| Chlamydia |
|
| TRANSMISSION |
Vaginal
sex, anal sex, oral sex, close genital contact, mother to
child at birth |
| SYMPTOMS
(clinical features) |
In
women:
Asymptomatic (80%)
Post-coital bleeding
Lower abdo pain
Purulent vaginal discharge
Mucopurulent cervicitis and/or cervical bleeding.
In
men:
Aspmtomatic in up to 50%
Urethral discharge
Dysuria
The severity of these is variable and may be so mild as
to be unnoticed by the patient. Rectal infection is usually
asymptomatic but may cause anal discharge and anorectal
discomfort.
Pharyngeal infections are asymptomatic |
| COMPLICATIONS |
- Pelvic
inflammatory disease
- Peri-hepatitis
(fitz-hugh-curtis syndrome) Tubal damage (infertility,
ectopic pregnancy)
- Chronic
pelvic pain
- Transmission
to neonate (conjunctivitis, pneumonia)
- Epididymo-orchitis
- Sexually
acquired reactive arthritis/reiters syndrome (commoner
in men)
|
| TESTS |
Women:
Cervical swab and a urethral swab
Men:
Urine sample for men together with a urethral swab. If anal
sex has taken place then a rectal swab should also be taken.
If oral sex then a pharyngeal swab should be taken.
|
| TREATMENT |
Recommended:
Doxycycline 100mgs twice a day for 7 days
or Azithromycin 1g orally in a single dose.
Alternatives:
Erythromycin 500mgs twice a day for 14 days
or Deteclo 300mgs twice a day for 7 days.
or Ofloxacin 200mgs twice a day for 7 days
|
| FOLLOW
UP |
Partner
notification:
Sexual contact should be traced back for 6 months or to
the last sexual partner whichever is the longer. It is routinely
acknowledged that it is perfectly reasonable to contact
partners as far back as a year.
Assessment
of treatment efficacy/exclusion of reinfection and health
education is an important part of follow up.
Test
of cures are usually recommended for pregnant women. |
| Gonorrhoea |
|
| TRANSMISSION |
Vaginal
sex
Anal sex
Oral sex
Close genital contact
Mother to child at birth |
| SYMPTOMS
(clinical features) |
In
women: frequently asymptomatic (50%).
Increased vaginal discharge
May present with abdo pain due to genital tract involvement
Urethral infection may cause dysuria (but not frequency)
Is a rare cause of intrarmenstrual bleeding or menorrhagia
Pharyngeal infection is usually asymptomatic. |
| COMPLICATIONS |
Infections
generally remain localised to the anogenital and pharyngeal
mucosae, but may spread to the upper genital infection to
cause epididymitis in men (1%) or pelvic inflammatory disease
(PID) in women (approx. 3%)
Much
less common are disseminated infections (DGI) These include:
septicaemia, arthritis, dermatitis, endocarditis and meningitis. |
| TESTS |
Up
to 80% of symptomatic urethral infection in men will be diagnosed
on a gram-stained smear, but only 50-70% of asymptomatic urethral
infection. Microscopy of the cervix and rectum is considered
less reliable (40-50%) In most women the diagnosis will be
made on culture from the cervix although in GC contacts the
urethra and rectum should also be sampled. In GC contacts
samples should be taken on two separate occasions before GC
is excluded. |
| TREATMENT |
If
the infection was acquired in the UK the first line treatment
is: Amoxycillin 3g + probenicid 1g orally as a single dose.
Imported infection should be assumed to be Penicillin resistant
when treated before antimicrobial sensitivity is known:
Ciprofloxacin 500mg orally as a single dose.
Alternative
regimens not usually used in the UK but valuable against
imported infections from SE Asia are: Ceftriaxone 250mg
im as a single dose, Spectinomycin 2g i/m as a single dose. |
| FOLLOW
UP |
Symptomatic
improvement with treatment does not guarantee eradication
of GC. There should be at least one test of cure (which
in women should include the rectum). And, the final test
of cure should take place 48-72 hours after the last antibiotic
therapy.
Patients
with uncomplicated infection should be seen at 24-48hrs
for a TOC which will pick up treatment failures.
All
patients should see the health adviser and contacts should
be traced for 3 months or to the last sexual partner (whichever
is longer) In some situations epidemiological treatment
may be given to named contacts where there is a likelihood
of poor compliance, risk of complication or infection of
others. |
| Warts |
More
than 80 different types of human papilloma virus. Some strains
have a particular prediliction for the genital area. Those
most commonly referred to are 6, 11, 16, 18, 31, 33.
But
approximately 30 different types are associated with genital
infection. |
| TRANSMISSION |
HPV
is passed through close physical contact (skin to skin), almost
always genital for genital warts. Autoinoculation from other
sites is unusual. |
| SYMPTOMS(clinical
features) |
Symptoms
in both sexes include:
Genital growths, which may be hard or soft and range from
solitary to multiple.
Bleeding especially urethral.
Occasional itching.
Sometimes pigmentation is present.
In
men: warts are found frequently on the penis, urethra,in
the perianal area and rarely on the scrotum.
In
women: the vulva, perianal, the cervix and vagina
(less frequently) and, infrequently the urethra are sites
for warts in women.
|
| COMPLICATIONS |
Genital
warts may be associated with abnormal cervical smears. HPV
16, 18, 31, 33 and several other genital strains are oncogenic.
There is an increased risk of cervical cancer and other genital
tract neoplasias in infected patients however extra genital
warts are most commonly caused by HPV 6 and 11 which are rarely
associated with dysplasia and do not cause genital or anal
cancers. |
| TESTS |
The
diagnosis for genital warts is usually clinical and based
on the very characteristic appearance of warts. If there is
any doubt about the diagnosis for example pigmentation, ulceration
other atypical appearance then a biopsy should be taken. |
| TREATMENT |
The
aim of the treatment is to eradicate visible warts. It is
not possible to eradicate the virus. The patient will remain
infectious even in the absence of visible warts.
Treatment
for simple external warts is: Podophyllin (avoid in pregnancy),
TCA (external keratinized warts), Cryotherapy (for few solitary
warts), Hyfrecater (for few recalcitrant solitary warts.
Treatment
may be used alone or in combination, once or twice weekly.
If not responding to treatment after a maximum of 6 weeks
review by doctor and consider changing therapy or referral
to a senior doctor.
Cervical
warts may be treated via colposcopy and oral warts with
cryotherapy.
|
| FOLLOW
UP |
Patients
should be monitored during treamtnet to check efficacy and
the need to change if not responding. A cervical smear should
be taken at presentation and repeated at 12 months. If this
is normal the woman can revert to standard screening. Approximately
60% of the contacts will also have genital warts. All contacts
should be traced and offered STI screening and advice. Female
contacts are normally offered a cervical smear and repeated
in 12 months. |
| Herpes |
|
| TRANSMISSION |
Causative
organism is the herpes simplex virus types 1 and 2. |
| SYMPTOMS
(clinical features) |
Herpes
can only be transmitted when an already infected individual
is shedding the virus which happens sporadically and not
necessarily in association with symptoms.
It
is transmitted through close physical contact, genital-genital
and oro-genital. Infection is acquired through intact mucous
membrane or when the virus comes in contact with damaged
keratinised epithelium. |
| COMPLICATIONS |
A
minority of people will develop a severe primary attack
or first clinical episode within 2-12 weeks of acquisition
of the virus. It may not be possible to distinguish between
a so-called primary attack, which implies new infection
or first clinical episode where the patient has acquired
genital herpes at some time in the past, but only recently
developed symptoms.
Some
develop minor lesions (blisters) only and 70-80% of people
have no symptoms at all. Primary infection usually more
severe in women. Febrile illness (prodrome) lasting 5-7
days Dysuria, urinary frequency, painful inguinal, lymphadenopathy,
tingling neuropathic pain, genital blisters, ulcers, fissures.
An
untreated episode may last 3 weeks or more.
Recurrent
episodes are usually mild and symptoms may include neuropathic
prodrome with tingling and burning, erythema, blisters,
ulcers. |
| TESTS |
Usually
only on the first episode and risk reduced with antiviral
therapy. Include acute urinary retention, which occurs predominantly
in women Constipation which may be a risk with first episode
of perianal infection. Aseptic meningitis.
Herpes
in pregnancy is usually only significant if the patient
is experiencing a primary attack. In early pregnancy the
usual outcome is either an unaffected foetus or a miscarriage.
At term there is a 50% risk of neonatal transmission. In
women with a history of genital herpes, the risk of transmission
is in the range of 0-4%. However most neonatal herpes occurs
in infants whose mothers have no history of genital herpes. |
| TREATMENT |
Patients
should be seen as soon as possible during an acute attack.
Swabs are taken from the lesion for HSV culture. A negative
culture does not exclude HSV. Other causes of genital ulceration
should be excluded especially syphilis. |
| FOLLOW
UP |
Treatment
for a primary or first episode if within 5 days of lesions
developing or beyond 5 days if new lesions are developing
commence treatment immediately. Valaciclovir 500mg bd for
5 days. Analgesics, laxatives, advice about urinating, lignocaine
gel.
A dilute
saline solution (eg 1 tsp salt in a tumbler of warm water/1teacup
of salt to medium bath) to relieve symptoms, reduce secondary
infection and promote healing.
Counselling
is of the utmost importance, may need to be repeated subsequently |
| Syphilis |
|
| TRANSMISSION |
Causative
organism spirochaete Treponema Pallidum |
| SYMPTOMS
(clinical features) |
Almost
exclusively sexual although can be passed from mother to child.
Sexual transmission occurs in the first two years of untreated
infection, although transmission to the foetus may occur up
to 10 years after primary infection. |
| COMPLICATIONS |
Primary
9-90 days
Macule-palule painless ulcer.
Heals spontaneously in 2-6 weeks.
Indurated with clear exudate.
Up to 50% may be atypical in some way e.g. multiple, painful,
purulent, extragenital.
Secondary
2-6 months
Transient variable skin rash which can affect the soles
and palms.
Generalised lymphadenopathy.
Condylomata lata-warty type lesions on the genitals.
Mucosal ulceration.
Latent
Serological diagnosis.
Late
syphilis
Cardiovascular, neurological, gummatous syphilis.
|
| TESTS |
Neurological
manifestations may occur at any time in the course of the
disease. The late manifestations can arise at anytime from
5 years after the primary infection in an individual who
has received no treatment or inadequate treatment.
For
diagnosis of primary syphilis the exudate from lesions should
be examined by dark field microscopy for spirochaetes. Repeat
dark field daily for 3 days if the clinical suspicion is
high.
Serological
tests do not become positive for at least 10-14 days after
appearance of the primary lesion. If strong suspicion repeat
FTA in 2 weeks. Repeat serology after 3 months in any case
of undiagnosed genital ulcerationIn secondary syphilis the
serology tests are always strongly positive.
Latent
and late syphilis diagnosis is based on a combination of
positive TPHA and FTA. With or without positive VDRL and
RPR. |
| TREATMENT |
Treatment
for early syphilis, (primary, secondary and early latent):
First line therapy: bicillin 800000 units (=procaine penicillin
G600,000 units) IM daily for 10 days.
If
unable to give Bicillin over the WE then give double dose
on Monday morning.
Penicillin
allergy: Doxycycline 200mg daily for 14 days
Or Tetracycline 500mgs QDS X 14days |
| FOLLOW
UP |
Review
at 3 months for repeat syphilis serology and continue 6
monthly follow up for 2 years for patients with primary
or secondary syphilis or yaws.
Partner
notification should take place for all partners for up to
two years prior to diagnosis (discuss with senior doctor). |
| Hepatitis
B |
|
| TRANSMISSION |
Causative
organism hepatitis B virus (small DNA virus). Endemic worldwide
with high carriage rates up to 20% particularly in South
and South east Asia, but also in Southern Europe, central
and South America, Africa and Eastern Europe. In the UK
carriage varies from 0.01-0.04% in blood donors to >
1% in IVDU and gay men.
About
10-100 times more infectious than HIVSexual transmission
occurs in unvaccinated gay men and correlates with multiple
partners, unprotected anal sex and also or anal sex (rimming).
Transmission also occurs after heterosexual contact e.g.
18% infection rate for regular partners of patients with
acute hepatitis B. Sex workers are also considered high
risk.
Other
routes of transmission areVertical transmission (mother
to child) Blood, blood products, drug users sharing needles
and equipment and occupational needlestick injuries. Infected
mothers can continue to breastfeed. |
| SYMPTOMS
(clinical features) |
Incubation
period of 40-160 days. Virtually all infants and children
have asymptomatic acute infection. Asymptomatic infection
is also found in 10-50% of adults in the acute phase and
is especially likely In those who are co infected with HIV.
Women tend to have more severe disease than men. Less than
1% of patients will get fulminant hepatitis 5-10% will develop
chronic infection but the rate is higher in those with asymptomatic
acute infection and those with HIV co infection.
Almost
all of infants born to Hep B positive mothers will become
chronic carriers unless immunised. 20-30% of this group
will go on to develop chronic hepatitis, cirrhosis or carcinoma
of the liver. Carriers with the e antigen have a higher
risk of developing complications. |
| COMPLICATIONS |
Mortality
is less than 1% for acute cases. Between 10-50% of chronic
carriers will develop cirrhosis leading to premature death
in approximately 50%. About 10% of cirrhotic patients will
progress to develop liver cancer. |
| TESTS |
Diagnosis
is made by serology. |
| TREATMENT |
Patients
who present acutely in the primary care setting can be monitored
and usually do not require hospital admission. In view of
the possibility of chronic infection serology should be
repeated after 6 months even if the LFT s are normal.
Patients
who develop e antibodies but remain HbsAg positive should
have annual liver function tests and referral considered
of abnormality develops. Persistent HBeAg Carriers should
be referred. |
| FOLLOW
UP |
Hepatitis
B testing should be considered in:
Gay men CSWsIVDU.
HIV positive patients.
Sexual assault victims.
People from countries where Hep B is common.
Needlestick injuries.
Sexual partners of positive or high risk patients.
If
non immune vaccinations should be offered to non immune
patients in most of the above groups. The main exceptions
are those who have been sexually assaulted and those born
in countries of high endemicity but not at continuing risk.
Vaccination
schedule is 0 mths, 1 mnth and 6 mths
Accelerated
vaccination is 0 mths, 1 mth and 3 mths. Test for antibody
response at 8-12. |
| |
|
| Hepatitis
C |
Causative
organism Hep C virus, genus hepacicvirus of the family flaviviridae. |
| TRANSMISSION |
Parenteral
spread accounts for the majority of cases through shared
needles, syringes and other drug using equipment in IVDUs.
Can also be transmitted via infected blood products and
needlestick injuries.
Sexual
transmission occurs at a low rate (approximately 0.2-2%
per year of relationship) but this rate increases if the
index patient is also HIV infected. Vertical mother to child
transmission also occurs at a low rate (5% or less) but
transmission rates for women co-infected with HIV are higher
at up to 40%. |
| SYMPTOMS
(clinical features) |
Usually
infection is acquired asymptomatically. Approximately 5% will
develop a hepatic illness which is usually mild. |
| COMPLICATIONS |
Acute
fulminant hepatitis is rare (< 1%). Approximately 50-85%
of infected patients become chronic carriers-a state which
is normally asymptomatic. Symptoms/signs are worse if there
is a high intake of alcohol or other liver disease.
Mortality
in acute hepatitis is very low. But 20% of carriers will
progress to severe liver disease after 20 years infection,
with an increased risk of liver cancer.
Pregnancy.There
is at present no way of reducing the risk of vertical transmission.
Women should be informed of the potential risk of transmission
in pregnancy. Breast feeding should continue as there appears
to be no additional risk of transmission. |
| TESTS |
Diagnosis
is based on the detection of Antibodies Anti HCV. There are
no easy tests for the carrier state. PCR is sometimes done
to detect active virus although this is not necessary before
referral to the liver specialist at the JR. |
| TREATMENT |
Anti
HCV positive patients should be offered a referral to the
JR for further investigation and possible treatment. Patients
referred must be prepared to undergo a liver biopsy. |
| FOLLOW
UP |
There
is currently no vaccine available to contacts of Hep C.
It
seems likely that if condoms are used consistently then
sexual transmission will be avoided although given the low
transmission rate monogamous partners may choose not to
use them. |
| |
|
| Molloscum
Contagiosum |
Causative
agent the Pox Virus |
| TRANSMISSION |
Transmission
is through direct skin to skin contact and may affect any
part of the body. It is a common childhood infection but in
adults is usually sexually acquired. |
| SYMPTOMS
(clinical features) |
After
an incubation period of 3-12 weeks, discreet pearly, papular,
smooth umbilicated lesions appear. The size of the lesions
rarely exceeds 5mm and if untreated there is usually spontaneous
regression after several months. |
| COMPLICATIONS |
Lesions
can become large and unsightly in immunocompromised patients. |
| TESTS |
Diagnosis
is based on clinical appearance. |
| TREATMENT |
Treatment
is for cosmetic reasons only as most lesions will resolve
spontaneously without treament.Treatment is usually by piercing
with an orange stick with the application of phenol. |
| FOLLOW
UP |
No
need for treatment or screening of sexual partners unless
another infection is present. |