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| Name | Class |
|---|---|
| Baxter Healthcare Corporation | INDUSTRY |
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Historically, innovations for acute kidney injury (AKI) and continuous renal replacement therapy (CRRT) have centered around an adult population. However, research has shown that over 10% of pediatric patients develop severe AKI within the first week in an intensive care unit (ICU). When a pediatric patient requires renal replacement therapy for AKI in the ICU, CRRT is usually the modality of choice. The HF20â„¢ is indicated for supporting patients weighing 8 to 20 kilograms, addressing a critical clinical need for critically ill children who require CRRT. Current US Food and Drug Administration (FDA) approved CRRT filters are designed for patients weighing more than 20 kg or less than 10 kg, leaving a gap in appropriately designed filters for pediatric patients.
A previous trial in the US showed that the HF20â„¢ is safe and effective, however the membrane composition of the HF20â„¢ used in that trial is different than what is currently manufacturer and available. Baxter Healthcare Corporation has received an Emergency Use Authorization (EUA) for the currently available HF20â„¢ to be used in the era of the COVID-19 pandemic, however participants do not need to be infected with the SAR-CoV-2 virus in order to be treated. The EUA for the HF20â„¢ allows for treatment for any children weighing between 8 and 20 kilograms in need of CRRT. This registry will collect clinical data related to the safety and efficacy of the HF20â„¢ filter for CRRT in pediatric patients weighing 8 to 20 kilograms at participating institutions, however participation in this registry is not a requirement in order to be treated with the HF20â„¢ filter.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| HF20â„¢ for Pediatric CRRT | Pediatric patients in an intensive care unit requiring CRRT for acute kidney injury (AKI) |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| HF20â„¢ | Device | HF20â„¢ will be used for CRRT |
|
| Measure | Description | Time Frame |
|---|---|---|
| Change in Blood Urea Nitrogen (BUN) | After 24 hours of CRRT with the HF20â„¢ filter as compared to baseline |
| Measure | Description | Time Frame |
|---|---|---|
| Change in Serum Creatinine | After 24 hours of CRRT with the HF20â„¢ filter as compared to baseline | |
| Change in Serum Bicarbonate/Carbon Dioxide | After 24 hours of CRRT with the HF20â„¢ filter as compared to baseline |
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Inclusion Criteria:
Receiving or plan to receive CRRT with the HF20â„¢ filter as standard of care
Acute kidney injury (AKI) or fluid overload as defined as one of the two below:
AKI defined as Kidney Disease Improving Global Outcomes (KDIGO) Stage 1 or higher by either:
Severe fluid overload defined as greater than 10 percent fluid accumulation based on ICU admission weight
Exclusion Criteria:
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Patients receiving CRRT with the HF20â„¢ filter as their standard care for AKI or fluid overload in an intensive care unit at a participating institution.
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| Name | Affiliation | Role |
|---|---|---|
| Stuart L Goldstein, MD | Children's Hospital Medical Center, Cincinnati | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Lucile Packard Children's Hospital Stanford | Palo Alto | California | 94304 | United States | ||
| Cincinnati Children's Hospital Medical Center |
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| ID | Term |
|---|---|
| D058186 | Acute Kidney Injury |
| ID | Term |
|---|---|
| D051437 | Renal Insufficiency |
| D007674 | Kidney Diseases |
| D014570 | Urologic Diseases |
| D052776 | Female Urogenital Diseases |
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| Cincinnati |
| Ohio |
| 45229 |
| United States |
| Seattle Children's | Seattle | Washington | 98105 | United States |
| D005261 |
| Female Urogenital Diseases and Pregnancy Complications |
| D000091642 | Urogenital Diseases |
| D052801 | Male Urogenital Diseases |