26 research outputs found

    Evaluation of discontinuation of antibacterial prophylaxis in children with vesicoureteral reflux

    Get PDF
    زمینه و هدف: ریفلاکس وزیکویورترال ( VUR ) مهمترین علت زمینه ساز عفونت ادراری در کودکان است. جهت جلوگیری از عفونت ادراری در کودکان با ریفلاکس وزیکویورترال، از آنتی بیوتیک پروفیلاکسی استفاده می شود که می تواند با عدم پذیرش خانواده به دلیل مصرف طولانی مدت دارو همراه باشد. این مطالعه با هدف مقایسه قطع و عدم قطع داروی پروفیلاکسی در کودکان با ریفلاکس وزیکویورترال درجه 1 و 2 انجام شده است. روش بررسی: در این مطالعه نیمه تجربی 54 کودک مبتلا به ریفلاکس وزیکویورترال درجه 1 یا 2 و بالای 5 سال که طی یکسال گذشته فاقد عفونت ادراری بودند به روش در دسترس انتخاب شدند. کودکان به صورت یک در میان به دو گروه قطع (32 کودک) و ادامه (21 کودک) درمان تقسیم و حداقل به مدت 12 ماه پیگیری شدند. میزان عود عفونت در دو گروه مورد مقایسه قرار گرفت. جهت بررسی آماری از آزمون های آماری کای دو ، t ، Logrank و تحلیل رگرسیون کاکسی استفاده شد. یافته ها: میانگین سن کودکان 5/2 ± 8/7 سال و 8/77 دختر بودند. در گروه قطع درمان 5 مورد و در گروه ادامه درمان 7 مورد عود عفونت وجود داشت (05/0 P> ). شانس عود عفونت در دختران 5/1 برابر پسران (05/0 P> ) و در کودکان زیر 7 سال 5 برابر کودکان بالای 7 سال بود (033/0= P ). نتیجه گیری: قطع دارو در کودکان بالای 5 سال با ریفلاکس وزیکویورترال درجه 1یا2 ریسک عود عفونت ادراری را افزایش نداده و قطع درمان پروفیلاکسی می تواند یک روش مطمئن و بی خطر باشد

    Rubinstein-Taybi Syndrome; A Case Report

    Get PDF
    ObjectiveRubinstein-Taybi Syndrome is a rare genetic disorder with characteristic featuresincluding downward slanting palpebral fissures, broad thumbs and halluces,and mental retardation. Systemic features may involve cardiac, auditory,ophthalmic, endocrine, nervous, renal and respiratory systems. This syndromeis sporadic in nature and has been linked to microdeletion at 16p 13.3 encodingCREB-binding protein gene (CREBBP). We report a 15-years-old girl, a knowncase of chronic renal failure, with downward slanting palpebral fissures towardthe ears, hypertelorism, short stature, beaked nose, micrognathia, strabismus,dental anomalies, large toes, broad thumbs, and mental retardation.Key words: Rubinstein-Taybi syndrome; chromosome 16p 13.3; mentalretardation; CBP gene.  

    Causes of Recurrent Urinary Tract Infection in Children on Prophylaxis

    Get PDF
     Introduction: Urinary tract infection (UTI) is a common pediatric problem. It has been estimated that 8% of girls and 2% of boys suffer from UTI during childhood. So, prevention of scar formation in high risk children is very important. This study was performed to evaluate the causes of recurrent urinary tract infection in children on prophylaxis. Materials & Methods: This study was performed on 141 cases in 126 children with recurrent UTI. A questionnaire was prepared and data including sex, age, grade of vesicoureteral reflux, and antibiotic used for prophylaxis were collected. Results: The mean age of the patients was 46.6±41.1 months; 24 % of the participants were male and 76% were female. The most common predisposing factor of recurrent UTI was vesicoureteral reflux. E.coli was the microorganism responsible for most of the cases (85.5%). In 85.5% of the children, Co-trimoxazole was used as prophylaxis. Drug resistance was the most common reason of recurrence. Conclusions: We conclude that girls are at higher risk of recurrent infection and regarding the high prevalence of Co-trimoxazole resistance, administration of this drug should be limited and with caution. Keywords: Urinary tract infections; Vesico-Ureteral Reflux; Drug resistance; Chil

    A case report of nephrotic syndrome with hemorrhage of intracerebral in cerebral venous thrombosis

    Get PDF
    Introduction: Cerebral vein thrombosis is a rare complication of nephrotic syndrome (NS).We report a known case of NS with hemorrhagic thrombosis. Case report: A boy with previous history of NS was admitted with headache and decrease of level of consciousness and his brain images were revealed hemorrhagic thrombosis Conclusions: Cerebral vein thrombosis must be considered in patients with history of NS (especially in new cases and during of relapses) and prevention of hemoconcentration is very important to decrease thrombosis risk

    Tacrolimus and diabetic ketoacidosis after kidney transplantation in a 15-year-old girl (Case Report)

    Get PDF
    Tacrolimus is a main drug for induction and maintenance immunosuppression for patients with kidney transplants in many centers. One of important side effect of drug is post-transplant diabetes mellitus. Of course, diabetes ketoacidosis (DKA) is rare. In this report, a 12-year-old girl with DKA was presented after 45 days of kidney transplantation

    CSWS Versus SIADH as the Probable Causes of Hyponatremia in Children With Acute CNS Disorders

    Get PDF
    How to Cite This Article: Sorkhi H, Salehi Omran MR, Barari Savadkoohi R, Baghdadi F, Nakhjavani N, Bijani A. CSWS versus SIADH as the probable Causes of Hyponatremia in Children with Acute CNS Disorders. Iran J Child Neurol. 2013 Summer;7(3): 34-39. ObjectiveThere is a major problem about the incidence, diagnosis, and differentiation of cerebral salt wasting syndrome (CSWS) and syndrome of inappropriate secretion of antidiuretic hormone (SIADH) in patients with acute central nervous system (CNS) disorders. According to rare reports of these cases, this study was performed in children with acute CNS disorders for diagnosis of CSWS versus SIADH.Materials & MethodsThis prospective study was done on children with acute CNS disorders. The definition of CSWS was hyponatremia (serum sodium ≤130 mEq/L), urine volume output ≥3 ml/kg/hr, urine specific gravity ≥1020 and urinary sodium concentration ≥100 mEq/L. Also, patients with hyponatremia (serum sodium ≤130 mEq/L), urine output < 3 ml/kg/hr, urine specific gravity ≥1020, and urinary sodium concentration >20 mEq/L were considered to have SIADH.ResultsOut of 102 patients with acute CNS disorders, 62 (60.8%) children were male with mean age of 60.47±42.39 months. Among nine children with hyponatremia (serum sodium ≥130 mEq/L), 4 children had CSWS and 3 patients had SIADH.In 2 cases, the cause of hyponatremia was not determined. The mean day of hyponatremia after admission was 5.11±3.31 days. It was 5.25±2.75 and 5.66± 7.23 days in children with CSWS and SIADH, respectively. Also, the urine sodium (mEq/L) was 190.5±73.3 and 58.7±43.8 in patients with CSWS and SIADH, respectively.ConclusionAccording to the results of this study, the incidence of CSWS was more than SIADH in children with acute CNS disorders. So, more attention is needed to differentiate CSWS versus SIADH in order to their different management.References1. Peters JP, Welt LG, Sims EAH. A salt wasting syndromeassociated with cerebral disease. Trans Assoc Am Physiciants 1957;63:57-64.2. Schwartz WB, Bennett W, Curelop S. A syndrome of renal sodium loss and hyponatremia probably resulting from inappropriate secretion of antiduretic hormone. Am J Med 1950:23(4); 529-42.3. Hasan D, Wijdicks EF, Vermeulen M. Hyponatremia is associated with cerebral ischemia in patients with aneurysmal subarachnoid hemorrhage. Ann Neurol 1990;27(1):106-8.4. Sherlock M, O’Sullivan E, Agha A, Behan LA, Rawluk D, Brennan P, et al. The incidence and pathophysiology of hyponatraemia after subarachnoid haemorrhage. Clin Endocrinol (Oxf). 2006;64(3):250-4.5. Wartenberg KE, Schmidt JM, Claassen J, Temes RE, Frontera JA, Ostapkovich N, et al. Impact of medical complications on outcome after subarachnoid hemorrhage. Crit Care Med 2006;34(3):617-23; quiz 624. 6. Qureshi AI, Suri MF, Sung GY, Straw RN, Yahia AM, Saad M, et al. Prognostic significance of hypernatremia and hyponatremia among patients with aneurysmal subarachnoid hemorrhage. Neurosurgery 2002;50(4):749-55.7. Bianchetti MG, Simonetti GD, Bettinelli A. Body fluids and salt metabolism - Part I. Ital J Pediatr 200919;35(1):36.8. Peruzzo M, Milani GP, Garzoni L, Longoni L, Simonetti GD, Bettinelli A, et al. Body fluids and salt metabolism - part II. Ital J Pediatr 2010;36(1):78.9. Moritz ML, Ayus JC. New aspects in the pathogenesis, prevention, and treatment of hyponatremic encephalopathy in children. Pediatr Nephrol. 2010;25(7):1225-38.10. Albanese A, Hindmarsh P, Stanhope R. Management ofhyponatraemia in patients with acute cerebral insults. Arch Dis Child 2001;85(3):246-51. 11. Brimioulle S, Orellana-Jimenez C, Aminian A, Vincent JL. Hyponatremia in neurological patients: cerebral salt wasting versus inappropriate antidiuretic hormone secretion. Intensive Care Med 2008;34(1):125-31.12. Yee AH, Burns JD, Wijdicks EF. Cerebral salt wasting: pathophysiology, diagnosis, and treatment. Neurosurg Clin N Am 2010;21(2):339-52.13. Palmer BF. Hyponatraemia in a neurosurgical patient: syndrome of inappropriate antidiuretic hormone secretion versus cerebral salt wasting. Nephrol Dial Transplant 2000;15(2):262-8.14. Rivkees SA. Differentiation appropriate antiduretic hormone secretion, inappropriate antiduretic secretion and cerebral salt wasting: the common, uncommon, and misnamed. Curr Opin Pediatr 2008;20(4):448-52.15. Sterns RH, Silver SM. Cerebral salt wasting versus SIADH:What difference? J Am Soc Nephrol 2008;19(2):194-6.16. Jiménez R, Casado-Flores J, Nieto M, García-Teresa MA. Cerebral salt wasting syndrome in children with acute central nervous system injury. Pediatr Neurol 2006;35(4):261-3.17. Bartter FC, Schwartz WB. Syndrome of inappropriate secretion of antidiuretic hormone. Am J Med 1967;42:790- 806.18. Verbalis JG. Pathogenesis of hyponatremia in an experimental model of the syndrome of inappropriate antidiuresis. Am J Physiol 1994;267(6 Pt 2):R1617-25.19. Harrigan MR. Cerebral salt wasting syndrome: a review.Neurosurgery 1996;38(1):152-60.20. Inatomi J, Yokoyama Y, Sekine T, Igarashi T. A case of cerebral salt-wasting syndrome associated with aseptic meningitis in an 8-year-old boy. Pediatr Nephrol 2008;23(4):659-62.21. Brookes MJ, Gould TH. Cerebral salt wasting syndrome in meningoencephalitis: a case report. J Neurol Neurosurg Psychiatry 2003;74(2):277.22. Cuardrado-Godia E, Cerda M, Rodriguez-Campello A, Puig de Dou J. Sindrome pierde sal cerebral en las infeccioned del sistema nervioso central. Med Clin (Barc) 2007;24:128(7);229-9.23. Roca-Ribas F, Ninno JE, Gasperin A, Lucas M, Liubia C. Cerebral salt wasting syndrome as a postoperative complication after surgical resection of acoustic neuroma. Otol Neurotol 2002;23:992-5.24. Bussmann C, Bast T, Rating D. Hyponatraemia in childrenwith acute CNS disease: SIADH or cerebral salt wasting? Childs Nerv Syst 2001;17(1-2):58-62.25. Hardesty DA, Kilbaugh TJ, Storm PB. Cerebral Salt Wasting Syndrome in Post-Operative Pediatric Brain Tumor Patients. Neurocrit Care 2012;17(3):382-7.26. Agha A, Thornton E, O’Kelly P, Tormey W, Phillips J, Thompson CJ. Posterior pituitary dysfunction after traumatic brain injury. J Clin Endocrinol Metab 2004;89(12):5987-92.27. Singh S, Bohn D, Carlotti AP, Cusimano M, Rutka JT, Halperin ML. Cerebral salt wasting: truths, fallacies, theories, and challenges. Crit Care Med. 2002 Nov;30(11):2575-9.28. Carlotti AP, Bohn D, Rutka JT, Singh S, Berry WA, Sharman A, et al. A method to estimate urinary electrolyte excretion in patients at risk for developing cerebral salt wasting. J Neurosurg 2001;95(3):420-4.29. International committee for Standardization in Haematology. Recommended methods for measurement of red-cell and plasma volume. J Nucl Med 1980:21(8);793-800.30. Byeon JH, Yoo G. Cerebral salt wasting syndrome after calvarial remodeling in craniosynostosis. J Korean Med Sci 2005;20(5):866–9. 31. Gutierrez OM, Lin HY. Refractory hyponatremia. Kidney Int 2007; 71(1):79-82. 32. Maesaka JK, Imbriano LJ, Ali NM, Ilamathi E. Is it cerebral or renal salt wasting? Kidney Int 2009; 76(9):934-8.33. Maesaka JK, Venkatesan J, Piccione JM, Decker R, Dreisbach AW, Wetherington JD. Abnormal urate transport in patients with intracranial disease. Am J Kidney Dis 1992;19(1):10-5.34. Berendes E, Walter M, Cullen P, Prien T, Van Aken H, Horsthemke J, et al. Secretion of brain natriuretic peptide in patients with aneurysmal subarachnoid haemorrhage. Lancet 1997 Jan 25;349(9047):245-9.35. Kurokawa Y, Uede T, Ishiguro M, Honda O, Honmou O,Kato T, et al. Pathogenesis of hyponatremia following subarachnoid hemorrhage due to ruptured cerebral aneurysm. Surg Neurol 1996;46(5):500-7.36. Khurana VG, Wijdicks EF, Heublein DM, McClelland RL, Meyer FB, Piepgras DG, et al. A pilot study of dendroaspis natriuretic peptide in aneurysmal subarachnoid hemorrhage. Neurosurgery 2004;55(1):69- 75.37. Kaneko T, Shirakami G, Nakao K, Nagata I, Nakagawa O, Hama N, et al. C-type natriuretic peptide (CNP) is the major natriuretic peptide in human cerebrospinal fluid. Brain Res 1993;612(1-2):104-9.38. Damaraju SC, Rajshekhar V, Chandy MJ. Validation study of a central venous pressure-based protocol for the management of neurosurgical patients with hyponatremia and natriuresis. Neurosurgery 1997;40(2):312-6.39. Sivakumar V, Rajshekhar V, Chandy MJ. Management ofneurosurgical patients with hyponatremia and natriuresis.Neurosurgery 1994;34(2):269-74; discussion 274

    Glomerular filtration rate determination by creatinine and cystatin-C in patients with acute pyelonephritis

    Get PDF
    Background: Measurement of glomerular filtration rate (GFR) and monitoring of it in any patient on nephrotoxic drugs is very important. Recently, cystatin C (cys-C) has been introduced as a better marker for determining and monitoring renal function than creatinine especially in a mild decrease of GFR. This study was done to assess the change of GFR measurement based on serum Cys-C and creatinine and their comparison in children with acute pyelonephritis on amikacin. Methods: All children with acute pyelonephritis who were admitted in Nephrology ward were enrolled in this study. Serum creatinine, serum cys-C and the GFR calculation based on them were measured in patients on the day of admission (day zero) and then on days 3 and 7 after the start of treatment with amikacin and p-value less than 0.05 was considered significant. Results: Among the 70 children, 61 patients were females and the others were males. Mean age was 42.66±41.53 months. Estimated GFR based on creatinine on day 0 (before amikacin administration), 3 and 7 were 72.41±20.89 ml/min/1.73 m2, 78.42±21.15 ml/min/1.73 m2 and 80.5±22.43 ml/min/1.73 m2, respectively. Moreover, GFR based on cys-C during these days were 116.23±58.9 ml/min/1.73 m2, 116.49±53.31 ml/min/1.73 m2 and 108.37±51.02 ml/min/1.73 m2, respectively (p<0.05). Conclusions: According to this study, decrease of GFR calculation based on Cys-C was seen and estimated GFR was not changed according to creatinine. So, we recommend the use of cys-C for the monitoring of renal function in any patient treated with nephrotoxic drugs such as amikacin

    Comparison of urinary tract infection after kidney transplantation between adult and children

    Get PDF
    Background: Urinary tract infection (UTI) is an important complication after kidney transplantation (KT). UTI may cause kidney damage and dysfunction especially in children. Therefore, the aim of this study was to evaluate the risk of UTI after KT in adult and children and compare of them. Methods: This study was done in Shaheed Beheshti Hospital (Babol Medical University). All patients, after KT and during one month after their operation were followed and divided to two groups (according their ages): more than 18 years old (adults) and under 18 years old (Children). Then, their urine samples were sent for culture every 2-3 days during admition and every week after discharged and more than 100000 single colony count were defined positive culture. Data were analyzed using t-test and p<0.05 was considered important. Results: There were 508 cases and 450 patients were adult and others were children. Among them, 109 (24%) adult and 8(13.8%) children had positive urine culture, respectively (P>0.05) .In adult groups, 62 (21.6%) male and 47(28.8%) female patients had positive culture. However, in children group, 2 (6.3%) boys and 6 (23.1%) girls had positive culture, respectively (P<0.05). Conclusions: According to positive culture, there was no difference between adult and children, but females had higher risk of positive U/C than males .So, more attention was needed after KT in females

    Bacterial Agents and Antibiotic Resistance Profile in Pyelonephritis; A Comparison between Children with and without Urinary Tract Abnormalities in the North of Iran

    Get PDF
    Background:      Pyelonephritis in children is a serious condition that is commonly encountered in clinical practice. Urinary tract abnormalities increase the risk of urinary tract infections (UTIs) and consequently antibiotic resistance. Our study aimed to evaluate the local trend in terms of bacterial uropathogen resistance in Babol, Iran, in children with pyelonephritis considering urinary tract abnormalities. Methods:      We recruited pediatric cases aged 1 month to 18 years who were admitted to Amirkola hospital with a diagnosis of pyelonephritis from 2016 to 2019. Children with negative urine cultures or incomplete imaging were excluded from the study. Causative agents were identified based on biochemical features. Antimicrobial in vitro resistance tests were performed using the disk diffusion agar test. Results:      A total of 105 children were included in the study. E. coli was the most common causative agent found in 93 (88.6%) patients. Most of the bacterial isolates were sensitive to amikacin and imipenem, and only 12.4% and 13.3% of isolates were resistant to this antibiotic. On the other hand, nalidixic acid represented the least effective treatment, with a resistance rate of 88.6%. A statistically significant difference was observed in resistance to nitrofurantoin and nalidixic acid between children with and without anomalies (p < 0.05). Conclusion:      High antibiotic resistance, especially in children with urinary tract anomalies, was identified for frequently used antibiotics. Our findings provide important implications regarding local patterns of uropathogens and antibiotic resistance in children with pyelonephritis
    corecore