Evaluation of the safety and effectiveness of combination therapy with 1% ivermectin solution in moderate to severe rosacea: a cohort study.

Kyzzhibek Keneshbek Kyzy, Aisuluu Omurzakova, Venera Azhikulova, Bukatcha Zainalieva, Dinara Abdulkasymova
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Abstract

Introduction. Rosacea is a common chronic dermatological disease that negatively affects the quality of life of patients.Hypothesis. Combination therapy with 1% ivermectin solution alongside systemic treatment methods is more effective in reducing the severity of moderate to severe papulopustular rosacea symptoms compared with traditional treatment methods alone.Aim. This study is aimed at finding new approaches to the treatment of moderate and severe forms of rosacea.Methodology. This research compared the main group receiving ivermectin with a control group getting conventional treatment to assess the safety and efficacy of 1% ivermectin combination therapy in 70 individuals with moderate to severe rosacea. At weeks 2, 4 and 8, the dynamics of clinical symptoms were evaluated using a 4-point scale.Results. The use of combination therapy with ivermectin led to a more pronounced improvement in the clinical picture. Already at week 4, a 48-54% decrease in symptoms was recorded in the main group, while in the control group, it was only by 25-30%. By week 8, an almost complete reduction of the main manifestations was observed in the main group (78-88% decrease). Regression analysis confirmed that combination therapy with ivermectin was a key factor determining a more substantial clinical improvement, regardless of age, gender and the initial severity of the patient's condition. In addition, a much more pronounced decrease in the number of Demodex ticks was recorded in the main group. The effectiveness of combination therapy with ivermectin did not depend on the demographic or clinical characteristics of patients, which makes it a universal method of treating rosacea. No serious side effects have been reported in any patient receiving combination therapy, which indicates its safety.Conclusion. This approach can be a valuable addition to existing strategies for the treatment of this chronic dermatological disease.

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评价1%伊维菌素溶液联合治疗中重度酒渣鼻的安全性和有效性:一项队列研究。
介绍。酒渣鼻是一种常见的慢性皮肤病,会对患者的生活质量产生负面影响。与传统治疗方法相比,1%伊维菌素溶液联合全身治疗在减轻中度至重度丘疹性酒渣鼻症状的严重程度方面更有效。本研究旨在寻找治疗中度和重度酒渣鼻的新方法。本研究比较了接受伊维菌素治疗的主组和接受常规治疗的对照组,以评估1%伊维菌素联合治疗70例中重度酒渣鼻患者的安全性和有效性。在第2、4和8周,使用4分制评估临床症状的动态。使用伊维菌素联合治疗导致临床画面更明显的改善。在第4周,主组的症状已经减轻了48-54%,而对照组仅减轻了25-30%。到第8周,观察到主组的主要表现几乎完全减轻(减少78-88%)。回归分析证实,与伊维菌素联合治疗是决定更实质性临床改善的关键因素,无论年龄、性别和患者病情的初始严重程度如何。此外,在主要组中记录到的蠕形螨数量下降更为明显。伊维菌素联合治疗的有效性不依赖于患者的人口统计学或临床特征,这使其成为治疗酒渣鼻的普遍方法。联合用药未见严重副作用,提示其安全性。这种方法可以成为治疗这种慢性皮肤病的现有策略的一个有价值的补充。
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