Table 1.
Full Cohort (n = 308) |
Validation Subgroup (n = 91) |
|||
---|---|---|---|---|
No. on Placebo | No. on Acyclovir | No. on Placebo | No. on Acyclovir | |
No self-reported recurrenceb | ||||
No diagnosed recurrence | 104 | 119 | 30 | 35 |
Diagnosed recurrence | 26 | 14 | 8 | 4 |
Self-reported recurrenceb | ||||
No diagnosed recurrence | 11 | 10 | 3 | 3 |
Diagnosed recurrence | 12 | 12 | 4 | 4 |
Sensitivityc | 0.32 | 0.46 | 0.33 | 0.50 |
Specificityd | 0.90 | 0.92 | 0.91 | 0.92 |
a Self-reported outcomes and physician records were available for all 308 participants. We sampled a synthetic validation subgroup of 91 participants for the purposes of illustration.
b Participants reported ocular HSV recurrences through a weekly diary and were seen by an ophthalmologist every 3 months. Self-reported recurrences were determined from data obtained from patient diaries, and physician-diagnosed recurrences were determined via examination by the study ophthalmologist.
c Sensitivity was the proportion of patients with a physician-diagnosed recurrence who also self-reported a recurrence.
d Specificity was the proportion of participants without a physician-diagnosed recurrence who did not self-report a recurrence.