Clinical outcome and follow-up of prenatal hydronephrosis |
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Authors: | Arye Blachar Yoram Blachar Pinhas M. Livne Loreta Zurkowski Deborah Pelet Benjamin Mogilner |
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Affiliation: | (1) School of Medicine, Ben-Gurion University of the Negev, Beer-Sheva, Israel;(2) Department of Pediatric Nephrology, Kaplan Hospital, 76100 Rehovot, Israel;(3) Department of Radiology, Kaplan Hospital, 76100 Rehovot, Israel;(4) Department of Nuclear Medicine, Kaplan Hospital, 76100 Rehovot, Israel;(5) Department of Neonatology, Kaplan Hospital, 76100 Rehovot, Israel;(6) Division of Pediatric Urology, Beilinson Hospital, Petah Tikva, Israel |
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Abstract: | Between 1987 and 1991, 160 hydronephrotic kidneys were diagnosed prenatally and confirmed postnatally in 100 infants. The aim of the study was to describe the natural history and management of primary hydronephrosis detected prenatally. We devised a new classification of obstructive uropathy outcome using ultrasonography and the diethylenetriamine penta-acetic acid scan. Accordingly, we classified the patients as having mild, moderate or severe hydronephrosis. Nine patients had pyeloplasties and 5 had ureteric reimplantations. We conclude that in most cases there is no need for immediate surgery, and that the initial approach to the management of congenital hydronephrosis should be conservative. We suggest that anti-bacterial prophylaxis be conventionally given to infants with vesicoureteral reflux and for the first 6 months of life to infants demonstrating moderate to severe newborn primary hydronephrosis.Presented by A.B. in partial fulfillment of the requirements for the M.D. degree at the School of Medicine, Soroka Medical Center-Ben Gurion University of the Negev, Beer-sheva, Israel. |
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Keywords: | Prenatal hydronephrosis Obstructive uropathy Sonography Diuretic renography Ureteropelvic junction stenosis Pyeloplasty |
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