You are in: eMedicine Specialties > Obstetrics and Gynecology > Infections CervicitisArticle Last Updated: May 3, 2007AUTHOR AND EDITOR INFORMATIONAuthor: Anita B Varkey, MD, Assistant Professor, Department of Medicine, Loyola University Medical Center; Associate Program Director, Internal Medicine Residency; Medical Director, General Internal Medicine Clinic, Loyola Outpatient Center Anita B Varkey is a member of the following medical societies: American College of Physicians and Society of General Internal Medicine Coauthor(s): Sabrina R Kendrick, MD, FACP, Assistant Professor, Department of Internal Medicine, Rush University Medical Center; Director, Screening Clinic, The CORE Center; Consulting Staff, Division of Infectious Diseases, John H Stroger Hospital of Cook County Editors: Jeffrey B Garris, MD, Chief, Assistant Professor, Department of Obstetrics and Gynecology, Division of Urogynecology and Reconstructive Pelvic Surgery, Tulane University School of Medicine; Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine; A David Barnes, MD, PhD, MPH, FACOG, Consulting Staff, Department of Obstetrics and Gynecology, Mammoth Hospital, Mammoth Lakes, California, Pioneer Valley Hospital, Salt Lake City, Utah, Warren General Hospital, Warren, Pennsylvania and Mountain West Hospital, Tooele, Utah; Frederick B Gaupp, MD, Consulting Staff, Department of Family Practice, Hancock Medical Center; Michel E Rivlin, MD, Associate Professor, Coordinator, Quality Assurance/Quality Improvement, Department of Obstetrics and Gynecology, University of Mississippi School of Medicine Author and Editor Disclosure Synonyms and related keywords: cervicitis, female lower genital tract infections, mucopurulent cervicitis, sexually transmitted diseases, STDs, vulvovaginitis, Chlamydia trachomatis, Neisseria gonorrhoeae, Trichomonas vaginalis, human papillomavirus, HPV, herpes simplex virus, HSV, pelvic inflammatory disease, PID, infertility, ectopic pregnancy, spontaneous abortion, cervical cancer, preterm delivery, condylomata acuminata, Papanicolaou test, Pap smear INTRODUCTIONBackgroundCervicitis is an inflammation of the uterine cervix. Infectious cervicitis might be caused by Chlamydia trachomatis, Neisseria gonorrhoeae, Trichomonas vaginalis, herpes simplex virus (HSV), or human papillomavirus (HPV). Noninfectious cervicitis might be caused by local trauma, radiation, or malignancy. The infectious etiologies are significantly more common than the noninfectious causes, and all possible infectious causes of cervicitis are sexually transmitted diseases (STDs). This article focuses on the infectious etiologies of cervicitis. PathophysiologyBecause the female genital tract is contiguous from the vulva to the fallopian tubes, there is some overlap between vulvovaginitis and cervicitis. Vulvovaginitis and cervicitis are commonly categorized as lower genital tract infections. Infections involving the endometrium and fallopian tubes are commonly categorized as upper genital tract infections and are not discussed in this article. FrequencyUnited StatesThe Centers for Disease Control and Prevention (CDC) estimates that 19 million STD infections occur annually, almost half of them among those aged 15-24 years. In addition to potentially severe health consequences, STDs pose a tremendous economic burden, with direct medical costs as high as $15.5 billion in a single year. Trichomoniasis is the most common curable STD in young, sexually active women. An estimated 7.4 million new cases occur each year in women and men. In 2003, 877,478 chlamydial infections were reported to the CDC, up from 834,555 cases reported in 2002. Because many cases are not reported or even diagnosed, it is estimated that actually 2.8 million new cases of chlamydia occur each year. Gonorrhea is the second most commonly reported infectious disease in the United States, with 335,104 cases reported in 2003. Much like chlamydia, gonorrhea is believed to be underreported. An estimated 718,000 new infections occur each year. The annual rate of infection by HSV and HPV is difficult to estimate because the vast majority of initial infections are asymptomatic or unrecognized. In the United States, seroprevalence studies show that 22% of adults have HSV type 2 antibodies, and currently, it is believed that over 500,000 new cases of genital herpes occurs annually. Approximately 20 million people are currently infected with HPV. At least 50% of sexually active men and women acquire a genital HPV infection at some point in their lives. By age 50 years, at least 80% of women will have acquired genital HPV infection. About 6.2 million Americans get a new genital HPV infection each year. InternationalWorldwide, more than 400 million adults become infected with an STD every year. Four STDs that are spread primarily through sexual contact are completely curable—trichomoniasis, chlamydia, syphilis, and gonorrhea. These infections account for 333 million STD infections, or about 80% of the worldwide total. Approximately 9% of all persons aged 15-44 years in North America contract 1 of these STDs annually, but the rate rises to 25% in sub-Saharan Africa. Worldwide, over 170 million cases of trichomoniasis are reported each year. Infection rates have been reported as high as 67% in Mongolia in 1988, 40-60% in Africa, and 40% in indigenous Australians older than age 40. Chlamydia is the next most common STD with approximately 92 million cases a year. Prevalence of chlamydia varies enormously across the world. In the 1990s, rates amongst pregnant women in Europe ranged from 2.7% in Italy to 8.0% in Iceland, while studies in South America found rates of 1.9% amongst teenagers in Chile and 2.1% amongst pregnant women in Brazil. In Asia, rates among pregnant women tend to be much higher: up to 17% in India and 26% in rural Papua New Guinea. In Africa, studies amongst pregnant women have revealed rates from 6% in Tanzania to 13% in Cape Verde. HPV, HSV, and gonorrhea each account for roughly 20-60 million cases of STDs per year. The prevalence of HPV, a cause of cervical cancer, varies roughly 20-fold internationally. Among the countries evaluated, Spain had the lowest prevalence of HPV; only 1.4% of women in Spain tested positive for HPV. The highest prevalence of HPV was seen in sub-Saharan Africa; 26% of the women in Nigeria tested positive for HPV. South America tended to have rates that were in between those of Europe and sub-Saharan Africa, while rates in Asia varied widely (with the lowest rates in Hanoi, Vietnam, and the highest in India and Korea). In a variety of studies, the seroprevalence of HSV-2 is higher in the United States (13-40%) than in Europe (7-16%), and the highest is in Africa (30-40%). Studies of pregnant women in Africa have found rates for gonorrhea ranging from 0.02% in Gabon to 3.1% in Central African Republic and 7.8% in South Africa. In the Western Pacific in the 1990s, the highest prevalence rates (>3%) were in Cambodia and Papua New Guinea. Other areas such as China, Vietnam, and the Philippines had rates of 1% or less. Between 1995 and 1999, a significant increase in gonorrhea incidence occurred in Eastern Europe, with the highest rates in Estonia, Russia, and Belarus. Mortality/MorbidityComplications from untreated infectious cervicitis depend on the pathogen. Morbidity includes pelvic inflammatory disease (PID), infertility, ectopic pregnancy, spontaneous abortion, cervical cancer, premature rupture of membranes, and preterm delivery. Perinatal and neonatal infections can cause mental retardation, blindness, low birth weight, stillbirth, meningitis, and death. The social stigma is strong and might expose women to verbal, emotional, or physical abuse from others, particularly male partners. RaceNo racial predilection exists. Known risk factors include urban residence and low socioeconomic status. SexMale urethritis is more often symptomatic; therefore, diagnosis is usually made earlier in males than in females. Females with cervicitis are most often asymptomatic, so they do not seek evaluation or treatment as readily. AgeIndividuals younger than age 25 and single marital status are both risk factors for cervicitis. Both biological (eg, postulated immaturity of the female reproductive tract) and behavioral factors (eg, greater number of partners, low awareness of acquired immunodeficiency syndrome (AIDS) and other STDs, and limited use of protection against STDs) are thought to contribute to this risk. Routine screening of sexually active adolescents and young adults is therefore recommended. CLINICALHistory
PhysicalThe physical examination should include a general survey; external inspection; and pelvic speculum, and bimanual examinations. In certain patients, a rectal examination should be performed.
CausesAll of the infectious etiologies of cervicitis are STDs. Risk factors include multiple sex partners, young age, single marital status, urban residence, low socioeconomic status, and alcohol or drug use. DIFFERENTIALSAdnexal Tumors Benign Cervical Lesions Benign Lesions of the Ovaries Candidiasis Cervical Cancer Cervicitis Chancroid Chlamydial Genitourinary Infections Cystitis, Nonbacterial Ectopic Pregnancy Endometritis Gonococcal Infections Gynecologic Pain Herpes Simplex HIV Disease Human Herpesvirus Type 6 Human Papillomavirus Malignant Vulvar Lesions Missed Abortion Oophoritis Ovarian Cancer Ovarian Cysts Pyelonephritis, Acute Radiation Cystitis Rectovaginal Fistula Salpingitis Trichomoniasis Trigonitis Tuberculosis Tuberculosis of the Genitourinary System Urinary Tract Infection, Females Uterine Cancer Vaginitis Vulvovaginitis
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| Drug Name | Ceftriaxone (Rocephin) |
|---|---|
| Description | Third-generation cephalosporin with broad-spectrum, gram-negative activity; lower efficacy against gram-positive organisms; higher efficacy against resistant organisms. Arrests bacterial growth by binding to one or more penicillin-binding proteins. |
| Adult Dose | 125 mg IM once |
| Pediatric Dose | Administer as in adults |
| Contraindications | Documented hypersensitivity |
| Interactions | Probenecid may increase levels; coadministration with ethacrynic acid, furosemide, and/or aminoglycosides may increase nephrotoxicity |
| Pregnancy | B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals |
| Precautions | Partner must be treated; adjust dose in renal impairment; caution in breastfeeding women and allergy to penicillin; also treat for chlamydia because 20-40% of patients with gonorrhea are co-infected; partner(s) must also be treated |
| Drug Name | Cefixime (Suprax) |
|---|---|
| Description | Third-generation cephalosporin effective in treating gonorrhea. By binding to one or more of the penicillin-binding proteins, it arrests bacterial cell wall synthesis and inhibits bacterial growth. However, it is not available in pill form in the US. |
| Adult Dose | 400 mg PO once |
| Pediatric Dose | <45 kg: Not established >45 kg: Administer as in adults |
| Contraindications | Documented hypersensitivity |
| Interactions | Coadministration of aminoglycosides increase nephrotoxicity; probenecid may increase effects; false-positive Clinitest results |
| Pregnancy | C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus |
| Precautions | Partner must be treated; adjust dose in renal impairment; colitis may occur |
| Drug Name | Spectinomycin (Trobicin) |
|---|---|
| Description | Inhibits protein synthesis in bacterial cells. Site of action is 30S ribosomal subunit and is structurally different from related aminoglycosides. Use if allergic to penicillin and quinolones. Do not use if oropharyngeal gonorrhea is suspected. |
| Adult Dose | 2 g IM once |
| Pediatric Dose | <45 kg: 40 mg/kg IM once >45 kg: Administer as in adults |
| Contraindications | Documented hypersensitivity |
| Interactions | None reported |
| Pregnancy | B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals |
| Precautions | Partner must be treated; benzyl alcohol used as a diluent is associated with fatal gasping syndrome in infants |
| Drug Name | Azithromycin (Zithromax) |
|---|---|
| Description | Semisynthetic macrolide antibiotic effective in treating chlamydia. Treats mild-to-moderate microbial infections. |
| Adult Dose | 1 g PO once |
| Pediatric Dose | <6 months: Not established >6 months: Administer as in adults |
| Contraindications | Documented hypersensitivity; hepatic impairment; use of pimozide |
| Interactions | May increase toxicity of theophylline, warfarin, and digoxin; effects are reduced with coadministration of aluminum and/or magnesium antacids; nephrotoxicity and neurotoxicity may occur when coadministered with cyclosporine |
| Pregnancy | B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals |
| Precautions | Partner must be treated; if pregnant, use erythromycin; site reactions can occur with IV route; bacterial or fungal overgrowth may result with prolonged antibiotic use; may increase hepatic enzymes and cholestatic jaundice; caution in patients with impaired hepatic function, prolonged QT intervals, or pneumonia; caution in patients who are hospitalized, elderly, or debilitated |
| Drug Name | Doxycycline (Vibramycin) |
|---|---|
| Description | Long-acting tetracycline derived from oxytetracycline. Effective in treating chlamydia. Inhibits protein synthesis and thus bacterial growth by binding to 30S and possibly 50S ribosomal subunits of susceptible bacteria. |
| Adult Dose | 100 mg PO bid for 7 d |
| Pediatric Dose | <8 years: Not recommended >8 years: Administer as in adults |
| Contraindications | Documented hypersensitivity; children <8 y; severe hepatic impairment |
| Interactions | Bioavailability decreases with antacids containing aluminum, calcium, magnesium, iron, or bismuth subsalicylate; tetracyclines can increase hypoprothrombinemic effects of anticoagulants; tetracyclines can decrease effects of PO contraceptives, causing breakthrough bleeding and increased risk of pregnancy |
| Pregnancy | D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus |
| Precautions | Partner must be treated; if pregnant, use erythromycin; photosensitivity may occur with prolonged exposure to sunlight or tanning equipment; reduce dose in renal impairment; consider drug serum level determinations in prolonged therapy; tetracycline use during tooth development (ie, last half of pregnancy through age 8 y) can cause permanent discoloration of teeth; Fanconilike syndrome may occur with outdated tetracyclines |
| Drug Name | Erythromycin base (E-Mycin) |
|---|---|
| Description | Inhibits bacterial growth, possibly by blocking dissociation of peptidyl t-RNA from ribosomes, causing RNA-dependent protein synthesis to arrest. |
| Adult Dose | 500 mg PO bid for 7 d |
| Pediatric Dose | <12 years: Not established >12 years: Administer as in adults |
| Contraindications | Documented hypersensitivity; hepatic dysfunction; current use of pimozide |
| Interactions | Decrease clearance of alfentanil, bromocriptine, carbamazepine, cyclosporine, digoxin, disopyramide, ergot alkaloids, methylprednisolone, protease inhibitor, theophylline, and triazolam; increases anticoagulant effect of warfarin; decreases metabolism of vinblastine; serum levels increased by protease inhibitors, increased levels and rhabdomyolysis with use of lovastatin and simvastatin |
| Pregnancy | B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals |
| Precautions | Partner must be treated; estolate formulation may cause cholestatic jaundice; adverse GI effects are common (administer doses pc); discontinue use if nausea, vomiting, malaise, abdominal colic, or fever occur |
| Drug Name | Erythromycin ethylsuccinate (E.E.S.) |
|---|---|
| Description | Inhibits bacterial growth, possibly by blocking dissociation of peptidyl t-RNA from ribosomes, causing RNA-dependent protein synthesis to arrest. |
| Adult Dose | 800 mg PO qid for 7 d |
| Pediatric Dose | <12 years: Not established >12 years: Administer as in adults |
| Contraindications | Documented hypersensitivity; hepatic dysfunction; current use of pimozide |
| Interactions | Decrease clearance of alfentanil, bromocriptine, carbamazepine, cyclosporine, digoxin, disopyramide, ergot alkaloids, methylprednisolone, protease inhibitor, theophylline, and triazolam; increases anticoagulant effect of warfarin; decreases metabolism of vinblastine; serum levels increased by protease inhibitors, increased levels and rhabdomyolysis with use of lovastatin and simvastatin |
| Pregnancy | B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals |
| Precautions | Partner must be treated; caution in liver disease; discontinue if GI distress, malaise, or fever occurs |
| Drug Name | Metronidazole (Flagyl) |
|---|---|
| Description | Synthetic antibacterial and antiprotozoal agent. Only drug proven effective in treating T vaginalis infections. |
| Adult Dose | 2 g PO once; alternatively, 500 mg PO bid for 7 d |
| Pediatric Dose | <1 year: 10-30 mg/kg/d PO for 5-8 d <12 years: 15 mg/kg/d PO in 3 divided doses for 7-10 d >12 years: Administer as in adults |
| Contraindications | Documented hypersensitivity; controversy exists about treatment during first trimester (category D) despite no proof of harm, some suggest waiting until second trimester to treat using 2 g PO x 1 or 500 mg PO bid for 7 d |
| Interactions | Avoid alcohol for 7 d (disulfiramlike reaction); effect decreased by phenobarbital and phenytoin; increases PT with warfarin; increases toxicity/serum level of lithium; serum level increased by cimetidine |
| Pregnancy | B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals |
| Precautions | Partner must be treated; adjust dose in hepatic disease; monitor for seizures and development of peripheral neuropathy |
Nucleoside analogs are initially phosphorylated by viral thymidine kinase to eventually form a nucleoside triphosphate. These molecules inhibit HSV polymerase with 30-50 times the potency of human alpha-DNA polymerase.
| Drug Name | Acyclovir (Zovirax) |
|---|---|
| Description | Synthetic purine nucleoside analog indicated for genital HSV infections. First episode, begin treating within 6 d after appearance of first symptoms. If recurrent attack, begin treating during prodrome or within 1 d after onset of lesions. Suppression requires daily treatment for 1 y. |
| Adult Dose | First episode: 400 mg PO tid for 7-10 d; alternatively 200 mg PO 5 times qd for 7-10 d Recurrent attack: 200 mg PO 5 times qd for 5 d; alternatively 400 mg PO tid for 5 d or 800 mg PO bid for 5 d Suppression: 400 mg PO bid for 1 y |
| Pediatric Dose | First episode: 400 mg PO tid for 7-10 d; not to exceed 80 mg/kg/d Recurrent attack: 400 mg PO tid for 5 d; alternatively, 800 mg PO bid for 5 d; not to exceed 80 mg/kg/d >12 years: Administer as in adults |
| Contraindications | Documented hypersensitivity |
| Interactions | Probenecid and zidovudine increase adverse CNS effects |
| Pregnancy | C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus |
| Precautions | Register pregnant patients on acyclovir at 1-800-722-9292; caution in renal failure or coadministration of nephrotoxic drugs |
| Drug Name | Famciclovir (Famvir) |
|---|---|
| Description | Prodrug for penciclovir (active moiety) indicated for genital HSV infections. For first episode, begin treating within 6 d after appearance of first symptoms. For recurrent attack, begin treating during prodrome or within 1 d after onset of lesions. Suppression requires daily treatment for 1 y. |
| Adult Dose | First episode: 250 mg PO tid for 7-10 d Recurrent attack: 125 mg PO bid for 5 d Suppression: 250 mg PO bid for 1 y |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity |
| Interactions | Cimetidine and probenecid increase toxicity/serum level of penciclovir; increases digoxin level |
| Pregnancy | B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals |
| Precautions | Register pregnant patients at 1-800-722-9292; caution in renal failure or coadministration of nephrotoxic drugs |
| Drug Name | Valacyclovir (Valtrex) |
|---|---|
| Description | Indicated for genital HSV infections. For first episode, begin treating within 6 d after appearance of first symptoms. For recurrent attack, begin treating during prodrome or within 1 d after onset of lesions. Suppression requires daily treatment for 1 y. |
| Adult Dose | First episode: 1 g PO bid for 7-10 d Recurrent attack: 500 mg PO bid for 5 d Suppression: 1 g PO qd for 1 y; alternatively, 500 mg PO qd for 1 y or 250 mg PO bid for 1 y |
| Pediatric Dose | <12 years: Not established >12 years: Administer as in adults |
| Contraindications | Documented hypersensitivity |
| Interactions | Cimetidine/probenecid decrease conversion rate to acyclovir |
| Pregnancy | B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals |
| Precautions | Register pregnant patients at 1-800-722-9292; monitor patients who are immunocompromised for thrombotic thrombocytopenic purpura/hemolytic uremic syndrome; adjust dose in renal impairment |
Indicated for genital/perianal warts.
| Drug Name | Imiquimod (Aldara), Podofilox (Condylox), Trichloroacetic acid, 5-fluorouracil |
|---|---|
| Description | Topical products for genital/perianal warts. Available as 5% topical cream. Podofilox is available as a 0.5% solution. Trichloroacetic acid is available in an 80-90% solution. 5-fluorouracil is available in a 5% cream. |
| Adult Dose | Imiquimod: Apply to warts qhs 3 times/wk for up to 16 wk, rinse treatment area with soap and water 6-10 h after application Podofilox: Apply to warts bid for 3 d, no therapy for 4 d, then repeat up to 4 cycles Trichloroacetic acid: Apply to warts and powder with talc or sodium bicarbonate (baking soda) to remove unreacted acid; may repeat weekly 5-fluorouracil cream: Apply daily, may use an applicator for urethral warts |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity |
| Interactions | None reported |
| Pregnancy | C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus |
| Precautions | In pregnancy, most lesions may be treated postpartally; however, consideration may be given to using topical liquid nitrogen qwk or surgical treatments (eg, excision, electrocauterization, laser vaporization); avoid contact with genital mucous membranes; burning, pain, inflammation, erosion, and pruritus have occurred |
Article Last Updated: May 3, 2007