Racial disparities in sepsis-related complications among hospitalized patients with Myelodysplastic Syndromes: A national inpatient sample analysis (2016–2022)

S Sooraj Srirangadhamu Gopu (1New York Medical College/Landmark Medical Center, Hematology-Oncology, Woonsocket, United States) J Jatin Thukral (Landmark Medical Center, Woonsocket, Cumberland, Rhode Island, United States) A Amanda Lussier (1New York Medical College/Landmark Medical Center, Hematology-Oncology, Woonsocket, United States) K Kanishka Uttam Chandani (4Mayo Clinic, Hematology-Oncology, Phoenix, United States) S Salman Ayub Jajja (NYMC-LANDMARK MEDICAL CENTER, RI, Woonsocket, Rhode Island, United States) D Dhruvi Joshi (Narendra Modi Medical College and Sheth L.G. Hospital, Ahmedabad, India) O Omar Alkasabrah (Landmark Medical center, Providence, Rhode Island, United States) A Ahmed Nadeem (1New York Medical College/Landmark Medical Center, Hematology-Oncology, Woonsocket, United States)

Abstract

Abstract Background: Myelodysplastic syndromes (MDS) are clonal hematopoietic disorders characterized by ineffective hematopoiesis, cytopenias, and an increased susceptibility to infections. Sepsis remains a common and serious cause of morbidity and mortality in this population. While racial disparities in sepsis-related outcomes have been described in the general population, their presence and magnitude among patients with MDS remain poorly understood. Methods: We performed a retrospective cohort study using the National Inpatient Sample (NIS) from 2016 to 2022 to identify adult hospitalizations with co-diagnoses of MDS and sepsis. Patients were stratified by race into White (reference), Black, Hispanic, Asian, Native American, and Other categories. Multivariable logistic regression models, adjusted for demographics, comorbidities, and hospital characteristics, were used to evaluate associations between race and seven key sepsis-related complications: septic shock, acute renal failure, respiratory failure, encephalopathy, disseminated intravascular coagulation (DIC), Clostridioides difficile infection (CDI), and fungal sepsis. Results: Among 78,549 hospitalizations for MDS with sepsis, significant racial disparities were observed. Asian patients had higher odds of developing septic shock (OR 1.26, 95% CI 1.05–1.50, p = 0.014), and both Black (OR 1.24, 95% CI 1.17–1.31, p < 0.001) and Asian (OR 1.14, 95% CI 1.04–1.24, p = 0.004) patients had increased odds of acute renal failure. Respiratory failure was less likely among Black (OR 0.84, 95% CI 0.79–0.90, p < 0.001) and Hispanic (OR 0.76, 95% CI 0.70–0.82, p < 0.001) patients. Encephalopathy was significantly more common in Black (OR 1.29, 95% CI 1.18–1.41, p < 0.001) and Other (OR 1.20, 95% CI 1.01–1.42, p = 0.042) patients. DIC was more frequent in Asian (OR 2.11, 95% CI 1.37–3.27, p = 0.001) and Hispanic (OR 1.53, 95% CI 1.09–2.14, p = 0.014) patients, with a borderline association in Black patients (OR 1.35, p = 0.082). No statistically significant racial differences were noted for CDI or fungal sepsis, although Asian patients trended toward lower odds of CDI (OR 0.64, p = 0.067), and Native American patients had high but non-significant odds for fungal sepsis (OR 3.03, p = 0.287). Conclusion: Our study highlights significant racial disparities in sepsis-related complications among hospitalized MDS patients. Black and Asian patients were more likely to experience acute renal failure and encephalopathy, while Asian and Hispanic patients had higher odds of developing DIC. Conversely, Black and Hispanic patients had lower risk of respiratory failure. These findings underscore the need for race-conscious approaches in sepsis management for patients with MDS and suggest that tailored interventions may be necessary to ensure equitable outcomes across racial groups. Keywords: Myelodysplastic syndromes, sepsis, racial disparities, acute kidney injury, encephalopathy, DIC, respiratory failure, fungal sepsis, National Inpatient Sample

Article Details

Journal Blood
Volume / Issue Vol. 146, Issue Supplement 1
Published November 03, 2025
Pages 8180-8180
ISSN 0006-4971
Publisher Elsevier BV

Journal Info

Blood

Elsevier BV

ISSN: 0006-4971 Health Sciences

Authors (8)

S

Sooraj Srirangadhamu Gopu

1New York Medical College/Landmark Medical Center, Hematology-Oncology, Woonsocket, United States

J

Jatin Thukral

Landmark Medical Center, Woonsocket, Cumberland, Rhode Island, United States

A

Amanda Lussier

1New York Medical College/Landmark Medical Center, Hematology-Oncology, Woonsocket, United States

K

Kanishka Uttam Chandani

4Mayo Clinic, Hematology-Oncology, Phoenix, United States

S

Salman Ayub Jajja

NYMC-LANDMARK MEDICAL CENTER, RI, Woonsocket, Rhode Island, United States

D

Dhruvi Joshi

Narendra Modi Medical College and Sheth L.G. Hospital, Ahmedabad, India

O

Omar Alkasabrah

Landmark Medical center, Providence, Rhode Island, United States

A

Ahmed Nadeem

1New York Medical College/Landmark Medical Center, Hematology-Oncology, Woonsocket, United States