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Module 14: Clinical & Applied Pharmacology Evidence Guide
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Page 1 Managing sexually transmitted infections: Beyond the 2015 guidelines 1.5 CONTACT HOURS 1.0 CONTACT HOUR Copyright (c) 2018 Wolters Kluwer Health, Inc. All rights reserved. Abstract: Guidelines for the prevention and management of sexually transmitted infections (STIs) are updated periodically while new science is continuously developed. Advanced practice registered nurses implement clinical decisions based on current guidelines and evidence. This article provides recent updates on managing STIs. By Versie Johnson-Mallard, PhD, WHNP, FAANP, FAAN; Kim Curry, PhD, FNP, FAANP; Rasheeta Chandler, PhD, FNP, FAANP; Ivy Alexander, PhD, ANP, FAAN; Elizabeth Kostas-Polston, PhD, WHNP, FAANP, FAAN; Susan Orsega, MSN, FNP, FAAN; and Nancy Fugate Woods, PhD, RN, FAAN D espite efforts to improve access to evidence- based reproductive healthcare services, out comes of sexually transmitted infection (STI) prevention efforts in the United States continue to lag behind other developed countries.1-3 Some progress in STI prevention and treatment services can be attributed to the Patient Protection and Affordable Care Act, which provides coverage for STI services for adolescent and young adult women up to 26 years of age. However, health disparities continue to exist regarding STI preva lence rates. Populations most burdened by STIs include 15- to 19-year-old adolescents, 20- to 24-year-old women, older adults, special populations (such as some transgender individuals), those who are incarcerated, and the homeless.1,2 Recommendations on STI prevention and manage ment are frequently updated by the CDC, United States Preventive Services Task Force (uspstf), and the World Health Organization (WHO).1,2,4,5 STI guidelines are not based on race or ethnicity, but in some cases, they are based on age, gender, culture, and sexual preference.6,7 For example, chlamydia is the most common reportable STI in the United States, whereas the human papilloma virus (HPV) is the most common STI in women.1,2 Varijanta / Thinkstock Keywords: men who have sex with men, MSM, prevention, reproductive health, sexual assault, sexually transmitted infections, STI, transgender 28 The Nurse Practitioner - Vol. 43, No. 8 www.tnpj.com Page 2 Managing sexually transmitted infections: Beyond the 2015 guidelines Respect and compassion are important to elicit accurate and pertinent information during screening and treatment of STIs. Copyright (c) 2018 Wolters Kluwer Health, Inc. All rights reserved. This article provides updates from the current STI prevention and management literature published since the 2015 CDC STI treatment guidelines were issued. Only those infections for which information has been updated since the most recent CDC guidelines are included. Notable updates include: - treatment regimens for Neisseria gonorrhea and geni tal warts - use of nucleic acid amplification (NAAT) test - update of HPV vaccine recommendation and coun seling messages - managing the care of transgender individuals - hepatitis C annual testing in those with HIV infections - retesting to detect repeat infections - recognition and treatment of urethritis/cervicitis caused by Mycoplasma genitalium (M. genitalium). STI prevention Primary prevention. To prevent the onset of STIs, active strategies of technology, behavior counseling, preven tion education, and vaccination should be implement ed before sexual debut.1,2,8,9 Research supports high intensity behavioral counseling and motivational in terviewing to augment information provided in pamphlets, handouts, and videos.10-12 Primary prevention also includes anticipatory guidance for parents of adolescents. Secondary prevention. Screening is an important secondary preven tion strategy and should include the use of age- and gender-appropriate, nonjudgmental strategies.1,13,14 During STI screening and treatment, nonjudgmental acknowledgment of adolescent, youth, and older adult engagement in behaviors that place them at high risk for STIs is a critical component of communication.12-14 Respect and compassion are important to elicit ac curate and pertinent information during screening and treatment of STIs.1,12-14 The uspstf, CDC, and WHO provide screening recommendations for viral and bacterial STIs.1,3-5 The uspstf recommends a combined approach to screen ing, which includes attention to individual's sexual history for behaviors that indicate increased risk.4,5 The CDC and WHO use an approach based on systematic review of the literature for individual disease or infec tion and population (national and global).1,2 The use of clinical prediction rules is an approach that is growing momentum. Clinical prediction rules combine an individualized risk assessment and popula tion approach to STI screening,which is similar to mea sures used to predict and manage several chronic diseases.6,7 Falasinnu and colleagues assessed differences in impact of individual-based and population-based approaches on over 35,000 individuals being screened for gonorrhea and chlamydia.6,7 Results indicated that this method would result in the detection of more cases of STIs while reducing the need for screening. Viral STIs HPV. It is widely accepted that high-risk HPV is a cancer-causing STI.15-17 The oncogenic high-risk geno types 16 and 18 cause most of the cervical, vulvar, vagi nal, anal, penile, and oropharyngeal cancers and cancer precursors.1,16,17 Low-risk genotypes 6 and 11 cause external genital warts, which are mostly benign in na ture; however, these warts tend to cause great emotional distress.1,2,16,17 HIV. The current recommendation for HIV pre vention is preexposure prophylaxis (PrEP).18-20 PrEP is an oral daily fixed-dose combination of two drugs: tenofovir disoproxil fumarate and emtricitabine.1,18,20 The drugs are recommended for use in HIV discordant heterosexual couples and men who have sex with men (MSM).1,20 Randomized placebo-controlled trials have estab lished risk for HIV transmission during sex, and I.V. drug use is substantially lowered for becoming infected with the HIV virus that causes AIDS when PrEP is used.1,20 Comprehensive guidance for use of HIV se roadaptive strategies, such as serosorting (choosing sex partners with similar HIV status) and strategic positioning (avoiding insertive anal sex if HIV posi tive) are behaviors that some MSM practice to prevent transmission.20 Seroadaptive strategies include: - limiting anal sex without a condom to partners with a similar HIV status - using a condom only with HIV serodiscordant partners - HIV-infected partner acting as a receptive partner for anal intercourse.20 www.tnpj.com The Nurse Practitioner - August 2018 29 Page 3 Copyright (c) 2018 Wolters Kluwer Health, Inc. All rights reserved. Managing sexually transmitted infections: Beyond the 2015 guidelines Sexual transmission of Zika virus23,25 Category Risk Transmission - Most commonly from symptomatic men to female partners Period of - May exceed 1 month after onset of symptoms contagiousness Body fl uids affected - Semen, saliva, blood, urine, and vaginal and cervical secretions Presentation of - May be asymptomatic or include mild symptoms such as fever, arthralgia, rashes, headaches infection - Guillain-Barre syndrome is a potential sequela Risk of infection to - Risks include microcephaly and other severe brain defects, miscar riage, ocular or hearing maternal child defects, and others health - Spontaneous miscarriage or stillbirth is possible sequela Prevention - Condom use if either partner has been exposed to Zika virus - Males should use condoms or abstain from sex for 6 months after onset of symptoms - Pregnant women should avoid travel to areas where Zika virus is present - Females should avoid sex for 8 weeks after onset of symptoms to avoid transmission to partners Counseling for seroadaptive strategies include sharing knowledge that home-testing HIV kits detect antibodies, not acute HIV infection. Serosorting and other adaptive behaviors carry greater HIV risk than consistent condom use.19,20 Hepatitis. Sexual transmission rates of hepatitis C are higher among individuals who engage in high-risk sexual practices, group sex, and use of drugs during sex.8,21 Screening for hepatitis C is recommended based on risk and for all individuals born between the years 1945 and 1965.21,22 Annual hepatitis C screening and diagnostic testing with assays is recommended among MSM with HIV.9,21,22 Zika. Infection with the Zika virus can be sexually transmitted.23-25 This mosquito-borne fl avivirus has infected as many as 1.3 million individuals in Brazil alone.24-27 Twenty countries or territories reported local transmission in 2018.25-27 Most Zika virus infections are characterized by subclinical or mild infl uenza-like illness.23-27 However, severe neurologic manifestations have been described, including Guillain-Barre syn drome in adults and microcephaly in babies born to infected mothers.25,27 Screening is not recommended to determine pres ence of the Zika virus.25-27 The prevention strategy for Zika includes avoidance of exposure via mosquito bites or body fluids, especially for pregnant women and men and women of childbearing age (see Sexual transmis sion of Zika virus).23-25 Risks to the unborn fetus include microcephaly, a severe brain defect, among other de fects, such as developmental delay and vision and hear ing problems.23-27 Viral RNA has been detected in breast milk, but transmission via breastfeeding has not been reported.27 Diagnosis remains suboptimal be cause lab tests are not widely available.26 Bacterial STIs Gonorrhea and Chlamydia. Sexually active women under the age of 25 years should be routinely screened for gonorrhea and chlamydia, as prevalence is highest among this age-group.2,6,7,15,28-30 However, current evi dence is insuffi cient to assess the balance of benefi t and harm of routine screening for chlamydia and gonorrhea in sexually active men.1,28 Gonorrhea treat ment and screening have experienced a paradigm shift.29,31-34 Fluoroquinolones are no longer recommended, and dual therapy is routinely recommended, prefer ably under direct observation; in addition, emerging resistance to oral cephalosporins has been document ed.1,28 Treatment for chlamydia has remained stable.11 Men and women in the younger age-group (between 15 and 24 years) are less likely to use condoms than older men and women, increasing the risk of repeated chlamydia and/or gonorrhea infections.6,7,12,15 Syphilis. In 2016, an advisory was issued on ocular syphilis outbreaks in San Francisco and Seattle, pri marily among HIV-positive homosexual men.30 In addition, if these men are diagnosed with syphilis, they should be tested for HIV.1 For rapid diagnostic testing of anti-HIV and anti-Treponema pallidum, a one-test device is on the horizon according to the WHO.13,35,36 Penicillin G benzathine and penicillin G procaine were in short supply in 2016.1 30 The Nurse Practitioner - Vol. 43, No. 8 www.tnpj.com Page 4 Managing sexually transmitted infections: Beyond the 2015 guidelines In 2016, the WHO issued new guidelines for treating chlamydia, gonorrhea, and syphilis based on emerging patterns of antibiotic therapy resistance. Copyright (c) 2018 Wolters Kluwer Health, Inc. All rights reserved. Penicillin G procaine is the recommended treat ment for congenital syphilis and an alternative treatment for neurosyphilis and ocular syphilis.30 Peni cillin G benzathine remains the first-line treatment for syphilis and is the only recommended treatment in pregnant women.1,2 Similarly in 2016, the WHO issued new guidelines for treating chlamydia, gonorrhea, and syphilis based on emerging patterns of resistance to antibiotic therapy.2,10,11 All individuals treated for syph ilis should have follow-up serologic testing.1 Trichomoniasis vaginalis (T. vaginalis). The parasitic protozoal infection T. vaginalis is included in this section as it is conventionally discussed along with bacterial infections. The CDC guidelines recommend screening women who seek care for vaginal dis charge concerns and possibly for those in high-prevalence settings.1 Routine screening for T. vaginalis in asymptomatic women with HIV infection is also recom mended because of the adverse reactions associated with T. vaginalis and HIV infection.1 Use of highly sensitive and specific NAAT testing is now recommended for detecting T. vaginalis.1 More over, individuals with positive NAAT testing should be retested after treatment. Retesting 3 months after diagnosis of chlamydia, gonorrhea, or T. vaginalis is advised to detect repeat infection.1 M. genitalium. Since being isolated in 1980, M. genitalium has become known as a signifi cant source of nongonococcal urethritis in men and as a signifi cant source of cervicitis, urethritis, and upper pelvic infections in women.32 Major symptoms in women include abdominal pain and dyspareunia. In men, urethritis and penile discharge are the most common symptoms.32 The only way of specifi cally diagnosing M. genitalium infection is via NAAT.1 If left untreated, the disease can cause preterm birth or spontaneous abortion and/or pelvic infl am matory disease (PID).1,33,34,35 A history of PID appears to be associated with subsequent development of non invasive tumors of uncertain malignant potential.34 Rasmussen and colleagues noted that women with two or more episodes of PID had twice the risk of develop ing these tumors.34 Special populations Adolescents. With a few exceptions specific to age and service type, all 50 states and the District of Columbia allow minors to consent for their own health services for STIs.1,35 No state requires parental consent for STI care, nor is there a requirement that providers notify parents that their adolescent minor has received STI services.1,35 It is important to note that constraints may exist even when the minor may consent, and parental notification may differ by state.1 Older adults. Men and women are living longer, healthier lives and are sexual beings well into older adulthood, as reflected in a rise in STI and HIV rates in the United States and internationally among this age cohort.36,37 Screening and education during clinical encounters should include consistent condom use as well as biological risk factors such as decreased im mune response, decreased estrogen, and psychosocial changes, as these all have a role in STI prevention among older adults.36 The CDC's routine HIV screen ing recommendations end at age 64 years.1 Screening is based on sexual risk assessment in older adults over age 65 years.1 Transgender individuals. Transgender women (also referred to as trans women) are a special population of individuals who were born with male anatomy but identify as women (see Summary of updates for special populations). Approximately 27.7% of all transgender women and 56.3% of Black transgender women in the United States are infected with HIV.38,39 Transgender men (also referred to as trans men) are individuals born with female anatomy but iden tify as men.40 There is a great deal of anatomic diver sity in this population, with many individuals who still have a vagina and cervix, and thus, are suscep tible to diseases of the female genital tract.41 Estab lishing rapport with the individual and discussing anatomical needs for screening are both important factors to ensuring the individual is appropriately screened.29,39-41 Immunizations Currently, immunizations are available for three STIs: hepatitis A, hepatitis B, and HPV.42 There are no re cent changes in recommendations for the hepatitis A www.tnpj.com The Nurse Practitioner - August 2018 31 Page 5 Copyright (c) 2018 Wolters Kluwer Health, Inc. All rights reserved. Managing sexually transmitted infections: Beyond the 2015 guidelines Summary of updates for special populations1,35-39 Special population Key points Adolescents - With a few exceptions specific to age and service type, minors may consent for their own health services for STIs - No parental consent is necessary for STI treatment - Parental notification of treatment is not required, however, it is important to note that constraints may exist even when the minor may consent, and parental notification may differ by state Older adults - Rise in STI and HIV rates internationally in older adults - Providers should screen/educate on condom use, biological risk factors for STIs, hormonal changes affecting sexual a ctivity, and psychosocial changes of aging - Screening for HIV in those over age 65 years is based on risk assessment Transgender - Transgender women have high rates of HIV infection individuals - There is much anatomic diversity in the transgender population - Female-to-male transgender individuals may be susceptible to female genital tract infections depending on their anatomy - Establishing a rapport to determine appropriate screening is key vaccine. In 2018, the CDC issued updated recom mendations for the hepatitis B vaccine. These updates include: - a universal recommendation for vaccination within 24 hours of birth for medically stable newborns of normal birthweight - testing pregnant women for the presence of hepatitis B DNA if they are positive for hepatitis B surface antigen (HBsAg) - serologic testing of infants whose mothers' hepatitis B status is unknown Confidentiality requirements related to STI treatment have been recently updated to include requirements for individuals with HIV. - single-dose revaccination of infants not respond ing to the initial vaccine series whose mothers are HBsAg positive - vaccination for those with chronic liver disease - removal of permissive language allowing delay of the birth dose until after a newborn is discharged from the hospital following birth.43 Recommendations for HPV vaccination were re vised in 2016.44 The CDC amended the 3-dose 9-valent HPV vaccine series to include a 2-dose series in those under the age of 15 years.44 In December 2015, the FDA granted approval to the manufacturer of the 9-valent vaccine to extend the indication to include males 16 through 26 years of age. Evidence supporting the ongoing use of the HPV vaccine is growing.45 After only 6 years of provider recommendation for HPV vaccina tion in the United States, HPV prevalence declined by 64% in adolescent females ages 14 to 19 years and by 34% in women ages 20 to 24 years.16,45 Confidentiality Confidentiality requirements related to STI treatment have been recently updated to include requirements for individuals with HIV.46 Individuals with HIV are protected against discrimination under provisions of the Americans with Disabilities Act of 1990, which assumes that indi viduals with HIV, whether symp tomatic or asymptomatic, "have physical impairments that substan tially limit one or more major life activities."46 A number of cases of discrimination based on HIV status have been litigated within the past 3 years.46 Conclusion As noted by the CDC, WHO, and FDA, the prevention, management, and treatment of STIs is an area of rap idly changing evidence requiring advance practice registered nurses (APRNs) to maintain awareness of up-to-date guidelines. APRNs are members of the primary prevention healthcare team responsible for guaranteeing confidentiality and ensuring that neces sary preventive services, immunizations, and PrEP services are delivered according to guidelines and cur rent evidence. 32 The Nurse Practitioner - Vol. 43, No. 8 www.tnpj.com Page 6 Copyright (c) 2018 Wolters Kluwer Health, Inc. All rights reserved. Managing sexually transmitted infections: Beyond the 2015 guidelines Without APRNs having a strong fundamental un derstanding of health consequences of missed or inap propriately diagnosed and treated STIs, patients can develop disease sequela. APRNs who use targeted edu cation campaigns geared toward specifi c age-groups and special populations, such as adolescents, are cham pions for preventing and decreasing STIs. During patient encounters, assessing each indi vidual's risk of STIs (sexual exposures, practices) pro vides the APRN an opportunity for focused patient education. Furthermore, educating individuals about the signs and symptoms of STIs reinforces importance of early treatment if an infection occurs. REFERENCES 1. Workowski KA, Bolan GA, Centers for Disease Control and Prevention. Sexually transmitted diseases treatment guidelines, 2015. MMWR Recomm Rep. 2015;64(RR-03):1-137. 2. World Health Organization. Global health sector strategy on sexually transmitted infections 2016-2021. 2016. www.apps.who.int/iris/bitstream/ handle/10665/246296/WHO-RHR-16.09-eng.pdf;jsessionid=3EC32A3E931 A398C94534B476E6CDB83?sequence=1. 3. Brener N. Sexually transmitted disease (STD) prevention education and services in a nationally representative sample of schools-United States, 2014. 2016. http://nphic.confex.com/cdc/std2016/videogateway.cgi/ id/12972?recordingid=12972. 4. Cantor AG, Pappas M, Daeges M, Nelson HD. Screening for syphilis: updated evidence report and systematic review for the US Preventive Services Task Force. JAMA. 2016;315(21):2328-2337. 5. U.S. Preventive Services Task Force. The guide to clinical preventive services. 2014. www.uspreventiveservicestaskforce.org/Page/Name/tools-and-resources for-better-preventive-care. 6. Falasinnu T, Gilbert M, Gustafson P, Shoveller J. A validation study of a clinical prediction rule for screening asymptomatic chlamydia and gonor rhoea infections among heterosexuals in British Columbia. Sex Transm Infect. 2016;92(1):12-18. 7. Falasinnu T, Gilbert M, Gustafson P, Shoveller J. An assessment of population-based screening guidelines versus clinical prediction rules for chlamydia and gonorrhea case fi nding. Prev Med. 2016;89:51-56. 8. Dustin LB, Bartolini B, Capobianchi MR, Pistello M. Hepatitis C virus: life cycle in cells, infection and host response, and analysis of molecular markers influencing the outcome of infection and response to therapy. Clin Microbiol Infect. 2016;22(10):826-832. 9. Aggarwal A, Hitchen TL, Ootes L, et al. HIV infection is infl uenced by dynamin at 3 independent points in the viral life cycle. Traff c. 2017;18(6): 392-410. 10. World Health Organization. WHO guidelines for the treatment of Neisseria gonorrhoeae. 2016. http://apps.who.int/iris/bitstream/hand le/10665/246114/9789241549691-eng.pdf?sequence=1. 11. World Health Organization. WHO guidelines for the treatment of Chlamydia trachomatis. 2016. http://apps.who.int/iris/bitstream/hand le/10665/246165/9789241549714-eng.pdf?sequence=1. 12. Miller SJ, Foran-Tuller K, Ledergerber J, Jandorf L. Motivational interview ing to improve health screening uptake: a systematic review. Patient Educ Couns. 2017;100(2):190-198. 13. Metsch LR, Feaster DJ, Gooden L, et al. Effect of risk-reduction counseling with rapid HIV testing on risk of acquiring sexually transmitted infections: the AWARE randomized clinical trial. JAMA. 2013;310(16):1701-1710. 14. LeFevre ML, U.S. Preventive Services Task Force. Screening for chlamydia and gonorrhea: U.S. Preventive Services Task Force recommendation state ment. Ann Intern Med. 2014;161(12):902-910. 15. Markowitz LE, Liu G, Hariri S, Steinau M, Dunne EF, Unger ER. Prevalence of HPV after introduction of the vaccination program in the United States. Pediatrics. 2016;137(3):e20151968. 16. Food and Drug Administration. December 10, 2014 approval letter -Gardasil 9. 2014. www.fda.gov/BiologicsBloodVaccines/Vaccines/ApprovedProducts/ ucm426520.htm. 17. Markowitz LE, Dunne EF, Saraiya M, et al. Human papillomavirus vac cination: recommendations of the Advisory Committee on Immunization Practices (ACIP). MMWR Recomm Rep. 2014;63(RR-05):1-30. 18. Spinner CD, Boesecke C, Zink A, et al. HIV pre-exposure prophylaxis (PrEP): a review of current knowledge of oral systemic HIV PrEP in hu mans. Infection. 2016;44(2):151-158. 19. Purcell DW, Higa D, Mizuno Y, Lyles C. Quantifying the harms and benefi ts from serosorting among HIV-negative gay and bisexual men: a systematic review and meta-analysis. AIDS Behav. 2017;21(10):2835-2843. 20. Kojima N, Klausner JD. Improving management of sexually transmitted infections in those who use pre-exposure prophylaxis for human immuno deficiency virus infection. AIDS. 2018;32(2):272-275. 21. Falade-Nwulia O, Sulkowski MS, Merkow A, Latkin C, Mehta SH. Under standing and addressing hepatitis C reinfection in the oral direct-acting antiviral era. J Viral Hepat. 2018;25(3):220-227. 22. Wuytack F, Lutje V, Tohme R, et al. Sexual Transmission of Hepatitis C Virus Infection in a Heterosexual Population, A Systematic Review. Dublin: National Clinical Effectiveness Committee, Department of Health; 2017. 23. Honein MA, Dawson AL, Petersen EE, et al. Birth defects among fetuses and infants of US women with evidence of possible Zika virus infection during pregnancy. JAMA. 2017;317(1):59-68. 24. Schuler-Faccini L, Roehe P, Zimmer ER, et al. ZIKA virus and neuroscience: the need for a translational collaboration. Mol Neurobiol. 2018;55(2):1551-1555. 25. Mead PS, Hills SL, Brooks JT. Zika virus as a sexually transmitted pathogen. Curr Opin Infect Dis. 2018;31(1):39-44. 26. Rather IA, Lone JB, Bajpai VK, Park YH. Zika virus infection during preg nancy and congenital abnormalities. Front Microbiol. 2017;8:581. 27. Colt S, Garcia-Casal MN, Pena-Rosas JP, et al. Transmission of Zika virus through breast milk and other breastfeeding-related bodily-fluids: a system atic review. PLoS Negl Trop Dis. 2017;11(4):e0005528. 28. Tuite AR, Gift TL, Chesson HW, Hsu K, Salomon JA, Grad YH. Impact of rapid susceptibility testing and antibiotic selection strategy on the emergence and spread of antibiotic resistance in gonorrhea. J Infect Dis. 2017;216(9):1141-1149. 29. Frecker H, Kives S, Yudin M. The prevalence of chlamydia in adoles cents at presentation to colposcopy: do new cervical cancer screening guidelines eliminate an STI screening opportunity? Am J Obstet Gynecol. 2015;215(12):886-887. 30. Marx GE, Dhanireddy S, Marrazzo JM, et al. Variations in clinical presenta tion of ocular syphilis: case series reported from a growing epidemic in the United States. Sex Transm Dis. 2016;43(8):519-523. 31. World Health Organization. Growing antibiotic resistance forces updates to recommended treatment for sexually transmitted infections. 2016. www. who.int/mediacentre/news/releases/2016/antibiotics-sexual-infections/en. 32. Jensen JS, Cusini M, Gomberg M, Moi H. 2016 European guideline on Mycoplasma genitalium infections. J Eur Acad Dermatol Venereol. 2016;30(10):1650-1656. 33. Shepherd S. Pelvic inflammatory disease. Medscape. 2017. http://emedicine. medscape.com/article/256448-overview. 34. Rasmussen CB, Kjaer SK, Albieri V, et al. Pelvic inflammatory disease and the risk of ovarian cancer and borderline ovarian tumors: a pooled analysis of 13 case-control studies. Am J Epidemiol. 2017;185(1):8-20. 35. Guttmacher Institute. Abortion rate. 2016. https://data.guttmacher.org/ states/trend?state=US&topics=68&dataset=data. 36. MacDonald J, Lorimer K, Knussen C, Flowers P. Interventions to increase condom use among middle-aged and older adults: a systematic review of theoretical bases, behaviour change techniques, modes of delivery and treat ment fi delity. J Health Psychol. 2016;21(11):2477-2492. 37. Johnson BK. Sexually transmitted infections and older adults. J Gerontol Nurs. 2013;39(11):53-60. 38. Neumann MS, Finlayson TJ, Pitts NL, Keatley J. Comprehensive HIV pre vention for transgender persons. Am J Public Health. 2017;107(2):207-212. 39. Raiford JL, Hall GJ, Taylor RD, Bimbi DS, Parsons JT. The role of structural barriers in risky sexual behavior, victimization and readiness to change HIV/STI-related risk behavior among transgender women. AIDS Behav. 2016;20(10):2212-2221. www.tnpj.com The Nurse Practitioner - August 2018 33 Page 7 Copyright (c) 2018 Wolters Kluwer Health, Inc. All rights reserved. Managing sexually transmitted infections: Beyond the 2015 guidelines INSTRUCTIONS Managing sexually transmitted infections: Beyond the 2015 guidelines DISCOUNTS and CUSTOMER SERVICE - Send two or more tests in any nursing journal published by Lippincott Williams & Wilkins together and deduct $0.95 from the price of each test. - We also offer CE accounts for hospitals and other healthcare facilities on nursingcenter.com. Call 1-800-787-8985 for details. PROVIDER ACCREDITATION Lippincott Professional Development will award 1.5 contact hours for this continuing nursing education activity. Lippincott Professional Development is accredited as a provider of continuing nursing edu cation by the American Nurses Credentialing Center's Commission on Accreditation. This activity is also provider approved by the California Board of Registered Nursing, Provider Number CEP 11749 for 1.5 contact hours. Lippincott Professional Development is also an approved provider of continuing nursing education by the District of Columbia, Georgia, and Florida CE Broker #50-1223. This activity has been assigned 1.0 pharmacology credits. For more than 263 additional continuing education articles related to Advanced Practice Nursing topics, go to NursingCenter.com/CE. Earn CE credit online: Go to www.nursingcenter.com/CE/NP and receive a certificate within minutes. TEST INSTRUCTIONS - To take the test online, go to our secure website at www. nursingcenter.com/ce/NP. View instructions for taking the test online there. - If you prefer to submit your test by mail, record your an- swers in the test answer section of the CE enrollment form on page 35. You may make copies of the form. Each question has only one correct answer. There is no minimum passing score required. Complete the registration information and course evalua- tion. Mail the completed form and registration fee of $17.95 to: Lippincott Professional Development CE Group, 74 Brick Blvd., Bldg. 4, Suite 206, Brick, NJ 08723. We will mail your certificate in 4 to 6 weeks. For faster service, include a fax number and we will fax your certificate within 2 business days of receiving your enrollment form. You will receive your CE certificate of earned contact hours and an answer key to review your results. - Registration deadline is June 5, 2020. 40. Scheim AI, Bauer GR, Travers R. HIV-related sexual risk among transgender men who are gay, bisexual, or have sex with men. J Acquir Immune Def c Syndr. 2017;74(4):e89-e96. 41. Stanton MC, Ali S, Chaudhuri S. Individual, social and community-level predictors of wellbeing in a US sample of transgender and gender non conforming individuals. Cult Health Sex. 2017;19(1):32-49. 42. Bluml BM, Brock KA, Hamstra S, Tonrey L. Evaluation of the impact of an innovative immunization practice model designed to improve population health: results of the project impact immunizations pilot. Popul Health Manag. 2018;21(1):55-62. 43. Schillie S, Vellozzi C, Reingold A, et al. Prevention of hepatitis B virus infec tion in the United States: recommendations of the Advisory Committee on Immunization Practices. CDC. 2018. www.cdc.gov/mmwr/volumes/67/rr/ pdfs/rr6701-H.pdf. 44. Meites E, Kempe A, Markowitz LE. Use of a 2-dose schedule for human pap illomavirus vaccination-updated recommendations of the Advisory Com mittee on Immunization Practices. Am J Transplant. 2017;17(3):834-837. 45. Petrosky E, Bocchini JA Jr, Hariri S, et al. Use of 9-valent human papilloma virus (HPV) vaccine: updated HPV vaccination recommendations of the advisory committee on immunization practices. MMWR Morb Mortal Wkly Rep. 2015;64(11):300-304. 46. Palmer C, Mickelson L. Falling through the cracks: the unique circum stances of HIV disease under recent Americans with Disabilities Act caselaw and emerging privacy policies. Law & Inequality: A Journal of Theory and Practice. 2017;21(2):219. Versie Johnson-Mallard is a department chair and associate professor at the University of Florida, Gainesville, Fla. Kim Curry is a clinical associate professor and associate dean, Student Affairs, at the University of Florida, College of Nursing, Gainesville, Fla. Rasheeta Chandler is an at Neill Hodgson School of Nursing, Emory University, Atlanta, Ga. Ivy Alexander is a professor and director of Advanced Practice Programs and director of the Adult-Gerontology Primary Care Track at the University of Connecticut, School of Nursing, Storrs, Conn. Elizabeth Kostas-Polston is an at Daniel K. Inouye Graduate School of Nursing, Bethesda, Md. Susan Orsega is a rear admiral at the United States Public Health Service (USPHS), Bethesda, Md. Nancy Fugate Woods is a Professor and dean emerita at the University of Washington, Department of Biobehavioral Nursing and Health Informatics, Seattle, Wash. The authors and planners have disclosed the following fi nancial relationships related to this article: Nancy Fugate Woods (scientific advisory board, Procter & Gamble; external ad visory board, CTSA Duke University; external advisory board, CTSA University of Pittsburgh; and consultancy, University of California, Davis). Ivy Alexander (board member, Pfizer; consultancy, Pfizer and WebMD; grants, HRSA ANA; lectures, MidlevelU, Planned Parenthood, Quinnipiac; and royal ties, Jones & Bartlett Publishers, NPACE). This article has been reviewed, and all potential or actual conflicts have been resolved. DOI-10.1097/01.NPR.0000541464.23795.5b 34 The Nurse Practitioner - Vol. 43, No. 8 www.tnpj.com