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