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Post-pyelonephritic renal scars are not associated with vesicoureteral reflux in children
1Hospital for Children and Adolescents, Helsinki University, Helsinki, Finland. seppo.taskinen@hus.fi
Insights
Renal scars in children after pyelonephritis are often caused by the infection itself, not urinary tract abnormalities. However, structural issues can lead to recurrent infections and potential kidney damage.
Area of Science:
- Pediatric Nephrology
- Urology
- Infectious Diseases
Background:
- Children with pyelonephritis face risks of renal damage.
- Early identification of risk factors for renal scarring is crucial.
Purpose of the Study:
- To evaluate clinical signs and urological abnormalities in predicting renal scars post-pyelonephritis in children.
- To determine the incidence and predictors of renal scarring after a first episode of pyelonephritis.
Main Methods:
- 64 hospitalized children with first pyelonephritis underwent ultrasonography and technetium-labeled dimercapto-succinic acid (DMSA) scintigraphy within 1 week.
- Voiding cystourethrography was performed at 8 weeks; follow-up DMSA scintigraphy at 2 years for 58 patients.
Main Results:
- 48% of patients showed parenchymal defects on initial DMSA.
- Renal scars were present in 21% of patients at 2-year follow-up; most did not have vesicoureteral reflux (VUR).
- Older age at infection correlated with renal scars; high-grade VUR with repeat infections showed kidney function deterioration.
Conclusions:
- Renal scars after initial pyelonephritis are primarily infection-related, not due to urinary tract abnormalities.
- Structural abnormalities can predispose to recurrent infections.
- New renal scars can develop post-pyelonephritis in all children, irrespective of sex or age.
Purpose:
Children with pyelonephritis are at risk for renal damage. We assess the value of clinical signs and urological abnormalities in predicting renal scars in children following pyelonephritis.
Materials And Methods:
A total of 64 hospitalized children (29 females and 35 males, median age 2.9 years) underwent ultrasonography and technetium labeled dimercapto-succinic acid (DMSA) scintigraphy imaging within 1 week following the diagnosis of the first pyelonephritis. Voiding cystourethrography was performed 8 weeks after the diagnosis. Followup DMSA scintigraphy was performed in 58 patients after 2 years of followup.
Results:
Urological abnormalities observed were vesicoureteral reflux (VUR, grade 2 or higher) in 11 patients (19%), nonrefluxing and nonobstructed megaureter in 2 (4%) and pyeloureteral obstruction in 1 (2%). The first DMSA scintigraphy showed parenchymal defects in 48% of patients. VUR did not increase the risk of renal defects. At 2 years after the infection 12 of the 58 patients (21%) had renal scars. Nine of these patients did not have VUR. However, 2 patients with high grade VUR and repeat infections demonstrated deterioration of kidney function during followup. The patients with renal scars were older than those without scars (3.1 vs 0.8 years, p = 0.0291) at the time of infection.
Conclusions:
Renal scars after first pyelonephritis are in most cases not associated with abnormalities of the urinary tract, but are caused by the infection itself. However, structural abnormalities may predispose to recurrent infections. Following pyelonephritis new renal scars may develop in all age groups in both sexes.
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