Table 3.
Model | No. of Outcomes | No. at Risk | Adjusted RRa | 95% CI | SE for ln(RR) |
---|---|---|---|---|---|
Complete data, physician- diagnosed recurrence | |||||
Acyclovir group | 26 | 155 | 0.68 | 0.44, 1.07 | 0.23 |
Placebo group | 38 | 153 | 1 | ||
Total | 64 | 308 | |||
Naive analysis | |||||
Acyclovir group | 22 | 155 | 0.93 | 0.55, 1.59 | 0.27 |
Placebo group | 23 | 153 | 1 | ||
Total | 45 | 308 | |||
Validation subgroupb | |||||
Acyclovir group | 8 | 46 | 0.61 | 0.27, 1.35 | 0.41 |
Placebo group | 12 | 45 | 1 | ||
Total | 20 | 91 | |||
Direct maximum likelihood (nondifferential) | 0.68 | 0.34, 1.38 | 0.36 | ||
Direct maximum likelihood (differential) | 0.65 | 0.31, 1.40 | 0.39 | ||
Multiple imputation (nondifferential) | 0.69 | 0.35, 1.36 | 0.35 | ||
Multiple imputation (differential) | 0.69 | 0.34, 1.41 | 0.36 |
Abbreviations: CI, confidence interval; ln(RR), natural log of the risk ratio; RR, risk ratio; SE, standard error.
a All models were adjusted for race, sex, age, and number of previous recurrences.
b Validation subgroup included 91 participants.