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按需使用非索罗定:延长释放抗毒蕈碱药物的新模式。

On-demand use of fesoterodine: a new paradigm for extended release antimuscarinics.

机构信息

Izmir Bozyaka Training and Research Hospital, Department of Urology, University of Health Sciences, Izmir, Turkey.

Department of Urology, Izmir Tinaztepe Galen Hospital, Izmir, Turkey.

出版信息

Int Urogynecol J. 2022 Aug;33(8):2127-2132. doi: 10.1007/s00192-022-05250-1. Epub 2022 Jun 6.

DOI:10.1007/s00192-022-05250-1
PMID:35666289
Abstract

INTRODUCTION AND HYPOTHESIS

We aimed to compare on-demand and continuous use of fesoterodine 4 mg concerning efficacy and adverse effects.

METHODS

A total of 100 patients who were diagnosed with non-neurogenic overactive bladder (OAB) syndrome were included in the study. All patients were evaluated with MMSE, ICIQ-SF, SEAPI quality of health and OAB-V8 questionnaires, at the beginning, 1st month and 4th month. Fesoterodine 4 mg was started for treatment. At the end of the 1st month, patients who obtained benefit from the treatment were 1:1 randomized into two groups. In group 1, fesoterodine 4 mg was given 1 × 1 in a standard manner whereas in group 2 patients took the pills on demand. Both groups were evaluated for efficacy and adverse events at 4 months.

RESULTS

Final analyses included 69 patients. At 4-month follow-up, OAB-V8 scores were significantly improved compared to 1 month in both groups. Again at h months, no difference was detected between the two groups for MMSE, ICIQ-SF and SEAPI scores. In continuous usage group, 4th month MMSE scores were significantly lower than 1st month scores. At 4 months, dry mouth and constipation were lower in the on-demand group compared to continuous usage group.

CONCLUSIONS

Compared to standard continuous usage, on-demand usage of fesoterodine showed similar efficacy with fewer adverse events.

摘要

介绍和假设

我们旨在比较按需使用和连续使用非索罗定 4 毫克在疗效和不良反应方面的差异。

方法

本研究共纳入 100 例诊断为非神经源性膀胱过度活动症(OAB)的患者。所有患者均接受 MMSE、ICIQ-SF、SEAPI 健康质量和 OAB-V8 问卷评估,在开始时、第 1 个月和第 4 个月。开始使用非索罗定 4 毫克进行治疗。在第 1 个月结束时,从治疗中获益的患者以 1:1 的比例随机分为两组。在第 1 组中,非索罗定 4 毫克以标准方式 1×1 给药,而在第 2 组中患者按需服用。两组均在第 4 个月时评估疗效和不良反应。

结果

最终分析包括 69 例患者。在第 4 个月随访时,与第 1 个月相比,两组 OAB-V8 评分均显著改善。同样在 h 个月时,两组间 MMSE、ICIQ-SF 和 SEAPI 评分无差异。在连续使用组中,第 4 个月的 MMSE 评分明显低于第 1 个月的评分。在第 4 个月时,按需组的口干和便秘发生率低于连续使用组。

结论

与标准连续使用相比,按需使用非索罗定显示出相似的疗效,不良反应更少。

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