壳聚糖碘治疗CINⅠ伴高危HPV感染的疗效观察
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  • 英文篇名:Clinical efficacy of Chitosan-iodine in treatment of CINⅠ with high-risk human papillomaviras infection in patients
  • 作者:郭大庆 ; 刘艳媚 ; 廖庆梅 ; 加子珍 ; 王祥珍
  • 英文作者:Guo Daqing;Liu Yanmei;Liao qingmei;Jia Zizhen;Wang xiangzhen;Nanshan District,Shenzhen Maternity and Child Care Department of Pharmacy;Nanshan District,Shenzhen Maternity and Child Care Department of Gynecology;Nanshan District,Shenzhen Xili people's Hospital Department of Gynecology;
  • 关键词:壳聚糖碘 ; 人乳头状瘤病毒 ; 宫颈上皮内瘤变 ; 临床疗效
  • 英文关键词:Chitosan-iodine;;Cervical intraepithelial neoplasia Ⅰ;;Human papillomavirus;;Clinical efficacy
  • 中文刊名:BFYX
  • 英文刊名:Journal of North Pharmacy
  • 机构:深圳市南山区妇幼保健院药剂科;深圳市南山区妇幼保健院妇科;深圳市南山区西丽人民医院妇科;
  • 出版日期:2016-03-01
  • 出版单位:北方药学
  • 年:2016
  • 期:v.13
  • 基金:2013年深圳市南山区科技计划区属事业单位研发项目(南科研卫2013058)
  • 语种:中文;
  • 页:BFYX201603025
  • 页数:2
  • CN:03
  • ISSN:15-1333/R
  • 分类号:42-43
摘要
目的:探讨壳聚糖碘治疗宫颈上皮内瘤变Ⅰ(CINⅠ)伴人乳头状瘤病毒(HPV)感染的临床疗效及安全性,为临床应用提供参考。方法:选取2014年10月~2015年6月科室确诊CINⅠ伴HPV感染的患者100例,随机分为治疗组和对照组,各50例,治疗组使用壳聚糖碘治疗,对照组未用药物治疗,观察治疗组的不良反应情况,对比两组患者治疗高危HPV感染转阴情况,所得数据采用SPSS16.0进行分析。结果:治疗组3个月及6个月HPV转阴率分别为74.0%、78.0%,对照组3个月及6个月HPV转阴率分别为48.0%、62.0%,差异有统计学意义(P<0.05),治疗组患者无严重不良反应发生。结论:壳聚糖碘治疗CIN1伴HPV感染疗效确切、不良反应小,值得临床推广应用。
        Objective:To investigate clinical efficacy and safety of Chitosan-iodine in treatment of high-risk human papillomaviras infection in patients with cervical intraepithelial neoplasia Ⅰ(CIN Ⅰ).Methods:A total of 100 patients diagnosed with CIN Ⅰ and cervical high-risk HPV infection during Oct.2014 to Jun.2015 were randomly divided into group treatment and group control with 50 cases in each group.Women of group treatment were received Chitosan-iodine,group control did not received any medication.The therapeutic results for high-risk HPV infection change to negative patients were compared between the two groups and adverse reactions were observed.Data obtained were analyzed using the software SPSS16.0.Results:The high-risk HPV infection change to negative rate were 74.0% within three month and 78.0% within six month respectively in group treatment,48.0% within three month and 62.0% within six month respectively in group control the difference was significant(P<0.05).There were no serious adverse reactions were observed in group treatment.Conclusion:Treatment of Chitosan-iodine for CIN Ⅰ with high-risk human papillomaviras infection in patients resulted in significant efficacy and few adverse reactions,which was worthy of clinical application.
引文
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