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影响膀胱输尿管反流内镜治疗成功的因素及两种基于葡聚糖omer的填充剂的比较:填充物质重要吗?

Factors affecting the success of endoscopic treatment of vesicoureteral reflux and comparison of two dextranomer based bulking agents: does bulking substance matter?

作者信息

Dogan Hasan Serkan, Altan Mesut, Citamak Burak, Bozaci Ali Cansu, Koni Artan, Tekgul Serdar

机构信息

Hacettepe University Faculty of Medicine, Department of Urology, Ankara, Turkey.

Hacettepe University Faculty of Medicine, Department of Urology, Ankara, Turkey.

出版信息

J Pediatr Urol. 2015 Apr;11(2):90.e1-5. doi: 10.1016/j.jpurol.2014.12.009. Epub 2015 Mar 2.

Abstract

INTRODUCTION

Among the interventional treatment modalities for vesicoureteral reflux (VUR), endoscopic subureteric injection seems to be the least invasive method with acceptable outcomes when applied in appropriate patients.

OBJECTIVE

The aim of the presented study is to investigate the parameters which may affect the outcomes of endoscopic injection and to compare the efficacy of two different bulking agents both composed of dextranomer-hyaluronic acid copolymer.

STUDY DESIGN

The data of patients who underwent endoscopic VUR treatment between 2003 and 2012 were retrospectively reviewed. Patients with history of previous open antireflux surgery, more than one failed endoscopic treatment for reflux, VUR caused by posterior urethral valve, duplex system and overt spinal dysraphism were excluded. Surgical technique was the classical STING method. One of the two dextranomer-hyaluronic acid copolymer agents was used (Deflux in 109 and Dexell in 131 patients). Both agents were composed of similar amounts of hyaluronic acid gel (15 mg in Deflux versus 17 mg in Dexell) but different sized dextranomer microspheres (80-250 μm in Deflux and 80-120 μm in Dexell). During the follow-up, ultrasonography was performed with 3-month interval, antibiotic prophylaxis was continued until the control voiding cystourethrography (VCUG) was taken. Patient based success was defined as the disappearance of reflux on control VCUG performed 3-6 months after the operation.

RESULTS

Data were available for 240 patients. Mean age and mean postoperative follow-up were 78 ± 41 months and 19 ± 18 months. The overall success rate was 73.2%. Gender, laterality, grade of VUR, presence of voiding dysfunction, renal scar and preoperative breakthrough infection (BTI) were not found to affect the outcome, whereas age younger than 54 months and previous history of failed endoscopic injection were found to negatively affect the outcome both in univariate and multivariate analysis. The postoperative UTI (5 febrile and 43 nonfebrile) rate was 20%. Both univariate and multivariate analysis showed that postoperative UTI was more common in patients with persisting reflux, with preoperative breakthrough infections and in girls. Patient characteristics, treatment outcome and postoperative UTI rate were similar regarding the used bulking agent. No ureteral obstruction was experienced within the follow-up period.

DISCUSSION

Our success rate for second injection is about 60%, which is significantly lower than for the patients who underwent first injection. We could not find any affecting factor for this difference. Contrary to the literature, our success rates were similar in different reflux grades. We can explain this finding that we value the intraoperative orifice configuration more than the grade which can be accepted as a patient selection bias. The lower success rate in children younger than 54 months can be explained by unstabilized bladder dynamics and higher voiding pressures in this age group, who are still in the toilet-training phase. Despite successful endoscopic treatment, UTI might occur. Postoperative UTI was more common in patients with persisting reflux, preoperative BTI and girls. The similar success rates of both bulking agents proved that dextranomer size does not affect the clinical outcome. Limitations of our study can be counted as follows: 1. the data do not include the number of patients in whom conversion to open surgery was decided intraoperatively because of the unfavorable orifice configuration, 2. our data do not include the injected volume records.

CONCLUSION

Endoscopic treatment of VUR has satisfying outcomes in properly selected cases. Younger age (<54 months) and previous history of failed injection history were found to be related to unfavorable results. Postoperative UTI occurs more frequently in patients with persisting reflux, preoperative breakthrough infection history and girls. The choice of one of the dextranomer-based substances does not affect the surgical outcome and postoperative UTI development.

摘要

引言

在膀胱输尿管反流(VUR)的介入治疗方式中,内镜下输尿管下注射似乎是侵入性最小的方法,应用于合适的患者时可获得可接受的结果。

目的

本研究的目的是调查可能影响内镜注射结果的参数,并比较两种均由葡聚糖微球 - 透明质酸共聚物组成的不同填充剂的疗效。

研究设计

回顾性分析2003年至2012年间接受内镜下VUR治疗的患者数据。排除既往有开放性抗反流手术史、内镜下反流治疗失败超过一次、后尿道瓣膜引起的VUR、重复系统和明显脊柱裂的患者。手术技术为经典的STING方法。使用两种葡聚糖微球 - 透明质酸共聚物填充剂之一(109例患者使用Deflux,131例患者使用Dexell)。两种填充剂均含有相似量的透明质酸凝胶(Deflux中为15mg,Dexell中为17mg),但葡聚糖微球大小不同(Deflux中为80 - 250μm,Dexell中为80 - 120μm)。随访期间,每隔3个月进行超声检查,预防性使用抗生素直至进行排尿性膀胱尿道造影(VCUG)检查。以患者为基础的成功定义为术后3 - 6个月进行的对照VCUG检查时反流消失。

结果

获得了240例患者的数据。平均年龄和术后平均随访时间分别为78±41个月和19±18个月。总体成功率为73.2%。未发现性别、患侧、VUR分级、排尿功能障碍、肾瘢痕和术前突破性感染(BTI)对结果有影响,而在单因素和多因素分析中均发现年龄小于54个月和既往内镜注射失败史对结果有负面影响。术后尿路感染(5例发热和43例非发热)发生率为20%。单因素和多因素分析均显示,持续反流、术前有突破性感染的患者以及女孩术后尿路感染更常见。关于所用填充剂,患者特征、治疗结果和术后尿路感染发生率相似。随访期间未发生输尿管梗阻。

讨论

我们第二次注射的成功率约为60%,明显低于首次注射的患者。我们未发现造成这种差异的任何影响因素。与文献相反,我们在不同反流分级中的成功率相似。我们可以这样解释这一发现,即我们更看重术中的开口形态而非分级,这可视为一种患者选择偏倚。54个月以下儿童成功率较低可解释为该年龄组膀胱动力学不稳定且排尿压力较高,他们仍处于如厕训练阶段。尽管内镜治疗成功,但仍可能发生尿路感染。持续反流、术前有BTI的患者以及女孩术后尿路感染更常见。两种填充剂的成功率相似,证明葡聚糖微球大小不影响临床结果。我们研究的局限性如下:1. 数据未包括因开口形态不佳而术中决定转为开放手术的患者数量;2. 我们的数据未包括注射量记录。

结论

内镜治疗VUR在合适选择的病例中具有令人满意的结果。发现年龄较小(<54个月)和既往注射失败史与不良结果相关。持续反流、术前有突破性感染史的患者以及女孩术后尿路感染更频繁发生。选择基于葡聚糖的物质之一不影响手术结果和术后尿路感染的发生。

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