一项关于膀胱疼痛综合征/间质性膀胱炎女性患者膀胱内注射透明质酸和硫酸软骨素与二甲亚砜疗效及安全性的随机、开放标签、多中心研究。

A randomized, open-label, multicenter study of the efficacy and safety of intravesical hyaluronic acid and chondroitin sulfate versus dimethyl sulfoxide in women with bladder pain syndrome/interstitial cystitis.

作者信息

Cervigni Mauro, Sommariva Monica, Tenaglia Raffaele, Porru Daniele, Ostardo Edoardo, Giammò Alessandro, Trevisan Silvia, Frangione Valeria, Ciani Oriana, Tarricone Rosanna, Pappagallo Giovanni L

机构信息

Catholic University, Rome, Italy.

G. Fornaroli Hospital, Magenta (MI), Italy.

出版信息

Neurourol Urodyn. 2017 Apr;36(4):1178-1186. doi: 10.1002/nau.23091. Epub 2016 Sep 21.

Abstract

AIMS

Intravesical instillation of hyaluronic acid (HA) plus chondroitin sulfate (CS) in women with bladder pain syndrome/interstitial cystitis (BPS/IC) has shown promising results. This study compared the efficacy, safety, and costs of intravesical HA/CS (Ialuril , IBSA) to dimethyl sulfoxide (DMSO).

METHODS

Randomized, open-label, multicenter study involving 110 women with BPS/IC. The allocation ratio (HA/CS:DMSO) was 2:1. Thirteen weekly instillations of HA (1.6%)/CS (2.0%) or 50% DMSO were given. Patients were evaluated at 3 (end-of-treatment) and 6 months. Primary endpoint was reduction in pain intensity at 6 months by visual analogue scale (VAS) versus baseline. Secondary efficacy measurements were quality of life and economic analyses.

RESULTS

A significant reduction in pain intensity was observed at 6 months in both treatment groups versus baseline (P < 0.0001) in the intention-to-treat population. Treatment with HA/CS resulted in a greater reduction in pain intensity at 6 months compared with DMSO for the per-protocol population (mean VAS reduction 44.77 ± 25.07 vs. 28.89 ± 31.14, respectively; P = 0.0186). There were no significant differences between treatment groups in secondary outcomes. At least one adverse event was reported in 14.86% and 30.56% of patients in the HA/CS and DMSO groups, respectively. There were significantly fewer treatment-related adverse events for HA/CS versus DMSO (1.35% vs. 22.22%; P = 0.001). Considering direct healthcare costs, the incremental cost-effectiveness ratio of HA/CS versus DMSO fell between 3735€/quality-adjusted life years (QALY) and 8003€/QALY.

CONCLUSIONS

Treatment with HA/CS appears to be as effective as DMSO with a potentially more favorable safety profile. Both treatments increased health-related quality of life, while HA/CS showed a more acceptable cost-effectiveness profile.

摘要

目的

膀胱内灌注透明质酸(HA)加硫酸软骨素(CS)对膀胱疼痛综合征/间质性膀胱炎(BPS/IC)女性患者已显示出有前景的结果。本研究比较了膀胱内灌注HA/CS(Ialuril,IBSA公司)与二甲基亚砜(DMSO)的疗效、安全性和成本。

方法

一项随机、开放标签、多中心研究,纳入110例BPS/IC女性患者。分配比例(HA/CS:DMSO)为2:1。给予13次每周一次的HA(1.6%)/CS(2.0%)或50% DMSO灌注。在3个月(治疗结束时)和6个月时对患者进行评估。主要终点是6个月时通过视觉模拟量表(VAS)测量的疼痛强度相对于基线的降低。次要疗效指标为生活质量和经济分析。

结果

在意向性治疗人群中,两个治疗组在6个月时与基线相比疼痛强度均显著降低(P < 0.0001)。在符合方案人群中,与DMSO相比,HA/CS治疗在6个月时疼痛强度降低幅度更大(平均VAS降低分别为44.77±25.07和28.89±31.14;P = 0.0186)。治疗组在次要结局方面无显著差异。HA/CS组和DMSO组分别有14.86%和30.56%的患者报告了至少1次不良事件。与DMSO相比,HA/CS治疗相关不良事件显著更少(1.35%对22.22%;P = 0.001)。考虑直接医疗成本,HA/CS相对于DMSO的增量成本-效果比在3735€/质量调整生命年(QALY)至8003€/QALY之间。

结论

HA/CS治疗似乎与DMSO一样有效,且安全性可能更有利。两种治疗均提高了与健康相关的生活质量,而HA/CS显示出更可接受的成本-效果情况。

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