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Patient Case Study: Targeting DED Inflammation

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Explore a case of dry eye disease (DED) with underlying inflammation and the potential role of XIIDRA® (lifitegrast ophthalmic solution) 5%.

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  • Overview

    Patients with dry eye with inflammation can present with tearing, redness, and fluctuating vision, signaling that they may need an anti-inflammatory Rx.1,2 Xiidra® (lifitegrast ophthalmic solution) 5% is designed to target the dry eye inflammatory cycle.3,4* It has delivered early symptom relief that builds over time.3† Dr Cecilia Koetting joins Dr Nathan Lighthizer, as he discusses a case of a patient with dry eye with inflammation where Xiidra may be a preferred treatment choice.

    *The exact mechanism of action of Xiidra in dry eye disease is not known.
    Xiidra significantly reduced symptoms of eye dryness at 2 weeks (based on Eye Dryness Score compared to vehicle) in 2 of 4 studies, with improvements observed at 6 and 12 weeks in all 4 studies.

    References: 

    1. Pflugfelder SC, de Paiva CS. The pathophysiology of dry eye disease: what we know and future directions for research. Ophthalmology. 2017;124(11S):S4-S13.
    2. Rao SK, Mohan R, Gokhale N, Matalia H, Mehta P. Inflammation and dry eye disease—where are we?. Int J Ophthalmol. 2022;15(5):820-827.
    3. Xiidra. Prescribing Information. Bausch & Lomb Inc.
    4. Donnenfeld ED, Perry HD, Nattis AS, Rosenberg ED. Lifitegrast for the treatment of dry eye disease in adults. Expert Opin Pharmacother. 2017;18(14):1517-1524.

    ©2025 Bausch + Lomb. XDR.0160.USA.25

  • Indication

    Xiidra® (lifitegrast ophthalmic solution) 5% is indicated for the treatment of signs and symptoms of dry eye disease (DED).

  • Important Safety Information

    • Xiidra is contraindicated in patients with known hypersensitivity to lifitegrast or to any of the other ingredients.
    • In clinical trials, the most common adverse reactions reported in 5-25% of patients were instillation site irritation, dysgeusia and reduced visual acuity. Other adverse reactions reported in 1% to 5% of the patients were blurred vision, conjunctival hyperemia, eye irritation, headache, increased lacrimation, eye discharge, eye discomfort, eye pruritus and sinusitis.
    • To avoid the potential for eye injury or contamination of the solution, patients should not touch the tip of the single-use container to their eye or to any surface.
    • Contact lenses should be removed prior to the administration of Xiidra and may be reinserted 15 minutes following administration.
    • Safety and efficacy in pediatric patients below the age of 17 years have not been established.

    You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch or call 1-800-FDA-1088

    Click here for full Prescribing Information.

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