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H1抗组胺药剂量加倍治疗慢性荨麻疹的疗效——越南经验

The Efficacy of a Two-Fold Increase of H1-Antihistamine in the Treatment of Chronic Urticaria - the Vietnamese Experience.

作者信息

Thi Huyen Tran, Thi Lan Pham, Van Thuong Nguyen, Minh Phuong Pham Thi, Trong Hao Nguyen, Van Tro Chau, Huu Sau Nguyen, Minh Trang Trinh, Huu Nghi Dinh, Van Tam Hoang, Cam Van Tran, Huyen My Le, Hau Khang Tran, Thanh Thuy Nguyen, Thi Phuong Hoang, Thuy Linh Nguyen, Gandolfi Marco, Satolli Francesca, Feliciani Claudio, Tirant Michael, Vojvodic Aleksandra, Lotti Torello

机构信息

National Hospital of Dermatology and Venereology, Hanoi, Vietnam.

Hanoi Medical University, Hanoi, Vietnam.

出版信息

Open Access Maced J Med Sci. 2019 Jan 28;7(2):259-263. doi: 10.3889/oamjms.2019.069. eCollection 2019 Jan 30.

Abstract

BACKGROUND

Chronic urticaria, a mast cell-driven condition, is common, debilitating and hard to treat. H1-antihistamines are the first line treatment of chronic urticaria, but often patients do not get satisfactory relief with the recommended dose. European guidelines recommend increased antihistamine doses up to four-fold.

AIM

We conducted this study to evaluate the efficacy of increased H1-antihistamine doses up to two-fold in Vietnamese chronic urticaria patients.

METHODS

One hundred and two patients with chronic urticaria were recruited for treatment with levocetirizine (n = 52) or fexofenadine (n = 50). Treatment started at the conventional daily dose of 5 mg levocetirizine or 180 mg fexofenadine for 2 weeks and then increased to 10 mg levocetirizine or 360 mg fexofenadine for 2 weeks if patients did not have an improvement in symptoms. At week 0, week 2 and week 4 wheal, pruritus, size of the wheal, total symptom scores, and associated side-effects were assessed.

RESULTS

With the conventional dose, the total symptom scores after week 2 decreased significantly in both groups compared to baseline figures, i.e. 7.4 vs 2.3 for levocetirizine group and 8.0 vs 2.6 for fexofenadine group (p < 0.05). However, there were still 26 patients in each group who did not have improvements. Of these 26 patients, after having a two-fold increase of the conventional dose, 11.5% and 38.5% became symptom-free at week 4 in levocetirizine group and fexofenadine group, respectively. At week 4 in both groups, the total symptom scores had significantly decreased when compared with those at week 2 (2.8 ± 1.5 versus 4.7 ± 1.6 in levocetirizine group; 2.1 ± 1.9 versus 5.1 ± 1.4 in fexofenadine group). In both groups, there was no difference in the rate of negative side effects between the conventional dose and the double dose.

CONCLUSION

This study showed that increasing the dosages of levocetirizine and fexofenadine by two-fold improved chronic urticaria symptoms without increasing the rate of negative side effects.

摘要

背景

慢性荨麻疹是一种由肥大细胞驱动的疾病,常见、使人虚弱且难以治疗。H1抗组胺药是慢性荨麻疹的一线治疗药物,但患者通常按推荐剂量使用时无法获得满意的缓解效果。欧洲指南建议将抗组胺药剂量增加至四倍。

目的

我们开展这项研究以评估将H1抗组胺药剂量增加至两倍对越南慢性荨麻疹患者的疗效。

方法

招募102例慢性荨麻疹患者,分别用左西替利嗪(n = 52)或非索非那定(n = 50)进行治疗。治疗开始时,左西替利嗪每日常规剂量为5 mg,非索非那定为180 mg,持续2周;如果患者症状无改善,则将左西替利嗪剂量增至10 mg,非索非那定增至360 mg,再持续2周。在第0周、第2周和第4周评估风团、瘙痒、风团大小、总症状评分及相关副作用。

结果

使用常规剂量时,两组在第2周后的总症状评分与基线数据相比均显著下降,即左西替利嗪组从7.4降至2.3,非索非那定组从8.0降至2.6(p < 0.05)。然而,每组仍有26例患者症状未改善。在这26例患者中,将常规剂量增加两倍后,左西替利嗪组和非索非那定组在第4周时分别有11.5%和38.5%的患者症状消失。在两组的第4周时,与第2周相比,总症状评分均显著下降(左西替利嗪组为2.8±1.5对4.7±1.6;非索非那定组为2.1±1.9对5.1±1.4)。两组中,常规剂量和双倍剂量的不良反应发生率无差异。

结论

本研究表明,将左西替利嗪和非索非那定剂量增加两倍可改善慢性荨麻疹症状,且不增加不良反应发生率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c7fb/6364734/78f6ce34a597/OAMJMS-7-259-g001.jpg

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