ADVERTISEMENT

If you are seeing this message, you may be experiencing temporary network problems. Please wait a few minutes and refresh the page. If the problem persists, you may wish to report it to your local Network Manager.

It is also possible that your web browser is not configured or not able to display style sheets. In this case, although the visual presentation will be degraded, the site should continue to be functional. We recommend using the latest version of Microsoft or Mozilla web browser to help minimise these problems.

Wiley InterScience

< Previous Abstract  |  Next Abstract >

Save Article to My Profile      Download Citation      Request Permissions

Abstract |  References  |  Full Text: HTML, PDF (Size: 91K)  | Related Articles | Citation Tracking

The clinical efficacy of tolterodine extended-release is maintained for 24 h in patients with overactive bladder
Roger Dmochowski, Karl Kreder*, Scott MacDiarmid, Martin Carlsson and Zhonghong Guan
Department of Urology, Vanderbilt University Medical Center, Nashville, TN,  *University of Iowa Hospitals and Clinics, Iowa City, IA,  Department of Urology, Wake Forest University Baptist Medical Center, Winston-Salem, NC and  Pfizer Inc, New York, NY, USA
Correspondence to  Roger Dmochowski, Department of Urology, Medical Center North, Room A 1302, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
e-mail: roger.dmochowski@vanderbilt.edu
Copyright © 2007 THE AUTHORS; JOURNAL COMPILATION © 2007 BJU INTERNATIONAL
KEYWORDS
bladder diaries • efficacy • overactive bladder • tolterodine extended-release

OBJECTIVE

AbstractINTRODUCTIONPATIENTS AND METHODSRESULTSDISCUSSIONREFERENCES

To assess the 24-h efficacy of tolterodine extended-release (ER) in patients with overactive bladder (OAB) and urgency urinary incontinence (UUI).

PATIENTS AND METHODS

We conducted a post hoc analysis of a 12-week, placebo-controlled trial of tolterodine-ER in patients with frequency (≥8 voids/24 h) and UUI (≥5 episodes/week) for ≥ 6 months. Seven-day bladder diaries were used to record diary endpoints; 24-h diary data were stratified by 6-h periods beginning at midnight.

RESULTS

Compared with placebo (508 patients), tolterodine-ER (507 patients) significantly and consistently increased volume voided per void and reduced UUI episodes and micturition frequency during each interval.

CONCLUSIONS

These results indicate that tolterodine-ER maintained clinical efficacy over 24 h and should be effective for OAB symptoms without regard to whether symptoms occur during the day or at night.


Accepted for publication 25 January 2007

DIGITAL OBJECT IDENTIFIER (DOI)
10.1111/j.1464-410X.2007.06926.x About DOI

Related Articles

  • Find other articles like this in Wiley InterScience
  • Find articles in Wiley InterScience written by any of the authors

Wiley InterScience is a member of CrossRef.

Cross Ref Member


Click here
Click Here