HSV Flashcards
Incidence of neonatal HSV disease in Australia
very low (3 per 100,000 live births)
Modes of transmission of HSV
- Intrapartum (most)
- True intrauterine infection (<5%)
- Postnatal from infected care giver (10%)
Major type of neonatal HSV infection
HSV-1 (>65%)
Risk of MTCT with HSV-1 greater than from HSV-2 (OR 16.5)
Risk of MTCT of HSV:
Past history, no clinical recurrence in pregnancy or labour
Very low (<0.04%)
Risk of MTCT of HSV:
Past history, clinical recurrence in pregnancy or delivery
Active lesions at delivery: 2%
(Likely lower in immunocompetent women in Australia)
Risk of MTCT of HSV:
No past history, primary first episode (sero-neg for both HSV 1&2 and genital swab +ve)
High risk (25-50%)
- However if type specific sero-conversion occurs well before delivery (<30/40) = risk same as for recurrent herpes
Risk of MTCT of HSV:
Non-primary first episode (i.e. positive serology but for the other type than current infection)
High risk (25-50%)
- Unless sero-conversion well before delivery in which case risk same as for recurrent herpes
Antenatal Management of women with a history of genital HSV (laboratory confirmed)
Consider suppressive antiviral therapy from 36 weeks’ if:
- multiple recurrent overt lesions
- frequent symptomatic recurrences
Suppressive antiviral therapy what and why?
Aciclovir 400mg TDS or valaciclovir 500mg BD reduces
1. Clinical recurrences
2. Asymptomatic shedding
3. Caesarean section
4. Virus in genital tract
*Underpowered to evaluate efficacy of preventing transmission to newborn
Intra-partum management of women with a history of genital HSV and no active lesions
- Proceed with vaginal delivery
- Avoid FSE, FBS, OVD if possible
Who to examine for genital herpes
All women admitted in labour (RANZCOG)
Intra-partum management of women with a history of genital HSV and active lesions
- Balance low risk of MTCT in vaginal delivery of women with recurrent disease, with risks of caesarean section
- CS reduces risk of HSV transmission at birth, but does not provide complete protection
Antenatal Management of primary genital HSV
- If diagnosis in early pregnancy, suppressive therapy from 36/40
- If diagnosis in third trimester
- suppressive therapy from 36/40
- delivery via CS (regardless of timing of ROM)
Scenarios with very low risk of neonatal HSV exposure and disease
- Mother with active recurrent genital herpes due to HSV2 at delivery
- Mother who had primary genital HSV2 and how has now developed HSV type specific IgG
No need to do neonatal surface swabs on these babies in Australia. Monitor for clinical disease.
Scenarios with possible high risk of neonatal HSV exposure and disease
- Mother with primary genital or sstemic infection close to delivery
- Infant born to mother with active genital herpes and no known past history of genital HSV
- Preterm infant born to mother with active genital herpes
- Infant born to immunocompromised mother with active genital herpes
Perform Ix including swabs, bloods, LP and commence IV aciclovir immediately