机构地区:[1]首都医科大学附属北京友谊医院皮肤性病科,北京100050 [2]河北省中医院皮肤科,石家庄050013 [3]湖北省第三人民医院(湖北省中山医院)皮肤科,武汉430030 [4]台州市中心医院(台州学院附属医院)皮肤科,台州318001 [5]北京坚毅恒泰医疗科技有限公司,北京100024
出 处:《中华皮肤科杂志》2022年第11期1021-1025,共5页Chinese Journal of Dermatology
摘 要:目的:评价一种含低聚麦芽糖X的皮肤护理软膏辅助治疗湿疹瘙痒的临床疗效和安全性。方法:采用多中心、随机、双盲、模拟剂对照临床研究,2021年3-9月于首都医科大学附属北京友谊医院、河北省中医院、湖北省第三人民医院及浙江省台州市中心医院4家医院皮肤科门诊收集轻、中度湿疹患者,采用随机数字表法随机分为两组,观察组外用一种含低聚麦芽糖X的皮肤护理软膏,模拟剂组外用该皮肤护理软膏模拟剂,每天瘙痒发作时即使用,连续使用14 d。分别于辅助治疗前和治疗7、14 d随访,根据湿疹面积及严重程度指数(EASI)、视觉模拟标尺法(VAS)等评价疗效,记录不良事件。主要采用χ^(2)检验和t检验进行疗效和安全性分析。结果:入组患者232例,男90例、女142例,年龄(40.13±13.36)岁;观察组156例,模拟剂组76例。辅助治疗前两组患者EASI评分[(2.07±2.24)分比(2.29±2.28)分]、VAS评分[(6.22±1.78)分比(6.20±1.79)分]差异均无统计学意义(t值分别为-0.70、0.06,P值分别为0.486、0.955)。治疗1 d,两组VAS评分相对各自基线的变化即有统计学意义(P值分别<0.001、=0.003)。治疗14 d,观察组VAS评分均值2.67分,显著低于模拟剂组3.35分(t=-2.28,P=0.024)。治疗7 d和14 d,与基线相比两组EASI评分均显著下降(均P<0.001),但两组间差异均无统计学意义(P=0.853、0.731)。两组均无器械相关不良事件发生。结论:含低聚麦芽糖X的皮肤护理软膏辅助治疗湿疹瘙痒安全、有效,可用于临床。Objective To evaluate the clinical efficacy and safety of a skin care ointment containing oligomeric maltose X in the adjuvant treatment of eczema-related pruritus.Methods A multicenter,randomized,double-blind,vehicle-controlled clinical study was conducted.From March to September 2021,outpatients with mild to moderate eczema were collected from departments of dermatology of 4 hospitals,including Beijing Friendship Hospital,Hebei Traditional Chinese Medical Hospital,the Third People′s Hospital of Hubei Province,and Taizhou Central Hospital in Zhejiang Province.The patients were randomly divided into two groups by using a random number table:observation group topically treated with a skin care ointment containing oligomeric maltose X,and vehicle control group topically treated with an ointment vehicle.The ointments were applied during the attacks of itching for 14 consecutive days.Visits were scheduled before,7,and 14 days after the start of the adjuvant treatment.The efficacy was evaluated according to the eczema area and severity index(EASI)and visual analog scale(VAS),and adverse events were recorded.The efficacy and safety analyses were conducted by using chi-square test and t test.Results Totally,232 patients with eczema were enrolled,including 90 males and 142 females,with the age being 40.13±13.36 years;156 patients were in the observation group,and 76 in the vehicle control group.Before the adjuvant treatment,there were no significant differences in EASI(2.07±2.24 points vs.2.29±2.28 points)or VAS(6.22±1.78 points vs.6.20±1.79 points)scores between the observation group and vehicle control group(t=-0.70,0.06,P=0.486,0.955,respectively).After one-day treatment,the VAS scores significantly decreased compared with the baseline scores in the two groups(P<0.001,P=0.003,respectively).After 14-day treatment,the VAS score was significantly lower in the observation group(2.67 points)than in the vehicle control group(3.35 points;t=-2.28,P=0.024).After 7-and 14-day treatment,the EASI scores significantly decre
关 键 词:湿疹 瘙痒症 麦芽糖 甘油 低聚麦芽糖X 随机对照试验
分 类 号:R758.23[医药卫生—皮肤病学与性病学]
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