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Postdiarrheal hemolytic and uremic syndrome with severe multiorgan involvement and associated early risk factors
M Oualha1, S Pierrepont2, P Krug2
1Pediatric intensive care unit, hôpital Necker-Enfants-Malades, Assistance publique-Hôpitaux de Paris, faculté de médecine, université Paris-Descartes, 149, rue de Sèvres, 75743 Paris cedex 15, France.
Insights
Severe forms of postdiarrheal hemolytic uremic syndrome (D+HUS) are linked to early inflammatory signs. Fever, high C-reactive protein (CRP), and elevated white blood cell (WBC) counts may predict severe outcomes in children with D+HUS.
Area of Science:
- Pediatric Nephrology
- Infectious Diseases
- Critical Care Medicine
Background:
- Postdiarrheal hemolytic uremic syndrome (D+HUS) is a serious complication of certain infections.
- Identifying factors predicting severe D+HUS is crucial for timely intervention.
Purpose of the Study:
- To identify early clinical and biological indicators of severe D+HUS in children.
- To aid practitioners in determining appropriate treatment strategies for D+HUS.
Main Methods:
- Retrospective study of 49 children diagnosed with D+HUS between 2001 and 2011.
- Severe D+HUS defined by death, major neurological/cardiovascular involvement, or sequelae.
- Multivariate analysis to correlate clinical/biological factors with severe outcomes.
Main Results:
- Thirty-five children had extrarenal involvement; 13 experienced severe forms.
- Major neurological involvement, dialysis, and sequelae were associated with prodromal fever, high CRP, and elevated WBC count, respectively.
- Three children died, and 32 required dialysis.
Conclusions:
- D+HUS is a multiorgan disease with delayed extrarenal involvement.
- Early clinical and biological inflammatory parameters are associated with severe D+HUS forms.
- These findings may help predict disease severity and guide treatment.
Aim:
Identifying early clinical and biological factors associated with severe forms of postdiarrheal hemolytic uremic syndrome (D+HUS) that may help practitioners determine appropriate treatment.
Methods:
This retrospective study was conducted in 49 children with D+HUS between 2001 and 2011. Severe forms were defined as occurrence of one of the following conditions: death, major neurological involvement, cardiovascular involvement, and/or the presence of sequelae (neurological, cardiovascular, pancreatic, or renal).
Results:
During the acute phase, 35 children exhibited at least one type of extrarenal involvement including 13 severe forms with a median delayed occurrence after admission of 4.5 days (range: 1-8) for comatose children and 5 days (range: 2-6) for cardiovascular involvement; 32 children required dialysis and three died. In multivariate analysis, (i) major neurological involvement (n=13), (ii) dialysis (n=32), and (iii) sequelae (n=12) were associated with (i) fever during the prodromal phase requiring dialysis at admission, (ii) C-reactive protein level (CRP) >22mg/L at admission, and (iii) major neurological involvement and a white blood cell count (WBC)>20×103/mm3 during the acute stage, respectively.
Conclusions:
D+HUS is a multiorgan disease with a delayed occurrence of life-threatening extrarenal organ involvement. Severe forms appear to be associated with early biological and clinical inflammatory parameters.
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