The use of extemporal dosage form with pyroctone olamine in the complex treatment of patients with seborrheic dermatitis

I. Odintsova, A. Diudiun
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Abstract

The purpose of the work is to evaluate the efficacy and tolerance of extemporal dosage form with pyroctone olamine in the local treatment of patients with seborrheic dermatitis. Under our supervision there were 78 patients with seborrheic dermatitis aged 18 to 57 years. The average age of the patients was 29.5±2.1 years. Comprehensive treatment of patients with seborrheic dermatitis in both groups depended on the severity of clinical manifestations, the duration of the disease, and information on the effectiveness of previous therapy. For external treatment of the main group of patients with seborrheic dermatitis, an extemporaneously prepared gel with pyrocton olamine was used. Local treatment of patients in the comparison group consisted of the appointment of 1% cream of clotrimazole. An analysis of the results shows good therapeutic, microbiological effectiveness and good tolerance of extemporaneously prepared gel with pyrocton olamine in the complex treatment of patients with seborrheic dermatitis. The period for resolving the clinical manifestations of seborrheic dermatitis among patients in the main group was 2.5±0.1 days shorter compared with patients in the comparison group. The intensity of clinical manifestations in patients with seborrheic dermatitis of the main group decreased twice on the second day of complex treatment. In control patients with comparative seborrheic dermatitis, similar therapeutic efficacy was achieved on the fourth to fifth day. Long-term results of the study showed that the recurrence of the disease among patients of the main group was 5 (6.4%), and in patients of in the comparison group was 14 (17.9%). Clinical studies have shown good therapeutic efficacy and tolerance of the extemporal gel with pyroctone olamine in the complex treatment of patients with seborrheic dermatitis, which gives reason to recommend this dosage form for wider use in the practice of dermatovenerologists.
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使用颞外剂型与丙酮胺在复杂治疗患者脂溢性皮炎
本研究的目的是评价外用吡丙酮胺局部治疗脂溢性皮炎患者的疗效和耐受性。在我们的监督下,78例患者患有脂溢性皮炎,年龄在18至57岁之间。患者平均年龄29.5±2.1岁。两组脂溢性皮炎患者的综合治疗取决于临床表现的严重程度、疾病的持续时间和既往治疗的有效性信息。对于主要组脂溢性皮炎患者的外部治疗,使用临时制备的热丙酮胺凝胶。对照组患者局部治疗为1%克霉唑乳膏预约。结果分析表明,临时制备的热丙酮胺凝胶在综合治疗脂溢性皮炎患者中具有良好的疗效、微生物学效果和良好的耐受性。脂溢性皮炎临床症状的缓解时间主组较对照组缩短2.5±0.1 d。综合治疗第2天,主组脂溢性皮炎患者临床表现强度下降2倍。在对照比较脂溢性皮炎患者中,在第4至第5天达到相似的治疗效果。长期研究结果显示,主组患者复发5例(6.4%),对照组复发14例(17.9%)。临床研究表明,在脂溢性皮炎患者的复杂治疗中,含有吡丙酮胺的颞外凝胶具有良好的治疗效果和耐受性,这就有理由推荐这种剂型在皮肤性科医生的实践中得到更广泛的应用。
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