Updated: Dec 8, 2008
Vaginitis (infection of the vagina) is the most common gynecologic condition encountered in the office. Vaginitis is defined as the spectrum of conditions that cause vulvovaginal symptoms such as itching, burning, irritation, and abnormal discharge.
The most common causes of vaginitis in symptomatic women are bacterial vaginosis (BV) (22-50%), vulvovaginal candidiasis (17-39%), and trichomoniasis (4-35%); yet, 7-72% of women with vaginitis may remain undiagnosed. Accurate diagnosis may be elusive and must be distinguished from other infectious and noninfectious causes.
For a related CME activity, see Screening Pregnant Women for Bacterial Vaginosis Not Recommended.
A complex and intricate balance of microorganisms maintains the normal vaginal flora. Important organisms include lactobacilli, corynebacteria, and yeast. Hormones further influence this microenvironment. A state of decreased estrogen, as occurs in prepuberty and postmenopause and following oophorectomy, can result in an altered risk of infection.
The normal postmenarchal and premenopausal vaginal pH is 3.8-4.2. At this pH, growth of pathogenic organisms usually is inhibited. Disturbance of the normal vaginal pH can alter the vaginal flora, leading to overgrowth of pathogens. Factors that alter vaginal environment include feminine hygiene products, contraceptives, vaginal medications, antibiotics, sexually transmitted diseases (STDs), sexual intercourse, and stress.
The worldwide prevalence of trichomoniasis is 174 million and accounts for 10-25% of vaginal infections.20
Recurrent vaginal infections can lead to chronic irritation, excoriation, and scarring. These, in turn, can lead to sexual dysfunction. Psychosocial and emotional stresses are not uncommon. In addition, chronic vaginal infection can facilitate the transmission of other STDs, including HIV. Complications of BV include endometritis, pelvic inflammatory disease (PID), and vaginal wound infections after gynecologic surgeries. In pregnancy, Trichomonas infection and BV are associated with increased risk of premature rupture of the membranes, preterm labor, low birth weight, and preterm delivery.
Vaginitis affects all races. The highest incidence of bacterial vaginosis is in African Americans (23%) and lowest in Asians (6%). The incidence is 9% in whites and 16% in Hispanics.19
All age groups are affected. The highest incidence is noted among young, sexually active women.
Patients with vaginitis almost always present with a chief complaint of abnormal vaginal discharge. A carefully documented history is essential in the diagnosis of vaginitis.
BV, vaginal candidiasis, and T vaginalis infection are thought to cause approximately 90% of all vaginal infections.
| Cervicitis | Ureaplasma Infection |
| Cystitis, Nonbacterial | Varicella-Zoster Virus |
| Cytomegalovirus | |
| Herpes Simplex | |
| Paget Disease |
Atrophic vaginitis
Cervical polyp
Contact dermatitis
Entamoeba histolytica
Excessive desquamation of normal vaginal epithelium
Foreign objects
Large cervical ectropion
Lichen sclerosis
Lichen simplex chronicus
Vaginal adenosis
Vaginal cancer
Vaginal intraepithelial neoplasia
Vaginal ulcers
Vaginal emphysematosa (multiple gas-filled cysts on the vaginal and cervical mucosa)
All women presenting with abnormal vaginal discharge should have a careful pelvic examination. Have patients take condition-specific tests, ie, colposcopy and cervical biopsies, for suspected cervical cancer.
T vaginalis infection can be confused with koilocytotic atypia, caused by the human papilloma virus, and may mimic findings of mild dysplasia. BV may produce inflammation and atypical squamous cells of undetermined significance (ASCUS) on Papanicolaou tests. Also, BV may be linked with cervical intraepithelial neoplasia (CIN).
T vaginalis infection
Bacterial vaginosis
Vaginal candidiasis
For resistant infections, consider an infectious disease consultation. Notification of the Centers for Disease Control and Prevention (CDC) may be warranted.
Acidophilus supplements in the diet may help prevent vaginitis, especially if patients are taking antibiotics.
Instruct patients to abstain from sexual activity and from douching until a diagnosis has been made. Patients also should abstain from unprotected sexual activity (sexual activity without proper male condom use) until the infection has been treated.
The goals of pharmacotherapy are to reduce morbidity, prevent complications, and eradicate the infection.
Metronidazole is the antimicrobial agent of choice to treat T vaginalis infections and bacterial vaginosis.
Causes chemical reduction reaction within anaerobic bacteria and sensitive protozoa. Readily absorbed and permeates all tissues, including cerebral spinal fluid, breast milk, and alveolar bone. Metabolized and excreted in liver and kidneys. Treatment of partners increases cure rates.
2 g PO as single dose (to treat trichomoniasis) or 500 mg PO bid for 7 d
Recurrence: 2 g PO qd for 3-5 d
15 mg/kg/d PO divided tid for 7 d; not to exceed adult dose
Possible increased toxicity with concurrent administration of cimetidine; may increase effects of anticoagulants; may increase toxicity of lithium and phenytoin; disulfiramlike reaction may occur with orally ingested ethanol; may cause psychosis with disulfiram; possible decreased effects with phenytoin and phenobarbital
Documented hypersensitivity; long-term blood dyscrasias
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Adjust dose in hepatic disease; monitor for seizures and development of peripheral neuropathy; may cause nausea, headaches, dry mouth or metallic taste in mouth, and reddish or dark-colored urine; rarely, vomiting, diarrhea, insomnia, weakness, dizziness, stomatitis, rash, urethral burning, vertigo, and paresthesias may occur; if pregnant, delaying use is recommended until after first trimester (however, no increased risk of congenital abnormalities, stillbirths, or low birth weight infants has been reported); try to avoid in breastfeeding women; the current STD guidelines published by the CDC recommend deferring use of metronidazole past the first trimester
Imidazole derivatives that exert a fungicidal effect by altering permeability of the fungal cell membrane. The mechanism of action also may involve alteration of RNA and DNA metabolism or an intracellular accumulation of peroxides toxic to fungal cell.
Damages fungal cell wall membrane by inhibiting biosynthesis of ergosterol. Membrane permeability is increased, causing nutrients to leak out, which results in fungal cell death. Metabolism occurs in the liver. Products available OTC are indicated. Recurrent infections usually are treated with intravaginal regimens for 10-14 d, followed by maintenance oral treatment for 6 mo. Dual Pak is not for use in children.
200-mg vaginal supp: Insert 1 qhs for 3 d
100-mg vaginal supp: Insert 1 qhs for 7 d
2% cream: Insert 1 applicator full (5 g) intravaginally qhs for 7 d
Monistat Dual Pak: 1200 mg vaginal insert once plus 2% cream for external use
Administer as in adults
May impair barrier contraceptives
Documented hypersensitivity
C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
If sensitivity or chemical irritation occurs, discontinue use; use only externally; avoid contact with eyes; adverse effects include vaginal burning, irritation, and dyspareunia
Broad-spectrum antifungal agent that inhibits yeast growth by altering cell membrane permeability, causing death of fungal cells.
100-mg tab: Insert 1 tab intravaginally qhs for 7 d or 2 tabs intravaginally for 3 d
500-mg tab: Insert 1 tab intravaginally once
1% cream: Insert 1 applicator full intravaginally qhs for 7-14 d
Children: Not established
Adolescents: Administer as in adults
May impair barrier contraceptives
Documented hypersensitivity
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Not for treatment of systemic fungal infections; avoid contact with the eyes; if irritation or sensitivity develops, discontinue use and institute appropriate therapy
Damages fungal cell wall membrane by inhibiting biosynthesis of ergosterol. Membrane permeability is increased, causing nutrients to leak out, which results in fungal cell death
0.4% cream: Insert 1 applicator full (5 g) intravaginally for 7 d
0.8% cream: Insert 1 applicator full (5 g) intravaginally qhs for 3 d
80-mg vaginal supp: Insert 1 qhs for 3 d
Not established
May impair barrier contraceptives
Documented hypersensitivity
C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
If sensitivity or chemical irritation occurs, discontinue use; use only externally; avoid contact with eyes; high doses may cause fever or flulike symptoms
Broad-spectrum antifungal agent that inhibits yeast growth by altering cell membrane permeability, causing death of fungal cells.
6.5% ointment: Insert 1 applicator full (5 g) intravaginally once
Not established
May impair barrier contraceptives
Documented hypersensitivity
C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
Avoid contact with eyes; if irritation or sensitivity develops, discontinue use
Broad-spectrum antifungal agent that inhibits yeast growth by altering cell membrane permeability, causing death of fungal cells.
2% cream: Insert 1 applicator full (5 g) intravaginally qhs for 3 d
Not established
May impair barrier contraceptives
Documented hypersensitivity
C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
Avoid contact with eyes; if irritation or sensitivity develops, discontinue use
Fungicidal and fungistatic antibiotic obtained from Streptomyces noursei. Effective against various yeasts and yeastlike fungi. Changes permeability of fungal cell membrane after binding to cell membrane sterols, causing cellular contents to leak.
100,000-U tab: Insert 1 tab intravaginally qd for 14 d
Administer as in adults
None reported
Documented hypersensitivity
C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
Do not use to treat systemic mycoses
Synthetic oral antifungal (broad-spectrum bistriazole) that selectively inhibits fungal cytochrome P-450 and sterol C-14 alpha demethylation.
150-mg tab PO as single dose
5 mg/kg PO as single dose; not to exceed 150 mg/d
Levels may increase with hydrochlorothiazides; fluconazole levels may decrease with chronic coadministration of rifampin; may increase concentrations of theophylline, phenytoin, tolbutamide, cyclosporine, glyburide, and glipizide; effects of anticoagulants may increase with fluconazole coadministration
Documented hypersensitivity; liver failure
C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
Monitor closely if rashes develop and discontinue drug if lesions progress; possible clinical hepatitis, cholestasis, and fulminant hepatic failure (including death) with underlying medical conditions (eg, AIDS, malignancy) and while taking multiple concomitant medications; not recommended for breastfeeding women; convenience and efficacy of the single-dose regimen should be weighed against the difficulties resulting from a higher incidence of adverse reactions reported with oral fluconazole versus intravaginal agents; causes nausea, vomiting, rashes, abdominal pain, headaches, and hepatic impairment
Imidazole broad-spectrum antifungal agent. Inhibits synthesis of ergosterol, causing cellular components to leak, which results in fungal cell death. Usually used for maintenance therapy for recurrent vulvovaginal candidiasis
100 mg (half of 200-mg tab) PO qd for up to 6 mo
<12 years: Not established
>12 years: Administer as in adults
Isoniazid may decrease bioavailability of ketoconazole; coadministration decreases effects of either rifampin or ketoconazole; may increase effect of anticoagulants; may increase toxicity of corticosteroids and cyclosporine (cyclosporine dosage can be adjusted); may decrease theophylline levels
Documented hypersensitivity; fungal meningitis
C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
Hepatotoxicity may occur; may reversibly decrease corticosteroid serum levels (adverse effects avoided with dose of 200-400 mg/d); administer antacid, anticholinergics, or H2-blockers at least 2 h after taking ketoconazole; may cause nausea, vomiting, rash, abdominal pain, headache, and elevation of serum transaminases; may lead to gynecomastia and decreased libido by inhibiting synthesis of adrenal steroids and androgens; starting maintenance ketoconazole therapy not recommended until culture confirms cause of vaginitis
Empiric antimicrobial therapy must be comprehensive and should cover all likely pathogens in the context of the clinical setting.
Lincosamide for treatment of serious skin and soft tissue staphylococcal infections. Also effective against aerobic and anaerobic streptococci (except enterococci). Inhibits bacterial growth, possibly by blocking dissociation of peptidyl tRNA from ribosomes, causing RNA-dependent protein synthesis to arrest. Widely distributes in the body without penetration of CNS. Protein bound and excreted by the liver and kidneys. For recurrent infections, administer a trial of alternative regimens. Used as an alternative treatment to metronidazole in pregnancy.
Insert 1 applicator full (5 g) intravaginally qhs for 7d
Alternatively, administer 300-mg tab PO bid for 7d
10-20 mg/kg/d PO divided tid for 7d; not to exceed adult dose
Increases duration of neuromuscular blockade induced by tubocurarine and pancuronium; erythromycin may antagonize effects of clindamycin; antidiarrheals may delay absorption of clindamycin
Documented hypersensitivity; regional enteritis; ulcerative colitis; hepatic impairment; antibiotic-associated colitis
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Adjust dose in severe hepatic dysfunction; no adjustment necessary in renal insufficiency; associated with severe and possibly fatal colitis (Clostridium difficile is causal organism and usually will resolve with vancomycin treatment); may cause nausea or rashes; occasionally, impaired liver function and neutropenia
Indicated for atrophic vaginitis resulting from diminished levels of circulating estrogens. A relative lack of estrogen also predisposes the vagina and vulva to infection.
Reserved for women experiencing vaginal changes secondary to a deficiency of estrogen.
Premarin: 0.625 mg topically or PO qd
Estrace 0.01% vaginal cream: 2-4 g intravaginally qd for 1-2 wk, then half the dose for 1-2 wk, then 1 g up to 3 times/wk as maintenance
Premarin vaginal cream: 2-4 g qd for 3 wk (with 1 wk off in between) for 3-6 mo
Dienestrol 0.01% cream: Insert 1-2 applicators full for 1-2 wk, then decrease dosage
Not established
May reduce hypoprothrombinemic effects of anticoagulants; levels may be reduced with coadministration of barbiturates, rifampin, and other agents that induce hepatic microsomal enzymes; an increase in corticosteroid levels may occur when administered concurrently with ethinyl estradiol; use of ethinyl estradiol with hydantoins may cause spotting, breakthrough bleeding, and pregnancy; increase in fluid retention caused by estrogen intake may reduce seizure control
Documented hypersensitivity; thrombophlebitis; undiagnosed vaginal bleeding; pregnancy
X - Contraindicated; benefit does not outweigh risk
Hepatic impairment, migraine, seizure disorders, cerebrovascular disorders, breast cancer, or thromboembolic disease
Boric acid can be used in the treatment of refractory, recurrent vaginal candidiasis.
Soothing to chafed skin, abrasions, burns, and other skin irritations. For recurrent infection, maintain treatment at qod initially, then decrease to 2 times per wk.
600 mg in a gelatin size 0 capsule intravaginally qd until culture results are negative (10-14 d)
Not recommended
Increases riboflavin excretion
Documented hypersensitivity; inflamed skin; pregnancy
X - Contraindicated; benefit does not outweigh risk
Excessive amount can lead to severe chemical vaginitis
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vaginitis, vaginal infection, Trichomonas vaginalis, vaginal candidiasis, Candida infection, bacterial vaginosis, BV, pelvic inflammatory disease, PID, yeast infection, vaginal pH
Hetal B Gor, MD, FACOG, Consulting Staff, Private Practice, Bergen County, New Jersey
Hetal B Gor, MD, FACOG is a member of the following medical societies: American College of Obstetricians and Gynecologists and Society of Laparoendoscopic Surgeons
Disclosure: Nothing to disclose.
Bruce A Meyer, MD, MBA, Vice President for Medical Affairs, Associate Dean for Health System Affairs and Director of the Faculty Practice Plan, Professor, Department of Obstetrics and Gynecology, University of Texas Southwestern Medical School
Bruce A Meyer, MD, MBA is a member of the following medical societies: American College of Obstetricians and Gynecologists, American College of Physician Executives, American Institute of Ultrasound in Medicine, Association of Professors of Gynecology and Obstetrics, Massachusetts Medical Society, Medical Group Management Association, and Society for Maternal-Fetal Medicine
Disclosure: Nothing to disclose.
Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine
Disclosure: Nothing to disclose.
Antonio V Sison, MD, Medical Director, Ob/Gyn Group, Robert Wood Johnson University Hospital at Hamilton
Antonio V Sison, MD is a member of the following medical societies: American College of Obstetricians and Gynecologists and Association of Professors of Gynecology and Obstetrics
Disclosure: Nothing to disclose.
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.
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.
The authors and editors of eMedicine gratefully acknowledge the contributions of previous author Phuong H Nguyen, MD and Susanne Ching, MD to the development and writing of this article.
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