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Oral acyclovir to prevent dissemination of varicella in immunocompromised children
Insights
Oral acyclovir effectively treats varicella in immunocompromised children. This study found oral acyclovir safe and effective, significantly reducing the need for intravenous treatment compared to historical placebo data.
Area of Science:
- Pediatric Infectious Diseases
- Virology
- Pharmacology
Background:
- Varicella (chickenpox) poses a significant risk to immunocompromised children.
- Intravenous acyclovir has been the standard treatment, but oral administration is desirable for ease of use.
- Assessing the efficacy and safety of oral acyclovir in this vulnerable population is crucial.
Purpose of the Study:
- To evaluate the safety and efficacy of oral acyclovir in treating varicella in immunocompromised children.
- To compare the outcomes of oral acyclovir treatment with historical placebo data.
Main Methods:
- Twenty-five immunocompromised children with varicella received oral acyclovir (800 mg, five times daily for 7 days).
- Outcomes were monitored for disease resolution, dissemination, and adverse events.
- Compared outcomes to a historical placebo group.
Main Results:
- All patients achieved disease healing with no evidence of dissemination.
- Only two patients required a switch to intravenous acyclovir, a statistically significant reduction (P < 0.01) compared to the historical placebo group (12/25).
- The only reported adverse event was mild, self-limiting diarrhea in nine patients.
Conclusions:
- Oral acyclovir is a safe and effective treatment option for varicella in immunocompromised children.
- Oral acyclovir significantly reduces the need for intravenous therapy.
- Close medical observation of patients receiving oral acyclovir is recommended.
Abstract:
Twenty-five immunocompromised children with varicella were treated with oral acyclovir 800 mg, five times daily for 7 days. Two patients were transferred from the oral to the intravenous route: one had signs of varicella pneumonitis on routine X-ray, the other had continuing new lesion formation on day 4 of oral treatment. The disease healed in all patients, with no other evidence of dissemination. In an historical placebo treated group, 12 of 25 patients were transferred to intravenous acyclovir. The reduction to two of 25 is statistically significant (P < 0.01). The mean peak plasma acyclovir concentration in these patients was 6.56 mumol/l. Mild, self-limiting diarrhoea in nine patients was the only adverse event considered to be related to acyclovir. It is concluded that immunocompromised children with varicella can be treated safely and effectively with oral acyclovir. All patients should be observed closely by a physician.
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