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首页> 外文期刊>Journal of Clinical Medicine Research >Long-Term Efficacy, Safety, and Tolerability of Modified Intravesical Oxybutynin Chloride for Neurogenic Bladder in Children
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Long-Term Efficacy, Safety, and Tolerability of Modified Intravesical Oxybutynin Chloride for Neurogenic Bladder in Children

机译:改良的膀胱内奥昔布宁氯化物治疗儿童神经源性膀胱的长期疗效,安全性和耐受性

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Background: Children with spinal cord disorders can present with neurogenic bladder, a condition in which the bladder partly or completely loses its ability to store urine and void at low pressure. A bladder with low compliance may cause urinary incontinence, which negatively impacts quality of life and renal function. Long-term high pressure neurogenic bladder can increase the risk of deterioration in renal function. Antimuscarinic pharmacotherapy with clean intermittent catheterization is currently considered one of the most effective treatments for these patients. However, some patients do not respond to oral medication or have unacceptable adverse events (AEs), which may result in medical withdrawal for these patients. Intravesical oxybutynin is an effective treatment with less AEs compared with oral medication. However, an important issue with this treatment is retention of the solution in the bladder. Moreover, as yet no data are available on the very long-term use and outcome of modified intravesical oxybutynin therapy. In the present study, we report on the efficacy, safety, and side effects of long-term modified intravesical oxybutynin therapy in children with neurogenic bladder. Methods: Modified intravesical oxybutynin (1.25 mg/5 mL, twice a day) was administered to four children (three boys and one girl) with neurogenic bladder (detrusor overactivity and/or low compliance bladder), who were previously unresponsive to or experienced intolerable AEs from oral medications. Results of pretreatment cystometrograms were compared to those from follow-up urodynamic studies. Anticholinergic AEs, occurrence of urinary tract infection, and degree of incontinence during this treatment were also evaluated. Results: After 1 year, bladder compliance improved in three of the four patients. After 3 years, detrusor overactivity was undetectable in all patients. Bladder compliance at 3 years and 10 years after initiation of therapy was similar for three patients, and they are continuing modified intravesical oxybutynin therapy. One patient discontinued therapy at 118 months due to worsening of bladder compliance and upper urinary tract infection. No anticholinergic systemic AEs were observed in any of the patients. Conclusions: These results suggest that modified intravesical oxybutynin is an effective and relatively safe long-term therapeutic option for children with neurogenic bladder.
机译:背景:患有脊髓疾病的儿童可出现神经源性膀胱,膀胱在低压下会部分或完全失去其储存尿液和排尿的能力。顺应性低的膀胱可能引起尿失禁,对生活质量和肾功能产生负面影响。长期高压神经源性膀胱会增加肾功能恶化的风险。目前,抗毒蕈碱药物疗法与干净的间歇性导管插入术被认为是这些患者最有效的治疗方法之一。但是,有些患者对口服药物无反应或发生不良不良事件(AE),这可能导致这些患者停药。与口服药物相比,膀胱内奥昔布宁是一种有效的治疗方法,AEs较少。然而,这种治疗的重要问题是溶液在膀胱中的保留。此外,目前尚无关于改良的膀胱内奥昔布宁治疗的长期使用和结果的数据。在本研究中,我们报告了长期改良的膀胱内奥昔布宁治疗神经源性膀胱患儿的疗效,安全性和副作用。方法:向患有神经原性膀胱(逼尿肌过度活动和/或低顺应性膀胱)的四名儿童(三个男孩和一个女孩)服用改良的膀胱奥昔布宁(1.25 mg / 5 mL,每天两次),以前对这些药物无反应或无法忍受口服药物引起的不良事件。将治疗前的膀胱造影图的结果与后续尿动力学研究的结果进行比较。还评估了抗胆碱能AE,尿路感染的发生以及在此治疗过程中的失禁程度。结果:一年后,四名患者中的三名患者的膀胱顺应性得到改善。 3年后,在所有患者中均未检测到逼尿肌过度活动。三名患者在开始治疗后3年和10年的膀胱顺应性相似,三名患者仍在继续进行膀胱内奥昔布宁改良治疗。一名患者由于膀胱顺应性恶化和上尿路感染恶化,在118个月时停止治疗。在任何患者中均未观察到抗胆碱能全身性AE。结论:这些结果表明,改良的膀胱奥昔布宁对神经源性膀胱患儿是一种有效且相对安全的长期治疗选择。

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