A型肉毒毒素膀胱内注射治疗神经系统患者:单中心经验

I. Apostolidis, E. Papaefstathiou, E. Ioannidou, P. Georgopoulos, K. Mytilekas, Marina Kalaitzi, A. Apostolidis
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引用次数: 0

摘要

目的:本研究的目的是提供关于膀胱内注射批准剂量200U肉毒杆菌素治疗神经源性耐药尿失禁患者的有效性和安全性的真实数据。可用的文献相对有限。材料和方法:我们分析了在学术神经病学门诊就诊的神经源性耐药尿失禁患者的常规收集的前瞻性数据。所有患者均接受至少一次200U肉毒杆菌素膀胱内注射,在尿动力学证实神经源性逼尿肌过度活动的同时记录尿路感染(UTI)的存在。患者在6周和24周进行尿动力学复查。每次重复治疗均遵循此方案,同时记录尿失禁的复发时间。结果:共治疗49例,男28例,女21例,平均年龄47.04±14.16岁;脊髓损伤18例(36.7%),多发性硬化症12例(24.54%),其余为其他神经系统疾病。15人接受了第二次肉毒杆菌注射,10人接受了第三次注射,6人接受了第四次注射,1人接受了第五次和第六次注射。42例(85.7%)患者证实尿失禁,14例(28.6%)患者在首次治疗前发现尿路感染。首次治疗后尿失禁主观治愈率为73.7%。在肉毒杆菌治疗前,性别、神经学诊断或尿路感染的存在与尿失禁的持续存在没有相关性。前两次治疗后的中位复发时间分别为6个月(四分位数间距= 5)和10.5个月(P = 0.31)。与基线相比,每次治疗后尿动力学记录的最大膀胱容量(P < 0.001)和第一次治疗后的最大逼尿肌压力(P < 0.05, Bonferonni校正)均有显著改善。尿路感染的存在不影响初次治疗后尿失禁复发时间和尿动力学改变。结论:在本队列中,在每次重复注射后出现持续临床和尿动力学变化的患者中,显著比例的患者膀胱内注射200U肉毒杆菌素可以完全治愈神经源性耐药尿失禁。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Intravesical botulinum toxin Type A injection therapy in neurological patients: A single center experience
Objectives: The objective of this study is to present real-life data on the efficacy and safety of the intravesical injection of the approved dose of 200U BOTOX in patients with drug-resistant incontinence of neurogenic etiology. Available literature is relatively limited. Materials and Methods: We analyzed routinely collected prospective data from the treatment of patients with neurogenic drug-resistant incontinence who attended an academic neurourology outpatient clinic. All patients received at least one intravesical injection of 200U BOTOX, following urodynamic confirmation of neurogenic detrusor overactivity while recording the presence of urinary tract infection (UTI). Patients were followedup at 6 and 24 weeks with urodynamic retests. This protocol was followed with each repeat treatment, while recording the relapse time of incontinence. Results: Forty-nine patients (28 males, 21 females, mean age 47.04 ± 14.16 years) were treated; 18 (36.7%) suffered from spinal cord injury, 12 (24.54%) from multiple sclerosis, and the rest from other neurological conditions. Fifteen received a 2nd Botox treatment, 10 a 3rd, 6 a 4th, and one a 5th and 6th session. Forty-two (85.7%) patients had urodynamically proven incontinence and in 14 (28.6%) an UTI was identified before the first treatment. Subjective cure of incontinence was recorded in 73.7% of patients after the first treatment. There was no correlation of gender, neurological diagnosis, or presence of UTI before the BOTOX treatment with the persistence of incontinence. The median relapse time after the first two treatments was 6 (interquartile range = 5) and 10.5 months, respectively (P = 0.31). Significant improvements were recorded urodynamically in maximum cystometric capacity after each treatment (P < 0.001) and in maximum detrusor pressure after the first session compared to baseline (P < 0.05, Bonferonni correction). The presence of UTI did not affect the incontinence relapse time or urodynamic changes after initial treatment. Conclusions: In the present cohort, intravesical administration of 200U BOTOX achieved complete cure of neurogenic drug-resistant incontinence in a significant proportion of patients with sustained clinical and urodynamic changes after each repeat injection.
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