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Hemolytic Uremic Syndrome-Induced Acute Kidney Injury Treated via Immunomodulation with the Selective Cytopheretic
H Rhodes Hambrick1,2, Kara Short3, David Askenazi3
1Division of Nephrology and Hypertension, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.
Insights
Selective cytopheretic device (SCD) therapy shows promise in treating pediatric Shiga-toxin associated-hemolytic uremic syndrome (STEC-HUS). This immunomodulatory treatment improved outcomes in three children with STEC-HUS-induced acute kidney injury (AKI).
Area of Science:
- Pediatric Nephrology
- Immunology
- Critical Care Medicine
Background:
- Shiga-toxin associated-hemolytic uremic syndrome (STEC-HUS) is a severe condition causing acute kidney injury (AKI) in children.
- HUS pathophysiology involves activated neutrophils damaging vascular endothelial cells, leading to significant morbidity and mortality.
- Therapeutic immunomodulation targeting neutrophils may offer a novel treatment approach.
Purpose of the Study:
- To evaluate the safety and efficacy of the selective cytopheretic device (SCD) in pediatric patients with STEC-HUS.
- To assess the impact of SCD therapy on multi-organ dysfunction and renal recovery in STEC-HUS.
Main Methods:
- Three pediatric patients with STEC-HUS requiring continuous renal replacement therapy (CRRT) were treated with the SCD.
- Patient 1 received 7 days of SCD and CRRT; patients 2 and 3 each received 24 hours of SCD therapy followed by dialysis.
Main Results:
- The patient treated for 7 days showed gradual recovery of multi-organ dysfunction and normal kidney/hematologic parameters at 60-day follow-up.
- Both patients treated for 24 hours demonstrated gradual improvement, with normalization or near-normalization of kidney function at 60 days.
- SCD treatment was well-tolerated with no device-related adverse events.
Conclusions:
- Selective cytopheretic device (SCD) therapy was associated with improvements in STEC-HUS-induced AKI and associated multisystem organ dysfunction.
- SCD is a potentially effective and safe immunomodulatory treatment for pediatric STEC-HUS.
- Further research is warranted to confirm these findings in larger cohorts.
Introduction:
Shiga-toxin associated-hemolytic uremic syndrome (STEC-HUS) is a severe cause of acute kidney injury (AKI) in children. Although most children recover, about 5% die and 30% develop chronic renal morbidity. HUS pathophysiology includes activated neutrophils damaging vascular endothelial cells. Therapeutic immunomodulation of activated neutrophils may alter the progression of disease. We present 3 pediatric patients treated with the selective cytopheretic device (SCD).
Methods:
We describe a 12 y.o. (patient 1) and two 2 y.o. twins (patients 2 and 3) with STEC-HUS requiring continuous renal replacement therapy (CRRT) who were enrolled in two separate studies of the SCD.
Results:
Patient 1 presented with STEC-HUS causing AKI and multisystem organ failure and received 7 days of SCD and CRRT treatment. After SCD initiation, the patient had gradual recovery of multi-organ dysfunction, with normal kidney and hematologic parameters at 60-day follow-up. Patients 2 and 3 presented with STEC-HUS with AKI requiring dialysis. Each received 24 h of SCD therapy. Thereafter, both gradually improved, with normalization (patient 2) and near-normalization (patient 3) of kidney function at 60-day follow-up.
Conclusion:
Immunomodulatory treatment with the SCD was associated with improvements in multisystem stigmata of STEC-HUS-induced AKI and was well-tolerated without any device-related adverse events.
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