dc.contributor.author | Bosáková, Alice | |
dc.contributor.author | Šalounová, Dana | |
dc.contributor.author | Havelka, Jaroslav | |
dc.contributor.author | Kraft, Otakar | |
dc.contributor.author | Širůček, Pavel | |
dc.contributor.author | Kočvara, Radim | |
dc.contributor.author | Hladík, Michal | |
dc.date.accessioned | 2018-08-21T08:48:49Z | |
dc.date.available | 2018-08-21T08:48:49Z | |
dc.date.issued | 2018 | |
dc.identifier.citation | Journal of Pediatric Urology. 2018, vol. 14, issue 3, art. no. 269.e1. | cs |
dc.identifier.issn | 1477-5131 | |
dc.identifier.issn | 1873-4898 | |
dc.identifier.uri | http://hdl.handle.net/10084/131192 | |
dc.description.abstract | Introduction
Static renal scintigraphy is the gold standard for detection of inflammatory changes in the renal parenchyma in acute pyelonephritis. Our aim was to determine whether diffusion-weighted magnetic resonance imaging (DW-MRI) was comparable with static renal scintigraphy (DMSA-SRS) to demonstrate acute renal parenchymal lesions.
Objective
To compare Tc-99m-dimercaptosuccinic acid static renal scintigraphy (DMSA-SRS) with diffusion-weighted magnetic resonance imaging (DW-MRI) for detecting acute inflammatory changes in the renal parenchyma in children with febrile urinary tract infection.
Methods
Thirty-one children (30 girls) aged 3-18 years with a first episode of febrile UTI without a previously detected congenital malformation of the urinary tract, were prospectively included. DMSA-SRS and DW-MRI were performed within 5 days of diagnosis to detect renal inflammatory lesions. The DW-MRI examination was performed without contrast agent and without general anesthesia. Late examinations were performed after 6 months using both methods to detect late lesions.
Results
DW-MRI confirmed acute inflammatory changes of the renal parenchyma in all 31 patients (100%), mostly unilateral. DMSA-SRS detected inflammatory lesions in 22 children (71%; p = 0.002). The lesions were multiple in 26/31 children (84%) on DW-MRI and in 9/22 (40%) on DMSA-SRS. At the control examination, scarring of the renal parenchyma was found equally by DW-MRI and DMSA-SRS in five patients (16%), three of whom were the same patients. The overall concordance of positive and negative late findings occurred in 87% of patients. There was correspondence in the anatomical location of acute and late lesions.
Discussion
The clinical significance of acute and late parenchymal findings on DWI-MR is yet to be determined. A limitation of our study is the age of the patients (older than 3 years) who are less sensitive to scar development; therefore, a smaller number of patients with scars could be analyzed during control examination. Further studies using the DW-MRI should confirm its reliability to detect acute and late lesions in younger children and infants and determine the clinical consequences.
Conclusion
DW-MRI has higher sensitivity for detecting acute renal inflammatory lesions and multifocal lesions than DMSA-SRS. The incidence of scars was low and corresponded with the anatomical location of acute and late lesions. | cs |
dc.language.iso | en | cs |
dc.publisher | Elsevier | cs |
dc.relation.ispartofseries | Journal of Pediatric Urology | cs |
dc.relation.uri | https://doi.org/10.1016/j.jpurol.2018.02.014 | cs |
dc.rights | © 2018 Journal of Pediatric Urology Company. Published by Elsevier Ltd. All rights reserved. | cs |
dc.subject | acute pyelonephritis | cs |
dc.subject | diffusion-weighted magnetic resonance imaging (DW-MRI) | cs |
dc.subject | Tc-99m DMSA renal scintigraphy | cs |
dc.title | Diffusion-weighted magnetic resonance imaging is more sensitive than dimercaptosuccinic acid scintigraphy in detecting parenchymal lesions in children with acute pyelonephritis: A prospective study | cs |
dc.type | article | cs |
dc.identifier.doi | 10.1016/j.jpurol.2018.02.014 | |
dc.type.status | Peer-reviewed | cs |
dc.description.source | Web of Science | cs |
dc.description.volume | 14 | cs |
dc.description.issue | 3 | cs |
dc.description.firstpage | art. no. 269.e1 | cs |
dc.identifier.wos | 000436511000035 | |