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Published on: November 7, 2017
Risk factors for poor renal prognosis in children with hemolytic uremic syndrome
Alessandra Gianviti1, Alberto E Tozzi, Laura De Petris
1Division of Nephrology and Dialysis, Bambino Gesù Children's Hospital and Institute for Scientific Research, Rome, Italy. gianviti@opbg.net
Insights
Absence of diarrhea and Shiga toxin-producing E. coli infection are key indicators of poor prognosis in children with hemolytic uremic syndrome (HUS). Early identification of these factors aids in timely treatment for high-risk patients.
Area of Science:
- Pediatric Nephrology
- Infectious Diseases
- Epidemiology
Background:
- Predicting outcomes in pediatric hemolytic uremic syndrome (HUS) remains challenging.
- Identifying early prognostic factors is crucial for timely intervention and improved patient outcomes.
Purpose of the Study:
- To identify reliable early predictors of poor renal prognosis in children with HUS.
- To facilitate prompt identification of high-risk children who may benefit from early specific treatments like plasmapheresis.
Main Methods:
- Survival analysis and proportional hazard models were used to evaluate prognostic factors at HUS onset.
- Factors assessed included age, prodromal diarrhea (D), leukocyte count, central nervous system (CNS) involvement, and Shiga toxin-producing E. coli (STEC) infection evidence.
- 387 HUS cases were analyzed, with 276 tested for STEC.
Main Results:
- Age, leukocyte count, and CNS involvement did not correlate with renal recovery time.
- Absence of prodromal diarrhea (D-) and lack of STEC infection (STEC-) were independently linked to poor renal prognosis.
- Only 34% of D-STEC- patients recovered normal renal function, compared to 65%-76% in other groups.
Conclusions:
- Absence of both diarrhea and STEC infection signifies the worst prognosis in HUS patients.
- Patients with diarrhea but without STEC infection (D-STEC+) show a significantly better prognosis.
Abstract:
Many factors have been proposed as predictors of poor renal prognosis in children with hemolytic uremic syndrome (HUS), but their role is still controversial. Our aim was to detect the most reliable early predictors of poor renal prognosis to promptly identify children at major risk of bad outcome who could eventually benefit from early specific treatments, such as plasmapheresis. Prognostic factors identifiable at onset of HUS were evaluated by survival analysis and a proportional hazard model. These included age at onset, prodromal diarrhea (D), leukocyte count, central nervous system (CNS) involvement, and evidence of Shiga toxin-producing Escherichia coli (STEC) infection. Three hundred and eighty-seven HUS cases were reported; 276 were investigated for STEC infection and 189 (68%) proved positive. Age at onset, leukocyte count, and CNS involvement were not associated with the time to recovery. Absence of prodromal D and lack of evidence of STEC infection were independently associated with a poor renal prognosis; only 34% of patients D(-)STEC(- )recovered normal renal function compared with 65%-76% of D(+)STEC(+), D(+)STEC(-) and D(-)STEC(+ )patients. In conclusion, absence of both D and evidence of STEC infection are needed to identify patients with HUS and worst prognosis, while D(-) but STEC(+) patients have a significantly better prognosis.
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