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Real‐life effectiveness of once‐daily calcipotriol and betamethasone dipropionate gel vs. ointment formulations in psoriasis vulgaris: final analysis of the 52‐week PRO‐long study
BACKGROUND: Topical therapies are the mainstay of treatment for psoriasis vulgaris. The fixed combination of calcipotriol (Cal) 50 μg/g plus betamethasone 0.5 mg/g (as dipropionate; BD) is a first‐line topical treatment and available as a gel or ointment. The use of these fixed combination products...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5049671/ https://www.ncbi.nlm.nih.gov/pubmed/26337069 http://dx.doi.org/10.1111/jdv.13230 |
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author | Lambert, J. Hol, C.W. Vink, J. |
author_facet | Lambert, J. Hol, C.W. Vink, J. |
author_sort | Lambert, J. |
collection | PubMed |
description | BACKGROUND: Topical therapies are the mainstay of treatment for psoriasis vulgaris. The fixed combination of calcipotriol (Cal) 50 μg/g plus betamethasone 0.5 mg/g (as dipropionate; BD) is a first‐line topical treatment and available as a gel or ointment. The use of these fixed combination products was compared in PRO‐long, a long‐term noninterventional study, for which interim results (4 and 12 weeks) have previously been reported. OBJECTIVE: To describe and compare patients’ perspectives on the fixed combination gel and ointment formulations; to include efficacy, adherence behaviour, treatment satisfaction and health‐related quality of life (HRQoL) aspects during long‐term real‐life psoriasis management. METHODS: PRO‐long was a multicentre, prospective, observational, 52‐week study of patients prescribed fixed combination Cal/BD gel or ointment in clinical practice. For final analysis the following were assessed at weeks 24, 36 and 52: differences in the proportion of patients with ‘mild’/‘very mild’ disease according to patient's global assessment of disease severity, adherence behaviour, treatment satisfaction (nine‐item treatment satisfaction questionnaire for medication) and HRQoL (Skindex‐29). RESULTS: Patients (n = 328) were prescribed once‐daily Cal/BD gel (n = 152) or ointment (n = 176). At week 52, a higher proportion of patients reported that the severity of their psoriasis was ‘mild’/‘very mild’ vs. baseline (gel: 60.2 vs. 47.1%; ointment: 58.8 vs. 42.4%), with greater treatment satisfaction reported in patients using gel vs. those using ointment. A higher proportion of patients found the gel ‘easy’ to use compared with the ointment (66.7 vs. 45.2%). Daily application of treatment took ≤5 min for 86.1% of patients using gel and 71.0% of patients using ointment. CONCLUSION: This real‐life study has demonstrated similar effectiveness between the Cal/BD formulations. However, over a 52‐week treatment period, patients reported greater treatment satisfaction with the gel, which was considered easier to use, faster to apply and overall a more convenient product. |
format | Online Article Text |
id | pubmed-5049671 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-50496712016-10-06 Real‐life effectiveness of once‐daily calcipotriol and betamethasone dipropionate gel vs. ointment formulations in psoriasis vulgaris: final analysis of the 52‐week PRO‐long study Lambert, J. Hol, C.W. Vink, J. J Eur Acad Dermatol Venereol Original Articles BACKGROUND: Topical therapies are the mainstay of treatment for psoriasis vulgaris. The fixed combination of calcipotriol (Cal) 50 μg/g plus betamethasone 0.5 mg/g (as dipropionate; BD) is a first‐line topical treatment and available as a gel or ointment. The use of these fixed combination products was compared in PRO‐long, a long‐term noninterventional study, for which interim results (4 and 12 weeks) have previously been reported. OBJECTIVE: To describe and compare patients’ perspectives on the fixed combination gel and ointment formulations; to include efficacy, adherence behaviour, treatment satisfaction and health‐related quality of life (HRQoL) aspects during long‐term real‐life psoriasis management. METHODS: PRO‐long was a multicentre, prospective, observational, 52‐week study of patients prescribed fixed combination Cal/BD gel or ointment in clinical practice. For final analysis the following were assessed at weeks 24, 36 and 52: differences in the proportion of patients with ‘mild’/‘very mild’ disease according to patient's global assessment of disease severity, adherence behaviour, treatment satisfaction (nine‐item treatment satisfaction questionnaire for medication) and HRQoL (Skindex‐29). RESULTS: Patients (n = 328) were prescribed once‐daily Cal/BD gel (n = 152) or ointment (n = 176). At week 52, a higher proportion of patients reported that the severity of their psoriasis was ‘mild’/‘very mild’ vs. baseline (gel: 60.2 vs. 47.1%; ointment: 58.8 vs. 42.4%), with greater treatment satisfaction reported in patients using gel vs. those using ointment. A higher proportion of patients found the gel ‘easy’ to use compared with the ointment (66.7 vs. 45.2%). Daily application of treatment took ≤5 min for 86.1% of patients using gel and 71.0% of patients using ointment. CONCLUSION: This real‐life study has demonstrated similar effectiveness between the Cal/BD formulations. However, over a 52‐week treatment period, patients reported greater treatment satisfaction with the gel, which was considered easier to use, faster to apply and overall a more convenient product. John Wiley and Sons Inc. 2015-09-03 2015-12 /pmc/articles/PMC5049671/ /pubmed/26337069 http://dx.doi.org/10.1111/jdv.13230 Text en © 2015 The Authors. Journal of the European Academy of Dermatology and Venereology published by John Wiley & Sons Ltd on behalf of European Academy of Dermatology and Venereology. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Articles Lambert, J. Hol, C.W. Vink, J. Real‐life effectiveness of once‐daily calcipotriol and betamethasone dipropionate gel vs. ointment formulations in psoriasis vulgaris: final analysis of the 52‐week PRO‐long study |
title | Real‐life effectiveness of once‐daily calcipotriol and betamethasone dipropionate gel vs. ointment formulations in psoriasis vulgaris: final analysis of the 52‐week PRO‐long study |
title_full | Real‐life effectiveness of once‐daily calcipotriol and betamethasone dipropionate gel vs. ointment formulations in psoriasis vulgaris: final analysis of the 52‐week PRO‐long study |
title_fullStr | Real‐life effectiveness of once‐daily calcipotriol and betamethasone dipropionate gel vs. ointment formulations in psoriasis vulgaris: final analysis of the 52‐week PRO‐long study |
title_full_unstemmed | Real‐life effectiveness of once‐daily calcipotriol and betamethasone dipropionate gel vs. ointment formulations in psoriasis vulgaris: final analysis of the 52‐week PRO‐long study |
title_short | Real‐life effectiveness of once‐daily calcipotriol and betamethasone dipropionate gel vs. ointment formulations in psoriasis vulgaris: final analysis of the 52‐week PRO‐long study |
title_sort | real‐life effectiveness of once‐daily calcipotriol and betamethasone dipropionate gel vs. ointment formulations in psoriasis vulgaris: final analysis of the 52‐week pro‐long study |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5049671/ https://www.ncbi.nlm.nih.gov/pubmed/26337069 http://dx.doi.org/10.1111/jdv.13230 |
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