Treatment of Chickenpox
For immunocompetent patients, oral acyclovir 800 mg four times daily for 5 days (or 20 mg/kg/dose up to 800 mg for children) should be initiated within 24 hours of rash onset for adolescents ≥13 years, adults, and high-risk groups, while immunocompromised patients require intravenous acyclovir 10 mg/kg every 8 hours for 7-10 days. 1, 2, 3
Who Requires Antiviral Treatment
Mandatory treatment groups include:
- Adolescents and adults ≥13 years of age 1, 4
- All immunocompromised patients (require IV formulation) 1, 4
- Children with chronic cutaneous or pulmonary disorders 1, 4
- Patients on long-term salicylate therapy 1, 4
- Patients receiving corticosteroid therapy 1, 4
Treatment is most effective when started within 24 hours of rash onset, with a clear gradation in clinical response correlating to timing—earlier initiation produces significantly better outcomes. 5, 6 Starting therapy on day 2 of rash still provides some benefit, but efficacy diminishes substantially after 24 hours. 5
Oral Acyclovir Dosing
For children <40 kg:
For adults and children >40 kg:
Five days of therapy is sufficient—extending to 7 days provides no additional clinical benefit. 5 The FDA-approved regimen specifies dosing every 4 hours while awake (5 times daily). 3
Intravenous Acyclovir for Severe Disease
Immunocompromised patients and those with severe disease require:
- 10 mg/kg IV every 8 hours for 7-10 days 1, 2, 7
- Some experts dose children >1 year based on body surface area: 500 mg/m²/dose IV every 8 hours 2
IV acyclovir halts disease progression in immunocompromised hosts and is potentially life-saving, as chickenpox in this population can be fatal. 7
Renal Dosing Adjustments
For creatinine clearance 10-25 mL/min: 800 mg every 8 hours 3
For creatinine clearance 0-10 mL/min: 800 mg every 12 hours 3
Hemodialysis patients: Administer an additional dose after each dialysis session due to 60% reduction in plasma concentrations during 6-hour dialysis. 3
Post-Exposure Prophylaxis
Varicella zoster immune globulin (VZIG) is the preferred prophylaxis for high-risk exposed individuals:
- Administer as soon as possible, up to 10 days after exposure (ideally within 96 hours) 1, 4
- Indicated for susceptible immunocompromised patients 1, 4
- Indicated for pregnant women without evidence of immunity 1
- Indicated for neonates born to mothers with varicella 5 days before to 2 days after delivery 1
- Indicated for premature infants <28 weeks gestation or <1,000 g regardless of maternal immunity 1
If VZIG is unavailable:
Critical caveat: Acyclovir is NOT indicated for routine prophylaxis in healthy individuals after exposure. 2 Delay varicella vaccination 5 months after VZIG administration. 1
Infection Control Measures
Isolate patients until all lesions have crusted over. 1, 4 This is the standard endpoint for contagiousness.
Healthcare workers without immunity exposed to VZV should be furloughed from days 10-21 after exposure. 1, 4
Special Populations
Pregnant women:
- Acyclovir is FDA pregnancy category B 2
- Routine use during pregnancy is not generally recommended 2
- For serious viral-mediated complications, IV acyclovir should be considered 2
- VZIG is recommended for VZV-susceptible pregnant women within 96 hours of exposure 8
HIV-infected children:
- Varicella vaccination is recommended for asymptomatic, non-immunosuppressed children (immunologic category 1) at 12-15 months 8, 1
- Live varicella vaccine is contraindicated in other HIV-infected children due to risk of disseminated infection 8, 1
Vaccination Considerations for Contacts
Vaccinate susceptible household contacts of immunocompromised patients to prevent transmission, provided they are HIV-seronegative and have no history of chickenpox. 8, 4 This creates a protective barrier around vulnerable individuals.
Important Clinical Caveats
Acyclovir does not eradicate latent virus or affect subsequent risk of herpes zoster (shingles). 2 Antibody titers after infection in treated children do not differ substantially from untreated patients. 2
Viral resistance has not been a clinical problem—viruses shed during oral acyclovir therapy retain normal susceptibility and thymidine kinase function. 5 However, the effect on latent virus resistance remains unassessed. 5
Antibody titers are unreliable in patients with nephrotic-range proteinuria or those receiving IVIG for determining immunity status. 1
Disease severity increases with age, and secondary household cases tend to be more severe than primary cases, supporting treatment of adolescents, adults, and secondary family cases. 7