RiVUR研究结果及其对膀胱输尿管反流处理的意义。

Tiffany Damm, Ranjiv Mathews
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摘要

膀胱输尿管反流(RiVUR)的随机干预研究是美国国立卫生研究院的一项努力,旨在确定膀胱输尿管反流(VUR)管理中最重要的问题,即抗生素预防是否降低了VUR患儿复发性尿路感染(UTI)的发生率?在RiVUR研究的初始阶段,进行了几项类似的研究,似乎表明抗生素预防在VUR中缺乏益处。然而,这些研究中很少有严格的方法和真正的随机化儿科队列研究在RiVUR。此外,其中许多研究纳入的儿童年龄范围很广,用于识别UTI和VUR的评估不一致。2011年,美国儿科学会(AAP)发布了一份评估2至24个月发热儿童首次尿路感染的指南声明,建议不要对所有确诊尿路感染的儿童进行排尿膀胱输尿管造影(VCUG)。AAP指南的目标是减少进行vcug的数量,并可能减少被诊断为低级别VUR的儿童的数量,这些儿童似乎没有引起肾损伤的可能性。RiVUR研究包括超过600名在第一次或第二次发热性尿路感染后确诊为VUR的儿童,随机分为甲氧苄氨嘧啶/磺胺甲恶唑(TMP/SMZ)或安慰剂预防组,研究时间为2年。总的来说,与安慰剂相比,使用预防措施的患者复发性发热性尿路感染的发生率降低了50%。对该研究的队列进行了额外的亚组分析;本综述还对这些因素进行了评估,以确定RiVUR研究对当前VUR管理的总体影响。
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The RiVUR Study Outcomes and Implications on the Management of Vesicoureteral Reflux.

The Randomized intervention for Vesicoureteral Reflux (RiVUR) study was an effort by the National Institute of Health to identify the most significant question on the management of vesicoureteral reflux (VUR), i.e. Did antibiotic prophylaxis reduce the incidence of recurrent urinary tract infections (UTI) in children with VUR? During the initial phases of the RiVUR study, several similar studies were performed that seemed to indicate a lack of benefit of antibiotic prophylaxis in VUR. However, few of these studies had the rigorous methodology and true randomization of the pediatric cohort that was studied in RiVUR. Additionally, many of these studies included children of wide age ranges and inconsistent assessments were used for identification of UTI and VUR. In 2011, the American Academy of Pediatrics (AAP) published a guideline statement for the evaluation of initial UTI in febrile children aged 2 to 24 months, which recommended against performing a Voiding Cystourethrogram (VCUG) in all children with a confirmed UTI. The goal of the AAP guidelines was to reduce the number of VCUGs being performed and potentially to reduce the number of children diagnosed with low grade VUR that seems to have low potential to cause renal injury. The RiVUR study included over 600 children identified with VUR after a 1st or 2nd febrile UTI randomized to prophylaxis with trimethoprim/sulfamethoxazole (TMP/SMZ), or placebo and followed over a study timeline for 2 years. Overall, a 50% reduction was noted in the incidence of recurrent febrile UTI with the utilization of prophylaxis as compared to placebo. Additional sub-group analyses have been performed on the cohorts of the study; these are also evaluated in this review to determine the overall impact of the RiVUR study on the current management of VUR.

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