首页|螺内酯口服联合米诺地尔外用治疗女性雄激素性脱发的有效性和安全性研究

螺内酯口服联合米诺地尔外用治疗女性雄激素性脱发的有效性和安全性研究

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目的 探究螺内酯口服联合米诺地尔外用治疗女性雄激素性脱发的有效性和安全性。方法 选取2021年9月至2022年12月福建医科大学附属龙岩第一医院皮肤科门诊收治的160例确诊的雄激素性脱发女性患者,采用随机摸球法分为两组。对照组80例,采取米诺地尔单一治疗,研究组80例,在对照组基础上联合螺内酯治疗,两组均治疗12个月。比较两组毛发平均密度,记录两组不良事件发生情况,治疗前及治疗12个月采用生活质量简表(WHOQOL-100)评价两组生活质量。结果 干预后,两组毛发平均密度均高于干预前,研究组高于对照组,差异有统计学意义(P<0。05)。研究组不良事件总发生率高于对照组,差异有统计学意义(P<0。05)。干预后,两组WHOQOL-100评分均高于干预前,研究组高于对照组,差异有统计学意义(P<0。05)。结论 螺内酯口服联合米诺地尔外用治疗女性雄激素性脱发具有较好的临床疗效及安全性,有助于提高患者生活质量。
Study on the effectiveness and safety of oral spironolactone combined with topical minoxidil in the treatment of androgenetic alopecia in women
Objective To investigate the effectiveness and safety of oral spironolactone combined with topical minoxidil in the treatment of androgenetic alopecia in women.Methods A total of 160 female patients with confirmed androgenetic alopecia admitted to the outpatient clinic of the Department of Dermatology of the Longyan First Affiliated Hospital of Fujian Medical University between September 2021 and December 2022 were selected,and were divided into two groups using the randomized touching ball method.80 patients in the control group were treated with minoxidil monotherapy,and 80 patients in the study group were treated with combined spironolactone on the basis of the treatment in the control group,with a treatment duration of 12 months for both groups.The average hair density of both groups was compared,and the occurrence of adverse events in both groups was recorded.The quality of life of both groups was evaluated using the World Health Organization Quality of Life-100 items(WHOQOL-100)before treatment and at 12 months after treatment.Results After the intervention,the average hair density of both groups was higher than that before the intervention,and the density was higher in the study group than that in the control group,with a statistically significant difference(P<0.05).The total incidence rate of adverse events was higher in the study group than in the control group,with a statistically significant difference(P<0.05).After the intervention,the WHOQOL-100 score of both groups was higher than that before the intervention,and the score was higher in the study group than that in the control group,with a statistically significant difference(P<0.05).Conclusion Oral spironolactone combined with topical minoxidil for the treatment of androgenetic alopecia in women shows high clinical effectiveness and safety,which helps to improve patients'quality of life.

SpironolactoneMinoxidilAndrogenetic alopeciaEffectivenessSafetyQuality of life

郭春燕、陈若玺、张强、林苑津、林冠廷

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福建医科大学附属龙岩第一医院皮肤科,福建龙岩 364000

厦门弘爱医院皮肤科,福建厦门 361016

螺内酯 米诺地尔 雄激素性脱发 有效性 安全性 生活质量

2024

中国医药科学
海峡两岸医药卫生交流协会 二十一世纪联合创新(北京)医药科学研究院

中国医药科学

影响因子:1.083
ISSN:2095-0616
年,卷(期):2024.14(21)