首页> 外文期刊>The Journal of Urology >The vesicoureteral reflux dysplasia syndrome in patients with posterior urethral valves.
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The vesicoureteral reflux dysplasia syndrome in patients with posterior urethral valves.

机译:尿道后瓣膜患者的输尿管反流发育不良综合征。

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PURPOSE: We retrospectively reviewed outcomes in children followed for posterior urethral valves and the vesicoureteral reflux dysplasia (VURD) syndrome. MATERIALS AND METHODS: Of 65 patients with posterior urethral valves 13 fulfilled the criteria for the VURD syndrome. Patients were assessed with diethylenetriamine pentaacetic acid and dimercapto-succinic acid scans at followup to evaluate stability of renal function, presence of renal scarring and drainage of the contralateral kidney. Student's t test and the chi-square test were used for statistical analysis, with p < or = 0.05 considered significant. RESULTS: Based on the dimercapto-succinic acid scan reports, patients were classified into group 1 (6 patients), in which the contralateral kidney had no evidence of scarring, and group 2 (7 patients), in which the contralateral kidney had evidence of scars. Patients in group 1 had no breakthrough urinary tract infections or history of urinary incontinence. There was no dilatation of the contralateralupper urinary tract, and 5 of 6 patients had prompt ureteral drainage on scans. They also attained a long-term serum creatinine of 0.6 +/- 0.0 mg/dl. Patients in group 2 had a significant incidence of breakthrough urinary tract infections (p < or = 0.03) and diurnal incontinence (p < or = 0.01). Hydroureteronephrosis and slow drainage were seen in 6 of 7 patients on scans. The long-term mean serum creatinine attained in this group was 0.9 +/- 0.3 mg/dl. CONCLUSIONS: About half of the patients with the VURD syndrome had renal scarring in the contralateral kidney. These patients had evidence of hydroureteronephrosis, slow drainage of the ureter in association with breakthrough urinary tract infections and diurnal incontinence. Although serum creatinine in patients with the VURD syndrome and renal scarring in the contralateral kidney was not statistically different from that in children with a normal contralateral kidney in the short term, in the long term the deleterious effects of renal scarring, viz hypertension, proteinuria and renal failure, are likely to manifest. The presence of the VURD syndrome may not always be as good a prognostic indicator as believed previously.
机译:目的:我们回顾性分析了后尿道瓣膜和膀胱输尿管反流发育不良(VURD)综合征患儿的结局。材料与方法:在65例后尿道瓣膜患者中,有13例符合VURD综合征标准。随访时对患者进行了二亚乙基三胺五乙酸和二巯基琥珀酸扫描,以评估肾功能的稳定性,是否存在肾脏瘢痕形成和对侧肾脏引流。使用Student's t检验和卡方检验进行统计学分析,p <或= 0.05被认为是显着的。结果:根据二巯基琥珀酸扫描报告,将患者分为第1组(6例),其中对侧肾脏无瘢痕迹象;第2组(7例),其中对侧肾脏有证据表明对侧肾脏无瘢痕形成。疤痕。第一组的患者无突破性尿路感染或尿失禁史。对侧上尿路没有扩张,并且6例患者中有5例在扫描时提示输尿管迅速引流。他们还获得了0.6 +/- 0.0 mg / dl的长期血清肌酐。第2组的患者发生突破性尿路感染(p <或= 0.03)和日尿失禁(p <或= 0.01)的发生率很高。扫描发现7例患者中有6例发现输尿管肾盂肾病和引流缓慢。该组的长期平均血清肌酐为0.9 +/- 0.3 mg / dl。结论:约一半的VURD综合征患者对侧肾脏有肾脏瘢痕形成。这些患者有输尿管肾盂积水,输尿管缓慢引流与突破性尿路感染和日尿失禁有关的证据。尽管短期内VURD综合征和对侧肾脏肾脏瘢痕形成患者的血清肌酐与正常对侧肾脏儿童的血清肌酐没有统计学差异,但从长期来看,肾脏瘢痕形成,即高血压,蛋白尿和肾功能衰竭,很可能会表现出来。 VURD综合征的存在可能并不总是像以前认为的那样好作为预后指标。

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