Home
August 2008 September 2008 October 2008
Su Mo Tu We Th Fr Sa
Week 36 1 2 3 4 5 6
Week 37 7 8 9 10 11 12 13
Week 38 14 15 16 17 18 19 20
Week 39 21 22 23 24 25 26 27
Week 40 28 29 30

Once-Daily Oxybutynin, Tolterodine Reduce Incontinence in Women With Overactive Bladder Show Comments PDF Print E-mail
Monday, 23 June 2003
NEW YORK (Reuters Health) - Extended-release oxybutynin and tolterodine are similarly effective for reducing urge urinary incontinence (UUI) and total incontinence episodes in women with overactive bladder, according to a report in the June issue of Mayo Clinic Proceedings.

NEW YORK (Reuters Health) - Extended-release oxybutynin and tolterodine are similarly effective for reducing urge urinary incontinence (UUI) and total incontinence episodes in women with overactive bladder, according to a report in the June issue of Mayo Clinic Proceedings. However, micturition frequency is significantly lower with oxybutynin.

In a randomized, double-blind study, Dr. Ananias C. Diokno, of William Beaumont Hospital, Royal Oak, Michigan, and colleagues compared the efficacy of extended-release formulations of oxybutynin and tolterodine in 790 women with overactive bladder. Patients received 10 mg/d oxybutynin or 4 mg/d tolterodine for 12 weeks.

The team reports that of 391 patients who received oxybutynin, 339 (87%) completed the study. Of 399 who received tolterodine, 357 (89%) completed the study.

Improvements in UUI episodes were similar between the groups. In the oxybutynin group, the mean weekly episodes of UUI decreased from 37.1 at baseline to 10.8. In the tolterodine group, the mean weekly episodes decreased from 36.7 to 11.2.

"Oxybutynin participants had a greater decrease in the mean weekly micturition frequency compared with tolterodine participants (28.4 versus 25.2, respectively, compared to means of 66.4 and 71.1, respectively; p = 0.003)," Dr. Diokno and colleagues report.

Twenty-three percent of oxybutynin patients and 16.8% of those on tolterodine reported total dryness in their last 7-day 24-hour voiding diary (p = 0.03).

Dry mouth was the most common adverse event, and was reported by 29.7% and 22.3% of patients in the oxybutynin and tolterodine groups, respectively (p = 0.02). Adverse events were generally mild, according to the authors. The rate of discontinuation of treatment due to adverse events was similar between the groups.

Dr. Diokno and colleagues say that the flexible dosing schedule of extended release oxybutynin is an advantage in achieving "the optimal balance between efficacy and tolerability because of the wide range of approved doses."

Mayo Clin Proc 2003; 78:687-695.


Copyright © 2003 Reuters Limited. All rights reserved. Republication or redistribution of Reuters Limited content, including by framing or similar means, is expressly prohibited without the prior written consent of Reuters Limited. Reuters Limited shall not be liable for any errors or delays in the content, or for any actions taken in reliance thereon.

Reader Comments

Please log-in or register in order to submit comments.

Powered by AkoComment!

 
User Rating: / 1
PoorBest


 
Visitor Ratings:
Patients:
5 (1 votes)