Skip to main content
. 2012 Jun 16;32(5):507–517. doi: 10.1007/s10792-012-9589-2

Table 1.

Studies demonstrating the efficacy and safety of loteprednol etabonate (LE) 0.5 % for postoperative inflammation

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)