Congenital lower urinary tract obstruction

先天性下尿路梗阻
  • 文章类型: Journal Article
    患有瓣膜膀胱综合征(PUV)的男孩需要对下尿路进行充分的治疗,以保持肾功能并改善长期预后。在一些患者中,进一步的手术可能是必要的,以改善膀胱容量和功能。输尿管细胞成形术(UCP)通常用小肠进行,或者,输尿管扩张.我们的目的是评估PUV男孩UCP治疗后的长期结果。在我们医院(2004-2019年)对10名PUV男孩进行了UCP。评估术前和术后数据与肾脏和膀胱功能的关系,SWRD得分,额外的手术,并发症,和长期随访。一次瓣膜消融和UCP之间的平均时间为3.5年(SD±2.0)。中位随访时间为64.5个月(IQR36.0~97.25)。年龄调整后的膀胱容量平均增加25%(从77%(SD±0.28)到102%(SD±0.46))。八个男孩自发地排尿。超声显示无严重肾积水(3-4级)。SWRD评分显示中位数从4.5(范围2-7)降至3.0(范围1-5)。不需要增强的转换。UCP是改善PUV男孩膀胱容量的安全有效方法。此外,自然排尿的可能性仍然保持。
    Boys with valve bladder syndrome (PUV) require adequate treatment of the lower urinary tract to preserve renal function and improve long-term outcomes. In some patients, further surgery may be necessary to improve bladder capacity and function. Ureterocytoplasty (UCP) is usually carried out with a small segment of intestine or, alternatively, with a dilated ureter. Our aim was to evaluate the long-term outcomes after UCP in boys with PUV. UCP had been performed in 10 boys with PUV at our hospital (2004-2019). Pre- and postoperative data were evaluated in relation to kidney and bladder function, the SWRD score, additional surgery, complications, and long-term follow-up. The mean time between primary valve ablation and UCP was 3.5 years (SD ± 2.0). The median follow-up time was 64.5 months (IQR 36.0-97.25). The mean increase in age-adjusted bladder capacity was 25% (from 77% (SD ± 0.28) to 102% (SD ± 0.46)). Eight boys micturated spontaneously. Ultrasounds showed no severe hydronephrosis (grade 3-4). The SWRD score showed a median decrease from 4.5 (range 2-7) to 3.0 (range 1-5). No conversion of augmentation was required. UCP is a safe and effective approach to improve bladder capacity in boys with PUV. In addition, the possibility of micturating naturally is still maintained.
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  • 文章类型: Journal Article
    Congenital lower urinary tract obstruction is associated with oligohydramnios and significant perinatal mortality and long-term chronic kidney disease. The counseling of families facing this diagnosis, especially when prenatal intervention is proposed, is fraught with ambiguity. This review aims to equip the provider with the current evidence behind the conventional and novel biomarkers predictive of chronic kidney disease. The relevant clinical predictors are categorized by when they are identified, antenatally or postnatally, and as either anatomic or chemical. They are considered for their prognostic value and the challenges in obtaining them, specifically the risk to the fetus in the case of prenatal biomarkers. Serum creatinine in infancy is the traditional chemical biomarker of kidney function and continues to be a consistent predictor of future serum creatinine. β-2 microglobulin may provide earlier information regarding fetal glomerular and tubular function and is also predictive of long-term serum creatinine. Renal parenchymal area is an anatomic surrogate of nephron mass that is used in both prenatal and postnatal settings. Understanding the anatomic and chemical biomarkers is essential for future refinement of the staging algorithm used to distinguish which patients may benefit from early in utero intervention.
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