BV, STIs etc Flashcards

1
Q

What is actinomycosis?

A

Actinomycosis is an uncommon, chronic granulomatous disease caused by filamentous, gram-positive, anaerobic bacteria. Actinomyces israelii is the major human pathogen.

Antibiotics that are commonly used in the treatment of PID (doxycycline, clindamycin, beta-lactams, fluoroquinolones) also have activity against actinomyces, although the treatment duration is longer (3 to 6 months).

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2
Q

Clinical features of PID

A
  • Bilateral lower abdominal tenderness (sometimes radiating to legs)
  • Abnormal vaginal or cervical discharge
  • Fever >38
  • Abnormal vaginal bleeding (IMB, PCB, BTB)
  • Deep dyspareunia
  • Cervical motion tenderness on bimanual VE
  • Adnexal tenderness on bimanual VE (with or without palpable mass)
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3
Q

Indication for hospitalisation for PID

A
  • Pregnancy
  • Lack of response or tolerance to oral medications
  • Non-adherence to therapy
  • Inability to take oral medications due to nausea and vomiting
  • Severe clinical illness (high fever, nausea, vomiting, severe abdominal pain)
  • Pelvic abscess, including tuboovarian abscess
  • Possible need for surgical intervention or diagnostic exploration for alternative etiology (appendicitis)
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4
Q

Indications for laparoscopy for PID

A
  • Sick patient with high suspicion of a competing diagnosis (usually appendicitis)
    • An acutely ill patient who has failed outpatient treatment for PID
    • Any patient not clearly improving after approximately 72 hours of inpatient PID treatment
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5
Q

How do you counsel a patient with PID?

A
  • Explanation of what treatment is being given and potential adverse effects
  • Remains a risk of future infertility, chronic pelvic pain and ectopic pregnancy
  • Repeat episodes of PID are associated with exponential increase in risk of infertility
  • Use of barrier contraception will significantly reduce risk of future PID
  • Advise full STI screen and discussion of safe sex practices
  • Advise screening of sexual contacts to prevent re-infection
  • More severe disease = greater risk of sequelae
  • Early treatment = lower risk of future fertility problems
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6
Q

What are the complications of PID?

A
  • Hydrosalpinx
  • TOA
  • Chronic pelvic pain
  • Ectopic pregnancy
  • Infertility
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7
Q

You are seeing a young woman who has been sexually assaulted. She has just spent two hours with a counselor and decided against the police report and forensic examination.

a) You take a medical history from this patient for NON forensic examination. What would you try to elicit in the history?

A

General principles:
• Acknowledge it difficult to talk of assault
• Permission to talk in own words
• Explain why information required
• Precise documentation
• Offer information about criminal nature of sexual assault and right to take legal action

Sexual assault history:
• Circumstances of the assault (date, time, location, use of weapons, force, restraints, or threats)
• Areas of trauma should be ascertained (mouth, breasts, vagina, and rectum)
• Specifics regarding oral, vaginal, or anorectal contact or penetration
• Presence or absence of ejaculation and/or condom use
• Bleeding on the part of either assailant or victim
• Whether the victim experienced loss of consciousness or memory loss
• Assailant’s physical description along with the assailant’s use of drugs or alcohol
• Recent consensual sexual activity before or after the assault including details

Gynaecological history:
• LMP and current contraception
• Previous STIs
• Previous pregnancies

Other history:
• Significant medical or surgical history (contraindications to emergency OCP)
• Medications and allergies
• D&A intake, smoking history
• Social history including relationships, living arrangements, work

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8
Q

b) List the immediate investigations and treatment you would do? (sexual assault)

A

Multidisciplinary team approach (obstetrician, psychologist, social worker)

Physical examination (chaperone or advocate present):
• Document any evidence of trauma
• Descriptive not diagnostic terms
• Photograph injuries on patient request
• Complete body examination
• Carefully attention to breasts, external genitalia, vagina, anus, and rectum
• Common sites of vaginal injury include the posterior vagina and the labia minora.
• Consider colposcopic examination can enhance detection of areas of milder genital trauma

Investigations:
• Trauma assessment;
o Radiographic imaging as indicated
• STI assessment;
o Any sites of contact (vagina, rectum, pharynx, mouth) can be swabbed for gonorrhea and chlamydia
o Wet prep vaginal smear can be examined to look for bacterial vaginosis and trichomonas.
o Baseline serologic tests for syphilis and hepatitis B should be done
o Baseline HIV test counseling with options of confidential/anonymous testing offered and explained
o Consider blood and urine drug screen
o Drug screening for flunitrazepam (Rohypnol, the “date rape drug”) and gamma-hydroxy butyrate (GHB) should be done selectively if the victim has amnesia for any time surrounding the event
• Pregnancy assessment
o Serum BhCG

Treatment:
• Trauma care;
o Fractures, soft tissue injuries, and other traumatic injuries should be treated appropriately.
• Sexually transmitted infections;
o Offer empiric antibiotic prophylaxis
 Patients often prefer immediate treatment
 Many assault victims will not return for a follow-up visit
 Empiric therapy includes ceftriaxone 250mg IM for gonorrhea and either azithromycin 1 gram PO (single dose) or doxycycline 100 mg PO bd for 1/52 for chlamydia.
 Metronidazole 2g PO (single dose) is also recommended to treat trichomoniasis.
o HBV empiric treatment following sexual assault is controversial
 Consider HBV vaccination +/- HBIG
o Prophylactic treatment with antiviral drugs for HIV following sexual assault is controversial
 Risks and benefits of HIV prophylaxis should be addressed with every patient
 Prophylaxis should be offered despite the presumed low risk of transmission and the lack of evidence proving the efficacy of antiretroviral drugs after sexual assault
 Antiretroviral drugs are best started within 4 hours of assault, and should probably not be prescribed >72 hours post incident
• Pregnancy:
o Postcoital emergency contraception should be offered without regard to the menstrual cycle
o Options include levononorgestrol, Yuzpe method, copper IUD
o Many patients will experience nausea and vomiting from the combination of antibiotics and contraceptives; antiemetics should be offered.
• Psychosocial issues;
o Sexual assault victims require extensive emotional support
o Victims should be offered mental health services.
o Acute crisis counselling should include safety planning
o Victims should be referred for ongoing counseling ideally through sexual assault crisis programs.
• Other;
o Consider notification to police

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9
Q

Rate of sexual violence amongst women

A

1 in 5 women have experienced a form of sexual violence

More common in younger women

78% of perpetrators are known by the woman

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10
Q

Likelihood of pregnancy depending on point in menstrual cycle?

A

Probability of pregnancy after unprotected intercourse by timing of coitus:

3 days before ovulation 15%,
1-2 days before ovulation 30%,
day of ovulation 12%,
1-2 days after ovulation NICE guideline says 8% SOGC says 8% pregnant 28% of women experience a delay of more than 3 days with their period

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11
Q

Sx of chlamydia?

A
75% asymptomatic 
PCB 
Dysuria 
Vaginal discharge 
Pain 
PID 
IMB
Reactive arthritis
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12
Q

Swabs for chlamydia?

A

If examined- endocervical swab preferable - NAAT (Nucleic Acid Amplification Test)

Otherwise self swab acceptable

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13
Q

Who should be tested for chlamydia?

A

<30 years and sexually active
partner change in the last 12 months
have had an STI in past 12 months
have had a sexual partner with an STI
at increased risk of complications of an STI e.g. termination of pregnancy (TOP) or intrauterine device (IUD) insertion
signs or symptoms suggestive of chlamydia
patient requests a sexual health check.

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14
Q

Treatment of chlamydia?

A

1g azithromycin stat

or 100mg BD Doxycycline 7/7

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15
Q

Cause of genital warts?

A

HPV 6 and 11

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16
Q

Treatment of genital warts?

A

Patient applied podophyllotoxin 0.15% cream or 0.5% paint topically applied, BD for 3 days, then 4 days off, repeated weekly for 4-6 cycles until resolution. Paint is more suited for use on external keratinised skin. Cream is best used in perianal area, introital area
OR
Patient applied imiquimod 5% cream topically, 3 times per week at bedtime (wash after 6-10 hours) until resolution (up to 16 weeks).

Complicated or disseminated infection: Consider referral for laser or diathermy

Indication for treatment is for sx/cosmesis not for cure

17
Q

Cause of gonorrhoea infection?

A

Neisseria gonorrhoeae, a Gram-negative intracellular diplococci (GNID) bacterium.

18
Q

Sx of gonorrhoeal infection?

A

Abnormal vaginal discharge
Dyspareunia with cervicitis
Conjunctivitis

PID
Disseminated disease:
- macular rash that may include necrotic pustules
- septic arthritis

19
Q

Ix of gonorrhoea?

A

Endocervical swab if examined, self swab if not

NAAT + culture for sensitivities

20
Q

Rx of gonorrhoea?

A

Ceftriaxone 500mg IMI, stat in 2mL 1% lignocaine
PLUS
Azithromycin 1g PO, stat

21
Q

Follow up of patients with gonorrhoea?

A

Review in 1 week provides an opportunity to:

Assess for symptom resolution
Confirm contact tracing has been undertaken or offer more contact tracing support
Provide further sexual health education and prevention counselling.

Test of Cure (TOC)
For pharyngeal, anal or cervical infection, TOC by Nucleic Acid Amplification Test (NAAT) should be performed 2 weeks after treatment is completed.

Retesting
Retest patients 3 months after exposure.

22
Q

Hepatitis A

A

Acute infection of the liver - doesn’t cause chronic hepatitis

Sx: Incubation period 15-50 days, mean of 28 days

Acute hepatitis: lethargy, nausea, fever, anorexia for a few days then jaundice, pale stools and dark urine

Usually asymptomatic in children, more severe illness in elderly and pregnant women, usually resolves in 1 month

23
Q

Hepatitis B

A

There is no such thing as a ‘healthy carrier’.
Infection causes acute, which may progress to chronic, hepatitis.

Transmission occurs from mother to child (vertical) via parenteral exposure (shared injection equipment) or through sexual or household contact (horizontal).
The risk of developing chronic hepatitis B is highest if infected at birth or <5 years (>90%). Infection as an adult has a <5% risk of progression to chronic hepatitis B.

24
Q

Rx for Herpes?

A

Initial episode: Valaciclovir 500mg PO, BD for 5 - 10 days

Can be reduced to 3/7 for recurrence

Other immediate management:
Written information and support
Simple analgesia and antipyretics
Saline bathing
Topical lignocaine reduces pain from erosions
Urinating in a bath or shower relieves superficial dysuria
Neuropathic bladder requires catheterisation until resolution
Encourage condom use with ongoing partners

25
Q

Syphillis- cause?

A

spirochete bacterium Treponema pallidum

26
Q

Symptoms of primary syphillis

A

Primary Syphilis

Incubation is usually 21 days (range 9-90)

Signs

Chancre (develops from a single papule)

Anogenital, single, painless and indurated with clean base, non-purulent

Can be multiple, painful and purulent (usually extra-genital)

Resolve over 3-8 weeks

27
Q

Symptoms of secondary syphillis

A

If primary syphilis is untreated 25% will develop secondary syphilis

Occurs 4-10 weeks after initial chancre

Multi-system

Signs

Rash

Widespread mucocutaneous
May be itchy
Can affect palms and soles
Mucous patches (buccal, lingual and genital)

Condylomata lata (highly infectious, mainly affecting perineum and anus)

Hepatitis

Splenomegaly

Glomerulonephritis

Neurological complications

Acute meningitis
Cranial nerve palsies
Uveitis
Optic neuropathy
Interstitial keratitis and retinal involvement
28
Q

Latent syphillis

A

Secondary syphilis will resolve spontaneously in 3–12 weeks and the disease enters an asymptomatic latent stage

Approximately 25% of patients will develop a recurrence of secondary disease during the early latent stage

29
Q

Late/tertiary syphillis

A

Occurs in approximately one third of untreated patients

20-40 years after intial infection

Divided into gummatous (mainly bone/skin), cardiovascular (aortitis) and neurological complications (decline in memory/cognitive functions/emotional lability etc)

30
Q

Early congenital syphillis

A

2/3 will be asymptomatic at birth but will develop signs within 5 weeks

Signs

Common:

rash
haemorrhagic rhinitis
generalised lymphadenopathy
hepatosplenomegaly
skeletal abnormalities
Other signs:
condylomata lata
vesiculobullous lesions
osteochondritis
periostitis
pseudoparalysis
mucous patches
perioral fissures
non-immune hydrops
glomerulonephritis
neurological ocular involvement,
haemolysis and thrombocytopenia
31
Q

Late congenital syphillis

A

Manifestations:

interstitial keratitis;
Clutton’s joints;
Hutchinson’s incisors;
mulberry molars (maldevelopment of cuspsof first molars);
high palatal arch;
rhagades (peri-oralfissures);
sensineural deafness;
frontal bossing;
short
maxilla;
protuberance of mandible;
saddlenose
deformity;
sterno-clavicular thickening;
paroxysmal
cold haemoglobinuria;
neurological involvement
(intellectual disability, cranial nerve palsies)
32
Q

Testing for syphillis

A

(i) Demonstration of T. pallidum from lesions or infected lymph nodes

Dark ground microscopy:

Should be performed by experienced observer
Is less reliable in examining rectal and non-penile genital lesions
Not suitable for examining oral lesions due to the presence of commensal treponemes
Polymerase chain reaction (PCR):

Can be used on oral or other lesions where commensal treponemes may also be present
Available at reference laboratories
May be helpful in diagnosis by demonstrating T.pallidum in tissue samples, vitreous fluid and cerebrospinal fluid (CSF)

(ii) Serological tests for syphilis

Treponemal antibody tests cannot differentiate syphilis cause by T. pallidum subspecies pallidum from endemic treponematoses (yaws, bejel and pinta)

(a) Primary screening tests

Treponemal EIA/CLIA (preferably that detects both IgG and IgM) or TPPA, which is preferred to TPHA.

Request anti-treponemal IgM test if primary syphilis is suspected.

The clinical utility is limited by suboptimal sensitivity - should not be used to stage disease or decide the duration treatment.

Rapid treponemal tests might be useful is some outreach settings, provided positive results are confirmed by laboratory tests.

(b) Confirmatory tests

Positive screening tests should be confirmed with a different treponemal test.

An IgG immunoblot is recommended as a supplementary confirmatory test when the standard confirmatory test does not confirm the positive screening test result. The FTA-abs is not recommended as a standard confirmatory test, although it may have a role in specialist laboratories.

A second specimen should always be tested to confirm positive results, and on the day that treatment is commenced so the peak RPR/VDRL is documented.

(c) Tests for assessing serological activity of syphilis

A quantitative RPR/VDRL should be performed when treponemal tests indicate syphilis to help stage the infection indicates the need for treatment in some cases, for example, where the patient has been previously treated and may have been re-infected.

An initial RPR/VDRL titre of 16 usually indicates active disease and the need for treatment, although serology must be interpreted in the light of the treatment history and clinical findings.

An RPR/VDRL titre of 16 or less does not exclude active infection, particularly in a patient with clinical signs suggestive of syphilis or where adequate treatment of syphilis is not documented.

A negative anti-treponemal IgM test does not exclude active infection, particularly in late disease.

33
Q

Antibiotics for syphillis?

A

Benzathine penicillin- dose dependent on stage of syphillis and whether pregnant or not

34
Q

Causes of vaginal discharge

A

Infections not associated with sex: Group B streptococcal vaginitis, bacterial vaginosis, Candida albicans
Non-infectious causes: hormonal contraception, physiological, cervical ectropion and cervical polyps, malignancy, foreign body (e.g. retained tampon), dermatitis, fistulae, allergic reaction, erosive lichen planus, desquamative inflammatory vaginitis, atrophic vaginitis in lactating and postmenopausal women
STI: Chlamydia trachomatis, Mycoplasma genitalium, Neisseria gonorrhoea, Trichomonas vaginalis, herpes simplex virus (HSV).

35
Q

Trichomoniasis- organism?

A

Trichomonas vaginalis, a protozoan which infects the vagina, urethra and paraurethral glands.

36
Q

Trichomoniasis- Symptoms? Rx?

A

Malodourous vaginal discharge - typically profuse and frothy
Vulval itch/soreness
Cervicitis

Pregnancy:
Associated with premature rupture of membranes, pre-term delivery and low birth weight
Post-partum sepsis

Rx: Metronidazole 2g PO with food, stat.

37
Q

Rx for recurrent candida?

A

Treat each episode with longer course of azole cream (rather than stat dose) and/or induction with fluconazole 150mg PO, for 3 doses, 3 days apart, followed by maintenance with fluconazole 100mg PO, weekly for 6 months

38
Q

Causes of anogenital ulcers

A
  • STIs: Herpes simplex viruses (HSV), syphilis, lymphogranuloma venereum (LGV), donovanosis, chancroid

• Other conditions: Fixed drug eruptions, aphthous ulcers, trauma, carcinoma, Crohn’s disease. Behcets.

39
Q

Causes of anogenital lumps

A

STIs: human papillomavirus (HPV), Molluscum contagiosum virus, herpes simplex virus (HSV), syphilis (may cause lymphadenopathy)

Other conditions: folliculitis, impetigo, immunological conditions, normal anatomical variations.