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Patient persistence with first-line antiglaucomatous monotherapy
PURPOSE: To identify the extent of persistence (period of time of continuous therapy with the drug prescribed) of glaucoma patients treated with prostaglandins (latanoprost, bimatoprost, or travoprost), or β-blocker (timolol) monotherapy. METHODS: An observational retrospective study of a 24-month f...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Dove Medical Press
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2861932/ https://www.ncbi.nlm.nih.gov/pubmed/20463793 |
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author | Arias, Alfonso Schargel, Konrad Ussa, Fernando Canut, Maria I Robles, Amelia y Belén Sánchez, Belén Martí |
author_facet | Arias, Alfonso Schargel, Konrad Ussa, Fernando Canut, Maria I Robles, Amelia y Belén Sánchez, Belén Martí |
author_sort | Arias, Alfonso |
collection | PubMed |
description | PURPOSE: To identify the extent of persistence (period of time of continuous therapy with the drug prescribed) of glaucoma patients treated with prostaglandins (latanoprost, bimatoprost, or travoprost), or β-blocker (timolol) monotherapy. METHODS: An observational retrospective study of a 24-month follow-up in 191 patients (from four centers) was done to identify the time elapsed until patients discontinued their antiglaucomatous treatment. The relevant information was extracted from patients’ medical charts. A descriptive analysis, a Kaplan–Meier survival analysis, and a Cox regression model were used to determine which drug was associated with greater patient persistence and to detect variables significantly influencing persistence. RESULTS: Descriptive analysis and survival curves showed that after 24 months, latanoprost was associated with a higher persistence in glaucoma treatment than the alternative agents: 81.6% versus 22.9% for bimatoprost, 65.4% for travoprost, and 60.5% for timolol (P < 0.0001). Persistence was significantly influenced by the antiglaucoma agent used as monotherapy (with a six-fold higher risk of treatment discontinuation during the follow-up period due to receiving bimatoprost instead of latanoprost; P < 0.0001) and patient age (P = 0.001). Even though comorbidities could not be directly related to persistence, their occurrence was related to patient age. The main reasons for treatment discontinuation were lack of efficacy, development of intolerance and/or adverse events, which were significant in the bimatoprost group, 28.6% (P < 0.001) and 48.6% (P < 0.001), respectively. CONCLUSIONS: Latanoprost shows higher patient persistence compared with travoprost, bimatoprost, and timolol in routine clinical practice, and could lead to better control of intraocular pressure and lower associated economic costs. |
format | Text |
id | pubmed-2861932 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-28619322010-05-12 Patient persistence with first-line antiglaucomatous monotherapy Arias, Alfonso Schargel, Konrad Ussa, Fernando Canut, Maria I Robles, Amelia y Belén Sánchez, Belén Martí Clin Ophthalmol Original Research PURPOSE: To identify the extent of persistence (period of time of continuous therapy with the drug prescribed) of glaucoma patients treated with prostaglandins (latanoprost, bimatoprost, or travoprost), or β-blocker (timolol) monotherapy. METHODS: An observational retrospective study of a 24-month follow-up in 191 patients (from four centers) was done to identify the time elapsed until patients discontinued their antiglaucomatous treatment. The relevant information was extracted from patients’ medical charts. A descriptive analysis, a Kaplan–Meier survival analysis, and a Cox regression model were used to determine which drug was associated with greater patient persistence and to detect variables significantly influencing persistence. RESULTS: Descriptive analysis and survival curves showed that after 24 months, latanoprost was associated with a higher persistence in glaucoma treatment than the alternative agents: 81.6% versus 22.9% for bimatoprost, 65.4% for travoprost, and 60.5% for timolol (P < 0.0001). Persistence was significantly influenced by the antiglaucoma agent used as monotherapy (with a six-fold higher risk of treatment discontinuation during the follow-up period due to receiving bimatoprost instead of latanoprost; P < 0.0001) and patient age (P = 0.001). Even though comorbidities could not be directly related to persistence, their occurrence was related to patient age. The main reasons for treatment discontinuation were lack of efficacy, development of intolerance and/or adverse events, which were significant in the bimatoprost group, 28.6% (P < 0.001) and 48.6% (P < 0.001), respectively. CONCLUSIONS: Latanoprost shows higher patient persistence compared with travoprost, bimatoprost, and timolol in routine clinical practice, and could lead to better control of intraocular pressure and lower associated economic costs. Dove Medical Press 2010 2010-04-26 /pmc/articles/PMC2861932/ /pubmed/20463793 Text en © 2010 Arias et al, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited. |
spellingShingle | Original Research Arias, Alfonso Schargel, Konrad Ussa, Fernando Canut, Maria I Robles, Amelia y Belén Sánchez, Belén Martí Patient persistence with first-line antiglaucomatous monotherapy |
title | Patient persistence with first-line antiglaucomatous monotherapy |
title_full | Patient persistence with first-line antiglaucomatous monotherapy |
title_fullStr | Patient persistence with first-line antiglaucomatous monotherapy |
title_full_unstemmed | Patient persistence with first-line antiglaucomatous monotherapy |
title_short | Patient persistence with first-line antiglaucomatous monotherapy |
title_sort | patient persistence with first-line antiglaucomatous monotherapy |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2861932/ https://www.ncbi.nlm.nih.gov/pubmed/20463793 |
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