Skip to main content
Erschienen in: Pediatric Radiology 2/2006

Open Access 01.09.2006 | ALARA

Applying the ALARA concept to the evaluation of vesicoureteric reflux

verfasst von: Richard S. Lee, David A. Diamond, Jeanne S. Chow

Erschienen in: Pediatric Radiology | Sonderheft 2/2006

Abstract

The voiding cystourethrogram (VCUG) is a widely used study to define lower urinary tract anatomy and to diagnose vesicoureteric reflux (VUR) in children. We examine the technical advances in the VCUG and other examinations for reflux that have reduced radiation exposure of children, and we give recommendations for the use of imaging studies in four groups of children: (1) children with urinary tract infection, (2) siblings of patients with VUR, (3) infants with antenatal hydronephrosis (ANH), and (4) children with a solitary functioning kidney. By performing examinations with little to no radiation, carefully selecting only the children who need imaging studies and judiciously timing follow-up examinations, we can reduce the radiation exposure of children being studied for reflux.

Introduction

The traditional method for diagnosing vesicoureteric reflux (VUR) is the fluoroscopic voiding cystourethrogram (VCUG). This study is primarily used to screen children who are at risk of VUR and to provide detailed anatomical information on the genitourinary system. Because this examination is mainly performed in children, who are at greatest risk of the harmful effects of ionizing radiation, we must find ways to achieve diagnostic accuracy while minimizing radiation dosage.
In this article, we review the technical advances in the diagnosis of VUR and present recommendations for the evaluation of four groups of children widely studied for reflux: (1) children with urinary tract infection (UTI), (2) siblings of patients with VUR, (3) infants with antenatal hydronephrosis (ANH), and (4) children with a solitary functioning kidney. In addition, we discuss the timing and frequency of imaging studies to detect VUR resolution. By defining patients at risk of reflux and determining the differences between patient groups, we can utilize studies judiciously and minimize radiation exposure. Our recommendations are based on the imaging studies available at our hospital. The ultimate choice of imaging modality depends on diagnostic availability, the individual patient and the referring physician’s preference.

Technical advances in voiding cystography

In the last two decades enormous strides have been made in reducing the radiation dosage in patients studied for VUR. The improvement has been a result of replacement of standard fluoroscopic machines with digital and pulsed fluoroscopy, judicious use of radionuclide cystograms (RNC), and the introduction and growing popularity of voiding urosonography (VUS).
A traditional VCUG exposes the patient to 100 times the radiation of an RNC. In the last 10 years, low-dose fluoroscopy techniques, including digital fluoroscopy and pulsed fluoroscopy, have led to a decrease in the radiation dose to the patient [15] while providing similar diagnostic quality images [610]. By changing from continuous to pulse fluoroscopy, the effective dose of radiation can be reduced by approximately 90% with minimal loss of resolution [10]. Pulsed fluoroscopy is now considered a requisite for optimal pediatric fluoroscopy [11].
Digital fluoroscopy offers the advantage of ‘image or screen save’so that the last image can be saved without additional radiation to the patient. Limiting the number of spot images and maximizing the number of image-save acquisitions decreases radiation [12]. Meticulous image coning also significantly decreases patient radiation exposure. Thus low magnification, low-pulse-per-second fluoroscopy and image-save acquisition should be used when performing a VCUG.
In our department, the effective radiation dose of a VCUG using modern low-dose fluoroscopic methods is approximately 10 times that of RNC (mentioned below). For example, the average effective dose of a VCUG in a 3-year-old patient is 3 mrem, compared to 0.5 mrem for an RNC. For comparison, the average effective dose of an airplane ride from Boston to San Francisco is 5 mrem. The average effective dose of the VCUG is variable and depends on the patient size, operator and machinery.
The main advantage of RNC over fluoroscopic VCUG is decreased radiation exposure of the patient. The sensitivity of RNC for detecting reflux is equal to or greater than that of VCUG; however, the spatial resolution and anatomic detail seen on an RNC are inferior to those seen on a VCUG. To increase the sensitivity of either test, a cyclic study should be performed in children younger than 1 year [13].
In order to avoid instrumentation, methods of indirect cystography have been tested. Indirect cystography uses intravenously injected Tc 99m pentetate, which is cleared by the kidneys into the bladder to assess for reflux without bladder catheterization. Unfortunately, this method has a high percentage of false-negative studies, so it is not recommended.
During the last two decades, in an effort to eliminate the radiation exposure intrinsic to RNC and VCUG, sonography has been used to evaluate reflux. Indirect US methods without the use of contrast agents avoid instrumentation but are significantly less sensitive [1416]. A normal non-contrast US scan of the urinary tract without contrast agent does not exclude reflux [17]. The availability of a stable US contrast agent that can be administered intravesically is a great breakthrough that has popularized VUS [18]. During contrast sonocystography, the bladder is filled through a catheter with a US contrast agent, and reflux is assessed by the sonographic appearance of contrast agent within the kidneys and ureters. The grading system is similar to that for a VCUG [19]. This method is not as popular in North America as elsewhere in the world. In some German institutions, this method has led to a significantly reduced number of VCUGs and the associated ionizing radiation [20].
There is a 92% concordance in VUR diagnosis on VUS and VCUG/RNC [18, 21, 22]. In comparison to VCUG, the sensitivity and specificity of VUS range from 88% to 100% and 86% to 100%, respectively [18]. Although comparable to VCUG and RNC in sensitivity and accuracy in detecting VUR [2330], VUS as compared to a VCUG does not provide comparable anatomic detail of the bladder, ureter, and urethra. Current recommendations for the use of VUS vary.
During MR cystography, images of the genitourinary tract are obtained before and after the intravesical administration of gadolinium and after voiding. The method is less sensitive than VCUG for detecting reflux and is experimental. The relative benefits of this examination are that it exposes the child to no additional radiation and can evaluate the kidneys for changes related to reflux nephropathy [31, 32]. However, the sedation or anesthesia often required in the young patients evaluated by MRI imposes medical risks and costs time and resources.

Children with urinary tract infection

Most UTIs in children are ascending and related to factors such as dysfunctional voiding or impaired lower tract defenses. The VCUG has been regarded as fundamental in evaluating the child with a well-documented UTI because it evaluates: (1) bladder and urethral anatomy, (2) bladder capacity, (3) ability of the bladder to empty, (4) presence of VUR, and (5) the grade of VUR.
Although cystitis alone does not pose a significant threat to the health of a child, a UTI combined with VUR can result in significant renal damage. VUR is present in 30–0% of children with a febrile UTI [33]. Studies demonstrate that on initial evaluation of children with a febrile UTI and VUR there is up to a 40% incidence of renal scarring [34]. Although the majority of VURs resolve spontaneously with time, the likelihood of resolution depends on age at diagnosis, laterality and VUR grade. In addition, as children get older, they are much less likely to have VUR, because if they had it, it has resolved (Fig. 1) [35]. The VCUG provides critical prognostic information by detecting and then defining the severity of VUR.
The VCUG is invasive in terms of instrumentation and radiation exposure; therefore, selectivity in its application is appropriate. The greatest reduction in radiation exposure occurs by avoiding the study altogether. Critical to determining which patients require a VCUG is the definition of a UTI. Urine specimens obtained by catheterization or suprapubic aspiration are the gold standard. Any significant pure growth from a catheterized specimen or suprapubic aspiration is regarded as positive. A bacterial count of >105 cfu/ml from a clean midstream collection has an 80% (and two such collections a 90%) likelihood of representing a true infection [35]. Specimens that are obtained by adhering a plastic bag to the perineum are useful only if no organisms grow, as any bacterial growth usually reflects perineal flora. Contamination rates range from 60% to 70% [36]. Results from catheterization through a phimotic foreskin can also be misleading.
In addition, clinical presentation, age, race and social factors contribute to selecting which patients should have a VCUG. The combined presence of fever (>38.5°C) [37] and UTI are important clinical findings, as they might indicate a pyelonephritis as opposed to cystitis, which typically does not produce fever. Pyelonephritis can result in significant kidney damage unless prompt antimicrobial therapy is instituted. Children with repetitive febrile UTI are at further increased risk of renal damage. Therefore, in the young child with a febrile UTI, cystographic evaluation to rule out VUR is most strongly warranted.
Recently, attempts to link biomarkers of inflammation such as procalcitonin, known to be associated with renal scarring, have shown promise in attempting to stratify patients by risk of renal damage [38]. Further investigation is needed to accurately stratify patients by their risk of renal damage.
The greatest risk of renal damage is during the first 2 years of life. Therefore, we recommend aggressive screening of children <2 years of age, because of their increased risk and inability to describe symptoms. For prepubertal boys with a well-documented UTI, the VCUG is the preferred diagnostic study so that the urethral anatomy might be defined. In less well-documented cases, an initial renal bladder US is reasonable. For prepubertal girls with pyelonephritis, the VCUG is recommended, whereas for prepubertal girls with recurrent lower UTI and the ability to describe symptoms (>5 years of age) an RNC is recommended. If the veracity of the diagnosis of UTI in a girl is questioned, a US is a proper initial study.
Postpubertal children are at minimal risk of renal scarring and do not require diagnostic imaging when presenting with cystitis. Similarly, because of the low incidence of reflux in black children, the black child between the age of 5 years and puberty presenting without fever but with infection do not require a VCUG [39]. In settings where parental vigilance is questionable, an aggressive approach should be considered.

Sibling vesicoureteric reflux

VUR is the most common heritable disorder of the genitourinary tract, but has not been linked to a particular chromosome or genetic defect. A recent research synthesis of 1,768 siblings of various ages showed a mean VUR incidence of 32% [40]. The research demonstrated that certain factors help predict the risk of sibling VUR. When stratified by sibling age, 44% of children <2 years of age have VUR, as opposed to 9% of children >6 years [40]. If the sex of the sibling or index patient is considered individually there is no statistically significant difference in VUR risk; however, if the sex of both patients is considered, female siblings of female index patients are at higher risk of VUR than their male counterparts [41]. Twins are at particularly increased risk, and monozygotic twins are at higher risk than dizygotic twins [42, 43]. Approximately two-thirds of sibling VURs are low-grade (I/II) and half are unilateral [40]. Sibling VUR shows an inverse relationship between age and grade of reflux [44]. Although the data are limited, siblings might have a higher resolution rate as compared to children discovered after a febrile UTI [40].
Although the incidence of VUR in siblings is significantly higher than in the general population, the majority of sibling VUR is asymptomatic (no history of UTI) and might be innocuous. Hollowell and Greenfield [40] determined from the literature an 11% incidence of renal damage documented by various radiographic modalities in which the majority of patients were asymptomatic [40]. Furthermore, Puri et al. [45] demonstrated that symptomatic siblings (history of febrile UTI) not only have higher grades of VUR but also an increased rate of reflux nephropathy (25%) as compared to reported data on asymptomatic siblings. Therefore, the early detection of VUR in asymptomatic siblings might decrease the incidence of renal damage [46].
Although the goal of screening for sibling VUR is the prevention of renal damage, no current genetic tests can determine who is at risk of renal damage, let alone which siblings will have VUR. Based on the literature, we have divided children into four groups for potential screening: (1) newborns to the age of toilet training, (2) prepubertal children older than toilet-training age, (3) postpubertal children, and (4) any symptomatic sibling. The age of toilet training is chosen because typically at this age children can describe their symptoms and parents can detect signs of UTI such as frequency.
All children should be initially screened by an extensive history including voiding habits and any unexplained febrile events. We recommend elective screening with RNC for both girls and boys, because RNC is a sensitive examination for VUR and confers a very low dose of radiation. In the future, VUS might be a viable alternative to the RNC.
Because the prevalence of VUR drops considerably with increasing age (Fig. 1) for prepubertal children older than toilet training age (group 2), we recommend an initial screening US scan. If the renal US scan demonstrates abnormalities, such as size discrepancy, renal malformation or scarring, dilated ureter, hydronephrosis or change in renal pelvis or ureteral caliber during the examination, we recommend an RNC. If VUR is discovered, the follow-up study at 1 year should be a VCUG to more clearly define the genitourinary anatomy.
We accept that ultrasonography is not as sensitive as DMSA for the detection of renal scars in patients with a history of acute pyelonephritis; however, the role of evaluating the asymptomatic patient sonographically as compared to DMSA has not been defined [4749]. If the sibling population has remained asymptomatic during the most vulnerable period for renal damage secondary to infection and reflux, the value of conducting a DMSA scan as the initial screening test is low.
Vulnerability to renal damage is thought to persist until puberty [50, 51]. Taking this into consideration, with the decreasing incidence of reflux with age and the possible higher resolution rate of reflux in siblings, we recommend that asymptomatic postpubertal boys and girls be screened with a renal US scan only (group 3). We especially recommend screening of girls because of the increased risk of UTI during their reproductive years and the deleterious effects of an upper UTI during pregnancy. If there are no renal abnormalities, we recommend no further investigation unless symptoms develop. If abnormalities are found on sonography, we recommend a VCUG or RNC. Symptomatic siblings (group 4) need to be studied aggressively and treated as any other child with a UTI.

Antenatal hydronephrosis and vesicoureteric reflux

ANH affects 1–% of all pregnancies and is one of the most common prenatally detected abnormalities; however, the clinical relevance of varying degrees of ANH is unclear [5261]. Although the prenatal US scan is noninvasive and without ionizing radiation, postnatal assessment can be invasive and expose the child to radiation. To date there are no large comprehensive prospective studies that have determined the risk of VUR with varying degrees of ANH. Similarly, there are no large studies that have examined both ANH and postnatal US (PNUS) findings to predict postnatal risk of VUR or kidney damage. There is general agreement that the postnatal evaluation of children with moderate to severe ANH that persists postnatally should include a VCUG. However, the postnatal management of children with mild ANH, any degree of ANH that resolves soon after birth, or a nonspecific history of ANH is controversial.
Numerous small series demonstrate that children with ANH have an increased risk of VUR as compared to the general population [6264]. Overall, boys are thought to be at greater risk of bilateral high-grade reflux than girls [65]. The largest single series that documented mild ANH and its relationship to VUR established a 15% incidence of VUR; however, this series only had 40 patients [63].
Attempts to stratify risk based on PNUS findings have not been successful [6264, 66, 67]. Many studies have shown that a normal postnatal US scan is not a reliable indicator or predictor for the exclusion of VUR [6870]. In one study, hydronephrosis on PNUS had a sensitivity of 63% and specificity of 66% for VUR on VCUG [63]. Although the data are limited, children with ANH and VUR seemingly have a more benign course with a higher resolution rate of VUR than children discovered to have VUR after a febrile infection [7173].
We provide the following recommendations for the evaluation of children with ANH with the understanding that the current literature is controversial and that the care of each child is individual. Children with bilateral severe ANH or a solitary kidney with any grade of ANH should undergo a PNUS shortly after birth, keeping in mind that physiologic dehydration within the first 5 days might decrease the degree of hydronephrosis. Those with any other grade of ANH should undergo a PNUS within the first month of life. Male and female children with moderate or severe ANH should undergo a VCUG. Children with mild ANH that persists after birth might be followed by US with or without a VCUG or RNC. Management of mild ANH that resolves is controversial and might require further imaging.

The solitary kidney

The incidence of VUR in patients with a multicystic dysplastic kidney (MCDK) or renal agenesis has been examined in a number of studies. It is logical to do so because the child’s renal function is entirely dependent upon the integrity of the solitary kidney such that reflux nephropathy would have devastating consequences.
The incidence of reflux to the contralateral kidney in a child with MCDK ranges from 13% to 28% [7477]. Reflux in the majority of children is mild to moderate in degree, and the spontaneous resolution rate is high. Renal agenesis has been evaluated in fewer studies, but the incidence of VUR appears comparable to that in MCDK (5–4%) [7476]. Without doubt, some of these cases might represent undetectable MCDK. For both MCDK and renal agenesis, RNC and VUS seem advisable as screening studies for VUR because the stakes in this group of patients with a solitary functioning kidney are particularly high.

Timing and frequency of radiologic intervention for the detection of VUR resolution

The majority of patients with primary VUR are managed medically with prophylactic antibiotics until either resolution of VUR or an indication for surgical intervention. The rate of VUR resolution by grade and laterality has been well-documented. Nonetheless, guidelines vary considerably regarding the frequency or type of diagnostic imaging needed to follow VUR until resolution [7881]. Although most pediatric urologists and pediatric radiologists recommend annual follow-up studies, this has not been rigorously tested.
The dilemma has recently been analyzed by modeling, in both a theoretical and retrospective cohort of children younger than 10 years with a diagnosis of primary VUR and febrile UTI, different strategies of VCUG follow-up and its effects on antibiotic exposure and cost [82]. Based on their analysis, the authors recommended that patients with mild VUR undergo a VCUG every 2 years during follow-up and every 3 years if reflux was moderate to severe. The authors made these recommendations by determining which timing strategy would most effectively decrease the number of VCUGs and cost per patient while minimizing increase in antibiotic exposure. Using a small retrospective cohort of patients with low-grade reflux and a resolution rate similar to that of published rates they applied their clinical algorithm and predicted that the number of VCUGs performed per patient would be reduced by 19% (P=0.001), the costs reduced by 6% (P=0.17), and the antibiotic exposure increased by 26% (P=0.001).
With less frequent VCUG follow-up, long-term antibiotic exposure will increase significantly in patients who are compliant. However, it is well-documented that adherence to medication regimens in children with chronic diseases is about 50% [83]. The longer they require medication, the less likely they are to adhere to the regimen [83]. Although it is difficult to quantify, it is possible that voiding cystography would serve as a reminder of VUR, which in turn would improve medication compliance before VUR resolution.
Without doubt, if we could stratify VUR patients by their risk of renal damage, we would significantly decrease the amount of diagnostic imaging performed during medical management. Some authors have recently questioned the conventional management of children with low-grade reflux who might be at a low risk of renal injury; however, it is still difficult to determine which children are at risk of damage [8486].
We recommend that patients with low-grade (I, II) primary VUR, regardless of laterality, be followed annually because of the higher resolution rate with lower grades of VUR. If the initial study to document VUR was an RNC, we recommend the first follow-up examination be a VCUG in order to detect any occult bladder or urethral abnormalities that would decrease the likelihood of VUR resolution (e.g. hutch diverticulum, posterior urethral valves). All subsequent follow-up studies should be an RNC, keeping in mind that grade I reflux is sometimes difficult to discern on RNC. For patients with moderate to severe VUR (≥III), a more prolonged resolution period is anticipated. Initially, anatomical abnormalities need to be ruled out with a VCUG. At the discretion of the urologist and taking into consideration family compliance, patient age, and the logistics of follow-up, an RNC might be performed every 18 months to 2 years until resolution or surgical intervention. For patients with bilateral disease, the higher grade of VUR is the rate-limiting step to resolution and, therefore, dictates the frequency of follow-up.
For children who undergo antireflux surgery, postoperative imaging should be an RNC. A VCUG is rarely indicated, and many pediatric urologists [87] no longer perform postoperative voiding studies at all. For those who are committed to documenting the success of surgery, the VUS might prove to be the ideal study in the future.

Conclusion

Significant technical innovations, such as digital pulsed fluoroscopy and VUS, and the judicious use of the studies emitting ionizing radiation have led to the overall decrease in radiation exposure in children being evaluated for VUR. In the future, advances in basic science such as genetic screening and biomarker discovery might help determine which children are at risk of reflux and renal damage, potentially replacing our current invasive and radiation-emitting examinations for reflux.

Acknowledgements

We would like to thank Rhonda Johnson and acknowledge her for her continued excellent work. We also thank Drs. Alan Retik and Robert Lebowitz for their insightful comments and suggestions.
Open Access This is an open access article distributed under the terms of the Creative Commons Attribution Noncommercial License ( https://​creativecommons.​org/​licenses/​by-nc/​2.​0 ), which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.

Unsere Produktempfehlungen

e.Med Interdisziplinär

Kombi-Abonnement

Für Ihren Erfolg in Klinik und Praxis - Die beste Hilfe in Ihrem Arbeitsalltag

Mit e.Med Interdisziplinär erhalten Sie Zugang zu allen CME-Fortbildungen und Fachzeitschriften auf SpringerMedizin.de.

e.Med Pädiatrie

Kombi-Abonnement

Mit e.Med Pädiatrie erhalten Sie Zugang zu CME-Fortbildungen des Fachgebietes Pädiatrie, den Premium-Inhalten der pädiatrischen Fachzeitschriften, inklusive einer gedruckten Pädiatrie-Zeitschrift Ihrer Wahl.

e.Med Radiologie

Kombi-Abonnement

Mit e.Med Radiologie erhalten Sie Zugang zu CME-Fortbildungen des Fachgebietes Radiologie, den Premium-Inhalten der radiologischen Fachzeitschriften, inklusive einer gedruckten Radiologie-Zeitschrift Ihrer Wahl.

Literatur
1.
Zurück zum Zitat Cleveland RH, Constantinou C, Blickman JG, et al (1992) Voiding cystourethrography in children: value of digital fluoroscopy in reducing radiation dose. AJR 158:137–42PubMed Cleveland RH, Constantinou C, Blickman JG, et al (1992) Voiding cystourethrography in children: value of digital fluoroscopy in reducing radiation dose. AJR 158:137–42PubMed
2.
Zurück zum Zitat Diamond DA, Kleinman PK, Spevak M, et al (1996) The tailored low dose fluoroscopic voiding cystogram for familial reflux screening. J Urol 155:681–82CrossRefPubMed Diamond DA, Kleinman PK, Spevak M, et al (1996) The tailored low dose fluoroscopic voiding cystogram for familial reflux screening. J Urol 155:681–82CrossRefPubMed
3.
Zurück zum Zitat Kleinman PK, Diamond DA, Karellas A, et al (1994) Tailored low-dose fluoroscopic voiding cystourethrography for the reevaluation of vesicoureteral reflux in girls. AJR 162:1151–154; discussion 1155–156PubMed Kleinman PK, Diamond DA, Karellas A, et al (1994) Tailored low-dose fluoroscopic voiding cystourethrography for the reevaluation of vesicoureteral reflux in girls. AJR 162:1151–154; discussion 1155–156PubMed
4.
Zurück zum Zitat Mooney RB, McKinstry J (2001) Paediatric dose reduction with the introduction of digital fluorography. Radiat Prot Dosimetry 94:117–20PubMed Mooney RB, McKinstry J (2001) Paediatric dose reduction with the introduction of digital fluorography. Radiat Prot Dosimetry 94:117–20PubMed
5.
Zurück zum Zitat Ward VL, Barnewolt CE, Strauss KJ, et al (2003) Radiation exposure and imaging quality: preliminary results of a comparison of variable-rate pulsed fluoroscopy with continuous fluoroscopy in a swine model of pediatric genitourinary abnormalities. In: Annual Meeting of Association of University Radiologists, Miami, Fla Ward VL, Barnewolt CE, Strauss KJ, et al (2003) Radiation exposure and imaging quality: preliminary results of a comparison of variable-rate pulsed fluoroscopy with continuous fluoroscopy in a swine model of pediatric genitourinary abnormalities. In: Annual Meeting of Association of University Radiologists, Miami, Fla
6.
Zurück zum Zitat Persliden J, Helmrot E, Hjort P, et al (2004) Dose and image quality in the comparison of analogue and digital techniques in paediatric urology examinations. Eur Radiol 14:638–44CrossRefPubMed Persliden J, Helmrot E, Hjort P, et al (2004) Dose and image quality in the comparison of analogue and digital techniques in paediatric urology examinations. Eur Radiol 14:638–44CrossRefPubMed
7.
Zurück zum Zitat Hernandez RJ, Goodsitt MM (1996) Reduction of radiation dose in pediatric patients using pulsed fluoroscopy. AJR 167:1247–253PubMed Hernandez RJ, Goodsitt MM (1996) Reduction of radiation dose in pediatric patients using pulsed fluoroscopy. AJR 167:1247–253PubMed
8.
Zurück zum Zitat Boland GW, Murphy B, Arellano R, et al (2000) Dose reduction in gastrointestinal and genitourinary fluoroscopy: use of grid-controlled pulsed fluoroscopy. AJR 175:1453–457PubMed Boland GW, Murphy B, Arellano R, et al (2000) Dose reduction in gastrointestinal and genitourinary fluoroscopy: use of grid-controlled pulsed fluoroscopy. AJR 175:1453–457PubMed
9.
Zurück zum Zitat Bazopoulos EV, Prassopoulos PK, Damilakis JE, et al (1998) A comparison between digital fluoroscopic hard copies and 105-mm spot films in evaluating vesicoureteric reflux in children. Pediatr Radiol 28:162–66CrossRefPubMed Bazopoulos EV, Prassopoulos PK, Damilakis JE, et al (1998) A comparison between digital fluoroscopic hard copies and 105-mm spot films in evaluating vesicoureteric reflux in children. Pediatr Radiol 28:162–66CrossRefPubMed
10.
Zurück zum Zitat Lederman HM, Khademian ZP, Felice M, et al (2002) Dose reduction fluoroscopy in pediatrics. Pediatr Radiol 32:844–48CrossRefPubMed Lederman HM, Khademian ZP, Felice M, et al (2002) Dose reduction fluoroscopy in pediatrics. Pediatr Radiol 32:844–48CrossRefPubMed
11.
Zurück zum Zitat Brown PH, Thomas RD, Silberberg PJ, et al (2000) Optimization of a fluoroscope to reduce radiation exposure in pediatric imaging. Pediatr Radiol 30:229–35CrossRefPubMed Brown PH, Thomas RD, Silberberg PJ, et al (2000) Optimization of a fluoroscope to reduce radiation exposure in pediatric imaging. Pediatr Radiol 30:229–35CrossRefPubMed
12.
Zurück zum Zitat Agrawalla S, Pearce R, Goodman TR (2004) How to perform the perfect voiding cystourethrogram. Pediatr Radiol 34:114–19CrossRefPubMed Agrawalla S, Pearce R, Goodman TR (2004) How to perform the perfect voiding cystourethrogram. Pediatr Radiol 34:114–19CrossRefPubMed
13.
Zurück zum Zitat Paltiel HJ, Rupich RC, Kiruluta HG (1992) Enhanced detection of vesicoureteral reflux in infants and children with use of cyclic voiding cystourethrography. Radiology 184:753–55PubMed Paltiel HJ, Rupich RC, Kiruluta HG (1992) Enhanced detection of vesicoureteral reflux in infants and children with use of cyclic voiding cystourethrography. Radiology 184:753–55PubMed
14.
Zurück zum Zitat Kopac M, Kenig A, Kljucevsek D, et al (2005) Indirect voiding urosonography for detecting vesicoureteral reflux in children. Pediatr Nephrol 20:1285–287CrossRefPubMed Kopac M, Kenig A, Kljucevsek D, et al (2005) Indirect voiding urosonography for detecting vesicoureteral reflux in children. Pediatr Nephrol 20:1285–287CrossRefPubMed
15.
Zurück zum Zitat Kosar A, Yesildag A, Oyar O, et al (2003) Detection of vesico-ureteric reflux in children by colour-flow Doppler ultrasonography. BJU Int 91:856–59CrossRefPubMed Kosar A, Yesildag A, Oyar O, et al (2003) Detection of vesico-ureteric reflux in children by colour-flow Doppler ultrasonography. BJU Int 91:856–59CrossRefPubMed
16.
Zurück zum Zitat Oak SN, Kulkarni B, Chaubal N (1999) Color flow Doppler sonography: a reliable alternative to voiding cystourethrogram in the diagnosis of vesicoureteral reflux in children. Urology 53:1211–214CrossRefPubMed Oak SN, Kulkarni B, Chaubal N (1999) Color flow Doppler sonography: a reliable alternative to voiding cystourethrogram in the diagnosis of vesicoureteral reflux in children. Urology 53:1211–214CrossRefPubMed
17.
Zurück zum Zitat DiPietro MA, Blane CE, Zerin JM (1997) Vesicoureteral reflux in older children: concordance of US and voiding cystourethrographic findings. Radiology 205:821–22PubMed DiPietro MA, Blane CE, Zerin JM (1997) Vesicoureteral reflux in older children: concordance of US and voiding cystourethrographic findings. Radiology 205:821–22PubMed
18.
Zurück zum Zitat Darge K (2002) Diagnosis of vesicoureteral reflux with ultrasonography. Pediatr Nephrol 17:52–0CrossRefPubMed Darge K (2002) Diagnosis of vesicoureteral reflux with ultrasonography. Pediatr Nephrol 17:52–0CrossRefPubMed
19.
Zurück zum Zitat Darge K, Troeger J (2002) Vesicoureteral reflux grading in contrast-enhanced voiding urosonography. Eur J Radiol 43:122–28CrossRefPubMed Darge K, Troeger J (2002) Vesicoureteral reflux grading in contrast-enhanced voiding urosonography. Eur J Radiol 43:122–28CrossRefPubMed
20.
Zurück zum Zitat Darge K, Ghods S, Zieger B, et al (2001) Reduction in voiding cystourethrographies after the introduction of contrast enhanced sonographic reflux diagnosis. Pediatr Radiol 31:790–95CrossRefPubMed Darge K, Ghods S, Zieger B, et al (2001) Reduction in voiding cystourethrographies after the introduction of contrast enhanced sonographic reflux diagnosis. Pediatr Radiol 31:790–95CrossRefPubMed
21.
Zurück zum Zitat Ascenti G, Zimbaro G, Mazziotti S, et al (2004) Harmonic US imaging of vesicoureteric reflux in children: usefulness of a second generation US contrast agent. Pediatr Radiol 34:481–87CrossRefPubMed Ascenti G, Zimbaro G, Mazziotti S, et al (2004) Harmonic US imaging of vesicoureteric reflux in children: usefulness of a second generation US contrast agent. Pediatr Radiol 34:481–87CrossRefPubMed
22.
Zurück zum Zitat Riccabona M, Mache CJ, Lindbichler F (2003) Echo-enhanced color Doppler cystosonography of vesicoureteral reflux in children. Improvement by stimulated acoustic emission. Acta Radiol 44:18–3CrossRefPubMed Riccabona M, Mache CJ, Lindbichler F (2003) Echo-enhanced color Doppler cystosonography of vesicoureteral reflux in children. Improvement by stimulated acoustic emission. Acta Radiol 44:18–3CrossRefPubMed
23.
Zurück zum Zitat Mentzel HJ, Vogt S, Patzer L, et al (1999) Contrast-enhanced sonography of vesicoureterorenal reflux in children: preliminary results. AJR 173:737–40PubMed Mentzel HJ, Vogt S, Patzer L, et al (1999) Contrast-enhanced sonography of vesicoureterorenal reflux in children: preliminary results. AJR 173:737–40PubMed
24.
Zurück zum Zitat Darge K, Troeger J, Duetting T, et al (1999) Reflux in young patients: comparison of voiding US of the bladder and retrovesical space with echo enhancement versus voiding cystourethrography for diagnosis. Radiology 210:201–07PubMed Darge K, Troeger J, Duetting T, et al (1999) Reflux in young patients: comparison of voiding US of the bladder and retrovesical space with echo enhancement versus voiding cystourethrography for diagnosis. Radiology 210:201–07PubMed
25.
Zurück zum Zitat Valentini AL, Salvaggio E, Manzoni C, et al (2001) Contrast-enhanced gray-scale and color Doppler voiding urosonography versus voiding cystourethrography in the diagnosis and grading of vesicoureteral reflux. J Clin Ultrasound 29:65–1CrossRefPubMed Valentini AL, Salvaggio E, Manzoni C, et al (2001) Contrast-enhanced gray-scale and color Doppler voiding urosonography versus voiding cystourethrography in the diagnosis and grading of vesicoureteral reflux. J Clin Ultrasound 29:65–1CrossRefPubMed
26.
Zurück zum Zitat Galia M, Midiri M, Pennisi F, et al (2004) Vesicoureteral reflux in young patients: comparison of voiding color Doppler US with echo enhancement versus voiding cystourethrography for diagnosis or exclusion. Abdom Imaging 29:303–08CrossRefPubMed Galia M, Midiri M, Pennisi F, et al (2004) Vesicoureteral reflux in young patients: comparison of voiding color Doppler US with echo enhancement versus voiding cystourethrography for diagnosis or exclusion. Abdom Imaging 29:303–08CrossRefPubMed
27.
Zurück zum Zitat Nakamura M, Wang Y, Shigeta K, et al (2002) Simultaneous voiding cystourethrography and voiding urosonography: an in vitro and in vivo study. Clin Radiol 57:846–49PubMed Nakamura M, Wang Y, Shigeta K, et al (2002) Simultaneous voiding cystourethrography and voiding urosonography: an in vitro and in vivo study. Clin Radiol 57:846–49PubMed
28.
Zurück zum Zitat Ascenti G, Zimbaro G, Mazziotti S, et al (2003) Vesicoureteral reflux: comparison between urosonography and radionuclide cystography. Pediatr Nephrol 18:768–71CrossRefPubMed Ascenti G, Zimbaro G, Mazziotti S, et al (2003) Vesicoureteral reflux: comparison between urosonography and radionuclide cystography. Pediatr Nephrol 18:768–71CrossRefPubMed
29.
Zurück zum Zitat Radmayr C, Oswald J, Klauser A, et al (2002) Contrast-medium enhanced reflux ultrasound in children. A comparison with radiologic imaging up to now. Urologe A 41:548–51CrossRefPubMed Radmayr C, Oswald J, Klauser A, et al (2002) Contrast-medium enhanced reflux ultrasound in children. A comparison with radiologic imaging up to now. Urologe A 41:548–51CrossRefPubMed
30.
Zurück zum Zitat Vassiou K, Vlychou M, Moisidou R, et al (2004) Contrast-enhanced sonographic detection of vesicoureteral reflux in children: comparison with voiding cystourethrography. Rofo 176:1453–457PubMed Vassiou K, Vlychou M, Moisidou R, et al (2004) Contrast-enhanced sonographic detection of vesicoureteral reflux in children: comparison with voiding cystourethrography. Rofo 176:1453–457PubMed
31.
Zurück zum Zitat Rodriguez LV, Spielman D, Herfkens RJ, et al (2001) Magnetic resonance imaging for the evaluation of hydronephrosis, reflux and renal scarring in children. J Urol 166:1023–027CrossRefPubMed Rodriguez LV, Spielman D, Herfkens RJ, et al (2001) Magnetic resonance imaging for the evaluation of hydronephrosis, reflux and renal scarring in children. J Urol 166:1023–027CrossRefPubMed
32.
Zurück zum Zitat Lee SK, Chang Y, Park NH, et al (2005) Magnetic resonance voiding cystography in the diagnosis of vesicoureteral reflux: comparative study with voiding cystourethrography. J Magn Reson Imaging 21:406–14CrossRefPubMed Lee SK, Chang Y, Park NH, et al (2005) Magnetic resonance voiding cystography in the diagnosis of vesicoureteral reflux: comparative study with voiding cystourethrography. J Magn Reson Imaging 21:406–14CrossRefPubMed
33.
Zurück zum Zitat International Reflux Study Committee (1981) Medical versus surgical treatment of primary vesicoureteral reflux: report of the International Reflux Study Committee. Pediatrics 67:392–00 International Reflux Study Committee (1981) Medical versus surgical treatment of primary vesicoureteral reflux: report of the International Reflux Study Committee. Pediatrics 67:392–00
34.
Zurück zum Zitat Downs SM (1999) Technical report: urinary tract infections in febrile infants and young children. The Urinary Tract Subcommittee of the American Academy of Pediatrics Committee on Quality Improvement. Pediatrics 103:e54CrossRefPubMed Downs SM (1999) Technical report: urinary tract infections in febrile infants and young children. The Urinary Tract Subcommittee of the American Academy of Pediatrics Committee on Quality Improvement. Pediatrics 103:e54CrossRefPubMed
35.
Zurück zum Zitat American Academy of Pediatrics (1999) Practice parameter: the diagnosis, treatment, and evaluation of the initial urinary tract infection in febrile infants and young children. American Academy of Pediatrics. Committee on Quality Improvement. Subcommittee on Urinary Tract Infection (1999) Pediatrics 103(4 Pt 1):843–52 American Academy of Pediatrics (1999) Practice parameter: the diagnosis, treatment, and evaluation of the initial urinary tract infection in febrile infants and young children. American Academy of Pediatrics. Committee on Quality Improvement. Subcommittee on Urinary Tract Infection (1999) Pediatrics 103(4 Pt 1):843–52
36.
Zurück zum Zitat Al-Orifi F, McGillivray D, Tange S, et al (2000) Urine culture from bag specimens in young children: are the risks too high? J Pediatr 137:221–26CrossRefPubMed Al-Orifi F, McGillivray D, Tange S, et al (2000) Urine culture from bag specimens in young children: are the risks too high? J Pediatr 137:221–26CrossRefPubMed
37.
Zurück zum Zitat Gelfand MJ, Koch BL, Cordero GG, et al (2000) Vesicoureteral reflux: subpopulations of patients defined by clinical variables. Pediatr Radiol 30:121–24CrossRefPubMed Gelfand MJ, Koch BL, Cordero GG, et al (2000) Vesicoureteral reflux: subpopulations of patients defined by clinical variables. Pediatr Radiol 30:121–24CrossRefPubMed
38.
Zurück zum Zitat Leroy S, Adamsbaum C, Marc E, et al (2005) Procalcitonin as a predictor of vesicoureteral reflux in children with a first febrile urinary tract infection. Pediatrics 115:e706–e709CrossRefPubMed Leroy S, Adamsbaum C, Marc E, et al (2005) Procalcitonin as a predictor of vesicoureteral reflux in children with a first febrile urinary tract infection. Pediatrics 115:e706–e709CrossRefPubMed
39.
Zurück zum Zitat Rushton GH (1999) Vesicoureteral reflux and scarring. In: Barratt TM, Avner ED, Harmon WE (eds) Pediatric nephrology. Lippincott Williams and Wilkins, Philadelphia, pp 851–57 Rushton GH (1999) Vesicoureteral reflux and scarring. In: Barratt TM, Avner ED, Harmon WE (eds) Pediatric nephrology. Lippincott Williams and Wilkins, Philadelphia, pp 851–57
40.
Zurück zum Zitat Hollowell JG, Greenfield SP (2002) Screening siblings for vesicoureteral reflux. J Urol 168:2138–141CrossRefPubMed Hollowell JG, Greenfield SP (2002) Screening siblings for vesicoureteral reflux. J Urol 168:2138–141CrossRefPubMed
41.
Zurück zum Zitat Noe HN (1992) The long-term results of prospective sibling reflux screening. J Urol 148(5 Pt 2):1739–742PubMed Noe HN (1992) The long-term results of prospective sibling reflux screening. J Urol 148(5 Pt 2):1739–742PubMed
42.
Zurück zum Zitat Wan J, Greenfield SP, Ng M, et al (1996) Sibling reflux: a dual center retrospective study. J Urol 156(2 Pt 2):677–79PubMed Wan J, Greenfield SP, Ng M, et al (1996) Sibling reflux: a dual center retrospective study. J Urol 156(2 Pt 2):677–79PubMed
43.
Zurück zum Zitat Kaefer M, Curran M, Treves ST, et al (2000) Sibling vesicoureteral reflux in multiple gestation births. Pediatrics 105(4 Pt 1):800–04CrossRefPubMed Kaefer M, Curran M, Treves ST, et al (2000) Sibling vesicoureteral reflux in multiple gestation births. Pediatrics 105(4 Pt 1):800–04CrossRefPubMed
45.
Zurück zum Zitat Puri P, Cascio S, Lakshmandass G, et al (1998) Urinary tract infection and renal damage in sibling vesicoureteral reflux. J Urol 160(3 Pt 2):1028–030; discussion 1038PubMed Puri P, Cascio S, Lakshmandass G, et al (1998) Urinary tract infection and renal damage in sibling vesicoureteral reflux. J Urol 160(3 Pt 2):1028–030; discussion 1038PubMed
46.
Zurück zum Zitat Houle AM, Cheikhelard A, Barrieras D, et al (2004) Impact of early screening for reflux in siblings on the detection of renal damage. BJU Int 94:123–25CrossRefPubMed Houle AM, Cheikhelard A, Barrieras D, et al (2004) Impact of early screening for reflux in siblings on the detection of renal damage. BJU Int 94:123–25CrossRefPubMed
47.
Zurück zum Zitat Ataei N, Madani A, Habibi R, et al (2005) Evaluation of acute pyelonephritis with DMSA scans in children presenting after the age of 5 years. Pediatr Nephrol 20:1439–444CrossRefPubMed Ataei N, Madani A, Habibi R, et al (2005) Evaluation of acute pyelonephritis with DMSA scans in children presenting after the age of 5 years. Pediatr Nephrol 20:1439–444CrossRefPubMed
48.
Zurück zum Zitat Wang YT, Chiu NT, Chen MJ, et al (2005) Correlation of renal ultrasonographic findings with inflammatory volume from dimercaptosuccinic acid renal scans in children with acute pyelonephritis. J Urol 173:190–94; discussion 194PubMedCrossRef Wang YT, Chiu NT, Chen MJ, et al (2005) Correlation of renal ultrasonographic findings with inflammatory volume from dimercaptosuccinic acid renal scans in children with acute pyelonephritis. J Urol 173:190–94; discussion 194PubMedCrossRef
49.
Zurück zum Zitat Moorthy I, Wheat D, Gordon I (2004) Ultrasonography in the evaluation of renal scarring using DMSA scan as the gold standard. Pediatr Nephrol 19:153–56CrossRefPubMed Moorthy I, Wheat D, Gordon I (2004) Ultrasonography in the evaluation of renal scarring using DMSA scan as the gold standard. Pediatr Nephrol 19:153–56CrossRefPubMed
50.
Zurück zum Zitat Smellie JM, Ransley PG, Normand IC, et al (1985) Development of new renal scars: a collaborative study. Br Med J (Clin Res Ed) 290:1957–960CrossRef Smellie JM, Ransley PG, Normand IC, et al (1985) Development of new renal scars: a collaborative study. Br Med J (Clin Res Ed) 290:1957–960CrossRef
51.
Zurück zum Zitat Shimada K, Matsui T, Ogino T, et al (1989) New development and progression of renal scarring in children with primary VUR. Int Urol Nephrol 21:153–58CrossRefPubMed Shimada K, Matsui T, Ogino T, et al (1989) New development and progression of renal scarring in children with primary VUR. Int Urol Nephrol 21:153–58CrossRefPubMed
52.
Zurück zum Zitat Sairam S, Al-Habib A, Sasson S, et al (2001) Natural history of fetal hydronephrosis diagnosed on mid-trimester ultrasound. Ultrasound Obstet Gynecol 17:191–96CrossRefPubMed Sairam S, Al-Habib A, Sasson S, et al (2001) Natural history of fetal hydronephrosis diagnosed on mid-trimester ultrasound. Ultrasound Obstet Gynecol 17:191–96CrossRefPubMed
53.
Zurück zum Zitat Ismaili K, Hall M, Donner C, et al (2003) Results of systematic screening for minor degrees of fetal renal pelvis dilatation in an unselected population. Am J Obstet Gynecol 188:242–46CrossRefPubMed Ismaili K, Hall M, Donner C, et al (2003) Results of systematic screening for minor degrees of fetal renal pelvis dilatation in an unselected population. Am J Obstet Gynecol 188:242–46CrossRefPubMed
54.
Zurück zum Zitat Grandjean H, Larroque D, Levi S (1999) The performance of routine ultrasonographic screening of pregnancies in the Eurofetus Study. Am J Obstet Gynecol 181:446–54CrossRefPubMed Grandjean H, Larroque D, Levi S (1999) The performance of routine ultrasonographic screening of pregnancies in the Eurofetus Study. Am J Obstet Gynecol 181:446–54CrossRefPubMed
55.
Zurück zum Zitat National Birth Defects Prevention Network (2004) Birth defects surveillance data from selected states, 1997–001. Birth Defects Research 70 (part A):677–71 National Birth Defects Prevention Network (2004) Birth defects surveillance data from selected states, 1997–001. Birth Defects Research 70 (part A):677–71
56.
Zurück zum Zitat Adra AM, Mejides AA, Dennaoui MS, et al (1995) Fetal pyelectasis: is it always ‘physiologic– Am J Obstet Gynecol 173:1263–266CrossRefPubMed Adra AM, Mejides AA, Dennaoui MS, et al (1995) Fetal pyelectasis: is it always ‘physiologic– Am J Obstet Gynecol 173:1263–266CrossRefPubMed
57.
Zurück zum Zitat Kapadia H, Lidefelt KJ, Erasmie U, et al (2004) Antenatal renal pelvis dilatation emphasizing vesicoureteric reflux: two-year follow-up of minor postnatal dilatation. Acta Paediatr 93:336–39CrossRefPubMed Kapadia H, Lidefelt KJ, Erasmie U, et al (2004) Antenatal renal pelvis dilatation emphasizing vesicoureteric reflux: two-year follow-up of minor postnatal dilatation. Acta Paediatr 93:336–39CrossRefPubMed
58.
Zurück zum Zitat Vanara F, Bergeretti F, Gaglioti P, et al (2004) Economic evaluation of ultrasound screening options for structural fetal malformations. Ultrasound Obstet Gynecol 24:633–39CrossRefPubMed Vanara F, Bergeretti F, Gaglioti P, et al (2004) Economic evaluation of ultrasound screening options for structural fetal malformations. Ultrasound Obstet Gynecol 24:633–39CrossRefPubMed
59.
Zurück zum Zitat Roberts T, Henderson J, Mugford M, et al (2002) Antenatal ultrasound screening for fetal abnormalities: a systematic review of studies of cost and cost effectiveness. BJOG 109:44–6CrossRefPubMed Roberts T, Henderson J, Mugford M, et al (2002) Antenatal ultrasound screening for fetal abnormalities: a systematic review of studies of cost and cost effectiveness. BJOG 109:44–6CrossRefPubMed
60.
Zurück zum Zitat Romano PS, Waitzman NJ (1998) Can decision analysis help us decide whether ultrasound screening for fetal anomalies is worth it? Ann N Y Acad Sci 847:154–72CrossRefPubMed Romano PS, Waitzman NJ (1998) Can decision analysis help us decide whether ultrasound screening for fetal anomalies is worth it? Ann N Y Acad Sci 847:154–72CrossRefPubMed
61.
Zurück zum Zitat Ewigman BG, Crane JP, Frigoletto FD, et al (1993) Effect of prenatal ultrasound screening on perinatal outcome. RADIUS Study Group. N Engl J Med 329:821–27CrossRefPubMed Ewigman BG, Crane JP, Frigoletto FD, et al (1993) Effect of prenatal ultrasound screening on perinatal outcome. RADIUS Study Group. N Engl J Med 329:821–27CrossRefPubMed
62.
Zurück zum Zitat Aksu N, Yavascan O, Kangin M, et al (2005) Postnatal management of infants with antenatally detected hydronephrosis. Pediatr Nephrol 20:1253–259CrossRefPubMed Aksu N, Yavascan O, Kangin M, et al (2005) Postnatal management of infants with antenatally detected hydronephrosis. Pediatr Nephrol 20:1253–259CrossRefPubMed
63.
Zurück zum Zitat Gloor JM, Ramsey PS, Ogburn PL Jr, et al (2002) The association of isolated mild fetal hydronephrosis with postnatal vesicoureteral reflux. J Matern Fetal Neonatal Med 12:196–00PubMed Gloor JM, Ramsey PS, Ogburn PL Jr, et al (2002) The association of isolated mild fetal hydronephrosis with postnatal vesicoureteral reflux. J Matern Fetal Neonatal Med 12:196–00PubMed
64.
Zurück zum Zitat Phan V, Traubici J, Hershenfield B, et al (2003) Vesicoureteral reflux in infants with isolated antenatal hydronephrosis. Pediatr Nephrol 18:1224–228CrossRefPubMed Phan V, Traubici J, Hershenfield B, et al (2003) Vesicoureteral reflux in infants with isolated antenatal hydronephrosis. Pediatr Nephrol 18:1224–228CrossRefPubMed
65.
Zurück zum Zitat Herndon CD, McKenna PH, Kolon TF, et al (1999) A multicenter outcomes analysis of patients with neonatal reflux presenting with prenatal hydronephrosis. J Urol 162(3 Pt 2):1203–208PubMed Herndon CD, McKenna PH, Kolon TF, et al (1999) A multicenter outcomes analysis of patients with neonatal reflux presenting with prenatal hydronephrosis. J Urol 162(3 Pt 2):1203–208PubMed
66.
Zurück zum Zitat Brophy MM, Austin PF, Yan Y, et al (2002) Vesicoureteral reflux and clinical outcomes in infants with prenatally detected hydronephrosis. J Urol 168(4 Pt 2):1716–719; discussion 1719CrossRefPubMed Brophy MM, Austin PF, Yan Y, et al (2002) Vesicoureteral reflux and clinical outcomes in infants with prenatally detected hydronephrosis. J Urol 168(4 Pt 2):1716–719; discussion 1719CrossRefPubMed
67.
Zurück zum Zitat McIlroy PJ, Abbott GD, Anderson NG, et al (2000) Outcome of primary vesicoureteric reflux detected following fetal renal pelvic dilatation. J Paediatr Child Health 36:569–73CrossRefPubMed McIlroy PJ, Abbott GD, Anderson NG, et al (2000) Outcome of primary vesicoureteric reflux detected following fetal renal pelvic dilatation. J Paediatr Child Health 36:569–73CrossRefPubMed
68.
Zurück zum Zitat Davey MS, Zerin JM, Reilly C, et al (1997) Mild renal pelvic dilatation is not predictive of vesicoureteral reflux in children. Pediatr Radiol 27:908–11CrossRefPubMed Davey MS, Zerin JM, Reilly C, et al (1997) Mild renal pelvic dilatation is not predictive of vesicoureteral reflux in children. Pediatr Radiol 27:908–11CrossRefPubMed
69.
Zurück zum Zitat Jaswon MS, Dibble L, Puri S, et al (1999) Prospective study of outcome in antenatally diagnosed renal pelvis dilatation. Arch Dis Child Fetal Neonatal Ed 80:F135–F138CrossRefPubMed Jaswon MS, Dibble L, Puri S, et al (1999) Prospective study of outcome in antenatally diagnosed renal pelvis dilatation. Arch Dis Child Fetal Neonatal Ed 80:F135–F138CrossRefPubMed
70.
Zurück zum Zitat Mahant S, Friedman J, MacArthur C (2002) Renal ultrasound findings and vesicoureteral reflux in children hospitalised with urinary tract infection. Arch Dis Child 86:419–20CrossRefPubMed Mahant S, Friedman J, MacArthur C (2002) Renal ultrasound findings and vesicoureteral reflux in children hospitalised with urinary tract infection. Arch Dis Child 86:419–20CrossRefPubMed
71.
Zurück zum Zitat Penido Silva JM, Oliveira EA, Diniz JS, et al (2006) Clinical course of prenatally detected primary vesicoureteral reflux. Pediatr Nephrol 21:86–1CrossRefPubMed Penido Silva JM, Oliveira EA, Diniz JS, et al (2006) Clinical course of prenatally detected primary vesicoureteral reflux. Pediatr Nephrol 21:86–1CrossRefPubMed
72.
Zurück zum Zitat Ylinen E, Ala-Houhala M, Wikstrom S (2003) Risk of renal scarring in vesicoureteral reflux detected either antenatally or during the neonatal period. Urology 61:1238–242; discussion 1242–243CrossRefPubMed Ylinen E, Ala-Houhala M, Wikstrom S (2003) Risk of renal scarring in vesicoureteral reflux detected either antenatally or during the neonatal period. Urology 61:1238–242; discussion 1242–243CrossRefPubMed
73.
Zurück zum Zitat Upadhyay J, McLorie GA, Bolduc S, et al (2003) Natural history of neonatal reflux associated with prenatal hydronephrosis: long-term results of a prospective study. J Urol 169:1837–841; discussion 1841; author reply 1841CrossRefPubMed Upadhyay J, McLorie GA, Bolduc S, et al (2003) Natural history of neonatal reflux associated with prenatal hydronephrosis: long-term results of a prospective study. J Urol 169:1837–841; discussion 1841; author reply 1841CrossRefPubMed
74.
Zurück zum Zitat Eckoldt F, Woderich R, Wolke S, et al (2003) Follow-up of unilateral multicystic kidney dysplasia after prenatal diagnosis. J Matern Fetal Neonatal Med 14:177–86PubMed Eckoldt F, Woderich R, Wolke S, et al (2003) Follow-up of unilateral multicystic kidney dysplasia after prenatal diagnosis. J Matern Fetal Neonatal Med 14:177–86PubMed
75.
Zurück zum Zitat Flack CE, Bellinger MF (1993) The multicystic dysplastic kidney and contralateral vesicoureteral reflux: protection of the solitary kidney. J Urol 150:1873–874PubMed Flack CE, Bellinger MF (1993) The multicystic dysplastic kidney and contralateral vesicoureteral reflux: protection of the solitary kidney. J Urol 150:1873–874PubMed
76.
Zurück zum Zitat Selzman AA, Elder JS (1995) Contralateral vesicoureteral reflux in children with a multicystic kidney. J Urol 153:1252–254CrossRefPubMed Selzman AA, Elder JS (1995) Contralateral vesicoureteral reflux in children with a multicystic kidney. J Urol 153:1252–254CrossRefPubMed
77.
Zurück zum Zitat Guarino N, Casamassima MG, Tadini B, et al (2005) Natural history of vesicoureteral reflux associated with kidney anomalies. Urology 65:1208–211CrossRefPubMed Guarino N, Casamassima MG, Tadini B, et al (2005) Natural history of vesicoureteral reflux associated with kidney anomalies. Urology 65:1208–211CrossRefPubMed
78.
Zurück zum Zitat Elder JS, Peters CA, Arant BS Jr, et al (1997) Pediatric Vesicoureteral Reflux Guidelines Panel summary report on the management of primary vesicoureteral reflux in children. J Urol 157:1846–851CrossRefPubMed Elder JS, Peters CA, Arant BS Jr, et al (1997) Pediatric Vesicoureteral Reflux Guidelines Panel summary report on the management of primary vesicoureteral reflux in children. J Urol 157:1846–851CrossRefPubMed
79.
Zurück zum Zitat Rushton GH (2004) Vesicoureteral reflux and scarring. In: Avner ED, Harmon WE, Niaudet P (eds) Pediatric nephrology. Lippincott Williams and Wilkins, Philadelphia, pp 1027–048 Rushton GH (2004) Vesicoureteral reflux and scarring. In: Avner ED, Harmon WE, Niaudet P (eds) Pediatric nephrology. Lippincott Williams and Wilkins, Philadelphia, pp 1027–048
80.
Zurück zum Zitat Elder JS (2000) Vesicoureteral reflux. In: Behrman RE, Kliegman RM, Jenson HB (eds) Nelson’s textbook of pediatrics. Saunders, Philadelphia, pp 1625–629 Elder JS (2000) Vesicoureteral reflux. In: Behrman RE, Kliegman RM, Jenson HB (eds) Nelson’s textbook of pediatrics. Saunders, Philadelphia, pp 1625–629
81.
Zurück zum Zitat Elder JS, Snyder HM, Peters C, et al (1992) Variations in practice among urologists and nephrologists treating children with vesicoureteral reflux. J Urol 148(2 Pt 2):714–17PubMed Elder JS, Snyder HM, Peters C, et al (1992) Variations in practice among urologists and nephrologists treating children with vesicoureteral reflux. J Urol 148(2 Pt 2):714–17PubMed
82.
Zurück zum Zitat Thompson M, Simon SD, Sharma V, et al (2005) Timing of follow-up voiding cystourethrogram in children with primary vesicoureteral reflux: development and application of a clinical algorithm. Pediatrics 115:426–34CrossRefPubMed Thompson M, Simon SD, Sharma V, et al (2005) Timing of follow-up voiding cystourethrogram in children with primary vesicoureteral reflux: development and application of a clinical algorithm. Pediatrics 115:426–34CrossRefPubMed
83.
84.
Zurück zum Zitat Cooper CS, Chung BI, Kirsch AJ, et al (2000) The outcome of stopping prophylactic antibiotics in older children with vesicoureteral reflux. J Urol 163:269–72; discussion 272–73CrossRefPubMed Cooper CS, Chung BI, Kirsch AJ, et al (2000) The outcome of stopping prophylactic antibiotics in older children with vesicoureteral reflux. J Urol 163:269–72; discussion 272–73CrossRefPubMed
85.
Zurück zum Zitat Thompson RH, Chen JJ, Pugach J, et al (2001) Cessation of prophylactic antibiotics for managing persistent vesicoureteral reflux. J Urol 166:1465–469CrossRefPubMed Thompson RH, Chen JJ, Pugach J, et al (2001) Cessation of prophylactic antibiotics for managing persistent vesicoureteral reflux. J Urol 166:1465–469CrossRefPubMed
86.
Zurück zum Zitat Hellerstein S, Nickell E (2002) Prophylactic antibiotics in children at risk for urinary tract infection. Pediatr Nephrol 17:506–10CrossRefPubMed Hellerstein S, Nickell E (2002) Prophylactic antibiotics in children at risk for urinary tract infection. Pediatr Nephrol 17:506–10CrossRefPubMed
87.
Zurück zum Zitat Grossklaus DJ, Pope JC, Adams MC, et al (2001) Is postoperative cystography necessary after ureteral reimplantation? Urology 58:1041–045CrossRefPubMed Grossklaus DJ, Pope JC, Adams MC, et al (2001) Is postoperative cystography necessary after ureteral reimplantation? Urology 58:1041–045CrossRefPubMed
Metadaten
Titel
Applying the ALARA concept to the evaluation of vesicoureteric reflux
verfasst von
Richard S. Lee
David A. Diamond
Jeanne S. Chow
Publikationsdatum
01.09.2006
Verlag
Springer-Verlag
Erschienen in
Pediatric Radiology / Ausgabe Sonderheft 2/2006
Print ISSN: 0301-0449
Elektronische ISSN: 1432-1998
DOI
https://doi.org/10.1007/s00247-006-0185-3

Weitere Artikel der Sonderheft 2/2006

Pediatric Radiology 2/2006 Zur Ausgabe

Ein Drittel der jungen Ärztinnen und Ärzte erwägt abzuwandern

07.05.2024 Medizinstudium Nachrichten

Extreme Arbeitsverdichtung und kaum Supervision: Dr. Andrea Martini, Sprecherin des Bündnisses Junge Ärztinnen und Ärzte (BJÄ) über den Frust des ärztlichen Nachwuchses und die Vorteile des Rucksack-Modells.

Endlich: Zi zeigt, mit welchen PVS Praxen zufrieden sind

IT für Ärzte Nachrichten

Darauf haben viele Praxen gewartet: Das Zi hat eine Liste von Praxisverwaltungssystemen veröffentlicht, die von Nutzern positiv bewertet werden. Eine gute Grundlage für wechselwillige Ärzte und Psychotherapeuten.

Akuter Schwindel: Wann lohnt sich eine MRT?

28.04.2024 Schwindel Nachrichten

Akuter Schwindel stellt oft eine diagnostische Herausforderung dar. Wie nützlich dabei eine MRT ist, hat eine Studie aus Finnland untersucht. Immerhin einer von sechs Patienten wurde mit akutem ischämischem Schlaganfall diagnostiziert.

Screening-Mammografie offenbart erhöhtes Herz-Kreislauf-Risiko

26.04.2024 Mammografie Nachrichten

Routinemäßige Mammografien helfen, Brustkrebs frühzeitig zu erkennen. Anhand der Röntgenuntersuchung lassen sich aber auch kardiovaskuläre Risikopatientinnen identifizieren. Als zuverlässiger Anhaltspunkt gilt die Verkalkung der Brustarterien.

Update Radiologie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.