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复方聚六亚甲基双胍治疗微小隐孢子虫性角结膜炎的临床研究。

Clinical trial of 0.02% polyhexamethylene biguanide versus placebo in the treatment of microsporidial keratoconjunctivitis.

机构信息

L. V. Prasad Eye Institute, Bhubaneswar, Orissa, India.

出版信息

Am J Ophthalmol. 2010 Jul;150(1):110-115.e2. doi: 10.1016/j.ajo.2010.01.038. Epub 2010 May 5.

Abstract

PURPOSE

To evaluate the efficacy of 0.02% polyhexamethylene biguanide (PHMB) in the treatment of keratoconjunctivitis caused by microsporidia.

DESIGN

Prospective, double-masked, randomized, placebo-controlled clinical trial.

METHODS

One hundred forty-five patients in a single-center, institutional setting were recruited. Patients with superficial keratoconjunctivitis and corneal scrapings with positive results for microsporidial spores were included. Patients with any known allergy to PHMB, and clinically suspected bacterial, viral, or fungal infection were excluded from the study. One hundred forty-five patients were treated at 4-hour intervals with either topical 0.02% PHMB (n = 72) or placebo (n = 73). The patients were followed-up on day 3 +/- 1, day 7 +/- 1, and weekly thereafter, until complete resolution of the corneal lesions. Patients with deterioration of clinical symptoms and signs were removed from the study and were treated with PHMB. Main outcome measures included resolution time, cure time, and final visual outcome.

RESULTS

Resolution time was defined as the amount of time until disappearance of corneal epithelial infiltrates. Cure time was defined as the interval until absence of conjunctival congestion, corneal epithelial lesion, and superficial punctate keratitis. Baseline characteristics showed no relevant difference between the groups. The mean resolution time was 4.9 +/- 2.2 days and 4.6 +/- 2.3 days in the PHMB and placebo groups, respectively (P = .49). The mean time for cure was 13.5 +/- 6.6 days and 9.4 +/- 5.1 days in PHMB and placebo groups, respectively (P = .004). There was no significant difference in the final visual outcome between the groups (P = .10). No serious adverse effects were noted.

CONCLUSIONS

Treatment of microsporidial keratoconjunctivitis with PHMB does not offer any significant advantage over placebo, suggesting self-limiting nature of the disease.

摘要

目的

评估 0.02%聚六亚甲基双胍(PHMB)治疗微小孢子虫引起的角结膜炎的疗效。

设计

前瞻性、双盲、随机、安慰剂对照临床试验。

方法

在一家单中心机构招募了 145 名患者。纳入患有浅层角结膜炎和角膜刮片有微小孢子虫孢子阳性结果的患者。已知对 PHMB 过敏的患者,以及临床疑似细菌、病毒或真菌感染的患者均被排除在研究之外。145 名患者每隔 4 小时接受局部 0.02% PHMB(n=72)或安慰剂(n=73)治疗。患者在第 3 天(±1 天)、第 7 天(±1 天)以及此后每周进行随访,直到角膜病变完全消退。出现临床症状和体征恶化的患者被从研究中移除,并接受 PHMB 治疗。主要观察指标包括消退时间、治愈时间和最终视力结果。

结果

消退时间定义为角膜上皮浸润消失所需的时间。治愈时间定义为结膜充血、角膜上皮病变和浅层点状角膜炎消失所需的时间。基线特征显示两组之间无明显差异。PHMB 和安慰剂组的平均消退时间分别为 4.9±2.2 天和 4.6±2.3 天(P=0.49)。治愈时间分别为 13.5±6.6 天和 9.4±5.1 天(P=0.004)。两组最终视力结果无显著差异(P=0.10)。未观察到严重不良事件。

结论

用 PHMB 治疗微小孢子虫性角结膜炎并没有比安慰剂提供任何显著优势,提示疾病具有自限性。

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