Abstract
Idiopathic antenatal hydronephrosis (IAHN), defined as antenatal hydronephrosis not associated with other morphologic renal tract abnormalities, is the most common abnormality detected by antenatal ultrasound. We performed a systematic review and meta-analysis to determine the outcome of IAHN. We screened three databases and bibliographies to identify English-language original peer-reviewed papers that reported serial postnatal renal ultrasonography in children with IAHN. Patients who stabilized and/or improved were extracted and pooled according to the individual grading systems used by each study. A systematic analysis of data extracted from 25 articles revealed overall resolution of pelviectasis in milder cases of IAHN (Society of Fetal Urology [SFU] grade 1–2; anterior posterior pelvic diameter [APPD]<12 mm). In contrast, IAHN of higher severity (grades 3–4; APPD>12 mm) resolved with a lower frequency. Meta-analysis of data extracted from seven papers showed stabilization of pelviectasis in 98% of patients with grades 1–2 (95% confidence interval [CI] 0.93–1.0; p =0.0008) and in 51% of patients with grades 3–4 (95% CI 0.34–0.68; p <0.00001). Grades 1–2 pelviectasis was five times more likely to stabilize than grades 3–4 pelviectasis (odds ratio [OR] 4.69; 95% CI 1.73–12.76; p =0.002). We conclude that in patients with IAHN and lesser degrees of pelvic dilatation, pelvic diameter decreases to the normal range or does not worsen with the vast majority of patients. Further studies are needed to define outcomes, particularly in more severe forms of IAHN.
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Dudley JA, Haworth JM, McGraw ME, Frank JD, Tizard EJ (1997) Clinical relevance and implications of antenatal hydronephrosis. Arch Dis Child Fetal Neonatal Ed 76:F31–34
Ismaili K, Avni FE, Piepsz A, Wissing KM, Cochat P, Aubert D, Hall M (2004) Current management of infants with fetal renal pelvis dilation: a survey by French-speaking pediatric nephrologists and urologists. Pediatr Nephrol 19:966–971
Alconcher L, Tombesi M (2004) Mild antenatal hydronephrosis: management controversies. Pediatr Nephrol 19:819–820
Altman DG (2001) Systematic reviews of evaluations of prognostic variables. BMJ 323:224–228
Stroup DF, Berlin JA, Morton SC, Olkin I, Williamson GD, Rennie D, Moher D, Becker BJ, Sipe TA, Thacker SB (2000) Meta-analysis of observational studies in epidemiology: a proposal for reporting. Meta-analysis Of Observational Studies in Epidemiology (MOOSE) group. JAMA 283:2008–2012
DerSimonian R, Laird N (1986) Meta-analysis in clinical trials. Control Clin Trials 7:177–188
Higgins JP, Thompson SG, Deeks JJ, Altman DG (2003) Measuring inconsistency in meta-analyses. BMJ 327:557–560
Fernbach SK, Maizels M, Conway JJ (1993) Ultrasound grading of hydronephrosis: introduction to the system used by the Society for Fetal Urology. Pediatr Radiol 23:478–480
Cheng AM, Phan V, Geary DF, Rosenblum ND (2004) Outcome of isolated antenatal hydronephrosis. Arch Pediatr Adolesc Med 158:38–40
O’Flynn KJ, Gough DC, Gupta S, Lewis MA, Postlethwaite RJ (1993) Prediction of recovery in antenatally diagnosed hydronephrosis. Br J Urol 71:478–480
Lam BC, Wong SN, Yeung CY, Tang MH, Ghosh A (1993) Outcome and management of babies with prenatal ultrasonographic renal abnormalities. Am J Perinatol 10:263–268
Kitawaga H, Pringle KC, Stone P, Flower J, Murakami N, Robinson R (1998) Postnatal follow-up of hydronephrosis detected by prenatal ultrasound: the natural history. Fetal Diagn Ther 13:19–25
Liang CC, Cheng PJ, Lin CJ, Chen HW, Chao AS, Chang SD (2002) Outcome of prenatally diagnosed fetal hydronephrosis. J Reprod Med 47:27–32
Dhillon HK (1998) Prenatally diagnosed hydronephrosis: the Great Ormond Street experience. Br J Urol 81 [Suppl 2]:39–44
Morin L, Cendron M, Crombleholme TM, Garmel SH, Klauber GT, D’Alton ME (1996) Minimal hydronephrosis in the fetus: clinical significance and implications for management. J Urol 155:2047–2049
Senanayake M, Semmens M (1996) Fetal hydronephrosis, a 1-year follow-up. Ceylon Med J 41:141–143
Gloor JM, Ogburn PL Jr, Breckle RJ, Morgenstern BZ, Milliner DS (1995) Urinary tract anomalies detected by prenatal ultrasound examination at Mayo Clinic Rochester. Mayo Clin Proc 70:526–531
Misra D, Kempley ST, Hird MF (1999) Are patients with antenatally diagnosed hydronephrosis being over-investigated and overtreated? Eur J Pediatr Surg 9:303–306
Blachar A, Blachar Y, Livne PM, Zurkowski L, Pelet D, Mogilner B (1994) Clinical outcome and follow-up of prenatal hydronephrosis. Pediatr Nephrol 8:30–35
Ransley PG, Dhillon HK, Gordon I, Duffy PG, Dillon MJ, Barratt TM (1990) The postnatal management of hydronephrosis diagnosed by prenatal ultrasound. J Urol 144:584–587; discussion 593–584
Josephson S, Dhillon HK, Ransley PG (1993) Post-natal management of antenatally detected, bilateral hydronephrosis. Urol Int 51:79–84
Grignon A, Filion R, Filiatrault D, Robitaille P, Homsy Y, Boutin H, Leblond R (1986) Urinary tract dilatation in utero: classification and clinical applications. Radiology 160:645–647
Rodriguez LV, Lock J, Kennedy WA, Shortliffe LM (2001) Evaluation of sonographic renal parenchymal area in the management of hydronephrosis. J Urol 165:548–551
Takla NV, Hamilton BD, Cartwright PC, Snow BW (1998) Apparent unilateral ureteropelvic junction obstruction in the newborn: expectations for resolution. J Urol 160:2175–2178
Brandell RA, Brock JW 3rd, Hamilton BD, Cartwright PC, Snow BW (1996) Unilateral hydronephrosis in infants: are measurements of contralateral renal length useful? J Urol 156:188–189
Cost GA, Merguerian PA, Cheerasarn SP, Shortliffe LM (1996) Sonographic renal parenchymal and pelvicaliceal areas: new quantitative parameters for renal sonographic follow-up. J Urol 156:725–729
Koff SA, Campbell K (1992) Nonoperative management of unilateral neonatal hydronephrosis. J Urol 148:525–531
Koff SA, Campbell KD (1994) The nonoperative management of unilateral neonatal hydronephrosis: natural history of poorly functioning kidneys. J Urol 152:593–595
Kletscher B, de Badiola F, Gonzalez R (1991) Outcome of hydronephrosis diagnosed antenatally. J Pediatr Surg 26:455–459; discussion 459–460
Hafez AT, McLorie G, Bagli D, Khoury A (2002) Analysis of trends on serial ultrasound for high-grade neonatal hydronephrosis. J Urol 168:1518–1521
Onen A, Jayanthi VR, Koff SA (2002) Long-term follow-up of prenatally detected severe bilateral newborn hydronephrosis initially managed nonoperatively. J Urol 168:1118–1120
Ulman I, Jayanthi VR, Koff SA (2000) The long-term follow-up of newborns with severe unilateral hydronephrosis initially treated nonoperatively. J Urol 164:1101–1105
Maizels M, Mitchell B, Kass E, Fernbach SK, Conway JJ (1994) Outcome of nonspecific hydronephrosis in the infant: a report from the Registry of the Society for Fetal Urology. J Urol 152:2324–2327
Egger M, Smoth GD, Altman DG (2001) Systematic reviews in health care: meta-analysis in context. BMJ publishing group, London
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Sidhu, G., Beyene, J. & Rosenblum, N.D. Outcome of isolated antenatal hydronephrosis: a systematic review and meta-analysis. Pediatr Nephrol 21, 218–224 (2006). https://doi.org/10.1007/s00467-005-2100-9
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DOI: https://doi.org/10.1007/s00467-005-2100-9