Phototherapie bei Psoriasis - effektiv, verträglich und kostengünstig

P. Lehmann
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Abstract

Background: The prevalence of narrow-band ultraviolet B (NB-UVB) use in Europe for moderate and severe psoriasis is unknown, because national registries for psoriasis do not monitor this treatment. Objectives: To quantify the use of phototherapy, biologics or conventional treatments in psoriasis, in a setting where European Medicines Agency (EMA) eligibility criteria for biologics were strictly applied, and phototherapy was included among first-line treatments. Methods: We followed a cohort of 1,090 patients who were referred to the only centre entitled to prescribe biologics and phototherapy during a 5-year period. Results: The cumulative number of treatment cycles was: 1,047 with NB-UVB phototherapy, 650 with systemic treatments and 239 with biologics; 754 patients received at least 1 course of NB-UVB phototherapy, 422 at least 1 course with a systemic treatment and 137 with a biologic; 595 patients were treated only with phototherapy. Conclusions: Regular use of NB-UVB as first-line treatment for moderate and severe psoriasis and adherence to the EMA eligibility criteria for biologics led to a relatively restricted use of biologics.
普利兹奖
背景:窄带紫外线B (NB-UVB)在欧洲治疗中重度牛皮癣的流行程度尚不清楚,因为国家牛皮癣登记处没有监测这种治疗。目的:在严格应用欧洲药品管理局(EMA)生物制剂资格标准的情况下,量化光疗、生物制剂或常规治疗在牛皮癣中的应用,光疗被纳入一线治疗。方法:我们跟踪了一组1090名患者,这些患者在5年期间被转诊到唯一有权开具生物制剂和光疗处方的中心。结果:NB-UVB光疗累计治疗周期1047次,全身治疗650次,生物制剂治疗239次;754例患者接受了至少1个疗程的NB-UVB光疗,422例接受了至少1个疗程的全身治疗,137例接受了生物制剂治疗;595例患者仅接受光疗治疗。结论:常规使用NB-UVB作为中重度牛皮癣的一线治疗,并遵守EMA的生物制剂资格标准,导致生物制剂的使用相对受限。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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