Pyrithione zinc aerosol Weng Observation Treatment of Psoriasis Vulgaris.doc

Pyrithione zinc aerosol Weng Observation Treatment of Psoriasis Vulgaris.doc

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Pyrithione zinc aerosol Weng Observation Treatment of Psoriasis Vulgaris

 PAGE \* MERGEFORMAT 6 Pyrithione zinc aerosol Weng Observation Treatment of Psoriasis Vulgaris [Keywords:] pyridine sulfur aerosol Weng zinc psoriasis Evaluation of topiramate for the treatment of sulfur aerosol Weng zinc psoriasis efficacy and safety of our hospital in October 2006 to October 2008, Aung zinc sulfur aerosol of topiramate treatment in clinical psoriasis observation. 1 Case and methods 1.1 Case of 144 patients were selected from the outpatient department, 73 male and female 71 cases, aged 18 to 65 years, mean (36 + -1.6 years, duration of 6 months to 30 years, mean (12 + -1.4 years. topiramate treatment divided by the order of S Weng zinc group and tazarotene group. the two groups were gender, age, disease course and compared before treatment, the difference was not statistically significant. one of the following conditions are not as observed Target: 3 months had received systemic corticosteroids, Victoria A acid drugs, immunosuppressive agents, NB-UVB or PUVA treatment, within 1 month received local corticosteroids or other anti-psoriasis treatment, regression of patients, the treatment of allergy medicine or related components, lesion area accounts for more than 20% body surface area. pregnant women, lactating women or women who desire fertility in recent years, with serious heart, liver, kidney, blood system disorders. 1.2 Methods Pyrithione Zinc Weng application in patients in the lesion area of #8203;#8203;topiramate Spain imported zinc aerosol sulfur Weng (Spain international pharmaceutical new chemical production, spray volume to thin drug coverage for the degree of surface lesions, 3 times a day . tazarotene group of patients in the lesion area before going to bed every night with tazarotene gel applied 1 time, and gently rub, in order to promote drug absorption. Both groups were to disable other oral drugs and topical drugs, 1 week follow-up, treatment time was 4 w. 1.3 Efficacy of selected indicators and criteria for

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