Despite various attempts by health care workers to reduce the morbidity and mortality of sexually transmitted diseases (STDs), more than 15 million persons acquire STDs each year in the United States.1 Family physicians play a critical role in efforts to prevent or, when prevention fails, to treat these infections. To assist in these endeavors, the Centers for Disease Control and Prevention (CDC)2 recently updated guidelines for the prevention and treatment of STDs.
Clinical Prevention Guidelines
Family physicians are in an excellent position to provide education and counseling on the prevention of STDs. Information should be individualized on the basis of the patient's stage of development and understanding of sexual issues.3 The information should be delivered with respect and compassion, and in a nonjudgmental manner.2 In addition to counseling patients who are being assessed for an STD, family physicians should address possible misconceptions about STD-protective behavior in adolescents and young adults. This type of counseling has been shown to reduce misconceptions, and it also may reduce the occurrence of risky sexual behaviors.4
A nonintensive systematic intervention performed in an outpatient setting (i.e., counseling during the physical examination or visit for refill of a contraceptive prescription) can be effective.5 Over the past 10 years, the use of condoms has increased among at-risk heterosexuals in the United States: this increase suggests that the message on STD prevention is being heard.6 However, to reduce the incidence of STDs, family physicians must continue providing education and counseling.
One of the most reliable methods of avoiding STD transmission is abstinence from sexual relations, including oral, vaginal, and anal sex.2 Education on abstinence can reduce risky sexual behaviors,7 particularly when information on sexual negotiation skills is included.8 Counseling about abstinence is crucial for patients who are receiving treatment for STDs or whose partners are undergoing treatment for STDs, and those who wish to avoid possible consequences of sexual intercourse, such as pregnancy or exposure to an STD.2
The other method for reducing the risk of STD exposure is to be in a long-term monogamous relationship with an uninfected partner. The CDC2 recommends that potential sexual partners be tested for STDs, including human immunodeficiency virus (HIV) infection, before they begin having sexual intercourse. If one of the partners is infected or the infection status is unknown, a new condom should be used for each action of insertive sexual intercourse.
|Education and counseling about safer sexual behaviors in persons at risk for STDs|
|Identification of asymptomatic persons with STDs, as well as symptomatic infected persons who are unlikely to seek diagnostic and treatment services|
|Effective diagnosis and treatment of persons with STDs|
|Evaluation, treatment, and counseling of sexual partners of persons with STDs|
|Preexposure immunizations for vaccine-preventable STDs in selected populations|
Preexposure vaccination is one of the most effective strategies for preventing the transmission of certain STDs. The CDC2 recommends that patients being evaluated for an STD receive a hepatitis B vaccine series if they were not immunized in the past. Vaccination is particularly important in adolescents, who generally do not consider themselves to be at risk for contracting hepatitis B.9 The CDC also recommends the administration of hepatitis A vaccine to illegal drug users and men who have sex with men.
Another preventive strategy is the screening of selected populations. The CDC currently recommends annual screening for chlamydial infection in all sexually active women 24 years of age and younger.2 [Evidence level C, consensus/expert guidelines] Screening is important even if these women are asymptomatic, because younger women are more susceptible to chlamydial infection than older women. Women older than 24 years should be screened if they are at risk for chlamydial infection (e.g., new sexual partner, history of multiple sexual partners).2
Nonoxynol 9 is a chemical compound that has been promoted as a potential aid in reducing the transmission of STDs. However, recent studies10,11 have found that this compound provides no protection against gonorrhea or chlamydial infection. In one study,12 the use of nonoxynol 9 actually increased the risk of contracting gonorrhea. Condoms lubricated with nonoxynol 9 have a short shelf life and cost more than other condoms; furthermore, their use may increase the risk of urinary tract infection.2 Because of these factors, the CDC2 recommends against using nonoxynol 9 or condoms lubricated with this compound for preventing the transmission of STDs.
Diseases Characterized by Urethritis and Cervicitis
The diagnosis and treatment of urethritis and cervicitis are discussed in detail in the CDC guidelines.2 New information includes the wider spread of quinolone resistance to Neisseria gonorrhoeae and the need for follow-up testing in women treated for chlamydial infection.
Since the last CDC recommendations were published, resistance to quinolones has spread to Hawaii and parts of the West Coast. Based on epidemiology, resistance to these drugs is believed to have originated in Asia and the Pacific region; the incidence of quinolone resistance has been high in these areas for some time. In Hawaii, quinolones are no longer recommended for the treatment of gonorrhea. The CDC2 suggests that, because of the increased prevalence of resistant N. gonorrhoeae, quinolone therapy is “inadvisable” in California as well.
Cephalosporins, specifically orally administered cefixime (Suprax) and intramuscularly administered ceftriaxone (Rocephin), are first-line agents for the treatment of gonococcal urethritis (Table 2).2 Ceftriaxone, which remains the agent of choice for other forms of gonococcal disease, is given intravenously to treat all serious or systemic infections.
|Disease||Preferred treatment||Alternative treatment|
|Uncomplicated gonorrhea||Cefixime (Suprax), 400 mg orally one time|
Ceftriaxone (Rocephin), 125 mg IM one time*
Ciprofloxacin (Cipro), 500 mg orally one time
Ofloxacin (Floxin), 400 mg orally one time
Levofloxacin (Levaquin), 250 mg orally one time
|Spectinomycin (Trobicin), 2 g IM one time|
|Ceftizoxime (Cefizox), 500 mg IM one time|
|Cefoxitin (Mefoxin), 2 g IM one time, plus probenecid, 1 g orally one time|
|Cefotaxime (Claforan), 500 mg IM one time|
|Gatifloxacin (Tequin), 400 mg orally one time|
|Norfloxacin (Noroxin), 800 mg orally one time|
|Lomefloxacin (Maxaquin), 400 mg orally one time|
|Chlamydial infection||Azithromycin (Zithromax), 1 g orally one time|
Doxycycline (Vibramycin), 100 mg orally twice daily for 7 days
|Erythromycin base, 500 mg orally four times daily for 7 days|
|Erythromycin ethylsuccinate (E.E.S.), 800 mg orally four times daily for 7 days|
|Ofloxacin, 300 mg orally twice daily for 7 days|
|Levofloxacin, 500 mg orally once daily for 7 days|
|Persistent urethritis||Metronidazole (Flagyl), 2 g orally one time, plus erythromycin base, 500 mg orally four times daily for 7 days, or erythromycin ethylsuccinate, 800 mg orally four times daily for 7 days|
Quinolones are safe and effective for treating nonresistant gonococcal infections. However, these drugs should be used with caution when an infection may have been acquired in or from Asia or the Pacific region. Ciprofloxacin (Cipro) and ofloxacin (Floxin) are options for the intravenous treatment of disseminated gonococcal infections and are given orally for the treatment of uncomplicated infections of the urethra, cervix, or rectum.2
Etiologic agents in nongonococcal urethritis include Chlamydia trachomatis, Mycoplasma genitalium, and Ureaplasma urealyticum. Rarely, nongonococcal urethritis is caused by Trichomonas vaginalis or herpes simplex virus (HSV).
The recommended treatment for non-gonococcal urethritis (e.g., chlamydial infection) is azithromycin (Zithromax) or doxycycline (Vibramycin). Alternatively, the infection can be treated with a seven-day course of erythromycin base or erythromycin ethylsuccinate (E.E.S), ofloxacin, or levofloxacin (Levaquin).2 The CDC encourages testing for C. trachomatis in all patients with urethritis and cervicitis, and recommends treatment of gonorrhea and chlamydial infection if empiric therapy is initiated before test results are known or when patients are likely to be lost to follow-up.2 [Evidence level C, consensus/expert guidelines]
Rarely, symptoms persist after routine therapy. Unfortunately, there is no proven effective treatment for persistent urethritis. Recommendations include repeating the initial therapy if the patient did not comply with the original treatment plan. If the patient was compliant, consideration can be given to swab testing for T. vaginalis and treatment with metronidazole (Flagyl) and erythromycin.
The updated CDC guidelines2 include follow-up strategies for use in women with chlamydial infection. Unless symptoms persist, testing for cure is unnecessary when a chlamydial infection is treated with azithromycin or doxycycline. If retesting is indicated, it should be delayed for more than three weeks after treatment is completed to reduce the possibility of a false-positive result.
The CDC2 notes that patients who have had a chlamydial infection are at high risk for reinfection. Therefore, all women with previous chlamydial infection should be retested three to four months after treatment. Regardless of whether their sexual partner has been treated, these women should be rescreened by no later than 12 months after the infection.2
Diseases Characterized by Genital Ulcers
HSV infection is the most common cause of genital ulcers in this country.13 Approximately 45 to 50 million Americans have genital herpes, and an estimated 1 million new cases occur each year.2,14 Primary infection occurs mostly in adolescents and young adults. Genital herpes is more common in women, blacks, and persons with multiple sexual partners.
Two HSV serotypes have been identified in humans. HSV-1 is the most common cause of oral herpes infection, and HSV-2 is the primary pathogen in sexually transmitted genital herpes. Both serotypes can be present at oral or genital sites.
HSV infection can be characterized by episodes of latency, with asymptomatic viral shedding, recurrent activation, and perinatal and sexual transmission.15 Along with most common genital ulcerative diseases, HSV infection increases the risk of HIV transmission and is believed to play an important role in the heterosexual spread of HIV.16
The diagnosis of genital herpes is best established by viral culture. In the updated guidelines, the CDC2 also recommends type-specific serologic testing to determine which HSV serotype has caused the genital infection. Knowing the HSV serotype is important in counseling patients about the potential for recurrent genital herpes, because recurrent episodes are less likely with the HSV-1 serotype than with the HSV-2 serotype. In addition, type-specific serologic tests may help confirm the diagnosis of genital herpes in patients with recurrent infection or with healing lesions, for which HSV culture results may be false-negative.
Diseases Characterized by Vaginal Discharge
Bacterial vaginosis, trichomoniasis, and candidiasis are the most common diseases associated with vaginal discharge. Patients with any of these diseases also may have vulvar itching or irritation and a vaginal odor.
|Acyclovir (Zovirax), 400 mg orally three times daily for 7 to 10 days, or 200 mg orally five times daily for 7 to 10 days|
|Famciclovir (Famvir), 250 mg orally three times daily for 7 to 10 days|
|Valacyclovir (Valtrex), 1 g orally twice daily for 7 to 10 days|
|Acyclovir, 400 mg orally three times daily for 5 days, or 200 mg orally five times daily for 5 days, or 800 mg orally twice daily for 5 days|
|Famciclovir, 125 mg orally twice daily for 5 days|
|Valacyclovir, 500 mg orally twice daily for 3 to 5 days, or 1 g orally once daily for 5 days|
|Acyclovir, 400 mg orally twice daily|
|Famciclovir, 250 mg orally twice daily|
|Valacyclovir, 500 mg orally once daily, or 1 g orally once daily|
Bacterial vaginosis is caused by the replacement of normal vaginal flora with an overgrowth of anaerobic microorganisms, Mycoplasma hominis, and Gardnerella vaginalis. This disease is the most frequent cause of vaginal discharge, but most affected women are asymptomatic.
The current controversy about bacterial vaginosis concerns screening for and treating this disease in pregnant women. The presence of bacterial vaginosis during pregnancy has been associated with premature rupture of membranes, preterm labor, preterm birth, chorioamnionitis, postpartum endometritis, and postcesarean section infection. However, routine screening for and treatment of bacterial vaginosis during the prenatal period have not been shown to reduce these adverse pregnancy outcomes.17–20 [References17 and18—Evidence level A, randomized controlled trials (RCTs); reference19—Evidence level A, meta-analysis; reference20—Evidence level A, systematic review of RCTs]
The CDC2 recommends screening for bacterial vaginosis in all symptomatic pregnant women, followed by treatment if indicated. Testing for bacterial vaginosis also may be performed in pregnant women who have a history of preterm labor, with treatment given if disease is present. However, the optimal treatment regimen for these patients has not been established.
Men with trichomoniasis tend to be asymptomatic, but infected women tend to have a diffuse, malodorous, yellow-green vaginal discharge that causes vulvar irritation. Trichomoniasis is diagnosed by the presence of moving flagellated organisms in vaginal secretions viewed under a microscope.
Topical agents administered vaginally do not provide adequate coverage for trichomoniasis. The recommended treatment for this infection is metronidazole, taken orally in a single 2-g dose. Alternatively, metronidazole can be administered in a dosage of 500 mg orally twice daily for seven days.2
|Uterine or adnexal tenderness|
|Cervical motion tenderness|
|Oral temperature >38.3°C (>101°F)|
|Abnormal cervical or vaginal mucopurulent discharge|
|Presence of white blood cells on saline microscopy of vaginal secretions|
|Laboratory documentation of cervical gonococcal or chlamydial infection|
|Elevated C-reactive protein level|
|Elevated erythrocyte sedimentation rate|
|Endometrial biopsy with histopathologic evidence of endometritis|
|Laparoscopic abnormalities consistent with PID|
|Transvaginal ultrasound or MRI study showing thickened, fluid-filled tubes, with or without free pelvic fluid or tubo-ovarian complex|
Vulvovaginal candidiasis usually presents as pruritus and vulvovaginal erythema. The diagnosis of this infection can be confirmed by finding budding yeast or hyphae under a microscope after a 10 percent potassium hydroxide solution has been added to vaginal secretions. Current treatment recommendations include a substantial number of over-the-counter (OTC) antifungal agents, as well as prescription fluconazole (Diflucan) taken orally in a single 150-mg dose.2
An important concern is that women frequently self-diagnose vulvovaginal candidiasis incorrectly.2,23 The CDC2 notes that unnecessary or inappropriate use of OTC antifungal agents can delay correct diagnosis and treatment of vulvovaginitis resulting from other causes. Hence, self-medication with antifungal agents should be done only for recurrence of symptoms in women who have been diagnosed with vulvovaginal candidiasis by a health care professional. Women who use OTC antifungal agents should be advised to seek medical care if their symptoms do not resolve or if their symptoms recur within two months after OTC antifungal treatment.
|Parenteral regimen A|
|Cefotetan (Cefotan), 2 g IV every 12 hours, or cefoxitin (Mefoxin), 2 g IV every 6 hours|
|Doxycycline (Vibramycin), 100 mg orally or IV every 12 hours|
|Parenteral regimen B|
|Clindamycin (Cleocin), 900 mg IV every 8 hours|
|Gentamicin, 2 mg per kg IV or IM (loading dose), followed by 1.5 mg per kg IM or IV every 8 hours (maintenance dosage; single daily dosing may be substituted)|
|Alternative parenteral regimens|
|Ofloxacin (Floxin), 400 mg IV every 12 hours, or levofloxacin (Levaquin), 500 mg IV once daily|
|with or without|
|Metronidazole (Flagyl), 500 mg IV every 8 hours, or ampicillinsulbactam (Unasyn), 3 g IV every 6 hours|
|Doxycycline, 100 mg orally or IV every 12 hours|
|Outpatient regimen A|
|Ofloxacin, 400 mg orally twice daily for 14 days, or levofloxacin, 500 mg orally once daily for 14 days|
|with or without|
|Metronidazole, 500 mg orally twice daily for 14 days|
|Outpatient regimen B|
|Ceftriaxone (Rocephin), 250 mg IM one time; or cefoxitin, 2 g IM, plus probenecid, I g orally administered concurrently; or other parenterally administered third-generation cephalosporin (e.g., ceftizoxime [Cefizox], cefotaxime [Claforan])|
|Doxycycline, 100 mg orally twice daily for 14 days|
|with or without|
|Metronidazole, 500 mg orally twice daily for 14 days|
PELVIC INFLAMMATORY DISEASE
Pelvic inflammatory disease (PID) encompasses a range of inflammatory disorders that affect the female upper genital tract. The most common causes are C. trachomatis and N. gonorrhoeae. Other possible causes include anaerobes, G. vaginalis, Haemophilus influenzae, enteric gram-negative rods, Streptococcus agalactiae, cytomegalovirus, M. hominis, and U. urealyticum.
The CDC has developed diagnostic criteria for PID (Table 4).2 The updated CDC guidelines2 state that to reduce morbidity from PID, empiric therapy should be initiated in patients who have uterine or adnexal tenderness or cervical motion tenderness (minimum diagnostic criteria), with treatment based on the individual patient's risk profile. In one recent study,24 adnexal tenderness was found to be the most sensitive diagnostic criterion. Additional criteria can be used to support the diagnosis of PID.2