Treatment of Shingles (Herpes Zoster)
For immunocompetent adults with shingles, initiate oral valacyclovir 1 gram three times daily or famciclovir 500 mg three times daily within 72 hours of rash onset, continuing treatment until all lesions have completely scabbed—typically 7-10 days but potentially longer if active lesions persist. 1
Antiviral Therapy Selection
First-Line Oral Options for Immunocompetent Patients
Valacyclovir 1000 mg three times daily for 7 days is the preferred first-line agent, offering superior bioavailability and less frequent dosing than acyclovir while significantly accelerating pain resolution compared to acyclovir (median 38 days vs 51 days) 1, 2, 3
Famciclovir 500 mg three times daily for 7 days is equally effective to valacyclovir, with comparable efficacy in reducing postherpetic neuralgia duration and requiring only three-times-daily dosing 1, 4, 5
Acyclovir 800 mg five times daily for 7-10 days remains an effective option but requires more frequent dosing (five times daily), which may reduce adherence 1, 6
Critical Treatment Timing
Treatment must be initiated within 72 hours of rash onset for optimal efficacy in reducing acute pain, accelerating lesion healing, and preventing postherpetic neuralgia 1, 2
However, treatment initiated beyond 72 hours may still provide benefit for pain reduction, particularly in elderly patients, so do not withhold antivirals if the patient presents late 1
Treatment Duration Endpoint
Continue antiviral therapy until all lesions have completely scabbed, not just for an arbitrary 7-day period—this is the key clinical endpoint 1
If lesions remain active beyond 7-10 days, extend treatment duration accordingly 1
Intravenous Therapy Indications
When to Escalate to IV Acyclovir
Switch to intravenous acyclovir 10 mg/kg every 8 hours for: 1
- Disseminated herpes zoster (multi-dermatomal involvement or visceral involvement)
- Immunocompromised patients with any herpes zoster
- Complicated facial zoster with suspected CNS involvement
- Severe ophthalmic disease with vision-threatening complications
- Patients unable to tolerate oral medications
IV Treatment Duration and Monitoring
Continue IV acyclovir for minimum 7-10 days and until all lesions have completely scabbed 1
Monitor renal function closely during IV therapy with dose adjustments for renal impairment 1
In immunocompromised patients, assess for thrombotic thrombocytopenic purpura/hemolytic uremic syndrome with high-dose therapy 1
Special Population Considerations
Immunocompromised Patients
All immunocompromised patients should receive IV acyclovir 10 mg/kg every 8 hours due to high risk of dissemination and complications 1
Consider temporary reduction in immunosuppressive medications for disseminated or invasive disease 1
Treatment duration may need extension beyond 7-10 days as lesions develop over longer periods (7-14 days) and heal more slowly 1
Monitor for acyclovir resistance if lesions persist despite treatment; if confirmed, switch to foscarnet 40 mg/kg IV every 8 hours 1
Facial/Ophthalmic Involvement
Facial zoster requires particular urgency given risk of ophthalmic and cranial nerve complications 1
Initiate oral valacyclovir 1 gram three times daily or famciclovir 500 mg three times daily within 72 hours, ideally within 48 hours 1
Escalate to IV acyclovir if there is suspected CNS involvement, severe ophthalmic disease, or multi-dermatomal distribution 1
Elevate the affected area to promote drainage of edema and keep skin well hydrated with emollients to avoid dryness and cracking 1
Renal Impairment
Dose adjustments are mandatory for all oral antivirals to prevent acute renal failure 1
For valacyclovir with CrCl 30-49 mL/min: 1000 mg every 12 hours; CrCl 10-29 mL/min: 1000 mg every 24 hours; CrCl <10 mL/min: 500 mg every 24 hours 2
Pain Management
Acute Pain Control
Antiviral therapy itself is the primary intervention for reducing acute zoster-associated pain duration and intensity 1, 3
Valacyclovir and famciclovir demonstrate superior pain reduction compared to acyclovir 7, 3
Adjunctive Corticosteroids
Prednisone may be considered as adjunctive therapy in select cases of severe, widespread shingles in immunocompetent patients only 1
Avoid prednisone in immunocompromised patients due to increased risk of disseminated infection 1
Contraindications include poorly controlled diabetes, history of steroid-induced psychosis, severe osteoporosis, or prior severe steroid toxicity 1
The risks of corticosteroids (infections, hypertension, myopathy, glaucoma, osteopenia) generally outweigh benefits in most patients 1
Vaccination Recommendations
Post-Recovery Vaccination
Recommend recombinant zoster vaccine (Shingrix) for all adults aged 50 years and older after recovery from acute shingles, regardless of prior herpes zoster episodes 1
Shingrix reduces risk of future herpes zoster by over 90% with a two-dose series 1
Vaccination is particularly important before initiating immunosuppressive therapies like JAK inhibitors 1
The recombinant vaccine (Shingrix) is preferred over live-attenuated vaccine (Zostavax), which is contraindicated in immunocompromised patients 1
Infection Control
Patients with shingles must avoid contact with susceptible individuals (those who have not had chickenpox or vaccination) until all lesions have crusted, as lesions are contagious 1
Lesions are most contagious in the first 24 hours when vesicular 1
Common Pitfalls to Avoid
Do not use topical antivirals—they are substantially less effective than systemic therapy and are not recommended 1
Do not stop treatment at exactly 7 days if lesions have not completely scabbed—continue until clinical endpoint is reached 1
Do not use acyclovir 400 mg three times daily—this dose is only appropriate for genital herpes or HSV suppression, not shingles (requires 800 mg five times daily) 1
Do not delay treatment waiting for laboratory confirmation in typical presentations—clinical diagnosis is sufficient in immunocompetent patients 1
Do not apply corticosteroid creams to active shingles lesions—this can worsen infection and increase dissemination risk, particularly in immunocompromised patients 1