Genital herpes
Last Updated: 2023-07-07
Author(s): Anzengruber F., Navarini A.
ICD11: 1A94.0
Primary or secondary infection due to herpes simplex virus II (in 80-90% of cases) or HSV I (10-20%).
- Vulvovaginitis herpetica
- Cervicitis herpetica
- Proctitis herpetica
- Urethritis herpetica
- Balanitis or balanoposthitis herpetica
Transmission through skin to skin contact, mostly sexual intercourse / oral sex.
Genital redness and swelling with (often grouped localised) herpetiform vesicles, erosions and haemorrhagic crusts, sometimes painful, often severe itching; reduced AZ, fever, restlessness, vomiting.
- Clinical manifestion (exclude meningismus)
- If needed:
- PCR or microtrack
- Biopsy is rarely helpful
- Possible "peripartum" infection of the newborn in women
- Secondary infection with bacteria or candida
- Healing after 3-4 weeks
- Recurrences occur mainly in the first year after initial infection, with males showing symptoms more frequently
Recommendations:
- 1st line therapy: valaciclovir, aciclovir, famaciclovir
- 2nd line therapy: foscarnet, cidofovir
- 3rd line therapy: L-lysine, aspirin, topical imiquimod
Systemic therapy
- Aciclovir
- dosage: 3x 5-10 (according to Lebwohl) mg/kg bw/d i.v. or 5x200mg per os depending on clinic
- contraindications: hypersensitivity, lactation
- adverse reactions (very common): headache
- CAVE:
- in elderly patients, there is an increased risk for the occurrence of reversible neurological disorders
- adjust dosage if renal function is impaired
- enough fluid intake
- Valaciclovir
- dosage: 2x500mg daily p.o.for 10 days (initial infection), 5 days (relapse)
- contraindications: hypersensitivity, lactation
- adverse reactions (common): headache, nausea
- CAVE:
- adjustment of dosage in impaired renal function
- hydration state
- Famciclovir
- dosage: 500 mg 2x/d
- in pat. >50, 500mg 3x/d should be given to prevent zoster neuralgia
- independent on meals
- interactions: probenecid
- contraindications: Pregnancy, lactation, hypersensitivity to famciclovir or penciclovir
- CAVE:
- In patients at risk of dehydration, especially elderly patients, adequate hydration should be ensured
- Efficacy may be reduced in black patients
- Brivudine
- off-label-use
- dosage: 125 mg 1x/d for 7 days
- interactions: 5-fluorouracil preparations (time interval at least 4 weeks)
- adverse reactions (common): nausea
- contraindications: 5-fluorouracil- therapy, pregnancy, lactation, hypersensitivity to ingredient, not tested in children and adolescents
Topical therapy
- desiccative topiclas, i.e. iodine solutions
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