Treatment of Varicella (Chickenpox)
Acyclovir is the recommended treatment for varicella, with dosing regimens varying based on patient age, immune status, and disease severity. 1, 2
Treatment Recommendations by Patient Population
Immunocompetent Children
- For children 2 years and older: Oral acyclovir 20 mg/kg per dose 4 times daily (80 mg/kg/day) for 5 days, not to exceed 800 mg per dose 2
- For children over 40 kg: Adult dosing of 800 mg 4 times daily for 5 days 2
- Treatment should be initiated at the earliest sign or symptom of chickenpox, preferably within 24 hours of rash onset 2, 3
- Early treatment with acyclovir has been shown to reduce fever duration, accelerate cutaneous healing, and decrease the number of lesions 3
Immunocompetent Adults
- Oral acyclovir 800 mg 4 times daily for 5 days 2
- Treatment is most effective when started within 24 hours of rash onset 1
- Acyclovir has been demonstrated to reduce the duration and severity of clinical illness in adults 1
Immunocompromised Patients
- Intravenous acyclovir is indicated for immunocompromised patients with varicella 2, 4
- The recommended dose is 10 mg/kg or 500 mg/m² every 8 hours for 7-10 days 4, 5
- IV acyclovir has been shown to decrease new lesion formation, reduce acute pain, halt dissemination, and lessen visceral complications in immunocompromised patients 6, 5
- Treatment should be initiated immediately upon diagnosis, as early treatment is essential for preventing serious complications 5
Special Populations
Pregnant Women
- For pregnant women with serious varicella complications (e.g., pneumonia), intravenous acyclovir should be considered 1
- Acyclovir is classified as a Category B drug in pregnancy 1
- A registry of 596 infants whose mothers received systemic acyclovir during first trimester showed no increased rate of birth defects 1
Neonates and Premature Infants
- For neonates whose mothers developed varicella from 5 days before to 2 days after delivery: Varicella-Zoster Immune Globulin (VZIG) is indicated 1
- For premature infants born at <28 weeks gestation or weighing <1,000g with postnatal exposure: VZIG regardless of maternal immunity 1
- For premature infants born at >28 weeks gestation with postnatal exposure whose mothers lack immunity: VZIG is indicated 1
Post-Exposure Prophylaxis
Immunocompromised Patients
- VZIG is recommended for post-exposure prophylaxis in immunocompromised patients without evidence of immunity 1
- Dosage: 125 units/10 kg of body weight, up to maximum of 625 units 1
- VZIG should be administered as soon as possible after exposure, ideally within 96 hours 1
- Patients receiving monthly high-dose IGIV (>400 mg/kg) within 3 weeks before exposure likely don't require VZIG 1
Healthy Individuals
- Acyclovir is not indicated for prophylactic use among otherwise healthy individuals after exposure 1
- Vaccination is the method of choice for post-exposure prophylaxis in healthy individuals without evidence of immunity 1
Important Clinical Considerations
- Treatment with acyclovir should be initiated within 24 hours of rash onset for maximum effectiveness 1, 2
- Acyclovir does not decrease transmission of varicella or reduce the duration of absence from school 1
- Adequate hydration and urine flow must be maintained during treatment, especially with high-dose IV therapy 6
- For patients with renal impairment, dose adjustment is necessary based on creatinine clearance 2
- Patients receiving hemodialysis require an additional dose after each dialysis session 2
- Acyclovir-resistant VZV strains may emerge in immunocompromised patients; foscarnet is the treatment of choice in such cases 7
Monitoring During Treatment
- Monitor mental status of patients receiving high-dose IV therapy 6
- For immunocompromised patients, monitor for progression of cutaneous dissemination and development of visceral complications 5
- In patients with renal impairment, monitor renal function during treatment 2
By following these evidence-based treatment recommendations, the morbidity and mortality associated with varicella infections can be significantly reduced, particularly in high-risk populations.