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Published on: December 3, 2017
Delay in diagnosis in poststreptococcal glomerulonephritis
Priya J Pais1, Theresa Kump, Larry A Greenbaum
1Department of Pediatrics, Medical College of Wisconsin and Children's Research Institute of Children's Hospital of Wisconsin, Milwaukee, WI, USA.
Insights
Diagnostic delays are common in children with poststreptococcal glomerulonephritis (PSGN), particularly when gross hematuria is absent. Early urinalysis is crucial for timely diagnosis of this kidney condition.
Area of Science:
- Pediatric Nephrology
- Infectious Diseases
Background:
- Poststreptococcal glomerulonephritis (PSGN) is a significant cause of acute kidney injury in children.
- Timely diagnosis of PSGN is essential to prevent complications and ensure appropriate management.
Purpose of the Study:
- To investigate the incidence and identify risk factors associated with delayed diagnosis in pediatric PSGN cases.
- To improve early detection strategies for PSGN in children.
Main Methods:
- Retrospective chart review of 52 children diagnosed with PSGN.
- Statistical analysis, including univariate and multivariate logistic regression, to identify risk factors for diagnostic delays exceeding 24 hours.
Main Results:
- A diagnostic delay occurred in 33% of children with PSGN.
- Absence of gross hematuria as a presenting symptom significantly increased the risk of diagnostic delay (3.8-fold increased relative risk).
- Children with a negative infection history were more likely to experience diagnostic delays.
Conclusions:
- Diagnostic delays are prevalent in pediatric PSGN, especially when gross hematuria is not an initial sign.
- Physicians should maintain a high index of suspicion for PSGN in children presenting with symptoms potentially related to volume overload.
- Urinalysis serves as a valuable initial tool for diagnosing PSGN.
Objective:
To determine the frequency and risk factors for diagnostic delays in children with poststreptococcal glomerulonephritis (PSGN).
Study Design:
We reviewed the charts of 52 children with PSGN, and identified children with a delay in diagnosis of more than 24 hours. We determined risk factors for delay in diagnosis using univariate and multivariate logistic regression.
Results:
17 children (33%) with PSGN had a delay in diagnosis. Delay in diagnosis occurred in 14% of children with gross hematuria as a presenting complaint and in 54% of children without gross hematuria as a presenting complaint (3.8 increased relative risk, 95% CI = 1.4 to 10; P = .02). A delay in diagnosis was more common in children with a negative infection history (P = .04). In multiple logistic regression, only the absence of gross hematuria as a presenting complaint was associated with a delay in diagnosis (P = .01). All children with a delay in diagnosis had microscopic hematuria on their initial urinalysis.
Conclusions:
Delay in diagnosis is common in children with PSGN, especially if visible hematuria is not a presenting complaint. Physicians should consider the possibility of PSGN in children with symptoms that may be secondary to volume overload. A urinalysis is a helpful initial diagnostic test.
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