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0.03%和0.1%他克莫司软膏治疗儿童春季角结膜炎的疗效与安全性比较。

Comparision of efficacy and safety of 0.03% and 0.1% tacrolimus ointment in children with vernal keratoconjunctivitis.

作者信息

Saha Bhawesh Chandra, Kumari Rashmi, Ambasta Anita

机构信息

Department of Ophthalmology, All India Institute of Medical Sciences, Patna, Bihar, India.

Assistant Professor, Department of Ophthalmology, All India Institute of Medical Sciences, Deoghar 814152, India.

出版信息

Ther Adv Ophthalmol. 2023 May 26;15:25158414231173532. doi: 10.1177/25158414231173532. eCollection 2023 Jan-Dec.

Abstract

BACKGROUND

Topical immunosuppressants such as tacrolimus in different concentrations are a breakthrough in the management of recalcitrant vernal keratoconjunctivitis (VKC); however, there is a lacks of comparative studies to guide their use in VKC management.

OBJECTIVE

To compare the efficacy and safety of tacrolimus 0.03% and 0.1% eye ointment in the treatment of recalcitrant VKC.

DESIGN

A retrospective comparative single-centre observational study.

METHOD

We reviewed records of a total of 48 recalcitrant VKC patients treated with two different strengths of tacrolimus ointment between April 2016 and March 2017. Of these, 39 fulfilled the inclusion criteria and were categorized into two groups, A and B, depending on the use of strength of tacrolimus (0.03% and 0.1%) used, respectively. Group A had 18 patients, while group B had 21 patients. Thirty-six patients, 18 from each group, were finally analysed and compared. Records of patients were explored for the subjective symptoms and objective sign score of the patient at baseline and at each time point. The main outcome measures were composite scoring and comparison of total subjective symptom scores (TSSSs) and total objective sign scores (TOSSs) within and between the groups at each follow-up. Percentage of patient with significant reduction in symptom and sign scores as compared with baseline was considered success of treatment. Chi-square and -tests were used for comparison of outcomes between both groups.

RESULTS

Mixed variety was most commonly encountered type of VKC. The signs and symptoms were significantly reduced in patients with treatment in both groups ( = 0.001) in all types of VKC. However, in group B, there was significant improvement in the size of papillae ( = 0.04) as compared baseline in contrast to group A. Side effects like burning and stinging in group B were significantly higher as compared with group A.

CONCLUSIONS

Both strengths of tacrolimus (0.03% and 0.1%) are effective in all forms of recalcitrant VKC. Papillary component of VKC responds better with higher strength (0.1%) but is associated with more significant side effects. Different strengths of tacrolimus can be used strategically depending upon the severity and clinical type of VKC to intensify outcome and minimize side effects.

摘要

背景

不同浓度的局部免疫抑制剂,如他克莫司,是顽固性春季角结膜炎(VKC)治疗的一项突破;然而,缺乏比较研究来指导其在VKC治疗中的应用。

目的

比较0.03%和0.1%他克莫司眼膏治疗顽固性VKC的疗效和安全性。

设计

一项回顾性比较单中心观察性研究。

方法

我们回顾了2016年4月至2017年3月期间用两种不同强度的他克莫司眼膏治疗的48例顽固性VKC患者的记录。其中,39例符合纳入标准,根据所用他克莫司的强度(0.03%和0.1%)分为A、B两组。A组有18例患者,B组有21例患者。最终对每组18例共36例患者进行分析和比较。探究患者在基线和每个时间点的主观症状和客观体征评分记录。主要结局指标是每次随访时组内和组间的综合评分以及总主观症状评分(TSSS)和总客观体征评分(TOSS)的比较。与基线相比,症状和体征评分显著降低的患者百分比被视为治疗成功。采用卡方检验和t检验比较两组的结局。

结果

混合型是最常见的VKC类型。在所有类型的VKC中,两组患者经治疗后体征和症状均显著减轻(P = 0.001)。然而,与A组相比,B组乳头大小与基线相比有显著改善(P = 0.04)。B组如烧灼感和刺痛感等副作用明显高于A组。

结论

两种强度的他克莫司(0.03%和0.1%)对所有形式的顽固性VKC均有效。VKC的乳头成分对较高强度(0.1%)反应更好,但副作用更明显。可根据VKC的严重程度和临床类型策略性地使用不同强度的他克莫司,以增强疗效并减少副作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c85b/10226287/47f790ab763c/10.1177_25158414231173532-fig1.jpg

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