Table 1.
Study parameters | Stewart et al. [13] | LE postoperative study group 2 1998 [2] | Grigorian et al. [31] | Stewart [30] |
---|---|---|---|---|
Comparator | Vehicle | Vehicle | 1 % (PA) | Fluorometholone acetate 0.1 % (FA) |
No. of patients | 203 | 227 | 20 | 30 |
Treatment duration (weeks) | 2 | 2 | 4 | 2 |
Patients with resolution of ACIa at final visit (%) | LE group—64 | LE group—55 | LE group—60 | LE group—60 |
Vehicle—29 | Vehicle—28 | PA group—50 | FA group—100 | |
Mean IOP at final visit | Mean decrease in IOP of 1–2 mmHg for both treatment groups | Mean decrease in IOP of 1–2 mmHg for both treatment groups | LE group—12 ± 3 mmHg | Not reported |
PA group—16 ± 1 mmHg | ||||
Clinically significant increases in IOP (≥10 mmHg) | n = 3 for loteprednol etabonate; n = 0 for vehicle | n = 0 for loteprednol etabonate; n = 1 for vehicle | Not reported | Not reported |
ACI anterior chamber inflammation, IOP intraocular pressure, LE loteprednol etabonate, PA prednisolone acetate, FA fluorometholone acetate
aResolution of ACI defined as anterior chamber cell count <5 and flare Grade 0 (none)