Literature DB >> 12017406

A multicenter, prospective, open-label study of tolterodine extended-release 4 mg for overactive bladder: the speed of onset of therapeutic assessment trial (STAT).

Paul Siami1, Larry S Seidman, Daniel Lama.   

Abstract

BACKGROUND: Antimuscarinic agents are the primary treatment for overactive bladder (OAB), but there is a lack of information regarding when maximum symptom relief and maximum perceived patient benefit occur.
OBJECTIVE: This study assessed the speed of onset of therapeutic benefit with tolterodine extended-release (ER) 4 mg.
METHODS: This 12-week, multicenter, prospective, open-label study enrolled patients with OAB who either had received no previous pharmacologic treatment for OAB (drug naive) or were receiving such treatment at enrollment (previously treated). Efficacy was assessed at 1, 4, and 12 weeks using a micturition diary and measures of patients' and physicians' perceptions of improvement. Safety was assessed in terms of adverse events and study withdrawals.
RESULTS: The intent-to-treat population included 1138 patients (302 men, 836 women; 88.4% white; age range, 18-91 years), 735 drug naive and 403 receiving treatment for OAB at enrollment. After 1 week, tolterodine ER 4 mg had produced a significant improvement in all efficacy variables in both groups of patients (P < 0.01); 72% of the maximum effect on urge incontinence was observed in both groups; and 84.7% of drug-naive patients and 83.6% of previously treated patients perceived a benefit from treatment. After 4 weeks, drug-naive and previously treated patients reported a respective 93% and 100% of the maximum effect on episodes of urge incontinence. Tolterodine was well tolerated, with dry mouth (mostly mild) the most commonly reported adverse event (15.5% in each group). The 330 (81.9%) patients who had reported unacceptable efficacy and the 87 (21.6%) patients who had reported unacceptable tolerability of previous OAB treatment responded favorably to tolterodine ER 4 mg.
CONCLUSIONS: Tolterodine ER 4 mg was effective and well tolerated in both drug-naive and previously treated patients with OAB. More than 80% of patients reported benefit from treatment after 1 week, but maximum symptom relief was achieved with longer treatment.

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Year:  2002        PMID: 12017406     DOI: 10.1016/s0149-2918(02)85137-2

Source DB:  PubMed          Journal:  Clin Ther        ISSN: 0149-2918            Impact factor:   3.393


  6 in total

1.  [Comment on the STAR study: Comparison of the efficacy and tolerance of solifenacin and tolterodine retard in the treatment of overactive bladder].

Authors:  M Goepel
Journal:  Urologe A       Date:  2006-07       Impact factor: 0.639

2.  The responsiveness of the Overactive Bladder Questionnaire (OAB-q).

Authors:  Karin S Coyne; Louis S Matza; Christine L Thompson
Journal:  Qual Life Res       Date:  2005-04       Impact factor: 4.147

3.  M2 mediated contractions of human bladder from organ donors is associated with an increase in urothelial muscarinic receptors.

Authors:  Alan S Braverman; Brett Lebed; Mitchell Linder; Michael R Ruggieri
Journal:  Neurourol Urodyn       Date:  2007       Impact factor: 2.696

4.  Efficacy of tolterodine on overactive bladder symptoms and sexual and emotional quality of life in sexually active women.

Authors:  Rebecca Rogers; Gloria Bachmann; Zhanna Jumadilova; Franklin Sun; Jon D Morrow; Zhonghong Guan; Tamara Bavendam
Journal:  Int Urogynecol J Pelvic Floor Dysfunct       Date:  2008-08-07

5.  The effect of mirabegron on patient-related outcomes in patients with overactive bladder: the results of post hoc correlation and responder analyses using pooled data from three randomized Phase III trials.

Authors:  D Castro-Diaz; C R Chapple; Z Hakimi; M B Blauwet; L Delgado-Herrera; W Lau; S Mujais
Journal:  Qual Life Res       Date:  2015-02-17       Impact factor: 4.147

6.  Efficacy and safety of fesoterodine 8 mg in subjects with overactive bladder after a suboptimal response to tolterodine ER.

Authors:  S A Kaplan; L Cardozo; S Herschorn; L Grenabo; M Carlsson; D Arumi; T J Crook; L Whelan; D Scholfield; F Ntanios
Journal:  Int J Clin Pract       Date:  2014-06-04       Impact factor: 2.503

  6 in total

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