eMedicine Specialties > Obstetrics and Gynecology > Infections

Cervicitis: Treatment & Medication

Author: Arthur T Ollendorff, MD, Associate Professor of Clinical Obstetrics and Gynecology, Residency Program Director, Department of Obstetrics and Gynecology, University of Cincinnati College of Medicine; Chief of Gynecology, Veterans Affairs Medical Center, Cincinnati
Contributor Information and Disclosures

Updated: Aug 3, 2009

Treatment

Medical Care

Treatment of all causes of cervicitis is medical. Treatment must include the patient's sexual partners to prevent reinfection. Treatment for infectious causes of cervicitis can be done presumptively (treatment with azithromycin or doxycycline) or with specific antibiotic treatment once the etiology is known.

Activity

  • No sexual activity for 7 days after initiating treatment
  • No sexual activity until partner has been treated

Medication

Oral antibiotics effectively cure gonorrhea, chlamydia, and T vaginalis infections. Oral antivirals reduce duration of symptoms, lesions, and viral shedding in the first and recurrent episodes of genital herpes infections. Initially, topical therapy is used for symptomatic genital wart removal. Other options include intralesional injection and surgery.

In April 2007, the Centers for Disease Control and Prevention (CDC) updated treatment guidelines for gonococcal infection and associated conditions.5 Fluoroquinolone antibiotics are no longer recommended to treat gonorrhea in the United States. The recommendation was based on analysis of new data from the CDC’s Gonococcal Isolate Surveillance Project (GISP). The data from GISP showed the proportion of fluoroquinolone-resistant gonorrhea (QRNG) cases in heterosexual men reached 6.7%, an 11-fold increase from 0.6% in 2001. The data were published in the April 13, 2007 issue of the Morbidity and Mortality Weekly Report. This limits treatment of gonorrhea to drugs in the cephalosporin class (eg, ceftriaxone 125 mg IM once as a single dose). Fluoroquinolones may be an alternative treatment option for disseminated gonococcal infection if antimicrobial susceptibility can be documented.

For more information, see the CDC’s Antibiotic-Resistant Gonorrhea Web site or Updated Gonococcal treatment recommendations (April 2007).

Antibiotics

Therapy must be comprehensive and cover all likely pathogens in the context of this clinical setting.


Ceftriaxone (Rocephin)

First-line therapy for gonococcal cervicitis. 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

125 mg IM once

Pediatric

Administer as in adults

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(s) must be treated; adjust dose in renal impairment; caution in allergy to penicillin; if chlamydia testing results are not available, also treat for chlamydia because 20-40% of patients with gonorrhea are co-infected


Cefixime (Suprax)

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. This medication is once again available in the United States.

Adult

400 mg PO once

Pediatric

<45 kg: Not established
>45 kg: Administer as in adults

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


Spectinomycin (Trobicin)

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. Alternative regimen for treatment of gonorrhea. Do not use if oropharyngeal gonorrhea is suspected.

Adult

2 g IM once

Pediatric

<45 kg: 40 mg/kg IM once
>45 kg: Administer as in adults

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


Azithromycin (Zithromax)

First-line therapy for chlamydia cervicitis. Semisynthetic macrolide antibiotic effective in treating chlamydia. Treats mild-to-moderate microbial infections.

Adult

1 g PO once

Pediatric

<6 months: Not established
>6 months: Administer as in adults

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; use of pimozide

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Partner must be treated; 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


Doxycycline (Vibramycin)

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

100 mg PO bid for 7 d

Pediatric

<8 years: Not recommended
>8 years: Administer as in adults

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

Documented hypersensitivity; children <8 y; severe hepatic impairment

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


Erythromycin base (E-Mycin)

Inhibits bacterial growth, possibly by blocking dissociation of peptidyl t-RNA from ribosomes, causing RNA-dependent protein synthesis to arrest. Alternative therapy for chlamydia cervicitis.

Adult

500 mg PO bid for 7 d

Pediatric

<12 years: Not established
>12 years: Administer as in adults

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

Documented hypersensitivity; hepatic dysfunction; current use of pimozide

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


Erythromycin ethylsuccinate (E.E.S.)

Inhibits bacterial growth, possibly by blocking dissociation of peptidyl t-RNA from ribosomes, causing RNA-dependent protein synthesis to arrest. Alternative regimen for chlamydia cervicitis.

Adult

800 mg PO qid for 7 d

Pediatric

<12 years: Not established
>12 years: Administer as in adults

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

Documented hypersensitivity; hepatic dysfunction; current use of pimozide

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


Metronidazole (Flagyl)

Synthetic antibacterial and antiprotozoal agent. First-line therapy for T vaginalis infections.

Adult

2 g PO once; alternatively, 500 mg PO bid for 7 d

Pediatric

<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

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

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

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

Antivirals

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.


Acyclovir (Zovirax)

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

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

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

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


Famciclovir (Famvir)

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

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

Not established

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


Valacyclovir (Valtrex)

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

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

<12 years: Not established
>12 years: Administer as in adults

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

Topical skin products

Indicated for genital/perianal warts.


Imiquimod (Aldara)

Indicated for genital/perianal warts. Induces secretion of interferon alpha and other cytokines; mechanism of action are unknown. May be more effective in women than in men.

Adult

Apply to warts qhs 3 times/wk for up to 16 wk, rinse treatment area with soap and water 6-10 h after application

Pediatric

<12 years: Not established
>12 years: Administer as in adults

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


Podofilox (Condylox)

Topical antimitotic which can be chemically synthesized or purified from plant families Coniferae and Berberidaceae (eg, species of Juniperus and Podophyllum). Exact mechanism of action is unknown.

Adult

Apply bid for 3 d, no therapy for 4 d, then repeat up to 4 cycles

Pediatric

Not established

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

Avoid contact with eyes; if eye contact, immediately flush eye with copious quantities of water and seek medical advice; not for use on mucous membranes of genital area including urethra, rectum and vagina; do not exceed frequency of application or duration of usage


Fluorouracil (Carac, Efudex, Fluoroplex)

Cycle-specific agent that has activity as single agent and has for many years been combined with biochemical modulator leucovorin. Shown to be effective in adjuvant setting. Classic antimetabolite anticancer drug with chemical structure similar to endogenous intermediates or building blocks of DNA or RNA synthesis. 5-FU inhibits tumor cell growth through at least 3 different mechanisms that ultimately disrupt DNA synthesis or cellular viability. These effects depend on intracellular conversion of 5-FU into 5-FdUMP, 5-FUTP, and 5-FdUTP. 5-FdUMP inhibits thymidylate synthase (key enzyme in DNA synthesis). 5-FUTP is incorporated into RNA and interferes with RNA processing, and 5-FdUTP is incorporated into DNA, leading to cytotoxic DNA strandbreaks.

Adult

Apply daily, may use an applicator for urethral warts

Pediatric

Not established

Documented hypersensitivity; potentially serious infections

Pregnancy

D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus

Precautions

Inflammatory reactions may occur with use of occlusive dressings; porous gauze dressing may be applied for cosmetic reasons without increase in reaction; patients should expect inflammatory reaction with crusting


Trichloroacetic acid (Tri-Chlor)

Cauterizes skin, keratin, and other tissues. Although caustic, causes less local irritation and systemic toxicity than others in the same class. However, response is often incomplete and recurrence occurs frequently.

Adult

Apply to warts and powder with talc or sodium bicarbonate (baking soda) to remove unreacted acid; may repeat weekly

Pediatric

Not established

Documented hypersensitivity; not for use on premalignant or malignant lesions

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

External use only; restrict use to treatment areas only

Antiprotozoal

Alternative therapy for trichomonas infections.


Tinidazole (Fasigyn, Tindamax)

5-nitroimidazole derivative used for susceptible protozoal infections. Nitro group is reduced by cell extract of Trichomonas. The free nitro radical generated is thought to be responsible for antiprotozoal activity against T vaginalis. Indicated to treat trichomoniasis caused by T vaginalis in both males and females.

Adult

Individual and sexual partner: 2 g PO once with food

Pediatric

<3 years: Not established
>3 years: 50 mg/kg PO qd for 3 d with food, not to exceed 2 g/dose

Limited data exist; interaction information based on experience with other nitroimidazole derivatives (ie, metronidazole); may prolong PT when coadministered with warfarin; avoid alcoholic beverages and preparations containing ethanol or propylene glycol during and 3 d following administration (may cause disulfiramlike reaction); may increase serum levels of lithium, phenytoin, cyclosporine, tacrolimus, and fluorouracil; CYP450 inducers (eg, phenobarbital, rifampin, phenytoin) may increase elimination; CYP450 inhibitors (eg, cimetidine, ketoconazole) may decrease elimination; concurrent administration with cholestyramine may decrease oral bioavailability; oxytetracycline may antagonize effect

Documented hypersensitivity; first trimester of pregnancy; breastfeeding women (recommend interruption during therapy and for 3 d following last dose)

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

X - Contraindicated; benefit does not outweigh risk

Precautions

Caution in blood dyscrasias, organic neurological dysfunction, late trimesters of pregnancy, seizure disorders, and hepatic and renal impairment
Carcinogenicity has been observed in mice and rats treated chronically with metronidazole (another nitroimidazole), although not observed with tinidazole, use cautiously; may cause metallic/bitter taste, nausea, anorexia, vomiting, weakness, fatigue, dizziness, or headache; if administered on day of hemodialysis, administer additional dose equivalent to one-half of recommended dose following dialysis

More on Cervicitis

Overview: Cervicitis
Differential Diagnoses & Workup: Cervicitis
Treatment & Medication: Cervicitis
Follow-up: Cervicitis
References

References

  1. Centers for Disease Control and Prevention. Chlamydia screening among sexually active young females enrollees of health plans - United States, 2000-2007. MMWR Weekly. April 17, 2009;58(14):362-365. [Full Text].

  2. Clifford GM, Gallus S, Herrero R, Munoz N, Snijders PJ, Vaccarella S. Worldwide distribution of human papillomavirus types in cytologically normal women in the International Agency for Research on Cancer HPV prevalence surveys: a pooled analysis. Lancet. Sep 17-23 2005;366(9490):991-8. [Medline].

  3. Wright TC Jr, Schiffman M, Solomon D, Cox JT, Garcia F, Goldie S. Interim guidance for the use of human papillomavirus DNA testing as an adjunct to cervical cytology for screening. Obstet Gynecol. Feb 2004;103(2):304-9. [Medline].

  4. Goldie SJ, Kim JJ, Wright TC. Cost-effectiveness of human papillomavirus DNA testing for cervical cancer screening in women aged 30 years or more. Obstet Gynecol. Apr 2004;103(4):619-31. [Medline].

  5. 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].

  6. American College of Obstetricians and Gynecologists. Cervical Cytology and Screening. August 2003. ACOG Practice Bulletin.

  7. Anderson JR. Genital tract infections in women. Med Clin North Am. Nov 1995;79(6):1271-98. [Medline].

  8. 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].

  9. Griffith WF, Stuart GS, Gluck KL, Heartwell SF. Vaginal speculum lubrication and its effects on cervical cytology and microbiology. Contraception. Jul 2005;72(1):60-4. [Medline].

  10. Katz VL, Lentz GM, Lobo RA, Gershenson DM. Comprehensive Gynecology. 5th ed. Mosby; 2007:598-600.

  11. Low N, Cowan F. Genital chlamydial infection. Clin Evid. Jun 2003;(9):1721-8. [Medline][Full Text].

  12. Schiffman M, Khan MJ, Solomon D, Herrero R, Wacholder S, Hildesheim A. A study of the impact of adding HPV types to cervical cancer screening and triage tests. J Natl Cancer Inst. Jan 19 2005;97(2):147-50. [Medline].

  13. Sexually Transmitted Disease Surveillance 2007. Centers for Disease Control and Prevention; December 2008. [Full Text].

  14. Soper DE. Sexually transmitted disease & pelvic inflammatory disease. Primary Care of Women. 1995:339-347.

  15. World Health Organization. Sexually Transmitted Infections. October 2007. WHO Fact Sheet. [Full Text].

Further Reading

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

Contributor Information and Disclosures

Author

Arthur T Ollendorff, MD, Associate Professor of Clinical Obstetrics and Gynecology, Residency Program Director, Department of Obstetrics and Gynecology, University of Cincinnati College of Medicine; Chief of Gynecology, Veterans Affairs Medical Center, Cincinnati
Arthur T Ollendorff, MD is a member of the following medical societies: American College of Obstetricians and Gynecologists and American Public Health Association
Disclosure: Nothing to disclose.

Medical Editor

Jeffrey B Garris, MD, Chief, Assistant Professor, Department of Obstetrics and Gynecology, Division of Urogynecology and Reconstructive Pelvic Surgery, Tulane University School of Medicine
Jeffrey B Garris, MD is a member of the following medical societies: American College of Obstetricians and Gynecologists, American Institute of Ultrasound in Medicine, American Medical Association, American Urological Association, Association of Professors of Gynecology and Obstetrics, Louisiana State Medical Society, Royal Society of Medicine, and Sigma Xi
Disclosure: Nothing to disclose.

Pharmacy Editor

Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine
Disclosure: eMedicine Salary Employment

Managing Editor

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)
A David Barnes, MD, PhD, MPH, FACOG is a member of the following medical societies: American College of Forensic Examiners, American College of Obstetricians and Gynecologists, American Medical Association, Association of Military Surgeons of the US, and Utah Medical Association
Disclosure: Nothing to disclose.

CME Editor

Frederick B Gaupp, MD, Consulting Staff, Department of Family Practice, Hancock Medical Center
Frederick B Gaupp, MD is a member of the following medical societies: American Academy of Family Physicians
Disclosure: Nothing to disclose.

Chief Editor

Michel E Rivlin, MD, Professor, Coordinator of Quality Assurance/Quality Improvement, Department of Obstetrics and Gynecology, University of Mississippi School of Medicine
Michel E Rivlin, MD is a member of the following medical societies: American College of Obstetricians and Gynecologists, American Medical Association, Mississippi State Medical Association, and Royal College of Surgeons of Edinburgh
Disclosure: Nothing to disclose.

 
 
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