical and sexual development, with the greatest variability in puberty [28]. However, there are no published studies in adolescents, and potential effects are extrapolated from data gained in adult women.
Currently used ARVs that interact with sex steroid hormones leading to significant changes in drug concentrations include non-nucleoside reverse transcriptase inhibitors (NNRTIs) such as nevirapine and efavirenz, as well as protease inhibitors (PIs) such as lopinavir, atazanavir, darunavir and ritonavir (Table 1). Other ARVs such as nucleoside/nucleotide analogue reverse transcriptase inhibitors (NRTIs) a common backbone of combined ART, the newer NNRTIs etravirine and rilpivirine [29,30], maraviroc (a CCR5 receptor agonist) [31], and integrase inhibitors [32] do not seem to have clinically significant interactions, despite their metabolic pathways. There are no data yet on the outcome of interactions between cobicistat, a CYP450 inhibitor used as a booster for integrase inhibitors, and sex steroid hormones.
Table 1.
Antiretrovirals/booster molecules entering into drug–drug interactions with sex steroid hormones, leading to significant changes in hormonal levels and having an impact on contraceptive and antiretroviral efficacy.
ARV | Ethinyl oestradiol changes | Progestin changes | Contraceptive efficacy | ARV efficacy |
---|---|---|---|---|
Non-nucleoside reverse transcriptase inhibitors | ||||
Nevirapine | ↓ | Insignificant ↓ | Not decreased | Not decreased |
Efavirenz | ↓ | Significant ↓ | Decreased | Decreased |
Protease inhibitors | ||||
Lopinavir | ↓ | Insignificant–significant ↑ | Not decreased | Not decreased |
Atazanavir | ↑/↓ | Significant ↑ | Not decreased | No data |
Darunavir | ↓ | Insignificant ↓ | Not decreased | No data |
Integrase inhibitor booster | ||||
Cobicistat | No sufficient data | No sufficient data | No sufficient data | No data |
A number of PK studies, as well as several case reports and observational studies, have explored the topic, trying to understand its clinical significance.
PK interactions between nevirapine, efavirenz and sex steroid hormones
Nevirapine-based ART does not seem to reduce the effectiveness of HC [33–35] in observational and PK studies, in spite of significant changes in hormonal levels [33,36]. As a result of the PK interaction, ethinyl oestradiol (EE2) levels in the combined hormonal pills used dropped significantly; however, the progestin levels (the main suppressor of ovulation) fell insignificantly [37]. Serum progesterone, a marker for ovulation, also remained consistent with anovulation. Nevirapine levels were not affected [34].
In contrast to nevirapine, efavirenz-based ART seems to reduce the effectiveness of HC, regardless of the method of hormone delivery – combined contraceptive pill, ‘emergency’ pill or implant – due to significant reduction in progestin concentrations [33,34,38,39]. Furthermore, these findings are supported by case reports of contraceptive failure of the hormonal implant, Implanon, in HIV-positive women on efavirenz-based therapy [40,41]. Efavirenz effectiveness might also have been compromised, as efavirenz levels were below the targeted therapeutic threshold in approximately 20% of the participants [34]. Some recent large cohort studies have looked at HC use, or more specifically use of the hormonal implant, from a different perspective, in women on efavirenz-based therapy [35,42]. They reported that due to the high contraceptive efficacy of the hormonal implant as a LARC, there is still a lower real-life pregnancy rate among women on efavirenz-based therapy and implant in comparison to those using short-acting methods or no method. And this is true in spite of the reduced contraceptive efficacy as a result of the drug–drug interaction. However, we consider the findings of the PK studies with efavirenz to have a higher priority. Whenever possible, for women using efavirenz-based ART, we recommend the use of another LARC method, such as the copper IUD or DMPA injection, the only hormonal contraceptive so far without demonstrated interaction with efavirenz [43]. Alternatively, a switch from efavirenz may be considered, as it seems to be the only ARV that has clinically significant interactions with sex steroid hormones. Additionally, HC might compromise the efficacy of efavirenz [34].
PK interactions between PIs and sex steroid hormones
PIs, including the most commonly used today, lopinavir/ritonavir [44,45], atazanavir/ritonavir [46–48] and darunavir/ritonavir [49], have PK interactions with sex steroid hormones and, as a result, hormone levels change significantly. Oestrogen levels increase or decrease although progestin levels (delivered through combined contraceptive pills, patch or implant) increase significantly, often by up to 100%. As discussed, progestin is the hormone contributing mainly to the contraceptive effect of HC [37]. Whenever tested, serum progesterone level, a marker for ovulation, also remained low, consistent with suppressed ovulation. PI levels do not seem to be affected significantly as a result of the PK interaction. Therefore, the studies conclude that the contraceptive effect does not seem to be decreased when administering HC with PI-based ART.
We assessed the PK interaction between EE2/desogestrel in combined oral contraceptive (COC) and lopinavir/ritonavir-based ART in female adolescents living with HIV, and we had a comparable outcome [50]. Additionally, we found high variability of hormonal levels, which warrants close monitoring.
PK interactions between DMPA and ARVs
In contrast to the concerns of DMPA use in relation to HIV infectivity, DMPA does not seem to have clinically significant interactions with any of the studied ARVs, including nevirapine, efavirenz [43] and in recently published results for lopinavir/ritonavir [51].
The simultaneous use of condoms, together with the EC, should always be promoted, regardless of PK interactions, for prevention of STIs.
Metabolic changes with HC and ART
The use of HC in the general population has been associated to different degree of unfavourable changes in carbohydrate metabolism [52–55], lipid profile [55–57], bone turnover markers reflecting bone health [58,59], and marker of inflammation and coagulation [53,54]. These metabolic markers can already be affected by HIV infection alone and/or antiretroviral therapy, or may affect the course of HIV infection. Not much is known about the cumulative effect of HIV, ART and HC on metabolism and inflammation. We found two papers on these issues: the first was an older study from Womack et al. comparing carbohydrate and lipid changes between women living with and without HIV infection and using HC [60]; in the second one Beksinska et al. point to the importance of looking into bone changes in women living with HIV and using progestin-only contraception [61]. In a recently completed assessment in female adolescents living with HIV on ART and using HC, we have confirmed the high prevalence of metabolic changes in this target group and, additionally, found further deterioration with HC in some of metabolic markers (unpublished data). There is an urgent need for additional research in this field, especially because of the tendency to start prescription of HC very early in a woman's life, and promoting its use during the reproductive age [52,53].
Copper IUD in adolescents living with HIV
In a recent study offering and assessing the uptake and continuation of use of EC by sexually active female adolescents in several locations in Thailand, we found a significant increase in the EC users from 29% at screening visit (prior to study entry) to 74% at week 48 [62]. No participant chose an IUD. The IUD is the most effective LARC method; it is inexpensive, with no or minimal primary systemic side effects, in contrast to HC. It is safe for use in HIV-positive women, as well as in nulliparous and women below 20 years of age [63]. Studies from Africa found that the insertion of an IUD did not significantly alter the prevalence of cervical shedding of HIV-1-infected cells [64], and that IUDs in HIV-positive women did not significantly increase the incidence of pelvic inflammatory disease, in comparison to women who chose to use hormonal contraception [65]. In women who used either the evonorgestrel IUD or the copper T380A IUD, the frequencies of CCR5+CD4+ T cells in the endometrium and cervix were diminished, suggesting that susceptibility to HIV infection would not be increased with IUD [66]. However, some healthcare providers are unnecessarily hesitant in using IUDs in young women [67]. Earlier reports showed higher incidence of adverse events such as dysmenorrhoea, expulsion and impaired restoration of fertility with prolonged use of IUDs in nulliparous and young women [68,69]. More recent studies have found that an IUD is a safe and effective long-term contraceptive method for the above-discussed population [67,70]. The continuation of use is also good – adolescents were six to 12 times more likely to have discontinued any short-acting contraceptive method in comparison to an IUD 6 months after initiation [71]. The main challenges related to IUD use in adolescents (and adult women), are related to acceptance of the method by healthcare providers and by users. Secondly, in contrast to HC, which is relatively easy to administer in any setting, IUD administration needs a clean and private setting with sterile instruments, in addition to a trained healthcare provider.
Challenges related to the strategies of delivery EC
In Thailand, about 80% of Thai women use modern contraception, among whom less than 1% chose a copper IUD [72], and in a cohort of HIV-positive Thai women, no one was using an IUD [73]. However, when the copper IUD was offered to women living with HIV free of charge at the HIV clinic, 44% of eligible women started using the method and more than 90% continued using it after the 6-month follow up visit [74].
Provision of knowledge on the advantages and disadvantages of the method by a trained and motivated healthcare provider, and access to the method in a setting linked with the HIV service delivery, seemed to be important factors that helped women to decide on IUD uptake [74]. Providing knowledge, not only to potential users but also to healthcare providers [75] and partners [76], might be beneficial for increasing IUD use. This approach can be applied to all other contraceptive methods as well. Linking reproductive health services with HIV care is considered to be effective, with no negative outcomes [77]. Although many international agencies, such as WHO and UNAIDS, have advocated for strong links between the two services, this is still rarely the case in practice in resource-limited settings [77]. Some even integrate family planning services for HIV-positive women with basic general gynaecological services [78,79]. These studies conclude that all aspects of sexual and reproductive healthcare in such centres had improved since the introduction of this integrated approach.
Similarly, health facilities should provide services for adolescent females in a youth-friendly manner and integrate HIV and contraceptive services [76]. WHO also recommends dedicated and integrated youth-friendly programmes, and in coordination with the specific health system context [80]. More specifically, in their ‘5S’ approach they discuss the importance of supportive polices, strategic information, service delivery models that are youth friendly, sustainable resources and a cross-sectoral approach. It is important to build on what already exists – modifying existing facilities and building the competencies and attitudes of existing health service providers [80]. In a recently completed project with sexually active female adolescents living with HIV in five health centres in Thailand, we provided safe sex education on EC methods and dual contraception through an adolescent-friendly educational movie, health brochures and individual counselling [62]. Individual counselling was the most appreciated method for delivering health messages compared to the educational movie and the brochures. We further offered and assessed the uptake and continuation of use of reversible EC, including COC pills, DMPA injection, hormonal implant and IUD. All activities were carried out at the HIV clinic of the paediatric department. There was a significant increase in the EC use from screening through to the last visit at 48 weeks, from 29% to 74%. However, fewer than one-third of the participants chose a LARC method by the end of the study. No one chose an IUD.
The uptake of contraceptives can be additionally improved by building community support for providing health education and contraception to adolescents outside the formal settings [81,82], through various outlets and well-trained social/healthcare workers. A Cochrane database review demonstrated that community-based interventions can improve the uptake even of copper IUD contraception [83]. Furthermore, adolescent-friendly clinics only are unlikely to attract all adolescents [81]. Outreach to adolescents in venues where they socialise can improve their access to contraceptive information and services – on the spot or through referral [84]. Use of modern technologies and social media could be additional ways of increasing contraceptive use among adolescents [81]. The authors emphasise the importance of further research in this area, particularly designing and testing programmes on how most effectively to deliver the service, especially to the most vulnerable individuals, as well as gaining the support of the community [81]. Additionally, a cost–benefit analysis may be required to ensure the applicability and continuity of such programmes [83].
Conclusions
Many adolescents living with or without HIV are sexually active and in need of continuous free access to a variety of contraceptive methods. Dual contraception, condom use together with reversible EC, seems to be the most effective option for female adolescents for protection against unintended pregnancy and sexually transmitted infections. When counselling on specific contraceptive choice, healthcare providers should be aware about possible interaction of some types of HC with the immune system, with possible changes in infectivity, as well as about drug interactions between mainly efavirenz and some types of progestins. Adding HC to HIV-positive status and ART could have additive effects on metabolism. At the same time, the possible disadvantages of using HC in women living with HIV should be balanced against the advantages of very reliable methods of preventing unintended pregnancies. To reach and deliver contraceptive services to more young women, it proves effective to organise adolescent-friendly clinics and/or integrate with HIV services. Diverse approaches, including community-based contraceptive service provision and the use of modern technologies, can complement the effort of providing contraceptive services to this target group of female adolescents living with or at risk from HIV.
Acknowledgements
Conflict of interest
The authors state that there are no conflicts of interest.
References
- 1. Chokephaibulkit K, Kariminia A, Oberdorfer P et al. Characterizing HIV manifestations and treatment outcomes of perinatally infected adolescents in Asia. Pediatr Infect Dis J 2014; 33: 291– 294. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2. Lolekha R, Boon-Yasidhi V, Leowsrisook P et al. Knowledge, attitudes, and practices regarding antiretroviral management, reproductive health, sexually transmitted infections, and sexual risk behavior among perinatally HIV-infected youth in Thailand. AIDS Care 2015; 27: 618– 628. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3. UNAIDS Report on the global AIDS epidemic, 2013. 2013. Available at: http://www.unaids.org/sites/default/files/en/media/unaids/contentassets/documents/epidemiology/2013/gr2013/UNAIDS_Global_Report_2013_en.pdf ( accessed February 2016).
- 4. Dellar RC, Dlamini S, Karim QA. Adolescent girls and young women: key populations for HIV epidemic control. J Int AIDS Soc 2015; 18: 19408. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5. Setse RW, Siberry GK, Gravitt PE et al. Correlates of sexual activity and sexually transmitted infections among human immunodeficiency virus-infected youth in the LEGACY cohort, United States, 2006. Pediatr Infect Dis J 2011; 30: 967– 973. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6. Tassiopoulos K, Moscicki AB, Mellins C et al. Sexual risk behavior among youth with perinatal HIV infection in the United States: predictors and implications for intervention development. Clin Infect Dis 2013; 56: 283– 290. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7. Kancheva Landolt NT, Lakhonphon S, Ananworanich J. Contraception in HIV-positive female adolescents. AIDS Res Ther 2011; 8: 19. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8. Koenig LJ, Nesheim S, Abramowitz S. Adolescents with perinatally acquired HIV: emerging behavioral and health needs for long-term survivors. Curr Opin Obstet Gynecol 2011; 23: 321– 327. [DOI] [PubMed] [Google Scholar]
- 9. Koenig LJ, Pals SL, Chandwani S et al. Sexual transmission risk behavior of adolescents With HIV acquired perinatally or through risky behaviors. J Acquir Immune Defic Syndr 2010; 55: 380– 390. [DOI] [PubMed] [Google Scholar]
- 10. Kenny J, Williams B, Prime K et al. Pregnancy outcomes in adolescents in the UK and Ireland growing up with HIV. HIV Med 2012; 13: 304– 308. [DOI] [PubMed] [Google Scholar]
- 11. Munjal I, Dobroszycki J, Fakioglu E et al. Impact of HIV-1 infection and pregnancy on maternal health: comparison between perinatally and behaviorally infected young women. Adolesc Health Med Ther 2013; 4: 51– 58. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12. Mugo NR, Heffron R, Donnell D et al. Increased risk of HIV-1 transmission in pregnancy: a prospective study among African HIV-1-serodiscordant couples. Aids 2011; 25: 1887– 1895. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13. Potter J, Santelli JS. Adolescent contraception: review and guidance for pediatric clinicians. Minerva Pediatr 2015; 67: 33– 45. [PubMed] [Google Scholar]
- 14. Centers for Disease Control Update to CDC's U.S. Medical Eligibility Criteria for Contraceptive Use, 2010: revised recommendations for the use of hormonal contraception among women at high risk for HIV infection or infected with HIV. MMWR Morb Mortal Wkly Rep 2012; 61: 449– 452. [PubMed] [Google Scholar]
- 15. World Health Organization Hormonal contraception and HIV. Technical statement 2012. 2012. Available at: http://www.who.int/reproductivehealth/publications/family_planning/rhr_12_8/en/ ( accessed February 2016). [PubMed]
- 16. Secura GM, Allsworth JE, Madden T et al. The Contraceptive CHOICE Project: reducing barriers to long-acting reversible contraception. Am J Obstet Gynecol 2010; 203: 115.e111– 117. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 17. Byrne EH, Anahtar MN, Cohen KE et al. Association between injectable progestin-only contraceptives and HIV acquisition and HIV target cell frequency in the female genital tract in South African women: a prospective cohort study. Lancet Infect Dis 2015. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18. Heffron R, Donnell D, Rees H et al. Use of hormonal contraceptives and risk of HIV-1 transmission: a prospective cohort study. Lancet Infect Dis 2012; 12: 19– 26. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19. Ralph LJ, McCoy SI, Shiu K, Padian NS. Hormonal contraceptive use and women's risk of HIV acquisition: a meta-analysis of observational studies. Lancet Infect Dis 2015; 15: 181– 189. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20. Morrison C, Fichorova RN, Mauck C et al. Cervical inflammation and immunity associated with hormonal contraception, pregnancy, and HIV-1 seroconversion. J Acquir Immune Defic Syndr 2014; 66: 109– 117. [DOI] [PubMed] [Google Scholar]
- 21. Morrison CS, Chen PL, Kwok C et al. Hormonal contraception and the risk of HIV acquisition: an individual participant data meta-analysis. PLoS Med 2015; 12: e1001778. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22. Morrison CS, Chen PL, Kwok C et al. Hormonal contraception and HIV acquisition: reanalysis using marginal structural modeling. Aids 2010; 24: 1778– 1781. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23. Hel Z, Stringer E, Mestecky J. Sex steroid hormones, hormonal contraception, and the immunobiology of human immunodeficiency virus-1 infection. Endocr Rev 2010; 31: 79– 97. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24. Fichorova RN, Chen PL, Morrison CS et al. The Contribution of Cervicovaginal Infections to the Immunomodulatory Effects of Hormonal Contraception. MBio 2015; 6: e00221– 00215. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25. Sciaranghella G, Wang C, Hu H et al. CCR5 Expression Levels in HIV-Uninfected Women Receiving Hormonal Contraception. J Infect Dis 2015; 212: 1397– 1401. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 26. Korhonen T, Tolonen A, Uusitalo J et al. The role of CYP2C and CYP3A in the disposition of 3-keto-desogestrel after administration of desogestrel. Br J Clin Pharmacol 2005; 60: 69– 75. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27. Wang B, Sanchez RI, Franklin RB et al. The involvement of CYP3A4 and CYP2C9 in the metabolism of 17 alpha-ethinylestradiol. Drug Metab Dispos 2004; 32: 1209– 1212. [DOI] [PubMed] [Google Scholar]
- 28. Kennedy M. Hormonal regulation of hepatic drug-metabolizing enzyme activity during adolescence. Clin Pharmacol Ther 2008; 84: 662– 673. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 29. Scholler-Gyure M, Kakuda TN, Woodfall B et al. Effect of steady-state etravirine on the pharmacokinetics and pharmacodynamics of ethinylestradiol and norethindrone. Contraception 2009; 80: 44– 52. [DOI] [PubMed] [Google Scholar]
- 30. Crauwels H, Heeswijk R, Cornelis L et al. Pharmacokinetic interaction study between TMC278, an NNRTI, and the contraceptives norethindrone plus ethinylestradiol. 12th European AIDS Conferenc. Cologne, Germany.
- 31. Abel S, Russell D, Whitlock LA et al. Effect of maraviroc on the pharmacokinetics of midazolam, lamivudine/zidovudine, and ethinyloestradiol/levonorgestrel in healthy volunteers. Br J Clin Pharmacol 2008; 65 Suppl 1: 19– 26. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32. Song IH, Borland J, Chen S et al. Dolutegravir Has No Effect on the Pharmacokinetics of Oral Contraceptives With Norgestimate and Ethinyl Estradiol. Ann Pharmacother 2015; 49: 784– 789. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 33. Landolt NK, Phanuphak N, Ubolyam S et al. Significant decrease of ethinylestradiol with nevirapine, and of etonogestrel with efavirenz in HIV-positive women. J Acquir Immune Defic Syndr 2014; 66: e50– 52. [DOI] [PubMed] [Google Scholar]
- 34. Landolt NK, Phanuphak N, Ubolyam S et al. Efavirenz, in contrast to nevirapine, is associated with unfavorable progesterone and antiretroviral levels when coadministered with combined oral contraceptives. J Acquir Immune Defic Syndr 2013; 62: 534– 539. [DOI] [PubMed] [Google Scholar]
- 35. Patel RC, Onono M, Gandhi M et al. Pregnancy rates in HIV-positive women using contraceptives and efavirenz-based or nevirapine-based antiretroviral therapy in Kenya: a retrospective cohort study. Lancet HIV 2015; 2: e474– 482. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 36. Mildvan D, Yarrish R, Marshak A et al. Pharmacokinetic interaction between nevirapine and ethinyl estradiol/norethindrone when administered concurrently to HIV-infected women. J Acquir Immune Defic Syndr 2002; 29: 471– 477. [DOI] [PubMed] [Google Scholar]
- 37. Wright KP, Johnson JV. Evaluation of extended and continuous use oral contraceptives. Ther Clin Risk Manag 2008; 4: 905– 911. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 38. Carten ML, Kiser JJ, Kwara A et al. Pharmacokinetic interactions between the hormonal emergency contraception, levonorgestrel (Plan B), and Efavirenz. Infect Dis Obstet Gynecol 2012; 2012: 137192. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 39. Sevinsky H, Eley T, Persson A et al. The effect of efavirenz on the pharmacokinetics of an oral contraceptive containing ethinyl estradiol and norgestimate in healthy HIV-negative women. Antivir Ther 2011; 16: 149– 156. [DOI] [PubMed] [Google Scholar]
- 40. Leticee N, Viard JP, Yamgnane A et al. Contraceptive failure of etonogestrel implant in patients treated with antiretrovirals including efavirenz. Contraception 2012; 85: 425– 427. [DOI] [PubMed] [Google Scholar]
- 41. Matiluko AA, Soundararjan L, Hogston P. Early contraceptive failure of Implanon in an HIV-seropositive patient on triple antiretroviral therapy with zidovudine, lamivudine and efavirenz. J Fam Plann Reprod Health Care 2007; 33: 277– 278. [DOI] [PubMed] [Google Scholar]
- 42. Pyra M, Heffron R, Mugo NR et al. Effectiveness of hormonal contraception in HIV-infected women using antiretroviral therapy. Aids 2015; 29: 2353– 2359. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 43. Cohn SE, Park JG, Watts DH et al. Depo-medroxyprogesterone in women on antiretroviral therapy: effective contraception and lack of clinically significant interactions. Clin Pharmacol Ther 2007; 81: 222– 227. [DOI] [PubMed] [Google Scholar]
- 44. Vieira CS, Bahamondes MV, Souza RM et al. Effect of antiretroviral therapy including lopinavir/ritonavir or efavirenz on etonogestrel-releasing implant pharmacokinetics in HIV-positive women. J Acquir Immune Defic Syndr 2014; 66: 378– 385. [DOI] [PubMed] [Google Scholar]
- 45. Vogler MA, Patterson K, Kamemoto L et al. Contraceptive efficacy of oral and transdermal hormones when co-administered with protease inhibitors in HIV-1-infected women: pharmacokinetic results of ACTG trial A5188. J Acquir Immune Defic Syndr 2010; 55: 473– 482. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 46. DuBois BN, Atrio J, Stanczyk FZ, Cherala G. Increased exposure of norethindrone in HIV+ women treated with ritonavir-boosted atazanavir therapy. Contraception 2015; 91: 71– 75. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 47. Zhang J, Chung E, Yones C et al. The effect of atazanavir/ritonavir on the pharmacokinetics of an oral contraceptive containing ethinyl estradiol and norgestimate in healthy women. Antivir Ther 2011; 16: 157– 164. [DOI] [PubMed] [Google Scholar]
- 48. Tackett D, Child M, Agarwala S et al. Atazanavir: a summary of two pharmacokinetic drug interaction studies in healthy subjects. Conference on Retroviruses and Opportunistic Infections. Boston, MA, USA. Abstract: 543.
- 49. Sekar VJ, Lefebvre E, Guzman SS et al. Pharmacokinetic interaction between ethinyl estradiol, norethindrone and darunavir with low-dose ritonavir in healthy women. Antivir Ther 2008; 13: 563– 569. [PubMed] [Google Scholar]
- 50. Kancheva Landolt N, Bunupuradah T, Kosalaraksa P et al. High variability of hormonal levels and no clinically relevant interaction between ethinyl estradiol, desogestrel and lopinavir/ritonavir in a small sample of HIV-positive adolescents. J Acquir Immune Defic 2016; in press. [DOI] [PubMed] [Google Scholar]
- 51. Luque AE, Cohn SE, Park JG et al. Depot medroxyprogesterone acetate in combination with a twice-daily lopinavir-ritonavir-based regimen in HIV-infected women showed effective contraception and a lack of clinically significant interactions, with good safety and tolerability: results of the ACTG 5283 study. Antimicrob Agents Chemother 2015; 59: 2094– 2101. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 52. Cortes ME, Alfaro AA. The effects of hormonal contraceptives on glycemic regulation. Linacre Q 2014; 81: 209– 218. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 53. Morin-Papunen L, Martikainen H, McCarthy MI et al. Comparison of metabolic and inflammatory outcomes in women who used oral contraceptives and the levonorgestrel-releasing intrauterine device in a general population. Am J Obstet Gynecol 2008; 199: 529.e521– 529.e510. [DOI] [PubMed] [Google Scholar]
- 54. Piltonen T, Puurunen J, Hedberg P et al. Oral, transdermal and vaginal combined contraceptives induce an increase in markers of chronic inflammation and impair insulin sensitivity in young healthy normal-weight women: a randomized study. Hum Reprod 2012; 27: 3046– 3056. [DOI] [PubMed] [Google Scholar]
- 55. Sheu WH, Hsu CH, Chen YS et al. Prospective evaluation of insulin resistance and lipid metabolism in women receiving oral contraceptives. Clin Endocrinol (Oxf) 1994; 40: 249– 255. [DOI] [PubMed] [Google Scholar]
- 56. Fotherby K. Oral contraceptives and lipids. BMJ 1989; 298: 1049– 1050. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 57. Krauss RM, Burkman RT Jr.. The metabolic impact of oral contraceptives. Am J Obstet Gynecol 1992; 167: 1177– 1184. [DOI] [PubMed] [Google Scholar]
- 58. Beksinska ME, Kleinschmidt I, Smit JA et al. Bone mineral density in young women aged 19–24 after 4–5 years of exclusive and mixed use of hormonal contraception. Contraception 2009; 80: 128– 132. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 59. Cromer BA, Scholes D, Berenson A et al. Depot medroxyprogesterone acetate and bone mineral density in adolescents–the Black Box Warning: a Position Paper of the Society for Adolescent Medicine. J Adolesc Health 2006; 39: 296– 301. [DOI] [PubMed] [Google Scholar]
- 60. Womack JA, Scherzer R, Cole SR et al. Hormonal contraception and metabolic outcomes in women with or at risk for HIV infection. J Acquir Immune Defic Syndr 2009; 52: 581– 587. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 61. Beksinska ME, Smit JA, Ramkissoon A. Progestogen-only injectable hormonal contraceptive use should be considered in analysis of studies addressing the loss of bone mineral density in HIV-positive women. J Acquir Immune Defic Syndr 2010; 54: e5. [DOI] [PubMed] [Google Scholar]
- 62. Kancheva Landolt N, Achalapong J, Kosalaraksa P et al. Strategies to improve the uptake of effective contraception in HIV-positive adolescents. 6th HIV and Women Workshop. February 2016. Boston, MA, USA. Abstract 08.
- 63. World Health Organization Medical eligibility criteria for contraceptive use. 5th edn. 2015. Available at: http://www.who.int/reproductivehealth/publications/family_planning/MEC-5/en/ ( accessed February 2016). [PubMed]
- 64. Richardson BA, Morrison CS, Sekadde-Kigondu C et al. Effect of intrauterine device use on cervical shedding of HIV-1 DNA. Aids 1999; 13: 2091– 2097. [DOI] [PubMed] [Google Scholar]
- 65. Stringer EM, Kaseba C, Levy J et al. A randomized trial of the intrauterine contraceptive device vs hormonal contraception in women who are infected with the human immunodeficiency virus. Am J Obstet Gynecol 2007; 197: 144.e141– 148. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 66. Achilles SL, Creinin MD, Stoner KA et al. Changes in genital tract immune cell populations after initiation of intrauterine contraception. Am J Obstet Gynecol 2014; 211: 489.e481– 489. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 67. Abraham M, Zhao Q, Peipert JF. Young Age, Nulliparity, and Continuation of Long-Acting Reversible Contraceptive Methods. Obstet Gynecol 2015; 126: 823– 829. [DOI] [PubMed] [Google Scholar]
- 68. Doll H, Vessey M, Painter R. Return of fertility in nulliparous women after discontinuation of the intrauterine device: comparison with women discontinuing other methods of contraception. Bjog 2001; 108: 304– 314. [DOI] [PubMed] [Google Scholar]
- 69. Zhang J, Feldblum PJ, Chi IC, Farr MG. Risk factors for copper T IUD expulsion: an epidemiologic analysis. Contraception 1992; 46: 427– 433. [DOI] [PubMed] [Google Scholar]
- 70. Gold MA, Johnson LM. Intrauterine devices and adolescents. Curr Opin Obstet Gynecol 2008; 20: 464– 469. [DOI] [PubMed] [Google Scholar]
- 71. Maslyanskaya S, Coupey SM, Chhabra R, Khan UI. Predictors of Early Discontinuation of Effective Contraception by Teens at High Risk of Pregnancy. J Pediatr Adolesc Gynecol 2015. [DOI] [PubMed] [Google Scholar]
- 72. UN data Contraceptive prevalence method. 2014. Available at: http://data.un.org/DocumentData.aspx?q=thailand+contraception&id=356 ( accessed March 2016).
- 73. Landolt NK, Phanuphak N, Pinyakorn S et al. Sexual life, options for contraception and intention for conception in HIV-positive people on successful antiretroviral therapy in Thailand. AIDS Care 2012; 24: 897– 904. [DOI] [PubMed] [Google Scholar]
- 74. Landolt NK, Phanuphak N, Teeratakulpisarn N et al. Uptake and continuous use of copper intrauterine device in a cohort of HIV-positive women. AIDS Care 2013; 25: 710– 714. [DOI] [PubMed] [Google Scholar]
- 75. Stubbs E, Schamp A. The evidence is in. Why are IUDs still out?: family physicians’ perceptions of risk and indications. Can Fam Physician 2008; 54: 560– 566. [PMC free article] [PubMed] [Google Scholar]
- 76. Hagey JM, Akama E, Ayieko J et al. Barriers and facilitators adolescent females living with HIV face in accessing contraceptive services: a qualitative assessment of providers’ perceptions in western Kenya. J Int AIDS Soc 2015; 18: 20123. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 77. Spaulding AB, Brickley DB, Kennedy C et al. Linking family planning with HIV/AIDS interventions: a systematic review of the evidence. Aids 2009; 23 Suppl 1: S79– 88. [DOI] [PubMed] [Google Scholar]
- 78. Samuel MI, Welch J, Tenant-Flowers M et al. Contraception and medical gynaecology for HIV-positive women in a one-stop clinic. Int J STD AIDS 2008; 19: 559– 560. [DOI] [PubMed] [Google Scholar]
- 79. Coyne KM, Hawkins F, Desmond N. Sexual and reproductive health in HIV-positive women: a dedicated clinic improves service. Int J STD AIDS 2007; 18: 420– 421. [DOI] [PubMed] [Google Scholar]
- 80. World Health Organization Adolescent Health: Service delivery models that are youth-friendly. Available at: http://www.euro.who.int/en/health-topics/Life-stages/child-and-adolescent-health/adolescent-health/5s-approach/service-delivery-models-that-are-youth-friendly ( accessed February 2016).
- 81. Chandra-Mouli V, McCarraher DR, Phillips SJ et al. Contraception for adolescents in low and middle income countries: needs, barriers, and access. Reprod Health 2014; 11: 1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 82. Denno DM, Hoopes AJ, Chandra-Mouli V. Effective strategies to provide adolescent sexual and reproductive health services and to increase demand and community support. J Adolesc Health 2015; 56: S22– 41. [DOI] [PubMed] [Google Scholar]
- 83. Arrowsmith ME, Aicken CR, Saxena S, Majeed A. Strategies for improving the acceptability and acceptance of the copper intrauterine device. Cochrane Database Syst Rev 2012; 3: Cd008896. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 84. Denno DM, Chandra-Mouli V, Osman M. Reaching youth with out-of-facility HIV and reproductive health services: a systematic review. J Adolesc Health 2012; 51: 106– 121. [DOI] [PubMed] [Google Scholar]