0.03%局部他克莫司治疗春性角膜结膜炎的安全性和有效性:一项非随机对照临床试验

Q2 Medicine
Mahmoud Eltagoury, Waleed Abou Samra, Ehab Ghoneim
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引用次数: 1

摘要

背景:春性角膜结膜炎(VKC)是一种双侧、复发性、慢性结膜炎症性疾病,有季节性加重。本研究旨在评价0.03%他克莫司眼膏治疗慢性VKC的疗效和安全性。方法:这是一项开放标签、前瞻性、非随机、比较介入研究,纳入了50名慢性VKC患者,他们被分为两组。第一组患者给予0.03%他克莫司眼膏,每日2次,连用2个月,然后每日1次,连用2个月,之后每隔一天1次,连用2个月。对照组给予标准抗过敏药物,0.1%氟美洛酮滴眼液,每日3次,连用2周后逐渐减量,随访期间0.1%奥洛他定每日2次。使用症状和体征的四分制评估疾病严重程度。通过分析症状和体征的变化以及临床摄影来评估治疗效果。结果:50例双侧慢性VKC患者完成随访。他克莫司组和对照组的平均(标准差)年龄具有可比性(16.20[5.10]岁vs . 16.48[4.19]岁,P > 0.05)。最常见的症状是瘙痒,最常见的体征是乳头肥大和结膜充血。两组患者治疗后症状和体征均明显减轻。他克莫司组在3个月和6个月时的平均综合症状评分和平均综合体征评分均有更显著的改善(P < 0.05)。在并发症方面,对照组在类固醇治疗2周后出现1例眼压升高(4%),而他克莫司组除有刺痛感报道外,无并发症,耐受性良好。结论:0.03%他克莫司眼膏治疗慢性双侧VKC有效、安全。它可以被认为是减少慢性VKC患者类固醇相关并发症的替代治疗方法。未来需要更长的随访期的双盲临床试验来证实我们的发现,并确定0.03%他克莫司软膏外用在VKC中的长期安全性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Safety and efficacy of topical tacrolimus 0.03% in the management of vernal keratoconjunctivitis: a non-randomized controlled clinical trial.

Safety and efficacy of topical tacrolimus 0.03% in the management of vernal keratoconjunctivitis: a non-randomized controlled clinical trial.

Safety and efficacy of topical tacrolimus 0.03% in the management of vernal keratoconjunctivitis: a non-randomized controlled clinical trial.

Safety and efficacy of topical tacrolimus 0.03% in the management of vernal keratoconjunctivitis: a non-randomized controlled clinical trial.

Background: Vernal keratoconjunctivitis (VKC) is a bilateral, recurrent, chronic conjunctival inflammatory disease with seasonal exacerbations. This study aimed to assess the efficacy and safety of tacrolimus 0.03% eye ointment in the management of chronic VKC.

Methods: This was an open-label, prospective, non-randomized, comparative interventional study that enrolled 50 patients with chronic VKC, who were allocated to one of two groups. The first group was treated with tacrolimus 0.03% eye ointment twice daily for 2 months then once daily for 2 months, followed by once every other day for another 2 months. The control group was treated with standard anti-allergic drugs, topical fluorometholone 0.1% eye drops three times daily for 2 weeks and gradually tapered for another 2 weeks, with topical olopatadine 0.1% administered twice daily during the follow-up period. Disease severity was assessed using a four-point scale for symptoms and signs. Treatment efficacy was assessed by analyzing changes in symptoms and signs, and by clinical photography.

Results: Fifty patients with bilateral chronic VKC completed the follow-up. The mean (standard deviation) ages of the tacrolimus and control groups were comparable (16.20 [5.10] years versus 16.48 [4.19] years, P > 0.05). The most commonly reported symptom was itching, and the most common signs were papillary hypertrophy and conjunctival hyperemia. All symptoms and signs were significantly reduced after treatment in both groups. The tacrolimus group showed a more significant improvement at 3 and 6 months in the mean composite symptom score (both P < 0.05) and in the mean composite sign score (both P < 0.05). Regarding complications, one case of increased intraocular pressure occurred in the control group (4%) after 2 weeks of steroid treatment, while there were no complications in the tacrolimus group, except for some reports of stinging sensation, which was well tolerated.

Conclusions: Treatment of chronic bilateral VKC with tacrolimus 0.03% eye ointment is effective and safe. It could be considered an alternative treatment to reduce steroid-associated complications in patients with chronic VKC. Future double-blinded clinical trials with a longer follow-up period are necessary to confirm our findings and to determine the long-term safety of topical tacrolimus 0.03% ointment in VKC.

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