Long-term safety, tolerability, and efficacy of fesoterodine treatment in men and women with overactive bladder symptoms

被引:10
|
作者
Scarpero, Harriette
Sand, Peter K. [1 ]
Kelleher, Con J. [2 ]
Berriman, Sandra [3 ]
Bavendam, Tamara [3 ]
Carlsson, Martin [3 ]
机构
[1] Univ Chicago, Pritzker Sch Med, NorthShore Univ HealthSyst, Chicago, IL 60637 USA
[2] St Thomas Hosp, London, England
[3] Pfizer Inc, New York, NY USA
关键词
Efficacy; Fesoterodine; Health-related quality of life; Overactive bladder; Safety; Tolerability; TERMINOLOGY; TOLTERODINE; THERAPY;
D O I
10.1185/03007995.2011.559581
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
To evaluate long-term safety, tolerability, and efficacy of fesoterodine for men and women with overactive bladder (OAB) symptoms. This was a post hoc analysis of data pooled from two open-label extensions (NCT00220402, NCT00220376) of double-blind studies. All subjects began open-label treatment with fesoterodine 8 mg once daily, with voluntary dose reduction to 4 mg and re-escalation to 8 mg each permitted once annually. Maximum allowable duration of open-label treatment ranged from 24 to 36 months. Safety and discontinuations were assessed throughout treatment; subject-reported treatment tolerability and 3-day bladder diaries were evaluated at open-label baseline and months 1, 4, 8, 12, and 24. A total of 185 men and 705 women enrolled; 83 men (45%%) and 356 women (50%%) continued open-label treatment for epsilon a parts per thousand yen24 months. Most men (84%%) and women (75%%) remained on fesoterodine 8 mg throughout open-label treatment. No new or unexpected safety signals were observed. Dry mouth was the most common treatment-emergent adverse event (men, 24%%; women, 32%%), rates of discontinuation due to dry mouth were low (men, 1%%; women, 2%%). Most men and women (epsilon a parts per thousand yen91%%) reported at least ''good'' tolerance. For men and women, statistically significant improvements in urgency urinary incontinence episodes, micturitions, urgency episodes, and mean voided volume per micturition achieved between double-blind baseline and open-label baseline were sustained or further improved through month 24; significant improvements in most OAB symptoms were observed between double-blind baseline and month 24 when subjects were stratified by double-blind treatment (placebo, tolterodine extended release 4 mg, fesoterodine 4 mg, fesoterodine 8 mg). Limitations include the lack of a placebo control and that subjects completing double-blind treatment may have been more likely to tolerate or respond to long-term fesoterodine treatment. Long-term fesoterodine treatment was well tolerated and associated with sustained improvements in OAB symptoms in men and women.
引用
收藏
页码:921 / 930
页数:10
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