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C. Brock Woodis, PharmD, BCACP, BCPS, CDE, BC-ADM, CPP Associate Professor Campbell University College of Pharmacy & Health Sciences Duke Family Medicine September 27, 2016 [email protected] I do not have any financial relevance related to this continuing education activity. Identify most likely causative pathogens for a variety of presented sexually transmitted infections (STIs) Recommend appropriate drug therapy for a variety of STIs based on specific laboratory and patientspecific data Formulate complete patient-specific treatment plans including monitoring for safety and efficacy for a variety of presented STIs Workowski KA and Bolan KA. Sexually transmitted diseases treatment guidelines. MMWR Recomm Rep 2015;64(No. RR-3):[1-137]. http://www.cdc.gov/std/tg2015/ Pocket guide Wall poster Growing antibiotic resistance forces updates to recommended treatment for sexually transmitted infections. World heath organization website. Updated Aug 30, 2016. Accessed Sept 22, 2016. http://www.who.int/reproductivehealth/topics/rtis/stis-new- treatment-guidelines/en/ Each day > 1 million sexually transmitted infections (STIs) are acquired worldwide Estimated 357 million new infections with 1 of 4 STIs occur each year: chlamydia, gonorrhea, syphilis and trichomoniasis > 500 million people are estimated to have genital infection with herpes simplex virus (HSV) > 290 million women have a human papillomavirus (HPV) infection Majority of STIs have no symptoms or only mild symptoms that may not be recognized as an STI Sexually transmitted infections fact sheet. World Health Organization website. Updated August 2016. Accessed Sept 22, 2016. STIs such as HSV type 2 and syphilis can increase the risk of HIV acquisition > 900 000 pregnant women were infected with syphilis resulting in approximately 350 000 adverse birth outcomes including stillbirth in 2012 STIs can have serious reproductive health consequences beyond the immediate impact of the infection itself (e.g., infertility or mother-to-child transmission) Drug resistance (especially for gonorrhea) is a major threat to reducing the impact of STIs worldwide Sexually transmitted infections fact sheet. World Health Organization website. Updated August 2016. Accessed Sept 22, 2016. STI transmission Variety of clinical syndromes and infections caused by pathogens which are acquired and transmitted through sexual activity Few STIs have been eradicated STIs have reemerged secondary to social trends of sexual activity ↑ numbers of adolescents engaging in unsafe sexual practices ↑ incidence of men who have sex with men (MSM) and women who have sex with women (WSW) Pharmacotherapy: A Pathophysiologic Approach. 9th ed. 2014;Chapter 95. Optimal detection and treatment of STIs depends on knowledgeable and competent clinicians Higher reported incidence of most major STIs in men, but complications of STIs are generally more frequent and severe in women Serious effects on maternal and child health during pregnancy Possible damage to reproductive organs, cancer, and transmission to fetus if untreated Pharmacotherapy: A Pathophysiologic Approach. 9th ed. 2014;Chapter 95. Partners Practices Prevention of pregnancy Protection from STIs Past history of STIs IMPORTANCE OF STI PREVENTION COUNSELING MMWR Recomm Rep 2015;64(No. RR-3):[1-137]. Sociocultural Host susceptibility Changes of causative pathogen Demographics STI transmission Economics Patterns of sexual behavior Pharmacotherapy: A Pathophysiologic Approach. 9th ed. 2014;Chapter 95. Treatment of infection based on microbiologic eradication Alleviation of signs and symptoms Prevention of sequelae Prevention of transmission, including advantages such as cost-effectiveness and other advantages (e.g. single-dose formulations) MMWR Recomm Rep 2015;64(No. RR-3):[1-137]. http://www.cdc.gov/std/ept Do not assume that patients (especially adolescents) consistently know how to use barrier methods of contraception ↑ of adolescents engaging in unsafe sexual practices, as well as men who have sex with men (MSM) and women who have sex with women (WSW) Optimal to treat both partners for an STI simultaneously Pharmacotherapy: A Pathophysiologic Approach. 9th ed. 2014;Chapter 95. All sexually active females aged 25 and younger, and older women at risk for STIs should be screened for chlamydia and gonorrhea At-risk women include those with new sexual partners, multiple partners, and inconsistent condom use USPSTF says not enough evidence to weigh the benefits and harms of such screening in men Recommends intensive behavioral counseling for all sexually active adolescents and for adults at increased risk for STIs Interventions include at least 2 hours of contact time, basic information about STIs, training in condom use, and goal setting Gram-stained smears Culture DNA hybridization probe Nucleic acid amplification tests (NAATs) Gram stain of male urethral specimen that demonstrates polymorphonuclear leukocytes with intracellular gram (-) diplococci considered diagnostic in men .MMWR Recomm Rep 2015;64(No. RR-3):[1-137]. Preferred drugs Dose Route Frequency Ceftriaxone PLUS 250 mg IM X 1 dose Azithromycin OR 1g PO X 1 dose Doxycycline 100 mg PO BID X 7 days Cefixime PLUS 400 mg PO X 1 dose Azithromycin OR 1g PO X 1 dose Doxycycline 100 mg PO BID X 7 days Alternative drugs MMWR Recomm Rep 2015;64(No. RR-3):[1-137]. CDC recommends combination therapy with ceftriaxone 250 mg IM X 1 dose + azithromycin 1 g PO X1 dose OR doxycycline 100 mg PO BID (in place of azithromycin) X 7 days as the most reliably effective treatment for uncomplicated gonorrhea CDC no longer recommends cefixime at any dose as a 1st-line regimen for treatment of gonococcal infections Cefixime Alternative agent Patient should return in 1 week for a test-of-cure at the site of infection Centers for disease control and prevention. 25 Sept 2012 <http://www.cdc.gov/std> Drug Dose Route Frequency Ceftriaxone PLUS 250 mg IM X 1 dose Azithromycin OR 1g PO X 1 dose Doxycycline 100 mg PO BID X 7 days MMWR Recomm Rep 2015;64(No. RR-3):[1-137]. Follow-up No “test-of-cure” unless cefixime used Retest 3 months after treatment to assess REINFECTION Cephalosporins are safe in pregnancy Management of sex partners MMWR Recomm Rep 2015;64(No. RR-3):[1-137]. Gonococcal conjunctivitis-ceftriaxone 1g IM X1 dose PLUS azithromycin 1 g PO X 1 dose Disemminated gonococcal infection (DGI) Results in petechial or pustular acral lesions, symmetrical arthralgia, tenosynsovitis, or septic arthritis Hospitalization initially Rule out endocarditis and meningitis Recommended-ceftriaxone 1 g IM or IV Q24H PLUS azithromycin 1 g PO X 1 dose then switch to cefixime 400 mg PO BID X 7 days Alternatives (in combination with azithromycin 1 g PO X 1 dose) ▪ Cefotaxime 1 g IV Q8H OR ▪ Ceftizoxime 1g IV Q8H MMWR Recomm Rep 2015;64(No. RR-3):[1-137]. Meningitis-ceftriaxone 1-2 g IV Q12H-24H X 10-14 days Endocarditis-ceftriaxone 1-2 g IV Q12H-24H X 4 weeks Both should also receive azithromycin 1 g PO X 1 dose MMWR Recomm Rep 2015;64(No. RR-3):[1-137]. Culture Enzyme immunoassay DNA hybridization probe Direct fluorescent monoclonal antibody test Urine or swab specimen of endocervix (women) Urethral swab or urine specimen (men) MMWR Recomm Rep 2015;64(No. RR-3):[1-137]. Resistance to azithromycin is emerging according to CDC findings CDC currently recommends a combination gonorrhea treatment with two antibiotics – an oral dose of azithromycin and single shot of ceftriaxone Combination therapy currently recommended by CDC is still effective No treatment failures have been reported in the United States Signs of emerging resistance to azithromycin suggests that this drug will be next in the long line of antibiotics to which gonorrhea bacteria have become resistant – a list that includes penicillin, tetracycline, and fluoroquinolones Antibiotic resistance threatens gonorrhea treatment. Centers for disease control and prevention website. Updated July 14, 2016. Accessed Sept 22, 2016. Preferred drugs Dose Route Frequency Azithromycin OR 1g PO X 1 dose Doxycycline 100 mg PO BID X 7 days Erythromycin base OR 500 mg PO QID X 7 days Erythromycin ethylsuccinate OR 800 mg PO QID X 7 days Levofloxacin OR 500 mg PO QDAY X 7 days Ofloxacin 300 mg PO BID X 7 days Alternative drugs MMWR Recomm Rep 2015;64(No. RR-3):[1-137]. Abstinence from intercourse for 7 days from when therapy was initiated Test-of-cure is not recommended Unlike test-of-cure, repeat C. trachomatis testing of recently infected men and women should be conducted 3 months after treatment Azithromycin recommended for pregnancy and chlamydial infection MMWR Recomm Rep 2015;64(No. RR-3):[1-137]. 3 IMPORTANT signs Uterine tenderness Cervical motion tenderness Adnexal tenderness Additional criteria Oral temperature > 38.3° (101°F) Abnormal cervical or vaginal discharge WBC presence on saline microscopy of vaginal secretions ↑ Erythrocyte sedimentation rate ↑ C-reactive protein MMWR Recomm Rep 2015;64(No. RR-3):[1-137]. General-signs/symptoms may vary from mild to severe Signs-vague Symptoms Lower abdominal or pelvic pain Malodorous vaginal discharge Abnormal uterine bleeding Dyspareunia Nausea and/or vomiting Fever MMWR Recomm Rep 2015;64(No. RR-3):[1-137]. Treatment for sexually active young women and other women at risk for STIs if they are experiencing pelvic or lower abdominal pain AND No other cause other than PID can be identified One or more of 3 IMPORTANT SIGNS are present on pelvic exam Additional criteria include oral temperature > 38.3°C, abnormal cervical or vaginal discharge, WBC presence on saline microscopy of vaginal secretions, ↑ ESR and CRP MMWR Recomm Rep 2015;64(No. RR-3):[1-137]. Therapy should provide empiric, broad spectrum coverage of likely pathogens N. gonorrhoeae C. trachomatis Microorganisms which comprise vaginal flora Gardnerella vaginalis Haemophilus influenzae Enteric gram (-) rods Streptococcus agalactiae Anaerobes MMWR Recomm Rep 2015;64(No. RR-3):[1-137]. Anaerobic bacteria have been isolated from the upper-reproductive tract of women who have PID Data from in vitro studies have revealed some anaerobes (e.g. Bacteroides fragilis) can cause tubal and epithelial destruction Bacterial vaginosis (BV) also present in many women who have PID Use of regimens with anaerobic activity should be considered for PID treatment MMWR Recomm Rep 2015;64(No. RR-3):[1-137]. If mild to moderate clinical severity, outpatient therapy has similar outcomes to inpatient management Hospitalize if ANY of the following factors present Surgical emergencies Pregnancy Does not respond to oral antimicrobial therapy Unable to follow or tolerate oral regimen Severe illness, N/V, high fever Tubo-ovarian abscess MMWR Recomm Rep 2015;64(No. RR-3):[1-137]. Drug Dose Route Frequency Cefotetan PLUS 2g IV Q12H Doxycycline OR 100 mg PO/IV Q12H Cefoxitin PLUS 2g IV Q6H Doxycycline 100 mg PO/IV Q12H May discontinue parenteral therapy 24 hours after clinical improvement, but oral therapy with doxycycline should continue to complete 14 days of therapy! MMWR Recomm Rep 2015;64(No. RR-3):[1-137]. Drug Dose Route Frequency Clindamycin PLUS 900 mg IV Q8H Gentamicin Loading dose: 2 mg/kg IBW Followed by maintenance dose of 1.5 mg/kg IV Q8H OR Single daily dose of 3-5 mg/kg IBW May discontinue parenteral therapy 24 hours after clinical improvement, but oral therapy with doxycycline at 100 mg PO BID or clindamycin 450 mg PO Q6H should continue to complete 14 days of therapy! MMWR Recomm Rep 2015;64(No. RR-3):[1-137]. Drug Dose Route Frequency Ceftriaxone PLUS 250 mg IM X1 dose Doxycycline WITH or WITHOUT 100 mg PO BID X 14 days Metronidazole 500 mg PO BID X 14 days Cefoxitin AND 2g IM X1 Probenecid PLUS 1g PO X1 Doxycycline WITH or WITHOUT 100 mg PO BID X 14 days Metronidazole 500 mg PO BID X 14 days OR MMWR Recomm Rep 2015;64(No. RR-3):[1-137]. Inflammation of the vagina, oftentimes caused by infection Usually characterized by discharge, itching, and odor Three infections most frequently associated with discharge BV- NOT an STI Trichomoniasis Vulvovaginal candidiasis (VVC)- NOT an STI MMWR Recomm Rep 2015;64(No. RR-3):[1-137]. BV diagnosed according to Amsel’s Diagnostic Criteria 3/4 criteria must be present Thin, white, homogenous discharge Clue cells on microscopy Vaginal pH > 4.5 Release of “fishy” odor once 10% KOH (i.e. “whiff test”) added to vaginal sample Alternatively, gram-stain vaginal smear may be used MMWR Recomm Rep 2015;64(No. RR-3):[1-137]. Drug Dose Route Frequency Metronidazole OR 500 mg PO BID X 7 days Metronidazole 0.75% gel OR 1 full applicator (5 g) Intravaginally QDAY X 5 days Clindamycin 2% cream 1 full applicator (5 g) Intravaginally QHS X 7 days MMWR Recomm Rep 2015;64(No. RR-3):[1-137]. Drug Dose Route Frequency Tinidazole OR 2g PO QDAY X 2 days Tinidazole OR 1g PO QDAY X 5 days Clindamycin OR 300 mg PO BID X 7 days Clindamycin ovules 100 mg Intravaginally QHS X 3 days MMWR Recomm Rep 2015;64(No. RR-3):[1-137]. Recommended regimen Dose Route Frequency Metronidazole OR 2g PO X1 Tinidazole 2g PO X1 500 mg PO BID X 7 days Alternative regimen Metronidazole MMWR Recomm Rep 2015;64(No. RR-3):[1-137]. A disulfiram-like reaction may occur if taken with alcohol Flushing, palpitations, tachycardia, nausea, vomiting, may occur with concurrent use Although the risk for most patients may be slight, caution is advised Alcoholic beverages should be avoided while taking metronidazole and for at least 1 day (metronidazole tablets) or 3 days (metronidazole capsules and extended release tablets) after discontinuing MMWR Recomm Rep 2015;64(No. RR-3):[1-137]. Drug Dose Route Frequency Butoconazole 2% sustained-release cream OR 5g Intravaginally X 1 day Fluconazole OR 150 mg PO X 1 day Tioconazole 6.5% ointment 5g Intravaginally X 1 day MMWR Recomm Rep 2015;64(No. RR-3):[1-137]. Drug Dose Route Frequency Clotrimazole 2% cream OR 5g Intravaginally QHS X 3 days Miconazole 200 mg vaginal suppository OR 1 suppository Intravaginally QHS X 3 days Terconazole 0.8% cream OR 5g Intravaginally QHS X 3 days Terconazole 80 mg vaginal suppository 1 suppository Intravaginally QHS X 3 days MMWR Recomm Rep 2015;64(No. RR-3):[1-137]. Drug Dose Route Frequency Clotrimazole 1% cream OR 5g Intravaginally QHS X 7-14 nights Clotrimazole 100 mg vaginal tab OR 1 tablet Intravaginally QHS X 7 nights Miconazole 2% cream OR 5g Intravaginally QHS X 7 nights Miconazole 100 mg vaginal tab OR 1 suppository Intravaginally QHS X 7 nights Terconazole 0.4% cream 5g Intravaginally QDAY X 7 days MMWR Recomm Rep 2015;64(No. RR-3):[1-137]. Stage General Site Signs/symptoms Primary Incubates 10-90 days External genitalia, mouth, throat Single, painless lesion (chancre) Secondary Develops 2-8 weeks Multisystem involvement due to lymphatic spread Pruritic or nonpruritic rash; flu-like symptoms Latent Develops 4-10 weeks Potentially multisystem (dormant) Asymptomatic Tertiary Develops in 30% of those untreated or inadequately treated CNS, heart, eyes, bones, and joints CV syphilis, neurosyphilis, gummatous lesions MMWR Recomm Rep 2015;64(No. RR-3):[1-137]. Stage Characteristics Adult Treatment Primary Solitary, painless chancre Benzathine PCN 2.4 million units X 1 dose Secondary Fatigue, diffuse rash on palms of hands and soles of feet, fever, lymphadenopathy Benzathine PCN 2.4 million units X 1 dose Early latent Involves 1st year after infection Benzathine PCN 2.4 million units X 1 dose Late latent Usually asymptomatic; resolved lesions; seropositive for T. pallidum Benzathine PCN 7.2 million units total 2.4 million units IM weekly X 3 weeks Tertiary Develops years after infection; may affect any organ in body (gummatous and CV syphilis treated same as tertiary) Benzathine PCN 7.2 million units total 2.4 million units IM weekly X 3 weeks Neurosyphilis and ocular syphilis CNS involvement (e.g. cognitive dysfunction, motor deficits, meningitis symptoms, etc.) Aqueous PCN G 3-4 million units IV Q4H X 10-14 days MMWR Recomm Rep 2015;64(No. RR-3):[1-137]. Am Fam Physician. 2003;68:283-290. Reaction which occurs secondary to spirochete lysis and pro-inflammatory cytokine cascades Can transpire as early as 2 hours after PCN administration and usually resolves within 24 hours Clinical presentation Fever Chills Tachycardia Tachypnea Treatment is supportive MMWR Recomm Rep 2015;64(No. RR-3):[1-137]. Syphilis infection during pregnancy can result in significant health problems for an infant Historical data indicate that up to 40% of pregnancies in women with untreated syphilis will result in miscarriage, stillbirth, or infant death Infants who live may develop severe illness, including skeletal abnormalities; hepatosplenomegaly; jaundice; anemia; optic atrophy; interstitial keratitis; sensorineural deafness; or meningitis, which can cause developmental delays and seizures All pregnant women should be screened for syphilis at their first prenatal visit Women at high risk should be rescreened early in their third trimester and again at delivery Pregnant women diagnosed with syphilis should be treated with penicillin immediately and should last 30 days prior to delivery Kidd S. Congenital Syphilis Is on the Rise? Reviewing Prevention Steps. Centers for disease control and prevention. Updated July 18, 2016. Accessed Sept 22, 2016. Patients should be advised tell sex partners about the infection and encourage them to get tested and treated to avoid reinfection Before discharging any newborn infant from the hospital, mothers should be tested for syphilis at least once during her pregnancy or at delivery If a woman delivers a stillborn infant, she should be tested for syphilis Safe sex practices should be discussed Partner with health departments, prenatal care providers, and other local organizations to address barriers to obtaining early and adequate prenatal care for the most vulnerable pregnant women in the community Kidd S. Congenital Syphilis Is on the Rise? Reviewing Prevention Steps. Centers for disease control and prevention. Updated July 18, 2016. Accessed Sept 22, 2016. Recommended treatment for syphilis and the only recommended treatment for pregnant women infected or exposed to syphilis is benzathine penicillin G) Pfizer, the sole manufacturer of Bicillin L-A® (penicillin G benzathine) in the United States is experiencing a manufacturing delay of this product CDC recommendations until shortage resolves Refrain from the use of Bicillin L-A® (penicillin G benzathine) for treatment of other infectious diseases (e.g., streptococcal pharyngitis) where other effective antimicrobials are available Adhere to the recommended dosing regimen of 2.4 million units of penicillin G benzathine IM for the treatment of primary, secondary and early latent syphilis (i.e., early syphilis) as outlined in the 2015 STD Treatment Guidelines(http://www.cdc.gov/std/tg2015/syphilis.htm) Additional doses to treat early syphilis do not enhance efficacy, including in patients living with HIV infection Contact your pharmacists/distributors to procure Bicillin L-A® (penicillin G benzathine), if you do not have product readily available If product reaches a critical supply level of three weeks or less, contact Pfizer Direct questions about syphilis clinical management to an infectious disease specialist or the on-line National Network of STD Clinical Prevention Training Centers (NNPTC) STD Clinical Consultation Network (https://www.stdccn.org ). Bicillin-LA (benzathine penicillin G) shortage. Centers for disease control and prevention. Updated June 28, 2016. Accessed Sept 22, 2016. Procaine Penicillin G IM is one of the recommended treatments for congenital syphilis and an alternative treatment for both neurosyphilis and ocular syphilis Other recommended treatment for congenital syphilis is aqueous crystalline penicillin G IV Pfizer, the sole manufacturer of this product in the United States, is experiencing manufacturing delays CDC is continuing to work with FDA’s Drug Shortage Staff and Pfizer to address this situation If Procaine Penicillin G is unavailable and until normal quantities of Procaine Penicillin G is available, CDC suggests using other available and recommended regimens of penicillin to treat congenital syphilis as outlined in the 2015 STD Treatment Guidelines(https://www.cdc.gov/std/tg2015/syphilis.htm) Procaine penicillin shortage. Centers for disease control and prevention. Updated Sept 19, 2016. Accessed Sept 22, 2016. Desired outcome is to curtail number of episodic prodromes and to minimize any side effects experienced due to antivirals Treatment is based on several factors Likelihood of patient compliance Whether it is the first or recurrent episode Host immunity Pregnancy MMWR Recomm Rep 2015;64(No. RR-3):[1-137]. Drug Dose Route Frequency Acyclovir OR 200 mg PO 5 X/day X 7-10 days Acyclovir OR 400 mg PO TID X 7-10 days Valacyclovir OR 1g PO BID X 7-10 days Famciclovir 250 mg PO TID X 7-10 days MMWR Recomm Rep 2015;64(No. RR-3):[1-137]. Drug Dose Route Frequency Acyclovir 400 mg PO TID X 5 days Acyclovir 800 mg PO BID X 5 days Acyclovir 800 mg PO TID X 2 days Valacyclovir 500 mg PO BID X 3 days Valacyclovir 1g PO QDAY X 5 days Famciclovir 125 mg PO BID X 5 days Famciclovir 1000 mg PO BID X 1 day Famciclovir 500 mg once, then 250 mg BID PO BID X 2 days MMWR Recomm Rep 2015;64(No. RR-3):[1-137]. Drug Dose Route Frequency Acyclovir OR 400 mg PO BID up to a year Valacyclovir OR 500 mg PO DAILY up to a year Valacyclovir OR 1g PO DAILY up to a year Famciclovir 250 mg PO BID up to a year MMWR Recomm Rep 2015;64(No. RR-3):[1-137]. Headache Confusion Nausea Vomiting Thrombocytopenia Renal insufficiency Rash Pruritus Fever MMWR Recomm Rep 2015;64(No. RR-3):[1-137]. Arthralgias Myalgias Thrombotic thrombocytopenic purpura (TTP) Hallucinations Somnolence Depression Drug Dose Side effects Acyclovir 5-10 mg/kg IV Q8H X 2-7 days See previous slide Foscarnet 40 mg/kg IV Q8-12H X 2-3 weeks or until clinical resolution attained Renal insufficiency, metabolic disturbances, hypophosphatemia Cidofovir 0.3%, 1%, and 3% topical agent used on a compassionate basis for acyclovirresistant herpes lesions (3-7 days) Application site reactions, lesion recrudescence Trifluridine 1% topical agent used for acyclovirresistant herpes infections X 7-14 days Transient burning or stinging, palpebral edema, superficial punctuate, keratopathy, changes in intraocular pressure MMWR Recomm Rep 2015;64(No. RR-3):[1-137]. Predominant symptom is pruritus Sarcoptes scabiei Treatment Drug Permethrin 5% cream Dose and Duration Apply to all areas of the body from neck down and wash off in 8-14 hours Ivermectin 200 mcg/kg PO; repeat in 2 weeks MMWR Recomm Rep 2015;64(No. RR-3):[1-137]. Most common viral STI in the United States Over 100 subtypes characterized 30 types associated with genital tract lesions Types 6 and 11 associated with development of low- grade dysplasia manifested as exophytic genital warts Most warts will regress spontaneously within 1-2 years of initial appearance, but reinfection common in young, sexually active populations MMWR Recomm Rep 2015;64(No. RR-3):[1-137]. Infection with several HPV subtypes (e.g. HPV-16 and HPV-18) is considered the major risk factor for development of cervical neoplasia (2nd most common cancer in women worldwide) HPV infection alone is insufficient to cause cervical cancer development Pap smear is most cost-effective and frequently used diagnostic test for HPV MMWR Recomm Rep 2015;64(No. RR-3):[1-137]. Three HPV vaccines marketed in the United States Cervarix® (HPV2)-bivalent vaccine for HPV-16 and HPV-18 Gardasil® (HPV4)-quadrivalent vaccine for HPV-6, -11, -16, and - 18 Gardasil-9 (HPV9)-nine-valent vaccine for HPV 6, 11, 16, 18, 31, 33, 45, 52, 58 Vaccines are indicated for preventing cervical precancers and cervical cancer in females 11 or 12 through 26 years of age (but can be started as early as 9) HPV4 and HPV9 also indicated in males to prevent genital warts (HPV-6 and -9) and anal cancers (HPV-16 and-18) Centers for disease control and prevention. 06 Oct 2015 <http://www.cdc.gov/std> Trade name Cervarix Gardasil Gardasil 9 Synonym HPV2 HPV4 HPV9 Components 16, 18 6, 11, 16, 18 6, 11, 16, 18, 31, 33, 45, 52, 58 Females Males and females Males and females None None None Not contraindicated Not contraindicated Not contraindicated Recommended Recommended Recommended Monitoring 30 min 30 min 30 min Side effects Injection-site reactions, bruising, syncope Injection-site reactions, bruising, syncope Injection-site reactions, bruising, syncope Drug interactions Belimumab, fingolimod, immosuppressants Belimumab, fingolimod, immosuppressants Belimumab, fingolimod, immosuppressants Indications Preservative Immunosuppression HIV infection Females All vaccines are recommended in a 3-dose series for routine vaccination at age 11 or 12 years For those aged 13 through 26 years, if not previously vaccinated Males HPV4 and HPV9 are recommended in a 3-dose series for routine vaccination at age 11 or 12 years, and for those aged 13 through 21 years, if not previously vaccinated Males aged 22 through 26 years may be vaccinated HPV4 is recommended for MSM through age 26 years or those who did not get any or all doses when they were younger Centers for disease control and prevention. 9 Oct 2015 <http://www.cdc.gov/std> Vaccination is recommended for immunocompromised persons (including those with HIV infection) through age 26 years for those who did not get any or all doses when they were younger A complete series for all vaccines consists of 3 doses 2nd dose should be administered 1–2 months after the first dose 3rd dose should be administered 6 months after the first dose (at least 24 weeks after the first dose) HPV vaccines are not recommended for use in pregnant women Pregnancy testing is not needed before vaccination If a woman is found to be pregnant after initiating the vaccination series, no intervention is needed Remainder of the 3-dose series should be delayed until completion of pregnancy Centers for disease control and prevention. 9 Oct 2015 <http://www.cdc.gov/std> Cervical cancer Most common HPV-associated cancer Almost all cervical cancer is caused by HPV Vulvar cancer-~50% are linked to HPV Vaginal cancer-~65% are linked to HPV Penile cancer-~35% are linked to HPV Anal cancer-~95% are linked to HPV Oropharyngeal cancers Cancers of the back of the throat, including the base of the tongue and tonsils ~60% are linked to HPV Many of these cancers may be related to tobacco and alcohol use Centers for disease control and prevention. 9 Oct 2015 <http://www.cdc.gov/std> Infection Recommended regimen Nongonococcal urethritis/cervicitis Azithromycin 1 g PO X 1 dose Chancroid (Haemophilus ducreyi) Azithromycin 1 g PO X 1 dose OR Ceftriaxone 250 mg IM X 1 dose OR Ciprofloxacin 500 mg PO BID X 3 days OR Erythromycin 500 mg PO TID X 7 days Lymphogranuloma venereum (C. trachomatis) Doxycycline 100 mg PO BID X 21 days HPV infection (genital warts) Podofilox 0.5% solution or gel applied BID X 3 days, followed by 4 days of no therapy, cycle repeated as necessary up to 4 cycles OR Imiquimod 5% cream applied QHS 3 times weekly for up to 16 weeks .MMWR Recomm Rep 2015;64(No. RR-3):[1-137]. Zika can be passed through sex from a person who has Zika to his or her sex partners Sex includes vaginal, anal, oral sex, and the sharing of sex toys Zika can be passed through sex, even if the person does not have symptoms at the time It can be passed from a person with Zika before their symptoms start, while they have symptoms, and after their symptoms end Though not well documented, the virus may also be passed by a person who carries the virus but never develops symptoms Studies are underway to find out how long Zika stays in the semen and vaginal fluids of people who have Zika, and how long it can be passed to sex partners It is known that Zika can remain in semen longer than in other body fluids, including vaginal fluids, urine, and blood Zika and sexual transmission. Centers for disease control and prevention. Updated Sept 1, 2016. Accessed Sept 22, 2016. Condoms can reduce the chance of getting Zika from sex Condoms include male and female condoms Dental dams (latex or polyurethane sheets) may also be used for certain types of oral sex (mouth to vagina or mouth to anus) Condoms should be used from start to finish, every time during vaginal, anal, and oral sex Not sharing sex toys can also reduce the risk of spreading Zika to sex partners Not having sex eliminates the risk of getting Zika from sex Zika and sexual transmission. Centers for disease control and prevention. Updated Sept 1, 2016. Accessed Sept 22, 2016. WHO has released new guidelines for treating gonorrhea, syphilis, and chlamydia given their increasing resistance to treatment Gonorrhea treatment changes Quinolones are no longer recommended given the high prevalence of resistance Dual therapy is preferred over single therapy Health authorities should advise providers to prescribe the antibiotic that would be most effective, taking into account current local patterns of resistance Oropharyngeal treatment recommendations and guidance on retreatment after treatment failure are included Syphilis-new guidelines strongly recommend a dose of benzathine penicillin, which has been in short supply, over procaine penicillin Chlamydia WHO developed recommendations for treating pregnant women Recommendations for preventing and treating chlamydia ophthalmia neonatorum Growing antibiotic resistance forces updates to recommended treatment for sexually transmitted infections. World heath organization website. Updated Aug 30, 2016. Accessed Sept 22, 2016. https://npin.cdc.gov/KABIChronicles Several STIs may be encountered in clinical practice Open communication with patients is essential to successful care Variety of medications are available for treatment Therapy must be chosen through a patientcentered approach C. Brock Woodis, PharmD, BCACP, BCPS, CDE, BC-ADM, CPP Associate Professor Campbell University College of Pharmacy & Health Sciences Duke Family Medicine September 27, 2016 [email protected]