Double anticholinergic therapy for refractory neurogenic and non-neurogenic detrusor overactivity in children: Long-term results of a prospective open-label study

被引:13
|
作者
Nadeau, Genevieve [1 ]
Schroeder, Annette [2 ]
Moore, Katherine [1 ]
Genois, Lucie [1 ]
Lamontagne, Pascale [1 ]
Hamel, Micheline [1 ]
Pellerin, Eve [1 ]
Bolduc, Stephane [1 ]
机构
[1] Univ Laval, CHUQ, Div Urol, Quebec City, PQ, Canada
[2] Hosp Sick Children, Dept Urol, Toronto, ON M5G 1X8, Canada
来源
关键词
BOTULINUM TOXIN; SACRAL NEUROMODULATION; URINARY-INCONTINENCE; BLADDER; ANTIMUSCARINICS; DYSFUNCTION; EFFICACY;
D O I
10.5489/cuaj.1362
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
Introduction: In this study, we optimize pharmacotherapy in children who failed anticholinergic monotherapy by simultaneous administration of 2 anticholinergics (oxybutynin and/or tolterodine and/or solifenacin). Methods: This report is an update of our previously published study on double anticholinergic regimen in children with refractory incontinence due to neurogenic (NDO) and non-neurogenic (DO) detrusor overactivity. Patients with an insufficient response (clinically/urodynamically) to an optimized dose of a single anticholinergic (oxybutynin or tolterodine) received a second anticholinergic (tolterodine or solifenacin), in addition to the pre-existing medication. The primary end-point was efficacy (continence) and the secondary end-points were tolerability and safety. The Patient Perception of Bladder Condition (PPBC) scale was used to rate subjective improvement of patients. Results: In total, 56 patients with DO (n = 31) or NDO (n = 25) were enrolled at a mean age of 11.4 +/- 3.5 years and were followed for a minimum of 3 months. The duration of double treatment was 36 +/- 23 months. Our results found that 23 patients became dry, 18 improved significantly and 15 improved moderately. Urodynamic capacity improved from 158 +/- 87 mL to 359 +/- 148 mL and maximal pressure of contractions decreased from 76 +/- 24 to 22 +/- 22 cmH(2)O (p < 0.0001). The overall success rate was 82%, since 10 patients discontinued treatment for unsatisfactory clinical response or bothersome side effects. No side effects were reported by 28 patients, mild side effects by 20, moderate side effects by 8; 2 patients withdrew from the study due to their side effects. Of the 35 patients who voided spontaneously, 8 developed post-void residuals (>20%). Conclusions: With a larger cohort and prospective follow-up, we reiterated that double anticholinergic regimen in children with DO or NDO refractory to anticholinergic monotherapy is a feasible and efficient approach.
引用
收藏
页码:175 / 180
页数:6
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