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Tolerability in Glaucoma Patients Switched from Preserved to Preservative-Free Prostaglandin-Timolol Combination: A Prospective Real-Life Study

PurposeTo evaluate the effect of switching from preserved prostaglandin analog-timolol fixed combinations (PG-timolol FCs) to preservative-free latanoprost-timolol FC (PF-LT) on intraocular pressure (IOP), ocular surface health, and tolerability in glaucoma and ocular hypertension (OH) patients with...

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Published in:Clinical ophthalmology (Auckland, N.Z.) N.Z.), 2022, Vol.16, p.3181-3192
Main Authors: Jandroković, Sonja, Vidas Pauk, Sania, Lešin Gaćina, Dina, Skegro, Ivan, Tomić, Martina, Masnec, Sanja, Kuzman, Tomislav, Kalauz, Miro
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container_title Clinical ophthalmology (Auckland, N.Z.)
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creator Jandroković, Sonja
Vidas Pauk, Sania
Lešin Gaćina, Dina
Skegro, Ivan
Tomić, Martina
Masnec, Sanja
Kuzman, Tomislav
Kalauz, Miro
description PurposeTo evaluate the effect of switching from preserved prostaglandin analog-timolol fixed combinations (PG-timolol FCs) to preservative-free latanoprost-timolol FC (PF-LT) on intraocular pressure (IOP), ocular surface health, and tolerability in glaucoma and ocular hypertension (OH) patients with the concurrent ocular surface disease (OSD). MethodsThis was a longitudinal, prospective, interventional, real-life study among 42 patients. Up to 3 visits were planned, at baseline, 30, and 90 days to assess efficacy on IOP decrease and local tolerance. The severity of OSD symptoms [Ocular Surface Disease Index (OSDI) questionnaire], subjective drug tolerability [visual analog scale (VAS)], conjunctival hyperemia (McMonnies scale), and tear break-up time (TBUT) were the main parameters assessed. ResultsData from 36 patients were available for statistical analysis. IOP was significantly reduced at day 30 and day 90 compared to baseline (16 vs 14 vs 14 mmHg, p < 0.001). Significant improvement was demonstrated in OSD symptoms, signs, and VAS scores from the baseline to the second and third visits. Median OSDI (27.1 vs 9.6 vs 4.2, p < 0.001), conjunctival hyperemia (2 vs 1 vs 1, p < 0.001), corneal surface staining (p < 0.001), and conjunctival staining scores (p < 0.001), and the percentage of patients with eyelid and periocular hyperemia (61.1 vs 12.5 vs 2.8%, p < 0.001), significantly decreased. TBUT (4 vs 5 vs 6 s, p < 0.001) and VAS score regarding tolerability (5 vs 2 vs 1, p < 0.001) significantly increased. ConclusionA switch from preserved PG-timolol FCs to PF-LT improved tolerability and optimized IOP control, providing better adherence with greater chances of treatment success.
doi_str_mv 10.2147/OPTH.S382497
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MethodsThis was a longitudinal, prospective, interventional, real-life study among 42 patients. Up to 3 visits were planned, at baseline, 30, and 90 days to assess efficacy on IOP decrease and local tolerance. The severity of OSD symptoms [Ocular Surface Disease Index (OSDI) questionnaire], subjective drug tolerability [visual analog scale (VAS)], conjunctival hyperemia (McMonnies scale), and tear break-up time (TBUT) were the main parameters assessed. ResultsData from 36 patients were available for statistical analysis. IOP was significantly reduced at day 30 and day 90 compared to baseline (16 vs 14 vs 14 mmHg, p < 0.001). Significant improvement was demonstrated in OSD symptoms, signs, and VAS scores from the baseline to the second and third visits. Median OSDI (27.1 vs 9.6 vs 4.2, p < 0.001), conjunctival hyperemia (2 vs 1 vs 1, p < 0.001), corneal surface staining (p < 0.001), and conjunctival staining scores (p < 0.001), and the percentage of patients with eyelid and periocular hyperemia (61.1 vs 12.5 vs 2.8%, p < 0.001), significantly decreased. TBUT (4 vs 5 vs 6 s, p < 0.001) and VAS score regarding tolerability (5 vs 2 vs 1, p < 0.001) significantly increased. ConclusionA switch from preserved PG-timolol FCs to PF-LT improved tolerability and optimized IOP control, providing better adherence with greater chances of treatment success.]]></description><identifier>ISSN: 1177-5467</identifier><identifier>DOI: 10.2147/OPTH.S382497</identifier><language>eng</language><ispartof>Clinical ophthalmology (Auckland, N.Z.), 2022, Vol.16, p.3181-3192</ispartof><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>780,784,4490,27925,37013</link.rule.ids></links><search><creatorcontrib>Jandroković, Sonja</creatorcontrib><creatorcontrib>Vidas Pauk, Sania</creatorcontrib><creatorcontrib>Lešin Gaćina, Dina</creatorcontrib><creatorcontrib>Skegro, Ivan</creatorcontrib><creatorcontrib>Tomić, Martina</creatorcontrib><creatorcontrib>Masnec, Sanja</creatorcontrib><creatorcontrib>Kuzman, Tomislav</creatorcontrib><creatorcontrib>Kalauz, Miro</creatorcontrib><title>Tolerability in Glaucoma Patients Switched from Preserved to Preservative-Free Prostaglandin-Timolol Combination: A Prospective Real-Life Study</title><title>Clinical ophthalmology (Auckland, N.Z.)</title><description><![CDATA[PurposeTo evaluate the effect of switching from preserved prostaglandin analog-timolol fixed combinations (PG-timolol FCs) to preservative-free latanoprost-timolol FC (PF-LT) on intraocular pressure (IOP), ocular surface health, and tolerability in glaucoma and ocular hypertension (OH) patients with the concurrent ocular surface disease (OSD). MethodsThis was a longitudinal, prospective, interventional, real-life study among 42 patients. Up to 3 visits were planned, at baseline, 30, and 90 days to assess efficacy on IOP decrease and local tolerance. The severity of OSD symptoms [Ocular Surface Disease Index (OSDI) questionnaire], subjective drug tolerability [visual analog scale (VAS)], conjunctival hyperemia (McMonnies scale), and tear break-up time (TBUT) were the main parameters assessed. ResultsData from 36 patients were available for statistical analysis. IOP was significantly reduced at day 30 and day 90 compared to baseline (16 vs 14 vs 14 mmHg, p < 0.001). Significant improvement was demonstrated in OSD symptoms, signs, and VAS scores from the baseline to the second and third visits. Median OSDI (27.1 vs 9.6 vs 4.2, p < 0.001), conjunctival hyperemia (2 vs 1 vs 1, p < 0.001), corneal surface staining (p < 0.001), and conjunctival staining scores (p < 0.001), and the percentage of patients with eyelid and periocular hyperemia (61.1 vs 12.5 vs 2.8%, p < 0.001), significantly decreased. TBUT (4 vs 5 vs 6 s, p < 0.001) and VAS score regarding tolerability (5 vs 2 vs 1, p < 0.001) significantly increased. ConclusionA switch from preserved PG-timolol FCs to PF-LT improved tolerability and optimized IOP control, providing better adherence with greater chances of treatment success.]]></description><issn>1177-5467</issn><fulltext>true</fulltext><rsrctype>report</rsrctype><creationdate>2022</creationdate><recordtype>report</recordtype><recordid>eNqVjU1OwzAUhL0AifKz4wBesnGxnTQO7FBF6QKJiGRfuckLGNl-xXaKegqujEFwAFajb_SNhpBLwedSlOr6qenW87aoZXmjjshMCKXYoqzUCTmN8Y3zSvJazchnhxaC3hpr0oEaTx-snnp0mjY6GfAp0vbDpP4VBjoGdLQJECHsMyb8g2zuga0CQG4wJv1itR-MZ51xaNHSJbqt8VlDf0vvfqQd9N8r-gzaskczAm3TNBzOyfGobYSL3zwjV6v7brlmu4DvE8S0cSb2YPMB4BQ3UklRFYov6uIf6hcG9F7q</recordid><startdate>20220101</startdate><enddate>20220101</enddate><creator>Jandroković, Sonja</creator><creator>Vidas Pauk, Sania</creator><creator>Lešin Gaćina, Dina</creator><creator>Skegro, Ivan</creator><creator>Tomić, Martina</creator><creator>Masnec, Sanja</creator><creator>Kuzman, Tomislav</creator><creator>Kalauz, Miro</creator><scope>7X8</scope></search><sort><creationdate>20220101</creationdate><title>Tolerability in Glaucoma Patients Switched from Preserved to Preservative-Free Prostaglandin-Timolol Combination: A Prospective Real-Life Study</title><author>Jandroković, Sonja ; Vidas Pauk, Sania ; Lešin Gaćina, Dina ; Skegro, Ivan ; Tomić, Martina ; Masnec, Sanja ; Kuzman, Tomislav ; Kalauz, Miro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_miscellaneous_27216370583</frbrgroupid><rsrctype>reports</rsrctype><prefilter>reports</prefilter><language>eng</language><creationdate>2022</creationdate><toplevel>online_resources</toplevel><creatorcontrib>Jandroković, Sonja</creatorcontrib><creatorcontrib>Vidas Pauk, Sania</creatorcontrib><creatorcontrib>Lešin Gaćina, Dina</creatorcontrib><creatorcontrib>Skegro, Ivan</creatorcontrib><creatorcontrib>Tomić, Martina</creatorcontrib><creatorcontrib>Masnec, Sanja</creatorcontrib><creatorcontrib>Kuzman, Tomislav</creatorcontrib><creatorcontrib>Kalauz, Miro</creatorcontrib><collection>MEDLINE - Academic</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jandroković, Sonja</au><au>Vidas Pauk, Sania</au><au>Lešin Gaćina, Dina</au><au>Skegro, Ivan</au><au>Tomić, Martina</au><au>Masnec, Sanja</au><au>Kuzman, Tomislav</au><au>Kalauz, Miro</au><format>book</format><genre>unknown</genre><ristype>RPRT</ristype><atitle>Tolerability in Glaucoma Patients Switched from Preserved to Preservative-Free Prostaglandin-Timolol Combination: A Prospective Real-Life Study</atitle><jtitle>Clinical ophthalmology (Auckland, N.Z.)</jtitle><date>2022-01-01</date><risdate>2022</risdate><volume>16</volume><spage>3181</spage><epage>3192</epage><pages>3181-3192</pages><issn>1177-5467</issn><abstract><![CDATA[PurposeTo evaluate the effect of switching from preserved prostaglandin analog-timolol fixed combinations (PG-timolol FCs) to preservative-free latanoprost-timolol FC (PF-LT) on intraocular pressure (IOP), ocular surface health, and tolerability in glaucoma and ocular hypertension (OH) patients with the concurrent ocular surface disease (OSD). MethodsThis was a longitudinal, prospective, interventional, real-life study among 42 patients. Up to 3 visits were planned, at baseline, 30, and 90 days to assess efficacy on IOP decrease and local tolerance. The severity of OSD symptoms [Ocular Surface Disease Index (OSDI) questionnaire], subjective drug tolerability [visual analog scale (VAS)], conjunctival hyperemia (McMonnies scale), and tear break-up time (TBUT) were the main parameters assessed. ResultsData from 36 patients were available for statistical analysis. IOP was significantly reduced at day 30 and day 90 compared to baseline (16 vs 14 vs 14 mmHg, p < 0.001). Significant improvement was demonstrated in OSD symptoms, signs, and VAS scores from the baseline to the second and third visits. Median OSDI (27.1 vs 9.6 vs 4.2, p < 0.001), conjunctival hyperemia (2 vs 1 vs 1, p < 0.001), corneal surface staining (p < 0.001), and conjunctival staining scores (p < 0.001), and the percentage of patients with eyelid and periocular hyperemia (61.1 vs 12.5 vs 2.8%, p < 0.001), significantly decreased. TBUT (4 vs 5 vs 6 s, p < 0.001) and VAS score regarding tolerability (5 vs 2 vs 1, p < 0.001) significantly increased. ConclusionA switch from preserved PG-timolol FCs to PF-LT improved tolerability and optimized IOP control, providing better adherence with greater chances of treatment success.]]></abstract><doi>10.2147/OPTH.S382497</doi></addata></record>
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title Tolerability in Glaucoma Patients Switched from Preserved to Preservative-Free Prostaglandin-Timolol Combination: A Prospective Real-Life Study
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