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Review

Critical appraisal of loteprednol ointment, gel, and suspension in the treatment of postoperative inflammation and pain following ocular and corneal transplant surgery

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Pages 379-387 | Published online: 10 Feb 2014

Figures & data

Figure 1 Loteprednol etabonate 0.5% ointment, Bausch and Lomb Incorporated, Rochester, NY, USA.

Figure 1 Loteprednol etabonate 0.5% ointment, Bausch and Lomb Incorporated, Rochester, NY, USA.

Figure 2 Loteprednol etabonate molecular structure: loteprednol etabonate is synthesized through structural modifications of a prednisolone-related compound.

Notes: Chemical name: chloromethyl 17α-[(ethoxycarbonyl)oxy]-11β-hydroxy-3-oxoandrosta-1,4-diene-17β-carboxylate. Active compound: loteprednol etabonate 5 mg (0.5%). Inactive compounds: mineral oil and white petrolatum.
Figure 2 Loteprednol etabonate molecular structure: loteprednol etabonate is synthesized through structural modifications of a prednisolone-related compound.

Figure 3 Change in intraocular pressure after treatment with Lotemax® ointment or vehicle.

Notes: Values shown are the mean ± the standard error of the mean. Lotemax 0.5%, Bausch and Lomb Incorporated, Rochester, NY, USA. Copyright © 2011. Reproduced from Dove Medical Press. Comstock TL, Paterno MR, Singh A, Erb T, Davis E. Safety and efficacy of loteprednol etabonate ophthalmic ointment 0.5% for the treatment of inflammation and pain following cataract surgery. Clin Ophthalmol. 2011;5:177–186.Citation42
Abbreviation: Lotemax, Ioteprednol etabonate.
Figure 3 Change in intraocular pressure after treatment with Lotemax® ointment or vehicle.

Table 1 Published clinical studies on Lotemax® and penetrating keratoplasty

Table 2 Comparative studies on efficacy and safety of Lotemax® 0.5% in resolution of postoperative inflammation