E-ISSN: 1308-5263
All-Cause and Exacerbation-Related Readmissions in Thrombotic Microangiopathy Requiring Plasmapheresis: A Population-Based Cohort Study [Turk J Hematol]
Turk J Hematol. Ahead of Print: TJH-43815 | DOI: 10.4274/tjh.galenos.2025.2025.0317

All-Cause and Exacerbation-Related Readmissions in Thrombotic Microangiopathy Requiring Plasmapheresis: A Population-Based Cohort Study

Alexander R. Thebert1, Toru Yoshino2, Sae X. Morita3, Misa Ito4, Ayman Qasrawi5, Hirotaka Kato6
1University of Kentucky College of Medicine, Department of Internal Medicine, Lexington, KY, USA
2Jacobi Medical Center, Albert Einstein College of Medicine, Department of Medicine, Bronx, NY, USA
3SBH Health System, Department of Medicine, Bronx, NY, USA
4University of Kentucky College of Medicine, Department of Internal Medicine and Pediatrics, Lexington, KY, USA
5University of Kentucky College of Medicine and Markey Cancer Center, Division of Hematology, Bone Marrow Transplant & Cellular Therapy, Lexington, KY, USA
6University of Kentucky College of Medicine, Division of Hospital Medicine, Lexington, KY, USA

Objective: Thrombotic microangiopathy (TMA) is a serious condition characterized by microangiopathic hemolytic anemia and thrombocytopenia, with high exacerbation rates. This study examined all-cause and exacerbation-related readmission risks among patients hospitalized with TMA requiring plasmapheresis.
Materials and Methods: A secondary analysis of the 2020 Nationwide Readmission Database was conducted, including discharge data from non-federal hospitals in 31 states. Patients aged 18 years or older admitted non-electively with a primary or secondary diagnosis of TMA requiring plasmapheresis were included. Exacerbation-related readmission was defined as subsequent admissions requiring plasmapheresis within 7 or 30 days post-discharge. Multivariable logistic regression and Cox proportional hazards models assessed readmission risks, adjusting for demographics, comorbidities, and predisposing factors.
Results: Among an estimated 1,393 patients, 791 (56.8%) had predisposing conditions. All-cause readmissions were more frequent in patients with predisposing conditions (26.2% vs. 21.9%), while exacerbation-related readmissions were more common in TMA-only patients (9.0% vs. 3.4% at 7 days; 13.7% vs. 6.4% at 30 days). Most exacerbations occurred within 14 days post-discharge. No patients treated with caplacizumab experienced exacerbation. TMA-only patients had a 2.1 times higher risk of 30-day exacerbation-related readmissions (adjusted hazard ratio 2.10, p = 0.04). Rural residence and patient-directed discharge were potential risk factors for exacerbation-related readmissions.
Conclusions: These findings highlight the need for improved post-discharge care and treatment strategies to prevent readmissions. Further studies should explore interventions to reduce exacerbation-related readmissions, particularly in high-risk populations.

Keywords: database, microangiopathy, nationwide, readmission, thrombotic

Corresponding Author: Hirotaka Kato, United States of America
Manuscript Language: English
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