Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/73118
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dc.contributor.authorKulwadee Laosakulen_US
dc.contributor.authorSiri Chiewchanviten_US
dc.contributor.authorMati Chuamanochanen_US
dc.contributor.authorNapatra Tovanabutraen_US
dc.date.accessioned2022-05-27T08:35:51Z-
dc.date.available2022-05-27T08:35:51Z-
dc.date.issued2022-04-01en_US
dc.identifier.issn14770962en_US
dc.identifier.issn09612033en_US
dc.identifier.other2-s2.0-85127307280en_US
dc.identifier.other10.1177/09612033221086878en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85127307280&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/73118-
dc.description.abstractBackground: The treatment of discoid lupus erythematosus (DLE) is often challenging, especially in patients who are refractory or intolerant to topical treatments and first-line systemic drugs, specifically antimalarial drugs. Although acitretin has been shown to be effective in patients with DLE in a few studies, there is no published study describing the long-term efficacy of acitretin with a validated score. Objectives: To evaluate the efficacy and safety of acitretin in patients with antimalarial-refractory/intolerant DLE. Methods: A prospective, open-label, uncontrolled study was conducted in patients with antimalarial-refractory/intolerant DLE. All patients were treated with an initial dosage of 10 mg acitretin daily. Clinical response was assessed using the Revised Cutaneous Lupus Erythematosus Disease Area and Severity Index (RCLASI) at weeks 4, 8, 12, and 24. Acitretin was increased to 25 mg daily unless an adequate response was achieved at week 8. Results: Fourteen patients were recruited. Of these, 10 were antimalarial-refractory and four were antimalarial-intolerant. The acitretin therapy was discontinued in one patient after 20 weeks of treatment because of active systemic disease. Of the 13 remaining patients, the mean RCLASI activity scores declined from 21 ± 9 at baseline to 9 ± 4 at week 24. A significant reduction in RCLASI was initially observed at week four and consistently noted at each follow-up visit (p ≤ 0.01). At the end of the study, a marked response was achieved in approximately 80% of patients. There were no statistically significant differences in the clinical response or in the requirement of the up-dosing of acitretin between the refractory and intolerance groups (p = 0.88 and p = 0.326, respectively). Age ≥50 years old, female sex, and generalized DLE were the favorable prognostic factors. No serious adverse events were noted. Conclusions: Acitretin appears to be an effective treatment with acceptable safety profiles for antimalarial-refractory/intolerant DLE.en_US
dc.subjectMedicineen_US
dc.titleAcitretin treatment in antimalarial-refractory/intolerant discoid lupus erythematosus: A prospective, open-label, uncontrolled studyen_US
dc.typeJournalen_US
article.title.sourcetitleLupusen_US
article.volume31en_US
article.stream.affiliationsFaculty of Medicine, Chiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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