Table 4.
P. aeruginosa (n = 110)*n (%) | All Other Bacteria (n = 384)*n (%) | Total n (%) | P† | |
---|---|---|---|---|
Change in antibiotic/addition of other antibiotic | 15 (14) | 53 (14) | 68 (14) | >0.99 |
Corneal perforation | 2 (2) | 13 (3) | 15 (3) | 0.54 |
Death | 2 (2) | 10 (3) | 12 (2) | >0.99 |
IOP elevated >25 but ≤35 mm Hg with medications within 1 week of therapy‡ | 4 (4) | 8 (2) | 12 (2) | 0.31 |
Increase in infiltrate size (>50%) and >1 mm in maximum diameter | 1 (1) | 12 (3) | 13 (3) | 0.32 |
No resolution of epithelial defect at 21 days or later | 19 (17) | 52 (14) | 71 (14) | 0.36 |
Progressive corneal thinning ≥50% of enrollment thickness | 1 (1) | 1 (0.3) | 2 (0.4) | 0.40 |
Recurrence of epithelial defect | 1 (1) | 7 (2) | 8 (2) | 0.69 |
Total subjects with any adverse events | 27 (25) | 76 (20) | 103 (21) | 0.29 |
Adverse events were recorded from enrollment until the 3-month follow-up. These values (n) reflect the number of cases at enrollment.
Fisher's exact test.
IOP elevation >35 was considered a serious adverse event. There were no cases of IOP elevation >35 in SCUT.