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参榆洗剂联合曲安奈德益康唑乳膏治疗足癣的疗效观察 被引量:2
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作者 孔韵莹 伍紫炫 朱铭华 《广州中医药大学学报》 CAS 2021年第1期52-57,共6页
【目的】观察参榆洗剂联合曲安奈德益康唑乳膏治疗浸渍糜烂型足癣的临床疗效。【方法】将64例浸渍糜烂型足癣患者随机分为治疗组和对照组,每组各32例。对照组给予曲安奈德益康唑乳膏外涂治疗,治疗组给予参榆洗剂浸泡联合曲安奈德益康唑... 【目的】观察参榆洗剂联合曲安奈德益康唑乳膏治疗浸渍糜烂型足癣的临床疗效。【方法】将64例浸渍糜烂型足癣患者随机分为治疗组和对照组,每组各32例。对照组给予曲安奈德益康唑乳膏外涂治疗,治疗组给予参榆洗剂浸泡联合曲安奈德益康唑乳膏外涂治疗,疗程为4周,并于疗程结束后4周进行随访。观察2组患者治疗前后临床症状总积分的变化情况,比较2组患者的病原清除情况和复发情况,评价2组患者的临床疗效和安全性。【结果】(1)治疗过程中,对照组脱落2例,治疗组无脱落病例,最终对照组30例、治疗组32例完成试验。(2)治疗4周后,治疗组的愈显率和总有效率分别为78.1%(25/32)和96.9%(31/32),对照组分别为56.7%(17/30)和90.0%(27/30);2组患者的总有效率比较,差异无统计学意义(P>0.05),但治疗组的愈显率和总体疗效均优于对照组,差异均有统计学意义(P<0.05)。(3)治疗后,2组患者的临床症状总积分均较治疗前明显降低(P<0.05),且治疗组的降低作用明显优于对照组,差异有统计学意义(P<0.05)。(4)治疗后,治疗组和对照组的病原清除率分别为90.6%(29/32)、86.7%(26/30),组间比较,差异无统计学意义(P>0.05)。(5)在疗程结束后4周,治疗组的复发率为9.4%(3/32),对照组为16.7%(5/30),组间比较,差异无统计学意义(P>0.05)。(6)治疗过程中,2组患者均无明显的不良事件发生。【结论】参榆洗剂联合曲安奈德益康唑乳膏治疗浸渍糜烂型足癣疗效确切,其疗效优于单纯使用曲安奈德益康唑乳膏治疗。 展开更多
关键词 中药外治法 参榆洗剂 曲安奈德益康唑乳膏 浸渍糜烂型足癣
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参榆外洗剂联合克霉唑栓对单纯性湿热下注型外阴阴道假丝酵母菌病中医证候、阴道微生态及灌洗液炎症因子的影响
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作者 刘松君 石吟 +1 位作者 蒋亦 程启媛 《浙江中医杂志》 2024年第11期978-979,共2页
目的:探讨参榆外洗剂联合克霉唑栓对单纯性湿热下注型外阴阴道假丝酵母菌病中医证候、阴道微生态及灌洗液炎症因子的影响。方法:选取门诊首次就诊且未经治疗的单纯性湿热下注型外阴阴道假丝酵母菌病患者共90例,采用完全随机对照法分组,... 目的:探讨参榆外洗剂联合克霉唑栓对单纯性湿热下注型外阴阴道假丝酵母菌病中医证候、阴道微生态及灌洗液炎症因子的影响。方法:选取门诊首次就诊且未经治疗的单纯性湿热下注型外阴阴道假丝酵母菌病患者共90例,采用完全随机对照法分组,分成观察组和对照组各45例,分别于治疗前和治疗后7天进行中医证候疗效评分,治疗后3月随访复发率,留取阴道分泌物和阴道灌洗液标本,测定阴道微生态系统评分和阴道灌洗液炎症因子[白介素-2(IL-2)、IL-6、干扰素-γ(INF-γ)和肿瘤坏死因子-α(TNF-α)]变化。结果:观察组中医证候疗效总有效率高于对照组,复发率低于对照组(P<0.05)。治疗后,观察组阴道微生态评分低于对照组(P<0.05);观察组阴道灌洗液炎症因子IL-2、TNF-α水平较对照组明显降低(P<0.05),IL-6较对照组有所升高(P<0.05)。结论:采用参榆外洗剂联合克霉唑栓治疗单纯性湿热下注型外阴阴道假丝酵母菌病有助于改善患者中医证候评分、阴道微生态指标及灌洗液细胞因子水平,复发率低,能提高临床疗效。 展开更多
关键词 参榆洗剂 克霉唑栓 外阴阴道假丝酵母菌病 阴道微生态 炎症因子
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Experimental Study on Acute Toxicity of Yusheng Xiaoyang Lotion in Mice
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作者 熊成欢 徐风 +2 位作者 蒋玲 熊静 刘明 《Agricultural Science & Technology》 CAS 2017年第5期843-845,共3页
[Objective] This study was carried out to provide toxicological basic data for the development and research of Yushen Xiaoyang Lotion.[Method]SPF SD mice, half male and half female, were divided into a blank control g... [Objective] This study was carried out to provide toxicological basic data for the development and research of Yushen Xiaoyang Lotion.[Method]SPF SD mice, half male and half female, were divided into a blank control group and a Yusheng Xiaoyang Lotion group randomly. The percutaneous acute toxicity of Yusheng Xiaoyang Lotion was observed by one time limited dose method, and ap-parent sign changes and death condition of mice after administration of the drug were recorded. After the test, all the animals were weighed and subjected to gross anatomy, and if there were abnormal phenomena, further histopathological examina-tion of should be done. Animals died during the test should be subjected to anato-my. [Result] All the mice survived and exhibited normal behavior,glossy hair and increase of body weight in accordance with growth law.No local and systematic toxicity responses on skin were observed. In visual observation after dissection, no pathologic changes on heart, liver, spleen, lung and kidney were observed. There were no significant differences in body weight between the Yusheng Xiaoyang Lo-tion group and the blank control group before administration,the 7th d after adminis-tration and the 14th after administration (P〉0.05). [Conclusion] In the transdermaldrug delivery acute toxicity test of Yusheng Xiaoyang Lotion on mice, no obvious toxic responses were observed under the total dose of 89.70 g/kg (equivalent to 120 times of the clinical daily dose for adults). 展开更多
关键词 Yusheng Xiaoyang Lotion MOUSE Acute toxicity test
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