QUELIMMUNE (SCD-PED) PediAtric SurVeillance REgistry
QUELIMMUNE is FDA-approved under an HDE for the treatment of pediatric patients (weight ≥10kg and age ≤22 years) with AKI due to sepsis or a septic condition on antibiotic therapy and requiring RRT. The purpose of this surveillance registry is to prospectively collect safety data among all patients treated with QUELIMMUNE under the HDE. More specifically, we intend on comparing the incidence of new (secondary) blood stream infections in the first 28 days after SCD-PED initiation to a comparator group of matched CKRT patients with sepsis who did not receive treatment with QUELIMMUNE
Inclusion Criteria:
- All patients initiated on QUELIMMUNE therapy under the HDE-approved indication
Exclusion Criteria:
- Weight <10kg
- Age >22 years
- Known allergy to any components of QUELIMMUNE
DEVICE: QUELIMMUNE (SCD-PED)
Acute Kidney Injury, Acute Kidney Injury Due to Sepsis
continuous kidney replacement therapy, continuous renal replacement therapy, acute kidney injury, organ failure, inflammation, dialysis