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Topical 3.0% diclofenac in 2.5% hyaluronan gel in the treatment of actinic keratoses

dc.contributor.authorWolf, John E.en_US
dc.contributor.authorTaylor, Joseph Richarden_US
dc.contributor.authorTschen, Eduardoen_US
dc.contributor.authorKang, Sewanen_US
dc.date.accessioned2010-04-01T14:53:21Z
dc.date.available2010-04-01T14:53:21Z
dc.date.issued2001-11en_US
dc.identifier.citationWolf, John E.; Taylor, Joseph Richard; Tschen, Eduardo; Kang, Sewan (2001). "Topical 3.0% diclofenac in 2.5% hyaluronan gel in the treatment of actinic keratoses." International Journal of Dermatology 40(11): 709-713. <http://hdl.handle.net/2027.42/65343>en_US
dc.identifier.issn0011-9059en_US
dc.identifier.issn1365-4632en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/65343
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=11737438&dopt=citationen_US
dc.description.abstractActinic keratoses (AKs) are epidermal skin lesions with the potential to develop into invasive squamous cell carcinoma (SCC). Treatment at an early stage may prevent development of SCC. Current treatment options are highly destructive and associated with significant side-effects. Early studies with topical diclofenac were encouraging and led to its evaluation for the treatment of actininic keratosis. Previous studies have demonstrated that 3% diclofenac in 2.5% hyaluronan gel is effective and well tolerated in the treatment of AK. The present study was designed to further explore the therapeutic potential of this gel. Methods This randomized, double-blind, placebo-controlled trial involved outpatients with a diagnosis of five or more AK lesions contained in one to three 5 cm 2 blocks. Patients received either active treatment (3% diclofenac gel in 2.5% hyaluronan gel) or inactive gel vehicle (hyaluronan) as placebo (0.5 g b.i.d. in each 5 cm 2 treatment area for 90 days). Assessments included the Target Lesion Number Score (TLNS), Cumulative Lesion Number Score (CLNS), and Global Improvement Indices rated separately by both the investigator (IGII) and patient (PGII). Results Results obtained from 96 patients at follow up (30 days after end of treatment) indicated that a significantly higher proportion of patients who received active treatment had a TLNS 0 compared to the placebo group (50% vs. 20%; P < 0.001). There was also a significant difference between the two groups in CLNS, with 47% of patients in the active treatment group having a CLNS 0 compared with only 19% in the placebo group ( P < 0.001). The proportion of patients with an IGII score of 4 (completely improved) at follow-up was 47% in the active treatment group compared with only 19% in the placebo group ( P < 0.001); for PGII these values were 41% vs. 17%, P < 0.001. Both treatments were well tolerated, with most adverse events related to the skin. Conclusions Topical 3% diclofenac in 2.5% hyaluronan gel was effective and well tolerated for the treatment of AK.en_US
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dc.format.extent3110 bytes
dc.format.mimetypeapplication/pdf
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dc.publisherBlackwell Science Ltden_US
dc.rightsInternational Society of Dermatologyen_US
dc.titleTopical 3.0% diclofenac in 2.5% hyaluronan gel in the treatment of actinic keratosesen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelDermatologyen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumFrom the Department of Dermatology, Baylor College of Medicine, Houston, Miami VA Medical Center and Department of Dermatology, University of Miami, Miami, Academic Dermatology Associates, Albuquerque, and the Department of Dermatology, University of Michigan, Ann Arbor, USAen_US
dc.identifier.pmid11737438en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/65343/1/j.1365-4362.2001.01324.x.pdf
dc.identifier.doi10.1046/j.1365-4362.2001.01324.xen_US
dc.identifier.sourceInternational Journal of Dermatologyen_US
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dc.owningcollnameInterdisciplinary and Peer-Reviewed


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