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Herpes Simplex in Pregnancy and Labour
Background
Genital HSV in pregnancy is clinically significant because of the risk of neonatal transmission — which carries high mortality and morbidity. The key determinants of risk are:
- Nature of infection at delivery: first episode vs. recurrent
- Presence of active genital lesions at the time of labour
- Gestational timing of primary acquisition
Neonatal herpes occurs in ~1:3,000–20,000 live births; 85% of cases are acquired at delivery, 10–15% postnatally from non-maternal sources, and only 5% in utero.
Risk of Neonatal Transmission
| Scenario | Transmission Risk |
|---|
| Recurrent genital HSV, vaginal delivery with active lesions | 2–5% |
| Primary/first-episode genital HSV at delivery, vaginal | 26–56% |
| Caesarean section (culture-positive cervix) | ~1% |
The 70% of mothers of neonates with HSV are asymptomatic at delivery with no prior history — so history-taking alone cannot reliably identify risk.
— Andrews' Diseases of the Skin, p. 429; Harrison's Principles of Internal Medicine 22E
Treatment in Pregnancy
First Episode / Primary Infection During Pregnancy
Antiviral treatment is recommended for all initial episodes of genital HSV in pregnancy (except possibly in the first month, where there may be an increased risk of spontaneous abortion).
- Acyclovir 400 mg orally three times daily for 10 days (standard dose)
- This is especially important for initial episodes in the third trimester
- IV acyclovir should be considered for severe/disseminated primary infection
Acyclovir is safe in pregnancy: "No adverse effects to the fetus or newborn have been attributable to acyclovir. Acyclovir can be used in all stages of pregnancy and among women who are breastfeeding." — Harrison's, p. 1547
Suppressive Therapy in Late Pregnancy
For women with recurrent genital herpes or a first-episode during pregnancy, suppressive therapy from 36 weeks gestation until delivery is recommended to:
- Reduce clinical recurrences at term
- Reduce the frequency of caesarean delivery for active HSV
- Reduce viral shedding at delivery
Regimens:
- Acyclovir 400 mg orally three times daily from ~34–36 weeks until delivery
- Valacyclovir 500 mg orally twice daily from ~34 weeks until delivery
Note: Suppressive therapy reduces the risk of needing caesarean section but may not fully prevent neonatal transmission.
— Harrison's, p. 1547; Andrews' Diseases of the Skin, p. 429; Fitzpatrick's Dermatology
Management During Labour
Caesarean Section Indications
Caesarean section is recommended when a woman presents in labour with:
- Active genital lesions (cervical, vaginal, or vulvar)
- Prodromal symptoms (tingling, burning in genital area)
This reduces transmission risk from ~8% to ~1% in culture-positive women. However, it does not prevent all neonatal herpes cases.
Caesarean section may not reliably prevent neonatal HSV when membranes have been ruptured for ≥24 hours. — Fitzpatrick's Dermatology
Intrapartum Precautions
- Avoid scalp electrodes in any delivery where cervical HSV shedding is possible — associated with up to sevenfold increased risk of neonatal infection
- Avoid vacuum-assisted delivery — increases relative risk of neonatal transmission 2–27 times
- Routine prenatal cultures are not recommended in recurrent herpes (they don't predict shedding at delivery); they may be of value in women with primary genital HSV during pregnancy
Preventing Maternal Acquisition During Pregnancy (Serodiscordant Couples)
If the woman is HSV-seronegative and her partner is HSV-positive:
- Barrier contraception (condoms) for all sexual contact
- Avoid orogenital contact if partner is HSV-1 positive and woman is HSV-1 negative
- Valacyclovir suppression of the infected partner can be considered
- Abstinence in the third trimester further reduces risk
These measures are important because acquisition of primary HSV near term carries the highest risk of neonatal disease.
Neonatal Treatment (if infected)
| Disease type | Treatment |
|---|
| SEM (skin, eyes, mouth) | IV acyclovir × 14 days |
| CNS disease | IV acyclovir × 21 days |
| Disseminated disease | IV acyclovir × 21 days |
Prognosis: localized SEM disease is rarely fatal with treatment; CNS/disseminated disease has 15–50% mortality even with treatment, and >50% of survivors have neurologic disability.
— Andrews' Diseases of the Skin, p. 429
Summary Table
| Clinical Situation | Management |
|---|
| Primary HSV in pregnancy | Acyclovir 400 mg TDS × 10 days; IV acyclovir if severe |
| Recurrent HSV, antepartum | Suppression from 36 wks: acyclovir 400 mg TDS or valacyclovir 500 mg BD |
| Active lesions/prodrome at labour onset | Caesarean section |
| No active lesions, recurrent HSV | Vaginal delivery can be considered |
| Intrapartum | Avoid scalp electrodes; avoid vacuum delivery |
| Neonatal HSV (SEM) | IV acyclovir 14 days |
| Neonatal HSV (CNS/disseminated) | IV acyclovir 21 days |