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中国真菌学杂志 2017, Vol. 12  Issue (2): 92-97.

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伏立康唑治疗播散性马尔尼菲蓝状菌病临床分析

魏金瑛1, 欧阳沿音2, 蔡双启3, 梁浩4, 曹存巍1   

  1. 1. 广西医科大学第一附属医院皮肤性病科 广西艾滋病防治研究重点实验室, 南宁 530021;
    2. 广西壮族自治区皮肤病医院, 南宁 530003;
    3. 广西医科大学第一附属医院呼吸疾病研究所, 南宁 530021;
    4. 广西医科大学公共卫生学院 & 生命科学研究院, 南宁 530021
  • 收稿日期:2016-12-08 出版日期:2017-04-28 发布日期:2017-04-28
  • 通讯作者: 曹存巍,E-mail:caocunwei@yeah.net E-mail:caocunwei@yeah.net
  • 作者简介:魏金瑛,女(汉族),硕士研究生在读.E-mail:13807725746@163.com
  • 基金资助:

    国家自然科学基金(81571971,81271804)

Administration of voriconazole in disseminated penicilliosis marneffei: a retrospective study

WEI Jin-ying1, OUYANG Yan-yin2, CAI Shuang-qi3, LIANG Hao4, CAO Cun-wei1   

  1. 1. Department of Dermatology and Venereology, The First Affiliated hospital of Guangxi Medical University, Guangxi Key Laboratory of AIDS Prevention and Treatment, Nanning 530021, China;
    2. Department of Dermatology, Guangxi Institute of Dermatology, Nanning 530003, China;
    3. Department of Respiratory, The First Affiliated Hospital of Guangxi Medical University, Nanning 530021, China;
    4. Guangxi Key Laboratory of AIDS Prevention and Treatment, School of Public Health & Life Sciences Institute, Guangxi Medical University, Nanning 530021, China
  • Received:2016-12-08 Online:2017-04-28 Published:2017-04-28

摘要:

目的 采用回顾性分析的方法探讨伏立康唑治疗播散性马尔尼菲蓝状菌病(PSM)的临床疗效及安全性。方法 收集2010年1月~2015年6月期间,诊断为PSM且使用伏立康唑作为初始抗真菌治疗的患者资料。伏立康唑近期疗效及安全性分别于治疗16周或治疗结束时予以评估,远期疗效及安全性则于治疗结束后6个月,12个月后予以评估。结果 共有17例患者采用伏立康唑进行初始治疗,3例患者未能完成疗程,在完成治疗的14例患者中,10例病情得到完全控制,3例部分控制,1例无效。在治疗结束6个月后随访的11例患者中,8例治愈,3例复发;治疗结束12月后访视的8例患者病情均无复发。所有患者在治疗期间及治疗结束后均未发生明显的毒副作用。结论 提示伏立康唑治疗播散性PSM具有较好的近期及远期临床疗效及安全性,可作为PSM治疗的一种新方法。

关键词: 伏立康唑, 马尔尼菲蓝状菌病, 疗效, 安全性

Abstract:

Objective The aim of this retrospective study is to evaluate the efficacy and safety of voriconazole in the treatment of Penicilliosis marneffei (PSM)patients with or without HIV infection in clinical setting.Methods The disseminated PSM patients who received intravenous voriconazole (6 mg/kg every 12 hours for the first 24 hours and then 4 mg/kg every 12 hours afterwards) as primary antifungal treatment were enrolled.The following duration of antifungal treatment varied at the discretion of investigators according to the response of the patients.Primary response was evaluated at Week 16 or at the end of treatment (EOT).Follow-up evaluations were performed at 6 months and 1 year after EOT.Results A total of seventeen patients enrolled in this study, three patients were not evaluable because the treatment discontinued prematurely.Among the remaining fourteen patients, thirteen had satisfied response to treatment, ten patients had complete response and three patients had partial response at Week 16.Only one patient was evaluated as failure.Follow-up assessments in eleven patients showed eight patients were cured and the remaining three patients relapsed at 6 months after EOT.Eight patients were assessed 1 year later, none of them relapsed.No adverse events associated to voriconazole were recorded during the treatment.Conclusion The results from our study suggest that voriconazole is an effective, well-tolerated therapeutic option for disseminated P.marneffei infection.

Key words: voriconazole, disseminated penicilliosis marneffei, efficacy, safety

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