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IMAGING
Imaging
in pediatric urinary tract infection: a 9-year local experience
Luk WH, Woo YH, Au-Yeung AW, Chan JC
Department of Diagnostic Radiology and Organ Imaging, United Christian
Hospital, Kowloon, Hong Kong
AJR Am J Roentgenol. 2009; 192: 1253-60
- Objective:
Urinary tract infection (UTI) is a common disease entity in children,
and a number of imaging options are offered for these patients. The
purpose of our study was to retrospectively describe the (99m)Tc-labeled
dimer captosuccinic acid (DMSA) renal scintigraphy, ultrasound, and
micturating cystourethrography (MCU) findings over a 9-year period.
- Materials
and Methods: All children younger than 10 years old who presented
to a local hospital in Hong Kong between July 1, 1997, and June 30,
2006, with culture-confirmed UTI and who subsequently underwent DMSA
scintigraphy, ultrasound, and MCU were identified. For the purpose of
this study, patients with underlying major congenital urinary tract
abnormalities were excluded. DMSA scintigraphy was regarded as the gold
standard for the diagnosis of renal scarring. DMSA scintigraphy, ultrasound,
and MCU findings and clinical outcomes were reviewed and analyzed.
- Results:
A total of 583 children were included in the study. Of these, 432 children
(74.1%) had normal findings on ultrasound and on MCU. Only 13 children
(3%) of this group had renal scarring as shown on DMSA scintigraphy.
The overall negative predictive value (NPV) for excluding renal scarring
of combined ultrasound and MCU reached 97%. The NPV was 97.7% in the
subgroup of patients 0 to 2 years old.
- Conclusion:
For children younger than 2 years with UTI in the absence of underlying
major congenital urinary tract abnormalities, we recommend that DMSA
scintigraphy may be withheld if findings on both ultrasound and MCU
examinations are normal.
- Editorial
Comment
The authors performed a retrospective study in order to evaluate the
potential role of combined ultrasound (US) and MCU as first-line imaging
tests in predicting renal scarring using DMSA scintigraphy as the gold
standard. In their cohort, almost 600 children were included. The performances
of US alone, MCU alone, and the techniques combined were systematically
evaluated and compared with the performance of DMSA scintigraphy. If
US alone was performed, the probability of missing renal scarring was
as high as 7.2% compared to 3.1 % with MCU alone. If MCU and US were
considered together, the probability of missing renal scarring could
be further reduced to 3.0%. A normal US and normal MCU therefore would
safely exclude renal scarring in most cases with a false-negative risk
of 2.3% in children younger than 2 years. The authors concluded that
DMSA scintigraphy may be withheld in children younger than 2 years in
the absence of major congenital urinary tract abnormalities. For children
with either positive US or positive MCU findings, further evaluation
with DMSA scintigraphy should be performed to determine whether scarring
is present.
In this study, DMSA scintigraphy was generally performed a minimum of
3 months after the onset of UTI. As we know there is on going debate
in order to establish the most adequate timing to perform DMSA scintigraphy
since pyelonephritis and renal scarring looks similar on DMSA scans
(1). In other words, it is difficult to determine at what time point
a scintigraphic defect should be considered permanent scarring rather
than potentially recovering pyelonephritis. Up to now there is no consensus
regarding the length of time after the initial episode of UTI that this
follow-up DMSA scanning for scarring should be performed. In the literature,
this length of time varies from 3 months to 12 months. As we can see,
we are still distant from following accurate strict guidelines in imaging
protocol in these children.
Reference
1. Lim R: Vesicoureteral reflux and urinary tract infection: evolving
practices and current controversies in pediatric imaging. AJR Am J Roentgenol.
2009; 192: 1197-208.
Dr.
Adilson Prando
Chief, Department of Radiology and
Diagnostic Imaging, Vera Cruz Hospital
Campinas, São Paulo, Brazil
E-mail: adilson.prando@gmail.com
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