Updated: Mar 6, 2008
Cervicitis is inflammation of the cervix. Patients usually present with cervical erythema and discharge.
Cervicitis is caused by a sexually transmitted bacterial infection. Infection of the cervix results in inflammation and may be accompanied by vulvovaginitis. Mucopurulent cervicitis is a clinical diagnosis, one typically characterized by friability of the cervix, mucopurulent discharge from the os, and increased numbers of polymorphs in endocervical secretions.1 An ascending infection can cause endometritis, salpingitis, tuboovarian abscess, or perihepatitis.
In the United States, the prevalence of chlamydial infection is 5-15% in sexually active teenagers and young adults, who are asymptomatic.2 The prevalence increases to almost 50% in symptomatic patients; however, the incidence of gonorrhea has declined steadily over the last 20 years.3 Adolescents and young adults continue to have the highest rates of infection, with a transmission risk of 20-50% per sexual contact. The incidence of co-infection with both gonorrheal and chlamydial organisms may be 15-20%.
Chlamydia trachomatis is the most prevalent bacterial pathogen that causes sexually transmitted infections worldwide. According to the World Health Organization (WHO), 50-70 million cases occur each year.
Primary morbidity results from ascending infection to the uterus and fallopian tubes (pelvic inflammatory disease) that leads to chronic abdominal pain and infertility.
Compared with older populations, sexually active adolescents and young adults have a higher incidence of both chlamydial and gonococcal cervicitis.
Elicit the patient's history of sexual activity, number of sexual partners, and type of contraception used (if any). An increased incidence of chlamydial cervicitis in women has been associated with use of oral (PO) contraceptives.
Upon physical examination, findings in the cervix include the following:
Child Abuse & Neglect: Sexual Abuse
Chlamydial Infections
Gonorrhea
Other causes of vaginal discharge
Physiologic leukorrheaAdvise patients to abstain from sexual activity until test results after therapy are negative and partners are treated. Advise them to use condoms when they resume sexual activity.
The Centers for Disease Control and Prevention (CDC) revised their treatment guidelines for sexually transmitted diseases in 2006.6 Therapy for cervicitis depends on the etiologic agent. Ceftriaxone is the recommended drug for gonorrhea; doxycycline is recommended for chlamydial cervicitis. Other effective antibiotics for treatment of gonorrheal disease include cefixime 400 mg. All are administered as single PO doses. For chlamydial infections, azithromycin 1 g PO as a single dose is an acceptable alternative to doxycycline 100 mg PO bid for 7 days.
Alternatives for patients presenting with ceftriaxone allergy include spectinomycin, ciprofloxacin, or norfloxacin. Fluoroquinolones are not approved by the US Food and Drug Administration (FDA) for use in children younger than 18 years and are no longer recommended for gonorrhea in the United States because of increased resistance. Erythromycin is recommended for patients with chlamydial infections who are unable to take doxycycline. A single dose of azithromycin 1 g PO is also highly effective for treatment of chlamydial disease. If a patient has clinical cervicitis, both ceftriaxone and azithromycin are recommended as empirical treatment. Acyclovir may be used for primary herpes infection, but it is not curative, and recurrences are common. Metronidazole is the drug of choice for infection by Trichomonas organisms.
Testing to determine the specific microorganism causing the infection is recommended because both chlamydial and gonococcal infections are reportable to state health departments. If diagnostic tools (eg, Gram stain, microscope) are unavailable, treat patients for both infections.
First choice for treatment for gonococcal cervicitis.
125 mg IM as single dose
Administer as adults
Concurrent use with furosemide or aminoglycosides may increase renal toxicity; decreases efficacy of PO contraceptives
Documented hypersensitivity; hyperbilirubinemic neonates
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Caution with history of penicillin allergy; mix with lidocaine 1% to decrease injection pain; reversible sonographic gallbladder anomalies reported
Treatment of choice for chlamydial cervicitis.
100 mg PO bid for 7 d
<8 years: Contraindicated
>8 years: Administer as in adults
Bioavailability decreases with antacids containing aluminum, calcium, magnesium, iron, or bismuth subsalicylate (administer doxycycline 1 h before or 2 h after); tetracyclines can increase hypoprothrombinemic effects of anticoagulants; tetracyclines can decrease effects of PO contraceptives, causing breakthrough bleeding and increasing risk of pregnancy; barbiturates, rifampin, phenytoin, or carbamazepine induce metabolism of doxycycline; milk or dairy products, calcium, and iron may decrease doxycycline absorption; administer 1 h before or 2-3 h after milk, dairy products, or iron ingested
Documented hypersensitivity; severe hepatic dysfunction; pregnancy
D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus
May cause photosensitivity (avoid prolonged exposure to sunlight or tanning equipment); associated with retardation of skeletal development in infants; use during tooth development (last half of pregnancy through age 8 y) can permanently discolor teeth
Synthetic antimicrobial agent active against most obligate anaerobes. Used in Trichomonas infection.
2 g PO as single dose
15 mg/kg/d PO divided q8h for 7 d; not to exceed 1 g/d
May increase toxicity of anticoagulants, lithium, and phenytoin; cimetidine may increase toxicity of metronidazole; disulfiram reaction may occur with PO ingested ethanol
Documented hypersensitivity; first trimester of pregnancy
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Pregnancy category X in first trimester; caution in breastfeeding and later stages of pregnancy; adjust dose in patients with hepatic disease; monitor for seizures and development of peripheral neuropathy; blood dyscrasias have been reported rarely
Macrolide antibiotic for treatment of C trachomatis infection.
1 g PO as single dose 1 h ac or 2 h pc
10 mg/kg PO as single dose; not to exceed 1 g/dose
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
Documented hypersensitivity; hepatic impairment; do not administer with pimozide
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Caution with hepatic dysfunction
Effective PO for treating gonococcal cervicitis. Arrests bacterial cell-wall synthesis and inhibits bacterial growth by binding to one or more penicillin-binding protein.
400 mg PO as single dose
<45 kg: 8 mg/kg PO as single dose
>45 kg: Administer as in adults
Coadministration of aminoglycosides increases nephrotoxicity; probenecid may increase effects of cefixime
Documented hypersensitivity
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Adjust dose in severe renal insufficiency (high doses may cause CNS toxicity); superinfections and promotion of nonsusceptible organisms may occur with prolonged use or repeated therapy; cross sensitivity exists with penicillins; administer with food to minimize adverse GI effects
Inhibits protein synthesis in bacterial cells. Site of action is 30S ribosomal subunit and structurally different from related aminoglycosides. Alternative antimicrobial in to treat urethral, endocervical, or rectal gonococcal infections in patients who cannot take cephalosporins or fluoroquinolones. Can be administered to pregnant women allergic to cephalosporins.
2 g IM as single dose
<45 kg and cannot tolerate ceftriaxone: 40 mg/kg IM as single dose; not to exceed 2 g/dose
>45 kg and cannot tolerate ceftriaxone: Administer as in adults
None reported
Documented hypersensitivity
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Benzyl alcohol used as diluent associated with fatal gasping syndrome in infants; antibiotics may mask or delay symptoms of incubating syphilis; perform serologic testing for syphilis in all patients with gonorrhea at time of diagnosis followed by additional testing after 3 mo; monitor clinical effects to detect resistance by N gonorrhea
Marrazzo JM. Mucopurulent cervicitis: no longer ignored, but still misunderstood. Infect Dis Clin North Am. Jun 2005;19(2):333-49, viii. [Medline].
Darville T. Chlamydia. Pediatr Rev. Mar 1998;19(3):85-91. [Medline].
Darville T. Gonorrhea. Pediatr Rev. Apr 1999;20(4):125-8. [Medline].
Simpson T, Oh MK. Urethritis and cervicitis in adolescents. Adolesc Med Clin. Jun 2004;15(2):253-71. [Medline].
Smith KR, Ching S, Lee H, et al. Evaluation of ligase chain reaction for use with urine for identification of Neisseria gonorrhoeae in females attending a sexually transmitted disease clinic. J Clin Microbiol. Feb 1995;33(2):455-7. [Medline].
CDC, Workowski KA, Berman SM. Sexually transmitted diseases treatment guidelines, 2006. MMWR Recomm Rep. Aug 4 2006;55(RR-11):1-94. [Medline]. [Full Text].
CDC. Update to CDC's sexually transmitted diseases treatment guidelines, 2006: fluoroquinolones no longer recommended for treatment of gonococcal infections. MMWR Morb Mortal Wkly Rep. Apr 13 2007;56(14):332-6. [Medline]. [Full Text].
Sexually transmitted diseases: gonorrhea, Chlamydia trachomatis, pelvic inflammatory disease and syphilis. In: Emans SJ, Laufer MR, Goldstein DP, et al, eds. Pediatric and Adolescent Gynecology. 4th ed. Philadelphia, PA: Lippincott-Raven; 1998:457-504.
Rome ES. Sexually transmitted diseases: testing and treating. Adolesc Med. Jun 1999;10(2):231-41, vi. [Medline].
Stuart GS, Castano PM. Sexually transmitted infections and contraceptives: selective issues. Obstet Gynecol Clin North Am. 30(4):795-808. [Medline].
cervicitis, cervix, gonococcal cervicitis, chlamydial cervicitis, vaginal discharge, sexually transmitted disease, STD, cervical infection, cervical inflammation, cervical erythema, vulvovaginitis, endometritis, salpingitis, tubo-ovarian abscess, perihepatitis, gonorrhea, Neisseria gonorrhea, Chlamydia trachomatis, C trachomatis, Neisseria gonorrhea, N gonorrhea vaginal bleeding, PID, pelvic inflammatory disease
Latha Chandran, MD, MPH, Associate Professor of Pediatrics, Associate Dean for Academic Affairs, Director, Division of General Pediatrics, State University of New York at Stony Brook School of Medicine
Latha Chandran, MD, MPH is a member of the following medical societies: American Academy of Pediatrics
Disclosure: Nothing to disclose.
Elizabeth Alderman, MD, Director of Fellowship Training Program, Director, Adolescent Ambulatory Service, Clinical Professor, Department of Pediatrics, Division of Adolescent Medicine, Albert Einstein College of Medicine and Montefiore Medical Center
Elizabeth Alderman, MD is a member of the following medical societies: Ambulatory Pediatric Association, American Academy of Pediatrics, North American Society for Pediatric and Adolescent Gynecology, and Society for Adolescent Medicine
Disclosure: Nothing to disclose.
Mary L Windle, PharmD, Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy, Pharmacy Editor, eMedicine.com, Inc
Disclosure: Pfizer Inc Stock Investment from broker recommendation; Avanir Pharma Stock Investment from broker recommendation
Wayne Wolfram, MD, MPH, Clinical Associate Professor, Departments of Pediatrics, Children's Hospital and University of Cincinnati
Wayne Wolfram, MD, MPH is a member of the following medical societies: American Academy of Emergency Medicine, American Academy of Pediatrics, and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.
Paul D Petry, DO, FACOP, FAAP, Consulting Staff, Freeman Pediatric Care, Freeman Health System
Paul D Petry, DO, FACOP, FAAP is a member of the following medical societies: American Academy of Osteopathy, American Academy of Pediatrics, American College of Osteopathic Pediatricians, and American Osteopathic Association
Disclosure: Nothing to disclose.
Maureen Strafford, MD, Arnold P Gold Foundation Associate Professor, Departments of Anesthesiology and Pediatrics, Tufts University and Tufts-New England Medical Center
Maureen Strafford, MD is a member of the following medical societies: American Medical Women's Association, American Pain Society, American Society of Anesthesiologists, International Anesthesia Research Society, Society for Education in Anesthesia, Society for Pediatric Anesthesia, and Society of Cardiovascular Anesthesiologists
Disclosure: Nothing to disclose.
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