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柳氮磺胺吡啶可改善银屑病。一项双盲分析。

Sulfasalazine improves psoriasis. A double-blind analysis.

作者信息

Gupta A K, Ellis C N, Siegel M T, Duell E A, Griffiths C E, Hamilton T A, Nickoloff B J, Voorhees J J

机构信息

Department of Dermatology, University of Michigan Medical Center, Ann Arbor 48109-0314.

出版信息

Arch Dermatol. 1990 Apr;126(4):487-93.

PMID:1690970
Abstract

In an 8-week double-blind trial of sulfasalazine for the treatment of moderate-to-severe psoriasis, 23 and 27 patients received the active and placebo tablets, respectively. At the end of the double-blind phase, there were 17 assessable patients receiving sulfasalazine; 7 (41%) had marked improvement, 7 (41%) had moderate improvement, and 3 (18%) demonstrated minimal change. Only 1 patient receiving placebo demonstrated moderate improvement, whereas the rest had minimal improvement or worsening of psoriasis. When the randomization code was broken, patients receiving sulfasalazine were allowed to continue therapy for an additional 4 weeks in an open manner, while those using placebo left the study. Six of 23 patients discontinued sulfasalazine therapy during the double-blind phase because of side effects, 4 due to the development of a cutaneous eruption and 2 due to nausea. Fourteen of 17 patients, who were assessable at the end of the 8-week double-blind phase, completed the additional 4 weeks of sulfasalazine therapy. Of these 14 patients, marked improvement occurred in 8 (57%), moderate improvement in 2 (14%), and minimal improvement in 4 (29%), compared with pretherapy. The low incidence of severe side effects makes sulfasalazine a consideration for oral therapy in patients whose disease severity does not justify use of methotrexate, etretinate, or psoralen plus UV-A, but whose disease severity is too widespread for safe and practical use of topical corticosteroids.

摘要

在一项为期8周的柳氮磺胺吡啶治疗中度至重度银屑病的双盲试验中,分别有23例和27例患者接受了活性片剂和安慰剂片剂治疗。在双盲阶段结束时,有17例可评估患者接受柳氮磺胺吡啶治疗;7例(41%)有显著改善,7例(41%)有中度改善,3例(18%)显示变化极小。仅1例接受安慰剂治疗的患者有中度改善,而其余患者银屑病改善极小或病情恶化。当随机分组代码被破解后,接受柳氮磺胺吡啶治疗的患者被允许以开放方式继续治疗4周,而使用安慰剂的患者则退出研究。23例患者中有6例在双盲阶段因副作用停止柳氮磺胺吡啶治疗,4例因出现皮疹,2例因恶心。在8周双盲阶段结束时可评估的17例患者中,有14例完成了额外4周的柳氮磺胺吡啶治疗。与治疗前相比,这14例患者中,8例(57%)有显著改善,2例(14%)有中度改善,4例(29%)有极小改善。严重副作用的发生率较低,这使得柳氮磺胺吡啶成为疾病严重程度不足以使用甲氨蝶呤、依曲替酯或补骨脂素加紫外线A,但疾病严重程度又广泛到无法安全实用地使用外用皮质类固醇的患者口服治疗的一个选择。

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