Table 1 |
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Characteristics of randomised controlled trials comparing acyclovir to placebo among immunocompetent children |
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|
Study |
Number of participants |
Age Range (mean) |
Acyclovir protocol |
Outcomes |
Quality |
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|
|
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|
Total |
Per group |
Jadad Score |
Allocation Concealment |
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|
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|
Balfour 1990 |
102 |
50 – acyclovir 50 – placebo |
5–16 years (8.1) |
5–7 years: 20 mg/kg 7–12 years: 15 mg/kg 12–16 years: 10 mg/kg 4x/days for 5-7 days |
• Days to fever, crusting, no new lesions, maximum number of lesions, decrease in number of lesions and cessation of itching • Maximum number of lesions |
4 |
Unclear |
|
Dunkle 1991 |
815 |
408 – acyclovir 407 – placebo |
2–12 years (5.2) |
20 mg/kg 4×/day for 5 days |
• Maximum number of lesions • Number with >500 lesions • Residual lesions at day 28 |
3 |
Unclear |
|
Balfour 1992 |
62 |
31 – acyclovir 31 – placebo |
13–18 years (14.8) |
800 mg 4×/day for 5 days |
• Days to maximum number of lesions and cessation of itching • Maximum number of lesions • Residual lesions at day 28 |
3 |
Unclear |
|
|
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Klassen et al. BMC Pediatrics 2002 2:9 doi:10.1186/1471-2431-2-9 |
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