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Role of Late DMSA Renal Scan in Detecting High-Grade Vesicoureteral Reflux
Alejandro Balestracci1, Micaela Montecuco2, Carla Serviddio2
1Nephrology Unit, Hospital General de Niños Pedro de Elizalde, Montes de Oca 40, CP 1270, Ciudad Autónoma de Buenos Aires, Argentina. abalestracci@yahoo.com.ar.
Insights
Late dimercaptosuccinic acid (DMSA) renal scans effectively identify high-grade vesicoureteral reflux (VUR) in children over 3 with a history of febrile urinary tract infection (fUTI). A normal DMSA scan can rule out high-grade VUR, potentially avoiding further imaging like voiding cystourethrogram (VCUG).
Area of Science:
- Pediatric Nephrology
- Diagnostic Imaging
- Urology
Background:
- Febrile urinary tract infections (fUTI) in children can indicate underlying vesicoureteral reflux (VUR).
- Timely diagnosis of high-grade VUR is crucial to prevent renal scarring and complications.
- Late dimercaptosuccinic acid (DMSA) renal scans are utilized for evaluating renal scarring and VUR.
Purpose of the Study:
- To assess the diagnostic performance of late DMSA scans in identifying high-grade VUR (grades III-V) in children over 3 years old with a history of fUTI.
- To determine if a normal late DMSA scan can reliably exclude high-grade VUR, thereby avoiding the need for voiding cystourethrogram (VCUG).
Main Methods:
- Retrospective diagnostic accuracy study analyzing clinical records of 122 children (3-18 years) with fUTI history.
- Exclusion of patients with pre-existing renal abnormalities or prior genitourinary imaging.
- Comparison of late DMSA scan findings with voiding cystourethrogram (VCUG) as the gold standard for VUR grading.
Main Results:
- Abnormal DMSA scans were significantly associated with all grades of VUR (p<0.00001) and specifically with high-grade VUR (p<0.00001).
- For high-grade VUR, late DMSA scans demonstrated 100% sensitivity and 100% negative predictive value (NPV).
- Overall VUR detection by DMSA had 93.1% sensitivity, 75% specificity, 92.3% NPV, and 77.1% positive predictive value (PPV).
Conclusions:
- A normal late DMSA scan in older children reliably predicts the absence of high-grade VUR.
- This finding suggests that a normal late DMSA scan can obviate the need for VCUG in this patient group.
- Late DMSA scan can serve as a valuable screening tool for children with fUTI who were not investigated promptly during the acute infection phase.
Objective:
To determine the performance of late dimercaptosuccinic acid (DMSA) renal scans in identifying high-grade (III-V) vesicoureteral reflux (VUR) in children aged over 3 y with a febrile urinary tract infection (fUTI) history that has not been timely investigated.
Methods:
In this retrospective study of diagnostic accuracy, the clinical records of children aged between 3 and 18 y with fUTI history evaluated consecutively at Nephrology Unit of Hospital General de Niños Pedro de Elizalde, Argentina between 2006 and 2016 were reviewed. Patients with previously diagnosed renal or urinary tract abnormalities or who underwent previous postnatal genitourinary imaging were excluded. Only those assessed by renal and bladder ultrasound (RBUS), voiding cystourethrogram (VCUG) and late 6-mo DMSA scan were analyzed. The ability of the scintigraphy in identifying high-grade VUR was determined by comparing its findings with those of VCUG.
Results:
In 122 children (median age 5.37 y, 88.5% girls) RBUS was abnormal in 53 (43.4%) and 58 (47.5%) had VUR (30 of high-grade). Abnormal DMSA scan findings (70 patients, 57.4%) were associated with all grade (p = 0.00001) and with high-grade VUR (p = 0.00001). Sensitivity, specificity, negative (NPV) and positive (PPV) predictive values of late DMSA scans for all grades VUR were 93.1%, 75%, 92.3% and 77.1%, respectively. Only 4 patients with low-grade VUR had normal scans. For high-grade VUR, sensitivity and NPV reached 100%.
Conclusions:
In older children, the normal late DMSA scan predicted the absence of high-grade VUR, obviating the need for a VCUG. This approach could be a possible strategy for children not studied at acute infection time.
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