When is the Best Time for Voiding Cystourethrogram in Urinary Tract Infection of Children?

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ORIGINAL REPORT When is the Best Time for Voiding Cystourethrogram in Urinary Tract Infection of Children? Abolfazl Mahyar 1, Parviz Ayazi 2, Saeid Tarlan 3, Alireza Moshiri 4, Monadi Hamidfar 5, and Ameneh Barikani 6 1 Department of Pediatrics, Qazvin University of Medical Sciences, Qazvin, Iran 2 Department of Pediatrics Infectious Diseases, Qazvin University of Medical Sciences, Qazvin, Iran 3 Department of Pediatric Surgery, Qazvin University of Medical Sciences, Qazvin, Iran 4 Department of Pediatric Nephrology, Qazvin University of Medical Sciences, Qazvin, Iran 5 Department of Emergency Medicine, Qazvin University of Medical Sciences, Qazvin, Iran 6 Department of Community Medicine, Qazvin University of Medical Sciences, Qazvin, Iran Received: 8 Sep. 2011; Received in revised form: 20 Nov. 2011; Accepted: 17 Jan. 2012 Abstract- This study was conducted to investigate whether the length of the interval between a urinary tract infection and the performance of the voiding cystourethrogram influences the presence or severity of vesicoureteral reflux (VUR). In this study 161 children with first episode of urinary tract infection were evaluated. Depending on time of performance of voiding cystourethrogram (), patients divided into two groups: early (within the first 7 days following treatment) and late (during second week or thereafter of the start of treatment). The prevalence and severity of vesicoureteral reflux in both groups were compared. Out of 161patients, the early and late groups consisted of 75 and 86 patients, respectively. The prevalence of vesicouretral reflux in the early and late groups was 25.3% and 30.2%, respectively. No significant difference was observed between two groups regarding prevalence (P=0.598) and severity (P=0.379) of vesicoureteral reflux. This study showed that the prevalence and severity of VUR is not affected by timing of. Therefore, it is recommended that in children with urinary tract infection, should be done following negative urine culture as soon as possible. 2012 Tehran University of Medical Sciences. All rights reserved. Acta Medica Iranica, 2012; 50(7): 468-472. Keywords: ; VUR; UTI; Children Introduction Urinary tract infection (UTI) results from bacterial invasion to the urinary tract system. It is one of the most important causes of chronic renal failure. To prevent serious complications, early diagnosis, proper treatment and elimination of risk factors is very important (1-6). Multiple risk factors increase predisposing to UTI including renal abnormalities, constipation, hypercalciuria and vesicoureteral reflux (VUR) (1,4). VUR results from abnormal backflow of urine from the bladder to ureter and in some instance to pelvis and calyx (1). Based on previous studies, the prevalence of VUR is 25 to 40% in children with UTI (1,7). Performance of voiding cystourethrography () is necessary for diagnosis and treatment of VUR. The timing of performance is controversial. Some authors recommend that should be done 4-6 weeks after treatment of UTI (8,9). But others believe that must be done as soon as possible (10,11). Due to the controversies, this study was performed to determine the time of performance of in children with UTI hospitalized in Qazvin children hospital, Qazvin (Iran). Materials and Methods In this cross-section study, 161 children with UTI that were admitted in Qazvin children's hospital during September 2008 to March 2010 were investigated. Qazvin children hospital is affiliated to Qazvin University of Medical Sciences, Iran. All patients were younger than 12 years. Inclusion criteria included: 1- first episode of UTI 2-positive urine culture (more than 10 5 colonies of one organism per ml of urine by clean catch method or more than 10 3 colonies of one organism Corresponding Author: Abolfazl Mahyar Department of Pediatric, Qods Children Hospital, Valiasr square, Qazvin, Iran Tel: +982813334807-9, Fax: +982813344088, E-mail: Abolfazl473@yahoo.com

A. Mahyar, et al. per ml of urine by catheterization or presence of any number of colonies of organism in urine culture taken by suprapubic method). Patients with negative urine culture, presence of more than one organism in urine culture and history of more than once episode of UTI were excluded. According to the time of performance of, patients were divided into two groups: early (within the first 7 days following treatment) and late (during second week or thereafter of the start of treatment). VUR was diagnosed in all children by contrast. All were performed by the radiologist of Qazvin children's hospital. Reflux was graded according to the International Study of Reflux in children (12). Patient's data were gathered from medical records including: symptoms, laboratory tests, imaging and results of. Two groups were compared and analyzed by Chi-square and Mann-Whitney test using SPSS software. P value < 0.05 was considered significant. Results Out of 161 children with urinary tract infection 35 (21.6%) were males and 126 (78.4%) females. Minimum and maximum ages were 12 days and 132 months, respectively with median 13 months. Minimum and maximum ages in male were 30 days and 96 months, respectively with median11 months. In females similar values were 12 days and 132 months, respectively with median of 18.5 months (P=0.063). Symptoms and signs in patients included fever 142 (88%), dysuria 92 (57%), abdominal pain 55 (34%), vomiting 45 (28%), urine frequency 10 (6%) and flank pain 4 (2%). Group early late P Abnormal laboratory findings included Active urinanalysis 125 (78%), increased ESR 122 (76.3%), leukocytosis 110 (78%), positive CRP 109 (68.2%). Ultrasonography and renal DMSA scan were abnormal in 36.6% and 35.5% of patients, respectively. Abnormal sonography included pyelocalyces dilation (83.08%), hydronephrosis (25%) and ureteral dilation (20%). Pyelocalyceal dilation was more prominent in the left side (68.04%). Abnormal DMSA scan included photopenia (90.07%), decreased uptake (70.83%) and renal scar (13.4%). Positive urine culture consisted: E.coli 145 (90%), klebsiella 9 (5.5%), proteus 4 (2.48%) and staphylococcus epidermis 2 (1.24%). Antibiogram of urine culture revealed that ceftriaxone (89.98%) was most and ampicillin (19%) was least effective medicine. Out of 161 patients that performed, 75 (46.6%) belonged to the early and 86 (53.4%) to the late groups (P=0.386). Time between UTI and performance of in late group was 8-14 days 30 (34.8%), 15-21 days 15 (14.4%), 22-28 days 20 (23.2%) more than 28 days 21 (24.4%). Statistically there was no significant difference between two groups regarding the sex and average of age, (Table 1). Of 161 patients was abnormal in 45 (27.9%). The prevalence of VUR in early and late groups were 19 (25.3%) and 26 (30.2%), respectively (Table 2). No significant difference was observed between the two groups regarding the prevalence (P=0.598), severity (P=0.379) and site of VUR (P=0.775) (Tables 2-4). No significant difference was observed comparing timing in two groups regarding sonography (P=0.413) and DMSA scan (P=1) (Tables 5 and 6). Table1. Gender distribution and age average in both groups. Gender Number Median (month) 95% Confidence interval boy 15 11 6.67 40.39 girl 60 24 23.75 37.66 total 75 24 22.92 35.62 boy girl total 20 66 86 0.703 10 12 12 0.283 8.96 17.78 17.67 29.33 31.92 29.36 Table 2. Comparison of two groups regarding the prevalence of vesicoureteral reflux. Reflux yes 19 25.3 26 30.2 no 56 74.7 60 69.8 total 75 100 86 100 Chi-square test, P=0.598 Acta Medica Iranica, Vol. 50, No. 7 (2012) 469

The best time for in UTI Grade Table 3. Comparison of two groups regarding the severity of vesicoureteral reflux. I 10 52.6 8 30.8 II 6 31.6 9 34.6 III 3 15.8 8 30.8 IV 0 0.0 1 308 total 19 100 26 100 Chi-square test, P=0.379 Reflux direction Table 4. Comparison the two groups regarding the reflux site. Right 9 47.4 14 53.8 Left 7 36.8 7 26.9 Both 3 15.8 5 19.2 Total 19 100 26 100 Chi-square test, P=0.775 Sonography Table 5. Comparison of two groups regarding the sonography findings. Normal Abnormal early 50 49 24 42.1 late 52 51 33 57.9 total 102 100 57 100 Chi-square test, P=0.413 Table 6. Comparison of two groups regarding the renal DMSA scan findings. Renal DMSA scan Normal Abnormal Early 55 45.8 17 42.1 Late 65 54.2 19 57.9 Total 120 100 36 100 Chi-square test, P=1 Discussion Vesicoureteral reflux is the most common anomaly of urinary system. It is one the most important risk factor of UTI (1). VUR is backflow of urine from the bladder to the ureter and in some instance to the pelvis and the calyx (1-4). There are two types of reflux: primary and secondary. Primary type is more common and has familial and hereditary origin, and results from malfunction of ureterovesical valve. Secondary type results from increased intravesical pressure due to conditions such as neurogenic bladder or posterior urethral valves (PUV) (1,13-17). is the method of choice for diagnosis of VUR. The timing of is controversial. Many researchers suggest postponing the until 4-6 weeks after treatment. They believe that acute infection and release of endotoxins lead to transient reflux. Also, this process results in over-estimation of the grade of reflux (8,18). This suggestion was based on the results of animal studies and to our knowledge this theory has not been proved on human (19). 470 Acta Medica Iranica, Vol. 50, No. 7 (2012)

A. Mahyar, et al. According to studies in recent years, the timing of affects neither the rate nor the grade of the VUR. Soccorso et al. showed that the prevalence and severity of reflux was not statistically significant in patients who performed in the first and 2 month following UTI (20). So, they recommended, should be done as soon as possible (20). McDonald et al. revealed that timing of did not influence the prevalence and severity of reflux during the first week and later. They mentioned that the traditional recommendation to perform the at 3 to 6 weeks after the diagnosis of UTI should be reconsidered (11). Results of other studies were in accordance with report of McDonald et al. (11). They recommended that should be performed as soon as possible (9,21,22). Elder believes that should be done at the end of treatment, when discharging the patient from hospital (3). The data of this study was in accordance with recent researches. Therefore we also suggest that should be performed as soon as possible. Early performance of has following advantages: 1- It eliminates the need for antibiotic prophylaxis until the performance. 2- It is more convenient to perform this procedure at the same time as other imaging procedures are being done. 3- The patients would not be missed for. 4- This strategy relieves parental anxiety regarding the presence of VUR and increases obedience. In conclusion, this study showed that the prevalence and severity of VUR is not affected by timing of. Therefore, it is recommended that in children with UTI, should be done following negative urine culture as soon as possible. References 1. Hansson S, Jodal U. Urinary tract infection. In: Avner ED, Harmon W, Niaudet P, editors. Pediatric Nephrology. 5 th ed. Philadelphia, PA: Lippincott Williams and Wilkins; 2004. p. 1007-25. 2. Watson AR, Taylor CM, McGraw M. Urinary tract infections. In: Forfar and Arneil's Textbook of Paediatrics. 6 th ed. Edinburgh: Churchill Livingstone; 2003. p. 613-20. 3. Elder JS. Vesicoureteral reflux. In: Kliegman RM, Behrman RE, Jenson HB, Stanton BF, editors. Nelson Textbook of Pediatrics. 18 th ed. Philadelphia, PA: Saunders Elsevier; 2007. p. 2228-33. 4. Leonardo CR, Filgueiras MF, Vasconcelos MM, Vasconcelos R, Marino VP, Pires C, Pereira AC, Reis F, Oliveira EA, Lima EM. Risk factors for renal scarring in children and adolescents with lower urinary tract dysfunction. Pediatr Nephrol 2007;22(11):1891-6. 5. Ayazi P, Moshiri SA, Mahyar A, Moradi M. The effect of vitamin A on renal damage following acute pyelonephritis in children. Eur J Pediatr 2011;170(3):347-50. 6. Ayazi P, Mahyar A, Jahani Hashemi H, Daneshi M, Karimzadeh T, Salimi F. Comparison of procalcitonin and C-Reactive protein tests in children with urinary tract infection. Iran J Pediatr 2009;19(4):381 6. 7. Cleper R, Krause I, Eisenstein B, Davidovits M. Prevalence of vesicoureteral reflux in neonatal urinary tract infection. Clin Pediatr (Phila) 2004;43(7):619-25. 8. Auer J, Seager LD. Experimental local bladder edema causing urine reflux into ureter and kidney. Proc Soc Exp Biol Med, 1936,35:361 9. Hellström M, Jacobsson B. Diagnosis of vesico-ureteric reflux. Acta Paediatr Suppl 1999;88(431):3-12. 10. Mahant S, To T, Friedman J. Timing of voiding cystourethrogram in the investigation of urinary tract infections in children. J Pediatr 2001;139(4):568-71. 11. McDonald A, Scranton M, Gillespie R, Mahajan V, Edwards GA. Voiding cystourethrograms and urinary tract infections: how long to wait? Pediatrics 2000;105(4):E50. 12. Lebowitz RL, Olbing H, Parkkulainen KV, Smellie JM, Tamminen-Möbius TE. International system of radiographic grading of vesicoureteric reflux. International Reflux Study in Children. Pediatr Radiol 1985;15(2):105-9. 13. Greenbaum LA, Mesrobian HG. Vesicoureteral reflux. Pediatr Clin North Am 2006;53(3):413-27, vi. 14. Ismaili K, Avni FE, Piepsz A, Collier F, Schulman C, Hall M. Vesicoureteric reflux in children. EAU-EBU Update Series 2006;4(4):129-40. 15. Devriendt K, Groenen P, Van Esch H, van Dijck M, Van de Ven W, Fryns JP, Proesmans W. Vesico-ureteral reflux: a genetic condition? Eur J Pediatr 1998;157(4):265-71. 16. Eccles MR, Jacobs GH. The genetics of primary vesicoureteric reflux. Ann Acad Med Singapore 2000;29(3):337-45. 17. Noe HN, Wyatt RJ, Peeden JN Jr, Rivas ML. The transmission of vesicoureteral reflux from parent to child. J Urol 1992;148(6):1869-71. 18. Hellström M, Jodal U, Mårild S, Wettergren B. Ureteral dilatation in children with febrile urinary tract infection or bacteriuria. AJR Am J Roentgenol 1987;148(3):483-6. 19. Craig JC, Knight JF, Sureshkumar P, Lam A, Onikul E, Roy LP. Vesicoureteric reflux and timing of micturating cystourethrography after urinary tract infection. Arch Dis Child 1997;76(3):275-7. 20. Soccorso G, Moss G, Roberts J, Godbole P. Infantile urinary tract infection and timing of micturating cystourethrogram. 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The best time for in UTI 21. Doganis D, Mavrikou M, Delis D, Stamoyannou L, Siafas K, Sinaniotis K. Timing of voiding cystourethrography in infants with first time urinary infection. Pediatr Nephrol 2009;24(2):319-22. 22. Sathapornwajana P, Dissaneewate P, McNeil E, Vachvanichsanong P. Timing of voiding cystourethrogram after urinary tract infection. Arch Dis Child 2008;93(3):229-3. 472 Acta Medica Iranica, Vol. 50, No. 7 (2012)