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38 Cards in this Set

  • Front
  • Back
Incubation period of HSV-1 and HSV-2
2-12 days
When are HSV antibodies detectable?
first several weeks of infection and the persis. Usually within 2-3 weeks after infection.
How many women report recognition of their HSV infection?
5-15%
Risk factors for HSV.
Female. Duration of sexual activity. Minority ethnicity. Previous genital infection. Family income. Number of sexual partners.
Percent of genital herpes caused by HSV-1
80%. Most pronounced in the adolescent and young adult populations.
Women with recurrent HSV who have an outbreak in pregnancy
75% at least one recurrence. 14% have prodromal symptoms or clinical recurrence at delivery.
_______ percent of HSV infected infants are born to mothers with no reported history of HSV infection.
80%
Classes of Neonatal HSV infection
1. disseminated disease (25%)
2. central nervous system disease (30%).
3. disease limited to skin, eyes, or mouth (45%).
Number of neonatal herpes infection caused by HSV-1.
1/3-1/2
Mortality of neonatal HSV
1. 30% for disseminated disease.
2. 4% central nervous system disease.
Long term effects of neonatal HSV.
20% of survivors have long-term neurologic sequelae.
How can the diagnosis of HSV be established?
1. Viral detection.
2. antibody detection.
Examples of HSV detection.
HSV culture and PCR
Advantages to PCR detection over HSV culture.
3-5X more likely to be positive than cultures.
Increased sensitivity over culture.
How to increase the positive predictive value of type-specific serologic HSV tests?
Repeat testing with different type-specific assay.
Most important in populations at low risk. (Because the positive predictive value is influenced by the prevalence of the disease in the population tested).
Fetal outcomes associated with primary HSV outbreak in pregnancy.
1. neonatal chorioretinitis.
2. microcephaly.
3 skin lesions.
Duration of treatment for primary outbreak of HSV
can extend up to 10 days if lesions incompletely healed.
Risk of vertical transmission with primary outbreak at time of delivery
30-60%
Reasons why vertical transmission more likey with primary outbreak.
1. Reduced transplacental passage of protective antibodies.
2. Neonatal exposure may be increased.
3. Higher concentration od longer duration of viral shedding.
Mean duration of viral shedding in primary HSV if untreated
15 days
Rate of transmission with vaginal delivery of women with recurrent lesions.
3%.
Why is transmission of recurrent HSV less than primary HSV?
In part due to transplacental passage of antiherpes antibodies.
Meta-analysis of acyclovir suppression for recurrent genital HSV.
1. recurrence at delivery reduced by 75%.
2. rate oc CD reduced by 40%.
3. Viral detection at delivery was reduced by 90%.
When is suppressive threapy recommended.
Start at 36 weeks for either primary or recurrent disease.
Which medication should be used for suppressive therapy.
Meta-analysis with acyclovir. But Several trials have demonstrated efficacy of valacyclovir.
How do doses for pregnant women differ than those for non-pregnant women.
1. Are higher in the trials for pregnant than non pregnant patients.
Doses of meds for primary outbreak.
1. Acyclovir 400 mg PO TID X 7-10 d.
2. Valacyclovir 1 gram PO BID x 7-10 d.
Doses of meds for recurrent episode of HSV.
1. Acyclovir 400 mg PO TID X 5 days OR 800 mg BID X 5 days
2. Valacyclovir 500 mg PO BID x 3 days OR 1 g PO daily X 5 days.
Daily suppression for HSV.
Acyclovir 400 mg PO TID
Valacyclovir 500 mg PO BID
Dosing for severe or disseminated HSV disease
5-10 mg/kg IV Q 8 hour X 2-7 days, the PO to complete 10 days.
3 main meds for HSV treatment.
Acyclovir, Valacyclovir, famciclovir
Mechanism of action of Acyclovir
inhibits viral thymidine kinase
Difference between Acyclovir and Valacyclovir.
Acyclovir bioavailability is 20%.
Valacyclovir is prodrug of Acyclovir and has 54% bioavailability.
Can achieve doses closer to IV acyclovir with Valacyclovir.
Benefits of Famciclovir.
Prodrug. Changes to penciclovir. 77% bioavailability. No published data in pregnancy.
How common is Acyclovir resistant HSV.
Not common in immunocompotent patients, but is seen in immunocompromised patients (6-7%).
Is there a role for routine screening for HSV during pregnancy or delivery?
1. Routine cultures in asymptomatic patient is not recommended. Does not predict shedding at time of delivery.
2. Not cost effective to run serologic tests to determine suppressive therapy unless in a particular population or specific patient.
When to deliver HSV positive with PPROM.
No consensus on gestation age where risks of prmaturity outweigh risks of HSV.
What invasive procedures are contraindicated in HSV positive women.
Trans cervical procedures should be delayed.
Avoid fetal scalp electrodes (6 X increased risk of neonatal infection).