Nephrology: Clinical
Nephrology 3: Dialysis and Diversity and Equity in Kidney Health
Chloe E. Douglas, MD (she/her/hers)
PGY-5 Pediatric Nephrology Fellow
University of Washington/Seattle Children's Hospital
Seattle, Washington, United States
The ages of the 3 cases were: Patient A, 5 days; Patient B, 3 days; Patient C, 11 years (Table 1). Both neonatal patients were on an extracorporeal membrane oxygenation (ECMO) device at the time of rise in PFH, while the third patient had a left ventricle assist device (LVAD). All patients received continuous renal replacement therapy (CRRT) for AKI and/or fluid overload. TPE in all patients was performed using membrane filtration with Prismaflex device. The mean peak PFH level at time of initiation was 449.3 mg/dL (range 297-628 mg/dL) and the mean level after the first TPE session was 228 mg/dL (range 36-427 mg/dL). Patient A underwent three sessions of TPE prior to clinical improvement and ECMO decannulation. Patient B had clinical deterioration unrelated to the TPE procedure and underwent only a single session. Patient C had persistent hemolysis requiring LVAD exchange which led to improvement in PFH. No TPE-related complications were observed.
Conclusion(s):
TPE was safely used to reduce severely elevated PFH levels in three pediatric patients with risk factors for significant tissue toxicity. The impact on clinical outcomes was less clear in this case series. Given the risks of elevated PFH levels, additional studies are needed, along with guidelines on the appropriate use of apheresis for mechanical red cell hemolysis.