Abstract: PUB224
LDL Apheresis in Recurrent FSGS After Kidney Transplantation in Adults
Session Information
Category: Transplantation
- 2002 Transplantation: Clinical
Authors
- Nguyen, Matthew Duy Thanh Luyen, Keck Medicine of USC, Los Angeles, California, United States
- Duong, Heidi, Keck Medicine of USC, Los Angeles, California, United States
- Su, Lauren, Keck Medicine of USC, Los Angeles, California, United States
- Voora, Santhi, Keck Medicine of USC, Los Angeles, California, United States
Background
LDL apheresis (LDL-A) is a promising treatment for recurrent focal segmental glomerulosclerosis (rFSGS) post kidney transplant. We present two cases treated with LDL-A who achieved sustained proteinuria remission (<0.3 g/day).
Methods
We retrospectively reviewed two adults with rFSGS. Both received thymoglobulin and standard triple immunosuppression. After standard treatment for rFSGS, they were treated with LDL-A (biweekly for week 1-3 and weekly for week 6-12) and prednisone (1mg/kg) at week 4. Response was categorized as complete (UPCR ≤0.3 g/day), partial (0.3–3.5 g/day), or no remission (>3.5 g/day).
Results
Case #1 is a 38-year-old Jehovah’s Witness male with renal failure due to biopsy-proven FSGS. Post-transplant, he had immediate graft function but developed renal failure due to rFSGS. He was treated with rituximab and plasmapheresis complicated by recurrent perinephric hematoma. He achieved clinical remission, but due to risk for bleeding with plasmapheresis, LDL-A was started, leading to sustained remission of proteinuria. (Table #1)
Case #2 is a 49-year-old male with rFSGS after living related kidney transplant. On post-operative day 3, he developed nephrotic range proteinuria. He was empirically treated with 15 sessions of plasmapheresis and rituximab with partial response. Kidney biopsy confirmed rFSGS. Due to persistent proteinuria, LDL-A was started with sustained remission of proteinuria. (Figure #1)
Conclusion
We present two cases with sustained remission of proteinuria in post-transplant rFSGS treated with LDL apheresis.