Suppr超能文献

A型肉毒毒素(丽舒妥)注射治疗儿童顽固性膀胱反射亢进后抗体的形成。

Antibody formation following botulinum toxin type A (Dysport) injection in children with intractable bladder hyper-reflexia.

机构信息

Pediatric Urology Research Center, Department of Pediatric Urology, Children's Hospital Medical Center, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

Urology. 2010 Jul;76(1):233-7. doi: 10.1016/j.urology.2010.03.023. Epub 2010 May 10.

Abstract

OBJECTIVES

To investigate the pattern of anti-Dysport antibody (ADA) formation after Dysport injection in patients with neuropathic bladder. Antibody formation may lead to failure or allergic reactions in patients undergoing Dysport injection.

METHODS

Forty-four children with neuropathic bladder were enrolled and classified into 3 groups: group I, without history of previous injection (n = 8); group II, with history of one or more injections (n = 7); and group III, who had been injected 3-36 months before this study (n = 29). Groups I and II were subjected to Dysport injection. Fifty-five age-matched healthy children were selected as controls. Urinary incontinence score was assessed before and 6 months after injection. Under cystoscopic guidance, Dysport (10 IU/kg) was injected into the detrusor muscle, sparing the trigone and ureteral orifices. ADA level was measured by enzyme-linked immunosorbent assay technique before injection and then monthly for at least 4 months in groups I and II, and for just once in group III and control subjects.

RESULTS

ADA level was increased 1-2 months after the last injection in 3 (38%) of group I and 5 (71%) of group II. However, ADA level in group III was not higher than controls. All patients had complete or partial improvement in urinary incontinence score except for 1 patient in group I. No resistance to treatment was detected.

CONCLUSIONS

Increment of ADA titer in patients is not permanent. Repeated injections will not boost the immune system to produce higher levels of antibody. Increased levels of ADA may not be associated with treatment failure at follow-up visit.

摘要

目的

研究神经源性膀胱患者接受 Dysport 注射后抗 Dysport 抗体(ADA)形成的模式。抗体形成可能导致接受 Dysport 注射的患者治疗失败或出现过敏反应。

方法

纳入 44 例神经源性膀胱患儿,分为 3 组:I 组,无既往注射史(n=8);II 组,有 1 次或多次注射史(n=7);III 组,在本研究前 3-36 个月接受过注射(n=29)。I 组和 II 组接受 Dysport 注射。选择 55 名年龄匹配的健康儿童作为对照组。在注射前和注射后 6 个月评估尿失禁评分。在膀胱镜引导下,将 Dysport(10IU/kg)注入逼尿肌,避开三角区和输尿管口。在 I 组和 II 组中,在注射前和注射后至少 4 个月每月测量一次 ADA 水平,而在 III 组和对照组中仅测量一次。

结果

I 组中有 3 名(38%)和 II 组中有 5 名(71%)患者在最后一次注射后 1-2 个月 ADA 水平升高。然而,III 组的 ADA 水平并不高于对照组。除 1 名 I 组患者外,所有患者的尿失禁评分均有完全或部分改善。未发现治疗耐药。

结论

患者 ADA 滴度的升高并非永久性的。重复注射不会增强免疫系统产生更高水平的抗体。ADA 水平的升高可能与随访时的治疗失败无关。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验