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Acute pyelonephritis and renal scarring in Kuwaiti children: a follow-up study using 99mTc DMSA renal scintigraphy
Mohamed Zaki1, Mona Badawi, Ghalia Al Mutari
1Pediatric Department, Farwania Hospital, Kuwait. redc66@yahoo.com
Insights
Acute pyelonephritis (APN) frequently causes renal scarring in Kuwaiti children. Girls and children over two years old are more susceptible to APN and subsequent kidney damage.
Area of Science:
- Pediatric Nephrology
- Diagnostic Imaging
Background:
- Acute pyelonephritis (APN) is a significant cause of renal scarring in children.
- Understanding the prevalence and risk factors for renal scarring post-APN is crucial for early intervention.
Purpose of the Study:
- To determine the prevalence of renal scarring in Kuwaiti Arab children following their first documented episode of APN.
- To identify risk factors associated with the development of renal scarring.
Main Methods:
- Prospective study of 82 Kuwaiti Arab children diagnosed with APN.
- (99m)Tc DMSA renal scans were performed at diagnosis and 6 months post-treatment.
- Micturition cystourethrogram (MCUG) was performed to assess for vesicoureteric reflux (VUR).
Main Results:
- 38% of children developed persistent renal parenchymal defects (scarring) 6 months after APN.
- Vesicoureteric reflux (VUR) was present in 32% of children, with 50% of these developing scars.
- Children over 2 years old and girls showed higher susceptibility to APN and renal scarring.
Conclusions:
- APN is a major contributor to renal scarring in the studied pediatric population.
- Risk factors include VUR, recurrent infections, older age at first APN, and female sex.
- Early diagnosis and management of APN are essential to prevent long-term renal damage.
Abstract:
The aim of this study was to determine the prevalence of renal scarring in a group of Kuwaiti Arab children with their first documented acute pyelonephritis (APN). Eighty-two Kuwaiti Arab children (10 males and 72 females) who had abnormal (99m)Tc DMSA renal scan findings of acute pyelonephritis were prospectively studied with the same imaging modality 6 months after treatment to identify those who developed renal scarring. A micturition cystourethrogram (MCUG) was performed for all of the children 1 month after diagnosis. Children were divided into 3 age groups (<2 years, 2-5 years and above 5 years). The follow-up DMSA renal scans 6 months after diagnosis revealed normalization of renal changes in 56% (46 patients), much improvement with residual renal abnormality in 6% (5 patients), and persistent parenchymal defects in 38% (31 patients). Vesicoureteric reflux (VUR) was found in 32% of children (26/82) and the majority were between grade I and III. Thirteen of those with VUR (50%) developed renal scars on follow-up. Fifty-three percent of the scarred kidneys (19/36) were drained by non-refluxing ureters. In this study, children older than 2 years had less VUR yet were more susceptible to APN and to the development of renal scars. Girls were more prone to developing APN and renal scarring than boys. This work shows that APN is a serious cause for renal scarring in our patients, particularly if associated with other risk factors such as recurrent infections and the female sex.
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