4.3 Review

The treatment of glaucoma using topical preservative-free agents: an evaluation of safety and tolerability

Journal

EXPERT OPINION ON DRUG SAFETY
Volume 20, Issue 4, Pages 453-466

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1080/14740338.2021.1873947

Keywords

BAK; benzalconium chloride; dry eye; glaucoma; intraocular pressure; IOP; ocular surface; ocular surface disease; OSD; preservative-free

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Preservative-free (PF) medications are an important treatment strategy for glaucoma, providing tangible clinical benefits by removing preservative toxicity. Evidence suggests that PF medications are at least equally efficacious and potentially have superior tolerability and safety compared to preserved medications in the short term. However, further research is needed to understand the long-term benefits of PF therapy.
Introduction: Preservative-free (PF) medications represent a valuable treatment strategy in the lifelong management of glaucoma. By removing preservative toxicity, PF formulations provide tangible clinical benefits to glaucoma patients worldwide. They improve tolerability and adherence, leading to a positive impact in long-term intraocular pressure (IOP) control. Areas covered: A critical review of the subject is provided, including selected evidence on the safety and tolerability of currently available topical PF formulations. Cumulative evidence confirms that topical PF medications are at least equally efficacious to their preserved equivalents. There is convincing short-term evidence for superior tolerability and safety of PF formulations compared to preserved medications. The long-term benefits and success of PF therapy requires further elucidation. Expert opinion: Successful stepwise administration of medical therapy for glaucoma remains elusive. There is a greater risk for ocular toxicity and therapy failure with preserved topical glaucoma therapy. Currently available and emerging PF therapy options potentially optimize lifelong stepwise glaucoma therapy and may enhance outcome. To avert complications from preservatives leading to poor adherence, ideally, future antiglaucoma therapy should become 100% PF. There are still key aspects of PF therapy that warrant further investigation.

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