Please use this identifier to cite or link to this item: https://observatorio.fm.usp.br/handle/OPI/2604
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dc.contributorSistema FMUSP-HC: Faculdade de Medicina da Universidade de São Paulo (FMUSP) e Hospital das Clínicas da FMUSP-
dc.contributor.authorBARBOSA, Joao A. B. A.-
dc.contributor.authorCHOW, Jeanne S.-
dc.contributor.authorBENSON, Carol B.-
dc.contributor.authorYORIOKA, Marco A.-
dc.contributor.authorBULL, Alexandre S.-
dc.contributor.authorRETIK, Alan B.-
dc.contributor.authorNGUYEN, Hiep T.-
dc.date.accessioned2013-10-02T19:36:25Z-
dc.date.available2013-10-02T19:36:25Z-
dc.date.issued2012-
dc.identifier.citationPRENATAL DIAGNOSIS, v.32, n.13, p.1242-1249, 2012-
dc.identifier.issn0197-3851-
dc.identifier.urihttps://observatorio.fm.usp.br/handle/OPI/2604-
dc.description.abstractObjectives Clinical significance and management of prenatal hydronephrosis (PNH) are sources of debate. Existing studies are flawed with biased cohorts or inconsistent follow-up. We aimed to evaluate the incidence of pathology in a large cohort of PNH and assess the biases and outcomes of this population. Methods We reviewed 1034 charts of fetuses with PNH. Records of delivered offspring were reviewed at a pediatric center and analyzed with respect to prenatal and postnatal pathology and management. Results Prenatal resolution of hydronephrosis occurred in 24.7% of pregnancies. On first postnatal ultrasound, some degree of dilatation was present in 80%, 88% and 95% of mild, moderate and severe PNH cases, respectively. At the end of follow-up, hydronephrosis persisted in 10%, 25% and 72% of children, respectively. Incidence of vesicoureteral reflux did not correlate with severity of PNH. Children with postnatal workup had more severe PNH than those without. Conclusions Despite prenatal resolution totalizing 25%, pelvic dilatation persisted on first postnatal imaging in most cases, thus justifying postnatal ultrasound evaluation. Whereas most mild cases resolved spontaneously, a quarter of moderate and more than half of severe cases required surgery. Patients with postnatal imaging and referral had more severe PNH, which could result in overestimation of pathology. (c) 2012 John Wiley & Sons, Ltd.-
dc.language.isoeng-
dc.publisherWILEY-BLACKWELL-
dc.relation.ispartofPrenatal Diagnosis-
dc.rightsrestrictedAccess-
dc.subject.otherisolated antenatal hydronephrosis-
dc.subject.otherprimary vesicoureteral reflux-
dc.subject.otherurinary-tract abnormalities-
dc.subject.otherultrasound-
dc.subject.othermild-
dc.subject.otherultrasonography-
dc.subject.othermetaanalysis-
dc.subject.othermanagement-
dc.subject.otherinfants-
dc.titlePostnatal longitudinal evaluation of children diagnosed with prenatal hydronephrosis: insights in natural history and referral pattern-
dc.typearticle-
dc.rights.holderCopyright WILEY-BLACKWELL-
dc.identifier.doi10.1002/pd.3989-
dc.identifier.pmid23090854-
dc.subject.wosGenetics & Heredity-
dc.subject.wosObstetrics & Gynecology-
dc.type.categoryoriginal article-
dc.type.versionpublishedVersion-
hcfmusp.author.externalCHOW, Jeanne S.:Childrens Hosp, Dept Radiol, Boston, MA 02115 USA-
hcfmusp.author.externalBENSON, Carol B.:Brigham & Womens Hosp, Dept Radiol, Boston, MA 02115 USA-
hcfmusp.author.externalRETIK, Alan B.:Childrens Hosp, Dept Urol, Boston, MA 02115 USA-
hcfmusp.author.externalNGUYEN, Hiep T.:Childrens Hosp, Dept Urol, Boston, MA 02115 USA-
hcfmusp.description.beginpage1242-
hcfmusp.description.endpage1249-
hcfmusp.description.issue13-
hcfmusp.description.volume32-
hcfmusp.origemWOS-
hcfmusp.origem.id2-s2.0-84870688606-
hcfmusp.origem.idWOS:000312142500003-
hcfmusp.publisher.cityHOBOKEN-
hcfmusp.publisher.countryUSA-
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dc.description.indexMEDLINE-
hcfmusp.citation.scopus44-
hcfmusp.scopus.lastupdate2024-04-12-
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