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75 Vaginitis
75 Vaginitis
Basics 4
Definition 4
Epidemiology 4
Aetiology 4
Pathophysiology 5
Prevention 6
Primary prevention 6
Screening 6
Secondary prevention 6
Diagnosis 7
Case history 7
Step-by-step diagnostic approach 7
Risk factors 9
History & examination factors 10
Diagnostic tests 12
Differential diagnosis 13
Diagnostic criteria 14
Treatment 16
Follow up 32
Recommendations 32
Complications 33
Prognosis 33
Guidelines 34
Diagnostic guidelines 34
Treatment guidelines 35
Evidence scores 37
References 39
Images 43
Disclaimer 45
Summary
◊ Bacterial vaginosis continues to be a leading cause of vaginitis; other common infectious causes include
trichomoniasis and candidiasis, although non-infectious causes are also possible.
◊ Affects all age groups of women, particularly during their reproductive years. Black women are most commonly
affected.
◊ Sexual partners of patients with Trichomonas vaginalis should be treated and offered screening for other STDs.
Vaginitis Basics
Definition
Vaginitis is inflammation of the vagina due to changes in the composition of the vaginal micro-environment from infection,
BASICS
irritants, or from hormonal deficiency (e.g., atrophic vaginitis). Bacterial vaginosis, trichomoniasis, and candidiasis are
types of infections that cause vaginitis.
Epidemiology
Vaginitis is the most common gynaecological diagnosis in the primary care setting.[2] Women presenting with vaginal
discharge account for approximately 10 million office visits each year. In approximately 90% of affected patients in the
US, this condition develops secondary to bacterial vaginosis, candidiasis, or trichomoniasis, of which bacterial vaginosis
is the most common.[3] The incidence of Trichomonas has decreased dramatically in the US during the past 15 years,
partially due to the use of metronidazole.[3] However, global data suggest that trichomoniasis is the most common
sexually transmitted infection worldwide.[4]
The incidence of vulvovaginal candidiasis has increased during the past decade, particularly the non-albicans Candida
strains.[5] In Graz, Austria, non-albicans candida was detected in 12.1% of samples from women diagnosed with vulvovaginal
candidiasis between 2000 and 2004.[6]
Black women report higher incidence of candidiasis infections compared with white women.[7]
A study of pregnant women in Havana, Cuba, revealed a prevalence of 42.3% for candidiasis and 9.84% for trichomoniasis.[8]
In Hanoi, Vietnam, the prevalence of lower genital tract infections in women, most of whom were married and sexually
monogamous, attending maternal and child health and family planning clinics was the following: Candida, 11.1%;
Trichomonas vaginalis, 1.3%; Chlamydia trachomatis, 4.4%; bacterial vaginosis, 3.5%.[9]
Atrophic vaginitis may affect up to 40% of postmenopausal women, but very few seek medical care.[10] [11]
Aetiology
An overgrowth of bacterial organisms such as Gardnerella vaginalis, Mobiluncus species, Mycoplasma hominis, Escherichia
coli, group B streptococci, and Peptostreptococcus species are proven to be the main cause of bacterial vaginosis.[12]
Candida albicans, the second-most common cause of vaginitis, is the principal yeast responsible for vulvovaginal candidiasis.
Species that are more resistant to treatment, like Candida glabrata and Candida tropicalis, are known to be aetiological
factors.
Trichomonas vaginalis, a highly transmissible flagellated protozoan, is associated with vaginitis. The micro-organism can
be identified in up to 80% of male partners.[13] [14]
Atrophic vaginitis occurs due to declining oestrogen levels, predominantly in women who are postmenopausal. In addition,
the micro-environment in the vagina is supported by the presence of oestrogen. In premenopausal women, atrophy is
rare, but may be due to interference with ovarian production of oestrogen: for example, anti-oestrogen medication or
surgery.[10] [11]
Situations that alter the vaginal environment, such as douching, poor or excessive hygiene, antibiotics, certain soaps,
tobacco, tampons, contraceptive devices, and HIV, will increase the chances of acquiring the condition.[1] [15]
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Vaginitis Basics
Pathophysiology
Altering the vaginal pH leads to overgrowth of normal micro-organisms present in the vagina. Hydrogen-peroxide producing
BASICS
lactobacilli are important in preventing overgrowth of the anaerobes normally present in the vaginal flora. During the
reproductive years, the normal pH of the vagina is 3.8 to 4.2; as long as this low pH is maintained, no overgrowth can
occur.
In postmenopausal women, declining estrogen levels lead to vaginal atrophy. The vaginal mucosa becomes thinner and
drier, less elastic and more prone to inflammation.
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Vaginitis Prevention
Primary prevention
Avoiding douching and irritants such as strong soaps or bubble baths can help prevent vaginitis. Male condoms may help
prevent spread of infection. Lactobacillus acidophilus supplements in the diet may help to prevent recurrence of infectious
vaginitis.[23]
Screening
Bacterial vaginosis
Bacterial vaginosis is known to increase the risk of pregnancy complications (for example, preterm premature rapture of
membranes, preterm birth) but the evidence does currently not support routine screening for bacterial vaginosis in
asymptomatic pregnant women.[12] [30] There is insufficient evidence to assess the trade-off between benefits and
harms of screening asymptomatic pregnant women at high risk of preterm delivery.
Although bacterial vaginosis occurs more commonly in women with female sexual partners, routine screening for bacterial
vaginosis is currently not recommended for this population.[12]
PREVENTION
Trichomonas
Screening for Trichomonas vaginalis should be considered in women at high risk for infection (i.e., women who have new
or multiple partners, have a history of STDs, exchange sex for payment, or use injection drugs).[12]
Although Trichomonas vaginalis infection is known to increase the risk of pregnancy complications (for example, preterm
premature rapture of membranes, preterm birth), the evidence does currently not support routine screening in
asymptomatic pregnant women at low risk of infection.[12]
Secondary prevention
In bacterial vaginosis, treatment of sexual partners is not recommended.6[B]Evidence
Patients who have bacterial vaginosis or trichomoniasis, and who are also HIV-positive, should receive the same treatment
regimen as those who are HIV-negative.[12]
Sexual partners of patients with Trichomonas vaginalis should be treated and offered screening for other STDs. Patients
should avoid sex until they and their sexual partners are cured, or should at least use condoms.
Vulvovaginal candidiasis is not usually acquired through sexual intercourse; treatment of sexual partners is not
recommended, but should be considered in women who have recurrent infection. If a male sexual partner presents with
symptoms (e.g., irritation), these may be managed with topical agents.[12]
Bacterial vaginosis and candidiasis are not typically sexually transmitted; however, they may occur concomitantly with
STDs (e.g., gonorrhoea and chlamydial infections) and therefore it is recommended to screen for STDs in all patients with
infective vaginitis.
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Vaginitis Diagnosis
Case history
Case history #1
A 25-year-old white woman presents with a malodorous vaginal discharge and pruritus for the last 15 days. She reports
the smell is worse after intercourse and the discharge is white. She is in a stable monogamous relationship and has
never been pregnant. She denies any significant medical or gynaecological history. She reports this is the first time
she has had these symptoms and is worried about STDs. Physical examination shows a white discharge in the posterior
vaginal fornix, but there is no vaginal erythema or bleeding.
Case history #2
A 46-year-old black woman presents with complaints of white vaginal discharge, dyspareunia, pruritus, and vulvar
burning, especially when she urinates. She reports the vaginal discharge looks like cottage cheese and has no odour.
She has a 10-year history of diabetes mellitus type 2, which is treated with metformin; she denies any other medical
history. She has not had similar symptoms in the past. On physical examination, the vaginal walls are covered by white
plaques with the appearance of cottage cheese. Upon detaching them from the base, an erythematous area is left.
Hyphae and budding yeast are noted on the wet mount. There is also an erythematous area in the upper third of the
vulva, near the urethra. There is no other abnormal finding on the physical examination.
Other presentations
Patients with atrophic vaginitis present postmenopause with symptoms of dryness, dyspareunia, vaginal spotting,
and, less commonly, dysuria. Atrophic vaginitis may occur in non-menopausal women with a history of chemotherapy,
radiotherapy, or oophorectomy.
Irritant or allergic vaginitis presents with similar symptoms of vulvodynia, dyspareunia, or pruritus, with or without a
history of atopy. Patients may report douching, and/or a recent change in soaps, contraceptive devices, tampons,
and medications.[1]
DIAGNOSIS
Step-by-step diagnostic approach
Diagnosis is based on clinical findings, and confirmed with vaginal samples. Patients frequently self-diagnose vaginitis
and treat with over-the-counter medications.
Sexual partners of patients with Trichomonas vaginalis should be offered screening for other STDs. Bacterial vaginosis
and candidiasis are not typically sexually transmitted; however, they may occur concomitantly with STDs (e.g., gonorrhoea
and chlamydial infections) and therefore it is recommended to screen for STDs in all patients with infective vaginitis.
History
Precipitating factors for vaginitis include douching, poor or excessive hygiene, and antibiotic, IUD, or OCP use. In
addition, a history of recent change in feminine hygiene products and/or soaps, or use of latex condoms or diaphragms,
may be suggestive of irritant or allergic vaginitis. Infective vaginitis is more common during the reproductive years,
whereas the menopause predisposes to atrophic vaginitis. Vulvovaginal candidiasis is more frequently seen in black
women, and women with diabetes or HIV. Weaker risk factors include smoking, more frequent intercourse, and
pregnancy.
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Vaginitis Diagnosis
The history should assess the entire spectrum of vaginal symptoms, including change in discharge, vaginal malodour,
itching, dyspareunia, and dysuria. Questions about the location of symptoms (vulva, vagina, and anus), duration, the
response to prior treatment including self-treatment and douching, and a sexual history regarding number of sexual
partners and prior sexually transmitted infections can yield important insights into the likely aetiology.[24]
Atrophic vaginitis is suggested by a history of dyspareunia, dryness, and dysuria in a postmenopausal woman and is
diagnosed clinically. Patients with vulvovaginal candidiasis often report a white, thick discharge like cottage cheese
that is odourless, whereas women with bacterial vaginosis report a malodorous, white discharge, which is often more
noticeable following sexual intercourse. In trichomoniasis, a sexually transmitted infection, the discharge is described
as green, yellow, or white; frothy; and odorous.
Vaginal bleeding may occur from cervicitis in trichomoniasis; rarely it is also related to vaginal dryness in atrophic
vaginitis.
Fever and abdominal pain are very rare presenting symptoms and are usually associated with comorbid STDs.
Irritant or allergic vaginitis is typically diagnosed clinically, and examination may demonstrate erythema with or without
oedema.[25]
Atrophic vaginitis is typically diagnosed clinically based on history and evidence of atrophy on examination (decreased
elasticity; dryness; friable, pale, shiny epithelium).
Candidiasis is typically diagnosed clinically with evidence of erythema and a thick, white, cottage cheese-like discharge
adherent to lateral vaginal walls, but may be confirmed by 10% potassium hydroxide (KOH) wet mount preparation
or culture.
If bacterial vaginosis or trichomoniasis is suspected, vaginal samples for vaginal pH, amine ('whiff') test, saline, and
KOH microscopy (wet mount) aid diagnosis, together with clinical findings. [Fig-1]
DIAGNOSIS
The pH and amine testing can be performed either through direct measurement or by colorimetric testing. It is
important that the swab for pH evaluations be obtained from the mid-portion of the vaginal side wall to avoid false
elevations in pH results caused by cervical mucus, blood, semen, or other products.[24]
Depending on institution preference, bacterial vaginosis may be diagnosed by vaginal Gram stain (Nugent criteria) or
by the presence of at least 3 Amsel criteria:[26] [27]
• Vaginal pH >4.5
• 'Whiff' test
• Clue cells (vaginal epithelial cells with distinctive stippled appearance in saline wet mount by being covered
with bacteria)[Fig-4]
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Vaginitis Diagnosis
In trichomoniasis, the wet mount reveals numerous WBCs and motile protozoa.[Fig-3] On inspection, the cervix may
have a punctate and papilliform appearance (strawberry cervix).
Laboratory tests
If the diagnosis is still uncertain, vaginal cultures or polymerase chain reaction tests for trichomoniasis or yeast may
be warranted for infections that are resistant to treatment. These techniques are not carried out routinely.
A Gram stain of vaginal secretions for Nugent scoring of the bacterial flora identifies patients with bacterial vaginosis.[27]
Other available tests for diagnosis include rapid tests for enzyme activity from bacterial vaginosis-associated
organisms.[12] [24] [28] [29]
STD testing is recommended in patients with recurrent infections and/or those who are at risk of exposure to STDs
(e.g., unprotected intercourse), and should include tests for gonorrhoea, chlamydia, syphilis, and HIV.[12] Bacterial
vaginosis and candidiasis are not typically sexually transmitted; however, they may occur concomitantly with STDs
(e.g., gonorrhoea and chlamydial infections) and therefore it is recommended to screen for STDs in all patients with
infective vaginitis.
Risk factors
Strong
douching
• May alter the flora micro-environment of the vagina, due to changes in pH.[1]
antibiotic use
• Recent course of antibiotics may precipitate vaginitis, especially candidiasis. Results in a misbalance in vaginal
DIAGNOSIS
flora.[16]
HIV infection
• Immunosuppression, particularly low CD4 count and high HIV viral load, is associated with vulvovaginal
candidiasis.[17]
diabetes
• There is a direct correlation between hyperglycaemia and incidence of vaginitis, particularly caused by Candida
albicans.[18]
black women
• Vulvovaginal candidiasis may be more common in this population. Unclear reason for race predilection.
IUD
• May alter the flora micro-environment of the vagina.[19]
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Vaginitis Diagnosis
OCP use
• Alters the hormonal balance and, therefore, the flora of the micro-environment. Associated with increased risk of
vulvovaginal candidiasis infection.
latex condom/diaphragm
• Allergic vaginitis may present in women allergic to latex.
reproductive age
• Infective vaginitis is more common in these women.
menopause
• Reduced oestrogen levels alter elasticity and pH of vagina, predisposing to atrophic vaginitis.[10]
Weak
tobacco
• Possible changes in vaginal pH; weak evidence.[20]
pregnancy
• Increases oestrogen levels, possibly altering the vaginal flora. The evidence for this association is weak.[22]
dysuria (common)
• Associated with candidiasis and trichomoniasis. Also associated with atrophic vaginitis.
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Vaginitis Diagnosis
pruritus (common)
• Associated with bacterial vaginosis, candidiasis, and trichomoniasis.
• Also a common complaint in allergic or irritant causes of vaginitis.
vulvodynia (common)
• A common complaint in women with allergic or irritant vaginitis.
dyspareunia (common)
• Commonly associated with atrophic vaginitis and candidiasis.
• A general presenting symptom for most types of vaginitis.
erythema (common)
• Commonly present in candidiasis and allergic or irritant vaginitis.
DIAGNOSIS
friable epithelium (common)
• May be noted on insertion of speculum in women with atrophic vaginitis.
fever (uncommon)
• Very uncommon; not necessarily indicative of severity.
• Possibly more common with trichomoniasis since it is related to other STDs.
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Vaginitis Diagnosis
Diagnostic tests
1st test to order
Test Result
vaginal pH elevated/normal
• The normal vaginal pH in women of childbearing age is 4.5.
• In postmenopausal women, the vaginal pH is generally in the 6.0 to 7.0 range.
• Elevated pH is seen in bacterial infections, including trichomoniasis, and in
atrophic vaginitis.
• Generally, Candida infections will present with a normal range pH.
amine 'whiff' test of vaginal secretions positive in bacterial vaginosis
• The presence of volatile amines (fishy odour) is not encountered in normal
vaginal fluids.
• The presence of a fishy odour following addition of 10% potassium hydroxide
(KOH) to the vaginal sample indicates a positive result for bacterial vaginosis.
wet mount microscopy of vaginal secretions identification of bacteria and
• Vaginal samples added to two different slides, one with saline solution and one yeast infections
with KOH solution.
• Bacterial vaginosis: clue cells (vaginal epithelial cells with distinctive stippled
appearance by being covered with bacteria) are present and are seen as vaginal
epithelial cells covered with many rods and cocci, with a granular
appearance.[Fig-4] The numbers of lactobacilli are decreased and WBCs are
absent.
• Candidiasis: hyphae and budding yeast are better seen with the KOH preparation
microscopy.[Fig-2]
• Trichomoniasis: a significant number of WBCs and epithelial cells are observed.
The parasite is a motile oval or fusiform-shaped protozoan 15 micrometres
long.[Fig-3]
Gram stain of vaginal secretions Lactobacillus morphotype
reduced or absent
• Scored in accordance to Nugent classification, which involves counting the
DIAGNOSIS
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Vaginitis Diagnosis
Test Result
VDRL may be positive
• Routine to exclude syphilis.
• Recommended in patients with recurrent infections and/or those who are at
risk of exposure to STDs (e.g., unprotected intercourse).
• Bacterial vaginosis and candidiasis are not typically sexually transmitted;
however, they may occur concomitantly with STDs (e.g., gonorrhoea and
chlamydial infections) and therefore it is recommended to screen for STDs in
all patients with infective vaginitis.
serum rapid plasma regain (RPR) test may be positive
• Routine to exclude syphilis.
• Recommended in patients with recurrent infections and/or those who are at
risk of exposure to STDs (e.g., unprotected intercourse).
• Bacterial vaginosis and candidiasis are not typically sexually transmitted;
however, they may occur concomitantly with STDs (e.g., gonorrhoea and
chlamydial infections) and therefore it is recommended to screen for STDs in
all patients with infective vaginitis.
Test Result
culture of vaginal secretions positive for
• Trichomoniasis results take approximately 3 days. Although this is the most trichomoniasis/candidiasis
specific and sensitive test for trichomoniasis, wet mount preparation remains infections
the first-line test as it is quicker.
• May aid diagnosis in treatment-resistant cases of Candida and trichomoniasis.
PCR for trichomoniasis on vaginal secretions positive if trichomoniasis
• PCR targeting the beta-tubulin genes of Trichomonas vaginalis.[28]
rapid enzyme tests of vaginal secretions positive for
trichomoniasis/bacterial
• Antitrichomonal IgA antibody in the vaginal secretions by micro-ELISA
DIAGNOSIS
vaginosis associated with
technique.[29]
Gardnerella vaginalis
• Detects proline iminopeptidase from Gardnerella vaginalis.[12]
Differential diagnosis
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Vaginitis Diagnosis
Other causes of vaginal • Vaginal discharge may be • Papanicolaou smear: positive for
discharge physiological, and is typically cervical cancer.
odorous, mucousy, and • CT of abdomen or pelvis with
white-to-yellowish. oral/IV contrast: demonstrates
• Other less common pathological malignancy.
causes include desquamative • Vaginal wall biopsy: features of
inflammatory vaginitis (associated acute and chronic desquamative
with purulent and copious inflammation.
discharge), pelvic irradiation,
fallopian tube cancer (palpable
pelvic mass and vaginal bleeding),
and cervical cancer (late-stage
disease may present with watery
or foul-smelling vaginal discharge
most likely from necrotic mass).
DIAGNOSIS
Diagnostic criteria
• Vaginal pH >4.5
• Whiff test
• Clue cells (vaginal epithelial cells with distinctive stippled appearance in saline wet mount by being covered with
bacteria)
Nugent criteria[27]
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Vaginitis Diagnosis
Vaginal Gram stain of the bacterial flora may help to identify patients with bacterial vaginosis. The Nugent score is derived
from an estimation of the different proportions of bacterial morphotypes present, to give a score between 0 and 10:
• <4 normal
• 4 to 6 intermediate
DIAGNOSIS
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Vaginitis Treatment
Bacterial vaginosis
Treatment is indicated in all symptomatic women with bacterial vaginosis.[12] Although bacterial vaginosis is known
to increase the risk of certain pregnancy and neonatal complications, the only established benefits of treatment in
both pregnant and non-pregnant women are to relieve vaginal symptoms, reduce signs of infection, and potentially
to decrease the risk of acquiring HIV and other STDs (for example, Chlamydia trachomatis, Neisseria gonorrhoeae,
viral STDs).
In non-pregnant women, metronidazole is the treatment of choice.[12] Both topical and oral metronidazole seem
equally effective but intravaginal metronidazole may be associated with fewer adverse events.[31] [32] 1[B]Evidence
Metronidazole single-dose oral therapy has the lowest efficacy for bacterial vaginosis and is no longer
recommended.3[A]Evidence
Vaginal clindamycin cream is a useful first-line alternative in patients with contraindications to metronidazole therapy
or those who cannot tolerate metronidazole.[32] 4[C]Evidence Second-line treatment options include oral tinidazole,
oral clindamycin, and vaginal clindamycin ovules. Tinidazole has a longer serum half-life than metronidazole and also
reaches higher levels in the genitourinary tract.
For persistent or recurrent infection, metronidazole is administered for a longer period of 4-6 months after completion
of a recommended regimen.[33] 2[B]Evidence Suppressive therapy has been shown to reduce the risk of recurrences
but this benefit might not persist after discontinuation.[33]
Pregnant women can be safely treated with oral metronidazole. Oral clindamycin is an effective alternative.[12]
Patients should avoid alcohol consumption during treatment with metronidazole and tinidazole, and for 24 and 72
hours respectively after receiving the last dose. Women of childbearing age need to be aware that due to its oil-based
formula, clindamycin cream might weaken latex condoms and diaphragms for 5 days after use.
Although non-antibiotic treatments are available (e.g., benzydamine), their safety and efficacy are not well supported
by long-term scientific data.[34] There is also no significant scientific evidence to support the use of antiseptics or
disinfectants in bacterial vaginosis.[35] [36]
Trichomoniasis
Treatment of trichomoniasis results in relief of symptoms, microbiologic cure, and reduction of transmission.[12]
Isolation of the micro-organism is not necessary in all cases: for example, in a symptomatic patient with a prior history
of trichomoniasis or a known disease in sexual partner.
Single-dose therapy with metronidazole is, in most cases, enough for pregnant and non-pregnant women, and treating
TREATMENT
For resistant organisms and persistent infection, a different treatment approach is required. This involves higher doses
of metronidazole or treatment with tinidazole. Tinidazole is available for the treatment of trichomoniasis, and may
be considered as an alternative to the traditional treatment with metronidazole.[37] Tinidazole has a longer serum
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Vaginitis Treatment
half-life than metronidazole and also reaches higher levels in the genitourinary tract. Several T vaginalis isolates have
lower minimum inhibitory concentrations (MICs) to tinidazole than metronidazole.[12]
Patients should avoid alcohol consumption during treatment with metronidazole and tinidazole, and for 24 and 72
hours respectively after receiving the last dose.[12]
Condom use, although not 100% effective, should be discussed with the patient as part of sexually transmitted disease
prevention.
Vulvovaginal candidiasis
Several therapeutic options are available, both intravaginally and orally. It is important to distinguish between
uncomplicated and complicated Candida vaginitis (recurrence, severity, infection with Candida species other than
Candida albicans, pregnancy, and immunocompromise, including diabetic patients).
For uncomplicated infection, treatment with oral or topical azole antifungal agents should be started.7[A]Evidence
For complicated infections, short-course antifungal therapy (oral or topical) for infection is initiated, followed by
maintenance therapy (oral or topical) for approximately 6 months.
Pregnant women are treated only with topical azoles, for no longer than 7 days.
If the patient has concomitant diabetes, improvement in glycaemic control will also prevent recurrence.
Atrophic vaginitis
Dyspareunia may be treated with lubricant gels before intercourse and these may be initiated immediately, to be
used until successful treatment is established with topical oestrogen. For patients on HRT, concomitant use of a
lubricant may be adequate in controlling symptoms. As with initiation of HRT, a detailed discussion with the patient
should take place to explain the intended local therapy. Benefits and risks of oestrogen therapy should be carefully
weighed for each individual patient, aiming to minimise both the amount of oestrogen and length of treatment.[38]
[39] The potential adverse effects versus associated benefits of the different formulations should be considered.
While oestrogen rings provide the freedom of every 3-month replacement, the vaginal creams may offer a significant
and immediate soothing effect to the atrophic area. The easiest applicable method, at the lowest dose, for each
individual patient also needs to be considered (e.g., a patient with joint deformities from arthritis may find it difficult
to apply an oestrogen cream every night, and an oestrogen ring may be the most appropriate approach for this
patient).
Consult your local pharmaceutical database for comprehensive drug information including contraindications, drug
interactions, and alternative dosing. ( see Disclaimer )
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Vaginitis Treatment
Acute ( summary )
Patient group Tx line Treatment
2nd tinidazole
1st clindamycin
Ongoing ( summary )
Patient group Tx line Treatment
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Vaginitis Treatment
Ongoing ( summary )
complicated vulvovaginal 1st antifungal therapy and consultation with an
candidiasis infectious disease specialist
TREATMENT
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Vaginitis Treatment
Treatment options
Acute
Patient group Tx line Treatment
non-pregnant: isolated acute episode
Primary options
OR
» metronidazole vaginal: (0.75% gel) insert 5 g (one
applicatorful) into the vagina once daily at night for
5 days
use.
Primary options
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Vaginitis Treatment
Acute
Patient group Tx line Treatment
» clindamycin vaginal: (2% cream) insert 5 g (one
applicatorful) into the vagina once daily at night for
7 days
Primary options
OR
» clindamycin vaginal: 100 mg ovule into the vagina
once daily at night for 3 days
2nd tinidazole
» Treatment is indicated in all symptomatic women
with bacterial vaginosis to relieve vaginal symptoms,
reduce signs of infection, and potentially to decrease
the risk of acquiring HIV and other STDs (for example,
Chlamydia trachomatis, Neisseria gonorrhoeae, viral
STDs).[12]
Primary options
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Vaginitis Treatment
Acute
Patient group Tx line Treatment
» Systemic metronidazole is the treatment of choice
but tinidazole is an effective alternative.[12] Usually, a
2 g single dose is enough for clearance. Tinidazole has
a longer serum half-life than metronidazole and also
reaches higher levels in the genitourinary tract.
Primary options
OR
» tinidazole: 2 g orally as a single dose
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Vaginitis Treatment
Acute
Patient group Tx line Treatment
irritation), these may be managed with topical agents.
[12]
Primary options
OR
» clotrimazole vaginal: (1% cream) insert 5 g (one
applicatorful) into the vagina once daily at night for
7-14 days
OR
» clotrimazole vaginal: 100 mg vaginal tablet into
the vagina once daily at night for 7 nights, or insert
200 mg (two vaginal tablets) into the vagina once
daily at night for 3 nights
OR
» miconazole vaginal: (2% cream) insert 5 g (one
applicatorful) into the vagina once daily at night for
7 days
OR
» miconazole vaginal: 100 mg vaginal suppository
into the vagina once daily at night for 7 days
OR
» miconazole vaginal: 200 mg vaginal suppository
into the vagina once daily at night for 3 days
OR
» miconazole vaginal: 1200 mg vaginal suppository
into the vagina once daily at night as a single dose
OR
» tioconazole vaginal: (6.5% ointment) insert 5 g
(one applicatorful) into the vagina once daily at
night as a single dose
OR
» fluconazole: 150 mg/dose orally as a single dose
TREATMENT
OR
» nystatin vaginal: 100,000 unit vaginal tablet into
the vagina once daily at night for 14 days
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Vaginitis Treatment
Acute
Patient group Tx line Treatment
complicated vulvovaginal 1st antifungal therapy
candidiasis » Several agents are available orally or
topically.7[A]Evidence
Primary options
OR
» fluconazole: 150 mg orally every 3 days for a total
of 3 doses
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Vaginitis Treatment
Acute
Patient group Tx line Treatment
Primary options
1st clindamycin
» Treatment is indicated in all symptomatic women
with bacterial vaginosis.[12] Although bacterial
vaginosis is known to increase the risk of certain
pregnancy and neonatal complications, the only
established benefits of treatment in pregnant women
are relief of vaginal symptoms, reduced signs of
infection, and potentially a decreased risk of acquiring
HIV and other STDs (for example, Chlamydia
trachomatis, Neisseria gonorrhoeae, viral STDs).
Primary options
Primary options
TREATMENT
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Vaginitis Treatment
Acute
Patient group Tx line Treatment
» Vulvovaginal candidiasis is not usually acquired
through sexual intercourse; treatment of sexual
partners is not recommended, but should be
considered in women who have recurrent infection. If
a male sexual partner presents with symptoms (e.g.,
irritation), these may be managed with topical
agents.[12]
Primary options
Primary options
OR
» oestrogens, conjugated vaginal: (0.625 mg/g)
insert 0.5 to 2 g into the vagina once daily at night
for 1-2 weeks
TREATMENT
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Vaginitis Treatment
Acute
Patient group Tx line Treatment
gels, often called emollients, are available without
prescription and are commonly used to restore vaginal
pH and to relieve vaginal irritation and pruritus, and to
increase vaginal moisture.
Ongoing
Patient group Tx line Treatment
non-pregnant: persistent or recurrent
symptoms
Primary options
Primary options
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Vaginitis Treatment
Ongoing
Patient group Tx line Treatment
OR
» tinidazole: 2 g orally once daily for 5 days
Primary options
OR
» fluconazole: 150 mg orally once weekly for 6
months
Primary options
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Vaginitis Treatment
Ongoing
Patient group Tx line Treatment
trichomoniasis 1st metronidazole
» If a single high dose of metronidazole treatment is
unsuccessful, high-dose metronidazole for 7 days is
recommended.
Primary options
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Vaginitis Treatment
Ongoing
Patient group Tx line Treatment
Primary options
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Vaginitis Treatment
Emerging
Vitamin C vaginal tablets
May be beneficial in the management of bacterial vaginitis, but there is very little evidence as yet and long-term studies
are required.[47]
TREATMENT
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Vaginitis Follow up
Recommendations
Monitoring
FOLLOW UP
Bacterial vaginosis
• Follow-up is not recommended if symptoms resolve. Recurrence of bacterial vaginosis is not unusual and women
should be advised to return for additional therapy if symptoms recur.2[B]Evidence
• A treatment regimen different from the original regimen may be used to treat recurrent disease.
Trichomoniasis
• Follow-up is not recommended if couples are asymptomatic after treatment. If symptoms persist, tinidazole is
a reasonable alternative.
Vulvovaginal candidiasis
• Patients should be instructed to follow up if symptoms persist or recur within 2 months of onset of initial
symptoms.
Patient instructions
Infective vaginitis
• Diet: Lactobacillus acidophilus supplements in the diet may help to prevent vaginitis.[23]
• Activity: abstinence from douching and sexual activity is recommended until completion of treatment. If the
patient remains sexually active, advise use of condoms as a precaution; some of the topical treatments are
oil-based and can break condoms (e.g., clindamycin cream is oil-based and might weaken latex condoms and
diaphragms for 5 days after use). Check with condom manufacturer.
• Alcohol: patients should avoid consuming alcohol while on metronidazole and for 24 hours after last dose.
• Pregnant women: topical clindamycin preparations should not be used in the second half of pregnancy.
Atrophic vaginitis
• Avoiding causative agents, such as feminine hygiene products, latex condoms/diaphragms, douching, and
irritants such as strong soaps or bubble baths, can help prevent vaginitis.
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Vaginitis Follow up
Complications
FOLLOW UP
Complications Timeframe Likelihood
bacterial vaginosis/Trichomonas-related: preterm birth variable medium
In pregnant women, bacterial vaginosis and trichomoniasis have been associated with premature deliveries.[48] [49]
5[C]Evidence However, current recommendations do not advise routine screening for bacterial vaginosis in pregnant
women at risk for preterm delivery.[30] [50]
In pregnant women, bacterial vaginosis and trichomoniasis have been associated with premature rupture of the
membranes.[49]
In pregnant women, bacterial vaginosis and trichomoniasis have been associated with low birth weight.[48] [49]
5[C]Evidence
Bacterial vaginosis raises the risks of infections with Neisseria gonorrhoeae, HIV, Chlamydia trachomatis, and Herpes
simplex virus-2;[12] trichomoniasis increases the risk of HIV-1 acquisition 1.52-fold.[51] [52]
Prognosis
Overall, with the proper treatment, the prognosis is very good for all types of vaginitis.
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Vaginitis Guidelines
Diagnostic guidelines
Europe
Summary: Provides recommendations on the diagnosis of Trichomonas vaginalis infection including presenting signs
and symptoms. Diagnostic tests include microscopy and culture on vaginal swabs in females, and urethral swabs or
first-void urine in males. PCR has been used but is not yet available in the UK.
Published by: British Association for Sexual Health and HIV Last published: 2012
Summary: Provides recommendations on the diagnosis of bacterial vaginosis at first presentation as well as recurrence.
Discusses 2 approaches to diagnosis, using the Amsel criteria or assessment of the Gram-stained vaginal smear with
the Hay/Ison criteria or the Nugent criteria.
Summary: Provides recommendations on the evaluation and diagnosis of women presenting with vaginal discharge.
Antenatal care
Published by: National Institute for Health and Care Excellence Last published: 2008
Summary: The guidelines state that pregnant women should not be offered routine screening and treatment for
asymptomatic bacterial vaginosis as evidence has shown that treatment does not reduce preterm birth risk or prevent
other adverse sequelae.
North America
Summary: Guidelines for the management of STDs, including recommendations for diagnosis of vaginitis.
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Vaginitis Guidelines
North America
Summary: Evidence-based recommendations on screening for vulvovaginal candidiasis, trichomoniasis, and bacterial
vaginosis.
Summary: Covers point-of-care testing of Chlamydia trachomatis and Trichomonas vaginalis infection, gonorrhoea
(Gram-stain), and bacterial vaginosis in pregnant women; no recommendations made due to insufficient evidence for
Candida.
GUIDELINES
Oceania
Treatment guidelines
Europe
Summary: Provides recommendations on the treatment of Trichomonas vaginalis infection and prevention of further
infection.
Summary: Provides treatment recommendations for women evaluated for vaginal discharge.
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Vaginitis Guidelines
Europe
Summary: Recommendations for management of bacterial vaginosis, trichomoniasis, and candidiasis based on
currently available evidence, including the management of persistent and recurrent infections.
Antenatal care
Published by: National Institute for Health and Care Excellence Last published: 2008
Summary: The guidelines, commissioned by the National Institute for Health and Clinical Excellence (NICE), state
that pregnant women should not be offered routine screening and treatment for asymptomatic bacterial vaginosis as
evidence has shown that treatment does not reduce preterm birth risk or prevent other adverse sequelae.
GUIDELINES
North America
Summary: Guidelines for the management of STDs, including recommendations for treatment of vaginitis.
Summary: Recommendations on the management of vulvovaginal candidiasis, trichomoniasis, and bacterial vaginosis.
Oceania
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Vaginitis Evidence scores
Evidence scores
1. Cure rates: there is medium-quality evidence that intravaginal antibacterial treatment with metronidazole gel or
clindamycin cream is more effective at increasing cure rates at 25-39 days compared with placebo in non-pregnant
women with bacterial vaginosis. Oral metronidazole has been associated with nausea and a metallic taste.
Evidence level B: Randomized controlled trials (RCTs) of <200 participants, methodologically flawed RCTs of >200
participants, methodologically flawed systematic reviews (SRs) or good quality observational (cohort) studies.
2. Recurrence: there is medium-quality evidence that recurrence of bacterial vaginosis is likely to occur after
antibacterial treatment.
Evidence level B: Randomized controlled trials (RCTs) of <200 participants, methodologically flawed RCTs of >200
participants, methodologically flawed systematic reviews (SRs) or good quality observational (cohort) studies.
3. Cure rates: there is good-quality evidence that a twice-daily regimen of the oral antibacterial metronidazole is more
effective at increasing cure rates at 7 days compared with a single dose.
Evidence level A: Systematic reviews (SRs) or randomized controlled trials (RCTs) of >200 participants.
4. Cure rates: there is poor-quality evidence that clindamycin may be as effective at increasing cure rates at 7-10 days
compared with metronidazole in non-pregnant women with bacterial vaginosis. Intravaginal clindamycin has been
associated with mild to severe colitis and with vaginal candidiasis.
Evidence level C: Poor quality observational (cohort) studies or methodologically flawed randomized controlled
trials (RCTs) of <200 participants.
5. Complications in pregnant women: there is poor-quality evidence that antibacterials may reduce the risk of low
birth weight in pregnant women who have had a previous preterm birth, but we don't know if they are more effective
at reducing the risk of preterm birth.
Evidence level C: Poor quality observational (cohort) studies or methodologically flawed randomized controlled
trials (RCTs) of <200 participants.
6. Preventative action: there is medium-quality evidence that treating a steady male partner with oral antibacterials
is no more effective at reducing the rate of recurring infections in women with bacterial vaginosis, who are also
receiving antibacterial treatment, than not treating the male partner.
Evidence level B: Randomized controlled trials (RCTs) of <200 participants, methodologically flawed RCTs of >200
participants, methodologically flawed systematic reviews (SRs) or good quality observational (cohort) studies.
7. Clinical cure: there is good-quality evidence that there is no difference in clinical cure rate between intravaginal
EVIDENCE SCORES
and oral azole treatments for candidiasis. However, adverse effects have been found for both types of treatment.
Evidence level A: Systematic reviews (SRs) or randomized controlled trials (RCTs) of >200 participants.
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Vaginitis Evidence scores
8. Clinical cure: there is good-quality evidence that intravaginal metronidazole is as effective as oral metronidazole
in treating bacterial vaginosis and results in fewer adverse events.
Evidence level A: Systematic reviews (SRs) or randomized controlled trials (RCTs) of >200 participants.
EVIDENCE SCORES
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Vaginitis References
Key articles
REFERENCES
• Workowski KA, Bolan GA; Centers for Disease Control and Prevention (CDC). Sexually transmitted diseases treatment
guidelines, 2015. MMWR Recomm Rep. 2015;64:1-137. Full text Abstract
• Chollet JA. Efficacy and safety of ultra-low-dose Vagifem (10 mcg). Patient Prefer Adherence. 2011;5:571-574. Full
text Abstract
References
1. Ness RB, Hillier SL, Richter HE, et al. Douching in relation to bacterial vaginosis, lactobacilli, and facultative bacteria
in the vagina. Obstet Gynecol. 2002;100:765-772. Full text Abstract
2. Egan ME, Lipsky MS. Diagnosis of vaginitis. Am Fam Physician. 2000;62:1095-1104. Abstract
4. World Health Organization. Global prevalence and incidence of selected curable sexually transmitted infections.
Geneva, Switzerland: WHO; 2001. Full text
6. Paulitsch A, Weger W, Ginter-Hanselmayer G, et al. A 5-year (2000-2004) epidemiological survey of Candida and
non-Candida yeast species causing vulvovaginal candidiasis in Graz, Austria. Mycoses. 2006;49:471-475. Abstract
7. Foxman B, Barlow R, D'Arcy H, et al. Candida vaginitis: self-reported incidence and associated costs. Sex Transm Dis.
2000;27:230-235. Abstract
8. Limia OF, Lantero MI. Prevalence of Candida albicans and Trichomonas vaginalis in pregnant women in Havana City
by an immunologic latex agglutination test. MedGenMed. 2004;6:50.
9. Anh PK, Khanh NT, Ha DT, et al. Prevalence of lower genital tract infection among women attending maternal and
child health and family planning clinics in Hanoi, Vietnam. Southeast Asian J Trop Med Public Health. 2003;34:367-373.
Abstract
10. Pandit L, Ouslander JG. Postmenopausal vaginal atrophy and atrophic vaginitis. Am J Med Sci. 1997;34:228-231.
Abstract
11. Bachmann GA, Nevadunsky NS. Diagnosis and treatment of atrophic vaginitis. Am Fam Physician. 2000;61:3090-3096.
Abstract
12. Workowski KA, Bolan GA; Centers for Disease Control and Prevention (CDC). Sexually transmitted diseases treatment
guidelines, 2015. MMWR Recomm Rep. 2015;64:1-137. Full text Abstract
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39
of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2015. All rights reserved.
Vaginitis References
13. Hobbs MM, Lapple DM, Lawing LF, et al. Methods for detection of Trichomonas vaginalis in the male partners of
infected women: implications for control of trichomoniasis. J Clin Microbiol. 2006;44:3994-3999. Full text Abstract
REFERENCES
14. Sena AC, Miller WC, Hobbs MM, et al. Trichomonas vaginalis infection in male sexual partners: implications for
diagnosis, treatment, and prevention. Clin Infect Dis. 2007;44:13-22. Abstract
15. Taha TE, Hoover DR, Dallabetta GA, et al. Bacterial vaginosis and disturbances of vaginal flora: association with
increased acquisition of HIV. AIDS. 1998;12:1699-1706. Abstract
16. Wilton L, Kollarova M, Heeley E, et al. Relative risk of vaginal candidiasis after use of antibiotics compared with
antidepressants in women: postmarketing surveillance data in England. Drug Saf. 2003;26:589-597. Abstract
17. Duerr A, Heilig CM, Meikle SF, et al. Incident and persistent vulvovaginal candidiasis among human immunodeficiency
virus-infected women: risk factors and severity. Obstet Gynecol. 2003;101:548-556. Full text Abstract
18. De Leon EM, Jacober SJ, Sobel JD, et al. Prevalence and risk factors for vaginal Candida colonization in women with
type 1 and type 2 diabetes. BMC Infect Dis. 2002;2:1. Abstract
19. Joesoef MR, Karundeng A, Runtupalit C, et al. High rate of bacterial vaginosis among women with intrauterine devices
in Manado, Indonesia. Contraception. 2001;64:169-172. Abstract
20. Smart S, Singal A, Mindel A. Social and sexual risk factors for bacterial vaginosis. Sex Transm Infect. 2004;80:58-62.
Full text Abstract
21. Otero L, Palacio V, Carreno F, et al. Vulvovaginal candidiasis in female sex workers. Int J STD AIDS. 1998;9:526-530.
Abstract
22. Tolosa JE, Chaithongwongwatthana S, Daly S, et al. The International Infections in Pregnancy (IIP) study: variations
in the prevalence of bacterial vaginosis and distribution of morphotypes in vaginal smears among pregnant women.
Am J Obstet Gynecol. 2006;195:1198-1204. Abstract
23. Van Kessel K, Assefi N, Marrazzo J, et al. Common complementary and alternative therapies for yeast vaginitis and
bacterial vaginosis: a systematic review. Obstet Gynecol Surv. 2003;58:351-358. Abstract
24. ACOG Committee on Practice Bulletins--Gynecology. ACOG Practice Bulletin. Clinical management guidelines for
obstetrician-gynecologists, Number 72, May 2006: Vaginitis. Obstet Gynecol. 2006;107:1195-1206. Abstract
25. Hainer BL, Gibson MV. Vaginitis. Am Fam Physician. 2011;83:807-815. Full text Abstract
26. Amsel R, Totten PA, Spiegel CA, et al. Nonspecific vaginitis: diagnostic criteria and microbial and epidemiologic
associations. Am J Med. 1983;74:14-22. Abstract
27. Nugent RP, Krohn MA, Hillier SL. Reliability of diagnosing bacterial vaginosis is improved by a standardized method
of gram stain interpretation. J Clin Microbiol. 1991;29:297-301. Full text Abstract
28. Madico G, Quinn TC, Rompalo A, et al. Diagnosis of Trichomonas vaginalis infection by PCR using vaginal swab
samples. J Clin Microbiol. 1998;36:3205-3210. Full text Abstract
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Vaginitis References
29. Sharma P, Malla N, Gupta I, et al. A comparison of wet mount, culture and enzyme linked immunosorbent assay for
the diagnosis of trichomoniasis in women. Trop Geogr Med. 1991;43:257-260. Abstract
REFERENCES
30. US Preventive Services Task Force. Screening for bacterial vaginosis in pregnancy to prevent preterm delivery: US
Preventive Services Task Force recommendation statement. Ann Intern Med. 2008;148:214-219. Full text Abstract
31. Brandt M, Abels C, May T, et al. Intravaginally applied metronidazole is as effective as orally applied in the treatment
of bacterial vaginosis, but exhibits significantly less side effects. Eur J Obstet Gynecol Reprod Biol. 2008;141:158-162.
Abstract
32. Oduyebo OO, Anorlu RI, Ogunsola FT, et al. The effects of antimicrobial therapy on bacterial vaginosis in non-pregnant
women. Cochrane Database Syst Rev. 2009;(3):CD006055. Full text Abstract
33. Sobel JD, Ferris D, Schwebke J, et al. Suppressive antibacterial therapy with 0.75% metronidazole vaginal gel to
prevent recurrent bacterial vaginosis. Am J Obstet Gynecol. 2006;194:1283-1289. Abstract
34. Boselli F, Petrella E, Campedelli A, et al. Efficacy and tolerability of fitostimoline (vaginal cream, ovules, and vaginal
washing) and of benzydamine hydrochloride (tantum rosa vaginal cream and vaginal washing) in the topical treatment
of symptoms of bacterial vaginosis. ISRN Obstet Gynecol. 2012;2012:183403. Full text Abstract
35. Verstraelen H, Verhelst R, Roelens K, et al. Antiseptics and disinfectants for the treatment of bacterial vaginosis: a
systematic review. BMC Infect Dis. 2012;12:148. Full text Abstract
36. Weissenbacher ER, Donders G, Unzeitig V, et al. A comparison of dequalinium chloride vaginal tablets (Fluomizin®)
and clindamycin vaginal cream in the treatment of bacterial vaginosis: a single-blind, randomized clinical trial of
efficacy and safety. Gynecol Obstet Invest. 2012;73:8-15. Full text Abstract
37. Nanda N, Michel RG, Kurdgelashvili G, et al. Trichomoniasis and its treatment. Expert Rev Anti Infect Ther.
2006;4:125-135. Abstract
38. Krychman ML. Vaginal estrogens for the treatment of dyspareunia. J Sex Med. 2011;8:666-674. Abstract
39. Chollet JA. Efficacy and safety of ultra-low-dose Vagifem (10 mcg). Patient Prefer Adherence. 2011;5:571-574. Full
text Abstract
40. Gülmezoglu AM, Azhar M. Interventions for trichomoniasis in pregnancy. Cochrane Database Syst Rev.
2011;(5):CD000220. Abstract
41. Castelo-Branco C, Cancelo MJ. Compounds for the treatment of atropic vaginitis. Expert Opin Ther Pat.
2008;18:1385-1394.
42. Henriksson L, Stjernquist M, Boquist L, et al. A one-year multicenter study of efficacy and safety of a continuous,
low-dose, estradiol-releasing vaginal ring (Estring) in postmenopausal women with symptoms and signs of urogenital
aging. Am J Obstet Gynecol. 1996;174:85-92. Abstract
43. Suckling J, Lethaby A, Kennedy R. Local oestrogen for vaginal atrophy in postmenopausal women. Cochrane Database
Syst Rev. 2006;(4):CD001500. Full text Abstract
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Vaginitis References
44. Wolner-Hanssen P, Krieger JN, Stevens CE, et al. Clinical manifestations of vaginal trichomoniasis. JAMA.
1989;261:571-576. Abstract
REFERENCES
45. Mølgaard-Nielsen D, Pasternak B, Hviid A. Use of oral fluconazole during pregnancy and the risk of birth defects. N
Engl J Med. 2013;369:830-839. Full text Abstract
46. Food and Drug Administration. FDA drug safety communication: FDA to review study examining use of oral fluconazole
(Diflucan) in pregnancy. April 2016. http://www.fda.gov/ (last accessed 28 April 2016). Full text
47. Petersen EE, Genet M, Caserini M, et al. Efficacy of vitamin C vaginal tablets in the treatment of bacterial vaginosis:
a randomised, double blind, placebo controlled clinical trial. Arzneimittelforschung. 2011;61:260-265. Abstract
48. Svare JA, Schmidt H, Hansen BB, et al. Bacterial vaginosis in a cohort of Danish pregnant women: prevalence and
relationship with preterm delivery, low birthweight and perinatal infections. BJOG. 2006;113:1419-1425. Abstract
49. McGregor JA, French JI, Parker R, et al. Prevention of premature birth by screening and treatment for common
genital tract infections: results of a prospective controlled evaluation. Am J Obstet Gynecol. 1995;173:157-167.
Abstract
50. Brocklehurst P, Gordon A, Heatley E, et al. Antibiotics for treating bacterial vaginosis in pregnancy.
Cochrane.Database.Syst.Rev. 2013;(1):CD000262. Full text Abstract
51. St John E, Mares D, Spear GT. Bacterial vaginosis and host immunity. Curr HIV/AIDS Rep. 2007;4:22-28. Abstract
52. McClelland RS, Sangare L, Hassan WM, et al. Infection with Trichomonas vaginalis increases the risk of HIV-1
acquisition. J Infect Dis. 2007;195:698-702. Full text Abstract
53. Menard JP. Antibacterial treatment of bacterial vaginosis: current and emerging therapies. Int J Womens Health.
2011;3:295-305. Full text Abstract
54. Nurbhai M, Grimshaw J, Watson M, et al. Oral versus intra-vaginal imidazole and triazole anti-fungal treatment of
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Abstract
This PDF of the BMJ Best Practice topic is based on the web version that was last updated: May 05, 2016.
42 BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use
of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2015. All rights reserved.
Vaginitis Images
Images
IMAGES
Figure 1: Trichomonas vaginitis with copious purulent discharge emanating from the cervical os
CDC Image Library
Figure 2: Vaginal smear identifying Candida albicans using a wet mount technique
CDC Image Library; Dr Stuart Brown
This PDF of the BMJ Best Practice topic is based on the web version that was last updated: May 05, 2016.
BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use
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of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2015. All rights reserved.
Vaginitis Images
Figure 3: Phase contrast wet mount micrograph of a vaginal discharge revealing the presence of Trichomonas vaginalis
protozoa
IMAGES
Figure 4: Photomicrograph revealing bacteria adhering to vaginal epithelial cells, known as clue cells
CDC Image Library; M. Rein
This PDF of the BMJ Best Practice topic is based on the web version that was last updated: May 05, 2016.
44 BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use
of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2015. All rights reserved.
Vaginitis Disclaimer
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This PDF of the BMJ Best Practice topic is based on the web version that was last updated: May 05, 2016.
BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use
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Contributors:
// Authors:
// Peer Reviewers:
David Chelmow, MD
Chair
Department of Obstetrics and Gynecology, Virginia Commonwealth University, Richmond, VA
DISCLOSURES: DC declares that he has no competing interests.
Jonathon Solnik, MD
Director
Minimally Invasive Gynecologic Surgery, Cedars-Sinai Medical Center, Los Angeles, CA
DISCLOSURES: JS declares that he has no competing interests.