Although lesions caused by herpes simplex virus (HSV) subtypes HSV-1 and HSV-2 differ in rates of recurrence and subclinical shedding, they are treated with the same antiviral regimens, based on the site of infection.[1, 2, 3, 4]
First episode
Previously, treatment was recommended in all patients, as symptoms could be severe and/or prolonged.[1, 3, 4] The latest guidelines state that oral antiviral drugs should be administered to patients presenting within 5 days of the start of the episode or while new lesions are still forming. The recommended regimens, all with a treatment duration of 5-10 days, are as follows:[5]
Topical agents are not recommended, as they are less effective than oral agents and easily generate resistance.
Recommended initial doses in HIV-positive patients are as follows:
First episode during pregnancy: Daily suppressive acyclovir 400 mg TID from 36 weeks’ gestation may prevent HSV lesions at term and hence the need for delivery via Caesarean section.
Regimens in adults and adolescents with a first clinical episode of genital HSV infection are as follows:[6]
Recurrent episodes
Initiate treatment during prodrome or within 24 hours of lesion appearance to ensure effectiveness.[1, 3, 4] Regimens are as follows:
Recurrent genital herpes[5]
Oral acyclovir, valacyclovir, and famciclovir are effective at reducing the duration and severity of recurrent genital herpes. The reduction in duration is a median of 1-2 days.
Short-course therapies should be tried in the first instance, as follows:
Alternative longer 5-day courses include the following:
Management of HIV-positive pregnant women with recurrent HSV infection: Women who are HIV antibody–positive and have a history of genital herpes should be offered daily suppressive acyclovir 400 mg TID from 32 weeks’ gestation to reduce the risk of HIV-1 transmission, especially if vaginal delivery is planned.
Recurrent clinical episode of genital HSV infection[6]
Dosages for adults, adolescents, and pregnant women are as follows:
Dosages for people living with HIV and people who are immunocompromised are as follows:
Episodic infection in immunocompromised patients/those with HIV infection
Recommended regimens for episodic infection in immunocompromised patients including those with HIV infection[1] are as follows:
Recommendations for HSV treatment in adult HSV‐seropositive solid-organ transplant recipients are as follows:[7]
Because prompt initiation of therapy is associated with improved outcomes, therapy should be started based on clinical diagnosis, pending laboratory confirmation. Therapy should be continued until all lesions are completely healed or at least 5‐7 days.[7]
Suppressive therapy
Daily suppressive antiviral therapy reduces the rate of outbreaks and of subclinical shedding. Use of once-daily valacyclovir has been demonstrated to reduce the rate of transmission to HSV-2–seronegative partners.[1, 3, 8, 4]
Suppressive therapy reduces the frequency of genital herpes recurrences by 70%-80% in patients who have frequent recurrences.[9]
In adults and adolescents with recurrent clinical episodes of genital HSV infection that are frequent (eg, 4-6 times per year or more), that are severe, or that cause distress, the WHO sexually transmitted infection (STI) guidelines suggest suppressive therapy over episodic therapy and reassessment after one year.[6]
The optimal total daily dose of suppressive acyclovir therapy is 800 mg.[5]
Recommended doses for adults, adolescents, and pregnant women are as follows:[5, 6]
Second-stage therapy for poorly controlled cases are as follows:[5]
Recommended drug regimens for daily suppressive treatment in immunocompromised/HIV-positive patients are as follows:[6, 5, 1]
If these options do not adequately control disease, the first option should be to double the dose. If control is still not achieved, famciclovir 500 mg PO BID can be tried.[5]
Antiviral-resistant HSV infection
If lesions persist or recur in a patient receiving antiviral treatment, HSV resistance should be suspected and a viral isolate obtained for sensitivity testing.[9]
All acyclovir-resistant strains are also resistant to valacyclovir, and most are resistant to famciclovir.[9]
Treatment for acyclovir-resistant genital herpes:[9] Foscarnet (40-80 mg/kg IV q8h until clinical resolution is attained) is a DNA polymerase inhibitor unrelated to acyclovir and its congeners that is available only for intravenous use and has been compounded for topical use.
Alternatives are as follows:[9, 10]
The following are regimens for acyclovir‐resistant HSV in adult HSV‐seropositive solid organ transplant recipients:[7]
Resistance should be laboratory‐confirmed, although empiric therapy can be started. Reduce immunosuppression, if possible.[7]
Herpes labialis
Episodic therapy
Initiate treatment within 48 hours of symptom onset.[3, 11, 12, 4, 13] Regimens include the following:
Episodic treatment for recurrent herpes labialis in immunocompetent patients is as follows:[14]
Episodic treatment for recurrent herpes labialis in HIV-infected/immunocompromised patients is as follows:[14]
Suppressive therapy
Regimens include the following:[3, 11, 4, 13]
Long-term suppressive therapy should be considered in patients with frequent and severe infections, specifically patients with herpes-associated erythema multiforme or eczema herpeticum.[14]
Long-term suppressive therapy for recurrent herpes labialis in immunocompetent patients is as follows:[14]
Stomatitis[15]
Herpes labialis prophylaxis[15]
Esophagitis: Duration typically 7-10 days[15]
A systematic review and meta-analysis of 4 studies showed that patients receiving topical corticosteroids in addition to antiviral therapy had a significantly lower recurrence rate of ulcerative lesions compared with those in the placebo group (OR, 0.50; 95% CI, 0.39-0.66; P< 0.001) and the antiviral treatment alone group (OR, 0.73, 95% CI, 0.58-0.92; P = 0.007). The healing time was also significantly shorter in combined therapy compared with placebo (P< 0.001).[16]
Severe HSV disease
Disseminated HSV disease or severe symptoms in the immunocompromised patient[1] : Acyclovir 5-10 mg/kg IV q8h for 2-7 days until clinical improvement is observed, followed by oral antiviral therapy, to complete at least 10 days total of therapy
HSV meningoencephalitis[3, 17] : Acyclovir 10-20 mg/kg IV q8h for 14-21 days should be given early to prevent extensive replication and subsequent CNS damage.
Early treatment should be started in any of the following situations:[18]
Encephalitis[15] : Acyclovir 10 mg/kg IV q8h for 14-21 days
Acute meningitis[15] : Acyclovir 10 mg/kg IV q8h for 7-10 days
Benign recurrent lymphocytic meningitis[15] : Acyclovir 10 mg/kg IV q8h for 7-10 days
Severe, visceral/disseminated/CNS disease in adult HSV‐seropositive solid organ transplant recipients, as follows:[7]
Neonatal HSV[3, 17, 19] : Acyclovir 20 mg/kg IV q8h
Duration of therapy is determined by the disease classification, as follows[20]
After completion of the recommended 14- or 21-day treatment course with intravenous acyclovir determined by patient's classification of neonatal HSV disease, patients are transitioned to oral acyclovir (300 mg/m2/dose TID) to complete a 6-month course of suppressive therapy.[20]
All infants with CNS involvement require repeat lumbar puncture to assess for clearance of the virus prior to termination of intravenous therapy.[20]
If HSV PCR continues to show viral DNA at approximately day 21 of therapy, intravenous acyclovir should be extended an additional week and a repeat lumbar puncture performed to obtain CSF for HSV PCR testing.[20]
See Herpes Simplex Viruses: Test Your Knowledge, a Critical Images slideshow, for more information on clinical, histologic, and radiographic imaging findings in HSV-1 and HSV-2.