Abstract: SA-PO820
Thrombotic Microangiopathy Multidisciplinary Team Assessment: Single-Center Case Series
Session Information
- C3G, TMA, MGRS, Amyloidosis, and More
October 26, 2024 | Location: Exhibit Hall, Convention Center
Abstract Time: 10:00 AM - 12:00 PM
Category: Glomerular Diseases
- 1402 Glomerular Diseases: Clinical, Outcomes, and Therapeutics
Authors
- Nguyen, Matthew Duy Thanh Luyen, University of California Irvine Nephrology Hypertension & Kidney Transplantation, Orange, California, United States
- Patel, Samir Dinesh, University of California Irvine Nephrology Hypertension & Kidney Transplantation, Orange, California, United States
- Al Ammary, Fawaz, University of California Irvine Nephrology Hypertension & Kidney Transplantation, Orange, California, United States
- Tran, Minh-Ha, University of California Irvine - Department of Medicine - Division of Transfusion Medicine, Irvine, California, United States
- Ciurea, Stefan Octavian, University of California Irvine - Department of Medicine - Division of Hematology & Oncology, Irvine, California, United States
- Desai, Sheetal, University of California Irvine - Department of Medicine - Division of Rheumatology, Irvine, California, United States
- Amin, Alpesh, University of California Irvine - Department of Medicine, Irvine, California, United States
- Zhao, Hongyu, University of California Irvine Nephrology Hypertension & Kidney Transplantation, Orange, California, United States
- Vadpey, Omid, University of California Irvine - Department of Medicine, Irvine, California, United States
- Truong, Tai, University of California Irvine Nephrology Hypertension & Kidney Transplantation, Orange, California, United States
- Abdelmalek, Antoinette, University of California Irvine Nephrology Hypertension & Kidney Transplantation, Orange, California, United States
- Perkins, Jordan, University of California Irvine Nephrology Hypertension & Kidney Transplantation, Orange, California, United States
- Ahdoot, Rebecca S., University of California Irvine Nephrology Hypertension & Kidney Transplantation, Orange, California, United States
- Malik, Fatima T., University of California Irvine Nephrology Hypertension & Kidney Transplantation, Orange, California, United States
- Ferrey, Antoney Joseph, University of California Irvine Nephrology Hypertension & Kidney Transplantation, Orange, California, United States
- Reddy, Uttam Gummadi, University of California Irvine Nephrology Hypertension & Kidney Transplantation, Orange, California, United States
- Tantisattamo, Ekamol, University of California Irvine Nephrology Hypertension & Kidney Transplantation, Orange, California, United States
- Chang, Yongen, University of California Irvine Nephrology Hypertension & Kidney Transplantation, Orange, California, United States
- Lau, Wei Ling, University of California Irvine Nephrology Hypertension & Kidney Transplantation, Orange, California, United States
- Khagi, Yulian, University of California Irvine - VA LBMC Department of Medicine - Division of Nephrology, Irvine, California, United States
- Lee, Lisa, University of California Irvine - Department of Medicine - Division of Hematology & Oncology, Irvine, California, United States
- Pakbaz, Zahra, University of California Irvine - Department of Medicine - Division of Hematology & Oncology, Irvine, California, United States
- Hanna, Ramy Magdy, University of California Irvine Nephrology Hypertension & Kidney Transplantation, Orange, California, United States
Background
Thrombotic Microangiopathies (TMAs) include an etiological diverse group of phenotypically similar disorders. While individually rare, they are seen as an aggregate with regularity. Prior reports suggested the importance of approaching TMAs in a multidisciplinary fashion. We present the design, structure, evaluation workflow and data in the initial 3-year period of the established University of California Irvine (UCI) TMA team.
Methods
This is a single-center retrospective case series of 51 diverse patients demonstrating demographics, diagnoses, triggers, treatments applied, and outcomes for patients with the diagnosis of TMA
Results
Of the 51 patients, 31 were females with an age range between 18 and 83. Twenty patients were diagnosed with atypical hemolytic uremic syndrome (aHUS). Five patients were diagnosed with Hematopoetic Stem Cell Transplant associated TMA (HSCT-TMA), 2 patients had Thrombotic Thrombocytopenic purpura (TTP). Of the 20 aHUS patients, 13 were treated with anti-complement blockade and 7 were evaluated for potential future use of complement blockade. All patients treated with anti-complement blockade (100%) demonstrated a hematologic response, 75% (9 of 12) of patients requiring renal replacement therapy remain off dialysis after 6-18 months of treatment with anti-complement blockade. HSCT-TMA patients were treated with anti-complement blockade had a less positive response.
Conclusion
This case series highlights the importance of TMA multidisciplinary team to improve diagnosis and optimize outcomes of this rare condition. Future research is needed to assist efficacy and implementation of TMA-multidisciplinary care.