Published in Glaucoma

Transforming Clinical Journeys with IYUZEH: When to Make the Switch to Preservative-Free Latanoprost for Optimal Management of Patients with Open-Angle Glaucoma

This post is sponsored by Théa Pharma, Inc.
7 min read

Glaucoma specialists Dr. Paula Newsome, OD and Dr. Jason Bacharach, MD share their perspectives and clinical experiences on when they switch patients to preservative-free latanoprost (IYUZEH [latanoprost ophthalmic solution] 0.005%) for optimal treatment and management of open-angle glaucoma.

Transforming Clinical Journeys with IYUZEH: When to Make the Switch to Preservative-Free Latanoprost for Optimal Management of Patients with Open-Angle Glaucoma
Eye drops are commonly used for the treatment and ongoing management of glaucoma, with many patients trying to find multiple formulations that prove effective in lowering their intraocular pressure (IOP). Preservatives, including benzalkonium chloride (BAK), are used in approximately 70% of ophthalmic formulations for their antimicrobial properties. However, research shows that long-term exposure to BAK can be toxic to the ocular surface and may cause irreparable damage.1
IYUZEH (latanoprost ophthalmic solution) 0.005% is a prostaglandin F2α analogue indicated for the reduction of elevated intraocular pressure in patients with open-angle glaucoma or ocular hypertension. Please see Important Safety Information within and full Prescribing Information here.

Optimizing eye health: why avoid overuse of preservatives?

Chronic preservative exposure impacts eye health in several ways, including damage to the ocular surface. This can lead to ocular surface disease, potentially causing itching, burning, and decreased vision.2 In addition to the significant impact on patients’ quality of life, research shows that those who experience side effects are less likely to adhere to their prescribed treatment regimen. As a result, up to one-third of patients are not getting the full benefit of their prescribed treatment because of poor adherence.3
From a surgical perspective, the results of the Preservative Exposure and Surgical Outcomes (PESO) study show a direct correlation between preoperative exposure to preservatives and poorer outcomes following filtration surgery, demonstrating the lasting impact of frequent preservative use and how it could damage the ocular surface.4
Consequently, as specialists, we have a duty to minimize or eliminate exposure to preservatives within our prescribed treatment regimen where appropriate. Recent advancements in formulation offer treatment options that enable us to reduce the preservative load of a treatment regimen and effectively manage patients’ glaucoma. By adopting this approach, we can protect patients’ eye health while lowering IOP and potentially safeguard future treatment interventions that a patient may require later in the treatment journey. In many cases, this can be achieved by switching patients to a preservative-free formulation for treatment.

Advancements in glaucoma care: when to switch to preservative-free

IYUZEH, recently available in the USA, is the first preservative-free latanoprost for the treatment of open-angle glaucoma and ocular hypertension. In clinical studies, IYUZEH demonstrated clinically meaningful IOP-lowering effects when compared with Xalatan, and was well tolerated throughout the trial.5 In the two clinical trials conducted with IYUZEH the most frequently reported ocular adverse reactions were conjunctival hyperemia and eye irritation. This provides patients with an option that offers the reduction of IOP with a lower incidence of ocular treatment-emergent adverse events.
Our goal is to understand the unique needs of each patient and create a tailored treatment plan that will lead to the best outcomes for that individual. Having a preservative-free option allows us to balance our patients’ overall health and well-being with their long-term treatment and management of glaucoma.
The patient’s IOP was stable; however, he was experiencing redness and irritation in his eyes. In addition to causing the patient significant eye discomfort, this also proved disruptive to his occupation. This made it crucial to address.
As the preservatives in the medication he was using may have been causing the redness, my recommendation was to switch to IYUZEH to reduce the preservative load. As treating the whole patient is very important to me, I also recommended an anti-inflammatory lifestyle to address other factors that could be contributing to increased IOP.
Overall, the patient was very happy with the new treatment regimen. With IYUZEH, his IOP was sustained at an acceptable level and the medication is being well tolerated, with him no longer experiencing redness and irritation.
Following a successful SLT procedure, this patient did not require drops for the first 4 years of her treatment journey. Initially, I prescribed a preserved prostaglandin, which proved effective in lowering IOP to 20–30% below baseline.
Looking forward, as the drops were effective in managing IOP, my priority in this case was to ensure a sustainable long-term treatment plan to continue preventing disease progression. As the patient was likely to remain on eye drops for the foreseeable future, my recommendation was to switch to IYUZEH to help protect the patient’s ocular surface against preventable damage known to be caused by frequent and prolonged exposure to preservatives.
Following the switch, IYUZEH is proving effective in sustaining the 20–30% reduction in IOP. The patient continues to have good overall eye health, and the treatment is being well tolerated.

Why switch to preservative-free IYUZEH?

IYUZEH has demonstrated consistent IOP-lowering effects and proven tolerability across multiple trials in the U.S. and Europe. In randomized, controlled clinical trials of patients with open-angle glaucoma or ocular hypertension with mean baseline IOP of 19-24 mmHg, IYUZEH lowered IOP by 3 – 8 mmHg versus 4 – 8 mmHg by Xalatan, which is preserved with BAK.
In addition, a recent real-world study (where 1872 patients from 6 European countries were treated with preservative-free latanoprost for 3 months) found that, of patients who had switched from a preservative-related treatment, the most common reasons for switching to IYUZEH included local intolerance, insufficient efficacy, possibly due to poor adherence, and poor compliance. In total, 95.3% of patients were satisfied or very satisfied with IYUZEH in terms of tolerability. Additionally, 89.5% of patients found IYUZEH to be easier than or as easy to use as their previous preserved treatment.6
Overall, these real-world data, in addition to our day-to-day clinical experience, highlight IYUZEH as a valuable choice of therapy to address tolerability issues and to help with sustainable long-term management of glaucoma, empowering us to provide optimal care for our patients.

Indications and Important Safety Information for IYUZEH

INDICATIONS AND USAGE

IYUZEH(latanoprost ophthalmic solution) 0.005% is a prostaglandin F2α analogue indicated for the reduction of elevated intraocular pressure in patients with open-angle glaucoma or ocular hypertension.

IMPORTANT SAFETY INFORMATION

CONTRAINDICATIONS

Known hypersensitivity to latanoprost or any other ingredients in this product.

WARNINGS AND PRECAUTIONS

IYUZEH may cause changes to pigmented tissues. Most frequently reported changes are increased pigmentation of the iris, periorbital tissue (eyelid), and eyelashes. Pigmentation is expected to increase as long as IYUZEH is administered. Iris pigmentation is likely to be permanent. Eyelid skin darkening and eyelash changes may be reversible.

IYUZEH may cause gradual change to eyelashes including increased length, thickness, and number of lashes. These changes are usually reversible upon discontinuation of treatment.

IYUZEH should be used with caution in patients with a history of intraocular inflammation (iritis/uveitis) and should generally not be used in patients with active intraocular inflammation.

IYUZEH should be used with caution in aphakic patients, in pseudophakic patients with a torn posterior lens capsule, or in patients with known risk factors for macular edema.

Reactivation of herpes simplex keratitis has been reported during treatment with latanoprost. IYUZEH should be used with caution in patients with a history of herpetic keratitis.

Contact lenses should be removed prior to the administration of IYUZEH and may be reinserted 15 minutes after administration.

ADVERSE REACTIONS

The most common adverse reactions (5% to 35%) for IYUZEH are: conjunctival hyperemia, eye irritation, eye pruritus, abnormal sensation in eye, foreign body sensation in eyes, vision blurred, and lacrimation increased.

DRUG INTERACTIONS

The combined use of two or more prostaglandins or prostaglandin analogs including IYUZEH is not recommended. It has been shown that administration of these prostaglandin drug products more than once daily may decrease the IOP lowering effect or cause paradoxical elevations in IOP.

Please click here for the full Prescribing Information.

  1. Goldstein MH, Silva FQ, Blender N, Tran T, Vantipalli S. Ocular benzalkonium chloride exposure: problems and solutions. Eye (Lond). 2022;36(2):361–368. doi:10.1038/s41433-021-01668-x.
  2. Kahook MY, Rapuano CJ, Messmer EM, Radcliffe NM, Galor A, Baudouin C. Preservatives and ocular surface disease: A review. Ocul Surf. 2024;34:213–224. doi: 10.1016/j.jtos.2024.08.001.
  3. Wolfram C, Stahlberg E, Pfeiffer N. Patient-reported nonadherence with glaucoma therapy. J Ocul Pharmacol Ther. 2019;35(4):223–228. doi:10.1089/jop.2018.0134.
  4. Boimer C, Birt CM. Preservative exposure and surgical outcomes in glaucoma patients: the PESO study. J Glaucoma. 2013;22(9):730–735. doi:10.1097/IJG.0b013e31825af67d.
  5. Bacharach J, Ahmed IIK, Sharpe ED, Korenfeld MS, Zhang S, Baudouin C. Preservative-free versus benzalkonium chloride-preserved latanoprost ophthalmic solution in patients with primary open-angle glaucoma or ocular hypertension: a phase 3 US clinical trial. Clin Ophthalmol. 2023;17:2575–2588. doi:10.2147/OPTH.S414015.
  6. Erb C, Stalmans I, Iliev M, Muñoz-Negrete FJ. Real-world study on patient satisfaction and tolerability after switching to preservative-free latanoprost. Clin Ophthalmol. 2021;15:931–938. doi:10.2147/OPTH.S295821.
Paula Newsome, OD, MS, FAAO, FAARM, CHC
About Paula Newsome, OD, MS, FAAO, FAARM, CHC

As the first African American female optometrist to practice in the state of North Carolina and the first to become a fellow in the American Academy of Optometry, being cutting-edge is a way of life for Dr. Paula Newsome. Dr. Newsome has provided free eye care to people on numerous continents, including Africa, South America, and North America, has run a private practice in Charlotte for over 20 years, has taught optometry courses in Atlanta, GA, and is featured in Optometric Management discussing Acuvue Vitas Contact Lenses.

Paula Newsome, OD, MS, FAAO, FAARM, CHC
Jason Bacharach, MD
About Jason Bacharach, MD

Dr. Bacharach founded North Bay Eye Associates in 1993. As the Director of Research at North Bay Eye Associates, he is the Principal Investigator in numerous pharmacology and device studies in an effort to increase the effectiveness of glaucoma management as well as numerous other ocular diseases.

Dr. Bacharach travels the world extensively to lecture. He has authored many articles in peer-reviewed literature and book chapters.

Jason Bacharach, MD
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Indications and Important Safety Information for IYUZEH
INDICATIONS AND USAGE
IYUZEH(latanoprost ophthalmic solution) 0.005% is a prostaglandin F2α analogue indicated for the reduction of elevated intraocular pressure in patients with open-angle glaucoma or ocular hypertension.