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神经源性膀胱患儿的肠膀胱扩大术:长期随访

Enterocystoplasty in children with neuropathic bladders: long-term follow-up.

作者信息

López Pereira P, Moreno Valle J A, Espinosa L, Alonso Dorrego J M, Burgos Lucena L, Martínez Urrutia M J, Lobato Romera R, Luz Picazo M, Viguer J M, Jaureguízar Monereo E

机构信息

Department of Pediatric Urology, University Hospital La Paz, P degrees Castellana 261, Madrid 28046, Spain.

出版信息

J Pediatr Urol. 2008 Feb;4(1):27-31. doi: 10.1016/j.jpurol.2007.07.009. Epub 2007 Sep 17.

Abstract

OBJECTIVE

This study assesses clinical outcome, after at least 8 years, of augmentation done before or at puberty in neuropathic bladders.

PATIENTS AND METHODS

A total of 29 children with neuropathic bladders who did not respond satisfactorily to clean intermittent catheterisation and anti-cholinergic therapy underwent enterocystoplasty at a mean age of 11.8 years (range 3-18). Twenty-one children (72.4%) had vesicoureteral reflux (VUR) and/or ureterohydronephrosis and 22 (75.8%) had dimercapto-succinic acid scars, but all had normal renal function. All patients were followed at regular intervals with urinary tract imaging, serum electrolytes, creatinine, urodynamic evaluation and 24-h urine collection. Urine cytology, cystoscopy and biopsy were performed at the end of follow-up.

RESULTS

Mean follow-up was 11 years (range 8-14.5) and mean age at the end of follow-up was 22.2 years (range 13.2-31). Urodynamic studies showed a significant improvement in bladder compliance in all patients. Upper urinary tract dilatation disappeared in all, VUR in 13/17 (76.4%), and no new renal scarring occurred in any patient. At the end of follow-up, renal function was normal in all according to serum creatinine, but cystatin C levels were normal in 27 and elevated in two. Significant proteinuria and low concentrations of renin and aldosterone were present in 80% and 82%, respectively. Only one patient had urinary tract infection, three had bladder stones, and in another a catheterisable channel was made. All patients were dry with normal urine cytology and cystoscopy, and no malignant lesions have been found in the biopsy specimens.

CONCLUSION

Enterocystoplasty has preserved renal function and resolved VUR and/or hydronephrosis in most patients. The future implications of proteinuria and the low serum levels of renin and aldosterone, as well as the best indicator for measuring renal function, have yet to be determined. Close, life-long follow-up, including cystoscopy, is necessary to prevent complications.

摘要

目的

本研究评估在神经性膀胱患者青春期前或青春期时进行膀胱扩大术至少8年后的临床结局。

患者与方法

共有29例神经性膀胱患儿,对清洁间歇性导尿和抗胆碱能治疗反应不佳,平均11.8岁(3 - 18岁)时接受了肠膀胱扩大术。21例患儿(72.4%)有膀胱输尿管反流(VUR)和/或输尿管肾盂积水,22例(75.8%)有二巯基琥珀酸瘢痕形成,但所有患儿肾功能均正常。所有患者定期接受泌尿系统影像学检查、血清电解质、肌酐、尿动力学评估及24小时尿液收集检查。随访结束时进行尿液细胞学检查、膀胱镜检查及活检。

结果

平均随访11年(8 - 14.5年),随访结束时平均年龄22.2岁(13.2 - 31岁)。尿动力学研究显示所有患者膀胱顺应性均有显著改善。所有患者上尿路扩张均消失,17例中的13例(76.4%)VUR消失,且无患者出现新的肾瘢痕形成。随访结束时,根据血清肌酐,所有患者肾功能均正常,但27例胱抑素C水平正常,2例升高。80%的患者存在显著蛋白尿,82%的患者肾素和醛固酮浓度较低。仅1例患者发生泌尿系统感染,3例有膀胱结石,另1例患者制作了可导尿通道。所有患者均无尿失禁,尿液细胞学检查和膀胱镜检查正常,活检标本未发现恶性病变。

结论

肠膀胱扩大术在大多数患者中保留了肾功能,解决了VUR和/或肾盂积水问题。蛋白尿以及肾素和醛固酮血清水平低的未来影响,以及测量肾功能的最佳指标,尚待确定。需要进行密切的终身随访,包括膀胱镜检查,以预防并发症。

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