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what are STIs
Sexually transmitted infections
bacteria, viruses, parasites, lice, mites etc.
passed through contact with susceptible surfaces e.g. mucus membranes, genital fluid, genital discharge, blood to blood etc.
where does information from STIs come from
data collected every quarter from sexual health clinic attendances
demographics, testing, positive infections, treatments and health promotion details
where are high rates of STIs seen in
young people aged 15-24
gay, bisexual and other men who have sex with men (GBMSM)
black caribbean ethnicity
risks factors to consider for STIs
Age
ethnicity
sexuality
geography
poverty and social exclusion
recent partner chnage/ concurrent partners
bacterial STIs
chlamydia
gonorrhoea
what pathogen causes chlamydia and what is the infectious vector
caused by chlamydia trachomatis
exposure to bacteria through infected secretions/discharge
sites of inoculation in chlamydia
mucus membranes
endocervical
urethral
rectal
rectal
pharynx
conjunctiva
possible spread of chlamydia
pelvic inflammatory disease
Fitz-hugh curtis (peri-hepatitis)
epididymo-orchitis
proctitis
sexually acquired reactive arthritis (SARA)
what pathogen causes gonorhhoea and what is the infectious vector
caused by neisseria gonorrhoea
exposure to bacteria through infected secretions/ discharge
sites of inoculation of gonorrhoea
mucus membranes
endocervical
urethral
rectal
pharynx
conjunctiva
possible spread of gonorrhoea
local
gland infection and abcesses
pelvic inflammatory disease
epididymo-orchitis
proctitis
reactive
SARA
systemic→ disseminated gonoccocal infection
presentation of bacterial STIs
discharge from genital tract/rectum
discomfort, inflammation, bleeding
pelvic pain, pain on sex, testicular pain
joint/skin problems
conjunctivitis
identification of chlamydia
too small to see with magnification light, difficult to culture
PCR test
identification of gonorrhoea
visible under gram stain with light microscope
gram negative
cultured in specific medium and CO2 rich envrionment
vaginal infections
trichomonas vaginalis
bacterial vaginosis
candida
pathogen and infectious vector of trichomonas vaginalis
protozoa
exposure through infected secretions
site of inoculation of trichomonas vaginalis and possible spread
site of inoculation
vaginal epithelium
endo-urethral
spread
vaginal cuff
infections
reported post hysterectomy
PID
pathogen and infectious vector associated with bacterial vaginosis
bacterial vaginosis associated bacteria
traditionally thought not sexually transmitted
alkinisation of vagina promotes growth of BVAB
site of inoculation and possible spread of bacterial vaginosis
inoculation→ vaginal epithelium
possible spread
linked with PID
possible causative agent associated with more severe disease
pathogen and infectious vector for candida
yeast→ candida albicans, non-albicans species
commensal
site of inoculation of candida and possible spread
inoculation
vaginal and vulval epithelium
sub prepuce
spread→ local hypersensitivity
presentation of trichomonas vaginalis
yellow, frothy discharge
itch
vaginal soreness
urethral irritation
presentation of bacterial vaginosis
thin, white discharge
odour
presentation of candidiasis
thick white clumpy discharge
itch
vaginal and vulva soreness
identification of vaginal diseases
trichomonas vaginalis→ visible using wet mount microscopy
bacterial vaginosis→ vaginal pH>4.5, gram stain with microscope shows
reduced lactobacilli, clue cells
candida→ gram stain with light microscope shows spores and hyphae
viral STIs
warts
molluscum contagiousum
herpes simplex
pathogen and infectious vector for warts
human papilloma virus types 6 and 11
skin to skin contact with viral shedding
site of inoculation and possible spread of warts
inoculation→ genital and perianal epithelium
spread→ vagina and cervix, endourethral, rectal mucosa
pathogen and infectious vector of molluscum contagiosum
pox virus
exposure to infectious lesions, auto-inoculation
site of inoculation and possible spread of molluscum contagiosum
inoculation→ any skin
possible spread→ widespread in immunocompromised
pathogen and infectious vector for herpes simplex
pathogen→ herpes simplex virus types 1 and 2
exposure to infectious lesions, asymptomatic shedding, autoinoculation
site of inoculation and possible spread of herpes simplex
inoculation→ any mucus membrane, damaged epithelium
systemic infection in pregnancy and neonatal period, HSV meningitis/encephalitis
identification of genital warts
clinical diagnosis
biopsy if unclear
HPV typing not commercially available
identification of molluscum
clinical diagnosis
biopsy if unclear
identification of herpes
PCR swab from visible ulcer or broken skin
serology will show antibody response
blood-borne infections
syphilis
HIV
pathogen and infectious vector of syphilis
bacteria treponema pallidum
mucus membrane exposure to bacteria via infectious lesions, blood to blood, vertical transmission
site of inoculation and possible spread of syphilis
primary chancre on mucous membrane, blood to blood, perinatal
spread
secondary syphilis, myriad of symptoms by systemic spread
identification of syphilis
treponemes visible with dark ground microscope
difficult to culture
test from wet skin lesion
serology looking for direct and indirect treponemal response
identification of HIV
first line→ 4th generation assay (45 day window)
point of care test or venous bloods to check for antigen and antibody to the virus (12 week window)
transmission of HIV
sexual
sharing needles, injection of drugs
occupational
blood products
vertical
HIV infection and viral replication
free virus enters CD4 cell through binding and fusion between virus and coreceptor
HIV RNA released into cell→ synthesised to DNA
integrated to cell DNA→ transcription and translation
new viral protein assembled→ budding of free virus
effects of HIV on immune system
loss of CD4+ cells
chronically elevated CD8+ cells but poor quality
early loss of memory T cells weakens recall response to antigens
stages of HIV
primary→ 2-6 weeks, nonspecific illness
secondary asymptomatic→ can last 5-10 yrs
secondary symptomatic→ immune system destruction, symptoms begin to appear
late stage/end stage/ AIDS defining→ presence of indicator diseases
aims of treatment of HIV
prevent further cell destruction to allow immune system recovery
prevent further formation
reduce complications from longstanding chronic inflammation