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594例皮肤真菌病患者使用益康唑的疗效评估(作者译)

[Evaluation of econazol in 594 cases of skin mycosis (author's transl)].

作者信息

Schwarz K J, Much T, Konzelmann M

出版信息

Dtsch Med Wochenschr. 1975 Jul 11;100(28):1497-500. doi: 10.1055/s-0028-1106606.

Abstract

A total of 594 patients were treated with the new antimycotic agent econazol (Pevaryl). The diagnosis was proven microscopically and on culture except in cases of pityriasis versicolor where it was proven microscopically only. Econazol was given to 130 patients as a 1% solution, to 128 patients as a 1% milk, and to 336 patients as a 1% spray solution. In 333 cases of foot mycosis or eczema marginatum econazol spray powder was given in addition. As measured by the cure rate the spray solution (92%) was not significantly more effective than the milk (89%) or the simple solution (87%). Criteria for cure included negative microscopy and fungal cultures a week after treatment had ceased as well as clinical cure. A total of 90% of all cases (n = 536) could be considered as cured microscopically and on culture after an average of 3.6 weeks (pityriasis versicolor) and 4.8 weeks (tinea pedis, manus, inguinocruralis). In a further 4.4% (n = 26) the fungus could be demonstrated microscopically despite a clinical cure and in 7 of these cases culture was also positive. The cure rate was independent of the responsible pathogen. The preparations were tolerated extremely well. In 7 cases, however, transient dermatitic irritations were seen in the inguinocrural region, mainly caused by the simple solution.

摘要

共有594例患者接受了新型抗真菌药物益康唑(派瑞松)治疗。除花斑糠疹仅通过显微镜检查确诊外,其余均经显微镜检查和培养确诊。130例患者使用1%溶液剂型的益康唑,128例患者使用1%乳剂,336例患者使用1%喷雾溶液剂型。在333例足癣或边缘性湿疹患者中,还加用了益康唑喷雾粉剂。以治愈率衡量,喷雾溶液剂型(92%)并不比乳剂(89%)或单纯溶液剂型(87%)显著更有效。治愈标准包括治疗停止一周后显微镜检查和真菌培养结果为阴性以及临床治愈。平均3.6周(花斑糠疹)和4.8周(足癣、手癣、股癣)后,所有病例中有90%(n = 536)经显微镜检查和培养可视为治愈。另有4.4%(n = 26)患者尽管临床治愈,但显微镜检查仍可发现真菌,其中7例培养结果也为阳性。治愈率与致病病原体无关。这些制剂的耐受性非常好。然而,有7例患者腹股沟区出现短暂性皮炎,主要由单纯溶液剂型引起。

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