2006
Low-Dose Acitretin Is Associated With Fewer Adverse Events Than High-Dose Acitretin in the Treatment of Psoriasis
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Cited by 59 publications
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Abstract
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“…Similar results are observed in other studies, that even with comparable efficacy of 25 and 50 mg acitretin, the benefit:risk ratio was in favor of 25 mg, thus, suggested the 25 mg as optimal dose (Dogra et al, 2013;Haushalter et al, 2012;Pearce et al, 2006). Low acitretin doses, namely 10 mg and 25 mg daily, are preferred as starting dosages that could be eventually increased (Berbis et al, 1989;Dogra et al, 2013;Haushalter et al, 2012;Pearce et al, 2006). According to blinded, placebo-controlled trials, we used the 25 mg daily dosage that could be considered therapeutically effective with a reduced risk of side effects.…”
Section: Discussion
supporting
confidence: 89%
Abstract
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“…Similar results are observed in other studies, that even with comparable efficacy of 25 and 50 mg acitretin, the benefit:risk ratio was in favor of 25 mg, thus, suggested the 25 mg as optimal dose (Dogra et al, 2013;Haushalter et al, 2012;Pearce et al, 2006). Low acitretin doses, namely 10 mg and 25 mg daily, are preferred as starting dosages that could be eventually increased (Berbis et al, 1989;Dogra et al, 2013;Haushalter et al, 2012;Pearce et al, 2006). According to blinded, placebo-controlled trials, we used the 25 mg daily dosage that could be considered therapeutically effective with a reduced risk of side effects.…”
Section: Discussion
supporting
confidence: 89%
“…In a randomized, double blind, parallel group, dose ranging study, testing 25, 35, and 50 mg/day acitretin dose, PASI 75 (at least 75% improvement of the baseline psoriasis area severity index, PASI score) response rate was higher in the 35 mg group (69% of treated patients), as compared with 25 mg‐ and 50 mg‐treated groups achieving PASI 75 in 47% and 53% of cases, respectively (Berbis et al, ). Similar results are observed in other studies, that even with comparable efficacy of 25 and 50 mg acitretin, the benefit:risk ratio was in favor of 25 mg, thus, suggested the 25 mg as optimal dose (Dogra et al, ; Haushalter et al, ; Pearce et al, ). Low acitretin doses, namely 10 mg and 25 mg daily, are preferred as starting dosages that could be eventually increased (Berbis et al, ; Dogra et al, ; Haushalter et al, ; Pearce et al, ).…”
Section: Discussion
supporting
confidence: 87%
Abstract
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“…[1315] In our study the maximum increase was noted in the 1 st and 2 nd week when patients were on 50 mg of acitretin, which steadily decreased with decreasing dosage. Similar findings were noted in a study by Pearce et al [16] Dogra et al noticed an increase in serum cholesterol and triglyceride levels above the upper limit of normal in 7 (11%) and 12 (20%) patients, respectively. [1] Though an increase in triglycerides, cholesterol and LDL was noted above the normal limits in many patients in our study [Figures 2 and 5], more than half returned to normal limits or near baseline levels with the reduction in dosage [Figure 3].…”
Section: Discussion
supporting
confidence: 89%
Abstract
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“…Common adverse effects observed in our study were mucocutaneous and musculoskeletal. Overall frequency of these adverse effects was dose dependent, which has also been noted in previous studies 23,24 . The mucocutaneous adverse effects resolved in majority of the patients with continued treatment indicating development of tolerance to these side‐effects.…”
Section: Discussion
supporting
confidence: 80%
