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Vaginal infection: not a classic STI, but strongly associated with sexual activity Curable

Bacterial Vaginosis

Bacterial vaginosis, or BV, is the most common cause of unusual vaginal discharge. It is not a classic STI but an imbalance of the bacteria that naturally live in the vagina: when the protective Lactobacillus decline and other bacteria overgrow, the result can be a thin gray discharge with a fishy odor, though many people notice nothing at all. BV is linked to douching and to sexual activity, and left untreated it can raise the risk of catching STIs and cause problems in pregnancy. Here is what BV is, what causes the imbalance, and how it is treated.

Most common vaginal infection
#1
Among people aged 15–44 in the United States, more common than yeast infections or trichomoniasis
Estimated U.S. cases
21.2 million
Women aged 14–49 annually; prevalence ~29% (CDC/NHANES), millions unaware
Often symptomless
~84%
of people with BV have no symptoms at all, it is frequently discovered only on routine testing
Curable with antibiotics
Yes
70–80% cure at 1 week; recurrence within 12 months affects ~50%

Understanding bacterial vaginosis

What is bacterial vaginosis?

Bacterial vaginosis is not a single pathogen, it is a microbial imbalance. A healthy vagina is dominated by Lactobacillus bacteria (primarily L. crispatus and L. iners) that produce lactic acid and hydrogen peroxide, maintaining a protective acidic environment (pH ≤4.5). When this balance breaks down, too little Lactobacillus, overgrowth of anaerobes including Gardnerella vaginalis, Prevotella species, Mobiluncus species, Mycoplasma hominis, and Bacteroides, the result is BV: elevated vaginal pH, a thin gray-white discharge, and the signature fishy amine odor. BV is diagnosed clinically using Amsel criteria (three of four features: thin homogeneous discharge, pH >4.5, positive whiff test, clue cells on wet-mount) or by Nugent score (Gram-stained vaginal smear) or molecular NAAT panel.

BV is the most common vaginal condition in people aged 15–44. The CDC estimates approximately 21.2 million cases in U.S. women aged 14–49, with roughly 84% experiencing no symptoms at all, making BV the most common vaginal condition most people have never heard of. Prevalence is notably higher among Black women (~50%) and Hispanic women than among white women, a disparity consistently documented in NHANES surveys and attributed to structural healthcare access inequities rather than biology. BV is not classically a sexually transmitted infection, but it is strongly and consistently associated with sexual activity: people who have never had sex rarely develop BV, new sexual partners increase risk, and female-female partners show high concordance.

The clinical stakes go well beyond discomfort. Untreated BV raises susceptibility to HIV acquisition by an estimated 60%, and increases risk of acquiring herpes, gonorrhea, chlamydia, and HPV by compromising the mucosal barrier. BV during pregnancy is linked to preterm labor, premature rupture of membranes, low birth weight, and postpartum endometritis. It also increases risk of post-procedure pelvic infection when untreated before gynecologic procedures (IUD insertion, endometrial biopsy, elective abortion). The good news: a single antibiotic course, oral or vaginal metronidazole, or vaginal clindamycin, clears BV with 70–80% efficacy at one week.

Recurrence is BV's defining challenge. Approximately 50% of women who are successfully treated experience a recurrence within 6–12 months. Standard antibiotics suppress the overgrowth but do not reliably restore Lactobacillus dominance, and re-exposure to BV-associated bacteria from untreated partners can re-establish the imbalance rapidly. Extended suppressive therapy, twice-weekly metronidazole gel for 16 weeks after acute treatment, with or without vaginal boric acid, reduces recurrence frequency in women with frequent episodes. Treating female partners concurrently in same-sex relationships also reduces recurrence.

Symptoms

What are the symptoms of bacterial vaginosis?

Approximately 84% of people with bacterial vaginosis have no symptoms at all: the infection is discovered incidentally during a routine pelvic exam, STI panel, or prenatal screening, or is not discovered at all. Many people with BV are unaware they have it for months or years. When symptoms do appear, they typically include a change in discharge character and a fishy odor that becomes more pronounced after sex (when semen raises vaginal pH, volatilizing amines) or during menstruation. There is no fixed incubation period. BV develops as a microbiome shift, not after a defined exposure window.

Common symptoms when present

  • Thin, gray-white, off-white, or grayish-yellow vaginal discharge: often described as watery or milky, coating the vaginal walls evenly
  • A fishy or musty odor: strongest after sex, after using douches, or during menstruation; caused by amine production from anaerobic bacteria
  • Mild vaginal itching or irritation, typically less intense than in a yeast infection
  • Mild burning with urination (less common than in yeast infections or UTIs)

What BV typically does NOT cause, distinguishing from other conditions

  • Thick, clumpy white discharge: that pattern is characteristic of a yeast infection (candidiasis), not BV
  • Intense external itching, swelling, or vulvar redness, more typical of yeast or contact irritation
  • Frothy, yellow-green, or gray-green discharge, suggests trichomoniasis rather than BV
  • Sores, ulcers, blisters, or lesions: those point to herpes simplex or syphilis, not BV

Because BV, yeast infections, and trichomoniasis produce nearly identical symptoms, never self-treat on symptoms alone. A clinician visit or at-home vaginal NAAT panel is the only accurate diagnostic path, treating the wrong condition delays recovery and may mask a real STI.

Left untreated

Why bacterial vaginosis is worth catching early

Increased HIV and STI acquisition risk

BV's most serious systemic consequence is dramatically elevated susceptibility to HIV and other STIs. Active BV disrupts the protective acidic, Lactobacillus-rich vaginal environment that acts as a chemical barrier. People with BV are an estimated 60% more likely to acquire HIV from an HIV-positive partner and are at meaningfully higher risk for herpes simplex virus, gonorrhea, chlamydia, and HPV. Treating BV promptly is therefore not just vaginal health care, it is a meaningful HIV and STI prevention measure.

Pelvic inflammatory disease (PID)

BV-associated anaerobic bacteria can ascend through the cervix into the upper reproductive tract, contributing to or triggering PID: infection and inflammation of the uterus, fallopian tubes, and ovaries. PID can cause chronic pelvic pain, tubal scarring, and permanent tubal damage leading to infertility and ectopic pregnancy risk. Untreated BV before gynecologic procedures (IUD insertion, dilation, endometrial biopsy) particularly elevates post-procedure PID risk.

Pregnancy complications

BV during pregnancy is strongly associated with preterm labor (before 37 weeks), premature rupture of membranes, low birth weight, and postpartum endometritis. The BV-associated bacteria produce enzymes (mucinases, sialidases) that may weaken amniotic membranes and trigger inflammatory cascades involved in preterm labor. Symptomatic pregnant people are treated regardless of trimester. Vaginal clindamycin cream is avoided after 22 weeks (associated with adverse neonatal outcomes in some studies); oral metronidazole or oral clindamycin is preferred in later pregnancy.

Post-procedure pelvic infection

Untreated BV before gynecologic procedures, including IUD insertion, endometrial biopsy, hysteroscopy, and surgical abortion, significantly raises the risk of ascending infection and post-procedure PID. Pre-procedure screening and treatment of BV is standard practice in most gynecologic settings and dramatically reduces complication rates.

High recurrence rate

Approximately 50% of women successfully treated for BV experience a recurrence within 6–12 months, the most frustrating aspect of BV management. Standard antibiotics suppress overgrowth but do not reliably restore Lactobacillus dominance; if Lactobacillus does not re-establish quickly, the imbalanced state returns. Re-exposure from an untreated partner, continued douching, or individual microbiome predisposition all contribute. Extended suppressive metronidazole gel (twice weekly for 16 weeks after acute treatment) is the best-evidenced intervention for frequent recurrence.

Healthcare access disparity and delayed diagnosis

Black women have approximately 50% BV prevalence, roughly double the rate of white women, a disparity documented across multiple NHANES surveys. Because BV is often asymptomatic, people without routine gynecologic care access may have prolonged untreated infection, accumulating HIV/STI susceptibility and pregnancy-complication risk over time. Expanding access to at-home vaginal NAAT panels and telehealth prescription services directly addresses this gap.

Treatment

How is bacterial vaginosis treated?

BV is cured with antibiotics. CDC first-line regimens, metronidazole (oral or vaginal gel) and clindamycin (vaginal cream), achieve cure rates of 70–80% at one week. All three are equivalent in efficacy; choice depends on tolerability, pregnancy status, and preference. Recurrence within 6–12 months affects approximately 50% of successfully treated women, the main clinical challenge, and extended suppressive therapy reduces recurrence frequency in women with frequent episodes.

Treat partners

Routine treatment of male partners is not currently universally recommended by CDC guidelines, multiple earlier RCTs failed to show benefit. However, a well-designed 2021 randomized controlled trial (Muzny et al.) found that treating male partners with oral metronidazole plus topical penile-area clindamycin cream significantly reduced BV recurrence in female partners over 12 weeks, reopening the clinical debate. Female partners (in same-sex or bisexual relationships) should be evaluated and treated concurrently. Gardnerella and BV-associated bacteria are efficiently shared between female partners, and simultaneous treatment substantially reduces recurrence risk.

In pregnancy

BV in pregnancy is treated to reduce the risk of preterm birth, premature rupture of membranes, and other complications. Recommended regimens: Metronidazole 500 mg orally twice daily × 7 days (preferred), OR clindamycin 300 mg orally twice daily × 7 days. Metronidazole 0.75% vaginal gel is considered safe in pregnancy as well. Vaginal clindamycin cream 2% should be avoided after 22 weeks of gestation, some studies have shown adverse neonatal outcomes (prematurity); oral regimens are preferred in later pregnancy. Metronidazole (both oral and vaginal) is considered safe throughout all trimesters, including the first.

Re-test after treatment

Routine test of cure is not needed if symptoms resolve completely after finishing the full antibiotic course. Retest if symptoms return or persist after completing treatment. Given the high recurrence rate (~50% within a year), many clinicians schedule a follow-up assessment at 1–3 months for patients with a history of recurrent BV, allowing early identification and treatment of relapse before it becomes symptomatic.

Resistance note: Metronidazole resistance in BV-associated anaerobes is uncommon but increasing in some Gardnerella strains. If metronidazole treatment fails after completing the full course, clindamycin (oral or vaginal) is the standard step-up. For persistently recurrent BV not responding to metronidazole or clindamycin, boric acid vaginal suppositories (which lower vaginal pH directly and create a hostile environment for anaerobes regardless of antibiotic sensitivity) plus a lactobacillus-supportive approach represents the most evidence-based alternative.

Prevention

How to prevent bacterial vaginosis

  • Avoid douching, entirely

    Douching is the single most important avoidable BV trigger. It washes out protective Lactobacillus, alkalinizes the vaginal environment, and can precipitate a BV episode within days. No form of vaginal douching provides any health benefit, the vagina is self-cleaning through natural secretions. Only warm water on the external vulva is appropriate. Products marketed for 'vaginal freshness' (douches, wipes, sprays) uniformly disrupt vaginal flora and increase infection risk.

  • Use condoms consistently

    Consistent condom use is associated with lower BV risk across multiple studies: likely by reducing exposure to new microbial species introduced by partners, preventing the pH-raising effect of semen with each encounter, and reducing risk of STIs (which co-occur with BV at higher rates). Condoms are also the most effective available measure to reduce the STI-acquisition risk that active BV creates. Using condoms consistently protects against BV's downstream consequences even when it does not prevent every episode.

  • Treat BV promptly and complete the full antibiotic course

    Complete all prescribed medication, oral metronidazole for 7 days, or the full vaginal regimen, even if symptoms resolve early. Stopping antibiotic treatment early leaves residual anaerobic overgrowth that can quickly re-establish before Lactobacillus recovers, setting up rapid recurrence. Prompt treatment also reduces the window of elevated HIV and STI susceptibility that active BV creates.

  • Consider suppressive therapy for recurrent BV

    If BV recurs three or more times per year, discuss extended suppressive therapy with your clinician. The best-evidenced protocol is: (1) complete a standard 7-day antibiotic course for the acute episode; (2) follow immediately with boric acid 600 mg vaginal suppositories daily × 21 days; (3) then twice-weekly metronidazole 0.75% vaginal gel for 16 weeks. Clinical trial data support this approach for substantially reducing recurrence frequency. This is a clinician-guided regimen, not an OTC self-treatment plan.

  • Treat female partners concurrently in same-sex relationships

    Gardnerella vaginalis and other BV-associated bacteria are efficiently shared between female partners during sex, making re-exposure a key driver of recurrence in women who have sex with women. If you have a female partner, concurrent evaluation and treatment of both partners when BV is diagnosed significantly reduces recurrence. This is supported by clinical evidence and recommended by most STI specialists, though not yet formally incorporated into all major guideline documents.

  • Avoid scented vaginal products and unnecessary chemicals near the vulva

    Scented soaps, bubble baths, vaginal deodorants, feminine wipes, and antibacterial body washes applied to the vulva or vaginal opening can alter the vaginal microbiome in similar ways to douching. Use only plain warm water on the external vulva. Avoid synthetic, tight-fitting underwear that traps warmth and moisture, cotton underwear is preferable. These behavioral modifications reduce chronic low-grade microbiome disruption.

Who is most at risk

Who is most at risk for bacterial vaginosis?

New or multiple sexual partners
New sexual partners are among the strongest risk factors for developing BV. Each new partner may introduce previously unexposed microbial species that compete with or displace Lactobacillus. Semen is alkaline (pH ~7.2–8.0) and temporarily elevates vaginal pH with each sexual encounter, facilitating anaerobic growth. Women who have ever had sex have dramatically higher BV rates than those who have not, though BV can develop without sexual activity. Consistent condom use is associated with lower BV risk.
Women with multiple male partners have approximately 2–3× higher BV prevalence than those with one partner
Douching
Vaginal douching is one of the most consistently documented modifiable risk factors for BV across epidemiological studies. Douching washes out protective Lactobacillus species, alkalinizes the vaginal environment, and can trigger a BV episode within days of a single use. Despite being practiced by an estimated 20–40% of U.S. women, douching provides no hygienic benefit and actively harms the vaginal microbiome. It should be avoided completely. The vagina is self-cleaning; only warm water on the external vulva is needed.
Douching is associated with approximately 2× increased BV risk in multiple prospective studies
Black and Hispanic race/ethnicity, structural healthcare disparity
Black women have approximately 50% BV prevalence, roughly double that of white women, and Hispanic women also show higher rates than white women. This disparity is not explained by biology or individual behavior differences; research consistently attributes it to structural factors: reduced access to routine gynecologic care, fewer opportunities for timely diagnosis and treatment (leading to prolonged untreated BV episodes), documented health effects of chronic stress and racial discrimination on immune function and the microbiome (allostatic load), and systemic differences in healthcare quality. This is a healthcare equity issue, not a measure of inherent susceptibility.
BV prevalence among Black women aged 14–49: ~50% vs. ~23% in white women (NHANES)
IUD use and recent antibiotics
Intrauterine device (IUD) use, particularly the copper IUD, is associated with modestly higher BV rates, possibly due to increased vaginal discharge and altered local immune environment. Recent broad-spectrum antibiotic therapy (especially amoxicillin-clavulanate, fluoroquinolones, or clindamycin) depletes Lactobacillus alongside the target pathogen, transiently creating a microbiome vulnerability that can shift toward BV. Cigarette smoking also independently increases BV risk through mechanisms that may include immune modulation and altered vaginal secretions.

Stats & rates

How common is bacterial vaginosis in the U.S.?

BV is the most common vaginal condition in people aged 15–44. The CDC estimates 21.2 million cases in U.S. women aged 14–49 annually, based on NHANES population surveys (BV is not a nationally reportable condition, so surveillance relies on survey data rather than case counts). Roughly 84% of those with BV are asymptomatic. Prevalence is significantly higher in Black women (~50%) and Hispanic women than in white women (~23%): a structural healthcare disparity, not a biologic one. BV is also common in women who have sex with women, with high partner concordance. Despite its prevalence, BV remains underdiagnosed due to high asymptomatic rates and limited primary-care awareness.

21.20M
Estimated U.S. cases annually (women aged 14–49) (2020)
#1
most common vaginal infection in the United States, ages 15–44

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Good to Know

Bacterial Vaginosis FAQs

Common questions about bacterial vaginosis, answered.

Is BV a sexually transmitted infection?

Not in the classical sense. BV is a disruption of the vaginal microbiome, a shift away from protective Lactobacillus-dominant flora toward an overgrowth of anaerobic bacteria, rather than the direct acquisition of a specific pathogen from a partner. It can develop in people who have never had sex (though this is uncommon), and treating a partner does not always prevent recurrence in the index patient. That said, sexual activity, particularly new or multiple partners, is a strong and consistent risk factor, and female-female partners show high BV concordance. Think of BV as sexually influenced but not classically sexually transmitted.

What is the difference between BV and a yeast infection?

Both cause vaginal discomfort and discharge, but the clinical fingerprints are distinct. BV produces thin, watery gray-white discharge with a characteristic fishy odor (especially after sex or menstruation), mild itch at most, and elevated vaginal pH above 4.5. A yeast infection (VVC) produces thick, clumpy white cottage-cheese discharge, intense vulvar itch and burning, no odor or a mild yeasty scent, and normal vaginal pH at or below 4.5. Because treatments are completely different, antibiotics for BV, antifungals for yeast, a clinician visit or molecular vaginal panel is the only reliable way to distinguish them. Studies show that fewer than one-third of women who self-treat for a presumed yeast infection actually have one.

Why does BV cause a fishy smell, and why is it worse after sex?

The fishy odor of BV is produced by volatile amines, specifically trimethylamine, putrescine, and cadaverine, released by the anaerobic bacteria that proliferate when Lactobacillus populations decline. These amines become volatile and therefore detectable by smell only in an alkaline environment. Semen is significantly alkaline (pH ~7.2–8.0), so intercourse temporarily elevates vaginal pH and instantly intensifies amine volatilization, making the fishy odor noticeably stronger right after sex. Menstrual blood is also alkaline, explaining odor flares during periods. This chemistry is exploited in the clinical whiff test: adding potassium hydroxide (KOH) to a vaginal sample immediately releases and amplifies the amine odor, confirming BV.

Can men carry or spread BV?

Men don't develop BV themselves, they have no vaginal microbiome to disrupt, but they can harbor BV-associated bacteria (Gardnerella vaginalis and others) under the foreskin and in the urethra without symptoms. These bacteria can be reintroduced into the female partner's vaginal environment during sex, contributing to BV recurrence. A landmark 2021 randomized controlled trial (Muzny et al.) found that treating male partners with oral metronidazole plus penile-area clindamycin cream significantly reduced BV recurrence in female partners over 12 weeks, suggesting male carriage is a meaningful recurrence driver. Routine male partner treatment is not yet universally recommended in major guidelines, but clinicians increasingly discuss it for women with frequent recurrent BV.

Why does BV keep coming back?

Recurrence is the central frustration of BV management, approximately 50% of successfully treated women experience a return within 6–12 months. Leading explanations include: (1) Antibiotics suppress anaerobic overgrowth but do not restore Lactobacillus dominance: if protective flora doesn't re-establish quickly, the microbiome reverts. (2) Re-exposure to BV-associated bacteria from an untreated partner (male or female). (3) Continued douching or scented product use. (4) Individual microbiome predisposition, some women's vaginal microbiomes appear inherently less stable and prone to dysbiosis. (5) Unrecognized non-albicans species if the original diagnosis was uncertain. Extended suppressive therapy, boric acid 21 days then twice-weekly metronidazole gel 16 weeks, is the most evidence-based recurrence-reduction protocol available.

Can BV resolve on its own without treatment?

Occasionally, yes, mild BV can resolve spontaneously if the vaginal microbiome naturally rebalances. However, this is unpredictable and often takes weeks. During any period of untreated BV, you remain at substantially elevated risk for HIV and STI acquisition (~60% higher HIV risk), and in pregnancy, untreated BV can cause preterm labor. If you have symptoms, are pregnant, or are about to have a gynecologic procedure, do not wait it out, a short antibiotic course resolves it quickly and removes downstream risk. Given the high asymptomatic rate, getting tested is more valuable than watching and waiting.

Is BV dangerous during pregnancy?

Yes, BV during pregnancy is associated with preterm labor, premature rupture of membranes, low birth weight, and postpartum endometritis (uterine infection after delivery). BV-associated bacteria produce enzymes that degrade cervical mucus and amniotic membranes, potentially triggering inflammatory pathways involved in preterm labor. Symptomatic pregnant people are treated with antibiotics regardless of trimester. Oral metronidazole is considered safe throughout pregnancy, including the first trimester. Vaginal clindamycin cream is avoided after 22 weeks due to rare associations with adverse neonatal outcomes; oral clindamycin is used instead when metronidazole is not tolerated. If you notice any abnormal discharge or vaginal odor during pregnancy, contact your OB or midwife promptly.

Does boric acid help with BV?

Yes: boric acid 600 mg vaginal suppositories play an evidence-based role in recurrent BV management, primarily as an adjunct to (not replacement for) antibiotics. Boric acid lowers vaginal pH directly, creating an acidic environment that suppresses anaerobic growth and supports Lactobacillus reestablishment. A validated recurrence-reduction protocol uses boric acid daily for 21 days following completion of the acute antibiotic course, then twice-weekly metronidazole vaginal gel for 16 weeks, with clinical trial data supporting meaningful recurrence reduction. Boric acid alone does not adequately treat an active acute BV episode. It is also NOT safe during pregnancy (embryotoxic: do not use at any trimester), is for intravaginal use only (oral ingestion is toxic), and is not FDA-approved for BV but is recommended in several clinical guideline addenda. Use only pharmaceutical-grade vaginal suppositories, not DIY preparations.

How is BV diagnosed? (Amsel criteria and Nugent score explained)

BV is diagnosed by three main methods. Amsel criteria (standard in primary care): four signs assessed together: (1) thin, gray-white homogeneous discharge; (2) vaginal pH above 4.5; (3) a positive whiff test (fishy amine odor when potassium hydroxide is added to the sample); (4) clue cells on saline wet-mount microscopy (vaginal epithelial cells whose borders appear stippled and indistinct, coated with adherent bacteria). Three of four positive findings confirms BV. Nugent score (research standard): a Gram-stained vaginal smear scored 0–10 based on the balance of Lactobacillus versus anaerobic morphotypes; 7–10 = BV. Molecular NAAT panel (highest accuracy): detects BV-associated bacteria and Lactobacillus depletion pattern from a single swab; available at most private labs and as at-home kits, no pelvic exam required for self-collected swabs.

How is BV treated? What antibiotics are used?

BV is treated with antibiotics. The CDC's 2021 STI Treatment Guidelines recommend three equivalent first-line options: (1) Metronidazole 500 mg orally twice daily for 7 days, the most extensively studied regimen; avoid alcohol during and 24 hours after. (2) Metronidazole 0.75% vaginal gel, one applicator once daily for 5 days: equivalent efficacy, lower systemic absorption, fewer systemic side effects. (3) Clindamycin 2% vaginal cream, one applicator nightly for 7 days, alternative for metronidazole intolerance; note that clindamycin cream is oil-based and degrades latex condoms for 5 days after use. Alternative single-dose option: secnidazole 2 g granules orally. Cure rates at one week: 70–80% for all regimens. Complete the full course even if symptoms improve early. Recurrence affects ~50% within a year, ask your clinician about suppressive therapy if this is not your first episode.

Does BV increase my risk of getting HIV or another STI?

Yes, substantially. BV disrupts the acidic, Lactobacillus-rich environment that serves as the vagina's chemical barrier against pathogens. People with active BV are an estimated 60% more likely to acquire HIV from an HIV-positive partner, and are at meaningfully elevated risk for herpes simplex virus, gonorrhea, chlamydia, HPV, and trichomoniasis. The mechanism is twofold: elevated vaginal pH makes pathogens more viable, and depleted Lactobacillus eliminates natural hydrogen peroxide and lactic acid production that inhibits many STI pathogens directly. Treating BV promptly and staying current with STI screening substantially lowers this compounded risk.

Why is BV more common in Black and Hispanic women?

CDC and NHANES data consistently show BV prevalence approximately twice as high among Black women (~50%) compared to white women (~23%), with Hispanic women showing intermediate rates, a disparity that has been documented for over two decades. Research consistently attributes this to structural and social factors, not biological differences or individual behavior: unequal access to routine gynecologic care means BV goes undetected longer; reduced ability to access timely treatment means untreated episodes persist; chronic stress from structural racism and discrimination has documented effects on immune function and vaginal microbiome stability (allostatic load); and historical medical mistrust, rooted in documented ethical failures in U.S. medical history, reduces healthcare engagement. Expanding access to low-cost or free vaginal NAAT panels, telehealth prescription services, and at-home testing directly addresses this disparity.

Does douching cause BV, and what should I use to clean down there?

Yes: douching is one of the strongest documented risk factors for BV, associated with approximately double the BV risk in prospective studies. Douching washes out the protective Lactobacillus-dominant flora, raises vaginal pH, and strips the natural defense mechanisms that keep anaerobic bacteria in check, sometimes precipitating a BV episode within days of a single douche. The vagina is entirely self-cleaning through natural secretions that maintain its acidic, healthy microbiome without external intervention. For external hygiene: warm water on the outer vulva is all that is needed or beneficial. Scented soaps, feminine washes, bubble baths, and intimate sprays applied near the vaginal opening have similar disrupting effects and should be avoided.

Medically Reviewed · Updated

Reviewed by Dr. Grace Lin, MD, FACOG · OB-GYN

Obstetrician-gynecologist focused on reproductive and sexual health for women: pregnancy, BV, yeast, trichomoniasis and HPV/cervical screening. Our editorial guidelines →

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