Cargando…
A prospective, multicenter, noninterventional study of Optive Plus(®) in the treatment of patients with dry eye: the prolipid study
OBJECTIVE: The aim was to evaluate the efficacy of Optive Plus(®), an artificial tear containing castor oil, in patients with dry eye, in a routine clinical setting. METHODS: This was a prospective, noninterventional study of patients with dry eye who switched from a prior therapy or who were naïve...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4069146/ https://www.ncbi.nlm.nih.gov/pubmed/24970993 http://dx.doi.org/10.2147/OPTH.S58464 |
_version_ | 1782322518548283392 |
---|---|
author | Kaercher, Thomas Thelen, Ulrich Brief, Gerrett Morgan-Warren, Robert J Leaback, Richard |
author_facet | Kaercher, Thomas Thelen, Ulrich Brief, Gerrett Morgan-Warren, Robert J Leaback, Richard |
author_sort | Kaercher, Thomas |
collection | PubMed |
description | OBJECTIVE: The aim was to evaluate the efficacy of Optive Plus(®), an artificial tear containing castor oil, in patients with dry eye, in a routine clinical setting. METHODS: This was a prospective, noninterventional study of patients with dry eye who switched from a prior therapy or who were naïve to treatment (n=1,209). Patients were issued Optive Plus(®) artificial tears. Dry eye severity, tear break-up time (TBUT), Schirmer score, Ocular Surface Disease Index (OSDI) score, and patient assessment of symptoms were recorded at baseline and at the follow-up visit (4 weeks after starting Optive Plus(®)). RESULTS: The cause of dry eye was determined to be aqueous deficiency, lipid deficiency, or a mixture of aqueous and lipid deficiency (in 19.5%, 20.1%, and 47.8%, respectively, of the total study population). The severity of dry eye decreased from baseline to the follow-up visit, showing a decrease of the more severe levels (2–4) and a concurrent increase in mild level (1) of the rating scale. Patients reported an improvement in dry eye symptoms over the duration of the study, specifically 74.2% (n=152), 85.4% (n=182), and 82.4% (n=417) of patients in the aqueous-deficient, lipid-deficient, and mixed-deficiency groups, respectively. TBUT was measured in 475 patients. Baseline measurements for mean and standard deviation were 9.0±3.5, 7.1±3.6, and 6.6±3.0 seconds for the aqueous-deficient, lipid-deficient, and mixed-deficiency groups, respectively. These increased to 10.5±3.5, 10.0±3.6, and 9.2±3.1 seconds at the final visit. Overall, 92.5% of all patients were satisfied with the use of Optive Plus(®), and 86% said they would purchase Optive Plus(®). Ten percent of patients reported adverse events, and 1.8% of all patients experienced treatment-related adverse events. CONCLUSION: Optive Plus(®) was well tolerated and effective in reducing the signs and symptoms of all types of dry eye but is recommended for lipid-deficient dry eye patients. |
format | Online Article Text |
id | pubmed-4069146 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-40691462014-06-26 A prospective, multicenter, noninterventional study of Optive Plus(®) in the treatment of patients with dry eye: the prolipid study Kaercher, Thomas Thelen, Ulrich Brief, Gerrett Morgan-Warren, Robert J Leaback, Richard Clin Ophthalmol Original Research OBJECTIVE: The aim was to evaluate the efficacy of Optive Plus(®), an artificial tear containing castor oil, in patients with dry eye, in a routine clinical setting. METHODS: This was a prospective, noninterventional study of patients with dry eye who switched from a prior therapy or who were naïve to treatment (n=1,209). Patients were issued Optive Plus(®) artificial tears. Dry eye severity, tear break-up time (TBUT), Schirmer score, Ocular Surface Disease Index (OSDI) score, and patient assessment of symptoms were recorded at baseline and at the follow-up visit (4 weeks after starting Optive Plus(®)). RESULTS: The cause of dry eye was determined to be aqueous deficiency, lipid deficiency, or a mixture of aqueous and lipid deficiency (in 19.5%, 20.1%, and 47.8%, respectively, of the total study population). The severity of dry eye decreased from baseline to the follow-up visit, showing a decrease of the more severe levels (2–4) and a concurrent increase in mild level (1) of the rating scale. Patients reported an improvement in dry eye symptoms over the duration of the study, specifically 74.2% (n=152), 85.4% (n=182), and 82.4% (n=417) of patients in the aqueous-deficient, lipid-deficient, and mixed-deficiency groups, respectively. TBUT was measured in 475 patients. Baseline measurements for mean and standard deviation were 9.0±3.5, 7.1±3.6, and 6.6±3.0 seconds for the aqueous-deficient, lipid-deficient, and mixed-deficiency groups, respectively. These increased to 10.5±3.5, 10.0±3.6, and 9.2±3.1 seconds at the final visit. Overall, 92.5% of all patients were satisfied with the use of Optive Plus(®), and 86% said they would purchase Optive Plus(®). Ten percent of patients reported adverse events, and 1.8% of all patients experienced treatment-related adverse events. CONCLUSION: Optive Plus(®) was well tolerated and effective in reducing the signs and symptoms of all types of dry eye but is recommended for lipid-deficient dry eye patients. Dove Medical Press 2014-06-17 /pmc/articles/PMC4069146/ /pubmed/24970993 http://dx.doi.org/10.2147/OPTH.S58464 Text en © 2014 Kaercher et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Kaercher, Thomas Thelen, Ulrich Brief, Gerrett Morgan-Warren, Robert J Leaback, Richard A prospective, multicenter, noninterventional study of Optive Plus(®) in the treatment of patients with dry eye: the prolipid study |
title | A prospective, multicenter, noninterventional study of Optive Plus(®) in the treatment of patients with dry eye: the prolipid study |
title_full | A prospective, multicenter, noninterventional study of Optive Plus(®) in the treatment of patients with dry eye: the prolipid study |
title_fullStr | A prospective, multicenter, noninterventional study of Optive Plus(®) in the treatment of patients with dry eye: the prolipid study |
title_full_unstemmed | A prospective, multicenter, noninterventional study of Optive Plus(®) in the treatment of patients with dry eye: the prolipid study |
title_short | A prospective, multicenter, noninterventional study of Optive Plus(®) in the treatment of patients with dry eye: the prolipid study |
title_sort | prospective, multicenter, noninterventional study of optive plus(®) in the treatment of patients with dry eye: the prolipid study |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4069146/ https://www.ncbi.nlm.nih.gov/pubmed/24970993 http://dx.doi.org/10.2147/OPTH.S58464 |
work_keys_str_mv | AT kaercherthomas aprospectivemulticenternoninterventionalstudyofoptiveplusinthetreatmentofpatientswithdryeyetheprolipidstudy AT thelenulrich aprospectivemulticenternoninterventionalstudyofoptiveplusinthetreatmentofpatientswithdryeyetheprolipidstudy AT briefgerrett aprospectivemulticenternoninterventionalstudyofoptiveplusinthetreatmentofpatientswithdryeyetheprolipidstudy AT morganwarrenrobertj aprospectivemulticenternoninterventionalstudyofoptiveplusinthetreatmentofpatientswithdryeyetheprolipidstudy AT leabackrichard aprospectivemulticenternoninterventionalstudyofoptiveplusinthetreatmentofpatientswithdryeyetheprolipidstudy AT kaercherthomas prospectivemulticenternoninterventionalstudyofoptiveplusinthetreatmentofpatientswithdryeyetheprolipidstudy AT thelenulrich prospectivemulticenternoninterventionalstudyofoptiveplusinthetreatmentofpatientswithdryeyetheprolipidstudy AT briefgerrett prospectivemulticenternoninterventionalstudyofoptiveplusinthetreatmentofpatientswithdryeyetheprolipidstudy AT morganwarrenrobertj prospectivemulticenternoninterventionalstudyofoptiveplusinthetreatmentofpatientswithdryeyetheprolipidstudy AT leabackrichard prospectivemulticenternoninterventionalstudyofoptiveplusinthetreatmentofpatientswithdryeyetheprolipidstudy |