Volume 13, Issue 2 pp. 105-108
Original Article

Comparison of the effectiveness and side-effects of tolterodine and oxybutynin in children with detrusor instability

NIZAMETTIN KILIC

NIZAMETTIN KILIC

The Medical Faculty of Uludag University, Departments of Paediatric Surgery, Paediatric Urology and Biostatistics, Bursa, Turkey

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EMIN BALKAN

EMIN BALKAN

The Medical Faculty of Uludag University, Departments of Paediatric Surgery, Paediatric Urology and Biostatistics, Bursa, Turkey

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SEMRA AKGOZ

SEMRA AKGOZ

The Medical Faculty of Uludag University, Departments of Paediatric Surgery, Paediatric Urology and Biostatistics, Bursa, Turkey

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NURI SEN

NURI SEN

The Medical Faculty of Uludag University, Departments of Paediatric Surgery, Paediatric Urology and Biostatistics, Bursa, Turkey

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HASAN DOGRUYOL

HASAN DOGRUYOL

The Medical Faculty of Uludag University, Departments of Paediatric Surgery, Paediatric Urology and Biostatistics, Bursa, Turkey

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First published: 06 March 2006
Citations: 38
Nizamettin Kiliç, md, Medical Faculty of Uludag University, Departments of Paediatric Surgery and Paediatric Urology, Gorukle, 16059, Bursa, Turkey. Email: [email protected]

Abstract

Background: Treatment with anticholinergic agents is the mainstay of therapy for detrusor instability (DI), a chronic and morbid condition characterized by urge urinary incontinence. The aim of this study is to assess the effectiveness and tolerability of tolterodine and oxybutynin in children with DI.

Methods: A total of 60 children with DI were enrolled, 30 (14 male, 16 female, mean age 7.97 ± 2.71 years) in the tolterodine group and 30 (12 male, 18 female, mean age 7.33 ± 2.23 years) in the oxybutynin group. In this prospective study we reviewed data from 60 children followed for at least 6 months. All of the patients in the study population had a history of dysfunctional voiding. Urodynamic investigations were conducted in all of the patients before and after anticholinergic treatment. Episodes of urge urinary incontinence and adverse events were also evaluated.

Results: Improvements in urge incontinence episodes were similar for the children who received tolterodine or oxybutynin. Improvements in the urodynamic parameters were also the same in the two groups. Adverse events were significantly lower in the tolterodine group (13 events in 13 patients) compared to the oxybutynin group (27 events in 20 patients; P = 0.027).

Conclusion: Reductions in urge urinary incontinence episodes were similar with tolterodine and oxybutynin in children with DI. Side-effects were more common with oxybutynin. Treatment of children with DI with tolterodine shows significantly better tolerability and this may enhance children's compliance during long-term treatment.

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