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不同剂量5% 5-盐酸氨酮戊酸光动力治疗面部中重度痤疮疗效观察 被引量:1

The Clinical Effect of Different Doses of 5% 5-Aminolevulinic Acid Photodynamic Therapy for Moderate and Severe Facial Acne
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摘要 目的观察不同剂量5%5-盐酸氨酮戊酸溶液光动力疗法(ALA-PDT)治疗面部中重度痤疮的安全性与疗效。方法 88例面部中重度痤疮患者随机2组,A组47例外用4.5 m L 5%5-ALA,B组41例外用2.2 m L 5%5-ALA,7~10 d重复治疗1次,连续治疗3次。每次治疗后及末次治疗后第1、4、8、12、24周进行疗效评价并记录不良反应。结果 81例患者完成全部治疗(A组45例,B组36例),治疗3次后A组有效率(100%)高于B组(8.89%),差异有统计学意义(P〈0.05);A组痊愈率(97.78%)高于B组(80.56%),差异有统计学意义(P〈0.05)。A组再次复发率为(9.09%)低于B组(38.46%),差异有统计学意义(P〈0.01)。不良反应A、B两组分别为33.33%、30.55%,差异无统计学意义(P〉0.05)。结论固定敷药时间时,外用4.5 m L 5%5-ALA-PDT疗效好,复发率低,不良反应未见明显增加。 Objective To observe the safety and efficacy of different doses of 5% 5- aminolevulinic acid photodynamic therapy( ALA-PDT) for moderate and severe facial acne.Methods 88 cases with moderate and severe facial acne were divided into Group A( 47 cases) and Group B( 41 cases).The Group A received 4.5ml of 5% 5- ALA and Group B received 2.2ml of 5% 5-ALA.They were repeated the treatment 1 times 7 ~ 10 days,3 times in a row.The efficacy and adverse reactions were evaluated after each time and 1,4,8,12 and 24 weeks after the last time.Results 81 patients completed the treatment( Group A of 45 cases,Group B of 36 cases).After 3 times of treatment,the effective rate of Group A( 100%) was higher than that of Group B( 88.89%) and the difference was statistically significant( P〈0.05).The recovery rate of Group A( 97.78%) was higher than that of Group B( 80.56%) and the difference was statistically significant( P〈0.05).The recurrence rate of Group A( 9.09%) was lower than that of Group B( 38.46%) and the difference was statistically significant( P〈0.01).The adverse reactions of Group A and Group B were respectively 33.33% and 30.55%.There was no statistical difference( P〉0.05).Conclusion 4.5 m L 5% 5- ALA- PDT has good curative effect,low recurrence rate and no significant increase in adverse reactions.
作者 陈奇 刘国艳
出处 《湖北民族学院学报(医学版)》 2016年第3期27-29,共3页 Journal of Hubei Minzu University(Medical Edition)
关键词 痤疮 5%5-盐酸氨酮戊酸溶液光动力 临床疗效 acne 5% 5-ALA-PDT clinical efficacy
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