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KEYWORDS
Discharge;
Vagina;
Vaginal discharge;
Vaginitis;
Vulvovaginitis
Summary
Vaginal discharge is a common symptom in women of reproductive age. The causes can be
divided into those that are infective or non-infective, the most common being the
infective agents. Initial assessment of a patient with vaginal discharge requires a thorough
history, including sexual history, examination, and testing for these common infections.
The non-sexually transmitted infections (STIs)bacterial vaginosis and candidiasisare
the most frequently encountered and these can often be diagnosed immediately by the
clinical findings and simple bedside tests. Persistence or recurrence of these infections is
also seen and might require repeated or prolonged courses of treatment.
The STIschlamydia, gonorrhoea and trichomoniasiscan also cause vaginal discharge
and diagnosis requires appropriate laboratory tests to be performed. Partner notification
and treatment is an essential part of the management.
In the absence of any infections, physiological discharge should be considered as a possible
cause.
& 2006 Elsevier Ltd. All rights reserved.
Introduction
Taking a history
Aetiology
Corresponding author. Tel.: +44 115 9691196;
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R. McCathie
Table 1
Table 2
History taking.
Associated symptoms
Itching, soreness, irritation
of vulva/vagina
Dysuria
Intermenstrual/post-coital
bleeding
Dyspareunia
Lower abdominal pain
Infective
Non-infective
Common causes
Physiological
Cervical ectropian
Cervical polyp
Retained tampon/condom
Retained products of
conception
Allergy
Sexual history
Recent change of sexual
partner
Symptoms in partner
Condom use
History of previous STIs
Other
Prescribed medication, e.g.
antibiotics, hormone
preparation
Treatment used already,
prescribed or shop bought
Personal hygiene practices,
e.g. douching, bubble baths
Box 1
Table 3
BV.
Risk factors
Complications
Younger age
Black ethnicity
Postpartum endometritis
Post-TOP (surgical)
endometritis and pelvic
inflammatory disease
Vaginal cuff cellulitis
following transvaginal
hysterectomy
Increased risk of preterm
birth, premature rupture
of membranes and late
miscarriage
Increased risk of acquiring
human immunodeficiency
virus
Vaginal douching
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Vaginal discharge: common causes and management
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Candida infection
Practice points
Recommended treatment regimens for BV:
Pregnancy
Diabetes mellitus
Immunosuppression
Antibiotic therapy
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214
R. McCathie
Practice points
Intravaginal treatment regimes for candida infection:
Chlamydia trachomatis
The prevalence of C. trachomatis in the UK was reported to
be 35% of sexually active women attending their GP. More
recently, a chlamydia screening pilot study showed higher
rates of 1014% in the under-25 age group.
The causative organism, C. trachomatis, has a unique
lifecycle rather similar to a virus due to its obligate
intracellular growth. Within the genital tract, the primary
site of infection in women is the cervix with the urethra also
infected in about 50% of cases. Other sites that can be
infected are the rectum, pharynx and the conjunctiva.
Chlamydia is an STI and therefore management requires
partner notification and treatment. The cumulative risk of
transmission between sexual partners is about 6070%. It
might also be associated with other STIs and therefore
testing for gonorrhoea, Trichomonas vaginalis and bloodborne STIs like syphilis and HIV should be considered.
Vaginal discharge, usually purulent in nature, can be a
presenting symptom of chlamydia in women; however, 80%
of those infected are asymptomatic. Other signs and
symptoms include post-coital bleeding, intermenstrual
bleeding, mucopurulent cervicitis and lower abdominal
pain. Box 3 lists the possible complications of chlamydia
and gonorrhoea infections. The risk of ascending infection is
increased with instrumentation such as TOP or IUD insertion,
therefore prior to any such event women should be tested
and treated if necessary.
Due to its unusual life cycle, diagnosis of chlamydia via
cell culture is extremely expensive and requires a high level
of expertise. It is performed in a few laboratories for
research and forensic purposes and is still currently used as a
gold standard; however, it has no role in routine
diagnostics. Until recently, the most common method used
for diagnosis was enzyme immunoassay (EIA). This test is
inexpensive and has a high specificity; however, the
sensitivity varies from 60% to 80% depending on the swab
and assay used. For the greatest sensitivity it is essential to
send a good cervical swab together with a urethral swab.
Over the past few years, most laboratories have switched
from using EIA to nucleic acid amplification tests (NAAT) for
chlamydia. The major advantages of NAAT tests are the
increased sensitivity and the possibility of using less-invasive
samples. Although it is more expensive than EIA, increased
government funding should mean that all laboratories in
England and Wales are able to provide this service in the
near future. A number of different sample sites have been
used for NAAT testing. Current evidence suggests vulvova-
Box 3
rhoea.
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Vaginal discharge: common causes and management
ginal swabs, either self-taken or clinician collected, or
cervical swabs have sensitivities of 490%. First-void urine
samples can also be used, although the sensitivity is not as
good (about 80%). The advent of NAAT tests has allowed
more widespread testing for chlamydia from non-genitourinary medicine settings and this should certainly be
encouraged, particularly in the under-25 age group.
Treatment for chlamydia should be offered to all women
with a positive chlamydia test. It is also appropriate to treat
women with clinical evidence of pelvic inflammatory disease
(PID) or mucopurulent cervicitis, and those who have been a
definite sexual contact of a male partner with chlamydia,
once tests for chlamydia and gonorrhoea have been sent.
Practice points
Recommended treatment regimens for C. trachomatis:
days
or
Erythromycin 500 mg orally twice daily for 14 days
(may be better tolerated).
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Of those women who are symptomatic, increased or
altered vaginal discharge is the most common symptom.
However, 50% of women with cervical infection can be
asymptomatic. Other symptoms and signs include dysuria,
mucopurulent cervicitis and lower abdominal pain. Postcoital and intermenstrual bleeding can also occur but are
quite unusual. The complications of gonorrhoea are as listed
above in Box 3. In comparison to Chlamydia, the consequences of untreated gonorrhoea during pregnancy are
more severe as there is a three- to six-fold increased risk of
preterm birth and a low-birth-weight baby. An extremely
rare complication of gonorrhoea (o1%) is haematogenous
dissemination, whereby the bacteria can seed into several
sites causing skin lesions, arthritis and tenosynovitis.
Diagnosis of gonorrhoea is established by culture of the
organism from a swab taken from the infected site. In
women, a cervical swab is required and pick up is increased
if a urethral swab is also sent. Within most genitourinary
clinics the swab can be immediately plated onto a selective
culture media before being sent to the laboratory but in
other settings a standard Amies swab or Stuarts swab should
be used and sent to the referring laboratory as soon as
possible. Culture is sensitive (490%), specific and inexpensive and allows antibiotic sensitivity to be performed. It is
currently the first choice for gonorrhoea diagnosis. More
recently, NAAT tests have become available to test for N.
gonorrhoeae. A number of different assays are being used
and validated at the current time but data suggests
sensitivities of 490% when compared to culture. The main
advantage of NAAT tests is that they allow less invasive
samples to be used and tests for both gonorrhoea and
chlamydia can thus be performed on a single sample.
Currently, NAAT testing for gonorrhoea is not being widely
used and culture remains the gold standard, although this
will undoubtedly be changing in the near future.
Treatment should be offered to all women with a positive
gonorrhoea test. It is also appropriate to treat women with
clinical evidence of PID or mucopurulent cervicitis, or who
have been a definite sexual contact of a male partner with
gonorrhoea, once the tests for gonorrhoea and chlamydia
have been sent.
Practice points
Neisseria gonorrhoeae
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216
on the antibiotic sensitivity from the culture. The complete
antibiotic guideline can be found in the National Guidelines
referred to at the end of the article.
Providing the patient is compliant and the organism is
shown to be sensitive to the antibiotic used, a repeat test
following treatment is not necessary. If a repeat test is
performed this should be done by culture 472 h after
completion of antibiotic therapy.
Trichomonas vaginalis
Infection with T. vaginalis is fairly uncommon in the UK,
although worldwide the rates are high and in Africa and Asia
it is a major cause of vaginal discharge. Prevalence rates of
up to 35% have been found in parts of Africa, where it is
usually the most common STI.
T. vaginalis is a flagellated protozoa, measuring 1020 mm
wide. Unlike chlamydia and gonorrhoea, it does not affect
any extragenital sites, but it is associated with vaginitis,
cervicitis, urethritis and PID. It is an STI and cure rates in
women are significantly improved if male partners receive
treatment. Testing for all other STIs should always be
considered, as 30% of women will also have chlamydia or
gonorrhoea.
Women infected with T. vaginalis might be asymptomatic
at the time of diagnosis; however, if left untreated they
often develop symptoms. The most common complaint is
vaginal discharge, classically described as green and frothy,
althoughpractically speakingit can be any colour. About
50% of women find the discharge to be malodorous and it
often has a pH of 44.5. Other signs and symptoms of
infection with T. vaginalis include vulval or vaginal itching,
evidence of a vaginitis or a cervicitis on speculum examination and, described in all textbooks but rarely seen,
punctuate haemorrhages of the cervix (so-called strawberry cervix). Symptoms might be worse during or just after
the menses.
Making a clinical diagnosis of T. vaginalis infection
is not easy as the symptoms and signs are not always
classical and the colour, smell and pH of the discharge
makes it difficult to differentiate from bacterial vaginosis.
Other diagnostic tools are therefore required. Within
genitourinary clinics the main method is direct visualisation
using microscopy of a sample of vaginal discharge on a
wet-slide (using saline). T. vaginalis can be seen to be
about the same size as a white blood cell and has a
characteristic motility; this has a sensitivity of about 80%. It
is a cheap test that provides an instant result, although it
requires immediate access to a microscope. The gold
standard for T. vaginalis diagnosis is culture. This requires
inoculation of a highly specific T. vaginalis culture medium
(usually liquid) and incubation at 3337 1C. This has a better
sensitivity than microscopy but a specific T. vaginalis culture
medium is not always available, it is more costly and
takes up to 7 days to get a diagnosis. A standard high vaginal
swab can be sent for culture, although the sensitivity of
this is lower.
A diagnosis of T. vaginalis can be reported on a
Papanicolaou (Pap) smear. However, this is neither a
sensitive nor specific test for T. vaginalis and the diagnosis
needs to be confirmed via another method before suggesting
R. McCathie
to patient that they have an STI. More recently, a NAAT test
for T. vaginalis has been developed. Initial data suggests
good sensitivity, although lower specificity than with
culture. This technique is not widely available.
First-line treatment of infection with T. vaginalis
requires systemic rather than topical treatment because,
as outlined above, the infection is not always confined
to the vagina but may involve other parts of the urogenital
tract.
Practice points
Recommended treatment regimens for T. vaginalis:
Practice points
In addition to medication, treatment for gonorrhoea,
chlamydia and T. vaginalis requires:
Physiological discharge
The question that many patients and physicians ask with
regard to vaginal discharge is what is normal? On
questioning, the majority of women accept that some
discharge is normal, although a substantial minority feel
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Vaginal discharge: common causes and management
that a healthy vagina should be dry. The quantity of the
discharge is certainly variable between populations and in
an individual varies with the menstrual cycle, usually
increasing midcycle. The consistency of the discharge also
varies during the cycle, having maximum viscosity in the
luteal phase and decreasing to a minimum at midcycle.
The colour of normal discharge is generally considered
to be white or clear but there are certainly many
women without any genitourinary pathology who would
describe their discharge as creamy or yellowy coloured.
Finally, it is generally assumed that discharge with an
offensive smell or that causes irritation must be pathological
in nature, although evidence shows this is not always
the case.
What does this mean to physicians trying to make a
diagnosis? First, it means that we often cannot make a
diagnosis based on the description of the discharge
alone. We must take a thorough history including sexual
history and assess the risks of a sexually transmitted
versus a non-sexually transmitted cause. Second, examination of the genital area, including speculum examination
and visualisation of the cervix, is almost always required.
Third, exclusion of the common causes of discharge by
diagnostic testing as outlined in this article is often
necessary. In the absence of any positive findings following
this process the likelihood is that the discharge is physiological in nature.
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Conclusion
Vaginal discharge can be a distressing and embarrassing
symptom for many women. The causes are numerous,
although there are clearly several particularly common
aetiologies, discussed within this article. These should be
considered and tested for at the outset, and treated
appropriately if required.
Further reading
1. British Association of Sexual Health and HIV (BASHH) Clinical
Effectiveness Group National Guidelines. Online. Available at:
http://www.bashh.org
2. Fenton KA, Ison CA, Johnson AP, Rudd E, Soltani M, Martin I, et al.
Ciprofloxacin resistance in Neisseria gonorrhoeae in England and
Wales in 2002. Lancet 2003;361:18679.
3. McMillan A, Ballard RC. Non-specific genital tract infection and
chlamydial infection, including lymphogranuloma venereum. In:
McMillan A, Young H, Ogilvie MM, Scott GR, editors. Clinical
practice in sexually transmissible infections. Elsevier Science
Limited; 2002. p. 281312.
4. Sobel JD, Wiesenfeld HC, Martens M, Danna P, et al. Maintenance
fluconazole therapy for recurrent vulvovaginal candidiasis. N
Engl J Med 2004;351:87683.
5. Wilson J. Managing recurrent bacterial vaginosis. Sex Transm
Infect 2004;80(1):811.