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Herpes Simplex Virus for the Physician Assistant Licensing Exam
  • Etiology:
    • Caused by herpes simplex virus types 1 and 2 (HSV-1 and HSV-2), both double-stranded DNA viruses in the Herpesviridae family.
    • HSV-1: Typically associated with orolabial infections but can cause genital lesions.
    • HSV-2: Primarily associated with genital herpes but may also cause oral infections.
  • Epidemiology:
    • HSV-1 is usually acquired in childhood through non-sexual contact, while HSV-2 is most commonly acquired during adolescence or adulthood via sexual contact.
Pathophysiology
  • Latency and Reactivation:
    • After initial infection, HSV establishes latency in sensory neurons (trigeminal ganglia for HSV-1, sacral ganglia for HSV-2).
    • Reactivation occurs due to triggers such as stress, immunosuppression, ultraviolet (UV) exposure, or hormonal changes, resulting in recurrent infections.
  • Transmission:
    • Transmitted via direct contact with infected mucosal surfaces or secretions.
    • Asymptomatic viral shedding contributes significantly to transmission, even in the absence of active lesions.
Clinical Manifestations
Primary HSV Infection
    • Systemic Symptoms: Often more intense than recurrent infections, with fever, malaise, lymphadenopathy, and myalgias.
    • Orolabial HSV-1:
    • Painful vesicles or ulcers on the lips, oral mucosa, or perioral skin.
hsv
    • Gingivostomatitis is common in children with primary HSV-1 infection.
    • Genital HSV-2:
    • Painful vesicles and ulcers on genital or perianal skin, often with dysuria and inguinal lymphadenopathy.
Recurrent HSV Infection
    • Orolabial Recurrence (HSV-1):
    • Manifests as cold sores, often preceded by tingling or itching.
    • Genital Recurrence (HSV-2):
    • Usually milder than the primary infection, with localized lesions often preceded by prodromal symptoms.
Complications
    • Herpetic Whitlow:
    • HSV infection of the finger, often seen in healthcare workers or patients with oral exposure.
    • Herpes Simplex Keratitis:
    • Corneal HSV infection, commonly HSV-1, presenting with dendritic ulcers and potential vision loss if untreated.
    • HSV Encephalitis:
    • Primarily HSV-1, affecting the temporal lobes and causing fever, altered mental status, focal neurological signs, and seizures.
    • Neonatal Herpes:
    • Acquired during delivery from mothers with active genital HSV, leading to disseminated disease, CNS infection, or localized skin/mucosal lesions in newborns.
Diagnosis
  • Polymerase Chain Reaction (PCR):
    • Preferred for detecting HSV in CNS infections and lesions due to high sensitivity and specificity.
  • Viral Culture:
    • Useful for early vesicular lesions but less sensitive than PCR.
  • Serology:
    • Detects HSV-1 and HSV-2 antibodies, useful for confirming prior exposure but not for acute diagnosis.
Treatment
Antiviral Therapy
    • Acyclovir, Valacyclovir, and Famciclovir:
    • First-line treatments that reduce symptoms and recurrence frequency.
    • Primary Infection:
    • Acyclovir: 400 mg PO three times daily for 7–10 days.
    • Valacyclovir: 1 g PO twice daily for 7–10 days.
    • Recurrent Infection:
    • Acyclovir: 400 mg PO three times daily for 5 days.
    • Valacyclovir: 500 mg PO twice daily for 3 days.
    • Suppressive Therapy:
    • For patients with frequent recurrences or those desiring to reduce transmission risk.
    • Acyclovir: 400 mg PO twice daily.
    • Valacyclovir: 500 mg or 1 g PO once daily.
Management of Complications
    • HSV Encephalitis: Requires high-dose IV acyclovir (10 mg/kg every 8 hours) for 14–21 days.
    • Neonatal Herpes: Requires immediate IV acyclovir treatment (20 mg/kg every 8 hours) for 14–21 days.
    • Herpetic Keratitis: Managed with topical antivirals like trifluridine or oral antivirals, and referral to ophthalmology.
Prevention and Reduction of Transmission
    • Condom Use: Reduces transmission but does not completely prevent it.
    • Partner Notification: Important to inform sexual partners; suppressive therapy can help lower transmission risk.
    • Cesarean Delivery: Recommended for pregnant women with active genital lesions at labor to prevent neonatal transmission.
Key Points
  • HSV-1 primarily causes orolabial infections, and HSV-2 is mainly responsible for genital infections, though both can affect either site.
  • Latency and Reactivation: HSV establishes latency in sensory ganglia, with reactivation triggered by stress or immunosuppression.
  • Diagnosis is confirmed with PCR, especially for CNS involvement; serology helps confirm past infection.
  • Treatment with acyclovir, valacyclovir, and famciclovir reduces symptoms and recurrence frequency.
  • Prevention involves condom use, partner notification, and cesarean delivery in cases of active maternal infection at the time of labor to protect neonates.