Efficacy, tolerability and safety of propiverine hydrochloride in comparison to oxybutynin in children with urge incontinence due to overactive bladder: Results of a multicentre observational cohort study

被引:41
作者
Alloussi, Schahnaz [2 ]
Muertz, Gerd [3 ]
Braun, Reinhard
Gerhardt, Ulrich
Heinrich, Martina [4 ]
Hellmis, Eva
Horn, Werner
Marschall-Kehrel, Daniela
Niklas, Kurt
Raabe, Michael
Roessler, Thomas
Seibt, Beatrix
Siemer, Stefan [5 ]
Schultz-Lampel, Daniela
Walter, Heiko
Wiedeking, Burkhard
Alloussi, Saladin [2 ]
Bock, Paul [6 ]
Strugala, Gerhard [3 ]
Madersbacher, Helmut [1 ]
机构
[1] Univ Kliniken Innsbruck, Landeskrankenhaus, Dept Neurourol, Innsbruck, Austria
[2] Krankenhaus Neunkirchen GmbH, Dept Urol & Paediat Urol, Dresden, Germany
[3] APOGEPHA Arzneimittel GmbH, Dresden, Germany
[4] Univ Saarland, Dr von Haunersches Kinderspital, Kinderchirurg Klin, D-6650 Homburg, Germany
[5] Univ Saarland, Dept Urol, D-6650 Homburg, Germany
[6] IFAG Basel AG, Basel, Switzerland
关键词
anticholinergics; children; overactive bladder; oxybutynin; propiverine; urinary incontinence; NEUROGENIC DETRUSOR OVERACTIVITY; URINARY-INCONTINENCE; ADOLESCENTS; CHLORIDE;
D O I
10.1111/j.1464-410X.2009.09129.x
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE To compare, in a retrospective observational cohort study, the efficacy, tolerability and safety of propiverine and oxybutynin in children with urge incontinence (UI) due to overactive bladder. PATIENTS AND METHODS Medical records were scrutinized for children with UI. As a primary efficacy outcome variable the achievement of continence after treatment with variable doses of propiverine or oxybutynin was assessed. Weekly UI episodes and daily voiding frequency were evaluated as secondary efficacy outcomes. Tolerability was evaluated by the rate of adverse events, adverse drug reactions caused by antimuscarinics and premature treatment termination. RESULTS At 16 study centres, 621 children aged 5-14 years with UI due to overactive bladder were enrolled. After anticholinergic treatment (437 propiverine, 184 oxybutynin) continence was achieved in 61.6% and 58.7% of the patients after 186 and 259 days, respectively. There were clinically relevant improvements in voiding frequency across treatment groups. Daily doses of propiverine were markedly below the recommendations (0.54 vs 0.8 mg/kg body weight), daily doses of oxybutynin were according to the recommendations (0.31 vs 0.2-0.4 mg/kg body weight) at treatment initiation. There was a significantly more favourable tolerability to propiverine than oxybutynin for the overall rate of adverse events (3.9% vs 16.3%, odds ratio 4.813), adverse drug reactions caused by propiverine or oxybutynin (2.8% vs 9.2%) and premature treatment termination due to adverse drug reactions (1.6% vs 4.4%). CONCLUSION Propiverine and oxybutynin are effective in children with UI due to overactive bladder. Sufficient treatment periods of at least 2, preferably 3-4, months are the crucial factors for a successful treatment. The tolerability profile of propiverine is better than for oxybutynin.
引用
收藏
页码:550 / 556
页数:7
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