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局部使用洗必泰和丙脒腙成功治疗棘阿米巴角膜炎

Successful medical therapy of Acanthamoeba keratitis with topical chlorhexidine and propamidine.

作者信息

Seal D, Hay J, Kirkness C, Morrell A, Booth A, Tullo A, Ridgway A, Armstrong M

机构信息

Tennent Institute of Ophthalmology, Western Infirmary, Glasgow, UK.

出版信息

Eye (Lond). 1996;10 ( Pt 4):413-21. doi: 10.1038/eye.1996.92.

Abstract

INTRODUCTION

Following laboratory studies on new potential chemotherapy for Acanthamoeba keratitis, when chlorhexidine and propamidine provided an additive in vitro effect, a series of 12 patients with culture-proven Acanthamoeba keratitis from three UK centres was monitored during and after therapy.

METHODS

In all cases the clinical diagnosis was confirmed by amoebal culture. In some instances identification of the protozoa by direct microscopy of corneal tissue was possible. The medication was provided topically in drop form until the keratitis had resolved. In vitro sensitivity to chlorhexidine and propamidine was performed on all isolates and compared with sensitivity to a range of other drugs used for treatment of the infection.

RESULTS

In vitro drug testing confirmed that trophozoites and cysts of all 12 Acanthamoeba isolates were fully sensitive to chlorhexidine and propamidine. Therapy was satisfactory for controlling and eradicating the acanthamoebal infection in all patients. Three patients developed discrete stromal infiltration at the site of infection that resolved 1 week after commencing therapy, with or without use of steroids. Two patients developed a late inflammatory effect in the stromal scar at 6 months, which resolved with steroids. No clinical evidence of chlorhexidine toxicity was found in any patients.

CONCLUSIONS

The combination of topical chlorhexidine and propamidine was very effective for treating Acanthamoeba keratitis provided the drugs were continued for a sufficient period. No drug toxicity or resistance of Acanthamoeba isolates was observed in the 12 treated patients.

摘要

引言

在对棘阿米巴角膜炎新的潜在化疗药物进行实验室研究后,当洗必泰和丙脒在体外产生相加作用时,对来自英国三个中心的12例经培养证实的棘阿米巴角膜炎患者在治疗期间及之后进行了监测。

方法

所有病例的临床诊断均通过阿米巴培养得以证实。在某些情况下,通过角膜组织直接显微镜检查可鉴定原生动物。药物以滴剂形式局部给药,直至角膜炎消退。对所有分离株进行了洗必泰和丙脒的体外敏感性检测,并与用于治疗该感染的一系列其他药物的敏感性进行了比较。

结果

体外药物检测证实,所有12株棘阿米巴的滋养体和包囊对洗必泰和丙脒均完全敏感。所有患者的棘阿米巴感染控制和根除治疗均令人满意。3例患者在感染部位出现离散的基质浸润,在开始治疗后1周消退,无论是否使用类固醇。2例患者在6个月时在基质瘢痕处出现迟发性炎症反应,使用类固醇后消退。未在任何患者中发现洗必泰毒性的临床证据。

结论

局部应用洗必泰和丙脒联合治疗棘阿米巴角膜炎非常有效,前提是持续用药足够时间。在12例接受治疗的患者中未观察到棘阿米巴分离株的药物毒性或耐药性。

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